-
1
-
-
0038457509
-
Melanoma etiology: Where are we?
-
2-s2.0-0038457509 10.1038/sj.onc.1206444
-
Tucker M. A., Goldstein A. M., Melanoma etiology: where are we? Oncogene 2003 22 20 3042 3052 2-s2.0-0038457509 10.1038/sj.onc.1206444
-
(2003)
Oncogene
, vol.22
, Issue.20
, pp. 3042-3052
-
-
Tucker, M.A.1
Goldstein, A.M.2
-
2
-
-
77958609747
-
Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: A GenoMEL study
-
2-s2.0-77958609747 10.1093/jnci/djq363
-
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-Scarr 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., Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. Journal of the National Cancer Institute 2010 102 20 1568 1583 2-s2.0-77958609747 10.1093/jnci/djq363
-
(2010)
Journal of the National Cancer Institute
, vol.102
, Issue.20
, pp. 1568-1583
-
-
Demenais, F.1
Mohamdi, H.2
Chaudru, V.3
Goldstein, A.M.4
Newton Bishop, J.A.5
Bishop, D.T.6
Kanetsky, P.A.7
Hayward, N.K.8
Gillanders, E.9
Elder, D.E.10
Avril, M.F.11
Azizi, E.12
Van Belle, P.13
Bergman, W.14
Bianchi-Scarr, G.15
Bressac-De Paillerets, B.16
Calista, D.17
Carrera, C.18
Hansson, J.19
Harland, M.20
Hogg, D.21
Höiom, V.22
Holland, E.A.23
Ingvar, C.24
Landi, M.T.25
Lang, J.M.26
Mackie, R.M.27
Mann, G.J.28
Ming, M.E.29
Njauw, C.J.30
Olsson, H.31
Palmer, J.32
Pastorino, L.33
Puig, S.34
Randerson-Moor, J.35
Stark, M.36
Tsao, H.37
Tucker, M.A.38
Van Der Velden, P.39
Yang, X.R.40
Gruis, N.41
more..
-
3
-
-
57449087434
-
Melanoma and genetics
-
2-s2.0-57449087434 10.1016/j.clindermatol.2008.09.005
-
Nelson A. A., Tsao H., Melanoma and genetics. Clinics in Dermatology 2009 27 1 46 52 2-s2.0-57449087434 10.1016/j.clindermatol.2008.09.005
-
(2009)
Clinics in Dermatology
, vol.27
, Issue.1
, pp. 46-52
-
-
Nelson, A.A.1
Tsao, H.2
-
4
-
-
85047700514
-
High- and low-penetrance cutaneous melanoma susceptibility genes
-
2-s2.0-33745169384 10.1586/14787210.6.5.657
-
Fargnoli M. C., Argenziano G., Zalaudek I., Peris K., High- and low-penetrance cutaneous melanoma susceptibility genes. Expert Review of Anticancer Therapy 2006 6 5 657 670 2-s2.0-33745169384 10.1586/14787210.6.5.657
-
(2006)
Expert Review of Anticancer Therapy
, vol.6
, Issue.5
, pp. 657-670
-
-
Fargnoli, M.C.1
Argenziano, G.2
Zalaudek, I.3
Peris, K.4
-
5
-
-
84856023369
-
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
-
2-s2.0-84856023369 10.1136/jmedgenet-2011-100156
-
Abdel-Rahman M. H., Pilarski R., Cebulla C. M., Massengill J. B., Christopher B. N., Boru G., Hovland P., Davidorf F. H., Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers. Journal of Medical Genetics 2011 48 12 856 859 2-s2.0-84856023369 10.1136/jmedgenet-2011-100156
-
(2011)
Journal of Medical Genetics
, vol.48
, Issue.12
, pp. 856-859
-
-
Abdel-Rahman, M.H.1
Pilarski, R.2
Cebulla, C.M.3
Massengill, J.B.4
Christopher, B.N.5
Boru, G.6
Hovland, P.7
Davidorf, F.H.8
-
6
-
-
80053385701
-
Germline BAP1 mutations predispose to malignant mesothelioma
-
2-s2.0-80053385701 10.1038/ng.912
-
Testa J. R., Cheung M., Pei J., Below J. E., Tan Y., Sementino E., Cox N. J., Dogan A. U., Pass H. I., Trusa S., Hesdorffer M., Nasu M., Powers A., Rivera Z., Comertpay S., Tanji M., Gaudino G., Yang H., Carbone M., Germline BAP1 mutations predispose to malignant mesothelioma. Nature Genetics 2011 43 10 1022 1026 2-s2.0-80053385701 10.1038/ng.912
-
(2011)
Nature Genetics
, vol.43
, Issue.10
, pp. 1022-1026
-
-
Testa, J.R.1
Cheung, M.2
Pei, J.3
Below, J.E.4
Tan, Y.5
Sementino, E.6
Cox, N.J.7
Dogan, A.U.8
Pass, H.I.9
Trusa, S.10
Hesdorffer, M.11
Nasu, M.12
Powers, A.13
Rivera, Z.14
Comertpay, S.15
Tanji, M.16
Gaudino, G.17
Yang, H.18
Carbone, M.19
-
7
-
-
80053386896
-
Germline mutations in BAP1 predispose to melanocytic tumors
-
2-s2.0-80053386896 10.1038/ng.910
-
Wiesner T., Obenauf A. C., Murali R., Fried I., Griewank K. G., Ulz P., Windpassinger C., Wackernagel W., Loy S., Wolf I., Viale A., Lash A. E., Pirun M., Socci N. D., Rütten A., Palmedo G., Abramson D., Offit K., Ott A., Becker J. C., Cerroni L., Kutzner H., Bastian B. C., Speicher M. R., Germline mutations in BAP1 predispose to melanocytic tumors. Nature Genetics 2011 43 10 1018 1022 2-s2.0-80053386896 10.1038/ng.910
-
(2011)
Nature Genetics
, vol.43
, Issue.10
, pp. 1018-1022
-
-
Wiesner, T.1
Obenauf, A.C.2
Murali, R.3
Fried, I.4
Griewank, K.G.5
Ulz, P.6
Windpassinger, C.7
Wackernagel, W.8
Loy, S.9
Wolf, I.10
Viale, A.11
Lash, A.E.12
Pirun, M.13
Socci, N.D.14
Rütten, A.15
Palmedo, G.16
Abramson, D.17
Offit, K.18
Ott, A.19
Becker, J.C.20
Cerroni, L.21
Kutzner, H.22
Bastian, B.C.23
Speicher, M.R.24
more..
