-
1
-
-
84892805731
-
Cancer statistics, 2014
-
Siegel R, Ma J, Zou Z, et al. Cancer statistics, 2014. CA Cancer J Clin 2014;64:9-29.
-
(2014)
CA Cancer J Clin
, vol.64
, pp. 9-29
-
-
Siegel, R.1
Ma, J.2
Zou, Z.3
-
2
-
-
1542611579
-
Global perspectives of contemporary epidemiological trends of cutaneous malignant melanoma
-
Lens MB, Dawes M. Global perspectives of contemporary epidemiological trends of cutaneous malignant melanoma. Br J Dermatol 2004;150:179-85.
-
(2004)
Br J Dermatol
, vol.150
, pp. 179-185
-
-
Lens, M.B.1
Dawes, M.2
-
3
-
-
33745650671
-
Cancer in 15-to 29-year-olds by primary site
-
Bleyer A, Viny A, Barr R. Cancer in 15-to 29-year-olds by primary site. Oncologist 2006;11:590-601.
-
(2006)
Oncologist
, vol.11
, pp. 590-601
-
-
Bleyer, A.1
Viny, A.2
Barr, R.3
-
4
-
-
84918790339
-
Measuring the societal burden of cancer: the cost of lost productivity due to premature cancer-related mortality in Europe
-
Hanly P, Soerjomataram I, Sharp L. Measuring the societal burden of cancer: the cost of lost productivity due to premature cancer-related mortality in Europe. Int J Cancer 2015;136:E136-45.
-
(2015)
Int J Cancer
, vol.136
, pp. E136-E145
-
-
Hanly, P.1
Soerjomataram, I.2
Sharp, L.3
-
5
-
-
74949143594
-
Final version of 2009 AJCC melanoma staging and classification
-
Balch CM, Gershenwald JE, Soong SJ, et al. Final version of 2009 AJCC melanoma staging and classification. J Clin Oncol 2009;27:6199-206.
-
(2009)
J Clin Oncol
, vol.27
, pp. 6199-6206
-
-
Balch, C.M.1
Gershenwald, J.E.2
Soong, S.J.3
-
6
-
-
11144340999
-
Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure
-
Gandini S, Sera F, Cattaruzza MS, et al. Meta-analysis of risk factors for cutaneous melanoma: II. Sun exposure. Eur J Cancer 2005;41:45-60.
-
(2005)
Eur J Cancer
, vol.41
, pp. 45-60
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
-
7
-
-
0035981152
-
Biological consequences of cyclobutane pyrimidine dimers
-
Vink AA, Roza L. Biological consequences of cyclobutane pyrimidine dimers. J Photochem Photobiol B 2001;65:101-4.
-
(2001)
J Photochem Photobiol B
, vol.65
, pp. 101-104
-
-
Vink, A.A.1
Roza, L.2
-
8
-
-
2642643719
-
Ultraviolet radiation of melanocytic nevi: a dermoscopic study
-
Hofmann-Wellenhof R, Soyer HP, Wolf IH, et al. Ultraviolet radiation of melanocytic nevi: a dermoscopic study. Arch Dermatol 1998;134:845-50.
-
(1998)
Arch Dermatol
, vol.134
, pp. 845-850
-
-
Hofmann-Wellenhof, R.1
Soyer, H.P.2
Wolf, I.H.3
-
9
-
-
0030856557
-
Critical effects of intense sun exposure on the expression of epiluminescence microscopy features of acquired melanocytic nevi
-
Stanganelli I, Bauer P, Bucchi L, et al. Critical effects of intense sun exposure on the expression of epiluminescence microscopy features of acquired melanocytic nevi. Arch Dermatol 1997;133:979-82.
-
(1997)
Arch Dermatol
, vol.133
, pp. 979-982
-
-
Stanganelli, I.1
Bauer, P.2
Bucchi, L.3
-
10
-
-
0028859278
-
UV-irradiated melanocytic nevi simulating melanoma in situ
-
Tronnier M, Wolff HH. UV-irradiated melanocytic nevi simulating melanoma in situ. Am J Dermatopathol 1995;17:1-6.
-
(1995)
Am J Dermatopathol
, vol.17
, pp. 1-6
-
-
Tronnier, M.1
Wolff, H.H.2
-
11
-
-
84880600207
-
Impact of sunscreens on preventing UVR-induced effects in nevi: in vivo study comparing protection using a physical barrier vs sunscreen
-
Carrera C, Puig-Butille JA, Aguilera P, et al. Impact of sunscreens on preventing UVR-induced effects in nevi: in vivo study comparing protection using a physical barrier vs sunscreen. JAMA Dermatol 2013;149:803-13.
