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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: . doi:10.1371/journal.pone.0072144 76   3 Cited 4 times in Scopus4 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 43   23 Cited 25 times in Scopus25 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 101   88 Cited 94 times in Scopus94 0
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 104 1 6 Cited 9 times in Scopus9 0
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 144   79 Cited 87 times in Scopus87 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 19   18 Cited 14 times in Scopus14 60
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 107   136 Cited 163 times in Scopus163 27
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 104   45 Cited 48 times in Scopus48 0
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 74   52 Cited 59 times in Scopus59 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 98 6 1 Cited 2 times in Scopus2 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 79   147 Cited 161 times in Scopus161 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 159 3 102 Cited 110 times in Scopus110 11
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 80   11 Cited 12 times in Scopus12 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 107   23 Cited 24 times in Scopus24 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 87   133 Cited 137 times in Scopus137 16
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-e100683. doi:10.1371/journal.pone.0100683 24   1 Cited 0 times in Scopus0 2
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 26 1 1 Cited 1 times in Scopus1 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 26 2 0 Cited 0 times in Scopus0 2
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 64   45 Cited 55 times in Scopus55 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 66 1 26 Cited 31 times in Scopus31 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 62   16 Cited 18 times in Scopus18 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 99   34 Cited 40 times in Scopus40 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 137   100 Cited 116 times in Scopus116 6
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 29 1 16 Cited 16 times in Scopus16 68
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.2010.06.009 120 3 221 Cited 223 times in Scopus223 9
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 51   16 Cited 17 times in Scopus17 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 25   0 Cited 0 times in Scopus0 2
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 70   41 Cited 40 times in Scopus40 0
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 46   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 64   132 0
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.2005.10.012 123   62 Cited 65 times in Scopus65 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 142 1 81 Cited 89 times in Scopus89 9
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)00868-3 210   18 Cited 20 times in Scopus20 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 41   15 Cited 15 times in Scopus15 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 49   123 Cited 126 times in Scopus126 6
Biondi, CA, Gartside, MG, Waring, P, Loffler, KA, Stark, MS, Magnuson, MA, Kay, GF and Hayward, NK (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 47   68 Cited 76 times in Scopus76 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 52   42 Cited 44 times in Scopus44 1
Larsen, J.E., Fong, K. M. and Hayward, N. K. (2007) Correction. New England Journal of Medicine, 356 2: 201-203. 77   Cited 0 times in Scopus0
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   18 Cited 17 times in Scopus17 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 39   51 Cited 63 times in Scopus63 0
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 55   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. 43   22
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 69   25 Cited 23 times in Scopus23 0
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 35   2 Cited 1 times in Scopus1 0
Tonks, ID, Mould, AW, Schroder, WA, Cotterill, A, Hayward, NK, Walker, GJ and Kay, GF (2010) Dual loss of Rb1 and Trp53 in the adrenal medulla leads to spontaneous pheochromocytoma. Neoplasia, 12 3: 235-243. doi:10.1593/neo.91646 69 1 5 Cited 5 times in Scopus5 0
Yang, Xiaohong R., Brown, Kevin, Landi, Maria T., Ghiorzo, Paola, Badenas, Celia, Xu, Mai, Hayward, Nicholas K., Calista, Donato, Landi, Giorgio, Bruno, William, Bianchi-Scarra, Giovanna, Aguilera, Paula, Puig, Susana, Goldstein, Alisa M. and Tucker, Margaret A. (2012) Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family. Pigment Cell & Melanoma Research, 25 2: 243-247. doi:10.1111/j.1755-148X.2012.00969.x 77   3 Cited 4 times in Scopus4 2
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 199   9 Cited 12 times in Scopus12 0
Hacker, E, Muller, HK, Hayward, N, Fahey, P and Walker, G (2010) Enhancement of DNA repair using topical T4 endonuclease V does not inhibit melanoma formation in Cdk4R24C⁄R24C⁄Tyr-NrasQ61K mice following neonatal UVR. Pigment Cell and Melanoma Research, 23 1: 121-128. doi:10.1111/j.1755-148X.2009.00643.x 96 1 8 Cited 8 times in Scopus8 0
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 46   35 Cited 36 times in Scopus36 0
Elliott, Katherine S., Zeggini, Eleftheria, McCarthy, Mark I., Gudmundsson, Julius, Sulem, Patrick, Stacey, Simon N., Thorlacius, Steinunn, Amundadottir, Laufey, Gronberg, Henrik, Xu, Jianfeng, Gaborieau, Valerie, Eeles, Rosalind A., Neal, David E., Donovan, Jenny L., Hamdy, Freddie C., Muir, Kenneth, Hwang, Shih-Jen, Spitz, Margaret R., Zanke, Brent, Carvajal-Carmona, Luis, Brown, Kevin M., Hayward, Nicholas K., Macgregor, Stuart, Tomlinson, Ian P. M., Lemire, Mathieu, Amos, Christopher I., Murabito, Joanne M., Isaacs, William B., Easton, Douglas F., Brennan, Paul, Barkardottir, Rosa B., Gudbjartsson, Daniel F., Rafnar, Thorunn, Hunter, David J., Chanock, Stephen J., Stefansson, Kari and Ioannidis, John P. A. (2010) Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies. PLoS One, 5 5: e10858-e10864. doi:10.1371/journal.pone.0010858 74 2 17 Cited 16 times in Scopus16 0

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