-
8
-
-
75549084094
-
Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma
-
2-s2.0-75549084094 10.1038/jid.2009.258
-
Duffy D. L., Zhao Z. Z., Sturm R. A., Hayward N. K., Martin N. G., Montgomery G. W., Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma. Journal of Investigative Dermatology 2010 130 2 520 528 2-s2.0-75549084094 10.1038/jid.2009.258
-
(2010)
Journal of Investigative Dermatology
, vol.130
, Issue.2
, pp. 520-528
-
-
Duffy, D.L.1
Zhao, Z.Z.2
Sturm, R.A.3
Hayward, N.K.4
Martin, N.G.5
Montgomery, G.W.6
-
9
-
-
77956301673
-
Genome-wide association studies of pigmentation and skin cancer: A review and meta-analysis
-
2-s2.0-77956301673 10.1111/j.1755-148X.2010.00730.x
-
Gerstenblith M. R., Shi J., Landi M. T., Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis. Pigment Cell and Melanoma Research 2010 23 5 587 606 2-s2.0-77956301673 10.1111/j.1755-148X.2010. 00730.x
-
(2010)
Pigment Cell and Melanoma Research
, vol.23
, Issue.5
, pp. 587-606
-
-
Gerstenblith, M.R.1
Shi, J.2
Landi, M.T.3
-
10
-
-
45549097424
-
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
-
Gudbjartsson D. F., Sulem P., Stacey S. N., ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nature Genetics 2008 40 8 886 891
-
(2008)
Nature Genetics
, vol.40
, Issue.8
, pp. 886-891
-
-
Gudbjartsson, D.F.1
Sulem, P.2
Stacey, S.N.3
-
11
-
-
67650073375
-
Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians
-
2-s2.0-67650073375 10.1002/ijc.24327
-
Nan H., Kraft P., Hunter D. J., Han J., Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians. International Journal of Cancer 2009 125 4 909 917 2-s2.0-67650073375 10.1002/ijc.24327
-
(2009)
International Journal of Cancer
, vol.125
, Issue.4
, pp. 909-917
-
-
Nan, H.1
Kraft, P.2
Hunter, D.J.3
Han, J.4
-
12
-
-
24744455058
-
Association between endothelin receptor B nonsynonymous variants and melanoma risk
-
2-s2.0-24744455058 10.1093/jnci/dji253
-
Soufir N., Meziani R., Lacapère J.-J., Bertrand G., Fumeron F., Bourillon A., Gérard B., Descamps V., Crickx B., Ollivaud L., Archimbaud A., Lebbe C., Basset-Seguin N., Saiag P., Grandchamp B., Association between endothelin receptor B nonsynonymous variants and melanoma risk. Journal of the National Cancer Institute 2005 97 17 1297 1301 2-s2.0-24744455058 10.1093/jnci/dji253
-
(2005)
Journal of the National Cancer Institute
, vol.97
, Issue.17
, pp. 1297-1301
-
-
Soufir, N.1
Meziani, R.2
Lacapère, J.-J.3
Bertrand, G.4
Fumeron, F.5
Bourillon, A.6
Gérard, B.7
Descamps, V.8
Crickx, B.9
Ollivaud, L.10
Archimbaud, A.11
Lebbe, C.12
Basset-Seguin, N.13
Saiag, P.14
Grandchamp, B.15
-
13
-
-
80054996042
-
Genome-wide association study identifies three new melanoma susceptibility loci
-
Barrett J. H., Iles M. M., Harland M., Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics 2011 43 1108 1113
-
(2011)
Nature Genetics
, vol.43
, pp. 1108-1113
-
-
Barrett, J.H.1
Iles, M.M.2
Harland, M.3
-
14
-
-
84855958422
-
Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk
-
2-s2.0-84855958422 10.1038/jid.2011.322
-
Law M. H., Montgomery G. W., Brown K. M., Martin N. G., Mann G. J., Hayward N. K., MacGregor S., Meta-analysis combining new and existing data sets confirms that the TERT-CLPTM1L locus influences melanoma risk. Journal of Investigative Dermatology 2012 132 2 485 487 2-s2.0-84855958422 10.1038/jid.2011.322
-
(2012)
Journal of Investigative Dermatology
, vol.132
, Issue.2
, pp. 485-487
-
-
Law, M.H.1
Montgomery, G.W.2
Brown, K.M.3
Martin, N.G.4
Mann, G.J.5
Hayward, N.K.6
Macgregor, S.7
-
15
-
-
80055002815
-
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3
-
Macgregor S., Montgomery G. W., Liu J. Z., Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature Genetics 2011 43 1114 1118
-
(2011)
Nature Genetics
, vol.43
, pp. 1114-1118
-
-
Macgregor, S.1
Montgomery, G.W.2
Liu, J.Z.3
-
16
-
-
59149091340
-
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
-
2-s2.0-59149091340 10.1038/ng.296
-
