Professor Nick Hayward

Honorary Professor

Royal Brisbane Clinical Unit
Faculty of Medicine

Overview

Qualifications

  • PhD, The University of Queensland
  • Master of Science, The University of Queensland
  • Bachelor of Science, The University of Queensland

Publications

  • Harland, Mark, Petljak, Mia, Robles-Espinoza, Carla Daniela, Ding, Zhihao, Gruis, Nelleke A., van Doorn, Remco, Pooley, Karen A., Dunning, Alison M., Aoude, Lauren G., Wadt, Karin A. W., Gerdes, Anne-Marie, Brown, Kevin M., Hayward, Nicholas K., Newton-Bishop, Julia A., Adams, David J. and Bishop, D. Timothy (2016) Germline TERT promoter mutations are rare in familial melanoma. Familial Cancer, 15 1: 139-144. doi:10.1007/s10689-015-9841-9

  • Wilmott, James S., Field, Matthew A., Johansson, Peter A., Kakavand, Hojabr, Shang, Ping, De Paoli-Iseppi, Ricardo, Vilain, Ricardo E., Pupo, Gulietta M., Tembe, Varsha, Jakrot, Valerie, Shang, Catherine A., Cebon, Jonathan, Shackleton, Mark, Fitzgerald, Anna, Thompson, John F., Hayward, Nicholas K., Mann, Graham J. and Scolyer, Richard A. (2015) Tumour procurement, DNA extraction, coverage analysis and optimisation of mutation-detection algorithms for human melanoma genomes. Pathology, 47 7: 683-693. doi:10.1097/PAT.0000000000000324

  • Rowe, C. J., Law, M. H., Palmer, J. M., MacGregor, S., Hayward, N. K. and Khosrotehrani, K. (2015) Survival outcomes in patients with multiple primary melanomas. Journal of the European Academy of Dermatology and Venereology, 29 11: 2120-2127. doi:10.1111/jdv.13144

View all Publications

Supervision

  • Doctor Philosophy

  • Doctor Philosophy

  • Master Philosophy

View all Supervision

Publications

Journal Article

  • Harland, Mark, Petljak, Mia, Robles-Espinoza, Carla Daniela, Ding, Zhihao, Gruis, Nelleke A., van Doorn, Remco, Pooley, Karen A., Dunning, Alison M., Aoude, Lauren G., Wadt, Karin A. W., Gerdes, Anne-Marie, Brown, Kevin M., Hayward, Nicholas K., Newton-Bishop, Julia A., Adams, David J. and Bishop, D. Timothy (2016) Germline TERT promoter mutations are rare in familial melanoma. Familial Cancer, 15 1: 139-144. doi:10.1007/s10689-015-9841-9

  • Wilmott, James S., Field, Matthew A., Johansson, Peter A., Kakavand, Hojabr, Shang, Ping, De Paoli-Iseppi, Ricardo, Vilain, Ricardo E., Pupo, Gulietta M., Tembe, Varsha, Jakrot, Valerie, Shang, Catherine A., Cebon, Jonathan, Shackleton, Mark, Fitzgerald, Anna, Thompson, John F., Hayward, Nicholas K., Mann, Graham J. and Scolyer, Richard A. (2015) Tumour procurement, DNA extraction, coverage analysis and optimisation of mutation-detection algorithms for human melanoma genomes. Pathology, 47 7: 683-693. doi:10.1097/PAT.0000000000000324

  • Rowe, C. J., Law, M. H., Palmer, J. M., MacGregor, S., Hayward, N. K. and Khosrotehrani, K. (2015) Survival outcomes in patients with multiple primary melanomas. Journal of the European Academy of Dermatology and Venereology, 29 11: 2120-2127. doi:10.1111/jdv.13144

  • Read, Jazlyn, Wadt, Karin A. W. and Hayward, Nicholas K. (2015) Melanoma genetics. Journal of Medical Genetics, 53 1: 1-14. doi:10.1136/jmedgenet-2015-103150

  • Wadt, K. A. W., Aoude, L. G., Johansson, P., Solinas, A., Pritchard, A., Crainic, O., Andersen, M. T., Kiilgaard, J. F., Heegaard, S., Sunde, L., Federspiel, B., Madore, J., Thompson, J. F., Mccarthy, S. W., Goodwin, A., Tsao, H., Jonsson, G., Busam, K., Gupta, R., Trent, J. M., Gerdes, A. -M., Brown, K. M., Scolyer, R. A. and Hayward, N. K. (2015) A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma. Clinical Genetics, 88 3: 267-272. doi:10.1111/cge.12501

  • Pritchard, Antonia L., Burel, Julie G., Neller, Michelle A., Hayward, Nicholas K., Lopez, J. Alejandro, Fatho, Martina, Lennerz, Volker, Woelfel, Thomas and Schmidt, Christopher W. (2015) Exome sequencing to predict neoantigens in melanoma. Cancer Immunology Research, 3 9: 992-998. doi:10.1158/2326-6066.CIR-15-0088

  • Law, Matthew H., Bishop, D. Timothy, Lee, Jeffrey E., Brossard, Myriam, Martin, Nicholas G., Moses, Eric K., Song, Fengju, Barrett, Jennifer H., Kumar, Rajiv, Easton, Douglas F., Pharoah, Paul D. P., Swerdlow, Anthony J., Kypreou, Katerina P., Taylor, John C., Harland, Mark, Randerson-Moor, Juliette, Akslen, Lars A., Andresen, Per A., Avril, Marie-Franoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brown, Kevin M., Debniak, Tadeusz, Duffy, David L., Elder, David E., Fang, Shenying, Friedman, Eitan, Galan, Pilar, Ghiorzo, Paola, Gillanders, Elizabeth M., Goldstein, Alisa M., Gruis, Nelleke A., Hansson, Johan, Helsing, Per, Hocevar, Marko, Hoeiom, Veronica, Ingvar, Christian, Kanetsky, Peter A., Chen, Wei V., Landi, Maria Teresa, Lang, Julie, Lathrop, G. Mark, Lubinski, Jan, Mackie, Rona M., Mann, Graham J., Molven, Anders, Montgomery, Grant W., Novakovic, Srdjan, Olsson, Hakan, Puig, Susana, Puig-Butille, Joan Anton, Qureshi, Abrar A., Radford-Smith, Graham L., van der Stoep, Nienke, van Doorn, Remco, Whiteman, David C., Craig, Jamie E., Schadendorf, Dirk, Simms, Lisa A., Burdon, Kathryn P., Nyholt, Dale R., Pooley, Karen A., Orr, Nick, Stratigos, Alexander J., Cust, Anne E., Ward, Sarah V., Hayward, Nicholas K., Han, Jiali, Schulze, Hans-Joachim, Dunning, Alison M., Bishop, Julia A. Newton, Demenais, Florence, Amos, Christopher I., MacGregor, Stuart and Iles, Mark M. (2015) Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 9: 987-995. doi:10.1038/ng.3373

  • Aoude, Lauren G., Heitzer, Ellen, Johansson, Peter, Gartside, Michael, Wadt, Karin, Pritchard, Antonia L., Palmer, Jane M., Symmons, Judith, Gerdes, Anne-Marie, Montgomery, Grant W., Martin, Nicholas G., Tomlinson, Ian, Kearsey, Stephen and Hayward, Nicholas K. (2015) POLE mutations in families predisposed to cutaneous melanoma. Familial Cancer, 14 4: 621-628. doi:10.1007/s10689-015-9826-8

