Professor Georgia Chenevix-Trench

Honorary Professor

Royal Brisbane Clinical Unit
Faculty of Medicine

Overview

Qualifications

  • PhD, Med.C.Virginia
  • Bachelor of Science, Dub

Publications

  • French, Juliet D., Johnatty, Sharon E., Lu, Yi, Beesley, Jonathan, Gao, Bo, Kalimutho, Murugan, Henderson, Michelle J., Russell, Amanda J., Kar, Siddhartha, Chen, Xiaoging, Hillman, Kristine M., Kaufmann, S, Sivakumaran H., O'Reilly, Martin, Wang, Chen, Korbie, Darren J., Lambrechts, Diether, Despierre, Evelyn, Van Nieuwenhuysen, Els, Lambrechts, Sandra, Vergote, Ignace, Karlan, Beth, Lester, Jenny, Orsulic, Sandra, Walsh, Christine, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Matsuo, Keitaro, Hosono, Satoyo, Pisterer, Jacobus, Hillemanns, Peter, Nakanishi, Toru, Yatabe, Yasushi, Goodman, Marc T., Lurie, Galine, Matsuno, Rayna K., Thompson, Pamela J., Pejovic, Tanja, Bean, Yukie, Heitz, Florian, Harter, Philipp, Du Bois, Andreas, Schwaab, Ira, Hogdall, Estrid, Kjaer, Susanne K., Jensen, Allan, Hogdall, Claus, Lundvall, Lene, Engelholm, Svend Aage, Brown, Bob, Flanagan, James M., Metcalf, Michelle D., Siddiqui, Nadeem, Sellers, Thomas, Fridley, Brooke, Cunningham, Julie, Schildkraut, Joellen M., Iversen, Ed, Weber, Rachel Palmieri, Brennan, Donal, Berchuck, Andrew, Pharoah, Paul, Harnett, Paul, Norris, Murray D., Haber, Michelle, Goode, Ellen L., Lee, Jason S., Khanna, Kum Kum, Meyer, Kerstin B., Chenevix-Trench, Georgia, DeFazio, Anna, Edwards, Stacey L. and MacGregor, Stuart (2016) Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Oncotarget, 7 6: 6353-6368. doi:10.18632/oncotarget.7047

  • Johnatty, Sharon E., Tyrer, Jonathan P., Kar, Siddhartha, Beesley, Jonathan, Lu, Yi, Gao, Bo, Fasching, Peter A., Hein, Alexander, Ekici, Arif B., Beckmann, Matthias W., Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Lambrechts, Sandrina, Rossing, Mary Anne, Doherty, Jennifer A., Chang-Claude, Jenny, Modugno, Francesmary, Ness, Roberta B., Moysich, Kirsten B., Levine, Douglas A., Kiemeney, Lambertus A., Massuger, Leon F. A. G., Gronwald, Jacek, Lubinski, Jan, Jakubowska, Anna, Cybulski, Cezary, Brinton, Louise, Lissowska, Jolanta, Wentzensen, Nicolas, Song, Honglin, Rhenius, Valerie, Campbell, Ian, Eccles, Diana, Sieh, Weiva, Whittemore, Alice S., McGuire, Valerie, Rothstein, Joseph H., Sutphen, Rebecca, Anton-Culver, Hoda, Ziogas, Argyrios, Gayther, Simon A., Gentry-Maharaj, Aleksandra, Menon, Usha, Ramus, Susan J., Pearce, Celeste L., Pike, Malcolm C., Stram, Daniel O., Wu, Anna H., Kupryjanczyk, Jolanta, Dansonka-Mieszkowska, Agnieszka, Rzepecka, Iwona K., Spiewankiewicz, Beata, Goodman, Marc T., Wilkens, Lynne R., Carney, Michael E., Thompson, Pamela J., Heitz, Florian, du Bois, Andreas, Schwaab, Ira, Harter, Philipp, Pisterer, Jacobus, Hillemanns, Peter, Karlan, Beth Y., Walsh, Christine, Lester, Jenny, Orsulic, Sandra, Winham, Stacey J., Earp, Madalene, Larson, Melissa C., Fogarty, Zachary C., Hogdall, Estrid, Jensen, Allan, Kjaer, Susanne Kruger, Fridley, Brooke L., Cunningham, Julie M., Vierkant, Robert A., Schildkraut, Joellen M., Iversen, Edwin S., Terry, Kathryn L., Cramer, Daniel W., Bandera, Elisa V., Orlow, Irene, Pejovic, Tanja, Bean, Yukie, Hogdall, Claus, Lundvall, Lene, McNeish, Ian, Paul, James, Carty, Karen, Siddiqui, Nadeem, Glasspool, Rosalind, Sellers, Thomas, Kennedy, Catherine, Chiew, Yoke-Eng, Berchuck, Andrew, MacGregor, Stuart, Pharoah, Paul D. P., Goode, Ellen L., deFazio, Anna, Webb, Penelope M. and Chenevix-Trench, Georgia (2015) Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium. Clinical Cancer Research, 21 23: 5264-5276. doi:10.1158/1078-0432.CCR-15-0632

  • Kondrashova,Olga, Love, Clare J., Lunke, Sebastian, Hsu, Arthur L., Waring, Paul M., Taylor, Graham R., Australian Ovarian Cancer Study (AOCS) Group, Chenevix-Trench, G. and Wyld, D. (2015) High-throughput amplicon-based copy number detection of 11 genes in formalin-fixed paraffin-embedded ovarian tumour samples by MLPA-seq. PLoS One, 10 11: 1-14. doi:10.1371/journal.pone.0143006

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Supervision

View all Supervision

Publications

Journal Article

  • French, Juliet D., Johnatty, Sharon E., Lu, Yi, Beesley, Jonathan, Gao, Bo, Kalimutho, Murugan, Henderson, Michelle J., Russell, Amanda J., Kar, Siddhartha, Chen, Xiaoging, Hillman, Kristine M., Kaufmann, S, Sivakumaran H., O'Reilly, Martin, Wang, Chen, Korbie, Darren J., Lambrechts, Diether, Despierre, Evelyn, Van Nieuwenhuysen, Els, Lambrechts, Sandra, Vergote, Ignace, Karlan, Beth, Lester, Jenny, Orsulic, Sandra, Walsh, Christine, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Matsuo, Keitaro, Hosono, Satoyo, Pisterer, Jacobus, Hillemanns, Peter, Nakanishi, Toru, Yatabe, Yasushi, Goodman, Marc T., Lurie, Galine, Matsuno, Rayna K., Thompson, Pamela J., Pejovic, Tanja, Bean, Yukie, Heitz, Florian, Harter, Philipp, Du Bois, Andreas, Schwaab, Ira, Hogdall, Estrid, Kjaer, Susanne K., Jensen, Allan, Hogdall, Claus, Lundvall, Lene, Engelholm, Svend Aage, Brown, Bob, Flanagan, James M., Metcalf, Michelle D., Siddiqui, Nadeem, Sellers, Thomas, Fridley, Brooke, Cunningham, Julie, Schildkraut, Joellen M., Iversen, Ed, Weber, Rachel Palmieri, Brennan, Donal, Berchuck, Andrew, Pharoah, Paul, Harnett, Paul, Norris, Murray D., Haber, Michelle, Goode, Ellen L., Lee, Jason S., Khanna, Kum Kum, Meyer, Kerstin B., Chenevix-Trench, Georgia, DeFazio, Anna, Edwards, Stacey L. and MacGregor, Stuart (2016) Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Oncotarget, 7 6: 6353-6368. doi:10.18632/oncotarget.7047

  • Johnatty, Sharon E., Tyrer, Jonathan P., Kar, Siddhartha, Beesley, Jonathan, Lu, Yi, Gao, Bo, Fasching, Peter A., Hein, Alexander, Ekici, Arif B., Beckmann, Matthias W., Lambrechts, Diether, Van Nieuwenhuysen, Els, Vergote, Ignace, Lambrechts, Sandrina, Rossing, Mary Anne, Doherty, Jennifer A., Chang-Claude, Jenny, Modugno, Francesmary, Ness, Roberta B., Moysich, Kirsten B., Levine, Douglas A., Kiemeney, Lambertus A., Massuger, Leon F. A. G., Gronwald, Jacek, Lubinski, Jan, Jakubowska, Anna, Cybulski, Cezary, Brinton, Louise, Lissowska, Jolanta, Wentzensen, Nicolas, Song, Honglin, Rhenius, Valerie, Campbell, Ian, Eccles, Diana, Sieh, Weiva, Whittemore, Alice S., McGuire, Valerie, Rothstein, Joseph H., Sutphen, Rebecca, Anton-Culver, Hoda, Ziogas, Argyrios, Gayther, Simon A., Gentry-Maharaj, Aleksandra, Menon, Usha, Ramus, Susan J., Pearce, Celeste L., Pike, Malcolm C., Stram, Daniel O., Wu, Anna H., Kupryjanczyk, Jolanta, Dansonka-Mieszkowska, Agnieszka, Rzepecka, Iwona K., Spiewankiewicz, Beata, Goodman, Marc T., Wilkens, Lynne R., Carney, Michael E., Thompson, Pamela J., Heitz, Florian, du Bois, Andreas, Schwaab, Ira, Harter, Philipp, Pisterer, Jacobus, Hillemanns, Peter, Karlan, Beth Y., Walsh, Christine, Lester, Jenny, Orsulic, Sandra, Winham, Stacey J., Earp, Madalene, Larson, Melissa C., Fogarty, Zachary C., Hogdall, Estrid, Jensen, Allan, Kjaer, Susanne Kruger, Fridley, Brooke L., Cunningham, Julie M., Vierkant, Robert A., Schildkraut, Joellen M., Iversen, Edwin S., Terry, Kathryn L., Cramer, Daniel W., Bandera, Elisa V., Orlow, Irene, Pejovic, Tanja, Bean, Yukie, Hogdall, Claus, Lundvall, Lene, McNeish, Ian, Paul, James, Carty, Karen, Siddiqui, Nadeem, Glasspool, Rosalind, Sellers, Thomas, Kennedy, Catherine, Chiew, Yoke-Eng, Berchuck, Andrew, MacGregor, Stuart, Pharoah, Paul D. P., Goode, Ellen L., deFazio, Anna, Webb, Penelope M. and Chenevix-Trench, Georgia (2015) Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium. Clinical Cancer Research, 21 23: 5264-5276. doi:10.1158/1078-0432.CCR-15-0632

  • Kondrashova,Olga, Love, Clare J., Lunke, Sebastian, Hsu, Arthur L., Waring, Paul M., Taylor, Graham R., Australian Ovarian Cancer Study (AOCS) Group, Chenevix-Trench, G. and Wyld, D. (2015) High-throughput amplicon-based copy number detection of 11 genes in formalin-fixed paraffin-embedded ovarian tumour samples by MLPA-seq. PLoS One, 10 11: 1-14. doi:10.1371/journal.pone.0143006