Rafnar T., Sulem P., Stacey S. N., Geller F., Gudmundsson J., Sigurdsson A., Jakobsdottir M., Helgadottir H., Thorlacius S., Aben K. K. H., Blöndal T., Thorgeirsson T. E., Thorleifsson G., Kristjansson K., Thorisdottir K., Ragnarsson R., Sigurgeirsson B., Skuladottir H., Gudbjartsson T., Isaksson H. J., Einarsson G. V., Benediktsdottir K. R., Agnarsson B. A., Olafsson K., Salvarsdottir A., Bjarnason H., Asgeirsdottir M., Kristinsson K. T., Matthiasdottir S., Sveinsdottir S. G., Polidoro S., Höiom V., Botella-Estrada R., Hemminki K., Rudnai P., Bishop D. T., Campagna M., Kellen E., Zeegers M. P., De Verdier P., Ferrer A., Isla D., Vidal M. J., Andres R., Saez B., Juberias P., Banzo J., Navarrete S., Tres A., Kan D., Lindblom A., Gurzau E., Koppova K., de Vegt F., Schalken J. A., van der Heijden H. F. M., Smit H. J., Termeer R. A., Oosterwijk E., van Hooij O., Nagore E., Porru S., Steineck G., Hansson J., Buntinx F., Catalona W. J., Matullo G., Vineis P., Kiltie A. E., Mayordomo J. I., Kumar R., Kiemeney L. A., Frigge M. L., Jonsson T., Saemundsson H., Barkardottir R. B., Jonsson E., Jonsson S., Olafsson J. H., Gulcher J. R., Masson G., Gudbjartsson D. F., Kong A., Thorsteinsdottir U., Stefansson K., Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nature Genetics 2009 41 2 221 227 2-s2.0-59149091340 10.1038/ng.296
-
(2009)
Nature Genetics
, vol.41
, Issue.2
, pp. 221-227
-
-
Rafnar, T.1
Sulem, P.2
Stacey, S.N.3
Geller, F.4
Gudmundsson, J.5
Sigurdsson, A.6
Jakobsdottir, M.7
Helgadottir, H.8
Thorlacius, S.9
Aben, K.K.H.10
Blöndal, T.11
Thorgeirsson, T.E.12
Thorleifsson, G.13
Kristjansson, K.14
Thorisdottir, K.15
Ragnarsson, R.16
Sigurgeirsson, B.17
Skuladottir, H.18
Gudbjartsson, T.19
Isaksson, H.J.20
Einarsson, G.V.21
Benediktsdottir, K.R.22
Agnarsson, B.A.23
Olafsson, K.24
Salvarsdottir, A.25
Bjarnason, H.26
Asgeirsdottir, M.27
Kristinsson, K.T.28
Matthiasdottir, S.29
Sveinsdottir, S.G.30
Polidoro, S.31
Höiom, V.32
Botella-Estrada, R.33
Hemminki, K.34
Rudnai, P.35
Bishop, D.T.36
Campagna, M.37
Kellen, E.38
Zeegers, M.P.39
De Verdier, P.40
Ferrer, A.41
Isla, D.42
Vidal, M.J.43
Andres, R.44
Saez, B.45
Juberias, P.46
Banzo, J.47
Navarrete, S.48
Tres, A.49
Kan, D.50
Lindblom, A.51
Gurzau, E.52
Koppova, K.53
De Vegt, F.54
Schalken, J.A.55
Van Der Heijden, H.F.M.56
Smit, H.J.57
Termeer, R.A.58
Oosterwijk, E.59
Van Hooij, O.60
Nagore, E.61
Porru, S.62
Steineck, G.63
Hansson, J.64
Buntinx, F.65
Catalona, W.J.66
Matullo, G.67
Vineis, P.68
Kiltie, A.E.69
Mayordomo, J.I.70
Kumar, R.71
Kiemeney, L.A.72
Frigge, M.L.73
Jonsson, T.74
Saemundsson, H.75
Barkardottir, R.B.76
Jonsson, E.77
Jonsson, S.78
Olafsson, J.H.79
Gulcher, J.R.80
Masson, G.81
Gudbjartsson, D.F.82
Kong, A.83
Thorsteinsdottir, U.84
Stefansson, K.85
more..
-
17
-
-
68149170036
-
New common variants affecting susceptibility to basal cell carcinoma
-
Stacey S. N., Sulem P., Masson G., New common variants affecting susceptibility to basal cell carcinoma. Nature Genetics 2009 41 909 914
-
(2009)
Nature Genetics
, vol.41
, pp. 909-914
-
-
Stacey, S.N.1
Sulem, P.2
Masson, G.3
-
18
-
-
0030218918
-
The genetics of pigmentation: From fancy genes to complex traits
-
2-s2.0-0030218918 10.1016/0168-9525(96)10031-7
-
Barsh G. S., The genetics of pigmentation: from fancy genes to complex traits. Trends in Genetics 1996 12 8 299 305 2-s2.0-0030218918 10.1016/0168-9525(96)10031-7
-
(1996)
Trends in Genetics
, vol.12
, Issue.8
, pp. 299-305
-
-
Barsh, G.S.1
-
19
-
-
6344290128
-
The genetics of sun sensitivity in humans
-
2-s2.0-6344290128 10.1086/425285
-
Rees J. L., The genetics of sun sensitivity in humans. American Journal of Human Genetics 2004 75 5 739 751 2-s2.0-6344290128 10.1086/425285
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.5
, pp. 739-751
-
-
Rees, J.L.1
-
20
-
-
14644429805
-
MC1R and the response of melanocytes to ultraviolet radiation
-
2-s2.0-14644429805 10.1016/j.mrfmmm.2004.09.014
-
Rouzaud F., Kadekaro A. L., Abdel-Malek Z. A., Hearing V. J., MC1R and the response of melanocytes to ultraviolet radiation. Mutation Research 2005 571 1-2 133 152 2-s2.0-14644429805 10.1016/j.mrfmmm.2004.09.014
-
(2005)
Mutation Research
, vol.571
, Issue.1-2
, pp. 133-152
-
-
Rouzaud, F.1
Kadekaro, A.L.2
Abdel-Malek, Z.A.3
Hearing, V.J.4
-
21
-
-
0035160974
-
The melanocortin-1 receptor: Red hair and beyond
-
2-s2.0-0035160974
-
Schaffer J. V., Bolognia J. L., The melanocortin-1 receptor: red hair and beyond. Archives of Dermatology 2001 137 11 1477 1485 2-s2.0-0035160974
-
(2001)
Archives of Dermatology
, vol.137
, Issue.11
, pp. 1477-1485
-
-
Schaffer, J.V.1
Bolognia, J.L.2
-
22
-
-
34247647905
-
Comprehensive evaluation of allele frequency differences of MC1R variants across populations