  • Akbani R., Akdemir K.C., Aksoy B.A., Albert M., Ally A., Amin S.B., Arachchi H., Arora A., Auman J.T., Ayala B., Baboud J., Balasundaram M., Balu S., Barnabas N., Bartlett J., Bartlett P., Bastian B.C., Baylin S.B., Behera M., Belyaev D., Benz C., Bernard B., Beroukhim R., Bir N., Black A.D., Bodenheimer T., Boice L., Boland G.M., Bono R., Bootwalla M.S., Bosenberg M., Bowen J., Bowlby R., Bristow C.A., Brockway-Lunardi L., Brooks D., Brzezinski J., Bshara W., Buda E., Burns W.R., Butterfield Y.S.N., Button M., Calderone T., Cappellini G.A., Carter C., Carter S.L., Cherney L., Cherniack A.D., Chevalier A., Chin L., Cho J., Cho R.J., Choi Y.-L., Chu A., Chudamani S., Cibulskis K., Ciriello G., Clarke A., Coons S., Cope L., Crain D., Curley E., Danilova L., D'Atri S., Davidsen T., Davies M.A., Delman K.A., Demchok J.A., Deng Q.A., Deribe Y.L., Dhalla N., Dhir R., Dicara D., Dinikin M., Dubina M., Ebrom J.S., Egea S., Eley G., Engel J., Eschbacher J.M., Fedosenko K.V., Felau I., Fennell T., Ferguson M.L., Fisher S., Flaherty K.T., Frazer S., Frick J., Fulidou V., Gabriel S.B., Gao J., Gardner J., Garraway L.A., Gastier-Foster J.M., Gaudioso C., Gehlenborg N., Genovese G., Gerken M., Gershenwald J.E., Getz G., Gomez-Fernandez C., Gribbin T., Grimsby J., Gross B., Guin R., Gutschner T., Hadjipanayis A., Halaban R., Hanf B., Haussler D., Haydu L.E., Hayes D.N., Hayward N.K., Heiman D.I., Herbert L., Herman J.G., Hersey P., Hoadley K.A., Hodis E., Holt R.A., Hoon D.S., Hoppough S., Hoyle A.P., Huang F.W., Huang M., Huang S., Hutter C.M., Ibbs M., Iype L., Jacobsen A., Jakrot V., Janning A., Jeck W.R., Jefferys S.R., Jensen M.A., Jones C.D., Jones S.J.M., Ju Z., Kakavand H., Kang H., Kefford R.F., Khuri F.R., Kim J., Kirkwood J.M., Klode J., Korkut A., Korski K., Krauthammer M., Kucherlapati R., Kwong L.N., Kycler W., Ladanyi M., Lai P.H., Laird P.W., Lander E., Lawrence M.S., Lazar A.J., Lazniak R., Lee D., Lee J.E., Lee J., Lee K., Lee S., Lee W., Leporowska E., Leraas K.M., Li H.I., Lichtenberg T.M., Lichtenstein L., Lin P., Ling S., Liu J., Liu O., Liu W., Long G.V., Lu Y., Ma S., Ma Y., Mackiewicz A., Mahadeshwar H.S., Malke J., Mallery D., Manikhas G.M., Mann G.J., Marra M.A., Matejka B., Mayo M., Mehrabi S., Meng S., Meyerson M., Mieczkowski P.A., Miller J.P., Miller M.L., Mills G.B., Moiseenko F., Moore R.A., Morris S., Morrison C., Morton D., Moschos S., Mose L.E., Muller F.L., Mungall A.J., Murawa D., Murawa P., Murray B.A., Nezi L., Ng S., Nicholson D., Noble M.S., Osunkoya A., Owonikoko T.K., Ozenberger B.A., Pagani E., Paklina O.V., Pantazi A., Parfenov M., Parfitt J., Park P.J., Park W.-Y., Parker J.S., Passarelli F., Penny R., Perou C.M., Pihl T.D., Potapova O., Prieto V.G., Protopopov A., Quinn M.J., Radenbaugh A., Rai K., Ramalingam S.S., Raman A.T., Ramirez N.C., Ramirez R., Rao U., Rathmell W.K., Ren X., Reynolds S.M., Roach J., Robertson A.G., Ross M.I., Roszik J., Russo G., Saksena G., Saller C., Samuels Y., Sander C., Sander C., Sandusky G., Santoso N., Saul M., Saw R.P., Schadendorf D., Schein J.E., Schultz N., Schumacher S.E., Schwallier C., Scolyer R.A., Seidman J., Sekhar P.C., Sekhon H.S., Senbabaoglu Y., Seth S., Shannon K.F., Sharpe S., Sharpless N.E., Shaw K.R.M., Shelton C., Shelton T., Shen R., Sheth M., Shi Y., Shiau C.J., Shmulevich I., Sica G.L., Simons J.V., Sinha R., Sipahimalani P., Sofia H.J., Soloway M.G., Song X., Sougnez C., Spillane A.J., Spychala A., Stretch J.R., Stuart J., Suchorska W.M., Sucker A., Sumer S.O., Sun Y., Synott M., Tabak B., Tabler T.R., Tam A., Tan D., Tang J., Tarnuzzer R., Tarvin K., Tatka H., Taylor B.S., Teresiak M., Thiessen N., Thompson J.F., Thorne L., Thorsson V., Trent J.M., Triche T.J., Tsai K.Y., Tsou P., Van Den Berg D.J., Van Allen E.M., Veluvolu U., Verhaak R.G., Voet D., Voronina O., Walter V., Walton J.S., Wan Y., Wang Y., Wang Z., Waring S., Watson I.R., Weinhold N., Weinstein J.N., Weisenberger D.J., White P., Wilkerson M.D., Wilmott J.S., Wise L., Wiznerowicz M., Woodman S.E., Wu C.-J., Wu C.-C., Wu J., Wu Y., Xi R., Xu A.W., Yang D., Yang L., Yang L., Zack T.I., Zenklusen J.C., Zhang H., Zhang J., Zhang W., Zhao X., Zhu J., Zhu K., Zimmer L., Zmuda E. and Zou L. (2015) Genomic Classification of Cutaneous Melanoma. Cell, 161 7: 1681-1696. doi:10.1016/j.cell.2015.05.044

  • Law, Matthew H., Rowe, Casey J., Montgomery, Grant W., Hayward, Nicholas K., MacGregor, Stuart and Khosrotehrani, Kiarash (2015) PARP1 polymorphisms play opposing roles in melanoma occurrence and survival. International Journal of Cancer, 136 10: 2488-2489. doi:10.1002/ijc.29280

  • Pritchard, Antonia L., Hastie, Marcus L., Neller, Michelle, Gorman, Jeffrey J., Schmidt, Chris W. and Hayward, Nicholas K. (2015) Exploration of peptides bound to MHC class I molecules in melanoma. Pigment Cell and Melanoma Research, 28 3: 281-294. doi:10.1111/pcmr.12357

  • Tembe, Varsha, Schramm, Sarah-Jane, Stark, Mitchell, Patrick, Ellis, Jayaswal, Vivek, Tang, Yue Hang, Barbour, Andrew, Hayward, Nicholas K., Thompson, John F., Scolyer, Richard A., Yang, Yee Hwa and Mann, Graham J. (2015) MicroRNA and mRNA expression profiling in metastatic melanoma reveal associations with BRAF mutation and patient prognosis. Pigment Cell and Melanoma Research, 28 3: 254-266. doi:10.1111/pcmr.12343

  • Barrett, Jennifer H., Taylor, John C., Bright, Chloe, Harland, Mark, Dunning, Alison M., Akslen, Lars A., Andresen, Per A., Avril, Marie-Francoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brossard, Myriam, Brown, Kevin M., Debniak, Tadeusz, Elder, David E., Friedman, Eitan, Ghiorzo, Paola, Gillanders, Elizabeth M., Gruis, Nelleke A., Hansson, Johan, Helsing, Per, Hocevar, Marko, Hoiom, Veronica, Ingvar, Christian, Landi, Maria Teresa, Lang, Julie, Lathrop, G. Mark, Lubinski, Jan, Mackie, Rona M., Molven, Anders, Novakovic, Srdjan, Olsson, Hakan, Puig, Susana, Anton Puig-Butille, Joan, van der Stoep, Nienke, van Doorn, Remco, van Workum, Wilbert, Goldstein, Alisa M., Kanetsky, Peter A., Pharoah, Paul D. P., Demenais, Florence, Hayward, Nicholas K., Newton Bishop, Julia A., Bishop, D. Timothy and Iles, Mark M. (2015) Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. International Journal of Cancer, 136 6: 1351-1360. doi:10.1002/ijc.29099

  • Aoude, Lauren G, Wadt, A.W, Pritchard, Antonia L and Hayward, Nicholas K (2015) Genetics of familial melanoma: 20 years after CDKN2A. Pigment Cell and Melanoma Research, 28 2: 148-160. doi:10.1111/pcmr.12333

  • Sargen, Michael R., Kanetsky, Peter A., Newton-Bishop, Julia, Hayward, Nicholas K., Mann, Graham J., Gruis, Nelleke A., Tucker, Margaret A., Goldstein, Alisa M., Bianchi-Scarra, Giovanna, Puig, Susana and Elder, David E. (2015) Histologic features of melanoma associated with CDKN2A genotype. Journal of the American Academy of Dermatology, 72 3: 496-507.e7. doi:10.1016/j.jaad.2014.11.014

  • Aoude, Lauren G., Pritchard, Antonia L., Robles-Espinoza, Carla Daniela, Wadt, Karin, Harland, Mark, Choi, Jiyeon, Gartside, Michael, Quesada, Victor, Johansson, Peter, Palmer, Jane M., Ramsay, Andrew J., Zhang, Xijun, Jones, Kristine, Symmons, Judith, Holland, Elizabeth A., Schmid, Helen, Bonazzi, Vanessa, Woods, Susan, Dutton-Regester, Ken, Stark, Mitchell S., Snowden, Helen, van Doom, Remco, Montgomery, Grant W., Martin, Nicholas G., Keane, Thomas M., Lopez-Otin, Carlos, Gerdes, Anne-Marie, Olsson, Hakan, Ingvar, Christian, Borg, Ake, Gruis, Nelleke A., Trent, Jeffrey M., Jonsson, Goran, Bishop, D. Timothy, Mann, Graham J., Newton-Bishop, Julia A., Brown, Kevin M., Adams, David J. and Hayward, Nicholas K. (2015) Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. Journal of the National Cancer Institute, 107 2: 1-7. doi:10.1093/jnci/dju408

  • Robles-Espinoza, Carla Daniela, Velasco-Herrera, Martin del Castillo, Hayward, Nicholas K. and Adams, David J. (2015) Telomere-regulating genes and the telomere interactome in familial cancers. Molecular Cancer Research, 13 2: 211-222. doi:10.1158/1541-7786.MCR-14-0305

  • Tiffen, Jessamy C., Gunatilake, Dilini, Gallagher, Stuart J., Gowrishankar, Kavitha, Heinemann, Anja, Cullinane, Carleen, Dutton-Regester, Ken, Pupo, Gulietta M., Strbenac, Dario, Yang, Jean Y., Madore, Jason, Mann, Graham J., Hayward, Nicholas K., McArthur, Grant A., Filipp, Fabian V. and Hersey, Peter (2015) Targeting activating mutations of EZH2 leads to potent cell growth inhibition in human melanoma by derepression of tumor suppressor genes. Oncotarget, 6 29: 27023-27036. doi:10.18632/oncotarget.4809

  • Aoude, Lauren G., Xu, Mai, Zhao, Zhen Zhen, Kovacs, Michael, Palmer, Jane M., Johansson, Peter, Symmons, Judith, Trent, Jeffrey M., Martin, Nicholas G., Montgomery, Grant W., Brown, Kevin M. and Hayward, Nicholas K. (2014) Assessment of PALB2 as a candidate melanoma susceptibility gene. PLoS One, 9 6: e100683.1-e100683.7. doi:10.1371/journal.pone.0100683

