Intergenic disease-associated regions are abundant in novel transcripts von Bartonicek, N, Clark, M B, Quek, X C, Torpy, J R, Pritchard, A L, Maag, J L V, Gloss, B S, Crawford, J, Taft, R J, Hayward, N K, Montgomery, G W, Mattick, J S, Mercer, T R, Dinger, M E

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Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study von 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-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Höiom, 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.

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Activation of the MAPK pathway is a common event in uveal melanomas although it rarely occurs through mutation of BRAF or RAS von ZUIDERVAART, W, VAN NIEUWPOORT, F, HAYWARD, N. K, GRUIS, N. A, STARK, M, DIJKMAN, R, PACKER, L, BORGSTEIN, A.-M, PAVEY, S, VAN DER VELDEN, P, OUT, C, JAGER, M. J

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A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma von 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., Jönsson, G., Busam, K., Gupta, R., Trent, J.M., Gerdes, A.-M., Brown, K.M., Scolyer, R.A., Hayward, N.K.

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Leptin and the risk of Barrett’s oesophagus von Kendall, B J, Macdonald, G A, Hayward, N K, Prins, J B, Brown, I, Walker, N, Pandeya, N, Green, A C, Webb, P M, Whiteman, D C

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Melanocytic Nevi, Solar Keratoses, and Divergent Pathways to Cutaneous Melanoma von Whiteman, David C., Watt, Peter, Purdie, David M., Hughes, Maria Celia, Hayward, Nicholas K., Green, Adèle C.

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Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype? von Palmer, James S., Duffy, David L., Box, Neil F., Aitken, Joanne F., O'Gorman, Louise E., Green, Adele C., Hayward, Nicholas K., Martin, Nicholas G., Sturm, Richard A.

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Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophrenia von HANDOKO, H. Y, NYHOLT, D. R, MOWRY, B. J, HAYWARD, N. K, NERTNEY, D. A, HANNAH, D. E, WINDUS, L. C, MCCORMACK, C. M, SMITH, H. J, FILIPPICH, C, JAMES, M. R

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Lack of augmentation of tumor spectrum or severity in dual heterozygous Men1 and Rb1 knockout mice von LOFFLER, K. A, BIONDI, C. A, HAYWARD, N. K, GARTSIDE, M. G, SEREWKO-AURET, M. M, DUNCAN, R, TONKS, I. D, MOULD, A. W, WARING, P, MULLER, H. K, KAY, G. F

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Genetics of melanoma predisposition von Hayward, Nicholas K

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Mice Lacking the Vascular Endothelial Growth Factor-B Gene (Vegfb) Have Smaller Hearts, Dysfunctional Coronary Vasculature, and Impaired Recovery From Cardiac Ischemia von Bellomo, Daniela, Headrick, John P, Silins, Ginters U, Paterson, Carol A, Thomas, Penny S, Gartside, Michael, Mould, Arne, Cahill, Marian M, Tonks, Ian D, Grimmond, Sean M, Townson, Steve, Wells, Christine, Little, Melissa, Cummings, Margaret C, Hayward, Nicholas K, Kay, Graham F

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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... von Zhu, Gu, Duffy, David L., Eldridge, Ann, Grace, Marlene, Mayne, Carol, O'Gorman, Louise, Aitken, Joanne F., Neale, Michael C., Hayward, Nicholas K., Green, Adele C., Martin, Nicholas G.

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Survival outcomes in patients with multiple primary melanomas von Rowe, C.J., Law, M.H., Palmer, J.M., MacGregor, S., Hayward, N.K., Khosrotehrani, K.

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Menin Associates with a Trithorax Family Histone Methyltransferase Complex and with the Hoxc8 Locus von Hughes, Christina M., Rozenblatt-Rosen, Orit, Milne, Thomas A., Copeland, Terry D., Levine, Stuart S., Lee, Jeffrey C., Hayes, D. Neil, Shanmugam, Kalai Selvi, Bhattacharjee, Arindam, Biondi, Christine A., Kay, Graham F., Hayward, Nicholas K., Hess, Jay L., Meyerson, Matthew

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Gene expression of lung squamous cell carcinoma reflects mode of lymph node involvement von Larsen, J. E, Pavey, S. J, Bowman, R, Yang, I. A, Clarke, B. E, Colosimo, M. L, Hayward, N. K, Fong, K. M

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Relevance of ultraviolet-induced N-ras oncogene point mutations in development of primary human cutaneous melanoma von van Elsas, A, Zerp, SF, van der Flier, S, Kruse, KM, Aarnoudse, C, Hayward, NK, Ruiter, DJ, Schrier, PI

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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 von Mould, A. W., Scotney, P., Greco, S. A., Hayward, N. K., Nash, A., Kay, G. F.

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Melanocyte transformation requires complete loss of all pocket protein function via a mechanism that mitigates the need for MAPK pathway activation von Tonks, I D, Mukhopadhyay, P, Schroder, W A, Sorolla, A, Mould, A W, Handoko, H Y, Ferguson, B, Muller, H K, Keith, P, Hayward, N K, Walker, G J, Kay, G F

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The CDKN2A (p16) gene and human cancer von Foulkes, W D, Flanders, T Y, Pollock, P M, Hayward, N K

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Genome Scan of Schizophrenia von Levinson, Douglas F., Mahtani, Melanie M., Nancarrow, Derek J., Brown, Donna M., Kruglyak, Leonid, Kirby, Andrew, Hayward, Nicholas K., Crowe, Raymond R., Andreasen, Nancy C., Black, Donald W., Silverman, Jeremy M., Endicott, Jean, Sharpe, Lawrence, Mohs, Richard C., Siever, Larry J., Walters, Marilyn K., Lennon, David P., Jones, Helen L., Nertney, Deborah A., Daly, Mark J., Gladis, Madeline, Mowry, Bryan J.

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