  • Guo X., Long J., Zeng C., Michailidou K., Ghoussaini M., Bolla M.K., Wang Q., Milne R.L., Shu X.-O., Cai Q., Beesley J., Kar S.P., Andrulis I.L., Anton-Culver H., Arndt V., Beckmann M.W., Beeghly-Fadiel A., Benitez J., Blot W., Bogdanova N., Bojesen S.E., Brauch H., Brenner H., Brinton L., Broekss A., Bruning T., Burwinkel B., Cai H., Canisius S., Chang-Claude J., Choi J.-Y., Couch F.J., Cox A., Cross S.S., Czene K., Darabi H., Devilee P., Droit A., Dork T., Fasching P.A., Fletcher O., Flyger H., Fostira F., Gaborieau V., Garcia-Closas M., Giles G.G., Grip M., Guenel P., Haiman C.A., Hamann U., Hartman M., Hollestelle A., Hopper J.L., Hsiung C.-N., Ito H., Jakubowska A., Johnson N., Kabisch M., Kang D., Khan S., Knight J.A., Kosma V.-M., Lambrechts D., Le Marchand L., Li J., Lindblom A., Lophatananon A., Lubinski J., Mannermaa A., Manoukian S., Margolin S., Marme F., Matsuo K., McLean C.A., Meindl A., Muir K., Neuhausen S.L., Nevanlinna H., Nord S., Olson J.E., Orr N., Peterlongo P., Putti T.C., Rudolph A., Sangrajrang S., Sawyer E.J., Schmidt M.K., Schmutzler R.K., Shen C.-Y., Shi J., Shrubsole M.J., Southey M.C., Swerdlow A., Teo S.H., Thienpont B., Toland A.E., Tollenaar R.A.E.M., Tomlinson I.P.M., Truong T., Tseng C.-C., Van Den Ouweland A., Wen W., Winqvist R., Wu A., Yip C.H., Zamora M.P., Zheng Y., Hall P., Pharoah P.D.P., Simard J., Chenevix-Trench G., Dunning A.M., Easton D.F., Zheng W., Eeles R.A., Al Olama A.A., Kote-Jarai Z., Benlloch S., Antoniou A., McGuffog L., Offit K., Lee A., Dicks E., Luccarini C., Tessier D.C., Bacot F., Vincent D., La Boissiere S., Robidoux F., Nielsen S.F., Cunningham J.M., Windebank S.A., Hilker C.A., Meyer J., Angelakos M., Maskiell J., Van Der Schoot E., Rutgers E., Verhoef S., Hogervorst F., Boonyawongviroj P., Siriwanarungsan P., Schrauder M., Rubner M., Oeser S., Landrith S., Williams E., Ryder-Mills E., Sargus K., McInerney N., Colleran G., Rowan A., Jones A., Sohn C., Schneeweiss A., Bugert P., Alvarez N., Bernstein L., Lacey J., Wang S., Ma H., Lu Y., Clague De Hart J., Deapen D., Pinder R., Lee E., Schumacher F., Horn-Ross P., Reynolds P., Nelson D., Park H., Ziegler H., Wolf S., Hermann V., Lo W.-Y., Justenhoven C., Ko Y.-D., Baisch C., Fischer H.-P., Pesch B., Rabstein S., Lotz A., Harth V., Heikkinen T., Erkkila I., Aaltonen K., Von Smitten K., Antonenkova N., Hillemanns P., Christiansen H., Myohanen E., Kemilainen H., Thorne H., Niedermayr E., Bowtell D., Chenevix-Trench G., De Fazio A., Gertig D., Green A., Webb P., Green A., Parsons P., Hayward N., Webb P., Whiteman D., Fung A., Yashiki J., Peuteman G., Smeets D., Van Brussel T., Corthouts K., Obi N., Heinz J., Behrens S., Eilber U., Celik M., Olchers T., Peissel B., Scuvera G., Zaffaroni D., Bonanni B., Feroce I., Maniscalco A., Rossi A., Bernard L., Tranchant M., Valois M.-F., Turgeon A., Heguy L., Yee P.S., Kang P., Nee K.I., Mariapun S., Sook-Yee Y., Lee D., Ching T.Y., Taib N.A.M., Otsukka M., Mononen K., Selander T., Weerasooriya N., Krol-Warmerdam E., Molenaar J., Blom J., Szeszenia-Dabrowska N., Peplonska B., Zatonski W., Chao P., Stagner M., Bos P., Blom J., Crepin E., Nieuwlaat A., Heemskerk A., Higham S., Cramp H., Connley D., Balasubramanian S., Brock I., Kerin M., Miller N., Kerbrat P., Arveux P., Le Scodan R., Raoul Y., Laurent-Puig P., Mulot C., Stegmaier C., Butterbach K., Karstens J.H., Flesch-Janys D., Seibold P., Vrieling A., Nickels S., Radice P., Pylkas K., Jukkola-Vuorinen A., Kauppila S., Conroy D., Baynes C., Chua K. and Pilarski R. (2015) Fine-scale mapping of the 4q24 locus identifies & pr two Independent loci associated with breast cancer risk. Cancer Epidemiology Biomarkers and Prevention, 24 11: 1680-1691. doi:10.1158/1055-9965.EPI-15-0363

  • Kar, Siddhartha P., Tyrer, Jonathan P., Li, Qiyuan, Lawrenson, Kate, Aben, Katja K. H., Anton-Culver, Hoda, Antonenkova, Natalia, Chenevix-Trench, Georgia, Baker, Helen, Bandera, Elisa V., Bean, Yukie T., Beckmann, Matthias W., Berchuck, Andrew, Bisogna, Maria, Bjorge, Line, Bogdanova, Natalia, Brinton, Louise, Brooks-Wilson, Angela, Butzow, Ralf, Campbell, Ian, Carty, Karen, Chang-Claude, Jenny, Chen, Yian Ann, Chen, Zhihua, Cook, Linda S., Cramer, Daniel, Cunningham, Julie M., Cybulski, Cezary, Dansonka-Mieszkowska, Agnieszka, Dennis, Joe, Dicks, Ed, Doherty, Jennifer A., Doerk, Thilo, du Bois, Andreas, Duerst, Matthias, Eccles, Diana, Easton, Douglas F., Edwards, Robert P., Ekici, Arif B., Fasching, Peter A., Fridley, Brooke L., Gao, Yu-Tang, Gentry-Maharaj, Aleksandra, Giles, Graham G., Glasspool, Rosalind, Goode, Ellen L., Goodman, Marc T., Grownwald, Jacek, Harrington, Patricia, Harter, Philipp, Hein, Alexander, Heitz, Florian, Hildebrandt, Michelle A. T., Hillemanns, Peter, Hogdall, Estrid, Hogdall, Claus K., Hosono, Satoyo, Iversen, Edwin S., Jakubowska, Anna, Paul, James, Jensen, Allan, Ji, Bu-Tian, Karlan, Beth Y., Kjaer, Susanne K., Kelemen, Linda E., Kellar, Melissa, Kelley, Joseph, Kiemeney, Lambertus A., Krakstad, Camilla, Kupryjanczyk, Jolanta, Lambrechts, Diether, Lambrechts, Sandrina, Le, Nhu D., Lee, Alice W., Lele, Shashi, Leminen, Arto, Lester, Jenny, Levine, Douglas A., Liang, Dong, Lissowska, Jolanta, Lu, Karen, Lubinski, Jan, Lundvall, Lene, Massuger, Leon, Matsuo, Keitaro, McGuire, Valerie, McLaughlin, John R., McNeish, Iain A., Menon, Usha, Modugno, Francesmary, Moysich, Kirsten B., Narod, Steven A., Nedergaard, Lotte, Ness, Roberta B., Nevanlinna, Heli, Odunsi, Kunle, Olson, Sara H., Orlow, Irene, Orsulic, Sandra, Weber, Rachel Palmieri, Pearce, Celeste Leigh, Pejovic, Tanja, Pelttari, Liisa M., Permuth-Wey, Jennifer, Phelan, Catherine M., Pike, Malcolm C., Poole, Elizabeth M., Ramus, Susan J., Risch, Harvey A., Rosen, Barry, Rossing, Mary Anne, Rothstein, Joseph H., Rudolph, Anja, Runnebaum, Ingo B., Rzepecka, Iwona K., Salvesen, Helga B., Schildkraut, Joellen M., Schwaab, Ira, Shu, Xiao-Ou, Shvetsov, Yurii B., Siddiqui, Nadeem, Sieh, Weiva, Song, Honglin, Southey, Melissa C., Sucheston-Campbell, Lara E., Tangen, Ingvild L., Teo, Soo-Hwang, Terry, Kathryn L., Thompson, Pamela J., Timorek, Agnieszka, Tsai, Ya-Yu, Tworoger, Shelley S., van Altena, Anne M., Van Nieuwenhuysen, Els, Vergote, Ignace, Vierkant, Robert A., Wang-Gohrke, Shan, Walsh, Christine, Wentzensen, Nicolas, Whittemore, Alice S., Wicklund, Kristine G., Wilkens, Lynne R., Woo, Yin-Ling, Wu, Xifeng, Wu, Anna, Yang, Hannah, Zheng, Wei, Ziogas, Argyrios, Sellers, Thomas A., Monteiro, Alvaro N. A., Freedman, Matthew L., Gayther, Simon A. and Pharoah, Paul D. P. (2015) Network-based integration of GWAS and gene expression identifies a HOX-centric network associated with serous ovarian cancer risk. Cancer Epidemiology Biomarkers and Prevention, 24 10: 1574-1584. doi:10.1158/1055-9965.EPI-14-1270