-
2-s2.0-34247647905 10.1002/humu.20476
-
Gerstenblith M. R., Goldstein A. M., Fargnoli M. C., Peris K., Landi M. T., Comprehensive evaluation of allele frequency differences of MC1R variants across populations. Human Mutation 2007 28 5 495 505 2-s2.0-34247647905 10.1002/humu.20476
-
(2007)
Human Mutation
, vol.28
, Issue.5
, pp. 495-505
-
-
Gerstenblith, M.R.1
Goldstein, A.M.2
Fargnoli, M.C.3
Peris, K.4
Landi, M.T.5
-
23
-
-
28044450150
-
Melanocortin-1 receptor structure and functional regulation
-
2-s2.0-28044450150 10.1111/j.1600-0749.2005.00278.x
-
García-Borrón J. C., Sánchez-Laorden B. L., Jiménez-Cervantes C., Melanocortin-1 receptor structure and functional regulation. Pigment Cell Research 2005 18 6 393 410 2-s2.0-28044450150 10.1111/j.1600-0749.2005.00278.x
-
(2005)
Pigment Cell Research
, vol.18
, Issue.6
, pp. 393-410
-
-
García-Borrón, J.C.1
Sánchez-Laorden, B.L.2
Jiménez-Cervantes, C.3
-
24
-
-
0035422250
-
The melanocortin-1-receptor gene is the major freckle gene
-
2-s2.0-0035422250
-
Bastiaens M., Ter Huurne J., Gruis N., Bergman W., Westendorp R., Vermeer B.-J., Bavinck J.-N. B., The melanocortin-1-receptor gene is the major freckle gene. Human Molecular Genetics 2001 10 16 1701 1708 2-s2.0-0035422250
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.16
, pp. 1701-1708
-
-
Bastiaens, M.1
Ter Huurne, J.2
Gruis, N.3
Bergman, W.4
Westendorp, R.5
Vermeer, B.-J.6
Bavinck, J.-N.B.7
-
25
-
-
0030782275
-
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair
-
2-s2.0-0030782275 10.1093/hmg/6.11.1891
-
Box N. F., Wyeth J. R., O'Gorman L. E., Martin N. G., Sturm R. A., Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair. Human Molecular Genetics 1997 6 11 1891 1897 2-s2.0-0030782275 10.1093/hmg/6.11.1891
-
(1997)
Human Molecular Genetics
, vol.6
, Issue.11
, pp. 1891-1897
-
-
Box, N.F.1
Wyeth, J.R.2
O'Gorman, L.E.3
Martin, N.G.4
Sturm, R.A.5
-
26
-
-
0034712537
-
Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair
-
2-s2.0-0034712537
-
Healy E., Flannagan N., Ray A., Todd C., Jackson I. J., Matthews J. N. S., Birch-Machin M. A., Rees J. L., Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair. The Lancet 2000 355 9209 1072 1073 2-s2.0-0034712537
-
(2000)
The Lancet
, vol.355
, Issue.9209
, pp. 1072-1073
-
-
Healy, E.1
Flannagan, N.2
Ray, A.3
Todd, C.4
Jackson, I.J.5
Matthews, J.N.S.6
Birch-Machin, M.A.7
Rees, J.L.8
-
27
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
2-s2.0-0028786945
-
Valverde P., Healy E., Jackson I., Rees J. L., Thody A. J., Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nature Genetics 1995 11 3 328 330 2-s2.0-0028786945
-
(1995)
Nature Genetics
, vol.11
, Issue.3
, pp. 328-330
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
Rees, J.L.4
Thody, A.J.5
-
28
-
-
58249125574
-
The contribution of melanocortin 1 receptor gene polymorphisms and the agouti signalling protein gene 8818A > G polymorphism to cutaneous melanoma and basal cell carcinoma in a Polish population
-
2-s2.0-58249125574 10.1111/j.1600-0625.2008.00760.x
-
Brudnik U., Branicki W., Wojas-Pelc A., Kanas P., The contribution of melanocortin 1 receptor gene polymorphisms and the agouti signalling protein gene 8818A > G polymorphism to cutaneous melanoma and basal cell carcinoma in a Polish population. Experimental Dermatology 2009 18 2 167 174 2-s2.0-58249125574 10.1111/j.1600-0625.2008.00760.x
-
(2009)
Experimental Dermatology
, vol.18
, Issue.2
, pp. 167-174
-
-
Brudnik, U.1
Branicki, W.2
Wojas-Pelc, A.3
Kanas, P.4
-
29
-
-
21244446712
-
MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a mediterranean population
-
2-s2.0-21244446712 10.1093/jnci/dji176
-
Landi M. T., Kanetsky P. A., Tsang S., Gold B., Munroe D., Rebbeck T., Swoyer J., Ter-Minassian M., Hedayati M., Grossman L., Goldstein A. M., Calista D., Pfeiffer R. M., MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a mediterranean population. Journal of the National Cancer Institute 2005 97 13 998 1007 2-s2.0-21244446712 10.1093/jnci/dji176
-
(2005)
Journal of the National Cancer Institute
, vol.97
, Issue.13
, pp. 998-1007
-
-
Landi, M.T.1
Kanetsky, P.A.2
Tsang, S.3
Gold, B.4
Munroe, D.5
Rebbeck, T.6
Swoyer, J.7
Ter-Minassian, M.8
Hedayati, M.9
Grossman, L.10
Goldstein, A.M.11
Calista, D.12
Pfeiffer, R.M.13
-
