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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: e72144. doi:10.1371/journal.pone.0072144     33 Cited 37 times in Scopus37 1
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     65 Cited 70 times in Scopus70 1
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     123 Cited 132 times in Scopus132 3
Wright, CM, Larsen, JE, Hayward, NK, Martins, MU, Tan, ME, Davidson, MR, Savarimuthu, SM, McLachlan, RE, Passmore, LH, Windsor, MN, Clarke, BE, Duhig, EE, Yang, IA, Bowman, RV and Fong, KM (2010) ADAM28: A potential oncogene involved in asbestos-related lung adenocarcinomas. Genes Chromosomes & Cancer, 49 8: 688-698. doi:10.1002/gcc.20779   1 17 Cited 21 times in Scopus21 3
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     89 Cited 97 times in Scopus97 3
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     98 Cited 104 times in Scopus104 63
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     241 Cited 275 times in Scopus275 32
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     54 Cited 60 times in Scopus60 0
Molven, Anders, Grimstvedt, Magne B., Steine, Solrun J., Harland, Mark, Avril, Marie-Fran├žoise, 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     65 Cited 72 times in Scopus72 0
Serewko-Auret, MM, Mould, AW, Loffler, KA, Duncan, R, Kay, GF and Hayward, NK (2010) Alterations in gene expression in MEN1-associated insulinoma development. Pancreas, 39 8: 1140-1146. doi:10.1097/MPA.0b013e3181dc67fc   6 5 Cited 5 times in Scopus5 1
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     162 Cited 180 times in Scopus180 0
Yokoyama, Satoru, Woods, Susan L., Boyle, Glen M., Aoude, Lauren G., MacGregor, Stuart, Zismann, Victoria, Gartside, Michael, Cust, Anne E., Haq, Rizwan, Harland, Mark, Taylor, John C., Duffy, David L., Holohan, Kelly, Dutton-Regester, Ken, Palmer, Jane M., Bonazzi, Vanessa, Stark, Mitchell S., Symmons, Judith, Law, Matthew H., Schmidt, Christopher, Lanagan, Cathy, O'Connor, Linda, Holland, Elizabeth A., Schmid, Helen, Maskiell, Judith A., Jetann, Jodie, Ferguson, Megan, Jenkins, Mark A., Kefford, Richard F., Giles, Graham G., Armstrong, Bruce K., Aitken, Joanne F., Hopper, John L., Whiteman, David C., Pharoah, Paul D., Easton, Douglas F., Dunning, Alison M., Newton-Bishop, Julia A., Montgomery, Grant W., Martin, Nicholas G., Mann, Graham J., Bishop, D. Timothy, Tsao, Hensin, Trent, Jeffrey M., Fisher, David E., Hayward, Nicholas K. and Brown, Kevin M. (2011) A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 480 7375: 99-103. doi:10.1038/nature10630     212 Cited 237 times in Scopus237 20
Shekar, SN, Duffy, DL, Youl, P, Baxter, AJ, Kvaskoff, M, Whiteman, DC, Green, AC, Hughes, MC, Hayward, NK, Coates, M and Martin, NG (2009) A Population-Based Study of Australian Twins with Melanoma Suggests a Strong Genetic Contribution to Liability. Journal of Investigative Dermatology, 129 9: 2211-2219. doi:10.1038/jid.2009.48     20 Cited 19 times in Scopus19 6
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     45 Cited 48 times in Scopus48 0
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     31 Cited 30 times in Scopus30 0
Sriram, Krishna B., Larsen, Jill E., Francis, Santiyagu M. Savarimuthu, Wright, Casey M., Clarke, Belinda E., Duhig, Edwina E., Brown, Kevin M., Hayward, Nicholas K., Yang, Ian A., Bowman, Rayleen V. and Fong, Kwun M. (2012) Array-comparative genomic hybridization reveals loss of SOCS6 is associated with poor prognosis in primary lung squamous cell carcinoma. Plos One, 7 2: e30398-1-e30398-12. doi:10.1371/journal.pone.0030398     20 Cited 19 times in Scopus19 0
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     194 Cited 207 times in Scopus207 31
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     4 Cited 5 times in Scopus5 1
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   1 3 Cited 3 times in Scopus3 1
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   2 3 Cited 3 times in Scopus3 1
Whiteman, DC, Parmar, P, Fahey, P, Moore, SP, Stark, M, Zhao, ZZ, Montgomery, GW, Green, AC, Hayward, NK, Webb, PM and Australian Canc Study (2010) Association of helicobacter pylori infection with reduced risk for esophageal cancer is independent of environmental and genetic modifiers. Gastroenterology, 139 1: 73-83. doi:10.1053/j.gastro.2010.04.009     78 Cited 92 times in Scopus92 1
Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A. M., Newton Bishop, J. A., Bishop, D. T., Kanetsky, P. A., Hayward, N. K., Gillanders, E., Elder, D. E., Avril, M. F., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarra, G., Brassac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Hoiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Lang, J. M., Mackie, R. M., Mann, G. J., Ming, M. E., Njauw, C. J., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M. A., van der Velden, P., Yang, X. R., Gruis, N. and Melanoma Genetics Consortium (2010) Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: A GenoMEL study. Journal of the National Cancer Institute, 102 20: 1568-1583. doi:10.1093/jnci/djq363   1 52 Cited 67 times in Scopus67 0
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     17 Cited 20 times in Scopus20 0
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     56 Cited 59 times in Scopus59 0
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     128 Cited 144 times in Scopus144 23
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   1 47 Cited 50 times in Scopus50 69
Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010) A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 1: 139-145. doi:10.1016/j.ajhg.2010.06.009   3 481 Cited 483 times in Scopus483 17
Barbour, Andrew P., Tang, Yue Hang, Armour, Nicola, Dutton-Regester, Ken, Krause, Lutz, Loffler, Kelly A., Lambie, Duncan, Burmeister, Bryan, Thomas, Janine, Smithers, B. Mark and Hayward, Nicholas K. (2014) BRAF mutation status is an independent prognostic factor for resected stage IIIB and IIIC melanoma: implications for melanoma staging and adjuvant therapy. European Journal of Cancer, 50 15: 2668-2676. doi:10.1016/j.ejca.2014.06.009     22 Cited 23 times in Scopus23 0
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     18 Cited 21 times in Scopus21 0
Tonks, Ian D., Walker, Graeme J., Mould, Arne W., Ferguson, Blake, Keith, Patricia, Hayward, Nicholas K. and Kay, Graham F. (2012) Brca1 is involved in establishing murine pigmentation in a p53 and developmentally specific manner. Pigment Cell & Melanoma Research, 25 4: 530-532. doi:10.1111/j.1755-148X.2012.01009.x     0 0 1
Teh, BT, Birrell, G, Farrell, A, Leonard, JH, Walters, MK, Palmer, JM, Ramsay, JR, Schlect, DJ, Furnival, C, Lavin, MF, Bennett, I and Hayward, NK (1997) Breast cancer in six women with neurofibromatosis type 1. Breast, 6 3: 155-160. doi:10.1016/S0960-9776(97)90558-0     6 Cited 8 times in Scopus8 0
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     56 Cited 54 times in Scopus54 0
Freitag, Daniel, Butterworth, Adam S, Willeit, Peter, Howson, Joanna M M, Burgess, Stephen, Kaptoge, Stephen, Young, Robin, Ho, Weang Kee, Wood, Angela M, Sweeting, Michael, Spackman, Sarah, Staley, James R, Ramond, Anna, Harshfield, Eric, Nielsen, Sune F, Grande, Peer, Lange, Leslie A, Bown, Matthew J, Jones, Gregory T, Scott, Robert A, Bevan, Steve, Porcu, Eleonora, Thorleifsson, Gudmar, Zeng, Lingyao, Kessler, Thorsten, Nikpay, Majid, Do, Ron, Zhang, Weihua, Hopewell, Jemma C, Kleber, Marcus, Delgado, Graciela E, Nelson, Christopher P, Goel, Anuj, Bis, Joshua C, Dehghan, Abbas, Ligthart, Symen, Smith, Albert V, Qu, Liming, van 't Hof, Femke.NG., de Bakker, Paul I W, Baas, Annette F, van Rij, Andre, Tromp, Gerard, Kuivaniemi, Helena, Ritchie, Marylyn D, Verma, Shefali S, Crawford, Dana C, Malinowski, Jennifer, de Andrade, Mariza, Kullo, Iftikhar J, Peissig, Peggy L, McCarty, Catherine A, Bottinger, Erwin P, Gottesman, Omri, Crosslin, David R, Carrell, David S, Rasmussen-Torvik, Laura J, Pacheco, Jennifer A, Huang, Jie, Timpson, Nicholas J, Kettunen, Johannes, Ala-Korpela, Mika, Mitchell, Gary F, Parsa, Afshin, Wilkinson, Ian B, Gorski, Mathias, Li, Yong, Franceschini, Nora, Keller, Margaux F, Ganesh, Santhi K, Langefeld, Carl D, Bruijn, Lucie, Brown, Matthew A, Evans, David M, Baltic, Svetlana, Ferreira, Manuel A, Baurecht, Hansjorg, Weidinger, Stephan, Franke, Andre, Lubitz, Steven A, Muller-Nurasyid, Martina, Felix, Janine, Smith, Nicholas L, Sudman, Marc, Thompson, Susan D, Zeggini, Eleftheria, Panoutsopoulou, Kalliope, Nalls, Mike A, Singleton, Andrew, Polychronakos, Constantin, Bradfield, Jonathan P, Hakonarson, Hakonarson, Easton, Douglas