  • Lawrenson, Kate, Li, Qiyan, Kar, Siddhartha, Seo, Ji-Heui, Tyrer, Jonathan, Spindler, Tassja J., Lee, Janet, Chen, Yibu, Karst, Alison, Drapkin, Ronny, Aben, Katja K. H., Anton-Culver, Hoda, Antonenkova, Natalia, Baker, Helen, Bandera, Elisa V., Bean, Yukie, Beckmann, Matthias W., Berchuck, Andrew, Bisogna, Maria, Bjorge, Line, Bogdanova, Natalia, Brinton, Louise A., Brooks-Wilson, Angela, Bruinsma, Fiona, Butzow, Ralf, Campbell, Ian G., Carty, Karen, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Chen, Anne, Chen, Zhihua, Cook, Linda S., Cramer, Daniel W., Cunningham, Julie M., Cybulski, Cezary, Dansonka-Mieszkowska, Agnieszka, Dennis, Joe, Dicks, Ed, Doherty, Jennifer A., Doerk, Thilo, Du Bois, Andreas, Duerst, Matthias, Eccles, Diana, Easton, Douglas T., Edwards, Robert P., Eilber, Ursula, Ekici, Arif B., Fasching, Peter A., Fridley, Brooke L., Gao, Yu-Tang, Gentry-Maharaj, Aleksandra, Giles, Graham G., Glasspool, Rosalind, Goode, Ellen L., Goodman, Marc T., Grownwald, Jacek, Harrington, Patricia, Harter, Philipp, Hasmad, Hanis Nazihah, Hein, Alexander, Heitz, Florian, Hildebrandt, Michelle A. T., Hillemanns, Peter, Hogdall, Estrid, Hogdall, Claus, Hosono, Satoyo, Iversen, Edwin S., Jakubowska, Anna, James, Paul, Jensen, Allan, Ji, Bu-Tian, Karlan, Beth Y., Kjaer, Susanne Kruger, Kelemen, Linda E., Kellar, Melissa, Kelley, Joseph L., Kiemeney, Lambertus A., Krakstad, Camilla, Kupryjanczyk, Jolanta, Lambrechts, Diether, Lambrechts, Sandrina, Le, Nhu D., Lee, Alice W., Lele, Shashi, Leminen, Arto, Lester, Jenny, Levine, Douglas A., Liang, Dong, Lissowska, Jolanta, Lu, Karen, Lubinski, Jan, Lundvall, Lene, Massuger, Leon F. A. G., Matsuo, Keitaro, McGuire, Valerie, McLaughlin, John R., Nevanlinna, Heli, McNeish, Ian, Menon, Usha, Modugno, Francesmary, Moysich, Kirsten B., Narod, Steven A., Nedergaard, Lotte, Ness, Roberta B., Azmi, Mat Adenan Noor, Odunsi, Kunle, Olson, Sara H., Orlow, Irene, Orsulic, Sandra, Weber, Rachel Palmieri, Pearce, Celeste L., Pejovic, Tanja, Pelttari, Liisa M., Permuth-Wey, Jennifer, Phelan, Catherine M., Pike, Malcolm C., Poole, Elizabeth M., Ramus, Susan J., Risch, Harvey A., Rosen, Barry, Rossing, Mary Anne, Rothstein, Joseph H., Rudolph, Anja, Runnebaum, Ingo B., Rzepecka, Iwona K., Salvesen, Helga B., Schildkraut, Joellen M., Schwaab, Ira, Sellers, Thomas A., Shu, Xiao-Ou, Shvetsov, Yurii B., Siddiqui, Nadeem, Sieh, Weiva, Song, Honglin, Southey, Melissa C., Sucheston, Lara, Tangen, Ingvild L., Teo, Soo-Hwang, Terry, Kathryn L., Thompson, Pamela J., Timorek, Agnieszka, Tsai, Ya-Yu, Tworoger, Shelley S., Van Altena, Anne M., Van Nieuwenhuysen, Els, Vergote, Ignace, Vierkant, Robert A., Wang-Gohrke, Shan, Walsh, Christine, Wentzensen, Nicolas, Whittemore, Alice S., Wicklund, Kristine G., Wilkens, Lynne R., Woo, Yin-Ling, Wu, Xifeng, Wu, Anna H., Yang, Hannah, Zheng, Wei, Ziogas, Argyrios, Monteiro, Alvaro, Pharoah, Paul D., Gayther, Simon A., Freedman, Matthew L., Grp, Australian Ovarian Canc Study, Bowtell, David, Webb, Penelope M. and Defazio, Anna (2015) Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer. Nature Communications, 6 1-14. doi:10.1038/ncomms9234

  • Kelemen L.E., Lawrenson K., Tyrer J., Li Q., Lee J.M., Seo J.-H., Phelan C.M., Beesley J., Chen X., Spindler T.J., Aben K.K.H., Anton-Culver H., Antonenkova N., Baker H., Bandera E.V., Bean Y., Beckmann M.W., Bisogna M., Bjorge L., Bogdanova N., Brinton L.A., Brooks-Wilson A., Bruinsma F., Butzow R., Campbell I.G., Carty K., Chang-Claude J., Chen Y.A., Chen Z., Cook L.S., Cramer D.W., Cunningham J.M., Cybulski C., Dansonka-Mieszkowska A., Dennis J., Dicks E., Doherty J.A., Dork T., Bois A.D., Durst M., Eccles D., Easton D.T., Edwards R.P., Eilber U., Ekici A.B., Engelholm S.A., Fasching P.A., Fridley B.L., Gao Y.-T., Gentry-Maharaj A., Giles G.G., Glasspool R., Goode E.L., Goodman M.T., Grownwald J., Harrington P., Harter P., Hasmad H.N., Hein A., Heitz F., Hildebrandt M.A.T., Hillemanns P., Hogdall E., Hogdall C., Hosono S., Iversen E.S., Jakubowska A., Jensen A., Ji B.-T., Karlan B.Y., Kellar M., Kelley J.L., Kiemeney L.A., Krakstad C., Kjaer S.K., Kupryjanczyk J., Lambrechts D., Lambrechts S., Le N.D., Lee A.W., Lele S., Leminen A., Lester J., Levine D.A., Liang D., Lissowska J., Lu K., Lubinski J., Lundvall L., Massuger L.F.A.G., Matsuo K., McGuire V., McLaughlin J.R., McNeish I., Menon U., Modugno F., Moes-Sosnowska J., Moysich K.B., Narod S.A., Nedergaard L., Ness R.B., Nevanlinna H., Adenan N.A.M., Odunsi K., Olson S.H., Orlow I., Orsulic S., Weber R.P., Paul J., Pearce C.L., Pejovic T., Pelttari L.M., Permuth-Wey J., Pike M.C., Poole E.M., Ramus S.J., Risch H.A., Rosen B., Rossing M.A., Rothstein J.H., Rudolph A., Runnebaum I.B., Rzepecka I.K., Salvesen H.B., Schildkraut J.M., Schwaab I., Shu X.-O., Shvetsov Y.B., Siddiqui N., Sieh W., Song H., Southey M.C., Sucheston L., Tangen I.L., Teo S.-H., Terry K.L., Thompson P.J., Tworoger S.S., Van Altena A.M., Nieuwenhuysen E.V., Vergote I., Vierkant R.A., Shan W.-G., Walsh C., Wentzensen N., Whittemore A.S., Wicklund K.G., Wilkens L.R., Sawicki W., Woo Y.-L., Wu X., Wu A.H., Yang H., Zheng W., Ziogas A., Sellers T.A., Freedman M.L., Chenevix-Trench G., Pharoah P.D.P., Gayther S.A. and Berchuck A. (2015) Genome-wide significant risk associations for mucinous ovarian carcinoma. Nature Genetics, 47 8: 888-897. doi:10.1038/ng.3336

  • Saunus, Jodi M., Quinn, MIchael C. J., Patch, Ann-Marie, Pearson, John V., Bailey, Peter J., Nones, Katia, McCart Reed, Amy E., Miller, David, Peter J. Wilson, Al-Ejeh, Fares, Mariasegaram, Mythily, Lau, Queenie, Withers, Teresa, Jeffree, Rosalind L., Reid, Lynne E., Da Silva, Leonard, Matsika, Admire, Niland, Colleen M., Cummings, Margaret C., Bruxner, Timothy J. C., Christ, Angelika N., Harliwong, Ivon, Idrisoglu, Senel, Manning, Suzanne, Nourse, Craig, Nourbakhsh, Ehsan, Wani, Shivangi, Anderson, Matthew J., Fink, J. Lynn, Holmes, Oliver, Kazakoff, Stephen, Leonard, Conrad, Newell, Felicity, Taylor, Darrin, Wood, Scott, Xu, Qinying, Kassahn, Karin S., Narayanan, Vairavan, Taib, Nur Aishah, Teo, Soo-Hwang, Chow, Yock Ping, kConFab, Jat, Parmjit S., Brandner, Sebastian, Flanagan, Adrienne M., Khanna, KumKum, Chenevix-Trench, Georgia, Grimmond, Sean M., Simpson, Peter T., Waddell, Nicola and Lakhani, Sunil R. (2015) Integrated genomic and transcriptomic analysis of human brain metastases identifies recurrently altered pathways of potential clinical significance. Journal of Pathology, 237 3: 363-378. doi:10.1002/path.4583

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  • Simpson, Peter T., Vargas, Ana Christina, Al-Ejeh, Fares, Khanna, Kum Kum, Chenevix-Trench, Georgia and Lakhani, Sunil R. (2011) Application of molecular findings to the diagnosis and management of breast disease: Recent advances and challenges. Human Pathology, 42 2: 153-165. doi:10.1016/j.humpath.2010.07.008

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  • Beesley, Jonathan, Johnatty, Sharon E., Chen, Xiaoqing, Spurdle, Amanda B., Peterlongo, Paolo, Barile, Monica, Pensotti, Valeria, Manoukian, Siranoush, Radice, Paolo, Australian Ovarian Cancer Study Group, Kathleen Cuningham Consortium for Research in Familial Breast Cancer and Chenevix-Trench, Georgia (2011) No evidence for an association between the earwax-associated polymorphism in ABCC11 and breast cancer risk in Caucasian women. Breast Cancer Research and Treatment, 126 1: 235-239. doi:10.1007/s10549-010-1292-2

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  • Mulligan, Anna Marie, Couch, Fergus J., Barrowdale, Daniel, Domchek, Susan M., Eccles, Diana, Nevanlinna, Heli, Ramus, Susan J., Robson, Mark, Sherman, Mark, Spurdle, Amanda B., Wappenschmidt, Barbara, Lee, Andrew, McGuffog, Lesley, Healey, Sue, Sinilnikova, Olga M., Janavicius, Ramunas, Hansen, Thomas V.O., Nielsen, Finn C., Ejlertsen, Bent, Osorio, Ana, Munoz-Repeto, Ivan, Duran, Mercedes, Godino, Javier, Pertesi, Maroulio, Benitez, Javier, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Pasini, Barbara, Papi, Laura, Ottini, Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Hamann, Ute, Verheus, Martijn, Meijers-Heijboer, Hanne E.J., Wijnen, Juul, Gomez Garcia, Encarna B., Nelen, Marcel R., Kets, C. Marleen, Seynaeve, Caroline, Tilanus-Linthorst, Madeleine M.A., van der Luijt, Rob B., van Os, Theo, Rookus, Matti, Frost, Debra, Jones, J. Louise, Evans, D. Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Donaldson, Alan, Dorkins, Huw, Gregory, Helen, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E., McCann, Emma, Murray, Alex, Peock, Susan, Godwin, Andrew, Schmutzler, Rita K., Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Deissler, Helmut, Gadzicki, Dorothea, Kast, Karin, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Schoenbuchner, Ines, Fiebig, Britta, Heinritz, Wolfram, Schafer, Dieter, Gevensleben, Heidrun, Caux-Moncoutier, Virginie, Fassy-Colcombet, Marion, Cornelis, Francois, Mazoyer, Sylvie, Leone, Melanie, Boutry-Kryza, Nadia, Hardouin, Agnes, Berthet, Pascaline, Muller, Daniele, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal, Coupier, Isabelle, Lebrun, Marine, Kientz, Caroline, Longy, Michel, Sevenet, Nicolas, Stoppa-Lyonnet, Dominique, Isaacs, Claudine, Caldes, Trinidad, de al Hoya, Miguel, Heikkinen, Tuomas, Aittomaki, Kristiina, Blanco, Ignacio, Lazaro, Conxi, Barkardottir, Rosa B., Soucy, Penny, Dumont, Martine, Simard, Jacques, Montagna, Marco, Tognazzo, Silvia, D'Andrea, Emma, Fox, Stephen, Yan, Max, Rebbeck, Timothy R., Olopade, Olufunmilayo I., Weitzel, Jeffrey N., Lynch,Henry T., Ganz, Patricia A., Tomlinson, Gail E., Wang, Xianshu, Fredericksen, Zachary, Pankratz, Vernon S., Lindor, Noralane M., Szabo, Csila, Offit, Kenneth, Sakr, Rita, Gaudet, Mia, Bhatia, Jasmine, Kauff, Noah, Singer, Christian F., Tea, Muy-Kheng, Gschwantler-Kaulich, Daphne, Fink-Retter, Anneliese, Mai, Phuong L., Greene, Mark H., Imyanitov, Evgeny, O'Malley, Frances P., Ozcelik, Hilmi, Glendon, Gordon, Toland, Amanda E., Gerdes, Anne-Marie, Thomassen, Mads, Kruse, Torben A., Jensen, Uffe Birk, Skytte, Anne-Bine, Caligo, Maria A., Soller, Maria, Henriksson, Karin, von Wachenfeldt, Anna, Arver, Brita, Stenmark-Askmalm, Marie, Karlsson, Per, Ding, Yuan Chun, Neuhausen, Susan L., Beattie, Mary, Pharoah, Paul D.P., Moysich, Kirsten B., Nathanson, Katherine L., Karlan, Beth Y., Gross, Jenny, John, Esther M., Daly, Mary B., Buys, Saundra M., Southey, Melissa C., Hopper, John L., Terry, Mary Beth, Chung, Wendy, Miron, Alexander F., Goldgar, David, Chenevix-Trench, Georgia, Easton, Douglas F., Andrulis, Irene L. and Antoniou, Antonis C. (2011) Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2. Breast Cancer Research, 13 6: R110.1-R110.20. doi:10.1186/bcr3052