  • Savarimuthu Francis, Santiyagu M., Davidson, Morgan R., Tan, Maxine E., Wright, Casey M., Clarke, Belinda E., Duhig, Edwina E., Bowman, Rayleen V., Hayward, Nicholas K ., Fong, Kwun M. and Yang, Ian A. (2014) MicroRNA-34c is associated with emphysema severity and modulates SERPINE1 expression. BMC Genomics, 15 1: . doi:10.1186/1471-2164-15-88

  • Dutton-Regester, K., Kakavand, H., Aoude, L.G., Stark, M.S., Gartside, M.G., Johansson, P., O'Connor, L., Lanagan, C., Tembe, V., Pupo, G.M., Haydu, L.E., Schmidt, C.W., Mann, G.J., Thompson, J.F., Scolyer, R.A. and Hayward, N.K. (2013) Melanomas of unknown primary have a mutation profile consistent with cutaneous sun-exposed melanoma. Pigment Cell and Melanoma Research, 26 6: 852-860. doi:10.1111/pcmr.12153

  • Cronin, J.C., Watkins-Chow, D.E., Incao, A., Hasskamp, J.H., Schonewolf, N., Aoude, L.G., Hayward, N.K., Bastian, B.C., Dummer, R., Loftus, S.K. and Pavan, W.J. (2013) SOX10 ablation arrests cell cycle, induces senescence, and suppresses melanomagenesis. Cancer Research, 73 18: 5709-5718. doi:10.1158/0008-5472.CAN-12-4620

  • Aoude, Lauren G., Wadt, Karin, Bojesen, Anders, Cruger, Dorthe, Borg, Ake, Trent, Jeffrey M., Brown, Kevin M., Gerdes, Anne-Marie, Jonsson, Goran and Hayward, Nicholas K. (2013) A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers. PloS One, 8 8: . doi:10.1371/journal.pone.0072144

  • Gartner, J.J., Parker, S.C.J., Prickett, T.D., Dutton-Regester, K., Stitzel, M.L., Lin, J.C., Davis, S., Simhadri, V.L., Jha, S., Katagiri, N., Gotea, V., Teer, J.K., Wei, X., Morken, M.A., Bhanot, U.K., Chen, G., Elnitski, L.L., Davies, M.A., Gershenwald, J.E., Carter, H., Karchin, R., Robinson, W., Robinson, S., Rosenberg, S.A., Collins, F.S., Parmigiani, G., Komar, A.A., Kimchi-Sarfaty, C., Hayward, N.K., Margulies, E.H. and Samuels, Y. (2013) Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma. Proceedings of the National Academy of Sciences of the United States of America, 110 33: 13481-13486. doi:10.1073/pnas.1304227110

  • Pritchard, A.L. and Hayward, N.K. (2013) Molecular pathways: Mitogen-activated protein kinase pathway mutations and drug resistance. Clinical Cancer Research, 19 9: 2301-2309. doi:10.1158/1078-0432.CCR-12-0383

  • Kendall, Bradley J., Macdonald, Graeme A., Hayward, Nicholas K., Prins, Johannes B., O'Brien, Suzanne, Whiteman, David C., Study of Digestive Health, Green. Adele C., Parsons, Peter G., Pavey, Sandra J., Purdie, David M. and Webb, Penelope M. (2013) The risk of Barrett's esophagus associated with abdominal obesity in males and females. International Journal of Cancer, 132 9: 2192-2199. doi:10.1002/ijc.27887

  • Hacker, Elke, Nagore, Eduardo, Cerroni, Lorenzo, Woods, Susan L., Hayward, Nicholas K., Chapman, Brett, Montgomery, Grant W., Soyer, H. Peter and Whiteman, David C. (2013) NRAS and BRAF mutations in cutaneous melanoma and the association with MC1R genotype: findings from spanish and austrian populations. Journal of Investigative Dermatology, 133 4: 1027-1033. doi:10.1038/jid.2012.385

  • Aoude, Lauren G., Vajdic, Claire M., Kricker, Anne, Armstrong, Bruce and Hayward, Nicholas K. (2013) Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases. Pigment Cell and Melanoma Research, 26 2: 1-3. doi:10.1111/pcmr.12046

  • Levine, D.M., Ek, W.E., Zhang, R., Liu, X., Onstad, L., Sather, C., Lao-Sirieix, P., Gammon, M.D., Corley, D.A., Shaheen, N.J., Bird, N.C., Hardie, L.J., Murray, L.J., Reid, B.J., Chow, W.-H., Risch ,H.A., Nyren, O., Ye, W., Liu, G., Romero, Y., Bernstein, L., Wu, A.H., Casson, A.G., Chanock, S.J., Harrington, P., Caldas, I., Debiram-Beecham, I., Caldas, C., Hayward, N.K., Pharoah, P.D., Fitzgerald, R.C., MacGregor, S., Whiteman, D.C. and Vaughan, T.L. (2013) A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Nature Genetics, 45 12: 1487-1493. doi:10.1038/ng.2796

  • Iles M.M., Law M.H., Stacey S.N., Han J., Fang S., Pfeiffer R., Harland M., MacGregor S., Taylor J.C., Aben K.K., Akslen L.A., Avril M.-F., Azizi E., Bakker B., Benediktsdottir K.R., Bergman W., Scarra G.B., Brown K.M., Calista D., Chaudru V., Fargnoli M.C., Cust A.E., Demenais F., De Waal A.C., Debniak T., Elder D.E., Friedman E., Galan P., Ghiorzo P., Gillanders E.M., Goldstein A.M., Gruis N.A., Hansson J., Helsing P., Hocevar M., Hoiom V., Hopper J.L., Ingvar C., Janssen M., Jenkins M.A., Kanetsky P.A., Kiemeney L.A., Lang J., Lathrop G.M., Leachman S., Lee J.E., Lubinski J., MacKie R.M., Mann G.J., Martin N.G., Mayordomo J.I., Molven A., Mulder S., Nagore E., Novakovic S., Okamoto I., Olafsson J.H., Olsson H., Pehamberger H., Peris K., Grasa M.P., Planelles D., Puig S., Puig-Butille J.A., Randerson-Moor J., Requena C., Rivoltini L., Rodolfo M., Santinami M., Sigurgeirsson B., Snowden H., Song F., Sulem P., Thorisdottir K., Tuominen R., Van Belle P., Van Der Stoep N., Van Rossum M.M., Wei Q., Wendt J., Zelenika D., Zhang M., Landi M.T., Thorleifsson G., Bishop D.T., Amos C.I., Hayward N.K., Stefansson K., Bishop J.A.N. and Barrett J.H. (2013) A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics, 45 4: 428-432. doi:10.1038/ng.2571

  • Liu H., Wang L.-E., Liu Z., Chen W.V., Amos C.I., Lee J.E., Iles M.M., Law M.H., Barrett J.H., Montgomery G.W., Taylor J.C., Macgregor S., Cust A.E., Bishop J.A.N., Hayward N.K., Bishop D.T., Mann G.J., Affleck P. and Wei Q. (2013) Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma risk. Carcinogenesis, 34 4: 885-892. doi:10.1093/carcin/bgs407

  • Qian, J., Liu, H., Wei, S., Liu, Z., Li,Y., Wang, L..-E., Chen, W.V., Amos, C.I., Lee, J.E., Iles, M.M., Law, M.H., Cust, A.E., Barrett, J.H., Montgomery, G.W., Taylor, J., Bishop, J.A.N., Macgregor, S., Bishop, D.T., Mann, G.J., Hayward, N.K. and Wei, Q. (2013) Association between putative functional variants in the PSMB9 gene and risk of melanoma - re-analysis of published melanoma genome-wide association studies. Pigment Cell and Melanoma Research, 26 3: 392-401. doi:10.1111/pcmr.12069

  • Puntervoll, H.E., Yang, X.R., Vetti, H.H., Bachmann, I.M., Avril, M.F., Benfodda, M., Catricala, C., Dalle, S., Duval-Modeste, A.B., Ghiorzo, P., Grammatico, P., Harland, M., Hayward, N.K., Hu, H.-H., Jouary, T., Martin-Denavit, T., Ozola, A., Palmer, J.M., Pastorino, L., Pjanova, D., Soufir, S., Steine, S.J., Stratigos, A.J., Thomas, L., Tinat, J., Tsao, H., Veinalde, R., Tucker, M.A., Paillerets, B.B., Newton-Bishop, J.A., Goldstein, A.M., Akslen, L.A. and Molven, A. (2013) Melanoma prone families with CDK4 germline mutation: Phenotypic profile and associations with MC1R variants. Journal of Medical Genetics, 50 4: 264-270. doi:10.1136/jmedgenet-2012-101455

  • Hacker, E., Boyce, Z., Kimlin, M.G., Wockner, L., Pollak, T., Vaartjes, S.A., Hayward, N.K. and Whiteman, D.C. (2013) The effect of MC1R variants and sunscreen on the response of human melanocytes in vivo to ultraviolet radiation and implications for melanoma. Pigment Cell and Melanoma Research, 26 6: 835-844. doi:10.1111/pcmr.12157

  • Wadt, K., Choi, J., Chung, J.-Y., Kiilgaard, J., Heegaard, S., Drzewiecki, K.T., Trent, J.M., Hewitt, S.M., Hayward, N.K., Gerdes, A.-M. and Brown, K.M. (2012) A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma. Pigment Cell and Melanoma Research, 25 6: 815-818. doi:10.1111/pcmr.12006