F, Thompson, Deborah, Tomlinson, Ian P, Dunlop, Malcolm, Hemminki, Kari, Morgan, Gareth, Eisen, Timothy, Goldschmidt, Hartmut, Allan, James M, Henrion, Marc, Whiffin, Nicola, Wang, Yufei, Chubb, Daniel, Iles, Mark M, Bishop, D Timothy, Law, Matthew H, Hayward, Nicholas K, Luo, Yang, Nejentsev, Sergey, Barbalic, Maja, Crossman, David, Sanna, Serena, Soranzo, Nicole, Markus, Hugh S, Wareham, Nicholas J, Rader, Daniel J, Reilly, Muredach, Assimes, Themistocles, Harris, Tamara B, Hofman, Albert, Franco, Oscar H, Gudnason, Vilmundur, Tracy, Russell, Psaty, Bruce M, Farrall, Martin, Watkins, Hugh, Hall, Alistair S, Samani, Nilesh J, Marz, Winfried, Clarke, Robert, Collins, Rory, Kooner, Jaspal S, Chambers, John C, Kathiresan, Sekar, McPherson, Ruth, Erdmann, Jeanette, Kastrati, Adnan, Schunkert, Heribert, Stefansson, Kari, Thorsteinsdottir, Unnur, Walston, Jeremy D, Tybjaerg-Hansen, Anne, Alam, Dewan S, Al Shafi Majumder, Abdullah, Angelantonio, Emanuele Di, Chowdhury, Rajiv, Nordestgaard, Borge G, Saleheen, Danish, Thompson, Simon G, Danesh, John and Houlston, Richard S (2015) Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A Mendelian randomisation analysis. The Lancet Diabetes and Endocrinology, 3 4: 243-253. doi:10.1016/S2213-8587(15)00034-0     43 Cited 45 times in Scopus45 32
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     9 Cited 10 times in Scopus10 0
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     151 Cited 159 times in Scopus159 3
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     87 Cited 90 times in Scopus90 0
Stark, Mitchell S., Tyagi, Sonika, Nancarrow, Derek J., Boyle, Glen M., Cook, Anthony L., Whiteman, David C., Parsons, Peter G., Schmidt, Christopher, Sturm, Richard A. and Hayward, Nicholas K. (2010) Characterization of the melanoma miRNAome by deep sequencing. PLoS One, 5 3: e9685-1-e9685-9. doi:10.1371/journal.pone.0009685   1 134 Cited 149 times in Scopus149 12
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     23 Cited 26 times in Scopus26 0
Jovanovic, Braslav, Egyhazi, Suzanne, Eskandarpour, Malihe, Ghiorzo, Paola, Palmer, Jane M., Bianchi Scarra, Giovanna, Hayward, Nicholas K. and Hansson, Johan (2010) Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations. Journal of Investigative Dermatology, 130 2: 618-620. doi:10.1038/jid.2009.287     25 Cited 23 times in Scopus23 0
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     149 Cited 158 times in Scopus158 6
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     90 Cited 94 times in Scopus94 0
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     49 Cited 53 times in Scopus53 7
Grimmond, SM, Palmer, JM, Walters, MK, Scott, C, Nancarrow, DJ, Teh, BT, Elmes, C, Pyke, C, Khoo, SK, Bennett, I, Wetzig, N and Hayward, NK (1996) Confirmation of a susceptibility locus on chromosome 13 in Australian breast cancer families. Human Genetics, 98 1: 80-85. doi:10.1007/s004390050164     8 Cited 7 times in Scopus7 6
Larsen, J.E., Fong, K. M. and Hayward, N. K. (2007) Correction. New England Journal of Medicine, 356 2: 201-203.     Cited 1 times in Scopus1
Bonazzi, Vanessa F., Nancarrow, Derek J., Stark, Mitchell S., Moser, Ralf J., Boyle, Glen M., Aoude, Lauren G., Schmidt, Christopher and Hayward, Nicholas K. (2011) Cross-platform array screening identifies COL1A2, THBS1, TNFRSF10D and UCHL1 as genes frequently silenced by methylation in melanoma. PLoS One, 6 10: 1-9. doi:10.1371/journal.pone.0026121     40 Cited 42 times in Scopus42 1
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     59 Cited 74 times in Scopus74 3
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     0 0
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.     25
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     27 Cited 27 times in Scopus27 3
Tonks, Ian D., Mould, Arne, Nurcombe, Victor, Cool, Simon M., Walker, Graeme J., Hacker, Elke, Keith, Patricia, Schroder, Wayne A., Cotterill, Andrew, Hayward, Nicholas K. and Kay, Graham F. (2009) Dual loss of Rb1 and Trp53 in melanocytes perturbs melanocyte homeostasis and genetic stability in vitro but does not cause melanoma or pigmentation defects in vivo. Pigment Cell and Melanoma Research, 22 3: 328-330. doi:10.1111/j.1755-148X.2009.00560.x     2 Cited 1 times in Scopus1 0

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