  • Lurie, Galina, Wilkens, Lynne R., Thompson, Pamela J., Shvetsov, Yurii B., Matsuno, Rayna K., Carney, Michael E., Palmieri, Rachel T., Wu, Anna H., Pike, Malcolm C., Pearce, Celeste L., Menon, Usha, Gentry-Maharaj, Aleksandra, Gayther, Simon A., Ramus, Susan J., Whittemore, Alice S., McGuire, Valerie, Sieh, Weiva, Pharoah, Paul D. P., Song, Honglin, Gronwald, Jacek, Jakubowska, Anna, Cybulski, Cezary, Lubinski, Jan, Schildkraut, Joellen M., Berchuck, Andrew, Kjaer, Susanne Kruger, Hogdall, Estrid, Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Chenevix-Trench, Georgia, Webb, Penelope M., Beesley, Jonathan, The Australian Ovarian Cancer Study and Australian Cancer Study Groups, Goodman, Marc T. and The Ovarian Cancer Association Consortium (2011) Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: Pooled analysis within the ovarian cancer association consortium. PLoS One, 6 6: e20703-1-e20703-7. doi:10.1371/journal.pone.0020703

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  • Verderio, Paolo, Pizzamiglio, Sara, Southey, Melissa C., Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, Beesley, Jonathan, Australian Ovarian Cancer Study Group, kConFab, Schmutzler, Rita K., Engel, Christoph, Burwinkel, Barbara, Bugert, Peter, Ficarazzi, Filomena, Manoukian, Siranoush, Barile, Monica, Wappenschmidt, Barbara, Chenevix-Trench, Georgia, Radice, Paolo and Peterlongo, Paolo (2010) A BRCA1 promoter variant (rs11655505) and breast cancer risk. Journal of Medical Genetics, 47 4: 268-270. doi:10.1136/jmg.2009.073544

  • Flanagan, James M., Cocciardi, Sibylle, Waddell, Nic, Johnstone, Cameron N., Marsh, Anna, Henderson, Stephen, Simpson, Peter, da Silva, Leonard, kConFab Investigators, Khanna, Kumkum, Lakhani, Sunil, Boshoff, Chris, Chenevix-Trench, Georgia, Brown, Melissa, Cummings, Margaret and Edwards, Stacey (2010) DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status. American Journal of Human Genetics, 86 3: 420-433. doi:10.1016/j.ajhg.2010.02.008

  • Phelan, Catherine M., Tsai, Ya-Yu, Goode, Ellen L., Vierkant, Robert A., Fridley, Brooke L., Beesley, Jonathan, Chen, Xiao Qing, Webb, Penelope M., Chanock, Stephen, Cramer, Daniel W., Moysich, Kirsten, Edwards, Robert P., Chang-Claude, Jenny, Garcia-Closas, Montserrat, Yang, Hannah, Wang-Gohrke, Shan, Hein, Rebecca, Green, Adele C., Lissowska, Jolanta, Carney, Michael E., Lurie, Galina, Wilkens, Lynne R., Ness, Roberta B., Pearce, Celeste Leigh, Wu, Anna H., Van Den Berg, David J., Stram, Daniel O., Terry, Kathryn L., Whiteman, David C., Whittemore, Alice S., DiCioccio, Richard A., McGuire, Valerie, Doherty, Jennifer A., Rossing, Mary Anne, Anton-Culver, Hoda, Ziogas, Argyrios, Hogdall, Claus, Hogdall, Estrid, Kjaer, Susanne Krüger, Blaakaer, Jan, Quaye, Lydia, Ramus, Susan J., Jacobs, Ian, Song, Honglin, Pharoah, Paul D. P., Iversen, Edwin S., Marks, Jeffrey R., Pike, Malcolm C., Gayther, Simon A., Cunningham, Julie M., Goodman, Marc T., Schildkraut, Joellen M., Chenevix-Trench, Georgia, Berchuck, Andrew and Sellers, Thomas A. (2010) Polymorphism in the GALNT1 gene and epithelial ovarian cancer in non-hispanic white women: The Ovarian Cancer Association Consortium. Cancer Epidemiology Biomarkers and Prevention, 19 2: 600-604. doi:10.1158/1055-9965.EPI-09-0861

  • Lakhani, Sunil R., Khanna, Kum K. and Chenevix-Trench, Georgia (2010) Are estrogen receptor-positive breast cancers in BRCA1 mutation carriers sporadic?. Breast Cancer Research, 12 2: 104-1-104-2. doi:10.1186/bcr2483

  • Milne, Roger L., Gaudet, Mia M., Spurdle, Amanda B., Fasching, Peter A., Couch, Fergus J., Benitez, Javier, Arias Perez, Jose Ignacio, Zamora, M. Pilar, Malats, Nuria, dos Santos Silva, Isabel, Gibson, Lorna J., Fletcher, Olivia, Johnson, Nichola, Anton-Culver, Hoda, Ziogas, Argyrios, Figueroa, Jonine, Brinton, Louise, Sherman, Mark E., Lissowska, Jolanta, Hopper, John L., Dite, Gillian S., Apicella, Carmel, Southey, Melissa C., Sigurdson, Alice J., Linet, Martha S., Schonfeld, Sara J., Freedman, D. Michal, Mannermaa, Arto, Kosma, Veli-Matti, Kataja, Vesa, Auvinen, Paivi, Andrulis, Irene L., Glendon, Gord, Knight, Julia A., Weerasooriya, Nayana, Cox, Angela, Reed, Malcolm W. R., Cross, Simon S., Dunning, Alison M., Ahmed, Shahana, Shah, Mitul, Brauch, Hiltrud, Ko, Yon-Dschun, Bruning, Thomas, GENICA Network, Lambrechts, Diether, Reumers, Joke, Smeets, Ann, Wang-Gohrke, Shan, Hall, Per, Dzene, Kamila, Liu, Jianjun, Irwanto, Astrid K., Chenevix-Trench, Georgia, Holland, Helene, kConFab, AOCS, Giles, Graham G., Baglietto, Laura, Severi, Gianluca, Bojensen, Stig E., Nordestgaard, Borge G., Flyger, Henrik, John, Esther M., West, Dee W., Whittemore, Alice S., Vachon, Celine, Olson, Janet E., Fredericksen, Zachary, Kosel, Matthew, Hein, Rebecca, Vrieling, Alina, Flesch-Janys, Dieter, Heinz, Judith, Beckmann, Matthias W., Heusinger, Katharina, Ekici, Arif B., Haeberle, Lothar, Humphreys, Manjeet K., Morrison, Jonathan, Easton, Doug F., Pharoah, Paul D., Garcia-Closas, Montserrat, Goode, Ellen L., Chang-Claude, Jenny, Brown, Melissa, Cummings, Margaret and Lakhani, Sunil (2010) Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study. Breast Cancer Research, 12 6: R110.1-R110.11. doi:10.1186/bcr2797

  • Doherty, Jennifer A., Rossing, Mary Anne, Cushing-Haugen, Kara L., Chen, Chu, Van Den Berg, David J., Wu, Anna H., Pike, Malcolm C., Ness, Roberta B., Moysich, Kirsten, Chenevix-Trench, Georgia, Beesley, Jonathan, Webb, Penelope M., Chang-Claude, Jenny, Wang-Gohrke, Shan, Goodman, Marc T., Lurie, Galina, Thompson, Pamela J., Carney, Michael E., Hogdall, Estrid, Kruger Kjaer, Susanne, Hogdall, Claus, Goode, Ellen L., Cunningham, Julie M., Fridley, Brooke L., Vierkant, Robert A., Berchuck, Andrew, Moorman, Patricia G., Schildkraut, Joellen M., Palmieri, Rachel T., Cramer, Daniel W., Terry, Kathryn L., Yang, Hannah P., Garcia-Closas, Montserrat, Chanock, Stephen, Lissowska, Jolanta, Song, Honglin, Pharoah, Paul D.P., Shah, Mitul, Perkins, Barbara, McGuire, Valerie, Whittemore, Alice S., Di Cioccio, Richard A., Gentry-Maharaj, Aleksandra, Menon, Usha, Gayther, Simon A., Ramus, Susan J., Ziogas, Argyrios, Brewster, Wendy, Anton-Culver, Hoda, The Australian Ovarian Cancer Study Management Group, The Australian Cancer Study (Ovarian Cancer) and Leigh Pearce, Celeste (2010) ESR1/SYNE1 polymorphism and invasive epithelial ovarian cancer risk: An Ovarian Cancer Association Consortium Study. Cancer Epidemiology, Biomarkers & Prevention, 19 1: 245-250. doi:10.1158/1055-9965.EPI-09-0729

  • Walker, Logan C., Fredericksen, Zachary S., Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S., Lindor, Noralane M., Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, kConFab, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Mazoyer, Sylvie, Giraud, Sophie, Frickeer, Jean-Pierre, Muller, Daniele, Delnatte, Capucine, GEMO Study Collaborators, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Schonbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B., Verheus, Martijn, Hooning, Maartje J., van den Ouweland, Ans M. W., Nelen, Marcel R., Ausems, Margreet G. E. M., Aalfs, Cora M., van Asperen, Christi J., Devilee, Peter, Gerrits, Monique M., Waisfisz, Quinten f, Szabo, Csilla I., ModSQuaD2, Easton, Douglas F., Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Harrington, Patricia, Evans, D. Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, EMBRACE, Rebbeck, Tim, Nathanson, Katherine L., Domchek, Susan M., Singer, Christian F., Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K., Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A., Caligo, Maria Adelaide, Olsson, Hakan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, SWE-BRCA47, Sinilnikova, Olga M., McGuffog, Lesley, Antoniou, Antonis C., Chenevix-Trench, Georgia, Spurdle, Amanda B. and Couch, Fergus J. (2010) Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers. Breast Cancer Research, 12 6: R1020-1-R102-10. doi:10.1186/bcr2785