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  • Bonazzi, V.F., Irwin, D.L and Hayward, N (2009) Identification of candidate tumor suppressor genes inactivated by promoter methylation in melanoma. Genes, Chromosomes & Cancer, 48 1: 10-21. doi:10.1002/gcc.20615

  • Walker, G.J., Kimlin, M.G., Hacker, E., Ravishankar, S., Muller, H.K., Beermann, F. and Hayward, N. K. (2009) Murine neonatal melanocytes exhibit a heightened proliferative response to ultraviolet radiation and migrate to the epidermal basal layer. Journal of Investigative Dermatology, 129 1: 184-193. doi:10.1038/jid.2008.210

  • Bloethner, Sandra, Mould, Arne, Stark, Mitchell and Hayward, Nicholas K. (2008) Identification of ARHGEF17, DENND2D, FGFR3, and RBI mutations in melanoma by inhibition of nonsense-mediated mRNA decay. Genes, Chromosomes and Cancer, 47 12: 1076-1085. doi:10.1002/gcc.20598

  • Smith, Eric, De Young, Neville J., Pavey, Sandra J., Hayward, Nicholas K., Nancarrow, Derek J., Whiteman, David C., Smithers, B. Mark, Ruszkiewicz, Andrew R., Clouston, Andrew D., Gotley, David C., Devitt, Peter G., Jamieson, Glyn G. and Drew, Paul A. (2008) Similarity of aberrant DNA methylation in Barrett's esophagus and esophageal adenocarcinoma. Molecular Cancer, 7 75.1-75.12. doi:10.1186/1476-4598-7-75

  • Fowler, Elizabeth V., Doecke, James, Simms, Lisa A., Zhao, Zhen Zhen, Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Florin, Timothy H., Montgomery, Grant W., Cavanaugh, Juleen A. and Radford-Smith, Graham L. (2008) ATG16L1 T300A shows strong associations with disease subgroups in a large Australian IBD population: Further support for significant disease heterogeneity. The American Journal of Gastroenterology, 103 10: 2519-2526. doi:10.1111/j.1572-0241.2008.02023.x

  • Zhao, Zhen Zhen, Painter, Jodie N., Palmer, James S., Webb, Penelope M., Hayward, Nicholas K., Whiteman, David C., Boomsma, Dorret I., Martin, Nicholas G., Duffy, David L. and Montgomery, Grant W. (2008) Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning. Human Reproduction, 23 10: 2372-2379. doi:10.1093/humrep/den268

  • Helbig, Ingo, Matigian, Nicholas A., Vadlamudi, Lata, Lawrence, Kate M., Bayly, Marta A., Bain, Sharon M., Diyagama, Dileepa, Scheffer, Ingrid E., Mulley, John C., Holloway, Andrew J., Dibbens, Leanne M., Berkovic, Samuel F. and Hayward, Nicholas K. (2008) Gene expression analysis in absence epilepsy using a monozygotic twin design. Epilepsia, 49 9: 1546-1554. doi:10.1111/j.1528-1167.2008.01630.x

  • Brown, K. M., MacGregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D. C., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Newton Bishop, J., Kefford, R. F., Giles, G. G., Armstrong, B. K., Aitken, J. F., Hopper, J. L., Martin, N. G., Trent, J. M., Mann, G. J. and Hayward, N. (2008) Common sequence variants on 20q11.22 confer melanoma susceptibility. Nature Genetics, 40 7: 838-840. doi:10.1038/ng.163

  • Doecke, James, Zhao, Zhen Zhen, Pandeya, Nirmala, Sadeghi, Shahram, Stark, Mitchell, Green, Adele C., Hayward, Nicholas K., Webb, Penlope M. and Whiteman, David C. (2008) Polymorphisms in MGMT and DNA repair genes and the risk of esophageal adenocarcinoma. International Journal of Cancer, 123 1: 174-180. doi:10.1002/ijc.23410

  • Hacker, E., Muller, K., Whiteman, D. C., Pavey, S., Hayward, N. and Walker, G. (2008) Reduced expression of IL-18 is a marker of ultraviolet radiation-induced melanomas. International Journal of Cancer, 123 1: 227-231. doi:10.1002/ijc.23389

  • Nancarrow, D.J., Handoko, H. Y., Smithers, B.M., Gotley, D. C., Drew, P.A., Watson, D.I., Clouston, A. D., Hayward, N. and Whiteman, D. C. (2008) Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays. Cancer Research, 68 11: 4163-4172. doi:10.1158/0008-5472.CAN-07-6710

  • Han, J., Kraft, P., Nan, H., Guo, Q., Chen, C., Qureshi, A., Hankinson, S.E., Hu, F.B., Duffy, D., Zhao, Z.Z., Martin, N. G., Montgomery, G., Hayward, N., Thomas, G., Hoover, R.N., Chanock, S. and Hunter, D.J. (2008) A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Plos Genetics, 4 5: e1000074. doi:10.1371/journal.pgen.1000074

  • Sturm, Richard A., Duffy, David L., Zhao, Zhen Zhen, Leite, Fabio P.N., Stark, Mitchell S., Hayward, Nicholas K., Martin, Nicholas G. and Montgomery, Grant W. (2008) A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye colour. The American Journal of Human Genetics, 82 2: 424-431. doi:10.1016/j.ajhg.2007.11.005

  • Mould, A. W., Scotney, P., Greco, S. A., Hayward, N., Nash, A. and Kay, G. F. (2008) Prophylactic but not therapeutic activity of a monoclonal antibody that neutralizes the binding of VEGF-B to VEGFR-1 in a murine collagen-induced arthritis model. Rheumatology, 47 3: 263-266. doi:10.1093/rheumatology/kem369

  • Kendall, B. J., Macdonald, Graeme A., Hayward, N. K., Prins, Johannes B., Brown, I., Walker, Niel, Pandeya, N., Green. A. C., Whiteman, D. C. and Study of Digestive Health (2008) Leptin and the risk of Barrett’s oesophagus. Gut, 57 4: 448-454. doi:10.1136/gut.2007.131243

  • Richmond-Sinclair, N.M., Lee, E., Cummings, M.C., Williamson, R., Muller, H.K., Green, A.C., Hayward, N.K. and Whiteman, D.C. (2008) Histologic and epidemiologic correlates of P-MAPK, Brn-2, pRb, p53 and p16 immunostaining in cutaneous melanomas. Melanoma research, 18 5: 336-345. doi:10.1097/CMR.0b013e32830d8329

  • Doecke, J D, Zhao, Z Z, Stark, M S, Green, A C, Hayward, N K, Montgomery, G W, Webb, P M and Whiteman, D C (2008) Single nucleotide polymorphisms in obesity-related genes and the risk of esophageal cancers. Cancer Epidemiology, Biomarkers & Prevention, 17 4: 1007-1012. doi:10.1158/1055-9965.EPI-08-0023

  • Baxter, A.J., Hughes, M.C., Kvaskoff, M, Siskind, V., Shekar, S., Aitken, J. F., Green, A. C., Duffy, D., Hayward, N., Martin, N. G. and Whiteman, D. C. (2008) The Queensland study of melanoma:Environmental and genetic associations (Q_MEGA): study design, baseline characteristics, and repeatability of phenotype and sun exposure measures. Twin Research and Human Genetics, 11 2: 183-196. doi:10.1375/twin.11.2.183

  • Larsen, J. E., Pavey, S., Passmore, L. H., Bowman, R., Clarke, B. E., Hayward, N. K. and Fong, K. M. (2007) Expression profiling defines a recurrence signature in lung squamous cell carcinoma. Carcinogenesis, 28 3: 760-766. doi:10.1093/carcin/bgl207

  • Nancarrow, Derek J., Handoko, Herlina Y., Stark, Mitchell S., Whiteman, David C. and Hayward, Nicholas K. (2007) SiDCoN: A tool to aide scoring of DNA copy number changes in SNP chip data. PLoS One, 2 10: . doi:10.1371/journal.pone.0001093

  • Matigian, N., Windus, L., Smith, H., Fillipich, C., Pantelis, C., McGrath, J. J., Mowry, B. and Hayward, N. (2007) Expression profiling in monozygotic twins discordant for bipolar disorder reveals dysregulation of the WNT signaling pathway. Molecular Psychiatry, 12 9: 815-825. doi:10.1038/sj.mp.4001998

  • Packer, Leisl M., Pavey, Sandra J., Boyle, Glen M., Stark, Mitchell S., Ayub, Ana L., Rizos, Helen and Hayward, Nicholas K. (2007) Gene expression profiling in melanoma identifies novel downstream effectors of p14ARF. International Journal of Cancer, 121 4: 784-790. doi:10.1002/ijc.22725

  • Johansson, Peter, Pavey, Sandra and Hayward, Nicholas (2007) Confirmation of a BRAF mutation-associated gene expression signature in melanoma. Pigment Cell and Melanoma Research, 20 3: 216-221. doi:10.1111/j.1600-0749.2007.00375.x

  • Larsen,J. E., Pavey, S., Passmore, L. H., Bowman, R. V., Hayward, N. K. and Fong, K. M. (2007) Gene expression signature predicts recurrence in lung adenocarcinoma. Clinical Cancer Research, 13 10: 2946-2954. doi:10.1158/1078-0432.CCR-06-2525

  • Pujana, M. A., Ruiz, A., Badenas, C., Puig-Butille, J-A., Nadal, M., Stark, M., Gomez, L., Valls, J., Sole, X., Hernandez, P., Cerrato, C., Madrigal, I., de Cid, R., Aguilar, H., Capella, G., Cal, S., James, M. R., Walker, G. J., Malvehy, J., Mila, M., Hayward, N. K., Estivill, X. and Puig, S. (2007) Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor. Genes, Chromosomes & Cancer, 46 2: 155-162. doi:10.1002/gcc.20396

  • McRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007) Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 4: 364-373. doi:10.1093/hmg/ddl456

  • Loffler, Kelly A., Biondi, Christine A., Gartside, Michael, Waring, Paul, Stark, Mitchell, Serewko-Auret, Magdalena M., Muller, H. Konrad, Hayward, Nicholas K. and Kay, Graham F. (2007) Broad tumor spectrum in a mouse model of multiple endocrine neoplasia type 1. International Journal of Cancer, 120 2: 259-267. doi:10.1002/ijc.22288

  • Larsen, J.E., Fong, K. M. and Hayward, N. K. (2007) Correction. New England Journal of Medicine, 356 2: 201-203.

