The University of Queensland

Absolute and relative estimates of genetic and environmental variance in brain structure volumes

Strike, Lachlan T., Hansell, Narelle K., Thompson, Paul M., de Zubicaray, Greig I., McMahon, Katie L., Zietsch, Brendan P. and Wright, Margaret J. (2019) Absolute and relative estimates of genetic and environmental variance in brain structure volumes. Brain Structure and Function, . doi:10.1007/s00429-019-01931-8

Multi-site meta-analysis of morphometry

Jahanshad, Neda, Faskowitz, Joshua I., Roshchupkin, Gennady, Hibar, Derrek, Gutman, Boris A, Tustison, Nicholas J., Adams, Hieab H. H., Niessen, Wiro, Vernooij, Meike W, Ikram, M Arfan, Zwiers, Marcel P., Vasquez, Alejandro Arias, Franke, Barbara, Kroll, Jennifer L., Mwangi, Benson, Soares, Jair C, Ing, Alex, Desrivieres, Sylvane, Schumann, Gunter, Hansell, Narelle K, de Zubicaray, Greig I., McMahon, Katie L., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2019) Multi-site meta-analysis of morphometry. IEEE/ACM Transactions on Computational Biology and Bioinformatics, . doi:10.1109/TCBB.2019.2914905

Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

Davies, Gail, Lam, Max, Harris, Sarah E., Trampush, Joey W., Luciano, Michelle, Hill, W. David, Hagenaars, Saskia P., Ritchie, Stuart J., Marioni, Riccardo E., Fawns-Ritchie, Chloe, Liewald, David C. M., Okely, Judith A., Ahola-Olli, Ari V., Barnes, Catriona L. K., Bertram, Lars, Bis, Joshua C., Burdick, Katherine E., Christoforou, Andrea, DeRosse, Pamela, Djurovic, Srdjan, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E., Hayward, Caroline, Hofer, Edith, Ikram, M. Arfan, Karlsson, Robert, Knowles, Emma, Lahti, Jari, Leber, Markus, Li, Shuo, Mather, Karen A., Melle, Ingrid, Morris, Derek, Oldmeadow, Christopher, Palviainen, Teemu, Payton, Antony, Pazoki, Raha, Petrovic, Katja, Reynolds, Chandra A., Sargurupremraj, Muralidharan, Scholz, Markus, Smith, Jennifer A., Smith, Albert V., Terzikhan, Natalie, Thalamuthu, Anbupalam, Trompet, Stella, van der Lee, Sven J., Ware, Erin B., Windham, B. Gwen, Wright, Margaret J., Yang, Jingyun, Yu, Jin, Ames, David, Amin, Najaf, Amouyel, Philippe, Andreassen, Ole A., Armstrong, Nicola J., Assareh, Amelia A., Attia, John R., Attix, Deborah, Avramopoulos, Dimitrios, Bennett, David A., Böhmer, Anne C., Boyle, Patricia A., Brodaty, Henry, Campbell, Harry, Cannon, Tyrone D., Cirulli, Elizabeth T., Congdon, Eliza, Conley, Emily Drabant, Corley, Janie, Cox, Simon R., Dale, Anders M., Dehghan, Abbas, Dick, Danielle, Dickinson, Dwight, Eriksson, Johan G., Evangelou, Evangelos, Faul, Jessica D., Ford, Ian, Freimer, Nelson A., Gao, He, Giegling, Ina, Gillespie, Nathan A., Gordon, Scott D., Gottesman, Rebecca F., Griswold, Michael E., Gudnason, Vilmundur, Harris, Tamara B., Hartmann, Annette M., Hatzimanolis, Alex, Heiss, Gerardo, Holliday, Elizabeth G., Joshi, Peter K., Kähönen, Mika, Kardia, Sharon L. R., Karlsson, Ida, Kleineidam, Luca, Knopman, David S., Kochan, Nicole A., Konte, Bettina, Kwok, John B., Le Hellard, Stephanie, Lee, Teresa, Lehtimäki, Terho, Li, Shu-Chen, Lill, Christina M., Liu, Tian, Koini, Marisa, London, Edythe, Longstreth, Will T., Lopez, Oscar L., Loukola, Anu, Luck, Tobias, Lundervold, Astri J., Lundquist, Anders, Lyytikäinen, Leo-Pekka, Martin, Nicholas G., Montgomery, Grant W., Murray, Alison D., Need, Anna C., Noordam, Raymond, Nyberg, Lars, Ollier, William, Papenberg, Goran, Pattie, Alison, Polasek, Ozren, Poldrack, Russell A., Psaty, Bruce M., Reppermund, Simone, Riedel-Heller, Steffi G., Rose, Richard J., Rotter, Jerome I., Roussos, Panos, Rovio, Suvi P., Saba, Yasaman, Sabb, Fred W., Sachdev, Perminder S., Satizabal, Claudia L., Schmid, Matthias, Scott, Rodney J., Scult, Matthew A., Simino, Jeannette, Slagboom, P. Eline, Smyrnis, Nikolaos, Soumaré, Aïcha, Stefanis, Nikos C., Stott, David J., Straub, Richard E., Sundet, Kjetil, Taylor, Adele M., Taylor, Kent D., Tzoulaki, Ioanna, Tzourio, Christophe, Uitterlinden, André, Vitart, Veronique, Voineskos, Aristotle N., Kaprio, Jaakko, Wagner, Michael, Wagner, Holger, Weinhold, Leonie, Wen, K. Hoyan, Widen, Elisabeth, Yang, Qiong, Zhao, Wei, Adams, Hieab H. H., Arking, Dan E., Bilder, Robert M., Bitsios, Panos, Boerwinkle, Eric, Chiba-Falek, Ornit, Corvin, Aiden, De Jager, Philip L., Debette, Stéphanie, Donohoe, Gary, Elliott, Paul, Fitzpatrick, Annette L., Gill, Michael, Glahn, David C., Hägg, Sara, Hansell, Narelle K., Hariri, Ahmad R., Ikram, M. Kamran, Jukema, J. Wouter, Vuoksimaa, Eero, Keller, Matthew C., Kremen, William S., Launer, Lenore, Lindenberger, Ulman, Palotie, Aarno, Pedersen, Nancy L., Pendleton, Neil, Porteous, David J., Räikkönen, Katri, Raitakari, Olli T., Ramirez, Alfredo, Reinvang, Ivar, Rudan, Igor, Dan Rujescu,, Schmidt, Reinhold, Schmidt, Helena, Schofield, Peter W., Schofield, Peter R., Starr, John M., Steen, Vidar M., Trollor, Julian N., Turner, Steven T., Van Duijn, Cornelia M., Villringer, Arno, Weinberger, Daniel R., Weir, David R., Wilson, James F., Malhotra, Anil, McIntosh, Andrew M., Gale, Catharine R., Seshadri, Sudha, Mosley, Thomas H., Bressler, Jan, Lencz, Todd and Deary, Ian J. (2019) Author correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 10 . doi:10.1038/s41467-019-10160-w

Genetic structure of IQ, phonemic decoding skill, and academic achievement

Lazaroo, Nikita K., Bates, Timothy C., Hansell, Narelle K., Wright, Margaret J., Martin, Nicholas G. and Luciano, Michelle (2019) Genetic structure of IQ, phonemic decoding skill, and academic achievement. Frontiers in Genetics, 10 . doi:10.3389/fgene.2019.00195

Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA

Bates, Timothy C., Maher, Brion S., Colodro-Conde, Lucía, Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Okbay, Aysu, Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2019) Social competence in parents increases children's educational attainment: Replicable genetically-mediated effects of parenting revealed by non-transmitted DNA. Twin Research and Human Genetics, . doi:10.1017/thg.2018.75

Are there distinct cognitive types?

Loehlin, John C., Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2018) Are there distinct cognitive types?. Intelligence, 70 7-11. doi:10.1016/j.intell.2018.07.002

Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

Smit, Dirk J. A., Wright, Margaret J., Meyers, Jacquelyn L., Martin, Nicholas G., Ho, Yvonne Y. W., Malone, Stephen M., Zhang, Jian, Burwell, Scott J., Chorlian, David B., de Geus, Eco J. C., Denys, Damiaan, Hansell, Narelle K., Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina E. M., Jahanshad, Neda, Thompson, Paul M., Whelan, Christopher D., Medland, Sarah E., Porjesz, Bernice, Lacono, William G. and Boomsma, Dorret I. (2018) Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Human Brain Mapping, 39 11: 4183-4195. doi:10.1002/hbm.24238

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence

Savage, Jeanne E., Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, Bryois, Julien, de Leeuw, Christiaan A., Nagel, Mats, Awasthi, Swapnil, Barr, Peter B., Coleman, Jonathan R. I., Grasby, Katrina L., Hammerschlag, Anke R., Kaminski, Jakob A., Karlsson, Robert, Krapohl, Eva, Lam, Max, Nygaard, Marianne, Reynolds, Chandra A., Trampush, Joey W., Young, Hannah, Zabaneh, Delilah, Hägg, Sara, Hansell, Narelle K., Karlsson, Ida K., Linnarsson, Sten, Montgomery, Grant W., Muñoz-Manchado, Ana B., Quinlan, Erin B., Schumann, Gunter, Skene, Nathan G., Webb, Bradley T., White, Tonya, Arking, Dan E., Avramopoulos, Dimitrios, Bilder, Robert M., Bitsios, Panos, Burdick, Katherine E., Cannon, Tyrone D., Chiba-Falek, Ornit, Christoforou, Andrea, Cirulli, Elizabeth T., Congdon, Eliza, Corvin, Aiden, Davies, Gail, Deary, Ian J., DeRosse, Pamela, Dickinson, Dwight, Djurovic, Srdjan, Donohoe, Gary, Conley, Emily Drabant, Eriksson, Johan G., Espeseth, Thomas, Freimer, Nelson A., Giakoumaki, Stella, Giegling, Ina, Gill, Michael, Glahn, David C., Hariri, Ahmad R., Hatzimanolis, Alex, Keller, Matthew C., Knowles, Emma, Koltai, Deborah, Konte, Bettina, Lahti, Jari, Le Hellard, Stephanie, Lencz, Todd, Liewald, David C., London, Edythe, Lundervold, Astri J., Malhotra, Anil K., Melle, Ingrid, Morris, Derek, Need, Anna C., Ollier, William, Palotie, Aarno, Payton, Antony, Pendleton, Neil, Poldrack, Russell A., Räikkönen, Katri, Reinvang, Ivar, Roussos, Panos, Rujescu, Dan, Sabb, Fred W., Scult, Matthew A., Smeland, Olav B., Smyrnis, Nikolaos, Starr, John M., Steen, Vidar M., Stefanis, Nikos C., Straub, Richard E., Sundet, Kjetil, Tiemeier, Henning, Voineskos, Aristotle N., Weinberger, Daniel R., Widen, Elisabeth, Yu, Jin, Abecasis, Goncalo, Andreassen, Ole A., Breen, Gerome, Christiansen, Lene, Debrabant, Birgit, Dick, Danielle M., Heinz, Andreas, Hjerling-Leffler, Jens, Ikram, M. Arfan, Kendler, Kenneth S., Martin, Nicholas G., Medland, Sarah E., Pedersen, Nancy L., Plomin, Robert, Polderman, Tinca J. C., Ripke, Stephan, van der Sluis, Sophie, Sullivan, Patrick F., Vrieze, Scott I., Wright, Margaret J. and Posthuma, Danielle (2018) Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Nature Genetics, 50 7: 912-919. doi:10.1038/s41588-018-0152-6

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function

Davies, Gail, Lam, Max, Harris, Sarah E., Trampush, Joey W., Luciano, Michelle, Hill, W. David, Hagenaars, Saskia P., Ritchie, Stuart J., Marioni, Riccardo E., Fawns-Ritchie, Chloe, Liewald, David C. M., Okely, Judith A., Ahola-Olli, Ari V., Barnes, Catriona L. K., Bertram, Lars, Bis, Joshua C., Burdick, Katherine E., Christoforou, Andrea, DeRosse, Pamela, Djurovic, Srdjan, Espeseth, Thomas, Giakoumaki, Stella, Giddaluru, Sudheer, Gustavson, Daniel E., Hayward, Caroline, Hofer, Edith, Ikram, M. Arfan, Karlsson, Robert, Knowles, Emma, Lahti, Jari, Leber, Markus, Li, Shuo, Mather, Karen A., Melle, Ingrid, Morris, Derek, Oldmeadow, Christopher, Palviainen, Teemu, Payton, Antony, Pazoki, Raha, Petrovic, Katja, Reynolds, Chandra A., Sargurupremraj, Muralidharan, Scholz, Markus, Smith, Jennifer A., Smith, Albert V., Terzikhan, Natalie, Thalamuthu, Anbupalam, Trompet, Stella, van der Lee, Sven J., Ware, Erin B., Windham, B. Gwen, Wright, Margaret J., Yang, Jingyun, Yu, Jin, Ames, David, Amin, Najaf, Amouyel, Philippe, Andreassen, Ole A., Armstrong, Nicola J., Assareh, Amelia A., Attia, John R., Attix, Deborah, Avramopoulos, Dimitrios, Bennett, David A., Böhmer, Anne C., Boyle, Patricia A., Brodaty, Henry, Campbell, Harry, Cannon, Tyrone D., Cirulli, Elizabeth T., Congdon, Eliza, Conley, Emily Drabant, Corley, Janie, Cox, Simon R., Dale, Anders M., Dehghan, Abbas, Dick, Danielle, Dickinson, Dwight, Eriksson, Johan G., Evangelou, Evangelos, Faul, Jessica D., Ford, Ian, Freimer, Nelson A., Gao, He, Giegling, Ina, Gillespie, Nathan A., Gordon, Scott D., Gottesman, Rebecca F., Griswold, Michael E., Gudnason, Vilmundur, Harris, Tamara B., Hartmann, Annette M., Hatzimanolis, Alex, Heiss, Gerardo, Holliday, Elizabeth G., Joshi, Peter K., Kähönen, Mika, Kardia, Sharon L. R., Karlsson, Ida, Kleineidam, Luca, Knopman, David S., Kochan, Nicole A., Konte, Bettina, Kwok, John B., Le Hellard, Stephanie, Lee, Teresa, Lehtimäki, Terho, Li, Shu-Chen, Liu, Tian, Koini, Marisa, London, Edythe, Longstreth, Will T., Lopez, Oscar L., Loukola, Anu, Luck, Tobias, Lundervold, Astri J., Lundquist, Anders, Lyytikäinen, Leo-Pekka, Martin, Nicholas G., Montgomery, Grant W., Murray, Alison D., Need, Anna C., Noordam, Raymond, Nyberg, Lars, Ollier, William, Papenberg, Goran, Pattie, Alison, Polasek, Ozren, Poldrack, Russell A., Psaty, Bruce M., Reppermund, Simone, Riedel-Heller, Steffi G., Rose, Richard J., Rotter, Jerome I., Roussos, Panos, Rovio, Suvi P., Saba, Yasaman, Sabb, Fred W., Sachdev, Perminder S., Satizabal, Claudia L., Schmid, Matthias, Scott, Rodney J., Scult, Matthew A., Simino, Jeannette, Slagboom, P. Eline, Smyrnis, Nikolaos, Soumaré, Aïcha, Stefanis, Nikos C., Stott, David J., Straub, Richard E., Sundet, Kjetil, Taylor, Adele M., Taylor, Kent D., Tzoulaki, Ioanna, Tzourio, Christophe, Uitterlinden, André, Vitart, Veronique, Voineskos, Aristotle N., Kaprio, Jaakko, Wagner, Michael, Wagner, Holger, Weinhold, Leonie, Wen, K Hoyan, Widen, Elisabeth, Yang, Qiong, Zhao, Wei, Adams, Hieab H. H., Arking, Dan E., Bilder, Robert M., Bitsios, Panos, Boerwinkle, Eric, Chiba-Falek, Ornit, Corvin, Aiden, De Jager, Philip L., Debette, Stéphanie, Donohoe, Gary, Elliott, Paul, Fitzpatrick, Annette L., Gill, Michael, Glahn, David C., Hägg, Sara, Hansell, Narelle K., Hariri, Ahmad R., Ikram, M. Kamran, Jukema, J. Wouter, Vuoksimaa, Eero, Keller, Matthew C., Kremen, William S., Launer, Lenore, Lindenberger, Ulman, Palotie, Aarno, Pedersen, Nancy L., Pendleton, Neil, Porteous, David J., Räikkönen, Katri, Raitakari, Olli T., Ramirez, Alfredo, Reinvang, Ivar, Rudan, Igor, Schmidt, Reinhold, Schmidt, Helena, Schofield, Peter W., Schofield, Peter R., Starr, John M., Steen, Vidar M., Trollor, Julian N., Turner, Steven T., Van Duijn, Cornelia M., Villringer, Arno, Weinberger, Daniel R., Weir, David R., Wilson, James F., Malhotra, Anil, McIntosh, Andrew M., Gale, Catharine R., Seshadri, Sudha, Mosley, Thomas H., Bressler, Jan, Lencz, Todd and Deary, Ian J. (2018) Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Nature Communications, 9 1: 2098. doi:10.1038/s41467-018-04362-x

Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium

Kong, Xiang-Zhen, Mathias, Samuel R., Guadalupe, Tulio, Glahn, David C., Franke, Barbara, Crivello, Fabrice, Tzourio-Mazoyer, Nathalie, Fisher, Simon E., Thompson, Paul M., Francks, Clyde, ENIGMA Laterality Working Group, Hansell, Narelle K., van Eijk, Liza, Strike, Lachlan and Wright, Margaret Jane (2018) Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA consortium. Proceedings of the National Academy of Sciences, 115 22: E5154-E5163. doi:10.1073/pnas.1718418115

The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families

Bates, Timothy C., Maher, Brion S., Medland, Sarah E., McAloney, Kerrie, Wright, Margaret J., Hansell, Narelle K., Kendler, Kenneth S., Martin, Nicholas G. and Gillespie, Nathan A. (2018) The Nature of Nurture: Using a Virtual-Parent Design to Test Parenting Effects on Children's Educational Attainment in Genotyped Families. Twin Research and Human Genetics, 21 2: 73-83. doi:10.1017/thg.2018.11

Genetic Complexity of Cortical Structure: Differences in Genetic and Environmental Factors Influencing Cortical Surface Area and Thickness

Strike, Lachlan T., Hansell, Narelle K., Couvy-Duchesne, Baptiste, Thompson, Paul M., de Zubicaray, Greig I., McMahon, Katie L. and Wright, Margaret J. (2018) Genetic Complexity of Cortical Structure: Differences in Genetic and Environmental Factors Influencing Cortical Surface Area and Thickness. Cerebral Cortex (New York, N.Y. : 1991), . doi:10.1093/cercor/bhy002

Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes

Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina M., Bolton, Jennifer L., Hayward, Caroline, Direk, Nese, Anderson, Anna, Huffman, Jennifer, Wilson, James F., Campbell, Harry, Rudan, Igor, Wright, Alan, Hastie, Nicholas, Wild, Sarah H., Velders, Fleur P., Hofman, Albert, Uitterlinden, Andre G., Lahti, Jari, Räikkönen, Katri, Kajantie, Eero, Widen, Elisabeth, Palotie, Aarno, Eriksson, Johan G., Kaakinen, Marika, Järvelin, Marjo-Riitta, Timpson, Nicholas J., Davey Smith, George, Ring, Susan M., Evans, David M., St Pourcain, Beate, Tanaka, Toshiko, Milaneschi, Yuri, Bandinelli, Stefania, Ferrucci, Luigi, Van Der Harst, Pim, Rosmalen, Judith Gm, Bakker, Stephen Jl, Verweij, Niek, Dullaart, Robin Pf, Mahajan, Anubha, Lindgren, Cecilia M., Morris, Andrew, Lind, Lars, Ingelsson, Erik, Anderson, Laura N., Pennell, Craig E., Lye, Stephen J., Matthews, Stephen G., Eriksson, Joel, Mellstrom, Dan, Ohlsson, Claes, Price, Jackie F., Strachan, Mark Wj, Reynolds, Rebecca M., Tiemeier, Henning, Ripke, Stephan, Mattheisen, Manuel, Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till Fm, Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan Tf, Bennett, David A., Berger, Klaus, Bigdeli, Tim B., Bybjerg-Grauholm, Jonas, Byrne, Enda M., Cai, Na, Castelao, Enrique, Clarke, Toni-Kim, Coleman, Jonathan Ri, Consortium, Converge, Craddock, Nick, Dannlowski, Udo, Davies, Gareth, Davies, Gail, De Geus, Eco. J. C., De Jager, Philip, Deary, Ian J., Degenhardt, Franziska, Dunn, Erin C., Ehli, Erik A., Eley, Thalia C., Escott-Price, Valentina, Esko, Tõnu, Finucane, Hilary K., Gill, Michael, Gordon, Scott D., Grove, Jakob, Hall, Lynsey S., Hansen, Thomas F., Søholm Hansen, Christine, Heath, Andrew C., Henders, Anjali K., Herms, Stefan, Hoffmann, Per, Homuth, Georg, Horn, Carsten, Hottenga, Jouke-Jan, Hougaard, David, Huang, Hailiang, Ising, Marcus, Jansen, Rick, Jorgenson, Eric, Kloiber, Stefan, Knowles, James A, Kretzschmar, Warren W., Krogh, Jesper, Kutalik, Zoltán, Lang, Maren, Lewis, Glyn, Li, Yihan, MacIntyre, Donald J., Madden, Pamela Af, Marchine, Jonathan, Mbarek, Hamdi, McGuffin, Peter, Mehta, Divya, Metspalu, Andres, Middeldorp, Christel M., Mihailov, Evelin, Milani, Lili, Montgomery, Grant W., Mostafavi, Sara, Mullins, Niamh, Nauck, Matthias, Ng, Bernard, Nordentoft, Merete, Nyholt, Dale R., O'Donovan, Michael C., O'Reilly, Paul F., Oskarsson, Hogni, Owen, Michael J., Paciga, Sara A., Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, Pedersen, Nancy L., Pergadia, Michele L., Peterson, Roseann E., Pettersson, Erik, Peyrot, Wouter J., Porteous, David J., Posthuma, Danielle, Potash, James B., Quiroz, Jorge A., Rice, John P., Riley, Brien P., Rivera, Margarita, Ruderfer, Douglas M., Saeed Mirza, Saira, Schoevers, Robert, Shen, Ling, Shi, Jianxin, Sigurdsson, Engilbert, Sinnamon, Grant Cb, Smit, Johannes H., Smith, Daniel J., Stephansson, Hreinn, Steinberg, Stacy, Strohmaier, Jana, Tansey, Katherine E., Teumer, Alexander, Thompson, Wesley, Thomson, Pippa A., Thorgeirsson, Thorgeir E., Treutlein, Jens, Trzaskowski, Maciej, Umbricht, Daniel, Van Der Auwera, Sandra, Van Grootheest, Gerard, Van Hemert, Albert M., Viktorin, Alexander, Völzke, Henry, Wang, Yunpeng, Webb, Bradley T., Weissman, Myrna M., Wellmann, Jürgen, Willemsen, Gonneke, Xi, Hualin S., Baune, Bernhard T., Blackwood, Douglas H. R., Boomsma, Dorret I., Børglum, Anders D., Buttenschøn, Henriette N., Cichon, Sven, Domenici, Enrico, Flint, Jonathan, Grabe, Hans J., Hamilton, Steven P., Kendler, Kenneth S., Li, Qingqin S., Lucae, Susanne, Magnusson, Patrik K., McIntosh, Andrew M., Mors, Ole, Bo Mortensen, Preben, Müller-Myhsok, Bertram, Penninx, Brenda Wjh, Perlis, Roy H., Preisig, Martin, Schaefer, Catherine, Smoller, Jordan W., Stephansson, Kari, Uher, Rudolf, Werge, Thomas, Winslow, Ashley R., Breen, Gerome, Levinson, Douglas F., Lewis, Cathryn M., Wray, Naomi R., Sullivan, Patrick F., McGrath, John, Hickie, Ian B., Hansell, Narelle K., Wright, Margaret J., Gillespie, Nathan A., Forstner, Andreas J., Schulze, Thomas G, Wüst, Stefan, Nöthen, Markus M., Baumgartner, Markus R., Walker, Brian R., Crawford, Andrew A., Colodro-Conde, Lucía, Medland, Sarah E., Martin, Nicholas G. and Rietschel, Marcella (2017) Hair Cortisol in Twins: Heritability and Genetic Overlap with Psychological Variables and Stress-System Genes. Scientific Reports, 7 1: 15351. doi:10.1038/s41598-017-11852-3

Investigating the relationship between iron and depression

Mills, Natalie T., Maier, Robert, Whitfield, John B., Wright, Margaret J., Colodro-Conde, Lucia, Byrne, Enda M., Scott, James G., Byrne, Gerard J., Hansell, Narelle K., Vinkhuyzen, Anna A. E., CouvyDuchesne, Baptiste, Montgomery, Grant W., Henders, Anjali K., Martin, Nicholas G., Wray, Naomi R. and Benyamin, Beben (2017) Investigating the relationship between iron and depression. Journal of Psychiatric Research, 94 148-155. doi:10.1016/j.jpsychires.2017.07.006

Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group

Brouwer, Rachel M., Panizzon, Matthew S., Glahn, David C., Hibar, David P., Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, de Zubicaray, Greig I., Franz, Carol E., Hansell, Narelle K., Hickie, Ian B., Koenis, Marinka M. G., Martin, Nicholas G., Mather, Karen A., McMahon, Katie L., Schnack, Hugo G., Strike, Lachlan T., Swagerman, Suzanne C., Thalamuthu, Anbupalam, Wen, Wei, Gilmore, John H., Gogtay, Nitin, Kahn, Rene S., Sachdev, Perminder S., Wright, Margaret J., Boomsma, Dorret I., Kremen, William S., Thompson, Paul M. and Hulshoff Pol, Hilleke E. (2017) Genetic influences on individual differences in longitudinal changes in global and subcortical brain volumes: results of the ENIGMA plasticity working group. Human Brain Mapping, 8 9: 4444-4458. doi:10.1002/hbm.23672

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts

Hagg, S., Zhan, Y., Karlsson, R., Gerritsen, L., Ploner, A., van der Lee, S. J., Broer, L., Deelen, J., Marioni, R. E., Wong, A., Lundquist, A., Zhu, G., Hansell, N. K., Sillanpaa, E., Fedko, I. O., Amin, N. A., Beekman, M., de Craen, A. J. M., Degerman, S., Harris, S. E., Kan, K-J, Martin-Ruiz, C. M., Montgomery, G. W., Adolfsson, A. N., Reynolds, C. A., Samani, N. J., Suchiman, H. E. D., Viljanen, A., von Zglinicki, T., Wright, M. J., Hottenga, J-J, Boomsma, D. I., Rantanen, T., Kaprio, J. A., Nyholt, D. R., Martin, N. G., Nyberg, L., Adolfsson, R., Kuh, D., Starr, J. M., Deary, I. J., Slagboom, P. E., van Duijn, C. M., Codd, V. and Pedersen, N. L. (2017) Short telomere length is associated with impaired cognitive performance in European ancestry cohorts. Translational Psychiatry, 7 4: 983-992. doi:10.1038/tp.2017.73