  • Arnold, Jeremy M., Choong, David Y. H., Thompson, Ella R., kConFab, Waddell, Nic, Lindeman, Geoffrey J., Visvader, Jane E., Campbell, Ian G., Chenevix-Trench, Georgia, Brown, Melissa, Cummings, Margaret and Edwards, Stacey (2010) Frequent somatic mutations of GATA3 in non-BRCA1/BRCA2 familial breast tumors, but not in BRCA1-, BRCA2- or sporadic breast tumors. Breast Cancer Research And Treatment, 119 2: 491-496. doi:10.1007/s10549-008-0269-x

  • Da Silva, Leonard, Simpson, Peter T., Smart, Chanek E., Cocciardi, Sibylle, Waddell, Nic, Lane, Annette, Morrison, Brian J., Vargas, Ana Cristina, Healey, Sue, Beesley, Jonathan, Pakkiri, Pria, Parry, Suzanne, Kurniawan, Nyoman, Reid, Lynne, Keith, Patricia, Faria, Paulo, Pereira, Emilio, Skalova, Alena, Bilous, Michael, Balleine, Rosemary L., Do, Hongdo, Dobrovic, Alexander, Fox, Stephen, Franco, Marcello, Reynolds, Brent, Khanna, Kum Kum, Cummings, Margaret, Chenevix-Trench, Georgia and Lakhani, Sunil R. (2010) HER3 and downstream pathways are involved in colonization of brain metastases from breast cancer. Breast Cancer Research, 12 4: R46-1-R46-11. doi:10.1186/bcr2603

  • Spurdle, Amanda B., Fahey, Paul, Chen, Xiaoqing, McGuffog, Lesley, kConFab, Easton, Douglas, Peock, Susan, Cook, Margaret, EMBRACE, Simard, Jacques, INHERIT, Rebbeck, Tim R., MAGIC, Antoniou, Antonis C. and Chenevix-Trench, Georgia (2009) Pooled analysis indicates that the GSTT1 deletion, GSTM1 deletion, and GSTP1 Ile105Val polymorphisms do not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers. Breast Cancer Research and Treatment, 122 1: 281-285. doi:10.1007/s10549-009-0601-0

  • G Chenevix-Trench and Spurdle, Amanda B. (2009) Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). British Journal of Cancer Management, 101 12: 2048-2054. doi:10.1038/sj.bjc.6605416

  • Whiteman, David C. and Georgia Chenevix-Trench (2009) Rare, Evolutionarily Unlikely Missense Substitutions in ATM Confer Increased Risk of Breast Cancer. American Journal of Human Genetics, 85 4: 427-446. doi:10.1016/j.ajhg.2009.08.018

  • Spurdle, Amanda B. and Georgia Chenevix-Trench (2009) No evidence that GATA3 rs570613 SNP modifies breast cancer risk. Breast Cancer Research and Treatment, 117 2: 371-379. doi:10.1007/s10549-008-0257-1

  • Spurdle, Amanda B. and G Chenevix-Trench (2009) The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. British Journal of Cancer, 101 8: 1456-1460. doi:10.1038/sj.bjc.6605279

  • Spurdle, Amanda B. and Georgia Chenevix-Trench (2009) Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers. Human Molecular Genetics, 18 22: 4442-4456. doi:10.1093/hmg/ddp372

  • Chenevix-Trench, Georgia (2009) A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nature Genetics, 41 9: 996-1000. doi:10.1038/ng.424

  • Spurdle, Amanda B. and Chenevix-Trench, Georgia (2009) Modification of Ovarian Cancer Risk by BRCA1/2-Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers. Cancer Research, 69 14: 5801-5810. doi:10.1158/0008-5472.CAN-09-0625

  • Spurdle, Amanda B. and Georgia Chenevix-Trench (2009) Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042. National Cancer Institute. Journal, 101 14: 1012-1018. doi:10.1093/jnci/djp167

  • Johnatty, Sharon E., Beesley, Jonathan, Chen, Xiaoqing, Spurdle, Amanda B., DeFazio, Anna, Webb, Penelope M. and Chenevix-Trench, Georgia (2009) Polymorphisms in the FGF2 Gene and Risk of Serous Ovarian Cancer: Results From the Ovarian Cancer Association Consortium. Twin Research and Human Genetics, 12 3: 269-275. doi:10.1375/twin.12.3.269

  • Rebbeck, TR, Antoniou, AC, Llopis, TC, Nevanlinna, H, Aittomaki, K, Simard, J, Spurdle, A B. and Chenevix-Trench, Georgia (2009) No association of TGFB1 L10P genotypes and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a multi-center cohort study. Breast Cancer Research and Treatment, 115 1: 185-192. doi:10.1007/s10549-008-0064-8

  • Spurdle, Amanda B., Deans, AJ, Duffy, David and Georgia Chenevix-Trench (2009) No evidence that CDKN1B (p27) polymorphisms modify breast cancer risk in BRCA1 and BRCA2 mutation carriers. Breast Cancer Research and Treatment, 115 2: 307-313. doi:10.1007/s10549-008-0083-5

  • Chenevix-Trench, Georgia and Spurdle, Amanda B. (2009) The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case–control and family analysis. Breast Cancer Research and Treatment, 115 1: 145-150. doi:10.1007/s10549-008-0045-y

  • Fasching, Peter A., Gayther, Simon, Pearce, Leigh, Schildkraut, Joellen M., Goode, Ellen, Thiel, Falk, Chenevix-Trench, Georgina, Chang-Claude, Jenny, Wang-Gohrke, Shan, Ramus, Susan, Pharoah, Paul and Berchuck, Andrew (2009) Role of genetic polymorphisms and ovarian cancer susceptibility. Molecular Oncology, 3 2: 171-181. doi:10.1016/j.molonc.2009.01.008

  • Georgia Chenevix-Trench (2009) Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nature Genetics, 41 5: 585-590. doi:10.1038/ng.354

  • Georgia Chenevix-Trench (2009) Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study. Human Molecular Genetics, 18 12: 2297-2304. doi:10.1093/hmg/ddp138

  • Dunning, A. M., Healey, C. S., Baynes, C., Maia, A. T., Scollen, S., Vega, A., Rodriguez, R., Barbosa-Morais, N. L., Ponder, B. A.J., Low, Y. L., Bingham, S., Haiman, C. A., Le Marchand, L., Broeks, A., Schmidt, M. K., Hopper, J., Southey, M., Beckmann, M. W., Fasching, P. A., Peto, J., Johnson, N., Bojesen, S. E., Nordestgaard, B., Milne, R. L., Benitez, J., Hamann, U., Ko, Y., Schmutzler, R. K., Burwinkel, B., Schurmann, P.., Dork, T, Heikkinen, T., Nevanlinna, H., Lindblom, A., Margolin, S., Mannermaa, A., Kosma, V. M., Chen, X. Q., Spurdle, A., Change-Claude, J., Flesch-Janys, D., Couch, F. J., Olson, J. E., Severi, G., Baglietto, L., Brresen-Dale, A. L., Kristensen, V., Hunter, D. J., Hankinson, S. E., Devilee, P., Vreeswijk, M., Lissowska, J., Brinton, L., Liu, J. J., Hall, P., Kang, D., Yoo, K. Y., Shen, C. Y., Yu, J. C., Anton-Culver, H., Ziogoas, A., Sigurdson, A., Struewing, J., Easton, D. F., Garcia-Closas, M., Humphreys, M. K., Morrison, J., Pharoah, P. D. P., Pooley, K. A. and Chenevix-Trench, G. (2009) Association of ESR1 gene tagging SNPs with breast cancer risk. Human Molecular Genetics, 18 6: 1131-1139. doi:10.1093/hmg/ddn429

  • Chenevix-Trench, Georgia (2009) Single Nucleotide Polymorphisms in the TP53 Region and Susceptibility to Invasive Epithelial Ovarian Cancer. Cancer Research, 69 6: 2349-2357. doi:10.1158/0008-5472.CAN-08-2902

  • Chenevix-Trench, Georgia (2009) Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium. Nature Publishing Group, 100 2: 412-420. doi:10.1038/sj.bjc.6604820

  • Arnold, JM, George, J, Tinker, AV, Tothill, R, Waddell, N, Simms, L, Locandro, B, Fereday, S, Traficante, N, Birrer, MJ, Defazio, A, Chenevix-Trench, G, Bowtelll, DDL and AOCS Study Grp (2008) Mutation of ERBB2 provides a novel alternative mechanism for the ubiquitous activation of RAS-MAPK in ovarian serous low malignant potential tumors. Molecular Cancer Research, 6 11: 1678-1690. doi:10.1158/1541-7786.MCR-08-0193

  • Ramus, Susan J., Vierkant, Robert A., Johnatty, Sharon E., Pike, Malcolm C., Van Den Berg, David J., Wu, Anna H., Pearce, Celeste Leigh, Menon, Usha, Gentry-Maharaj, Aleksandra, Gayther, Simon A., DiCioccio, Richard A., McGuire, Valerie, Whittemore, Alice S., Song, Honglin, Easton, Douglas F., Pharoah, Paul D. P., Garcia-Closas, Montserrat, Chanock, Stephen, Lissowska, Jolanta, Brinton, Louise, Terry, Kathryn L., Cramer, Daniel W., Tworoger, Shelly S., Hankinson, Susan E., Berchuck, Andrew, Moorman, Patricia G., Schildkraut, Joellen M., Cunningham, Julie M., Liebow, Mark, Kjaer, Susanne Krueger, Hogdall, Estrid, Hogdall, Claus, Blaaker, Jan, Ness, Roberta B., Moysich, Kirsten B., Edwards, Robert P., Carney, Michael E., Lurie, Galina, Goodman, Marc T., Wang-Gohrke, Shan, Kropp, Silke, Chang-Claude, Jenny, Webb, Penelope M., Chen, Xiaoqing, Beesley, Jonathan, Chenevix-Trench, Georgia and Goode, Ellen L. (2008) Consortium analysis of 7 candidate SNPs for ovarian cancer. International Journal of Cancer, 123 2: 380-388. doi:10.1002/ijc.23448

  • Waddell, N, Ten Haaf, A, Marsh, A, Johnson, J, Walker, LC, Gongora, M, Brown, M, Grover, P, Girolami, M, Grimmond, S, Chenevix-Trench, G, Spurdle, AB and kConFab Investigators (2008) BRCA1 and BRCA2 missense variants of high and low clinical significance influence lymphoblastoid cell line post-irradiation gene expression. PLoS Genetics, 4 5: Article Number: e1000080. doi:10.1371/journal.pgen.1000080

  • Spurdle, A.B., Lakhani, S.R., Healey, S., Parry, S., Da Silva, L. M., Brinkworth, R.I., Hopper, J.L., Brown, M.A., Babikyan, D., Chenevix-Trench, G., Tavtigian, S.V. and Goldgar, D.E. (2008) Clinical classification of BRCA1 and BRCA2 DNA sequence variants: The value of cytokeratin profiles and evolutionary analysis - A report from the kConFab Investigators. Journal of Clinical Oncology, 26 10: 1657-1663. doi:10.1200/JCO.2007.13.2779

  • Wayte, Nicola, Da Silva, Leonard, Chenevix-Trench, Georgia and Lakhani, Sunil R. (2008) What's in a cancer syndrome? Genes, phenotype and pathology. Pathology, 40 3: 247-259. doi:10.1080/00313020801911553