-
(2013)
JAMA Dermatol
, vol.149
, pp. 803-813
-
-
Carrera, C.1
Puig-Butille, J.A.2
Aguilera, P.3
-
12
-
-
79951999964
-
Reduced melanoma after regular sunscreen use: randomized trial follow-up
-
Green AC, Williams GM, Logan V, et al. Reduced melanoma after regular sunscreen use: randomized trial follow-up. J Clin Oncol 2011;29:257-63.
-
(2011)
J Clin Oncol
, vol.29
, pp. 257-263
-
-
Green, A.C.1
Williams, G.M.2
Logan, V.3
-
13
-
-
11144298761
-
Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi
-
Gandini S, Sera F, Cattaruzza MS, et al. Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur J Cancer 2005;41:28-44.
-
(2005)
Eur J Cancer
, vol.41
, pp. 28-44
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
-
14
-
-
25144506469
-
Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors
-
Gandini S, Sera F, Cattaruzza MS, et al. Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors. Eur J Cancer 2005;41:2040-59.
-
(2005)
Eur J Cancer
, vol.41
, pp. 2040-2059
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
-
15
-
-
27744522710
-
High constant incidence rates of second cutaneous melanomas
-
Levi F, Randimbison L, Te VC, et al. High constant incidence rates of second cutaneous melanomas. Int J Cancer 2005;117:877-9.
-
(2005)
Int J Cancer
, vol.117
, pp. 877-879
-
-
Levi, F.1
Randimbison, L.2
Te, V.C.3
-
16
-
-
26044481446
-
Clinicopathological features of and risk factors for multiple primary melanomas
-
Ferrone CR, Ben Porat L, Panageas KS, et al. Clinicopathological features of and risk factors for multiple primary melanomas. JAMA 2005;294:1647-54.
-
(2005)
JAMA
, vol.294
, pp. 1647-1654
-
-
Ferrone, C.R.1
Ben Porat, L.2
Panageas, K.S.3
-
17
-
-
42649138270
-
Lessons from the skin-cutaneous features of familial cancer
-
Winship IM, Dudding TE. Lessons from the skin-cutaneous features of familial cancer. Lancet Oncol 2008;9:462-72.
-
(2008)
Lancet Oncol
, vol.9
, pp. 462-472
-
-
Winship, I.M.1
Dudding, T.E.2
-
18
-
-
27244435224
-
Population-based analysis of prognostic factors and survival in familial melanoma
-
Florell SR, Boucher KM, Garibotti G, et al. Population-based analysis of prognostic factors and survival in familial melanoma. J Clin Oncol 2005;23:7168-77.
-
(2005)
J Clin Oncol
, vol.23
, pp. 7168-7177
-
-
Florell, S.R.1
Boucher, K.M.2
Garibotti, G.3
-
19
-
-
0025847504
-
Hereditary cutaneous malignant melanoma: a 20-year family update
-
Anderson DE, Badzioch MD. Hereditary cutaneous malignant melanoma: a 20-year family update. Anticancer Res 1991;11:433-7.
-
(1991)
Anticancer Res
, vol.11
, pp. 433-437
-
-
Anderson, D.E.1
Badzioch, M.D.2
-
20
-
-
21144439424
-
Role of the CDKN2A locus in patients with multiple primary melanomas
-
Puig S, Malvehy J, Badenas C, et al. Role of the CDKN2A locus in patients with multiple primary melanomas. J Clin Oncol 2005;23:3043-51.
-
(2005)
J Clin Oncol
, vol.23
, pp. 3043-3051
-
-
Puig, S.1
Malvehy, J.2
Badenas, C.3
-
21
-
-
16844385347
-
Melanoma genetics and the development of rational therapeutics
-
Chudnovsky Y, Khavari PA, Adams AE. Melanoma genetics and the development of rational therapeutics. J Clin Invest 2005;115:813-24.
-
(2005)
J Clin Invest
, vol.115
, pp. 813-824
-
-
Chudnovsky, Y.1
Khavari, P.A.2
Adams, A.E.3
-
22
-
-
33746691847
-
Cellular senescence and DNA repair
-
Lou Z, Chen J. Cellular senescence and DNA repair. Exp Cell Res 2006;312:2641-6.
-
(2006)
Exp Cell Res
, vol.312
, pp. 2641-2646
-
-
Lou, Z.1
Chen, J.2
-
23
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Cannon-Albright LA, Goldgar DE, Meyer LJ, et al. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science 1992;258:1148-52.
-
(1992)
Science
, vol.258
, pp. 1148-1152
-
-
Cannon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
-
26
-
-
33847282821
-
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
-
Goldstein AM, Chan M, Harland M, et al. Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents. J Med Genet 2007;44:99-106.