Novel genetic loci associated with hippocampal volume

Hibar, Derrek P., Adams, Hieab H. H., Jahanshad, Neda, Chauhan, Ganesh, Stein, Jason L., Hofer, Edith, Renteria, Miguel E., Bis, Joshua C., Arias-Vasquez, Alejandro, Ikram, M. Kamran, Desrivieres, Sylvane, Vernooij, Meike W., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beecham, Ashley H., Beiser, Alexa, Bernard, Manon, Blanton, Susan H., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M., Carmichael, Owen, Chakravarty, M. Mallar, Chen, Qiang, Ching, Christopher R. K., Chouraki, Vincent, Cuellar-Partida, Gabriel, Crivello, Fabrice, Den Braber, Anouk, Doan, Nhat Trung, Ehrlich, Stefan, Giddaluru, Sudheer, Goldman, Aaron L., Gottesman, Rebecca F., Grimm, Oliver, Griswold, Michael E., Guadalupe, Tulio, Gutman, Boris A., Hass, Johanna, Haukvik, Unn K., Hoehn, David, Holmes, Avram J., Hoogman, Martine, Janowitz, Deborah, Jia, Tianye, Jorgensen, Kjetil N., Karbalai, Nazanin, Kasperaviciute, Dalia, Kim, Sungeun, Klein, Marieke, Kraemer, Bernd, Lee, Phil H., Liewald, David C. M., Lopez, Lorna M., Luciano, Michelle, Macare, Christine, Marquand, Andre F, Matarin, Mar, Mather, Karen A., Mattheisen, Manuel, McKay, David R., Milaneschi, Yuri, Munoz Maniega, Susana, Nho, Kwangsik, Nugent, Allison C., Nyquist, Paul, Loohuis, Loes M. 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M., Van Rooij, Daan, Walton, Esther, Westlye, Lars T., Whelan, Christopher D., Windham, Beverly G., Winkler, Anderson M., Wittfeld, Katharina, Woldehawariat, Girma, Wolf, Christiane, Wolfers, Thomas, Yanek, Lisa R., Yang, Jingyun, Zijdenbos, Alex, Zwiers, Marcel P., Agartz, Ingrid, Almasy, Laura, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arepalli, Sampath, Assareh, Amelia A., Barral, Sandra, Bastin, Mark E., Becker, Diane M., Becker, James T., Bennett, David A., Blangero, John, Van Bokhoven, Hans, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Brunner, Han G., Buckner, Randy L., Buitelaar, Jan K., Bulayeva, Kazima B., Cahn, Wiepke, Calhoun, Vince D., Cannon, Dara M., Cavalleri, Gianpiero L., Cheng, Ching-Yu, Cichon, Sven, Cookson, Mark R., Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Czisch, Michael, Dale, Anders M., Davies, Gareth E., De Craen, Anton J. M., De Geus, Eco J. C., De Jager, Philip L., De Zubicaray, Greig I., Deary, Ian J., Debette, Stephanie, Decarli, Charles, Delanty, Norman, Depondt, Chantal, Destefano, Anita, Dillman, Allissa, Djurovic, Srdjan, Donohoe, Gary, Drevets, Wayne C., Duggirala, Ravi, Dyer, Thomas D., Enzinger, Christian, Erk, Susanne, Espeseth, Thomas, Fedko, Iryna O., Fernandez, Guillen, Ferrucci, Luigi, Fisher, Simon E., Fleischman, Debra A., Ford, Ian, Fornage, Myriam, Foroud, Tatiana M., Fox, Peter T., Francks, Clyde, Fukunaga, Masaki, Gibbs, J. Raphael, Glahn, David C., Gollub, Randy L., Goring, Harald H. H., Green, Robert C., Gruber, Oliver, Gudnason, Vilmundur, Guelfi, Sebastian, Haberg, Asta K., Hansell, Narelle K., Hardy, John, Hartman, Catharina A., Hashimoto, Ryota, Hegenscheid, Katrin, Heinz, Andreas, Le Hellard, Stephanie, Hernandez, Dena G., Heslenfeld, Dirk J., Ho, Beng-Choon, Hoekstra, Pieter J., Hoffmann, Wolfgang, Hofman, Albert, Holsboer, Florian, Homuth, Georg, Hosten, Norbert, Hottenga, Jouke-Jan, Huentelman, Matthew, Pol, Hilleke E. Hulshoff, Ikeda, Masashi, Jack, Clifford R., Jenkinson, Mark, Johnson, Robert, Joensson, Erik G., Jukema, J. 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Bruce, Potkin, Steven G., Psaty, Bruce M., Reppermund, Simone, Rietschel, Marcella, Roffman, Joshua L., Romanczuk-Seiferth, Nina, Rotter, Jerome I., Ryten, Mina, Sacco, Ralph L., Sachdev, Perminder S., Saykin, Andrew J., Schmidt, Reinhold, Schmidt, Helena, Schofield, Peter R., Sigursson, Sigurdur, Simmons, Andrew, Singleton, Andrew, Sisodiya, Sanjay M., Smith, Colin, Smoller, Jordan W., Soininen, Hilkka, Steen, Vidar M., Stott, David J., Sussmann, Jessika E., Thalamuthu, Anbupalam, Toga, Arthur W., Traynor, Bryan J., Troncoso, Juan, Tsolaki, Magda, Tzourio, Christophe, Uitterlinden, Andre G., Hernandez, Maria C. Valdes, Van Der Brug, Marcel, Van Der Lugt, Aad, Van Der Wee, Nic J. A., Van Haren, Neeltje E. M., Van 'T Ent, Dennis, Van Tol, Marie-Jose, Vardarajan, Badri N., Vellas, Bruno, Veltman, Dick J., Volzke, Henry, Walter, Henrik, Wardlaw, Joanna M., Wassink, Thomas H., Weale, Michael E., Weinberger, Daniel R., Weiner, Michael W., Wen, Wei, Westman, Eric, White, Tonya, Wong, Tien Y., Wright, Clinton B., Zielke, Ronald H., Zonderman, Alan B., Martin, Nicholas G., Van Duijn, Cornelia M., Wright, Margaret J., Longstreth, W. T., Schumann, Gunter, Grabe, Hans J., Franke, Barbara, Launer, Lenore J., Medland, Sarah E., Seshadri, Sudha, Thompson, Paul M. and Ikram, M. Arfan (2017) Novel genetic loci associated with hippocampal volume. Nature Communications, 8 13624. doi:10.1038/ncomms13624

Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal

Loehlin, John C., Hansell, Narelle K., Wright, Margaret J. and Martin, Nicholas G. (2016) Genetic and environmental contributions to cognitive structure in Australian twins: a reappraisal. Intelligence, 59 24-31. doi:10.1016/j.intell.2016.05.007

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Adams, Hieab H. H., Hibar, Derrek P., Chouraki, Vincent, Stein, Jason L., Nyquist, Paul A., Renteria, Miguel E., Trompet, Stella, Arias-Vasquez, Alejandro, Seshadri, Sudha, Desrivieres, Sylvane, Beecham, Ashley H., Jahanshad, Neda, Wittfeld, Katharina, Van der Lee, Sven J., Abramovic, Lucija, Alhusaini, Saud, Amin, Najaf, Andersson, Micael, Arfanakis, Konstantinos, Aribisala, Benjamin S., Armstrong, Nicola J., Athanasiu, Lavinia, Axelsson, Tomas, Beiser, Alexa, Bernard, Manon, Bis, Joshua C., Blanken, Laura M. E., Blanton, SusanH., Bohlken, Marc M., Boks, Marco P., Bralten, Janita, Brickman, Adam M., Carmichael, Owen, Chakravarty, M. Mallar, Chauhan, Ganesh, Chen, Qiang, Ching, Christopher R. K., Cuellar-Partida, Gabriel, Braber, Anouk Den, Doan, Nhat Trung, Ehrlich, Stefan, Filippi, Irina, Ge, Tian, Giddaluru, Sudheer, Goldman, Aaron L., Gottesman, Rebecca F., Greven, Corina U., Grimm, Oliver, Griswold, Michael E., Guadalupe, Tulio, Hass, Johanna, Haukvik, Unn K., Hilal, Saima, Hofer, Edith, Hoehn, David, Holmes, Avram J., Hoogman, Martine, Janowitz, Deborah, Jia, Tianye, Kasperaviciute, Dalia, Kim, Sungeun, Klein, Marieke, Kraemer, Bernd, Lee, Phil H., Liao, Jiemin, Liewald, David C. M., Lopez, Lorna M., Luciano, Michelle, Macare, Christine, Marquand, Andre, Matarin, Mar, Mather, Karen A., Mattheisen, Manuel, Mazoyer, Bernard, McKay, David R., McWhirter, Rebekah, Milaneschi, Yuri, Mirza-Schreiber, Nazanin, Muetzel, Ryan L., Maniega, Susana Munoz, Nho, Kwangsik, Nugent, Allison C., Loohuis, Loes M. Olde, Oosterlaan, Jaap, Papmeyer, Martina, Pappa, Irene, Pirpamer, Lukas, Pudas, Sara, Putz, Benno, Rajan, Kumar B., Ramasamy, Adaikalavan, Richards, Jennifer S., Risacher, Shannon L., Roiz-Santianez, Roberto, Rommelse, Nanda, Rose, Emma J., Royle, Natalie A., Rundek, Tatjana, Samann, Phillip G., Satizabal, Claudia L., Schmaal, Lianne, Schork, Andrew J., Shen, Li, Shin, Jean, Shumskaya, Elena, Smith, Albert V., Sprooten, Emma, Strike, Lachlan T., Teumer, Alexander, Thomson, Russell, Tordesillas-Gutierrez, Diana, Toro, Roberto, Trabzuni, Daniah, Vaidya, Dhananjay, Van der Grond, Jeroen, Van der Meer, Dennis, Van Donkelaar, Maejolein M. J., Van Eijk, Kristel R., Van Erp, Thero G. M., Van Rooij, Daan, Walton, Esther, Westlye, Lars T., Whelan, Christopher D., Windham, Beverly G., Winkler, Anderson M., Woldehawariat, Girma, Wolf, Christiane, Wolfers, Thomas, Xu, Bing, Yanek, Lisa R., Yang, Jingyun, Zijdenbos, Aijdenbos, Zwiers, Marcel P., Agartz, Ingrid, Aggarwal, Neelum T., Almasy, Laura, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arepalli, Sampath, Assareh, Amelia A., Barral, Sandra, Bastin, Mark E., Becker, Diane M., Becker, James T., Bennett, David A., Blangero, John, van Bokhoven, Hans, Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Brunner, Han G., Buckner, Randy L., Buitelaar, Jan K., Bulayeva, Kazima B., Cahn, Wiepke, Calhoun, Vince D., Cannon, Dara M., Cavalleri, Gianpiero L., Chen, Christopher, Cheng, Ching-Yu, Cichon, Sven, Cookson, Mark R., Corvin, Aiden, Crespo-Facorro, Benedicto, Curran, Joanne E., Czisch, Michael, Dale, Anders M., Davies, Gareth E., De Geus, Eco J. C., De Jager, Philip L., de Zubicaray, Greig I., Delanty, Norman, Depondt, Chantal, Destefano, Anita L., Dillman, Allissa, Djurovic, Srdjan, Donohoe, Gary, Drevets, Wayne C., Duggirala, Ravi, Dyer, Thomas D., Erk, Susanne, Espeseth, Thomas, Evans, Denis A., Fedko, Iryna O., Fernandez, Guillen, Ferrucci, Luigi, Fisher, Simon E., Fleischman, Debra A., Ford, Ian, Foroud, Tatiana M., Fox, Peter T., Francks, Clyde, Fukunaga, Masaki, Gibbs, J. Raphael, Glahn, David C., Gollub, Randy L., Goring, Harald H. H., Grabe, Hans J., Green, Robert C., Gruber, Oliver, Gudnason, Vilmundur, Guelfi, Sebastian, Hansell, Narelle K., Hardy, John, Hartman, Catharina A., Hashimoto, Ryota, Hegenscheid, Katrin, Heinz, Adreas, Le Hellard, Stephanie, Hernandez, Dena G., Heslenfeld, Dirk J., Ho, Beng-Choon, Hoekstra, Pieter J., Hoffmann, Wolfgang, Hofman, Albert, Holsboer, Florian, Homuth, Georg, Hosten, Norbert, Hottenga, Jouke-Jan, Pol, Hilleke E. Hulshoff, Ikeda, Masashi, Ikram, M. Kamran, Jack, Clifford R., Jenkinson, Mark, Johnson, Robert, Jonsson, Erik G., Jukema, J. Wouter, Kahn, Rene S., Kanai, Ryota, Kloszewska, Iwona, Knopman, David S., Kochunov, Peter, Kwok, John B., Lawrie, Stephen M., Lemaitre, Herve, Liu, Xinmin, Longo, Dan L., Longstreth Jr., W. T., Lopez, Oscar L., Lovestone, Simon, Martinez, Oliver, Martinot, Jean-Luc, Mattay, Venkata S., McDonald, Colm, McIntosh, Andrew M., McMahon, Katie L., McMahon, Francis J., Mecocci, Patrizia, Melle, Ingrid, Meyer-Lindenberg, Andreas, Mohnke, Sebastian, Montgomery, Grant W., Morris, Derek W., Mosley, Thomas H., Muhleisen, Thomas W., Muller-Myhsok, Bertram, Nalls, Michael A., Nauck, Matthias, Nichols, Thomas E., Niessen, Wiro J., Nothen, Markus M., Nyberg, Lars, Ohi, Kazutaka, Olvera, Rene L., Ophoff, Roel A., Pandolfo, Massimo, Paus, Tomas, Pausova, Zdenka, Penninx, Brenda W. J. H., Pike, G. Bruce, Potkin, Steven G., Psaty, Bruce M., Reppermund, Simone, Rietschel, Marcella, Roffman, Joshua L., Romanczuk-Seiferth, Nina, Rotter, Jerome I., Ryten, Mina, Sacco, Ralph L., Sachdev, Perminder S., Saykin, Andrew J., Schmidt, Reinhold, Schofield, Peter R., Sigurdsson, Sigurdur, Simmons, Andy, Singleton, Andrew, Sisodiya, Sanjay M., Smith, Colin, Smoller, Jordan W., Soininen, Hilkka, Srikanth, Velandai, Steen, Vidar M., Stott, David J., Sussmann, Jessika E., Thalamuthu, Anbupalam, Tiemeier, Henning, Toga, Arthur W., Traynor, Bryan J., Troncoso, Juan, Turner, Jessica A., Tzourio, Christophe, Uitterlinden, Andrew G., Hernandez, Maria C. Valdes, Van der Brug, Marcel, Van der Lugt, Aad, Van der Wee, Nic J. A., Van Duijn, Cornelia M., Van Haren, Neeltje E.M., Van't Ent, Dennis, Van Tol, Marie-Jose, Vardarajan, Badri N., Veltman, Dick J., Vernooij, Meike W., Volzke, Henry, Walter, Henrik, Wardlaw, Joanna M., Wassink, Thomas H., Weale, Michael E., Weinberger, Daniel R., Weiner, Michael W., Wen, Wei, Westman, Eric, White, Tonya, Wong, Tien Y., Wright, Clinton B., Zielke, H. Ronald, Zonderman, Alan B., Deary, Ian J., Decarli, Charles, Schmidt, Helena, Martin, Nicholas G., De Craen, Anton J.M., Wright, Margaret J., Launer, Lenore J., Schumann, Gunter, Fornage, Myriam, Franke, Barbara, Debette, Stephanie, Medland, Sarah E., Ikram, M. Arfan and Thompson, Paul M. (2016) Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nature Neuroscience, 19 12: 1569-1582. doi:10.1038/nn.4398

Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins

Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Frank, Josef, Hansell, Narelle K., Wright, Margaret J., McGrath, John J., Witt, Stephanie H., Rietschel, Marcella and Martin, Nicholas G. (2016) Hair cortisol and its association with psychological risk factors for psychiatric disorders: a pilot study in adolescent twins. Twin Research and Human Genetics, 19 5: 438-446. doi:10.1017/thg.2016.50

Genome-wide association study of working memory brain activation

Blokland, Gabriella A. M., Wallace, Angus K., Hansell, Narelle K., Thompson, Paul M., Hickie, Ian B., Montgomery, Grant W., Martin, Nicholas G., McMahon, Katie L., de Zubicaray, Greig I. and Wright, Margaret J. (2016) Genome-wide association study of working memory brain activation. International Journal of Psychophysiology, 115 98-111. doi:10.1016/j.ijpsycho.2016.09.010

When does socioeconomic status (SES) moderate the heritability of IQ? No evidence for g × SES interaction for IQ in a representative sample of 1176 Australian adolescent twin pairs

Bates, Timothy C., Hansell, Narelle K., Martin, Nicholas G. and Wright, Margaret J. (2016) When does socioeconomic status (SES) moderate the heritability of IQ? No evidence for g × SES interaction for IQ in a representative sample of 1176 Australian adolescent twin pairs. Intelligence, 56 2: 10-15. doi:10.1016/j.intell.2016.02.003