30
-
-
33749481705
-
Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma
-
2-s2.0-33749481705 10.1158/0008-5472.CAN-06-1634
-
Kanetsky P. A., Rebbeck T. R., Hummer A. J., Panossian S., Armstrong B. K., Kricker A., Marrett L. D., Millikan R. C., Gruber S. B., Culver H. A., Zanetti R., Gallagher R. P., Dwyer T., Busam K., From L., Mujumdar U., Wilcox H., Begg C. B., Berwick M., Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma. Cancer Research 2006 66 18 9330 9337 2-s2.0-33749481705 10.1158/0008-5472.CAN-06-1634
-
(2006)
Cancer Research
, vol.66
, Issue.18
, pp. 9330-9337
-
-
Kanetsky, P.A.1
Rebbeck, T.R.2
Hummer, A.J.3
Panossian, S.4
Armstrong, B.K.5
Kricker, A.6
Marrett, L.D.7
Millikan, R.C.8
Gruber, S.B.9
Culver, H.A.10
Zanetti, R.11
Gallagher, R.P.12
Dwyer, T.13
Busam, K.14
From, L.15
Mujumdar, U.16
Wilcox, H.17
Begg, C.B.18
Berwick, M.19
-
31
-
-
70349237926
-
Melanocortin receptor 1 variants and melanoma risk: A study of 2 European populations
-
2-s2.0-70349237926 10.1002/ijc.24548
-
Scherer D., Nagore E., Bermejo J. L., Figl A., Botella-Estrada R., Thirumaran R. K., Angelini S., Hemminki K., Schadendorf D., Kumar R., Melanocortin receptor 1 variants and melanoma risk: a study of 2 European populations. International Journal of Cancer 2009 125 8 1868 1875 2-s2.0-70349237926 10.1002/ijc.24548
-
(2009)
International Journal of Cancer
, vol.125
, Issue.8
, pp. 1868-1875
-
-
Scherer, D.1
Nagore, E.2
Bermejo, J.L.3
Figl, A.4
Botella-Estrada, R.5
Thirumaran, R.K.6
Angelini, S.7
Hemminki, K.8
Schadendorf, D.9
Kumar, R.10
-
32
-
-
77949794236
-
Interactions between ultraviolet light exposure and DNA repair gene polymorphisms may increase melanoma risk
-
di Lucca J., Guedj M., Lacapère J. J., Interactions between ultraviolet light exposure and DNA repair gene polymorphisms may increase melanoma risk. British Journal of Dermatology 2010 162 891 893
-
(2010)
British Journal of Dermatology
, vol.162
, pp. 891-893
-
-
Di Lucca, J.1
Guedj, M.2
Lacapère, J.J.3
-
33
-
-
80053383840
-
Assessment of tyrosinase variants and skin cancer risk in a large cohort of French subjects
-
2-s2.0-80053383840 10.1016/j.jdermsci.2011.07.003
-
Hu H.-H., Guedj M., Descamps V., Jouary T., Bourillon A., Ezzedine K., Taieb A., Bagot M., Bensussan A., Saiag P., Grandchamp B., Basset-Seguin N., Soufir N., Assessment of tyrosinase variants and skin cancer risk in a large cohort of French subjects. Journal of Dermatological Science 2011 64 2 127 133 2-s2.0-80053383840 10.1016/j.jdermsci.2011.07.003
-
(2011)
Journal of Dermatological Science
, vol.64
, Issue.2
, pp. 127-133
-
-
Hu, H.-H.1
Guedj, M.2
Descamps, V.3
Jouary, T.4
Bourillon, A.5
Ezzedine, K.6
Taieb, A.7
Bagot, M.8
Bensussan, A.9
Saiag, P.10
Grandchamp, B.11
Basset-Seguin, N.12
Soufir, N.13
-
34
-
-
84865518526
-
MC1R, SLC45A2 and TYR genetic variants involved in melanoma susceptibility in Southern European populations: Results from a Meta-analysis
-
2-s2.0-84858823717 10.1016/j.ejca.2012.03.006
-
Ibarrola-Villava M., Hu H.-H., Guedj M., Fernandez L. P., Descamps V., Basset-Seguin N., Bagot M., Benssussan A., Saiag P., Fargnoli M. C., Peris K., Aviles J. A., Lluch A., Ribas G., Soufir N., MC1R, SLC45A2 and TYR genetic variants involved in melanoma susceptibility in Southern European populations: results from a Meta-analysis. European Journal of Cancer 2012 48 2183 2191 2-s2.0-84858823717 10.1016/j.ejca.2012.03.006
-
(2012)
European Journal of Cancer
, vol.48
, pp. 2183-2191
-
-
Ibarrola-Villava, M.1
Hu, H.-H.2
Guedj, M.3
Fernandez, L.P.4
Descamps, V.5
Basset-Seguin, N.6
Bagot, M.7
Benssussan, A.8
Saiag, P.9
Fargnoli, M.C.10
Peris, K.11
Aviles, J.A.12
Lluch, A.13
Ribas, G.14
Soufir, N.15
-
35
-
-
1442332032
-
Identification of four novel melanocortin 1 receptor (MC1R) gene variants in a Mediterranean population
-
2-s2.0-1442332032
-
Fargnoli M. C., Chimenti S., Keller G., Höfler H., Peris K., Identification of four novel melanocortin 1 receptor (MC1R) gene variants in a Mediterranean population. Human Mutation 2003 21 6 655 2-s2.0-1442332032
-
(2003)
Human Mutation
, vol.21
, Issue.6
, pp. 655
-
-
Fargnoli, M.C.1
Chimenti, S.2
Keller, G.3
Höfler, H.4
Peris, K.5
-
36
-
-
7244247169
-
Novel MC1R variants in Ligurian melanoma patients and controls
-
2-s2.0-7244247169
-
