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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. 7   2 Cited 1 times in Scopus1
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. 56   56 Cited 62 times in Scopus62
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. 49 1 4 Cited 5 times in Scopus5
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. 99   75 Cited 81 times in Scopus81
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. 51   100 Cited 104 times in Scopus104
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. 52   34 Cited 36 times in Scopus36
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. 44   43 Cited 45 times in Scopus45
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. 74 6 0 Cited 1 times in Scopus1
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. 52   140
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. 59 3 22 Cited 26 times in Scopus26
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. 42   6 Cited 8 times in Scopus8
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. 89   20 Cited 20 times in Scopus20
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. 38   86 Cited 94 times in Scopus94
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. 42   17 Cited 24 times in Scopus24
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. 42 1 12 Cited 14 times in Scopus14
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. 35   15 Cited 16 times in Scopus16
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. 51   24 Cited 27 times in Scopus27
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. 77   78 Cited 86 times in Scopus86
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. 83 3 70 Cited 73 times in Scopus73
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. 29   14 Cited 15 times in Scopus15
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: . 8   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. 48   35 Cited 32 times in Scopus32
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. 25   9
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. 41   121
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. 87   48 Cited 48 times in Scopus48
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. 97 1 42 Cited 50 times in Scopus50
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. 181   14 Cited 15 times in Scopus15
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. 27   9 Cited 8 times in Scopus8
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. 33   93 Cited 93 times in Scopus93
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. 17   61 Cited 65 times in Scopus65
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. 34   34 Cited 36 times in Scopus36
Larsen, J.E., Fong, K. M. and Hayward, N. K. (2007) Correction. New England Journal of Medicine, 356 2: 201-203. 110   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. 24   7 Cited 7 times in Scopus7
de Snoo, Femke A. and Hayward, Nicholas K. (2005) Cutaneous melanoma susceptibility and progression genes. Cancer Letters, 230 2: 153-186. 24   40 Cited 50 times in Scopus50
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. 33   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   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. 36   23 Cited 20 times in Scopus20
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. 20   2 Cited 1 times in Scopus1
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. 44 1 4 Cited 4 times in Scopus4
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. 8   1 Cited 1 times in Scopus1
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. 32   9 Cited 12 times in Scopus12
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. 70 1 7 Cited 7 times in Scopus7
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. 24   31 Cited 32 times in Scopus32
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. 34 2 10 Cited 4 times in Scopus4
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. 22   15
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. 23   53 Cited 57 times in Scopus57
Krauthammer, M., Kong, Y., Ha, B.H., Evans, P., Bacchiocchi, A., McCusker, J.P., Cheng, E., Davis, M.J., Goh, G., Choi, M., Ariyan, S., Narayan, D., Dutton-Regester, K., Capatana, A., Holman, E.C., Bosenberg, M., Sznol, M., Kluger, H.M., Brash, D.E., Stern, D.F., Materin, M.A., Lo, R.S., Mane, S., Ma, S., Kidd, K.K., Hayward, N.K., Lifton, R.P., Schlessinger, J., Boggon, T.J. and Halaban, R. (2012) Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma. Nature Genetics, 44 9: 1006-1014. 27   13 Cited 0 times in Scopus0
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. 32   22 Cited 26 times in Scopus26
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. 41   8 Cited 10 times in Scopus10
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. 54   48 Cited 49 times in Scopus49

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