The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume

Lupton, Michelle K., Strike, Lachlan, Hansell, Narelle K., Wen, Wei, Mather, Karen A., Armstrong, Nicola J., Thalamuthu, Anbupalam, McMahon, Katie L., de Zubicaray, Greig I., Assareh, Amelia A., Simmons, Andrew, Proitsi, Petroula, Powell, John F., Montgomery, Grant W., Hibar, Derrek P., Westman, Eric, Tsolaki, Magda, Kloszewska, Iwona, Soininen, Hilkka, Mecocci, Patrizia, Velas, Bruno, Lovestone, Simon, Brodaty, Henry, Ames, David, Trollor, Julian N., Martin, Nicholas G., Thompson, Paul M., Sachdev, Perminder S. and Wright, Margaret J. (2016) The effect of increased genetic risk for Alzheimer's disease on hippocampal and amygdala volume. Neurobiology of Aging, 40 68-77. doi:10.1016/j.neurobiolaging.2015.12.023

Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population

Clarke, T-K, Lupton, M. K., Fernandez-Pujals, A. M., Starr, J., Davies, G., Cox, S., Pattie, A., Liewald, D. C., Hall, L. S., MacIntyre, D. J., Smith, B. H., Hocking, L. J., Padmanabhan, S., Thomson, P. A., Hayward, C., Hansell, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Porteous, D. J., Deary, I. J. and McIntosh, A. M. (2016) Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population. Molecular Psychiatry, 21 3: 419-425. doi:10.1038/mp.2015.12

Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences

Hill, W. D., Davies, G., Liewald, D. C., Payton, A., McNeil, C. J., Whalley, L. J., Horan, M., Ollier, W., Starr, J. M., Pendleton, N., Hansel, N. K., Montgomery, G. W., Medland, S. E., Martin, N. G., Wright, M. J., Bates, T. C. and Deary, I. J. (2016) Examining non-syndromic autosomal recessive intellectual disability (NS-ARID) genes for an enriched association with intelligence differences. Intelligence, 54 80-89. doi:10.1016/j.intell.2015.11.005

Heritability of the network architecture of intrinsic brain functional connectivity

Sinclair, Benjamin, Hansell, Narelle K., Blokland, Gabriella A. M., Martin, Nicholas G., Thompson, Paul M., Breakspear, Michael, de Zubicaray, Greig I., Wright, Margret J. and McMahon, Katie L. (2015) Heritability of the network architecture of intrinsic brain functional connectivity. NeuroImage, 121 243-252. doi:10.1016/j.neuroimage.2015.07.048

Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait

Franic, Sanja, Groen-Blokhuis, Maria M., Dolan, Conor V., Kattenberg, Mathijs V., Pool, Rene, Xiao, Xiangjun, Scheet, Paul A., Ehli, Erik A., Davies, Gareth E., van der Sluis, Sophie, Abdellaoui, Abdel, Hansell, Narelle K., Martin, Nicholas G., Hudziak, James J., van Beijsterveldt, Catherina E. M., Swagerman, Suzanne C., Pol, Hilleke E. Hulshoff, de Geus, Eco J. C., Bartels, Meike, Ropers, H. Hilger, Hottenga, Jouke-Jan and Boomsma, Dorret I. (2015) Intelligence: Shared genetic basis between Mendelian disorders and a polygenic trait. European Journal of Human Genetics, 23 10: 1378-1383. doi:10.1038/ejhg.2015.3

Genome-wide autozygosity is associated with lower general cognitive ability

Howrigan, D.P., Simonson, M.A., Davies, G., Harris, S.E., Tenesa, A., Starr, J.M., Liewald, D.C., Deary, I.J., McRae, A., Wright, M.J., Montgomery, G.W., Hansell, N., Martin, N.G., Payton, A., Horan, M., Ollier, W.E., Abdellaoui, A., Boomsma, D.I., DeRosse, P., Knowles, E.E.M., Glahn, D.C., Djurovic, S., Melle, I., Andreassen, O.A., Christoforou, A., Steen, V.M., Hellard, S.L., Sundet, K., Reinvang, I., Espeseth, T., Lundervold, A.J., Giegling, I., Konte, B., Hartmann, A.M., Rujescu, D., Roussos, P., Giakoumaki, S., Burdick, K.E., Bitsios, P., Donohoe, G., Corley, R.P., Visscher, P.M., Pendleton, N., Malhotra, A.K., Neale, B.M., Lencz, T. and Keller, M.C. (2015) Genome-wide autozygosity is associated with lower general cognitive ability. Molecular Psychiatry, 21 6: 837-843. doi:10.1038/mp.2015.120

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

van Den Berg, Stephanie M., de Moor, Marleen H.M., Verweij, Karin J.H., Krueger, Robert F., Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K., Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D., Hansell, Narelle K., Hart, Amy B., Seppala, Ilkka, Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abdellaoui, Abdel, Abecasis, Goncalo R., Adkins, Daniel E., Agrawal, Arpana, Allik, Juri, Appel, Katja, Bigdeli, Timothy B., Busonero, Fabio, Campbell, Harry, Costa, Paul T., Smith, George Davey, Davies, Gail, de Wit, Harriet, Ding, Jun, Engelhardt, Barbara E., Eriksson, Johan G., Fedko, Iryna O., Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette M., Heath, Andrew C., Heinonen, Kati, Henders, Anjali K., Homuth, Georg, Hottenga, Jouke-Jan, Iacono, William G., Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John P., Kirkpatrick, Matthew G., Latvala, Antti, Lehtimaki, Terho, Liewald, David C., Madden, Pamela A.F., Magri, Chiara, Magnusson, Patrik K.E., Marten, Jonathan, Maschio, Andrea, Mbarek, Hamdi, Medland, Sarah E., Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant W., Nauck, Matthias, Nivard, Michel G., Ouwens, Klaasjan G., Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Raback, Laura, Raitakari, Olli T., Realo, Anu, Rose, Richard J., Ruggiero, Daniela, Schmidt, Carsten O., Slutske, Wendy S., Sorice, Rossella, Starr, John M., St Pourcain, Beate, Sutin, Angelina R., Timpson, Nicholas J., Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Wouda, Jasper, Wright, Margaret J., Zgaga, Lina, Generation Scotland, Porteous, David, Minelli, Alessandra, Palmer, Abraham A., Rujescu, Dan, Ciullo, Marina, Hayward, Caroline, Rudan, Igor, Metspalu, Andres, Kaprio, Jaakko, Deary, Ian J., Raikkonen, Katri, Wilson, James F., Keltikangas-Jarvinen, Liisa, Bierut, Laura J., Hettema, John M., Grabe, Hans J., Penninx, Brenda W.J.H., van Duijn, Cornelia M., Evans, David M., Schlessinger, David, Pedersen, Nancy L., Terracciano, Antonio, McGue, Matt, Martin, Nicholas G. and Boomsma, Dorret I. (2015) Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics, 46 2: 170-182. doi:10.1007/s10519-015-9735-5

Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder

De Moor, Marleen H.M, Van Den Berg, Stephanie M, Verweij, Karin J.H, Krueger, Robert F, Luciano, Michelle, Arias Vasquez, Alejandro, Matteson, Lindsay K, Derringer, Jaime, Esko, Tonu, Amin, Najaf, Gordon, Scott D, Hansell, Narelle K, Hart, Amy B, Seppala, Ilkka, Huffman, Jennifer E, Konte, Bettina, Lahti, Jari, Lee, Minyoung, Miller, Mike, Nutile, Teresa, Tanaka, Toshiko, Teumer, Alexander, Viktorin, Alexander, Wedenoja, Juho, Abecasis, Goncalo R, Adkins, Daniel E, Agrawal, Arpana, Allik, Juri, Appel, Katja, Bigdeli, Timothy B, Busonero, Fabio, Campbell, Harry, Costa, Paul T, Davey Smith, George, Davies, Gail, De Wit, Harriet, Ding, Jun, Engelhardt, Barbara E, Eriksson, Johan G, Fedko, Iryna O, Ferrucci, Luigi, Franke, Barbara, Giegling, Ina, Grucza, Richard, Hartmann, Annette M, Heath, Andrew C, Heinonen, Kati, Henders, Anjali K, Homuth, Georg, Hottenga, Kouke-Jan, Iacono, William G, Janzing, Joost, Jokela, Markus, Karlsson, Robert, Kemp, John P, Kirkpatrick, Matthew G, Latvala, Antti, Lehtimaki, Terho, Liewald, David C, Madden, Pamela A.F, Magri, Chiara, Magnusson, Patrik K.E, Marten, Jonathan, Maschio, Andrea, Medland, Sarah E, Mihailov, Evelin, Milaneschi, Yuri, Montgomery, Grant W, Nauck, Matthias, Ouwens, Klaasjan, Palotie, Aarno, Pettersson, Erik, Polasek, Ozren, Qian, Yong, Pulkki-Raback, Laura, Raitakari, Olli T, Realo, Anu, Rose, Richard J, Ruggiero, Daniela, Schmidt, Carsten O, Slutske, Wendy S, Sorice, Rossella, Starr, John M, St Pourcain, Beate, Sutin, Angelina R, Timpson, Nicholas J, Trochet, Holly, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Margaret J, Wouda, Jasper, Wright, Margaret J, Zgaga, Lina, Porteous, David, Minelli, Alessandra, Palmer, Abraham A, Rujescu, Dan, Ciullo, Marina, Hayward, Caroline, Rudan, Igor, Metspalu, Andres, Kaprio, Jaakko, Deary, Ian, Raikkonen, Katri, Wilson, James F, Keltikangas-Jarvinen, Liisa, Bierut, Laura J, Hettema, John M, Grabe, Hans J, Van Duijn, Cornelia M, Evans, David M, Schlessinger, David, Pedersen, Nancy L, Terracciano, Antonio, McGue, Matt, Penninx, Brenda W.J.H, Martin, Nicholas G and Boomsma, Dorret I (2015) Meta-analysis of genome-wide association studies for neuroticism, and the polygenic association with major depressive disorder. JAMA Psychiatry, 72 7: 642-650. doi:10.1001/jamapsychiatry.2015.0554

Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls

Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, McGrath, John, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2015) Retinal microvessels reflect familial vulnerability to psychotic symptoms: A comparison of twins discordant for psychotic symptoms and controls. Schizophrenia Research, 164 1-3: 47-52. doi:10.1016/j.schres.2015.01.045

Common genetic variants influence human subcortical brain structures

Hibar, Derrek P, Stein, Jason L, Renteria, Miguel E, Arias-Vasquez, Alejandro, Desrivieres, Sylvane, Jahanshad, Neda, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Andersson, Micael, Aribisala, Benjamin S, Armstrong, Nicola J, Bernard, Manon, Bohlken, Marc M, Boks, Marco P, Bralten, Janita, Brown, Andrew A, Mallar Chakravarty M., Chen, Qiang, Ching, Christopher R.K., Cuellar-Partida, Gabriel, Den Braber, Anouk, Giddaluru, Sudheer, Goldman, Aaron L, Grimm, Oliver, Guadalupe, Tulio, Hass, Johanna, Woldehawariat, Girma, Holmes, Avram J, Hoogman, Martine, Janowitz, Deborah, Jia, Tianye, Kim, Sungeun, Klein, Marieke, Kraemer, Bernd, Lee, Phil H, Olde Loohuis, Loes M, Luciano, Michelle, MacAre, Christine, Mather, Karen A, Mattheisen, Manuel, Milaneschi, Yuri, Nho, Kwangsik, Papmeyer, Martina, Ramasamy, Adaikalavan, Risacher, Shannon L, Roiz-Santianez, Roberto, Rose, Emma J, Salami, Alireza, Samann, Philipp G, Schmaal, Lianne, Schork, Andrew J, Shin, Jean, Strike, Lachlan T, Teumer, Alexander, Van Donkelaar, Marjolein. J, Van Eijk, Kristel R, Walters, Raymond K, Westlye, Lars T, Whelan, Christopher D, Winkler, Anderson M, Zwiers, Marcel P, Alhusaini, Saud, Athanasiu, Lavinia, Ehrlich, Stefan, Hakobjan, Marina M. H, Hartberg, Cecilie B, Haukvik, Unn K, Heister, Angelien J.G.A.M, Hoehn, David, Kasperaviciute, Dalia, Liewald, David C.M, Lopez, Lorna M, Makkinje, Remco R.R, Matarin, Mar, Naber, Marlies A.M, Reese McKay, D, Needham, Margaret, Nugent. Allison C, Putz, Benno, Royle, Natallie A, Shen, Li, Sprooten, Emma, Trabzuni, Daniah, Van Der Marel, Saskia S.L, Van Hulzen, Kimm J.E, Walton, Esther, Wolf, Christiane, Almasy, Laura, Ames, David, Arepalli, Sampath, Assareh, Amelia A, Bastin, Mark E, Brodaty, Henry, Bulayeva, Kazima B, Carless, Melanie A, Cichon, Sven, Corvin, Aiden, Curran, Joanne E, Czisch, Michael, De Zubicaray, Greig I, Dillman, Allissa, Duggirala, Ravi, Dyer, Thomas D, Erk, Susanne, Fedko, Iryna O, Ferrucci, Luigi, Foroud, Tatiana M, Fox, Peter T, Fukunaga, Masaki, Raphael Gibbs, J, Goring, Harald H.H, Green, Robert C, Guelfi, Sebastian, Hansell, Narelle K, Hartman, Catharina A, Hegenscheid, Katrin, Heinz, Andreas, Hernandez, Dena G, Heslenfeld, Dirk J, Hoekstra, Pieter J, Holsboer, Florian, Homuth, Georg, Hottenga, Jouke-Jan, Ikeda, Masashi, Jack, Clifford R, Jenkinson, Mark, Johnson, Robert, Kanai, Ryota, Keil, Maria, Kent, Jack W, Kochunov, Peter, Kwok, John B, Lawrie, Stephen M, Liu, Xinmin, Longo, Dan L, McMahon, Katie L, Meisenzahl, Eva, Melle, Ingrid, Mohnke, Sebastian, Montgomery, Grant W, Mostert, Jeanette C, Muhleisen, Thomas W, Nalls, Michael A, Nichols, Thomas E, Nilsson, Lars G, Nothen, Markus M, Ohi, Kazutaka, Olvera, Rene L, Perez-Iglesias, Rocio, Bruce Pike, G, Potkin, Steven G, Reinvang, Ivar, Reppermund, Simone, Rietschel, Marcella, Romanczuk-Seiferth, Nina, Rosen, Glenn D, Rujescu, Dan, Schnell, Knut, Schofield, Peter R, Smith, Colin, Steen, Vidar M, Sussmann. Jessika E, Thalamuthu, Anbupalam, Toga, Arthur W, Traynor, Bryan J, Troncoso, Juan, Turner, Jessica A, Valdes Hernandez, Maria C, Van 'T Ent, Dennis, Van Der Brug, Marcel, Van Der Wee, Nic J.A, Van Tol, Marie-Jose, Veltman, Dick J, Wassink, Thomas H, Westman, Eric, Zielke, Ronald H, Zonderman, Alan B, Ashbrook, David G, Hager, Reinmar, Lu, Lu, McMahon, Francis J, Morris, Derek W, Williams, Robert W, Brunner, Han G, Buckner, Randy L, Buitelaar, Jan K, Cahn, Wiepke, Calhoun, Vince D, Cavalleri, Gianpiero L, Crespo-Facorro, Benedicto, Dale, Anders M, Davies, Gareth E, Delanty, Norman, Depondt, Chantal, Djurovic, Srdjan, Drevets, Wayne C, Espeseth, Thomas, Gollub, Randy L, Ho, Beng-Choon, Hoffmann, Wolfgang, Hosten, Norbert, Kahn, Rene S, Le Hellard, Stephanie, Meyer-Lindenberg, Andreas, Muller-Myhsok, Bertram, Nauck, Matthias, Nyberg, Lars, Pandolfo, Massimo, Penninx, Brenda W.J.H, Roffman, Joshua L, Sisodiya, Sanjay M, Smoller, Jordan W, Van Bokhoven, Hans, Van Haren, Neeltje E. M, Volzke, Henry, Walter, Henrik, Weiner, Michael W, Wen, Wei, White, Tonya, Agartz, Ingrid, Andreassen, Ole A, Blangero, John, Boomsma, Dorret I, Brouwer, Rachel M, Cannon, Dara M, Cookson, Mark R, De Geus, Eco.J.C, Deary, Ian J, Donohoe, Gary, Fernandez, Guillen, Fisher, Simon E, Francks, Clyde, Glahn, David C, Grabe, Hans J, Gruber, Ole A, Hardy, John, Hashimoto, Ryota, Hulshoff Pol, Hilleke E, Jonsson, Erik G, Kloszewska, Iwona, Lovestone, Simon, Mattay, Venkata S, Mecocci, Patrizia, McDonald, COlm, McIntosh, Andrew M, Ophoff, Roel A, Paus, Tomas, Pausova, Zdenka, Ryten, Mina, Sachdev, Perminder S, Saykin, Andrew J, Simmons, Andy, Singleton, Andrew, Soininen, Hilkka, Wardlaw, Joanna M, Weale, Michael E, Weinberger, Daniel R, Adams, Hieab H.H, Launer, Lenore J, Seiler, Stephan, Schmidt, Reinhold, Chauhan, Ganesh, Satizabal, Claudia L, Becker, James T, Yanek, Lisa, Van Der Lee, Sven J, Ebling, Maritza, Fischl, Bruce, Longstreth, W.T, Greve, Douglas, Schmidt, Helena, Nyquist, Paul, Vinke, Louis N, Van Duijn, Cornelia M, Xue, Luting, Mazoyer, Bernard, Bis, Joshua C, Gudnason, Vilmundur, Seshadri, Sudha, Ikram, M.Arfan, Martin, Nicholas G, Wright, Margaret J, Schumann, Gunter, Franke, Barbara, Thompson, Paul M and Medland, Sarah E (2015) Common genetic variants influence human subcortical brain structures. Nature, 520 7546: 224-229. doi:10.1038/nature14101