Pastorino L., Cusano R., Bruno W., Lantieri F., Origone P., Barile M., Gliori S., Shepherd G. A., Sturm R. A., Scarra G. B., Novel MC1R variants in Ligurian melanoma patients and controls. Human Mutation 2004 24 1 103 2-s2.0-7244247169
-
(2004)
Human Mutation
, vol.24
, Issue.1
, pp. 103
-
-
Pastorino, L.1
Cusano, R.2
Bruno, W.3
Lantieri, F.4
Origone, P.5
Barile, M.6
Gliori, S.7
Shepherd, G.A.8
Sturm, R.A.9
Scarra, G.B.10
-
37
-
-
33847095560
-
Determination of phenotype associated SNPs in the MC1R gene
-
2-s2.0-33847095560 10.1111/j.1556-4029.2006.00361.x
-
Branicki W., Brudnik U., Kupiec T., Wolañska-Nowak P., Wojas-Pelc A., Determination of phenotype associated SNPs in the MC1R gene. Journal of Forensic Sciences 2007 52 2 349 354 2-s2.0-33847095560 10.1111/j.1556-4029.2006. 00361.x
-
(2007)
Journal of Forensic Sciences
, vol.52
, Issue.2
, pp. 349-354
-
-
Branicki, W.1
Brudnik, U.2
Kupiec, T.3
Wolañska-Nowak, P.4
Wojas-Pelc, A.5
-
38
-
-
0032918729
-
High polymorphism at the human melanocortin 1 receptor locus
-
2-s2.0-0032918729
-
Rana B. K., Hewett-Emmett D., Jin L., Chang B. H.-J., Sambuughin N., Lin M., Watkins S., Bamshad M., Jorde L. B., Ramsay M., Jenkins T., Li W.-H., High polymorphism at the human melanocortin 1 receptor locus. Genetics 1999 151 4 1547 1557 2-s2.0-0032918729
-
(1999)
Genetics
, vol.151
, Issue.4
, pp. 1547-1557
-
-
Rana, B.K.1
Hewett-Emmett, D.2
Jin, L.3
Chang, B.H.-J.4
Sambuughin, N.5
Lin, M.6
Watkins, S.7
Bamshad, M.8
Jorde, L.B.9
Ramsay, M.10
Jenkins, T.11
Li, W.-H.12
-
39
-
-
0038050991
-
DNA polymorphism and selection at the melanocortin-1 receptor gene in normally pigmented Southern African individuals
-
2-s2.0-0038050991
-
John P. R., Makova K., Li W.-H., Jenkins T., Ramsay M., DNA polymorphism and selection at the melanocortin-1 receptor gene in normally pigmented Southern African individuals. Annals of the New York Academy of Sciences 2003 994 299 306 2-s2.0-0038050991
-
(2003)
Annals of the New York Academy of Sciences
, vol.994
, pp. 299-306
-
-
John, P.R.1
Makova, K.2
Li, W.-H.3
Jenkins, T.4
Ramsay, M.5
-
40
-
-
0035834431
-
Thr40 and Met122 are new partial loss-of-function natural mutations of the human melanocortin 1 receptor
-
Jiménez-Cervantes C., Germer S., González P., Sánchez J., Sánchez C. O., García-Borrón J. C., Thr40 and Met122 are new partial loss-of-function natural mutations of the human melanocortin 1 receptor. FEBS Letters 2001 508 1 44 48
-
(2001)
FEBS Letters
, vol.508
, Issue.1
, pp. 44-48
-
-
Jiménez-Cervantes, C.1
Germer, S.2
González, P.3
Sánchez, J.4
Sánchez, C.O.5
García-Borrón, J.C.6
-
41
-
-
1842339332
-
A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes
-
2-s2.0-1842339332 10.1038/ng0397-311
-
Våge D. I., Lu D., Klungland H., Lien S., Adalsteinsson S., Cone R. D., A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpes. Nature Genetics 1997 15 3 311 315 2-s2.0-1842339332 10.1038/ng0397-311
-
(1997)
Nature Genetics
, vol.15
, Issue.3
, pp. 311-315
-
-
Våge, D.I.1
Lu, D.2
Klungland, H.3
Lien, S.4
Adalsteinsson, S.5
Cone, R.D.6
-
42
-
-
17644432720
-
Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure
-
2-s2.0-17644432720 ARTICLE E13
-
Matichard E., Verpillat P., Meziani R., Gérard B., Descamps V., Legroux E., Burnouf M., Bertrand G., Bouscarat F., Archimbaud A., Picard C., Ollivaud L., Basset-Seguin N., Kerob D., Lanternier G., Lebbe C., Crickx B., Grandchamp B., Soufir N., Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure. Journal of medical genetics 2004 41 2, article e13 2-s2.0-17644432720
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.2
-
-
Matichard, E.1
Verpillat, P.2
Meziani, R.3
Gérard, B.4
Descamps, V.5
Legroux, E.6
Burnouf, M.7
Bertrand, G.8
Bouscarat, F.9
Archimbaud, A.10
Picard, C.11
Ollivaud, L.12
Basset-Seguin, N.13
Kerob, D.14
Lanternier, G.15
Lebbe, C.16
Crickx, B.17
Grandchamp, B.18
Soufir, N.19
-
43
-
-
0036550115
-
Four novel variants in MC1R in red-haired South African individuals of European descent: S83P, Y152X, A171D, P256S
-
2-s2.0-0036550115
-
John P. R., Ramsay M., Four novel variants in MC1R in red-haired South African individuals of European descent: S83P, Y152X, A171D, P256S. Human Mutation 2002 19 4 461 462 2-s2.0-0036550115
-
(2002)
Human Mutation
, vol.19
, Issue.4
, pp. 461-462
-
-
John, P.R.1
Ramsay, M.2
-
44
-
-
40349087179
-