  • Beesley, Jonathan, Jordan, Susan J., Spurdle, Amanda B., Song, Honglin, Ramus, Susan J., Kjaer, Suzanne Kruger, Hogdall, Estrid, DiCioccio, Richard A., McGuire, Valerie, Whittemore, Alice S., Gayther, Simon A., Pharoah, Paul D.P., Webb, Penelope M., Chenevix-Trench, Georgia, Australian Ovarian Cancer Study Group, Australian Cancer Study (Ovarian Cancer) and Australian Breast Cancer Family Study (2007) Association Between Single-Nucleotide Polymorphisms in Hormone Metabolism and DNA Repair Genes and Epithelial Ovarian Cancer: Results from two Australian Studies and an Additional Validation Set. Cancer Epidemiology Biomarkers and Prevention, 16 12: 2557-2565. doi:10.1158/1055-9965.EPI-07-0542

  • Antoniou, Antonis C., Sinilnikova, Olga M., Simard, Jacques, Léoné, Mélanie, Dumont, Martine, Neuhausen, Susan L., Struewing, Jeffery P., Stoppa-Lyonnet, Dominique, Barjhoux, Laure, Hughes, David J., Coupier, Isabelle, Belotti, Muriel, Lasset, Christine, Bonadona, Valérie, Bignon, Yves-Jean, Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO), Rebbeck, Timothy R., Wagner, Theresa, Lynch, Henry T., Domchek, Susan M., Nathanson, Katherine L., Garber, Judy E., Weitzel, Jeffrey, Narod, Steven A., Tomlinson, Gail, Olopade, Olufunmilayo I., Godwin, Andrew, Isaacs, Claudine, Jakubowska, Anna, Lubinski, Jan, Gronwald, Jacek, Górski, Bohdan, Byrski, Tomasz, Huzarski, Tomasz, Peock, Susan, Cook, Margaret, Baynes, Caroline, Murray, Alexandra, Rogers, Mark, Daly, Peter A., Dorkins, Huw, Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers (EMBRACE), Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, German Consortium for Hereditary Breast and Ovarian Cancer (GCHBOC), Spurdle, Amanda B., Chen, Xiaoqing, Waddell, Nicola, Cloonan, Nicole, The Kathleen Cuningham Consortium for Research into Familial Breast Cancer (kConFab), Kirchhoff, Tomas, Offit, Kenneth, Offit, Kenneth, Friedman, Eitan, Kaufmann, Bella, Laitman, Yael, Galore, Gilli, Rennert, Gad, Lejbkowicz, Flavio, Raskin, Leon, Andrulis, Irene L., Ilyushik, Eduard, Ozcelik, Hilmi, Devilee, Peter, Vreeswijk, Maaike P. G., Greene, Mark H., Prindiville, Sheila A., Osorio, Ana, Benítez, Javier, Zikan, Michal, Szabo, Csilla I., Kilpivaara, Outi, Nevanlinna, Heli, Hamann, Ute, Durocher, Francine, Arason, Adalgeir, Couch, Fergus J., Easton, Douglas F. and Chenevix-Trench, Georgia (2007) RAD51 135G->C modifies breast cancer risk among BRCA2 mutation carriers: Results from a combined analysis of 19 studies. American Journal of Human Genetics, 81 6: 1186-1200. doi:10.1086/522611

  • Lovelock, Paul K., Spurdle, Amanda B., Mok, Myth T. S., Farrugia, Daniel J., Lakhani, Sunil R., Healey, Sue, Arnold, Stephen, Buchanan, Daniel, kConFab Investigators, Couch, Fergus J., Henderson, Berik R., Goldgar, David E., Tavtigian, Sean V., Chenevix-Trench, Georgia and Brown, Melissa A (2007) Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?. Breast Cancer Research, 9 6: R82: 1-13. doi:10.1186/bcr1826

  • Marsh, Anna, Healey, Sue, Lewis, Aaron, Spurdle, Amanda B., Kedda, Mary Anne, Khanna, Kum Kum, Mann, Graham J., Pupo, Gulietta M., Lakhani, Sunil R. and Chenevix-Trench, Georgia (2007) Mutation analysis of five candidate genes in familial breast cancer. Breast Cancer Research & Treatment, 105 3: 377-389. doi:10.1007/s10549-006-9461-z

  • Lovelock, Paul K., Wong, Ee Ming, Sprung, Carl N., Marsh, Anna, Hobson, Karen, French, Juliet D., Southey, Melissa, kConFab Investigators, Sculley, Tom, Pandeya, Nirmala, Brown, Melissa A., Chenevix-Trench, Georgia, Spurdle, Amanda B. and McKay, Michael J. (2007) Prediction of BRCA1 and BRCA2 mutation status using post-irradiation assays of lymphoblastoid cell lines is compromised by inter-cell-line phenotypic variability. Breast Cancer Research and Treatment, 104 3: 257-266. doi:10.1007/s10549-006-9415-5

  • Easton, Douglas F., Pooley, Karen A., Dunning, Alison M., Pharoah, Paul D. P., Thompson, Deborah, Ballinger, Dennis G., Struewing, Jeffery P., Morrison, Jonathan, Field, Helen, Luben, Robert, Wareham, Nicholas, Ahmed, Shahana, Healey, Catherine S., Bowman, Richard, SEARCH collaborators, Meyer, Kerstin B., Haiman, Christopher A., Kolonel, Laurence K., Henderson, Brian E., Marchand, Loic Le, Brennan, Paul, Sangrajrang, Suleeporn, Gaborieau, Valerie, Odefrey, Fabrice, Shen, Chen-Yang, Wu, Pei-Ei, Wang, Hui-Chun, Eccles Diana, Evans, D. Gareth, Peto, Julian, Fletcher, Olivia, Johnson, Nichola, Seal, Sheila, Stratton, Michael R., Rahman, Nazneen, Chenevix-Trench, Georgia, Bojesen, Stig E., Nordestgaard, Børge G., Axelsson, Christen K., Garcia-Closas, Montserrat, Brinton, Louise, Chanock, Stephen, Lissowska, Jolanta, Peplonska, Beata, Nevanlinna, Heli, Fagerholm, Rainer, Eerola, Hannaleena, Kang, Daehee, Yoo, Keun-Young, Noh, Dong-Young, Ahn, Sei-Hyun, Hunter, David J., Hankinson, Susan E., Cox, David G., Hall, Per, Wedren, Sara, Liu, Jianjun, Low, Yen-Ling, Bogdanova, Natalia, Schurmann, Peter, Dork, Thilo, Tollenaar, Rob A. E. M., Jacobi, Catharina E., Devilee, Peter, Klijn, Jan G. M., Sigurdson, Alice J., Doody, Michele M., Alexander, Bruce H., Zhang, Jinghui, Cox, Angela, Brock, Ian W., MacPherson, Gordon, Reed, Malcolm W. R., Couch, Fergus J., Goode, Ellen L., Olson, Janet E., Meijers-Heijboer, Hanne, van den Ouweland, Ans, Uitterlinden, Andre´, Rivadeneira, Fernando, Milne, Roger L., Ribas, Gloria, Gonzalez-Neira, Anna, Benitez, Javier, Hopper, John L., McCredie, Margaret, Southey, Melissa, Giles, Graham G., Schroen, Chris, Justenhoven, Christina, kConFab, AOCS Management Group, Mannermaa, Arto, Kosma, Veli-Matti, Kataja, Vesa, Hartikainen, Jaana, Day, Nicholas E., Cox, David R., Ponder, Bruce A. J., Spurdle, Amanda B., Beesley, Jonathan, Brown, Melissa, Cummings, Margaret, Lakhani, Sunil, Armes, Jane and Ward, Robyn (2007) Genome-wide association study identifies novel breast cancer susceptibility loci. Nature, 447 7148: 1087-1093. doi:10.1038/nature05887

  • Pagan, Julia K., Arnold, Jeremy, Hanchard, Kim J., Kumar, Raman, Bruno, Tiziana, Jones, Mathew J.K., Richard, Derek J., Forrest, Alistair, Spurdle, Amanda, Verdin, Eric, Crossley, Merlin, Fanciulli, Maurizio, Chenevix-Trench, Georgia, Young, David B. and Khanna, Kum Kum (2007) A novel corepressor, BCoR-L1, represses transcription through an interaction with CtBP. Journal of Biological Chemistry, 282 20: 15248-15257. doi:10.1074/jbc.M700246200

  • Spurdle, Amanda B., Chang, Jiun-Horng, Byrnes, Graham B., Chen, Xiaoqing, Dite, Gillian S., McCredie, Margaret R.E., Giles, Graham G., Southey, Melissa C., Chenevix-Trench, Georgia and Hopper, John L. (2007) A systematic approach to analysing gene-gene interactions: Polymorphisms at the microsomal epoxide hydrolase EPHX and glutathione S-transferase GSTM1, GSTT1, and GSTP1 loci and breast cancer risk. Cancer Epidemiology Biomarkers & Prevention, 16 4: 769-774. doi:10.1158/1055-9965.EPI-06-0776

  • Greenman, Christopher, Stephens, Philip, Smith, Raffaella, Dalgliesh, Gillian L., Hunter, Christopher, Bignell, Graham, Davies, Helen, Teague, John, Butler, Adam, Claire Stevens, Edkins, Sarah, O'Meara, Sarah, Vastrik, Imre, Schmidt, Esther E., Avis, Tim, Barthorpe, Syd, Bhamra, Gurpreet, Buck, Gemma, Choudhury, Bhudipa, Cole, Jodie, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jon, Jenkinson, Andy, Jones, David, Menzies, Andy, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, Dave, Shepherd, Rebecca, Small, Alexandra, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Cahill, Daniel P., Louis, David N., Goldstraw, Peter, Nicholson, Andrew G., Brasseur, Francis, Looijenga, Leendert, Weber, Barbara L., Chiew, Yoke-Eng, Defazio, Anna, Greaves, Mel F., Green, Anthony R., Campbell, Peter, Birney, Ewan, Easton, Douglas F., Chenevix-Trench, Georgia, Tan, Min-Han, Khoo, Sok Kean, Teh, Bin Tean, Yuen, Siu Tsan, Leung, Suet Yi, Wooster, Richard, Futreal, P. Andrew and Stratton, Michael R. (2007) Patterns of somatic mutation in human cancer genomes. Nature, 446 7132: 153-158. doi:10.1038/nature05610

  • Chenevix-Trench, Georgia, Milne, Roger L., Antoniou, Antonis C., Couch, Fergus J., Easton, Douglas F. and Goldgar, David E. (2007) An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2(CIMBA). Breast Cancer Research, 9 2: 1-4. doi:10.1186/bcr1670

  • Lose, Felicity, Arnold, Jeremy, Young, David B., Brown, Carolyn J., Mann, Graham J., Pupo, Gulietta M., Khanna, Kum Kum, Chenevix-Trench, Georgia and Spurdle, Amanda B. (2007) BCoR-L1 variation and breast cancer. Breast Cancer Research, 9 4: 1-12. doi:10.1186/bcr1759

  • Waddell, Nic, Jonnalagadda, Jyoti, Marsh, Anna, Grist, Scott, Jenkins, Mark, Hobson, Karen, Taylor, Malcolm, Lindeman, Geoff J., Tavtigian, Sean V., Suthers, Graeme, Goldgar, David, Oefner, Peter J., kConFab Investigators, Taylor, Darrin, Grimmond, Sean, Khanna, Kum Kum and Chenevix-Trench, Georgia (2006) Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling. Genes Chromosomes and Cancer, 45 12: 1169-1181. doi:10.1002/gcc.20381