Genetic basis of a cognitive complexity metric

Hansell, Narelle K., Halford, Graeme S., Andrews, Glenda, Shum, David H. K., Harris, Sarah E., Davies, Gail, Franic, Sanja, Christoforou, Andrea, Zietsch, Brendan, Painter, Jodie, Medland, Sarah E., Ehli, Erik A., Davies, Gareth E., Steen, Vidar M., Lundervold, Astri J., Reinvang, Ivar, Montgomery, Grant W., Espeseth, Thomas, Pol, Hilleke E. Hulshoff, Starr, John M., Martin, Nicholas G., Le Hellard, Stephanie, Boomsma, Dorret I., Deary, Ian J. and Wright, Margaret J. (2015) Genetic basis of a cognitive complexity metric. PLoS One, 10 4: 1-19. doi:10.1371/journal.pone.0123886

Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life

Strohmaier, Jana, van Dongen, Jenny, Willemsen, Gonneke, Nyholt, Dale R., Zhu, Gu, Codd, Veryan, Novakovic, Boris, Hansell, Narelle, Wright, Margaret J., Rietschel, Liz, Streit, Fabian, Henders, Anjali K., Montgomery, Grant W., Samani, Nilesh J., Gillespie, Nathan A., Hickie, Ian B., Craig, Jeffrey M., Saffery, Richard, Boomsma, Dorret I., Rietschel, Marcella and Martin, Nicholas G. (2015) Low birth weight in MZ twins discordant for birth weight is associated with shorter telomere length and lower IQ, but not anxiety/depression in later life. Twin Research and Human Genetics, 18 2: 198-209. doi:10.1017/thg.2015.3

Genetics and brain morphology

Strike, Lachlan T, Couvy-Duchesne, Baptiste, Hansell, Narelle K, Cuellar-Partida, Gabriel, Medland, Sarah E and Wright, Margaret J (2015) Genetics and brain morphology. Neuropsychology Review, 25 1: 63-96. doi:10.1007/s11065-015-9281-1

Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

Mills, Natalie T., Wright, Margaret J., Henders, Anjali K., Eyles, Darryl W., Baune, Bernhard T., McGrath, John J., Byrne, Edna M., Hansell, Narelle K., Birosova, Eva, Scott, James G., Martin, Nicholas G., Montgomery, Grant W., Wray, Naomi R. and Vinkhuyzen, Anna A. E. (2015) Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins. Twin Research and Human Genetics, 18 1: 28-35. doi:10.1017/thg.2014.70

Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults

Meier, Madeline H., Gillespie, Nathan A., Hansell, Narelle K., Hewitt, Alex W., Hickie, Ian B., Lu, Yi, MacGregor, Stuart, Medland, Sarah E., Sun, Cong, Wong, Tien Y., Wright, Margaret J., Zhu, Gu, Martin, Nicholas G. and Mackey, David A. (2014) Associations between depression and anxiety symptoms and retinal vessel caliber in adolescents and young adults. Psychosomatic Medicine, 76 9: 732-738. doi:10.1097/PSY.0000000000000117

Genetic architecture of subcortical brain regions: common and region-specific genetic contributions

Rentería, M. E., Hansell, N. K., Strike, L. T., McMahon, K. L., de Zubicaray, G. I., Hickie, Ian B., Thompson, Paul M., Martin, N. G., Medland, S. E. and Wright, M. J. (2014) Genetic architecture of subcortical brain regions: common and region-specific genetic contributions. Genes, Brain and Behavior, 13 8: 821-830. doi:10.1111/gbb.12177

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent, Karjalainen, Juha, Laibson, David, Lichtenstein, Paul, Liewald, David C., Magnusson, Patrik K. E., Martin, Nicholas G., McGue, Matt, McMahon, George, Pedersen, Nancy L., Pinker, Steven, Porteous, David J., Posthuma, Danielle, Rivadeneira, Fernando, Smithk, Blair H., Starr, John M., Tiemeier, Henning, Timpsonm, Nicholas J., Trzaskowskin, Maciej, Uitterlinden, Andre G., Verhulst, Frank C., Ward, Mary E., Wright, Margaret J., Smith, George Davey, Deary, Ian J., Johannesson, Magnus, Plomin, Robert, Visscher, Peter M., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014) Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 38: 13790-13794. doi:10.1073/pnas.1404623111

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)

Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent, Karjalainen, Juha, Laibson, David, Lichtenstein, Paul, Liewald, David C., Magnusson, Patrik K. E., Martin, Nicholas G., McGue, Matt, McMahon, George, Pedersen, Nancy L., Pinker, Steven, Porteous, David J., Posthuma, Danielle, Rivadeneira, Fernando, Smith, Blair H., Starr, John M., Tiemeier, Henning, Timpson, Nicholas J., Trzaskowski, Maciej, Uitterlinden, Andre G., Verhulst, Frank C., Ward, Mary E., Wright, Margaret J., Smith, George Davey, Deary, Ian J., Johannesson, Magnus, Plomin, Robert, Visscher, PeterM., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014) Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 4: E380-E380. doi:10.1073/pnas.1424631112

Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory

van den Berg, Stephanie M., de Moor, Marleen H. M., McGue, Matt, Pettersson, Erik, Terracciano, Antonio, Verweij, Karin J. H., Amin, Najaf, Derringer, Jaime, Esko, Tonu, van Grootheest, Gerard, Hansell, Narelle K., Huffman, Jennifer, Konte, Bettina, Lahti, Jari, Luciano, Michelle, Matteson, Lindsay K., Viktorin, Alexander, Wouda, Jasper, Agrawal, Arpana, Allik, Jueri, Bierut, Laura, Broms, Ulla, Campbell, Harry, Smith, George Davey, Eriksson, Johan G., Ferrucci, Luigi, Franke, Barbera, Fox, Jean-Paul, de Geus, Eco J. C., Giegling, Ina, Gow, Alan J., Grucza, Richard, Hartmann, Annette M., Heath, Andrew C., Heikkilae, Kauko, Iacono, William G., Janzing, Joost, Jokela, Markus, Kiemeney, Lambertus, Lehtimaki, Terho, Madden, Pamela A. F., Magnusson, Patrik K. E., Northstone, Kate, Nutile, Teresa, Ouwens, Klaasjan G., Palotie, Aarno, Pattie, Alison, Pesonen, Anu-Katriina, Polasek, Ozren, Pulkkinen, Lea, Pulkki-Raback, Laura, Raitakari, Olli T., Realo, Anu, Rose, Richard J., Ruggiero, Daniela, Seppala, Ilkka, Slutske, Wendy S., Smyth, David C., Sorice, Rossella, Starr, John M., Sutin, Angelina R., Tanaka, Toshiko, Verhagen, Josine, Vermeulen, Sita, Vuoksimaa, Eero, Widen, Elisabeth, Willemsen, Gonneke, Wright, Margaret J., Zgaga, Lina, Rujescu, Dan, Metspalu, Andres, Wilson, James F., Ciullo, Marina, Hayward, Caroline, Rudan, Igor, Deary, Ian J., Raikkonen, Katri, Vasquez, Alejandro Arias, Costa, Paul T., Keltikangas-Jarvinen, Liisa, van Duijn, Cornelia M., Penninx, Brenda W. J. H., Krueger, Robert F., Evans, David M., Kaprio, Jaakko, Pedersen, Nancy L., Martin, Nicholas G. and Boomsma, Dorret I. (2014) Harmonization of neuroticism and extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of item response theory. Behavior Genetics, 44 4: 295-313. doi:10.1007/s10519-014-9654-x

A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations

Roussotte, Florence F., Jahanshad, Neda, Hibar, Derrek P., Sowell, Elizabeth R., Kohannim, Omid, Barysheva, Marina, Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Toga, Arthur W., Jack Jr, Clifford R., Weiner, Michael W., Thompson, Paul M. and ADNI (2014) A commonly carried genetic variant in the delta opioid receptor gene, OPRD1, is associated with smaller regional brain volumes: replication in elderly and young populations. Human Brain Mapping, 35 4: 1226-1236. doi:10.1002/hbm.22247

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

Benyamin, B., St Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franic, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J., Harris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., de Geus, E. J. C., Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe, V. W. V., Starr, J. M., Verhulst, F. C., Pennell, C., Tiemeier, H., Iacono, W. G., Palmer, L. J., Montgomery, G. W., Martin, N. G., Boomsma, D. I., Posthuma, D., McGue, M., Wright, M. J., Davey Smith, G., Deary, I. J., Plomin, R. and Visscher, P. M. (2014) Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19 2: 253-258. doi:10.1038/mp.2012.184

Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins

Hill, W. D., Davies, G., Van De Lagemaat, L. N., Christoforou, A., Marioni, R. E., Fernandes, C. P. D., Liewald, D. C., Croning, M. D. R., Payton, A., Craig, L. C. A., Whalley, L. J., Horan, M., Ollier, W., Hansell, N. K., Wright, M. J., Martin, N. G., Montgomery, G. W., Steen, V. M., Le Hellard, S., Espeseth, T., Lundervold, A. J., Reinvang, I., Starr, J. M., Pendleton, N., Grant, S. G. N., Bates, T. C. and Deary, I. J. (2014) Human cognitive ability is influenced by genetic variation in components of postsynaptic signalling complexes assembled by NMDA receptors and MAGUK proteins. Translational Psychiatry, 4 1: 1-8. doi:10.1038/tp.2013.114

Heritability of resting state EEG functional connectivity patterns

Schutte, Nienke M., Hansell, Narelle K., de Geus, Eco J. C., Martin, Nicholas G., Wright, Margaret J. and Smit, Dirk J. A. (2013) Heritability of resting state EEG functional connectivity patterns. Twin Research and Human Genetics, 16 5: 962-969. doi:10.1017/thg.2013.55

The relationship of reading ability to creativity: positive, not negative associations

Ritchie, Stuart J., Luciano, Michelle, Hansell, Narelle K., Wright, Margaret J. and Bates, Timothy C. (2013) The relationship of reading ability to creativity: positive, not negative associations. Learning and Individual Differences, 26 171-176. doi:10.1016/j.lindif.2013.02.009

No association between general cognitive ability and rare copy number variation

McRae, Allan F., Wright, Margaret J., Hansell, Narelle K., Montgomery, Grant W. and Martin, Nicholas G. (2013) No association between general cognitive ability and rare copy number variation. Behavior Genetics, 43 3: 202-207. doi:10.1007/s10519-013-9587-9

Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

Jahanshad, Neda, Rajagopalan, Priya, Hua, Xue, Hibar, Derrek P., Nir, Talia M., Toga, Arthur W., Jack, Jr, Clifford R., Saykin, Andrew J., Green, Robert C., Weiner, Michael W., Medland, Sarah E., Montgomery, Grant W., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Martin, Nicholas G., Wright, Margaret J., Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2013) Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Proceedings of the National Academy of Sciences of the United States of America, 110 12: 4768-4773. doi:10.1073/pnas.1216206110

A study of changes in genetic and environmental influences on weight and shape concern across adolescence

Wade, Tracey D., Hansell, Narelle K., Crosby, Ross D., Bryant-Waugh, Rachel, Treasure, Janet, Nixon, Reginald, Byrne, Susan and Martin, Nicholas G. (2013) A study of changes in genetic and environmental influences on weight and shape concern across adolescence. Journal of Abnormal Psychology, 122 1: 119-130. doi:10.1037/a0030290

A genome-wide association study for reading and language abilities in two population cohorts

Luciano, M., Evans, D. M., Hansell, N. K., Medland, S. E., Montgomery, G. W., Martin, N. G., Wright, M. J. and Bates, T. C. (2013) A genome-wide association study for reading and language abilities in two population cohorts. Genes, Brain and Behavior, 12 6: 645-652. doi:10.1111/gbb.12053

Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects

Hibar, Derrek P., Stein, Jason L., Ryles, April B., Kohannim, Omid, Jahanshad, Neda, Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J., Saykin, Andrew J., Jack, lifford R., Weiner, Michael W., Toga, Arthur W. and Thompson, Paul M. (2013) Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Brain Imaging and Behavior, 7 2: 102-115. doi:10.1007/s11682-012-9199-7

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

Amin, Najaf, Hottenga, Jouke-Jan, Hansell, Narelle K., Janssens, A. Cecile J. W., de Moor, Marleen H. M., Madden, Pamela A. F., Zorkoltseva, Irina V., Penninx, Brenda W., Terracciano, Antonio, Uda, Manuela, Tanaka, Toshiko, Esko, Tonu, Realo, Anu, Ferrucci, Luigi, Luciano, Michelle, Davies, Gail, Metspalu, Andres, Abecasis, Goncalo R., Deary, Ian J., Raikkonen, Katri, Bierut, Laura J., Costa, Paul T., Saviouk, Viatcheslav, Zhu, Gu, Kirichenko, Anatoly V., Isaacs, Aaron, Aulchenko, Yurii S., Willemsen, Gonneke, Heath, Andrew C., Pergadia, Michele L., Medland, Sarah E., Axenovich, Tatiana I., de Geus, Eco, Montgomery, Grant W., Wright, Margaret J., Oostra, Ben A., Martin, Nicholas G., Boomsma, Dorret I. and van Duijn, Cornelia M. (2013) Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions. European Journal of Human Genetics, 21 8: 876-882. doi:10.1038/ejhg.2012.263

Discovery and replication of gene influences on brain structure using LASSO regression

Kohannim, Omid, Hibar, Derrek P., Stein, Jason L., Jahanshad, Neda, Hua, Xue, Rajagopalan, Priya, Toga, Arthur W., Jack Jr., Clifford R., Weiner, Michael W., de Zubicaray, Greig I., McMahon, Katie L., Hansell, Narelle K., Martin, Nicholas G., Margaret J. Wright, Thompson, Paul M. and The Alzheimer’s Disease Neuroimaging Initiative (2012) Discovery and replication of gene influences on brain structure using LASSO regression. Frontiers in Neuroscience, 6 AUG: 115.1-115.13. doi:10.3389/fnins.2012.00115

Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins

Hibar, Derrek P., Jahanshad, Neda, Stein, Jason L., Kohannim, Omid, Toga, Arthur W., Medland, Sarah E., Hansell, Narelle K., McMahon, Katie L., de Zubicaray, Greig I., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012) Alzheimer's disease risk gene, GAB2, is associated with regional brain volume differences in 755 young healthy twins. Twin Research and Human Genetics, 15 3: 286-295. doi:10.1017/thg.2012.15

Identification of common variants associated with human hippocampal and intracranial volumes

Stein, Jason L., Medland, Sarah E., Vasquez, Alejandro Arias, Hibar, Derrek P., Senstad, Rudy E., Winkler, Anderson M., Toro, Roberto, Appel, Katja, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Brown, Andrew A., Cannon, Dara M., Chakravarty, M. Mallar, Christoforou, Andrea, Domin, Martin, Grimm, Oliver, Hollinshead, Marisa, Holmes, Avram J., Homuth, Georg, Hottenga, Jouke-Jan, Langan, Camilla, Lopez, Lorna M., Hansell, Narelle K., Hwang, Kristy S., Kim, Sungeun, Laje, Gonzalo, Lee, Phil H., Liu, Xinmin, Loth, Eva, Lourdusamy, Anbarasu, Mattingsdal, Morten, Mohnke, Sebastian, Maniega, Susana Muñoz, Nho, Kwangsik, Nugent, Allison C., O'Brien, Carol, Papmeyer, Martina, Pütz, Benno, Ramasamy, Adaikalavan, Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roddey, J. Cooper, Rose, Emma J., Ryten, Mina, Shen, Li, Sprooten, Emma, Strengman, Eric, Teumer, Alexander, Trabzuni, Daniah, Turner, Jessica, van Eijk, Kristel, van Erp, Theo G. M., van Tol, Marie-Jose, Wittfeld, Katharina, Wolf, Christiane, Woudstra, Saskia, Aleman, Andre, Alhusaini, Saud, Almasy, Laura, Binder, Elisabeth B., Brohawn, David G., Cantor, Rita M., Carless, Melanie A., Corvin, Aiden, Czisch, Michael, Curran, Joanne E., Davies, Gail, de Almeida, Marcio A. A., Delanty, Norman, Depondt, Chantal, Duggirala, Ravi, Dyer, Thomas D., Erk, Susanne, Fagerness, Jesen, Fox, Peter T., Freimer, Nelson B., Gill, Michael, Göring, Harald H. H., Hagler, Donald J., Hoehn, David, Holsboer, Florian, Hoogman, Martine, Hosten, Norbert, Jahanshad, Neda, Johnson, Matthew P., Kasperaviciute, Dalia, Kent Jr., Jack W., Kochunov, Peter, Lancaster, Jack L., Lawrie, Stephen M., Liewald, David C., Mandl, René, Matarin, Mar, Mattheisen, Manuel, Meisenzahl, Eva, Melle, Ingrid, Moses, Eric K., Mühleisen, Thomas W., Nauck, Matthias, Nöthen, Markus M., Olvera, Rene L., Pandolfo, Massimo, Pike, G. Bruce, Puls, Ralf, Reinvang, Ivar, Rentería, Miguel E., Rietschel, Marcella, Roffman, Joshua L., Royle, Natalie A., Rujescu, Dan, Savitz, Jonathan, Schnack, Hugo G., Schnell, Knut, Seiferth, Nina, Smith, Colin, Steen, Vidar M., Hernández, Maria C. Valdés, Van den Heuvel, Martijn, van der Wee, Nic J., Van Haren, Neeltje E. M., Veltman, Joris A., Völzke, Henry, Walker, Robert, Westlye, Lars T., Whelan, Christopher D., Agartz, Ingrid, Boomsma, Dorret I., Cavalleri, Gianpiero L., Dale, Anders M., Djurovic, Srdjan, Drevets, Wayne C., Hagoort, Peter, Hall, Jeremy, Heinz, Andreas, Jack Jr., Clifford R., Foroud, Tatiana M, Le Hellard, Stephanie, Macciardi, Fabio, Montgomery, Grant W., Poline, Jean Baptiste, Porteous, David J., Sisodiya, Sanjay M., Starr, John M., Sussmann, Jessika, Toga, Arthur W., Veltman, Dick J., Walte, Henrik, Weiner, Michael W., the Alzheimer's Disease Neuroimaging Initiative (ADNI), EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study Group (SYS), Bis, Joshua C., Ikram, M. Arfan, Smith, Albert V., Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Launer, Lenore J., DeCarli, Charles, Seshadri, Sudha, Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, Andreassen, Ole A., Apostolova, Liana G., Bastin, Mark E., Blangero, John, Brunner, Han G., Buckner, Randy L., Cichon, Sven, Coppola, Giovanni, de Zubicaray, Greig I., Deary, Ian J., Donohoe, Gary, de Geus, Eco J. C., Espeseth, Thomas, Fernández, Guillén, Glahn, David C., Grabe, Hans J., Hardy, John, Pol, Hilleke E. Hulshoff, Jenkinson, Mark, Kahn, René S., McDonald, Colm, McIntosh, Andrew M., McMahon, Francis J., McMahon, Katie L., Meyer-Lindenberg, Andreas, Morris, Derek W., Müller-Myhsok, Bertram, Nichols, Thomas E., Ophoff, Roel A., Paus, Tomas, Pausova, Zdenka, Penninx, Brenda W., Potkin, Steven G., Sämann, Philipp G., Saykin, Andrew J., Schumann, Gunter, Smoller, Jordan W., Wardlaw, Joanna M., Weale, Michael E., Martin, Nicholas G., Franke, Barbara, Wright, Margaret J., Thompson, Paul M., for the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, Danoy, Patrick and Brown, Matthew A. (2012) Identification of common variants associated with human hippocampal and intracranial volumes. Nature Genetics, 44 5: 552-561. doi:10.1038/ng.2250

Longevity candidate genes and their association with personality traits in the elderly

Luciano, Michelle, Lopez, Lorna M., de Moor, Marleen H. M., Harris, Sarah E., Davies, Gail, Nutile, Teresa, Krueger, Robert F., Esko, Tonu, Schlessinger, David, Toshiko, Tanaka, Derringer, Jaime L., Realo, Anu, Hansell, Narelle K., Pergadia, Michele L., Pesonen, Anu-Katriina, Sanna, Serena, Terracciano, Antonio, Madden, Pamela A. F., Penninx, Brenda, Spinhoven, Philip, Hartman, Catherina A., Oostra, Ben A., Janssens, A. Cecile J. W., Eriksson, Johan G., Starr, John M., Cannas, Alessandra, Ferrucci, Luigi, Metspalu, Andres, Wright, Margeret J., Heath, Andrew C., van Duijn, Cornelia M., Bierut, Laura J., Raikkonen, Katri, Martin, Nicholas G., Ciullo, Marina, Rujescu, Dan, Boomsma, Dorret I. and Deary, Ian J. (2012) Longevity candidate genes and their association with personality traits in the elderly. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159 B 2: 192-200. doi:10.1002/ajmg.b.32013

Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins

Hansell, N. K., Wright, M. J., Medland, S. E., Davenprot, T. A., Wray, N. R., Martin, N. G. and Hickie, I. B. (2012) Genetic co-morbidity between neuroticism, anxiety/depression and somatic distress in a population sample of adolescent and young adult twins. Psychological Medicine, 42 6: 1249-1260. doi:10.1017/S0033291711002431

Meta-analysis of genome-wide association studies for personality

de Moor, M. H. M., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Toshiko, T., Penninx, B. W. J. H., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J.-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A., Sullivan, P., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A., Lin, P., Grucza, R., Nutile, T., Ciullo, M., Rujescu, D., Giegling, I., Konte, B., Widen, E., Cousminer, D. L., Eriksson, J. G., Palotie, A., Peltonen, L., Luciano, M., Tenesa, A., Davies, G., Lopez, L. M., Hansell, N. K., Medland, S. E., Ferrucci, L., Schlessinger, D., Montgomery, G. W., Wright, M. J., Aulchenko, Y. S., Janssens, A. C. J. W., Oostra, B. A., Metspalu, A., Abecasis, G. R., Deary, I. J., Raikkonen, K., Bierut, L. J., Martin, N. G., van Duijn, C. M. and Boomsma, D. I. (2012) Meta-analysis of genome-wide association studies for personality. Molecular Psychiatry, 17 3: 337-349. doi:10.1038/mp.2010.128

The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior

Miller, Geoffrey, Zhu, Gu, Wright, Margaret J., Hansell, Narelle K. and Martin, Nicholas G. (2012) The heritability and genetic correlates of mobile phone use: a twin study of consumer behavior. Twin Research and Human Genetics, 15 1: 97-106. doi:10.1375/twin.15.1.97

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking

Terracciano, A., Esko, T., Sutin, A. R., de Moor, M. H. M., Meirelles, O., Zhu, G., Tanaka, T., Giegling, I., Nutile, T., Realo, A., Allik, J., Hansell, N. K., Wright, M. J., Montgomery, G. W., Willemsen, G., Hottenga, J-J, Friedl, M., Ruggiero, D., Sorice, R., Sanna, S., Cannas, A., Raikkonen, K., Widen, E., Palotie, A., Eriksson, J. G., Cucca, F., Krueger, R. F., Lahti, J., Luciano, M., Smoller, J. W., van Duijn, C. M., Abecasis, G. R., Boomsma, D. I., Ciullo, M., Costa, P. T., Jr., Ferrucci, L., Martin, N. G., Metspalu, A., Rujescu, D., Schlessinger, D. and Uda, M. (2011) Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Translational Psychiatry, 1 10: e49-e49. doi:10.1038/tp.2011.42

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search

Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M, McMahon, K. L., de Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack Jr, C. R., Weiner. M. W., Toga. A. W., Thompson, P. M. and The Alzheimer’s Disease Neuroimaging Initiative (2011) Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Molecular Psychiatry, 16 9: 927-937. doi:10.1038/mp.2011.32

Genome-wide association reveals dopamine-related genetic effects on caudate volume

Stein, J. L., Hibar, D. P., Madsen, S. K., Khamis, M., McMahon, K. L., De Zubicaray, G. I., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J., Saykin, A. J., Jack, C. R., Weiner, M. W., Toga, A. W. and Thompson, P. M. (2011) Genome-wide association reveals dopamine-related genetic effects on caudate volume. Molecular Psychiatry, 16 9: 881-881. doi:10.1038/mp.2011.98

BDNF gene effects on brain circuitry replicated in 455 twins

Chiang, M. C., Barysheva, M., Toga, A. W., Medland, S. E., Hansel, N. K., James, M. R., McMahon, K. L., de Zubicaray, G. I., Martin, N. G., Wright, M. J. and Thompson, P. M. (2011) BDNF gene effects on brain circuitry replicated in 455 twins. NeuroImage, 55 2: 448-454. doi:10.1016/j.neuroimage.2010.12.053

Whole genome association scan for genetic polymorphisms influencing information processing speed

Luciano, Michelle, Hansell, Narelle K., Lahti, Jari, Davies, Gail, Medland, Sarah E., Raikkonen, Katri, Tenesa, Albert, Widen, Elisabeth, McGhee, Kevin A., Palotie, Aarno, Liewald, David, Porteous, David J., Starr, John M., Montgomery, Grant W., Martin, Nicholas G., Eriksson, Johan G., Wright, Margaret J. and Deary, Ian J. (2011) Whole genome association scan for genetic polymorphisms influencing information processing speed. Biological Psychology, 86 3: 193-202. doi:10.1016/j.biopsycho.2010.11.008

Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms

Martin, Nicolas W., Benyamin, Beben, Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Bates, Timothy C. (2011) Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms. Journal of the American Academy of Child and Adolescent Psychiatry, 50 1: 55-62.e4. doi:10.1016/j.jaac.2010.10.010

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects

Rizzi, Thais S., Arias-Vasquez, Alejandro, Rommelse, Nanda, Kuntsi, Jonna, Anney, Richard, Asherson, Philip, Buitelaar, Jan, Banaschewski, Tobias, Ebstein, Richard, Ruano, Dina, van der Sluis, Sophie, Markunas, Christina A., Garrett, Melanie E., Ashley-Koch, Allison E., Kollins, Scott H., Anastopoulos, Arthur D., Hansell, Narelle K., Wright, Margaret J., Montgomery, Grant W., Martin, Nicholas G., Harris, Sarah E., Davies, Gail, Tenesa, Albert, Porteous, David J., Starr, John M., Deary, Ian J., St. Pourcain, Beate, Smith, George Davey, Timpson, Nicholas J., Evans, David M., Gill, Michael, Miranda, Ana, Mulas, Fernando, Oades, Robert D., Roeyers, Herbert, Rothenberger, Aribert, Sergeant, Joseph, Sonuga-Barke, Edmund, Steinhausen, Hans Christoph, Taylor, Eric, Faraone, Stephen V., Franke, Barbara and Posthuma, Danielle (2011) The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 156 2: 145-157. doi:10.1002/ajmg.b.31149