-
(2007)
J Med Genet
, vol.44
, pp. 99-106
-
-
Goldstein, A.M.1
Chan, M.2
Harland, M.3
-
27
-
-
84927571470
-
Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling
-
Potrony M, Puig-Butillé JA, Aguilera P, et al. Increased prevalence of lung, breast, and pancreatic cancers in addition to melanoma risk in families bearing the cyclin-dependent kinase inhibitor 2A mutation: implications for genetic counseling. J Am Acad Dermatol 2014;71:888-95.
-
(2014)
J Am Acad Dermatol
, vol.71
, pp. 888-895
-
-
Potrony, M.1
Puig-Butillé, J.A.2
Aguilera, P.3
-
28
-
-
77954656426
-
Influence of loss of function MC1R variants in genetic susceptibility of familial melanoma in Spain
-
de Torre C, Garcia-Casado Z, Martinez-Escribano JA, et al. Influence of loss of function MC1R variants in genetic susceptibility of familial melanoma in Spain. Melanoma Res 2010;20:342-8.
-
(2010)
Melanoma Res
, vol.20
, pp. 342-348
-
-
de Torre, C.1
Garcia-Casado, Z.2
Martinez-Escribano, J.A.3
-
29
-
-
81055156168
-
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma
-
Pedace L, De Simone P, Castori M, et al. Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma. Cancer Epidemiol 2011;35:e116-20.
-
(2011)
Cancer Epidemiol
, vol.35
, pp. e116-e120
-
-
Pedace, L.1
De Simone, P.2
Castori, M.3
-
30
-
-
70449512620
-
Role of key-regulator genes in melanoma susceptibility and pathogenesis among patients from South Italy
-
Casula M, Muggiano A, Cossu A, et al. Role of key-regulator genes in melanoma susceptibility and pathogenesis among patients from South Italy. BMC Cancer 2009;9:352.
-
(2009)
BMC Cancer
, vol.9
, pp. 352
-
-
Casula, M.1
Muggiano, A.2
Cossu, A.3
-
31
-
-
70349792450
-
Clinical genetic testing for familial melanoma in Italy: a cooperative study
-
Bruno W, Ghiorzo P, Battistuzzi L, et al. Clinical genetic testing for familial melanoma in Italy: a cooperative study. J Am Acad Dermatol 2009;61:775-82.
-
(2009)
J Am Acad Dermatol
, vol.61
, pp. 775-782
-
-
Bruno, W.1
Ghiorzo, P.2
Battistuzzi, L.3
-
32
-
-
82255192207
-
Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma
-
Nikolaou V, Kang X, Stratigos A, et al. Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma. Br J Dermatol 2011;165:1219-22.
-
(2011)
Br J Dermatol
, vol.165
, pp. 1219-1222
-
-
Nikolaou, V.1
Kang, X.2
Stratigos, A.3
-
33
-
-
84877059923
-
Analysis of Latvian familial melanoma patients shows novel variants in the noncoding regions of CDKN2A and that the CDK4 mutation R24H is a founder mutation
-
Veinalde R, Ozola A, Azarjana K, et al. Analysis of Latvian familial melanoma patients shows novel variants in the noncoding regions of CDKN2A and that the CDK4 mutation R24H is a founder mutation. Melanoma Res 2013;23:221-6.
-
(2013)
Melanoma Res
, vol.23
, pp. 221-226
-
-
Veinalde, R.1
Ozola, A.2
Azarjana, K.3
-
34
-
-
37349115968
-
Germline CDKN2A/p16 mutations are rare in multiple primary and familial malignant melanoma in German patients
-
Lukowsky A, Schafer-Hesterberg G, Sterry W, et al. Germline CDKN2A/p16 mutations are rare in multiple primary and familial malignant melanoma in German patients. J Dermatol Sci 2008;49:163-5.
-
(2008)
J Dermatol Sci
, vol.49
, pp. 163-165
-
-
Lukowsky, A.1
Schafer-Hesterberg, G.2
Sterry, W.3
-
35
-
-
84925612085
-
Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition
-
Wadt KA, Aoude LG, Krogh L, et al. Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition. PLoS One 2015;10:e0122662.
-
(2015)
PLoS One
, vol.10
-
-
Wadt, K.A.1
Aoude, L.G.2
Krogh, L.3
-
36
-
-
84939253160
-
CDKN2a mutation-negative melanoma families have increased risk exclusively for skin cancers but not for other malignancies
-
Helgadottir H, Höiom V, Tuominen R, et al. CDKN2a mutation-negative melanoma families have increased risk exclusively for skin cancers but not for other malignancies. Int J Cancer 2015;137:2220-6.
-
(2015)
Int J Cancer
, vol.137
, pp. 2220-2226
-
-
Helgadottir, H.1
Höiom, V.2
Tuominen, R.3
-
38
-
-
84920875735
-
Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma
-
de Ávila AL, Krepischi AC, Moredo LF, et al. Germline CDKN2A mutations in Brazilian patients of hereditary cutaneous melanoma. Fam Cancer 2014;13:645-9.