  • Smith, Paula, McGuffog, Lesley, Easton, Douglas F., Mann, Graham J., Pupo, Gulietta M., Newman, Beth, Chenevix-Trench, Georgia, Szabo, Csilla, Southey, Melissa, Renard, Helene, Odefrey, Fabrice, Lynch, Henry, Stoppa-Lyonnet, Dominique, Couch, Fergus, Hopper, John L., Giles, Graham G., McCredie, Margaret R. E., Buys, Saundra, Andrulis, Irene, Senie, Ruby, Goldgar, David E., Oldenburg, Rogier, Kroeze-Jansema, Karin, Kraan, Jaennelle, Meijers-Heijboer, Hanne, Klijn, Jan G.M, van Asperen, Christi, van Leeuwen, Inge, Vasen, Hans F. A., Cornelisse, Cees J., Devilee, Peter, Baskcomb, Linda, Seal, Sheila, Barfoot, Rita, Mangion, Jon, Hall, Anita, Edkins, Sarah, Rapley, Elizabeth, Wooster, Richard, Chang-Claude, Jenny, Eccles, Diana, Evans, D. Gareth, Futreal, P. Andrew, Nathanson, Katherine L., Weber, Barbara L., Rahman, Nazneen and Stratton, Michael R. (2006) A genome wide linkage search for breast cancer susceptibility genes. Genes Chromosomes and Cancer, 45 7: 646-655. doi:10.1002/gcc.20330

  • Lovelock P. K., Healey, S., Au, W., Sum, E, Y. M., Tesoriero, A., Wong, E. M., Hinson, S., Brinkworth, R., Bekessy, A., Diez, O., Izatt, L., Solomon, E., Jenkins, M., Renard, H., Hopper, J., Waring, P., kConFab Investigators, Tavtigian, S. V., Goldgar, D., Lindeman, G J ., Visvader, J. E., Couch, F. J., Henderson, B. R., Southey, M., Chenevix-Trench, G., Spurdle, A. B. and Brown, M. A. (2006) Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants. Journal of Medical Genetics, 43 1: 74-83. doi:10.1136/jmg.2005.033258

  • Fleming, Jean S., Beaugie, Clare R., Haviv, Izhak, Chenevix-Trench, Georgia and Tan, Olivia L. (2006) Incessant ovulation, inflammation and epithelial ovarian carcinogenesis: Revisiting old hypotheses. Molecular and Cellular Endocrinology, 247 1-2: 4-21. doi:10.1016/j.mce.2005.09.014

  • Chenevix-Trench, Georgia, Healey, Sue, Lakhani, Sunil, Waring, Paul, Cummings, Margaret, Brinkworth, Ross, Deffenbaugh, Amie M., Burbidge, Lynn Anne, Pruss, Dmitry, Judkins, Thad, Scholl, Tom, Bekessy, Anna, Marsh, Anna, Lovelock, Paul, Wong, Ming, Tesoriero, Andrea, Renard, Helene, Southey, Melissa, Hopper, John L., Yannoukakos, Koulis, Brown, Melissa, kConFab Investigators, Easton, Douglas, Tavtigian, Sean V., Goldgar, David and Spurdle, Amanda B. (2006) Genetic and Histopathologic Evaluation of BRCA1 and BRCA2 DNA Sequence Variance of Unknown Clinical Significance. Cancer Research, 66 4: 2019-2027. doi:10.1158/0008-5472.CAN-05-3546

  • Lose, Felicity, Lovelock, Paul, Chenevix-Trench, Georgia, Mann, Graham J., Pupo, Gulietta M. and Spurdle, Amanda B. (2006) Variation in the RAD51 gene and familial breast cancer. Breast Cancer Research, 8 3: R26-1-R26-7. doi:10.1186/bcr1415

  • Lewis, Aaron G., Flanagan, James, Marsh, Anna, Pupo, Gulietta M., Mann, Graham, Spurdle, Amanda B., Lindeman, Geoffrey J., Visvader, Jane E., Brown, Melissa A., Chenevix-Trench, Georgia and KConFab, Kathleen Cuningham Foundation (2005) Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer. Breast Cancer Research, 7 6: R1005-R1016. doi:10.1186/bcr1336

  • Pettigrew, Christopher, Wayte, Nicola, Lovelock, Paul K., Tavtigian, Sean V, Chenevix-Trench, Georgia, Spurdle, Amanda B. and Brown, Melissa A. (2005) Evolutionary conservation analysis increases the colocalization of predicted exonic splicing enhancers in the BRCA1 gene with missense sequence changes and in-frame deletions, but not polymorphisms. Breast Cancer Research, 7 6: R929-R939. doi:10.1186/bcr1324

  • Marsh, A., Wicking, C. A., Wainwright, B. J. and Chenevix-Trench, G. (2005) DHPLC analysis of patients with nevoid basal cell carcinoma syndrome reveals novel PTCH missense mutations in the serol-sensing domain. Human Mutation, 26 3: 283-293. doi:10.1002/humu.9365

  • Thompson, Deborah, Antoniou, Antonis C., Jenkins, Mark, Marsh, Anna, Chen, Xiaoqing, Wayne, Tierney, Tesoriero, Andrea, Milne, Roger, Spurdle, Amanda, Thorstenson, Yvonne, Southey, Melissa, Giles, Graham G., kConFab Investigators,, Khanna, Kum Kum, Sambrook, Joseph, Oefner, Peter, Goldgar, David, Hopper, John L., Easton, Doug and Chenevix-Trench, Georgia (2005) Two ATM variants and breast cancer risk. Human Mutation, 25 6: 594-595. doi:10.1002/humu.9344

  • Arnold, J. M., Huggard, P. R., Cummings, M., Ramm, G. A. and Chenevix-Trench, G. (2005) Reduced expression of chemokine (C-C motif) ligand-2 (CCL2) in ovarian adenocarcinoma. British Journal of Cancer, 92 11: 2024-2031. doi:10.1038/sj.bjc.6602596

  • Webb, Penelope, Hopper, John L., Newman, Beth, Chen, Xiaoqing, Kelemen, Livia, Giles, Graham G., Southey, Melissa C., Chenevix-Trench, Georgia and Spurdle, Amanda B. (2005) Double-strand break repair gene polymorphisms and risk of breast or ovarian cancer. Cancer Epidemiology Biomarkers and Prevention, 14 2: 319-323. doi:10.1158/1055-9965.EPI-04-0335

  • Jekimovs, C. R., Chen, X., Arnold, J., Gatei, M., Richardson, D. J., kConFab Investigators, Spurdle, A. B., Khanna, K. K. and Chenevix-Trench, G. (2005) Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals. British Journal Of Cancer, 92 4: 784-790. doi:10.1038/sj.bjc.6602381

  • Tesoriero, A. A., Wong, E. M., Jenkins, M. A., Hopper, J. L., KConFab, K. C. F., Brown, M. A., Chenevix-Trench, G., Spurdle, A. B. and Southey, M. C. (2005) Molecular characterization and cancer risk associated with BRCA1 and BRCA2 splice site variants identified in multiple-case breast cancer families. Human Mutation, 26 5: 495-495. doi:10.1002/humu.9379

  • Kelemen, Livia, Spurdle, Amanda B., Purdie, David M., Gertig, Dorota and Chenevix-Trench, Georgia (2005) RAD52 Y415X truncation polymorphism and epithelial ovarian cancer risk in Australian women. Cancer Letters, 218 2: 191-197. doi:10.1016/j.canlet.2004.09.023

  • Khanna, Kum Kum and Chenevix-Trench, Georgia (2004) ATM and Genome Maintenance: Defining Its Role in Breast Cancer Susceptibility. Journal of Mammary Gland Biology and Neoplasia, 9 3: 247-262. doi:10.1023/B:JOMG.0000048772.92326.a1

  • Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, Dite, Gillian S., Cui, Jisheng, McCredie, Margaret R. E., Giles, Graham G., Ellis-Steinborner, Sarah, Venter, Deon J., Newman, Beth, Southey, Melissa C. and Chenevix-Trench, Georgia (2002) The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years. Cancer Epidemiology Biomarkers & Prevention, 11 4: 413-416.

  • Chenevix-Trench, Georgia, Spurdle, Amanda B., Gatei, Magtouf, Kelly, Helena, Marsh, Anna, Chen, Xiaoqing, Donn, Karen, Cummings, Margaret C., Nyholt, Dale, Jenkins, Mark A., Scott, Clare, Pupo, Gulietta M., Dork, Thilo, Bendix, Regina, Kirk, Judy, Tucker, Katherine, McCredie, Margaret R. E., Hopper, John L., Sambrook, Joseph, Mann, Graham J. and Khanna, Kum Kum (2002) Dominant negative ATM mutations in breast cancer families. Journal of the National Cancer Institute, 94 3: 205-215. doi:10.1093/jnci/94.3.205

  • Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, McCredie, Margaret R. E., Giles, Graham G., Newmann, Beth, Chenevix-Trench, Georgia and Khanna, KumKum (2002) No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer. Breast Cancer Research, 4 6: R15/1-R15/6. doi:10.1186/bcr534

  • Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, McCredie, Margaret R. E., Giles, Graham G., Venter, Deon J., Southey, Melissa C. and Chenevix-Trench, Georgia (2002) The progesterone receptor exon 4 Va1660Leu G/T polymorphism and risk of breast cancer in Australian women. Cancer Epidemiology Biomarkers & Prevention, 11 5: 439-443.

  • Spurdle, Amanda B., Hopper, John L., Chen, Xiaoqing, Dite, Gillian S., McCredie, Margaret R. E., Giles, Graham G., Venter, Deon J., Southey, Melissa C., Purdie, David M. and Chenevix-Trench, Georgia (2001) The steroid 5α-reductase type II TA repeat polymorphism is not associated with risk of breast or ovarian cancer in Australian women. Cancer Epidemiology, Biomarkers and Prevention, 10 12: 1287-1293.