  • Larsen, Jill E., Fong, Kwun M. and Hayward, Nicholas K. (2007) Refining prognosis in non–small-cell lung cancer. The New England Journal of Medicine, 356 2: 190-190.

  • Zhu, Gu, Montgomery, Grant W., James, Michael R., Trent, Jeff M., Hayward, Nicholas K., Martin, Nicholas G. and Duffy, David L. (2007) A genome-wide scan for naevus count: Linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics, 15 1: 94-102. doi:10.1038/sj.ejhg.5201729

  • Duffy, D. L., Montgomery, G. W., Chen, W., Zhao, Z. Z., Le, L., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2007) A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation. American Journal of Human Genetics, 80 2: 241-252. doi:10.1086/510885

  • Zuidervaart, W., Pavey, S., van Nieuwpoort, F. A., Packer, L., Out, C., Maat, W., Jager, M. J., Gruis, N. A. and Hayward, N. K. (2007) Expression of Wnt5a and its downstream effector beta-catenin in uveal melanoma. Melanoma Research, 17 6: 380-386. doi:10.1097/CMR.0b013e3282f1d302

  • Goldstein, Alisa M., Chan, May, Harland, Mark, Hayward, Nicholas K., Demenais, Florence, Bishop, D. Timothy, Azizi, Esther, Bergman, Wilma, Bianchi-Scarra, Giovanna, Bruno, William, Calista, Donato, Cannon Albright, Lisa A., Chaudru, Valerie, Chompret, Agnes, Cuellar, Francisco, Elder, David E., Ghiorzo, Paola, Gillanders, Elizabeth M., Gruis, Nelleke A., Hansson, Johan, Hogg, David, Holland, Elizabeth A., Kanetsky, Peter A., Kefford, Richard F., Landi, Maria T., Lang, Julie, Leachman, Sancy A., MacKie, Rona M., Magnusson, Veronica, Mann, Graham J., Bishop, Julia Newton, Palmer, Jane M., Puig, Susana, Puig-Butille, Joan A., Stark, Mitchell, Tsao, Hensin, Tucker, Margaret A., Whitaker, Linda, Yakobson, Emanuel, Ingvar, Christian, Borg, Ake, Westerdahl, Johan, Masback, Anna, Olsson, Hakan, Malvehy, Josep, Badenas, Celia, Cervera, Ramedios, Martí, Rosa, Brunet-Vidal, Joan, Yang, Guang, Martin, Nicholas, Whiteman, David, Green, Adele, Aitken, Joanne, Minghetti, Paola, Mantelli, Michela, Pastorino, Lorenza, Nasti, Sabina, Gargiulo, Sara, Gliori, Sara, Mistry, Sushila, Randerson-Moor, Juliette, de Snoo, Femke A., ter Huurne, Jeanet A. C., van der Rhee, Jasper, van Mourik, Leny, van Nieuwpoort, Frans, van der Drift, Clasine, Bressac-De Paillerets, Brigitte, Avril, Marie-Francoise, Grange, F., Sassolas, B., Boitier, F., Chevrant-Breton, J., Lasset, C., Dugast, C., Vabres, P., Ganguly, Arupa, Ming, Michael, Van Belle, Patricia, Platz, Anton, Egyhazi, Suzanne, Tuominen, Rainer, Linden, Diana, Schmid, Helen, Scope, Alon, Pavlotsky, Felix, Friedman, Eitan and Eliason, Mark (2007) Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. Journal of Medical Genetics, 44 2: 99-106. doi:10.1136/jmg.2006.043802

  • Larsen, J.E., Pavey, S.J., Bowman, R., Yang, I.A., Clarke, B.E., Colosimo, M.L., Hayward, N.K. and Fong, K.M. (2007) Gene expression of lung squamous cell carcinoma reflects mode of lymph node involvement. The European Respiratory Journal, 30 1: 21-25. doi:10.1183/09031936.00161306

  • Stark, M. and Hayward, N. (2007) Genome-wide loss of heterozygosity and copy number analysis in melanoma using high-denisty single-nucleotide polymorphism arrays. Cancer Research, 67 6: 2632-2642. doi:10.1158/0008-5472.CAN-06-4152

  • Mould, Arne W., Duncan, Russell, Serewko-Auret, Magdalena, Loffler, Kelly A., Biondi, Christine, Gartside, Michael, Kay, Graham F. and Hayward, Nicholas K. (2007) Global expression profiling of murine MEN1-associated tumors reveals a regulatory role for menin in transcription, cell cycle and chromatin remodelling. International Journal of Cancer, 121 4: 776-783. doi:10.1002/ijc.22734

  • Loffler, K. A., Biondi, C. A., Gartside, M. G., Serewko-Auret, M. M., Duncan, R., Tonks, I. D., Mould, A. W., Waring, P., Muller, H. K., Kay, G. F. and Hayward, N. K. (2007) Lack of augmentation of tumor spectrum or severity in dual heterozygous Men1 and Rb1 knockout mice. Oncogene, 26 27: 4009-4017. doi:10.1038/sj.onc.1210163

  • Lang, J, Hayward, N, Goldgar, D, Tsao, H, Hogg, D, Palmer, J, Stark, M, Tobias, ES and MacKie, R (2007) The M531 mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestry. Genes Chromosomes & Cancer, 46 3: 277-287. doi:10.1002/gcc.20410

  • Goldstein, Alisa M., Chan, May, Harland, Mark, Gillanders, Elizabeth M., Hayward, Nicholas K., Avril, Marie-Francoise, Azizi, Esther, Bianchi-Scarra, Giovanna, Bishop, D. Timothy, Bressac-de Paillerets, Brigitte, Bruno, William, Calista, Donato, Cannon Albright, Lisa A., Demenais, Florence, Elder, David E., Ghiorzo, Paola, Gruis, Nelleke A., Hansson, Johan, Hogg, David, Holland, Elizabeth A., Kanetsky, Peter A., Kefford, Richard F., Landi, Maria Teresa, Lang, Julie, Leachman, Sancy A., MacKie, Rona M., Magnusson, Veronica, Mann, Graham J., Niendorf, Kristin, Newton Bishop, Julia, Palmer, Jane M., Puig, Susana, Puig-Butille, Joan A., de Snoo, Femke A., Stark, Mitchell, Tsao, Hensin, Tucker, Margaret A., Whitaker, Linda, Yakobson, Emanuel, The Lund Melanoma Study Group and Melanoma Genetics Consortium (GenoMEL) (2006) High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL. Cancer research, 66 20: 9818-9828. doi:10.1158/0008-5472.CAN-06-0494

  • Packer, Leisl, Pavey, Sandra, Parker, Andrew, Stark, Mitchell, Johansson, Peter, Clarke, Belinda, Pollock, Pamela, Ringner, Markus and Hayward, Nicholas (2006) Osteopontin is a Downstream Effector of the PI3-kinase Pathway in Melanomas that is Inversely Correlated with Functional PTEN. Carcinogenesis, 27 9: 1778-1786. doi:10.1093/carcin/bgl016

  • Pavey, Sandra, Zuidervaart, Wieke, van Nieuwpoort, Frans, Packer, Leisl, Jager, Martine, Gruis, Nelleke and Hayward, Nicholas (2006) Increased p21-activated kinase-1 expression is associated with invasive potential in uveal melanoma. Melanoma Research, 16 4: 285-296. doi:10.1097/01.cmr.0000222589.30117.f2

  • Curtin, John A., Stark, Mitchell S., Pinkel, Daniel, Hayward, Nicholas K. and Bastian, Boris C. (2006) PI3-Kinase Subunits Are Infrequent Somatic Targets in Melanoma. Journal of Investigative Dermatology, 126 7: 1660-1663. doi:10.1038/sj.jid.5700311

  • Stark, M., Puig-Butille, J. A., Walker, G., Badenas, C., Malvehy, J., Hayward , N. and Puig, S. (2006) Mutation of the tumour suppressor p33ING1b is rare in melanoma. British Journal of Dermatology, 155 1: 94-99. doi:10.1111/j.1365-2133.2006.07274.x

  • Holliday, Elizabeth G., Handoko, Herlina Y., James, Michael R., McGrath, J. J., Nertney, Deborah A., Tirupati, Sujit, Thara, Rangaswamy, Levinson, Douglas F., Hayward, Nicholas K., Mowry, Bryan J. and Nyholt, Dale R. (2006) Association study of the dystrobrevin-binding gene with schizophrenia in Australian and Indian samples. Twin Research and Human Genetics, 9 4: 531-539. doi:10.1375/183242706778025035

  • McCurdy, Richard D., Feron, Francois, Perry, Chris, Chant, David C., McLean, Duncan, Matigian, Nick, Hayward, Nicholas K., McGrath, John J. and Mackay-Sim, Alan (2006) Cell cycle alterations in biopsied olfactory neuroepithelium in schizophrenia and bipolar I disorder using cell culture and gene expression analyses. Schizophrenia Research, 82 2-3: 163-173. doi:10.1016/j.schres.2005.10.012