MC1R variants associated susceptibility to basal cell carcinoma of skin: Interaction with host factors and XRCC3 polymorphism
-
2-s2.0-40349087179 10.1002/ijc.23257
-
Scherer D., Bermejo J. L., Rudnai P., Gurzau E., Koppova K., Hemminki K., Kumar R., MC1R variants associated susceptibility to basal cell carcinoma of skin: Interaction with host factors and XRCC3 polymorphism. International Journal of Cancer 2008 122 8 1787 1793 2-s2.0-40349087179 10.1002/ijc.23257
-
(2008)
International Journal of Cancer
, vol.122
, Issue.8
, pp. 1787-1793
-
-
Scherer, D.1
Bermejo, J.L.2
Rudnai, P.3
Gurzau, E.4
Koppova, K.5
Hemminki, K.6
Kumar, R.7
-
45
-
-
33745208440
-
MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas
-
2-s2.0-33745208440 10.1038/sj.jid.5700263
-
Liboutet M., Portela M., Delestaing G., Vilmer C., Dupin N., Gorin I., Saiag P., Lebbé C., Kerob D., Dubertret L., Grandchamp B., Basset-Seguin N., Soufir N., MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas. Journal of Investigative Dermatology 2006 126 7 1510 1517 2-s2.0-33745208440 10.1038/sj.jid.5700263
-
(2006)
Journal of Investigative Dermatology
, vol.126
, Issue.7
, pp. 1510-1517
-
-
Liboutet, M.1
Portela, M.2
Delestaing, G.3
Vilmer, C.4
Dupin, N.5
Gorin, I.6
Saiag, P.7
Lebbé, C.8
Kerob, D.9
Dubertret, L.10
Grandchamp, B.11
Basset-Seguin, N.12
Soufir, N.13
-
46
-
-
0033927855
-
Evidence for variable selective pressures at MC1R
-
2-s2.0-0033927855 10.1086/302863
-
Harding R. M., Healy E., Ray A. J., Ellis N. S., Flanagan N., Todd C., Dixon C., Sajantila A., Jackson I. J., Birch-Machin M. A., Rees J. L., Evidence for variable selective pressures at MC1R. American Journal of Human Genetics 2000 66 4 1351 1361 2-s2.0-0033927855 10.1086/302863
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.4
, pp. 1351-1361
-
-
Harding, R.M.1
Healy, E.2
Ray, A.J.3
Ellis, N.S.4
Flanagan, N.5
Todd, C.6
Dixon, C.7
Sajantila, A.8
Jackson, I.J.9
Birch-Machin, M.A.10
Rees, J.L.11
-
47
-
-
66749100686
-
Identification and functional analysis of novel variants of the human melanocortin 1 receptor found in melanoma patients
-
Pérez-Oliva A. B., Fernéndez L. P., Detorre C., Identification and functional analysis of novel variants of the human melanocortin 1 receptor found in melanoma patients. Human Mutation 2009 30 811 822
-
(2009)
Human Mutation
, vol.30
, pp. 811-822
-
-
Pérez-Oliva, A.B.1
Fernéndez, L.P.2
Detorre, C.3
-
48
-
-
33645014606
-
Identification of novel functional variants of the melanocortin 1 receptor gene originated from Asians
-
2-s2.0-33645014606 10.1007/s00439-006-0141-1
-
Nakayama K., Soemantri A., Jin F., Dashnyam B., Ohtsuka R., Duanchang P., Isa M. N., Settheetham-Ishida W., Harihara S., Ishida T., Identification of novel functional variants of the melanocortin 1 receptor gene originated from Asians. Human Genetics 2006 119 3 322 330 2-s2.0-33645014606 10.1007/s00439-006-0141-1
-
(2006)
Human Genetics
, vol.119
, Issue.3
, pp. 322-330
-
-
Nakayama, K.1
Soemantri, A.2
Jin, F.3
Dashnyam, B.4
Ohtsuka, R.5
Duanchang, P.6
Isa, M.N.7
Settheetham-Ishida, W.8
Harihara, S.9
Ishida, T.10
-
49
-
-
26444597589
-
Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees
-
2-s2.0-26444597589 10.1158/1055-9965.EPI-04-0777
-
Chaudru V., Laud K., Avril M.-F., Minière A., Chompret A., Bressac-De Paillerets B., Demenais F., Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees. Cancer Epidemiology Biomarkers and Prevention 2005 14 10 2384 2390 2-s2.0-26444597589 10.1158/1055-9965.EPI-04-0777
-
(2005)
Cancer Epidemiology Biomarkers and Prevention
, vol.14
, Issue.10
, pp. 2384-2390
-
-
Chaudru, V.1
Laud, K.2
Avril, M.-F.3
Minière, A.4
Chompret, A.5
Bressac-De Paillerets, B.6
Demenais, F.7
-
50
-
-
67650400328
-
Aberrant trafficking of human melanocortin 1 receptor variants associated with red hair and skin cancer: Steady-state retention of mutant forms in the proximal Golgi
-
2-s2.0-67650400328 10.1002/jcp.21804
-
Sánchez-Laorden B. L., Herraiz C., Valencia J. C., Hearing V. J., Jiménez-Cervantes C., García-Borrón J. C., Aberrant trafficking of human melanocortin 1 receptor variants associated with red hair and skin cancer: steady-state retention of mutant forms in the proximal Golgi. Journal of Cellular Physiology 2009 220 3 640 654 2-s2.0-67650400328 10.1002/jcp.21804
-
(2009)
Journal of Cellular Physiology
, vol.220