  • Boonchai, Waranya, Green, Adele, Ng, Jack, Dicker, Anthony and Chenevix-Trench, Georgia (2001) Basal cell carcinoma in chronic arsenicism occurring in Queensland, Australia after ingestion of an asthma medication. Journal of the American Academy of Dermatology, 43 4: 664-669. doi:10.1067/mjd.2000.107939

  • Spurdle, Amanda B., Webb, Penelope M., Purdie, David M., Chen, Xiaoqing, Green, Adele and Chenevix-Trench, Georgia (2001) No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer. Carcinogenesis, 22 5: 717-721. doi:10.1093/carcin/22.5.717

  • Francis-Thickpenny, K. M., Richardson, D. ., van Ee, C. C., Love, D.R., Winship, I. M., Baguley, B. C., Chenevix-Trench, G. and Shelling, A. N. (2001) Analysis of the TGF beta functional pathway in epithelial ovarian carcinoma. British Journal of Cancer, 85 5: 687-691. doi:10.1054/bjoc.2001.1950

  • Arnold, J. M., Mok, S. C., Purdie, D. and Chenevix-Trench, G. (2001) Decreased expression of the Id3 gene at 1p36.1 in ovarian adenocarcinomas. British Journal of Cancer, 84 3: 352-359. doi:10.1054/bjoc.2000.1620

  • Spurdle, Amanda B., Webb, Penelope M., Purdie, David M., Chen, Xiaoqing, Green, Adele and Chenevix-Trench, Georgia (2001) Polymorphisms at the glutathione S-transferase GSTM1, GSTT1 and GSTP1 loci: risk of ovarian cancer by histological subtype. Carcinogenesis, 22 1: 67-72. doi:10.1093/carcin/22.1.67

  • Arnold, J. M., Cummings, M., Purdie, D. and Chenevix-Trench, G. (2001) Reduced expression of intercellular adhesion molecule-1 in ovarian adenocarcinomas. British Journal of Cancer, 85 9: 1351-1358. doi:10.1054/bjoc.2001.2075

  • Marsh, Anna, Spurdle, Amanda B., Turner, Bruce C., Fereday, Sian, Thorne, Heather, Pupo, Gulietta M., Mann, Graham J., Hopper, John L., Sambrook, Joseph F., Chenevix-Trench, Georgia, Australian Breast Canc Family Stud and K Cunningham Fdn Consortium Res Fa (2001) The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia. Breast Cancer Research, 3 5: 346-349. doi:10.1186/bcr319

  • Spurdle, Amanda B., Purdie, David M., Webb, Penelope M., Chen, Xiaoqing, Green, Adele and Chenevix-Trench, Georgia (2001) The microsomal epoxide hydrolase Tyr113His polymorphism: Association with risk of ovarian cancer. Molecular Carcinogenesis, 30 1: 71-78. doi:10.1002/1098-2744(200101)30:1<71::AID-MC1015>3.0.CO;2-9

  • Spurdle, Amanda B., Hopper, John L., Dite, Gillian S, Chen, Xiaoqing, Cui, Jisheng, McCredie, Margaret R. E., Giles, Graham G., Southey, Melissa C., Venter, Deon J., Easton, Douglas F. and Chenevix-Trench, Georgia (2000) CYP17 promoter polymorphism and breast cancer in Australian women under age forty years. Journal of the National Cancer Institute, 92 20: 1674-1681. doi:10.1093/jnci/92.20.1674

  • Evans, T, Boonchai, W, Shanley, S, Smyth, I, Gillies, S, Georgas, K, Wainwright, B, Chenevix-Trench, G and Wicking, C (2000) The spectrum of patched mutations in a collection of Australian basal cell carcinomas. Human Mutation, 16 1: 43-48. doi:10.1002/1098-1004(200007)16:1<43::AID-HUMU8>3.0.CO;2-7

  • Imyanitov, EN, Togo, AV, Suspitsin, EN, Grigoriev, MY, Pozharisski, KM, Turkevich, EA, Hanson, KP, Hayward, NK, Chenevix-Trench, G, Theillet, C and Lavin, MF (2000) Evidence for microsatellite instability in bilateral breast carcinomas. Cancer Letters, 154 1: 9-17. doi:10.1016/S0304-3835(99)00444-9

  • Osborne, R., Hopper, J. L., Kirk, J. M., Chenevix-Trench, G., Thorne, H. J. and Sambrook, J.P. (2000) kConFab: a research resource of Australasian breast cancer families. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer. Medical Journal of Australia, 172 9: 463-464.

  • Boonchai, Waranya, Walsh, Michael, Cummings, Margaret and Chenevix-Trench, Georgia (2000) Expression of p53 in arsenic-related and sporadic basal cell carcinoma. Archives of Dermatology, 136 2: 195-198. doi:10.1001/archderm.136.2.195

  • Wilson, PJ, McGlinn, E, Marsh, A, Evans, T, Arnold, J, Wright, K, Biden, K, Young, J, Wainwright, B, Wicking, C and Chenevix-Trench, G (2000) Sequence variants of DLC1 in colorectal ovarian tumours. Human Mutation, 15 2: 156-165. doi:10.1002/(SICI)1098-1004(200002)15:2

  • Spurdle, A. B., Webb, P. M., Chen, X. D., Martin, N. G., Giles, G. G., Hopper, J. L. and Chenevix-Trench, G. (2000) Androgen receptor EXON 1 CAG repeat length and risk of ovarian cancer. International Journal of Cancer, 87 5: 637-643. doi:10.1002/1097-0215(20000901)87:5<637::AID-IJC3>3.0.CO;2-R

  • Spurdle, Amanda B., Chen, Xiaoqing, Abbazadegan, Mohammed, Martin, Nicholas, Khoo, Soo-Keat, Hurst, Terry, Ward, Bruce, Webb, Penelope M. and Chenevix-Trench, Georgia (2000) CYP17 promotor polymorphism and ovarian cancer risk. International Journal of Cancer, 86 3: 436-439. doi:10.1002/(SICI)1097-0215(20000501)86:3<436::AID-IJC21>3.0.CO;2-A

  • Boonchai, W., Walsh, M., Cummings, M. C. and Chenevix-Trench, G. (2000) Expression of b-catenin, a key mediator of the wnt signaling pathway, in basal cell carcinoma. Archives of Dermatology, 136 7: 937-938. doi:10.1001/archderm.136.7.937

  • Bianco, T., Chenevix-Trench, G., Walsh, D. C. A., Cooper, J. E. and Dobrovic, A. (2000) Tumour-specific distribution of BRCA1 promoter region methylation supports a pathogenetic role in breast and ovarian cancer. Carcinogenesis, 21 2: 147-151. doi:10.1093/carcin/21.2.147

  • Hopper, John L., Chenevix-Trench, Georgia, Jolley, Damien J., Dite, Gillian S., Jenkins, Mark A., Venter, Deon J., McCredie, Margaret R. E. and Giles, Graham G. (1999) Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the co-operative family registry for breast cancer studies (CFRBCS). Journal of the National Cancer Institute. Monographs, 26 95-100.

  • Wright, Kim, Wilson, Peter, Morland, Sarah, Campbell, Ian, Walsh, Michael, Hurst, Terry G., Ward, Bruce G., Cummings, Margaret C. and Chenevix-Trench, Georgia (1999) Beta-catenin mutation and expression analysis in ovarian cancer: Exon 3 mutations and nuclear translocation in 16% of endometrioid tumour. International Journal of Cancer, 82 5: 625-629. doi:10.1002/(SICI)1097-0215(19990827)82:5

  • Imyanitov, Evgeny N., Birrell, Geoff W., Filippovich, Igor, Sorokina, Natasha, Arnold, Jeremy, Mould, Michelle A., Wright, Kim, Walsh, Michael, Mok, Samuel C ., Lavin, Martin F., Chenevix-Trench, Georgia and Khanna, Kum Kum (1999) Frequent loss of heterozygosity at 1p36 in ovarian adenocarcinomas but the gene encoding p73 is unlikely to be the target. Oncogene, 18 32: 4640-4642. doi:10.1038/sj.onc.1202863

  • Spurdle, A. B., Dite, G. S., Chen, X. Q., Mayne, C. J., Southey, M. C., Batten, L. E., Chy, H., Trute, L, McCredie, M. R. E., Giles, G. G., Armes, J., Venter, D. J., Hopper, J. L. and Chenevix-Trench, G. (1999) Androgen receptor exon 1 CAG repeat length and breast cancer in women before age forty years. Journal of the National Cancer Institute, 91 11: 961-966. doi:10.1093/jnci/91.11.961

  • Georgas, K. M., Burridge, Linda M., Smith, K., Holmes, Greg P., Chenevix-Trench, G., Ioannou, P. A. and Little, M. H. (1999) Assignment of the human slit homologue SLIT2 to human chromosome band 4p15.2. Cytogenetics and Cell Genetics, 86 3-4: 246-247. doi:10.1159/000015351

  • Smyth, I., Narang, M. A., Evans, T. M., Heimann, C., Nakamura, Y., Chenevix-Trench, G., Pietsch, T., Wicking, C. A. and Wainwright, B. J. (1999) Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene in basal cell carcinoma and medulloblastoma on chromosome 1p32. Human Molecular Genetics, 8 2: 291-297. doi:10.1093/hmg/8.2.291

  • Wicking, C, Gillies, S, Smyth, I, Shanley, S, Fowles, L, Ratcliffe, J, Wainwright, B and ChenevixTrench, G (1997) De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype. American Journal of Medical Genetics Part A, 73 3: 304-307. doi:10.1002/(SICI)1096-8628(19971219)73:3<304::AID-AJMG14>3.0.CO;2-N

Conference Publication

  • Saunus, J. M., Quinn, M. C. J., Patch, A. M., Pearson, J. V., Bailey, P. J., Cloonan, N., Nones, K., Miller, D., Mariasegaram, M., Lau, Q., Jeffree, L., Khanna, K. K., Chenevix-Trench, G., Grimmond, S. M., Simpson, P. T., Waddell, N. and Lakhani, S. R. (2015). Genomic and transcriptomic landscapes of human brain metastases. In: 15th International Biennial Congress of the Metastasis Research Society, Heidelberg, Germany, (236-236). June 28th–July 1st, 2014. doi:10.1007/s10585-015-9708-3

  • Brown, M. A., Chenevix-Trench, G., Lovelock, P. K., Pettigrew, C., Spurdle, A. B., Tavtigian, S. and Wayte, N. J. (2005). Evolutionary conservation analysis may help identify functional exonic splice enhancer motifs in BRCA1 and BRCA2. In: Proceedings of the Familial Cancer 2005: Research and Practice. Familial Cancer 2005: Research and Practice, Couran Cove, Queensland, (). 30 August - 3 September, 2005.

  • Chenevix-Trench, G., Healey, S. C., Lakhani, S., Brinkworth, R. I., KConFab, K. C. F., Marsh, A., Brown, M. A., Easton, D. F., Tavtigian, S., Goldgar, D. E. and Spurdle, A. B. (2005). Genetic and immunohistopathological evaluation of BRCA1 and BRCA2 unclassified variants. In: Proceedings of the Familial Cancer 2005: Research and Practice. Familial Cancer 2005: Research and Practice, Couran Cove, Queensland, (). 30 August - 3 September, 2005.

  • Brown, M. A., Chenevix-Trench, G., French, J. D., Hobson, K., KConFab Investigators, Lovelock, P. K., Marsh, A., McKay, M., Pandeya, N., Sculley, T., Southey, M. C., Sprung, C. N., Spurdle, A. B. and Wong, E. M. (2005). Prediction of BRCA1 and BRCA2 mutation status using post-irradiation assays of lymphoblastoid cell lines is compromised by inter-cell line phenotypic variability. In: Proceedings of the Familial Cancer 2005: Research and Practice. Familial Cancer 2005: Research and Practice, Couran Cove, (). 30 August - 3 September, 2005.

  • Wright, K., Walsh, M. D., Cummings, M. C. and Chenevix-Trench, G. (1999). The E-cadherin-catenin system in ovarian cancer. In: Biochim Biophys Acta: Abstracts of the 11th Lorne Cancer Conference. 11th Lorne Cancer Conference, Lorne, Victoria, Australia, (721-721). 11th - 14th February, 1999.

PhD and MPhil Supervision

Current Supervision

  • Doctor Philosophy — Principal Advisor

  • Doctor Philosophy — Associate Advisor

  • Doctor Philosophy — Associate Advisor

  • Doctor Philosophy — Associate Advisor

Completed Supervision