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

Middeldorp, C. M., de Moor, M. H. M., McGrath, L. M., Gordon, S. D., Blackwood, D. H., Costa, P. T., Terracciano, A., Krueger, R. F., de Geus, E. J. C., Nyholt, D. R., Tanaka, T., Esko, T., Madden, P. A. F., Derringer, J., Amin, N., Willemsen, G., Hottenga, J-J., Distel, M. A., Uda, M., Sanna, S., Spinhoven, P., Hartman, C. A, Ripke, S., Sullivan, P. F., Realo, A., Allik, J., Heath, A. C., Pergadia, M. L., Agrawal, A., Lin, P., Grucza, R. A., Widen, E., Cousminer, D. L., Eriksson, J. G., Palotie, A., Barnett, J. H., Lee, P. H., Luciano, M., Tenesa, A., Davis, G., Lopez, L. M., Hansell, N. K., Medland, S. E., Ferrucci, L., Schlessinger, D., Montgomery, Grant G., Wright, M. J., Aulchenko, Y. S., Janssens, A. C. J. W., Oostra, B. A., Metspalu, A., Abecasis, G. R., Deary, I. J., Raikkonen, K., Bierut, L. J., Martin, N. G., Wray, N. R., van Duijn, C. M., Smoller, J. W., Penninx, B. W. J. H. and Boomsma, D. I. (2011) The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Translational Psychiatry, 1 10: e50.1-e50.8. doi:10.1038/tp.2011.45

Heritability of head size in Dutch and Australian twin families at ages 0-50 years

Smit, Dirk J. A., Luciano, Michelle, Bartels, Meike, van Beijsterveldt, Catharine E. M., Wright, Margaret J., Hansell, Narelle K., Brunner, Han G., Estourgie-van Burk, G. Frederiek, de Geus, Eco J. C., Martin, Nicholas G. and Boomsma, Dorret I. (2010) Heritability of head size in Dutch and Australian twin families at ages 0-50 years. Twin Research And Human Genetics, 13 4: 370-380. doi:10.1375/twin.13.4.370

Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness

Lu, Yi, Dimasi, David P., Hysi, Pirro G., Hewitt, Alex W., Burdon, Kathryn P., Toh, Tze'Yo, Ruddle, Jonathan B., Li, Yi Ju, Mitchell, Paul, Healey, Paul R., Montgomery, Grant W., Hansell, Narelle, Spector, Timothy D., Martin, Nicholas G., Young, Terri L., Hammond. Christopher J., Macgregor, Stuart, Craig, Jamie E. and Mackey, David A. (2010) Common genetic variants near the brittle cornea syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. PLoS Genetics, 6 5: e1000947.1-e1000947.10. doi:10.1371/journal.pgen.1000947

A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations

Lind, Penelope A., Macgregor, Stuart, Vink, Jacqueline M., Pergadia, Michele L., Hansell, Narelle K., de Moor, Marleen H. M., Smit, August B., Hottenga, Jouke-Jan, Richter, Melinda M., Heath, Andrew C., Martin, Nicholas G., Willemsen, Gonneke, de Geus, Eco J. C., Vogelzangs,Nicole, Penninx, Brenda W., Whitfield, John B., Montgomery, Grant W., Boomsma, Dorret I. and Madden, Pamela A. F. (2010) A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations. Twin Research And Human Genetics, 13 1: 10-29. doi:10.1375/twin.13.1.10

Genetic contribution to individual variation in binocular rivalry rate

Miller, Steven M., Hansell, Narelle K., Ngo, Trung T., Liu, Guang B., Pettigrew, John D., Martin, Nicholas G. and Wright, Margaret J. (2010) Genetic contribution to individual variation in binocular rivalry rate. Proceedings of the National Academy of Sciences of the United States of America, 107 6: 2664-2668. doi:10.1073/pnas.0912149107

Linkage analysis of alcohol dependence symptoms in the community

Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Gordon, Scott D., Lind, Penelope A., Pergadia, Michele L., Montgomery, Grant W., Madden, Pamela A. F., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2010) Linkage analysis of alcohol dependence symptoms in the community. Alcoholism: Clinical and Experimental Research, 34 1: 158-163. doi:10.1111/j.1530-0277.2009.01077.x

Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans

Medland, S, Nyholt, D, Painter, JN, McEnvoy, BP, Allan McRae, Zhu, G, Gordon, SD, Ferreira, MAR, Wright, MJ, Henders, AK, Campbell MJ, Duffy, D, Hansell, N K, Macgregor, S, Slutske, WS, Heath, AC, Montgomery, GW and Martin, NG (2009) Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans. American Journal of Human Genetics, 85 5: 750-755. doi:10.1016/j.ajhg.2009.10.009

Alcohol consumption indices of genetic risk for alcohol dependence

Julia D. Grant, Arpana Agrawal, Kathleen K. Bucholz, Pamela A.F. Madden, Michele L. Pergadia, Elliot C. Nelson, Michael T. Lynskey, Richard D. Todd, Alexandre A. Todorov, Narelle K. Hansell, John B. Whitfield, Nicholas G. Martin and Andrew C. Heath (2009) Alcohol consumption indices of genetic risk for alcohol dependence. Biological Psychiatry, 66 8: 795-800. doi:10.1016/j.biopsych.2009.05.018

Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?

Martin, Nicolas W., Hansell, Narelle K., Wainwright, Mark A., Shekar, Sri N., Medland, Sarah E., Bates, Timothy C., Burt, Jennifer S., Martin, Nicholas G. and Wright, Margaret J. (2009) Genetic covariation between the author recognition test and reading and verbal abilities: What can we learn from the analysis of high performance?. Behavior Genetics, 39 4: 417-426. doi:10.1007/s10519-009-9275-y

Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis

Stuart Macgregor, Penelope A. Lind, Kathleen K. Bucholz, Narelle K. Hansell, Pamela A.F. Madden, Melinda M. Richter, Grant W. Montgomery, Nicholas G. Martin, Andrew C. Heath and John B. Whitfield (2009) Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis. Human Molecular Genetics, 18 3: 580-593. doi:10.1093/hmg/ddn372

Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?

Narelle K. Hansell, Arpana Agrawal, John B. Whitfield, Katherine I. Morley, Scott D. Gordon, Penelope A. Lind, Michele L. Pergadia, Grant W. Montgomery, Pamela A. F. Madden, Richard D. Todd, Andrew C. Heath and Nicholas G. Martin (2009) Can We Identify Genes For Alcohol Consumption In Samples Ascertained For Heterogeneous Purposes?. Alcoholism: Clinical and Experimental Research, 33 4: 729-739. doi:10.1111/j.1530-0277.2008.00890.x

Autosomal linkage analysis for cannabis use behaviors in Australian adults

Agrawal, Arpana, Morley, Katherine I., Hansell, Narelle K., Pergadia, Michele L., Montgomery, Grant W., Statham, Dixie J., Todd, Richard D., Madden, Pamela A. F., Heath, Andrew C., Whitfield, John, Martin, Nicholas G. and Lynskey, Michael T. (2008) Autosomal linkage analysis for cannabis use behaviors in Australian adults. Drug and Alcohol Dependence, 98 3: 185-190. doi:10.1016/j.drugalcdep.2008.05.009

Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence

Hansell, Narelle K., Agrawal, Arpana, Whitfield, John B., Morley, Katherine I., Zhu, Gu, Lind, Penelope A., Pergadia, Michele L., Madden, Pamela A., Todd, Richard D., Heath, Andrew C. and Martin, Nicholas G. (2008) Long-term stability and heritability of telephone interview measures of alcohol consumption and dependence. Twin Research and Human Genetics, 11 3: 287-305. doi:10.1375/twin.11.3.287

QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes

Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Montgomery, Grant W., Geffen, Gina M. and Martin, Nicholas (2008) QTLs identified for P3 amplitude in a non-clinical sample: Importance of neurodevelopmental and neurotransmitter genes. Biological Psychiatry, 63 9: 864-873. doi:10.1016/j.biopsych.2007.09.002

Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta

Zietsch, Brendan P., Hansen, Jonathan L., Hansell, Narelle K, Geffen, Gina M., Martin, Nicholas G. and Wright, Margaret J. (2007) Common and specific genetic influences on EEG power bands delta, theta, alpha, and beta. Biological Psychology, 75 2: 154-164. doi:10.1016/j.biopsycho.2007.01.004

Effect of the BDNF V166M polymorphism on working memory in healthy adolescents

Hansell, N. K., James, M. R., Duffy, D. L., Birley, A. J., Luciano, M., Geffen, G. M., Wright, M. J., Montgomery, G. W. and Martin, N. G. (2007) Effect of the BDNF V166M polymorphism on working memory in healthy adolescents. Genes, Brain and Behavior, 6 3: 260-268. doi:10.1111/j.1601-183X.2006.00254.x

Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample

Smit, Christine M., Wright, Margaret J., Hansell, Narelle K., Geffen, Gina M. and Martin, Nicholas G. (2006) Genetic variation of individual alpha frequency (IAF) and alpha power in a large adolescent twin sample. International Journal of Psychophysiology, 61 2: 235-243. doi:10.1016/j.ijpsycho.2005.10.004

Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

Hansell, N. K., Medland, S. E., Ferreira, A. R., Geffen, G. M., Zhu, G., Montgomery, G. W., Duffy, D. L., Wright, M.J. and Martin, N. G. (2006) Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task. Behavior Genetics, 36 1: 29-44. doi:10.1007/s10519-005-9002-2

Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ

Hansell, N. K., Wright, M. J., Luciano, M., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2005) Genetic covariation between event-related potential (ERP) and behavioral non-ERP measures of working-memory, processing speed, and IQ. Behavior Genetics, 35 6: 695-706. doi:10.1007/s10519-005-6188-2

Bladder neck mobility is a heritable trait

Dietz, H. P., Hansell, N. K., Grace, M. E., Eldridge, A.M., Clarke, B. and Martin, N. G. (2005) Bladder neck mobility is a heritable trait. BJOG: An International Journal of Obstetrics and Gynaecology, 112 3: 334-339. doi:10.1111/j.1471-0528.2004.00428.x

Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins

Hansell, NK, Pang, D, Heath, AC, Martin, NG and Whitfield, JB (2005) Erythrocyte aldehyde dehydrogenase activity: Lack of association with alcohol use and dependence or alcohol reactions in Australian twins. Alcohol and Alcoholism, 40 5: 343-348. doi:10.1093/alcalc/agh168

Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave

Hansell, Narelle K., Wright, Margaret J., Geffen, Gina M., Geffen, Laurie B. and Martin, Nicholas G. (2004) Genetic influences on cognitive processes associated with distraction: An event-related potential study of the slow wave. Australian Journal of Psychology, 56 2: 89-98. doi:10.1080/0049530410001734856

Genetic covariation of pelvic organ and elbow mobility in twins and their sisters

Hansell, N. K., Dietz, H. P., Treloar, S. A., Clarke, B. and Martin, N. G. (2004) Genetic covariation of pelvic organ and elbow mobility in twins and their sisters. Twin Research, 7 3: 254-260. doi:10.1375/136905204774200532

Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task

Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2002) Genetic sources of covariation among P3(00) and online performance variables in a delayed-response working memory task. Biological Psychology, 61 1-2: 183-202. doi:10.1016/S0301-0511(02)00058-3

Genetic influence on ERP slow wave measures of working memory

Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001) Genetic influence on ERP slow wave measures of working memory. Behavior Genetics, 31 6: 603-614. doi:10.1023/A:1013301629521

Genetic influence on the variance in P3 amplitude and latency

Wright, M. J., Hansell, N. K., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2001) Genetic influence on the variance in P3 amplitude and latency. Behavior Genetics, 31 6: 555-565. doi:10.1023/A:1013393327704

Genetics of cognition: Outline of a collaborative twin study

Wright, M. J., Eco, D., Ando, J, Luciano, M., Posthuma, D., Ono, Y., Hansell, N. K., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G. M., Geffen, L. B., Kanba, S., Miyake, A., Martin, N. G. and Boomsa, D. I. (2001) Genetics of cognition: Outline of a collaborative twin study. Twin Research, 4 1: 48-56. doi:10.1375/twin.4.1.48

Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study

Smit, Dirk, Wright, Margareth, Meyers, Jacquelyn, Martin, Nicholas, Ho, Yvonne, Malone, Stephen, Zhang, Jian, Burwell, Scott, Chorlian, David, de Geus, Eco, Denys, Damiaan, Hansell, Narelle, Hottenga, Jouke-Jan, McGue, Matt, van Beijsterveldt, Catharina, Jehanshad, Neda, Thompson, Paul, Whelan, Chris, Medland, Sarah, Porjesz, Bernice, Iacono, William and Boomsma, Dorret (2018). Psychiatric Liability Genes are Linked to Oscillatory Brain Activity: A Genome-Wide Association Study. In: 73rd Annual Scientific Convention and Meeting of the Society-of-Biological-Psychiatry (SOBP), New York NY United States, (S336-S336). 10-12 May 2017.

A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait

Cuéllar-Partida, Gabriel, Ngo, Trung T., Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). A perceptual endophenotype for mental illness: Characterising normal genetic variation in the trait. In: BLiSS 2017 — Brisbane Life Science ECR Symposium, Translational Research Institute, Brisbane, (). 24 November 2017.

Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder

Trung Ngo,, Renteria, Miguel E., Conde, Lucia Colodro, Couvy-Duchesne, Baptiste, Cuellar-Partida, Gabriel, Hansen, Narelle K., Medland, Sarah E., Miller, Steven M., Wright, Margaret J. and Martin, Nicholas G. (2017). Binocular rivalry rate as a novel candidate endophenotype for bipolar disorder. In: 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, Canada, (S305-S305). 16-20 October 2015.

GWAS of complementary perceptual endophenotype measures: How do they rate?

Ngo, Trung T., Cuéllar-Partida, Gabriel, Couvy-Duchesne, Baptiste, Rentería, Miguel E., Colodro Conde, Lucia, Gordon, Scott D., Hansell, Narelle K., Medland, Sarah E., Wright, Margaret J. and Martin, Nicholas G. (2017). GWAS of complementary perceptual endophenotype measures: How do they rate?. In: Australasian Society for Bipolar & Depressive Disorders (ASBDD) 2017 Conference, Deakin Edge, Melbourne, (48-48). 15–17 September 2017.