, Issue.3
, pp. 640-654
-
-
Sánchez-Laorden, B.L.1
Herraiz, C.2
Valencia, J.C.3
Hearing, V.J.4
Jiménez-Cervantes, C.5
García-Borrón, J.C.6
-
51
-
-
70349438983
-
Melanocortin 1 receptor mutations impact differentially on signalling to the cAMP and the ERK mitogen-activated protein kinase pathways
-
2-s2.0-70349438983 10.1016/j.febslet.2009.09.023
-
Herraiz C., Jiménez-Cervantes C., Zanna P., García- Borrón J. C., Melanocortin 1 receptor mutations impact differentially on signalling to the cAMP and the ERK mitogen-activated protein kinase pathways. FEBS Letters 2009 583 19 3269 3274 2-s2.0-70349438983 10.1016/j.febslet.2009.09. 023
-
(2009)
FEBS Letters
, vol.583
, Issue.19
, pp. 3269-3274
-
-
Herraiz, C.1
Jiménez-Cervantes, C.2
Zanna, P.3
García- Borrón, J.C.4
-
52
-
-
0036451652
-
Loss-of-function variants of the human melanocortin-1 receptor gene in melanoma cells define structural determinants of receptor function
-
Sánchez-Más J., Olivares-Sánchez C., Ghanem G., Loss-of-function variants of the human melanocortin-1 receptor gene in melanoma cells define structural determinants of receptor function. European Journal of Biochemistry 2002 269 6133 6141
-
(2002)
European Journal of Biochemistry
, vol.269
, pp. 6133-6141
-
-
Sánchez-Más, J.1
Olivares-Sánchez, C.2
Ghanem, G.3
-
53
-
-
0344603629
-
Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair
-
2-s2.0-0344603629 10.1006/bbrc.1999.0935
-
Schiöth H. B., Phillips S. R., Rudzish R., Birch-Machin M. A., Wikberg J. E. S., Rees J. L., Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair. Biochemical and Biophysical Research Communications 1999 260 2 488 491 2-s2.0-0344603629 10.1006/bbrc.1999.0935
-
(1999)
Biochemical and Biophysical Research Communications
, vol.260
, Issue.2
, pp. 488-491
-
-
Schiöth, H.B.1
Phillips, S.R.2
Rudzish, R.3
Birch-Machin, M.A.4
Wikberg, J.E.S.5
Rees, J.L.6
-
54
-
-
6344275551
-
Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair
-
2-s2.0-6344275551 10.1111/j.0022-202X.2004.23444.x
-
Ringholm A., Klovins J., Rudzish R., Phillips S., Rees J. L., Schiöth H. B., Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair. Journal of Investigative Dermatology 2004 123 5 917 923 2-s2.0-6344275551 10.1111/j.0022-202X.2004.23444.x
-
(2004)
Journal of Investigative Dermatology
, vol.123
, Issue.5
, pp. 917-923
-
-
Ringholm, A.1
Klovins, J.2
Rudzish, R.3
Phillips, S.4
Rees, J.L.5
Schiöth, H.B.6
-
55
-
-
43049148341
-
MC1R variants, melanoma and red hair color phenotype: A meta-analysis
-
2-s2.0-43049148341 10.1002/ijc.23396
-
Raimondi S., Sera F., Gandini S., Iodice S., Caini S., Maisonneuve P., Fargnoli M. C., MC1R variants, melanoma and red hair color phenotype: a meta-analysis. International Journal of Cancer 2008 122 12 2753 2760 2-s2.0-43049148341 10.1002/ijc.23396
-
(2008)
International Journal of Cancer
, vol.122
, Issue.12
, pp. 2753-2760
-
-
Raimondi, S.1
Sera, F.2
Gandini, S.3
Iodice, S.4
Caini, S.5
Maisonneuve, P.6
Fargnoli, M.C.7
-
56
-
-
0035722059
-
Melanocortin 1 receptor (MC1R) gene variants are associated with an increased risk for cutaneous melanoma which is largely independent of skin type and hair color
-
2-s2.0-0035722059 10.1046/j.0022-202X.2001.01421.x
-
Kennedy C., Ter Huurne J., Berkhout M., Gruis N., Bastiaens M., Bergman W., Willemze R., Bouwes Bavinck J. N., Melanocortin 1 receptor (MC1R) gene variants are associated with an increased risk for cutaneous melanoma which is largely independent of skin type and hair color. Journal of Investigative Dermatology 2001 117 2 294 300 2-s2.0-0035722059 10.1046/j.0022-202X.2001.01421. x
-
(2001)
Journal of Investigative Dermatology
, vol.117
, Issue.2
, pp. 294-300
-
-
Kennedy, C.1
Ter Huurne, J.2
Berkhout, M.3
Gruis, N.4
Bastiaens, M.5
Bergman, W.6
Willemze, R.7
Bouwes Bavinck, J.N.8
-
57
-
-
79960912284
-
Melanocortin 1 receptor and risk of cutaneous melanoma: A meta-analysis and estimates of population burden
-
2-s2.0-79960912284 10.1002/ijc.25804
-
Williams P. F., Olsen C. M., Hayward N. K., Whiteman D. C., Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden. International Journal of Cancer 2011 129 7 1730 1740 2-s2.0-79960912284 10.1002/ijc.25804
-
(2011)
International Journal of Cancer
, vol.129
, Issue.7
, pp. 1730-1740
-
-
Williams, P.F.1
Olsen, C.M.2
Hayward, N.K.3
Whiteman, D.C.4
|