  • Mah, S., Nelson, M. R., DeLisi, L. E., Reneland, R. H., Markward, N., James, M. R., Nyholt, D. R., Hayward, N., Handoko, H., Mowry, B., Kammerer, S. and Braun, A. (2006) Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. Molecular Psychiatry, 11 5: 471-478. doi:10.1038/sj.mp.4001785

  • Palmer, J. S., Zhao, Z. Z., Hoekstra, C., Hayward, N. K., Webb, P. M., Whiteman, D. C., Martin, N. G., Boomsma, D. I., Duffy, D. L. and Montgomery, G. W. (2006) Novel variants in growth differentiation factor 9 in mothers of dizygotic twins. Journal of Clinical Endocrinology And Metabolism, 91 11: 4713-4716. doi:10.1210/jc.2006-0970

  • James, Michael R., Dumeni, Troy, Stark, Mitchell S., Duffy, David L., Montgomery, Grant W., Martin, Nicholas G. and Hayward, Nicholas K. (2006) Rapid screening of 4000 individuals for germ-line variations in the BRAF gene. Clinical Chemistry, 52 9: 1675-1678. doi:10.1373/clinchem.2006.070169

  • Hacker, E., Muller, H. K., Irwin, N., Gabrielli, B., Lincoin, D., Pavey, S., Powell, M. B., Malumbres, M., Barbacid, M., Hayward, N. and Walker, G. (2006) Spontaneous and UV radiation-induced multiple metastatic melanomas in Cdk4(R24C/R24C)/TPras mice. Cancer Research, 66 6: 2946-2952. doi:10.1158/0008-5472.CAN-05-3196

  • de Snoo, Femke A. and Hayward, Nicholas K. (2005) Cutaneous melanoma susceptibility and progression genes. Cancer Letters, 230 2: 153-186. doi:10.1016/j.canlet.2004.12.033

  • James, Michael R., Roth, Richard B., Shi, Michael M., Kammerer, Stefan, Nelson, Matthew R., Stark, Mitchell S., Dumenil, Troy, Montgomery, Grant W., Hayward, Nicholas K., Martin, Nicholas G., Braun, Andreas and Duffy, David L. (2005) BRAF Polymorphisms and Risk of Melanocytic Neoplasia. Journal of Investigative Dermatology, 125 6: 1252-1258. doi:10.1111/j.0022-202X.2005.23937.x

  • Hacker, Elke, Irwin, Nicole, Muller, H. Konrad, Powell, Marianne Broome, Kay, Graham, Hayward, Nicholas and Walker, Graeme (2005) Neonatal ultraviolet radiation exposure is critical for malignant melanoma induction in pigmented tpras transgenic mice. Journal of Investigative Dermatology, 125 5: 1074-1077. doi:10.1111/j.0022-202X.2005.23917.x

  • Mould, Arne W., Greco, Sonia A., Cahill, Marian M., Tonks, Ian D., Bellomo, Daniela, Patterson, Carol, Zournazi, Anna, Nash, Andrew, Scotney, Pierre, Hayward, Nicholas K. and Kay, Graham F. (2005) Transgenic overexpression of vascular endothelial growth factor-B isoforms by endothelial cells potentiates postnatal vessel growth in vivo and in vitro. Circulation Research, 97 6: e60-e70. doi:10.1161/01.RES.0000182631.33638.77

  • Molven, Anders, Grimstvedt, Magne B., Steine, Solrun J., Harland, Mark, Avril, Marie-Françoise, Hayward, Nicholas K. and Akslen, Lars A. (2005) A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. Genes, Chromosomes and Cancer, 44 1: 10-18. doi:10.1002/gcc.20202

  • Tonks, Ian D., Hacker, Elke, Irwin, Nicole, Muller, H. Conrad, Keith, Patricia, Mould, Arne, Zournazi, Anna, Pavey, Sandra, Hayward, Nicholas K., Walker, Graeme and Kay, Graham F. (2005) Melanocytes in conditional Rb–/– mice are normal in vivo but exhibit proliferation and pigmentation defects in vitro. Pigment Cell and Melanoma Research, 18 4: 252-264. doi:10.1111/j.1600-0749.2005.00245.x

  • Zuidervaart, W., van Nieuwpoort, F., Stark, M., Dijkman, R., Packer, L., Borgstein, A. -M., Pavey, S., van der Velden, P., Out, C., Jager, M. J., Hayward, N. K. and Gruis, N. A. (2005) Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS. British Journal of Cancer, 92 11: 2032-2038. doi:10.1038/sj.bjc.6602598

  • Chin, David, Boyle, Glen M., Kane, Anthony J., Theile, David, Hayward, Nicholas K., Parsons, Peter G. and Coman, William B. (2005) Invasion and metastasis markers in cancers. British Journal of Plastic Surgery, 58 4: 466-474. doi:10.1016/j.bjps.2004.12.025

  • Handoko, H. Y., Nyholt, D. R., Hayward, N. K., Nertney, D. A., Hannah, D. E., Windus, L. C., McCormack, C. M., Smith, H. J., Filippich, C., James, M. R. and Mowry, B. J. (2005) Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia. Molecular Psychiatry, 10 6: 589-597. doi:10.1038/sj.mp.4001606

  • Cardinal, J. W., Bergman, L., Hayward, N., Sweet, A., Warner, J., Marks, L., Learoyd, D., Dwight, T., Robinson, B., Epstein, M., Smith, M., Teh, B. T., Cameron, D. P. and Prins, J. B. (2005) A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of Medical Genetics, 42 1: 69-74. doi:10.1136/jmg.2003.017319

  • Walker, Graeme J., Indsto, James O., Sood, Raman, Faruque, Mezbah U., Hu, Ping, Pollock, Pam M., Duray, Paul, Holland, Elizabeth A., Brown, Kevin, Kefford, Richard F., Trent, Jeffrey M., Mann, Graham J. and Hayward, Nicholas K. (2004) Deletion mapping suggests that the 1p22 melanoma susceptibility gene is a tumor suppressor localized to a 9-Mb interval. Genes, Chromosomes & Cancer, 41 1: 56-64. doi:10.1002/gcc.20056

  • Pavey, Sandra, Johansson, Peter, Packer, Leisl, Taylor, Jennifer, Stark, Mitchell, Pollock, Pamela M., Walker, Graeme J., Boyle, Glen M., Harper, Ursula, Cozzi, Sarah-Jane, Hansen, Katherine, Yudt, Laura, Schmidt, Chris, Hersey, Peter, Ellem, Kay A. O., O'Rourke, Michael G. E., Parsons, Peter G., Meltzer, Paul, Ringnér, Markus and Hayward, Nicholas K. (2004) Microarray expression profiling in melanoma reveals a BRAF mutation signature. Oncogene, 23 23: 4060-4067. doi:10.1038/sj.onc.1207563

  • Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M. and Martin, N. G. (2004) A genome scan for eye color in 502 twin families: Most variation is due to a QTL on chromosome 15q. Twin Research, 7 2: 197-210. doi:10.1375/136905204323016186

  • Biondi, C. A., Gartside, M. G., Waring, P., Loffler, K. A., Stark, M. S., Magnuson, M. A., Kay, G. F. and Hayward, N. K. (2004) Conditional inactivation of the Men1 gene leads to pancreatic and pituitary tumorigenesis but does not affect normal development of these tissues. Molecular And Cellular Biology, 24 8: 3125-3131. doi:10.1128/MCB.24.8.3125-3131.2004

  • James, Michael R., Hayward, Nicholas K., Dumenil, Troy, Montgomery, Grant W., Martin, Nicholas G. and Duffy, David L. (2004) Epidermal Growth Factor Gene (EGF) Polymorphism and Risk of Melanocytic Neoplasiay. Journal of Investigative Dermatology, 123 4: 760-762. doi:10.1111/j.0022-202X.2004.23305.x

  • Ghiorzo, P., Villaggio, B., Sementa, A. R., Hansson, J., Platz, A., Nicolo, G., Spina, B., Canepa, M, Palmer, J. M., Hayward, N. K. and Bianchi-Scarra, G. (2004) Expression and localization of mutant p16 proteins in melanocytic lesions from familial melanoma patients. Human Pathology, 35 1: 25-33. doi:10.1016/j.humpath.2003.08.017

  • Duffy, D. L., Box, N. F., Chen, W., Palmer, J. S., Montgomery, G. W., James, M. R., Hayward, N. K., Martin, N. G. and Sturm, R. A. (2004) Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Human Molecular Genetics, 13 4: 447-461. doi:10.1093/hmg/ddh043

  • Hughes, C. M., Rozenblatt-Rosen, O., Milne, T. A., Copeland, T. D., Levine, S. S., Lee, J. C., Hayes, D. N., Shanmugam, K. S., Bhattacharjee, A., Biondi, C. A., Kay, G. F., Hayward, N. K., Hess, J. L. and Meyerson, M. (2004) Menin associates with a trithorax family histone methyltransferase complex and with the Hoxc8 locus. Molecular Cell, 13 4: 587-597. doi:10.1016/S1097-2765(04)00081-4

  • Whiteman, D. C., Watt, P., Purdie, D. M., Hughes, M. C., Hayward, N. K. and Green, A. C. (2003) RESPONSE: Re: Melanocytic Nevi, Solar Keratoses, and Divergent Pathways to Cutaneous Melanoma. Journal of the National Cancer Institute, 95 23: 1801-1802. doi:10.1093/jnci/djg128