Heritability of hair cortisol and genetic overlap with psychological variables

Streit, Fabian, Rietschel, Liz, Zhu, Gu, McAloney, Kerrie, Frank, Josef, Couvy-Duchesne, Baptiste, Witt, Stephanie H., Binz, Tina, McGrath, John, Hickie, Ian B., Hansell, Narelle K., Wright, Margaret J., Gillespie, Nathan, Forstner, Andreas J., Schulze, Thomas G., Wüst, Stefan, Nöthen, Markus M., Baumgartner, Markus, Walker, Brian R., Crawford, Andrew A., Conde, Lucia Colodro, Medland, Sarah E., Martin, Nicholas G. and Rietschel, Marcella (2017). Heritability of hair cortisol and genetic overlap with psychological variables. In: 47th Annual Conference of the International Society of Psychoneuroendocrinology, Zurich, Switzerland, (80-80). 7-9 September, 2017.

Association of psychiatric profile measures with binocular rivalry rate (BRR): Implications for slow BRR as an endophenotype for bipolar disorder

Ngo, T. T., Couvy-Duchesne, B., Cuéllar-Partida, G., Rentería, M. E., Colodro Conde, L., Gordon, S. D., Hansell, N. K., Law, P. C. F., Miller, S. M., Medland, S. E., Wright, M. J. and Martin, N. G. (2016). Association of psychiatric profile measures with binocular rivalry rate (BRR): Implications for slow BRR as an endophenotype for bipolar disorder. In: Abstracts from the ISTS Satellite Meeting June 20, 2016, Brisbane. International Society for Twin Studies Satellite Meeting, QIMR Berghofer Medical Research Institute, Brisbane, Australia, (518-518). 20 June 2016. doi:10.1017/thg.2016.66

Genetic contributions to brain structure

Strike, Lachlan, Hansell, Narelle, Couvy-Duchesne, Baptiste, Thompson, Paul, Martin, Nicholas, de Zubicaray, Greig, McMahon, Katie and Wright, Margaret (2016). Genetic contributions to brain structure. In: 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, (808-808). 20-23 June 2016. doi:10.1007/s10519-016-9812-4

Genetic covariation among hippocampal subfields

Hansell, Narelle, Strike, Lachlan, McMahon, Katie, Martin, Nicholas, de Zubicaray, Greig, Thompson, Paul and Wright, Margaret (2016). Genetic covariation among hippocampal subfields. In: 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, (786-786). 20-23 June 2016. doi:10.1007/s10519-016-9812-4

Hair cortisol and its Association with Symptoms of Depression, Neuroticism and Perceived Stress in Adolescent Twins

Rietschel, Liz, Streit, Fabian, Zhu, Gu, McAloney, Kerrie, Kirschbaum, Clemens, Hansell, Narelle K., Wright, Margie, McGrath, John J., Witt, Stephanie, Rietschel, Marcella and Martin, Nicholas G. (2016). Hair cortisol and its Association with Symptoms of Depression, Neuroticism and Perceived Stress in Adolescent Twins. In: IEPA 10th International Conference on Early Intervention in Mental Health – “Looking Back, Moving Forward”, Milan, Italy, (217-217). 20th – 22nd October, 2016. doi:10.1111/eip.12397

Power of multivariate GWAS: real case scenarios using brain phenotypes from MRI

Couvy-Duchesne, Baptiste, Strike, Lachlan, Hansell, Narelle, Martin, Nicholas, McMahon, Katie, de Zubicaray, Greig, Thompson, Paul and Wright, Margaret (2016). Power of multivariate GWAS: real case scenarios using brain phenotypes from MRI. In: 46th Annual Meeting of the Behavior Genetics Association, Brisbane, Australia, (777-777). 20-23 June 2016. doi:10.1007/s10519-016-9812-4

Genetic influences on longitudinal changes in subcortical volumes: results of the ENIGMA Plasticity Working Group

Pol, Hilleke Hulshoff, Brouwer, Rachel, Glahn, David, Hibar, Derrek, Hua, Xue, Jahanshad, Neda, Abramovic, Lucija, Franz, Carol, Hansell, Narelle, Koenis, Marinka, Mather, Karen, Panizzon, Matthew, Strike, Lachlan, Swagerman, Suzanne, Wen, Wei, Boomsma, Dorret, Gilmore, John, Gogtay, Nitin, Kahn, Rene S., Kremen, William, Sachdev, Perminder, Wright, Margaret and Thompson, Paul (2015). Genetic influences on longitudinal changes in subcortical volumes: results of the ENIGMA Plasticity Working Group. In: 45th Annual Meeting of the Behavior Genetics Association, San Diego, United States, (662-663). Jun 20, 2015.

Genome-wide association for reading and language abilities in two population cohorts

Luciano, Michelle, Evans, David, Hansell, Narelle, Medland, Sarah, Montgomery, Grant, Martin, Nick G., Wright, Margaret and Bates, Timothy (2013). Genome-wide association for reading and language abilities in two population cohorts. In: 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille, France, (530-530). 28 June-2 July 2013.

Human cognitive ability is influenced by genetic variation in components of postsynaptic signaling complexes assembled by MAGUK proteins

Hill, William, Davies, Gail, Van de Lagemaat, Louie, Christoforou, Andrea, Fernandes, Carla, Liewald, David, Croning, Mike, Payton, Antony, Craig, Leone, Whalley, Lawrence, Horan, Michael, Ollier, William, Hansell, Narelle, Wright, Margaret, Martin, Nick G., Montgomery, Grant, Steen, Vidar, Le Hellard, Stephanie, Espeseth, Thomas, Lundervold, Astri, Reinvang, Ivar, Starr, John, Pendleton, Neil, Grant, Seth, Bates, Timothy and Deary, Ian (2013). Human cognitive ability is influenced by genetic variation in components of postsynaptic signaling complexes assembled by MAGUK proteins. In: 43rd Annual Meeting of the Behavior Genetics Association, Marseille, France, (521-522). 28 June - 2 July 2013 3.

Diffusion imaging protocol effects on genetic associations

Jahanshad, Neda, Kohannim, Omid, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansell, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Diffusion imaging protocol effects on genetic associations. In: 2012 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012 - Proceedings. International Symposium on Biomedical Imaging, Barcelona, Spain, (944-947). 2-5 May 2012. doi:10.1109/ISBI.2012.6235712

Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome

Jahanshad, Neda, Hibar, Derrek, Ryles, April, Toga, Arthur W., McMahon, Katie L., de Zubicaray, Greig I., Hansel, Narelle K., Montgomery, Grant W., Martin, Nicholas G., Wright, Margaret J. and Thompson, Paul M. (2012). Discovery of genes that affect human brain connectivity: a genome-wide analysis of the connectome. In: 2012 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro: Proceedings. 9th International Symposium on Biomedical Imaging, Barcelona, Spain, (542-545). 2-5 May 2012. doi:10.1109/ISBI.2012.6235605

Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder

Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder. In: Abstracts of the 5th Biennial Conference of the International Society for Bipolar Disorders. 5th Biennial Conference of the International Society for Bipolar Disorders, Istanbul, Turkey, (103-103). 14–17 March 2012. doi:10.1111/j.1399-5618.2012.00981.x

Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder

Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Wright, M. J. and Martin, N. G. (2012). Genetic contribution to individual variation in binocular rivalry, an endophenotype for bipolar disorder. In: Special Issue: Abstracts of the 5th Biennial Conference of the International Society for Bipolar Disorders. 5th Biennial Conference of the International-Society-for-Bipolar-Disorders, Istanbul, Turkey, (s103-s103). 14-17 March 2012. doi:10.1111/j.1399-5618.2012.00981.x

Robust identification of partial-correlation based networks with applications to cortical thickness data

Wheland, D., Joshi, A., McMahon, K., Hansell, N., Martin, N., Wright, M., Thompson, P., Shattuck, D. and Leahy, R. (2012). Robust identification of partial-correlation based networks with applications to cortical thickness data. In: 2012 9th IEEE International Symposium on Biomedical Imaging : From Nano to Macro : proceedings. 9th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, ISBI 2012, Barcelona, Spain, (1551-1554). 2 - 5 May 2012. doi:10.1109/ISBI.2012.6235869

Increasing GWAS sample size using item response theory: A pilot study of the personality consortium

de Moor, Marleen, van den Berg, Stephanie, Wouda, Jasper, Verweij, Karin, Hansell, Narelle, Martin, Nick G. and Boomsma, Dorret (2011). Increasing GWAS sample size using item response theory: A pilot study of the personality consortium. In: Behavior Genetics. 41st Annual Meeting of the Behaviour-Genetics-Association, Newport Ri, (899-900). Jun 06-09, 2011.

A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults

Hansell, Narelle K., Hickie, Ian B., Davenport, Tracey A., Hadzi-Pavlovic, Dusan, Wray, Naomi R., Martin, Nicholas G. and Wright, Margaret J. (2010). A study of genetic influence on SPHERE (somatic and psychological health report) measures collected in adolescents and young adults. In: Behavior Genetics Association 40th Annual Meeting Abstracts. 40th Annual Meeting of Behavior Genetics Association, Pennsylvania, PA, U.S.A., (795-795). May 2009. doi:10.1007/s10519-010-9392-7

Genetic contribution to individual variation in binocular rivalry rate

Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). Genetic contribution to individual variation in binocular rivalry rate. In: Proceedings of the Australian Neuroscience Society and Australian Physiological Society Joint Meeting. ANS/AuPS 2010 — 30th Annual Meeting of the Australian Neuroscience Society, in conjunction with the 50th Anniversary Meeting of the Australian Physiological Society, Sydney Convention & Exhibition Centre, Darling Harbour, Sydney, (173-173). 31 January – 3 February 2010.

Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder

Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). Genetic contribution to individual variation in binocular rivalry rate, an endophenotype for bipolar disorder. In: Proceedings of the 18th World Congress of Psychiatric Genetics. 18th World Congress of Psychiatric Genetics, Athens, Greece, (). 3–7 October 2010.

The genetics of binocular rivalry

Miller, S. M., Hansell, N. K., Ngo, T. T., Liu, G. B., Pettigrew, J. D., Martin, N. G. and Wright, M. J. (2010). The genetics of binocular rivalry. In: Proceedings of the 7th FENS Forum of European Neuroscience. 7th FENS Forum of European Neuroscience, Amsterdam, The Netherlands, (139.14-139.14). 3–7 July, 2010.

Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits

de Moor, Marleen H. M., Boomsma, Dorret, I, de Geus, Eco J. C., Willemsen, Gonneke, Hottenga, Jouke-Jan, Distel, Marijn A., Abecasis, Goncalo R., Terracciano, Antonio, McCrae, Robert R., Costa, Paul T., Hartman, Catharina A., Spinhoven, Philip, Penninx, Brenda W., Esko, Tonu, Allik, Jueri, Realo, Anu, Metspalu, Andres, Hansell, Narelle K., Medland, Sarah E., Wray, Naomi R., Wright, Margie J., Martin, Nicholas G., Amin, Najaf, Aulchenko, Yurii S., Janssens, A. Cecile, Oostra, Ben A. and van Duijn, Cornelia M. (2009). Meta-analysis of genome-wide association results in > 10.000 individuals for the big five personality traits. In: 39th Annual Meeting of the Behavior Genetics Association, Mineapolis, MN, United States, (643-643). 17-20 June 2009 .

Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology

Wright, Margaret J., Luciano, Michelle, Hansell, Narelle K., Geffen, Gina M., Montgomery, Grant W. and Martin, Nicholas G. (2006). Genome-wide scan for loci influencing the P3: An endophenotype for psychopathology. In: Alcoholism-Clinical And Experimental Research: World Congress on Alcohol Research (ISBRA 2006). World Congress on Alcohol Research (ISBRA 2006), Sydney, Australia, (62A-62A). 10 - 13 September 2006. doi:10.1111/j.1530-0277.2006.00197.x

A genomic wide screen of the P3(00) ERP component: Preliminary findings

Wright, M. J., Luciano, M., Hansell, N. K., Geffen, G. M. and Martin, N. G. (2004). A genomic wide screen of the P3(00) ERP component: Preliminary findings. In: Behavior Genetics Association 34th Annual Meeting , Aix en Provence, France, (666-666). June 2004.

Linkage analyses of ERP slow wave measures of working memory

Hansell, Narelle K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2004). Linkage analyses of ERP slow wave measures of working memory. In: Behavior Genetics Association 34th Annual Meeting Abstracts. 34th Annual Meeting of the Behavior Genetics Association, Provence, France, (643-644). 27 - 30 June 2004. doi:10.1007/s10519-004-5590-5

Bladder neck mobility is a heritable trait

Dietz, H. P., Hansell, N., Grace, M., Eldridge, A., Martin, N. and Clarke, B. (2003). Bladder neck mobility is a heritable trait. In: M. M. Karram, International Urogynecology Journal: 28th Annual IUGA Meeting. 28th Annual IUGA Meeting, Buenos Aires, Argentina, (S74-S74). 28-31 October, 2003. doi:10.1007/s00192-003-1108-6

ERP endophenotypes of cognitive ability: A genetic study

Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B. and Martin, N. G. (2003). ERP endophenotypes of cognitive ability: A genetic study. In: Australian Journal of Psychology: The Abstracts of the 3rd Victorian Postgraduates in Psychology Conference. 3rd Victorian Postgraduates in Psychology Conference, RMIT University, Victoria, (19-19). 23 Nov 2002.

Genetic variation in brain function

de Geus, E, Posthuma, D, Hansell, N, Malone, SM and Mulder, E (2002). Genetic variation in brain function. In: Psychophysiology. , , (S3-S3). .

ERP phenotypes in a genetic study of working memory

Wright, M. J., Hansell, N. K., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). ERP phenotypes in a genetic study of working memory. In: -, -, (S14-S14). 2000.

Genetic influences on ERP slow wave measures of working memory in adolescent twins

Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). Genetic influences on ERP slow wave measures of working memory in adolescent twins. In: Behavior Genetics Association Meeting Abstracts. Behavior Genetics Association Meeting, -, (407-407). 2000.

Psychophysiological phenotypes of cognition: The P3 and SW components

Wright, M. J., Hansell, N., Geffen, G. M., Geffen, L., Smith, G. and Martin, N. (2000). Psychophysiological phenotypes of cognition: The P3 and SW components. In: Behavior Genetics: Behavior Genetics Association Meeting Abstracts. 30th Annual Meeting of the Behavior Genetics Association, Burlington, Vermont, USA, (422-422). June 29 - July 1, 2000. doi:10.1023/A:1017371222025

Reliability and stability of P3 and slow wave elicited in a working memory task

Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A. and Martin, N. G. (2000). Reliability and stability of P3 and slow wave elicited in a working memory task. In: -, -, (14-14). 2000.

A genetic investigation of brain function and cognitive ability

Hansell, Narelle Kaye (2003). A genetic investigation of brain function and cognitive ability PhD Thesis, School of Psychology, The University of Queensland.