  • Handoko, H. Y., Nancarrow, D. J., Hayward, N. K., Ohaeri, J. U., Aghanwa, H., McGrath, J. J., Levinson, D. F., Johns, C., Walters, M. K., Nertney, D. A., Srinivasan, T. N., Thara, R. and Mowry, B. J. (2003) Tumor necrosis factor haplotype analysis amongst schizophrenia probands from four distinct populations in the Asia-Pacific region. American Journal of Medical Genetics Part B - Neuropsychiatric Genetics, 121B 1: 1-6. doi:10.1002/ajmg.b.20059

  • Vajdic, C, Kricker, A, Duffy, DL, Aitken, JF, Stark, M, ter Huurne, JAC, Martin, NG, Armstrong, BK and Hayward, NK (2003) Ocular melanoma is not associated with CDKN2A or MC1R variants - a population-based study. Melanoma Research, 13 4: 409-413. doi:10.1097/01.cmr.0000056244.56735.28

  • Whiteman, D. C., Watt, P., Purdie, D. M., Hughes, M. C., Hayward, N. K. and Green, A. C. (2003) Melanocytic nevi, solar keratoses, and divergent pathways to cutaneous melanoma. Journal of The National Cancer Institute, 95 11: 806-812. doi:10.1093/jnci/95.11.806

  • Hayward, Nicholas K. (2003) Genetics of melanoma predisposition. Oncogene, 22 20: 3053-3062. doi:10.1038/sj.onc.1206445

  • Vajdic, C. M., Hutchins, A-M., Kricker, A., Aitken, J. F., Armstrong, B. K., Hayward, N. K. and Armes, J. E. (2003) Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based study. Cancer Genetics & Cytogenetics, 144 1: 12-17. doi:10.1016/S0165-4608(02)00868-3

  • Pollock, Pamela M., Harper, Ursula L., Hansen, Katherine S., Yudt, Laura M., Stark, Mitchell, Robbins, Christiane M., Moses, Tracy Y., Hostetter, Galen, Wagner, Urs, Kakareka, John, Salem, Ghadi, Pohida, Tom, Heenan, Peter, Duray, Paul, Kallioniemi, Olli, Hayward, Nicholas K., Trent, Jeffrey M. and Meltzer, Paul S. (2003) High frequency of BRAF mutations in nevi. Nature Genetics, 33 1: 19-20. doi:10.1038/ng1054

  • Gillanders, Elizabeth, Juo, Suh-Hang Hank, Holland, Elizabeth A., Jones, MaryPat, Nancarrow, Derek, Freas-Lutz, Diana, Sood, Raman, Park, Naeun, Faruque, Mezbah, Markey, Carol, Kefford, Richard F., Palmer, Jane, Bergman, Wilma, Bishop, D. Timothy, Tucker, Margaret A., Bressac-de Paillerets, Brigitte, Hansson, Johan, The Lund Melanoma Study Group, Stark, Mitchell, Gruis, Nelleke, Newton Bishop, Julia, Goldstein, Alisa M., Bailey-Wilson, Joan E., Mann, Graham J., Hayward, Nicholas, Trent, Jeffrey, Martin, Nicholas G. and The Melanoma Genetics Consortium (2003) Localization of a novel melanoma susceptibility locus to 1p22. American Journal of Human Genetics, 73 2: 301-313. doi:10.1086/377140

  • Mould, Arne W., Tonks, Ian D., Cahill, Marian M., Pettit, Allison R., Thomas, Ranjeny, Hayward, Nicholas K. and Kay, Graham F. (2003) Vegfb gene knockout mice display reduced pathology and synovial angiogenesis in both antigen-induced and collagen-induced models of arthritis. Arthritis and Rheumatism, 48 9: 2660-2669. doi:10.1002/art.11232

  • Fung, David C.Y., Holland, Elizabeth A., Becker, Therese M., Hayward, Nicholas K., Bressac-de Paillerets, Brigitte, Mann, Graham J. and Melanoma Genetics Consortium (2003) eMelanoBase: An online locus-specific variant database for familial melanoma. Human Mutation, 21 1: 2-7. doi:10.1002/humu.10149

  • Pollock, P. M., Walker, G. J., Glendening, J. M., Noy, T. Q., Bloch, N. C., Fountain, J. W. and Hayward, N. K. (2002) PTEN inactivation is rare in melanoma tumours but occurs frequently in melanoma cell lines. Melanoma Research, 12 6: 565-575. doi:10.1097/00008390-200212000-00006

  • Kefford, R., Bishop, J. N., Tucker, M., Bressac-de-Paillerets, B., Bianchi-Scarra, G., Bergman, W., Goldstein, A., Puig, S., Mackie, R., Elder, D., Hansson, J., Hayward, N., Hogg, D., Olsson, H. and Melanoma Genetics Consortium (2002) Genetic testing for melanoma. Lancet Oncology, 3 11: 653-654. doi:10.1016/S1470-2045(02)00894-X

  • Walker, Graeme J. and Hayward, Nicholas K. (2002) Pathways to Melanoma Development: Lessons from the Mouse. Journal of Investigative Dermatology, 119 4: 783-792. doi:10.1046/j.1523-1747.2002.00217.x

  • Whiteman, David C., Zhou, Xiao-Ping, Cummings, Margaret C., Pavey, Sandra, Hayward, Nicholas K. and Eng, Charis (2002) Nuclear PTEN expression and clinicopathologic features in a population-based series of primary cutaneous melanoma. International Journal of Cancer, 99 1: 63-67. doi:10.1002/ijc.10294

  • Walker, Graeme J. and Hayward, Nicholas K. (2002) p16INK4A and p14ARF tumour suppressors in melanoma: lessons from the mouse. Lancet, 359 9300: 7-8. doi:10.1016/S0140-6736(02)07271-9

  • Bishop, D. T., Demenais, F., Goldstein, A. M., Bergman, W., Newton Bishop, J., Bressac-de Paillerets, B., Chompret, A., Ghiorzo, P., Gruis, N., Hansson, J., Harland, M., Hayward, N., Holland, E. A., Mann, G. J. and Mantelli, M. (2002) Geographical variation in the penetrance of CDKN2A mutations for melanoma. Journal of the National Cancer Institute, 94 12: 894-903.

  • Irwin, N., Walker, G. and Hayward, N. (2002) Lack of TTC4 mutations in melanoma. Journal of Investigative Dermatology, 119 1: 186-187. doi:10.1046/j.1523-1747.2002.18181.x

  • Pavey, S. J., Cummings, M. C., Whiteman, D. C., Castellano, M., Walsh, M. D., Gabrielli, B. G., Green, A. and Hayward, N. K. (2002) Loss of p16 expression is associated with histological features of melanoma invasion. Melanoma Research, 12 6: 539-547. doi:10.1097/01.cmr.0000043154.28051.9f

  • Youl, Philippa, Aitken, Joanne, Hayward, Nicholas, Hogg, David, Liu, Ling, Lassam, Norman, Martin, Nicholas and Green, Adele (2002) Melanoma in adolescents: A case-control study of risk factors in Queensland, Australia. International Journal of Cancer, 98 1: 92-98. doi:10.1002/ijc.10117

  • Pollock, P. M. and Hayward, N. (2002) Mutations in exon 3 of the beta-catenin gene are rare in melanoma cell lines. Melanoma Research, 12 2: 183-186. doi:10.1097/00008390-200204000-00013

  • Biondi, C., Gartside, M., Tonks, I., Paterson, C., Hayward, N. K. and Kay, G. F. (2002) Targeting and conditional inactivation of the murine Men1 locus using the Cre recombinase: LoxP system. Genesis, 32 2: 150-151. doi:10.1002/gene.10061

  • Wanstall, J. C., Gambino, A., Jeffery, T. K., Cahill, M. M., Bellomo, D., Hayward, N. K. and Kay, G. F. (2002) Vascular endothelial growth factor-B-deficient mice show impaired development of hypoxic pulmonary hypertension. Cardiovascular Research, 55 2: 361-368. doi:10.1016/S0008-6363(02)00440-6

  • Pollock, Pamela M., Stark, Mitchell S., Palmer, Jane M., Walters, Marilyn K., Aitken, Joanne F., Martin, Nicholas G. and Hayward, Nicholas K. (2001) Mutation analysis of the CDKN2A promoter in Australian melanoma families. Genes Chromosomes and Cancer, 32 1: 89-94. doi:10.1002/gcc.1170

  • Welch, John, Millar, Doug, Goldman, Alana, Heenan, Peter, Stark, Mitchell, Eldon, Michael, Clark, Susan, Martin, Nicholas G. and Hayward, Nicholas K. (2001) Lack of Genetic and Epigenetic Changes in CDKN2A in Melanocytic Nevi [Letter to the editor]. Journal of Investigative Dermatology, 117 2: 383-384. doi:10.1046/j.0022-202x.2001.01391.x

  • Cook, AL, Pollock, PM, Welch, J, Walsh, MD, Bowman, RV, Bauman, KC, Hayward, NK and Leonard, JH (2001) CDKN2A is not the principal target of deletions on the short arm of chromosome 9 in neuroendocrine (Merkel cell) carcinoma of the skin. International Journal of Cancer, 93 3: 361-367. doi:10.1002/ijc.1352

  • Pollock, P. M., Welch, J. and Hayward, N. K. (2001) Evidence for three tumor suppressor loci on chromosome 9p involved in melanoma development. Cancer Research, 61 3: 1154-1161.

  • Whiteman, D. and Hayward, N. (2001) Impact of the human genome project on medical genetics. Today's Life Science, 13 38-43.

  • Box, N. F., Duffy, D. L., Chen, W., Stark, M., Martin, N. G., Sturm, R. A. and Hayward, N. K. (2001) MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. American Journal of Human Genetics, 69 4: 765-773. doi:10.1086/323412

  • Walker, G. and Hayward, N. (2001) No evidence of a role for activating CDK2 mutations in melanoma. Melanoma Research, 11 4: 343-348. doi:10.1097/00008390-200108000-00004

  • Williams, S. J. and Hayward, N. K. (2001) The impact of the Human Genome Project on medical genetics. Trends In Molecular Medicine, 7 5: 229-231. doi:10.1016/S1471-4914(01)02001-9

  • Mowry, B., Kelly, R. W., Nancarrow, D. J., Lennon, D. P., Nertney, D. A., Jones, H. L., O'Brien, M. F., Thornley, C. E., Walters, M. K., Crowe, R. R., Silverman, J. M., Endicott, J., Sharpe, L., Hayward, N. K., Gladis, M. M., Foote, S. J. and Levinson, D. F. (2000) Second state of a genome scan of schizophrenia: Study of five positive regions in an expanded sample. American Journal of Medical Genetics (Neuropsychiatric Genetics), 96 6: 864-869. doi:10.1002/1096-8628(20001204)96:6

  • 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

  • Bellomo, D., Headrick, J. P., Silins, G. U., Paterson, C. A., Thomas, P. S., Gartside, M., Mould, A., Cahill, M. M., Tonks, I. D., Grimmond, S. M., Wells, C. A., Little, M. H., Cummings, M. C., Hayward, N. K. and Kay, G. F. (2000) Mice lacking the vascular endothelial growth factor-B gene (Vegfb) have smaller hearts, dysfunctional coronary vasculature, and impaired recovery from cardiac ischemia. Circulation Research, 86 2: E29-E35.

  • Leonard, JH, Cook, AL, Nancarrow, D, Hayward, N, Van Gele, M, Van Roy, N and Speleman, F (2000) Deletion mapping on the short arm of chromosome 1 in Merkel cell carcinoma. Cancer Detection & Prevention, 24 6: 620-627.

  • Bergman, L., Teh, B. T., Cardinal, J., Palmer, J. H., Walters, M. A., Shepherd, J. R. W., Cameron, D. J. and Hayward, N. (2000) Identification of MEN1 gene mutations in families with MEN1 and related disorders. British Journal of Cancer, 83 8: 1009-1014. doi:10.1054/bjoc.2000.1380

  • Palmer, JS, Duffy, DL, Box, NF, Aitken, JF, O'Gorman, LE, Green, AC, Hayward, NK, Martin, NG and Sturm, RA (2000) Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?. American Journal of Human Genetics, 66 1: 176-186. doi:10.1086/302711

  • Nancarrow, D. J., Levinson, D. F., Taylor, J. J., Hayward, N., Walters, M. K., Lennon, D. P., Nertney, D. A., Jones, H. T., Brown, D. M., Kirby, A., Kruglyak, L., Crowe, R. R., Andreasen, N. C., Black, D. W., Silverman, J. M., Mohs, R. C., Siever, L. J., Endicott, J., Sharpe, L., Mowry, B. and Mahtani, M. M. (2000) No support for linkage to the bipolar regions on chromosomes 4p, 18p or 18q in 43 schizophrenia pedigrees. American Journal of Medicaletics (Neuropsych Geniatric Genetics), 96 2: 224-227. doi:10.1002/ajmg.b.30108

  • Zhu, G, Duffy, DL, Eldridge, A, Grace, M, Mayne, C, O'Gorman, L, Aitken, JF, Neale, MC, Hayward, NK, Green, AC and Martin, NG (1999) A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. American Journal of Human Genetics, 65 2: 483-492. doi:10.1086/302494

  • Forrest, A. R. R., McCormack, A. K., DeSouza, C. P. C., Sinnamon, J. M., Tonks, I. D., Hayward, N. K., Ellem, K. A. O. and Gabrielli, B. G. (1999) Multiple splicing variants of cdc25B regulate G2/M progression. Biochemical and Biophysical Research Communications, 260 2: 510-515. doi:10.1006/bbrc.1999.0870

  • Aitken, J., Welch, J., Duffy, D., Milligan, A., Green, A., Martin, N. G. and Hayward, N. (1999) CDKN2A variants in a population-based sample of Queensland families with melanoma. Journal of the National Cancer Institute, 91 5: 446-452. doi:10.1093/jnci/91.5.446

  • Walker, GJ, Gabrielli, BG, Castellano, M and Hayward, NK (1999) Functional reassessment of p16 variants using a transfection-based assay. International Journal of Cancer, 82 2: 305-312. doi:10.1002/(SICI)1097-0215(19990719)82:2<305::AID-IJC24>3.0.CO;2-Z

Conference Publication

  • Kendall, B. J., Macdonald, G. A., Hayward, N. K., Prins, J. B., O'Brien, S., Whiteman, D. C. and Study Digestive Hlth (2011). Obesity, central obesity and the risk of Barrett's oesophagus. In: Abstracts of Australian Gastroenterology Week 2011. Australian Gastroenterology Week 2011, Brisbane, Qld, Australia, (76-76). 12–15 September, 2011. doi:10.1111/j.1440-1746.2011.06825.x

  • Kendall, B. J., Macdonald, G. A., Hayward, N. K., Prins, J. B., O'Brien, S., Whiteman, D. C. and Study Of Digestive Health (2011). Type 2 diabetes mellitus and the risk of Barrett's oesophagus. In: Abstracts of Australian Gastroenterology Week 2011. Australian Gastroenterology Week 2011, Brisbane, Qld, Australia, (76-76). 12–15 September, 2011. doi:10.1111/j.1440-1746.2011.06825.x

  • Kendall, B. J., MacDonald, G. A., Hayward, N. K., Prins, J. B., O'Brien, S., Whiteman, D. C. and for the Study of Digestive Health (2010). Daytime sleepiness, gastro-oesophageal reflux and Barrett's oesophagus: A case-control study. In: Australian Gastroenterology Week 2010, Broadbeach, Qld., Australia, (A41-A41). 20-23 October 2010. doi:10.1111/j.1440-1746.2010.06451.x

  • Kendall, B. J., Macdonald, G. A., Hayward, N. K., Prins, J. B., O'Brien, S., Whiteman, D. C. and for the Study of Digestive Health (2010). Metabolic syndrome and the risk of Barrett's oesophagus. In: Australian Gastroenterology Week 2010, Broadbeach, Qld., Australia, (A78-A78). 20-23 October 2010. doi:10.1111/j.1440-1746.2010.06453.x

  • Kendall, B. J., MacDonald, G. A., Hayward, N. K., Green, A. C., Webb, P. M. and Whiteman, D. C. (2009). Undiagnosed coeliac disease and risk of oesophageal squamous cell carcinoma. In: Abstracts of the Australia & New Zealand Medical & Surgical Gastrointestinal Week 2009. The Australia & New Zealand Medical & Surgical Gastrointestinal Week 2009, Sydney, Australia, (A339-A339). 21-24 October 2009. doi:10.1111/j.1440-1746.2009.06061.x

  • McCurdy, R. D., Feron, F., Perry, C., Chant, D. C., McLean, D., Matigian, N., Hayward, N. K., McGrath, J. J. and Mackay-Sim, A. (2006). Functional and molecular alterations to cell cycle are seen in biopsied olfactory neuroepithelium from patients with schizophrenia and bipolar I disorder. In: Schizophrenia Research : Abstracts of the XIIIth Biennial Winter Workshop on Schizophrenia Research. XIIIth Biennial Winter Workshop on Schizophrenia Research, Davos, Switzerland, (198-198). 4-10 February, 2006. doi:10.1016/j.schres.2006.01.006

  • Larsen, J., Pavey, S., Passmore, L., Bowman, R., Hayward, N., Zimmerman, P. and Fong, K. (2005). Expression profiling of metastatic recurrence in primary bronchogenic squamous cell. In: Lung Cancer. Abstract of the 11th World Conference on Lung Cancer. 11th World Conference on Lung Cancer 2005, Barcelona, Spain, (S133-S133). 3-6 July 2005. doi:10.1016/S0169-5002(05)80568-9

  • Schmidt, Christopher, Martinez, Nathan R., Neller, Michelle, Lai, M., Lopez, Jose Alejandro, Lanagan, Catherine M., O'Connor, Linda E., Nicholas, D., Johnson, Maree K., See, Janet L., Hallt, S., Slater, Gregory J., O'Rourke, Michael G. E., Pavey, Sandra, Hayward, Nick and Ellem, Kay A. O. (2005). Towards a response model for dendritic cell immunotherapy of advanced metastatic melanoma. In: Abstracts fo the 35th Annual Scientific Meeting of the Australasian Society for Immunology and 14th International HLA & Immunogenetics Workshop. 35th Annual SCientific Meeting of the Australasian-Society-for-Immunology/14th International HLA and Immunogenetics Workshops, Melbourne, VIC, Australia, (533-533). 29 November - 2 December 2005. doi:10.1111/j.1399-0039.2005.00523.x

  • Whiteman, D., Green, A., Hayward, N., Pavey, S., Purdie, D. and Webb, P. (2003). Molecular epidemiology of Barret's esophagus and cancer: A population-based case-control study. In: Cancer Epidemiology Biomarkers & Prevention.. 2nd Annual AACR International Conference on Frontiers in Cancer Prevention Research, Phoenix, Arizona,, (1349S-1350S). 26-30 October 2003.

Other Outputs

  • Hayward, Nicholas Kim (1983). Phenacetin metabolites and DNA damage PhD Thesis, School of Molecular and Microbial Sciences, The University of Queensland. doi:10.14264/uql.2014.581

Grants (Administered at UQ)

PhD and MPhil Supervision

Current Supervision

  • Doctor Philosophy — Principal Advisor

  • Doctor Philosophy — Principal Advisor

  • Master Philosophy — Principal Advisor

Completed Supervision