-
(2014)
Fam Cancer
, vol.13
, pp. 645-649
-
-
de Ávila, A.L.1
Krepischi, A.C.2
Moredo, L.F.3
-
39
-
-
84872684625
-
Genetic variations of patients with familial or multiple melanoma in Southern Brazil
-
Grazziotin TC, Rey MC, Bica CG, et al. Genetic variations of patients with familial or multiple melanoma in Southern Brazil. J Eur Acad Dermatol Venereol 2013;27:e179-85.
-
(2013)
J Eur Acad Dermatol Venereol
, vol.27
, pp. e179-e185
-
-
Grazziotin, T.C.1
Rey, M.C.2
Bica, C.G.3
-
40
-
-
33750567811
-
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
-
Goldstein AM, Chan M, Harland M, et al. High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. Cancer Res 2006;66:9818-28.
-
(2006)
Cancer Res
, vol.66
, pp. 9818-9828
-
-
Goldstein, A.M.1
Chan, M.2
Harland, M.3
-
41
-
-
0034790609
-
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect
-
Auroy S, Avril MF, Chompret A, et al. Sporadic multiple primary melanoma cases: CDKN2A germline mutations with a founder effect. Genes Chromosomes Cancer 2001;32:195-202.
-
(2001)
Genes Chromosomes Cancer
, vol.32
, pp. 195-202
-
-
Auroy, S.1
Avril, M.F.2
Chompret, A.3
-
42
-
-
84928727401
-
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom
-
Harland M, Cust AE, Badenas C, et al. Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom. Hered Cancer Clin Pract 2014;12:20.
-
(2014)
Hered Cancer Clin Pract
, vol.12
, pp. 20
-
-
Harland, M.1
Cust, A.E.2
Badenas, C.3
-
43
-
-
0037134702
-
Geographical variation in the penetrance of CDKN2A mutations for melanoma
-
Bishop DT, Demenais F, Goldstein AM, et al. Geographical variation in the penetrance of CDKN2A mutations for melanoma. J Natl Cancer Inst 2002;94:894-903.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 894-903
-
-
Bishop, D.T.1
Demenais, F.2
Goldstein, A.M.3
-
44
-
-
0033836334
-
Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden)
-
Vasen HF, Gruis NA, Frants RR, et al. Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden). Int J Cancer 2000;87:809-11.
-
(2000)
Int J Cancer
, vol.87
, pp. 809-811
-
-
Vasen, H.F.1
Gruis, N.A.2
Frants, R.R.3
-
45
-
-
84864143250
-
Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers
-
Mukherjee B, Delancey JO, Raskin L, et al. Risk of non-melanoma cancers in first-degree relatives of CDKN2A mutation carriers. J Natl Cancer Inst 2012;104:953-6.
-
(2012)
J Natl Cancer Inst
, vol.104
, pp. 953-956
-
-
Mukherjee, B.1
Delancey, J.O.2
Raskin, L.3
-
46
-
-
84860282103
-
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families
-
Ghiorzo P, Fornarini G, Sciallero S, et al. CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. J Med Genet 2012;49:164-70.
-
(2012)
J Med Genet
, vol.49
, pp. 164-170
-
-
Ghiorzo, P.1
Fornarini, G.2
Sciallero, S.3
-
47
-
-
0034596343
-
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
-
Borg A, Sandberg T, Nilsson K, et al. High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families. J Natl Cancer Inst 2000;92:1260-6.
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1260-1266
-
-
Borg, A.1
Sandberg, T.2
Nilsson, K.3
-
48
-
-
84905579541
-
High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families
-
Helgadottir H, Hoiom V, Jonsson G, et al. High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families. J Med Genet 2014;51:545-52.
-
(2014)
J Med Genet
, vol.51
, pp. 545-552
-
-
Helgadottir, H.1
Hoiom, V.2
Jonsson, G.3
-
49
-
-
0029664339
-
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
-
Zuo L, Weger J, Yang Q, et al. Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma. Nat Genet 1996;12:97-9.
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
-
50
-
-
84878886596
-
Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
-
Puntervoll HE, Yang XR, Vetti HH, et al. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. J Med Genet 2013;50:264-70.
-
(2013)
J Med Genet
, vol.50
, pp. 264-270
-
-
Puntervoll, H.E.1
Yang, X.R.2
Vetti, H.H.3
-
51
-
-
84890378293
-
A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers
-
Aoude LG, Wadt K, Bojesen A, et al. A BAP1 mutation in a Danish family predisposes to uveal melanoma and other cancers. PLoS One 2013;8:e72144.
-
(2013)
PLoS One
, vol.8
-
-
Aoude, L.G.1
Wadt, K.2
Bojesen, A.3
-
52
-
-
84856023369
-
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
-
Abdel-Rahman MH, Pilarski R, Cebulla CM, et al. Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers. J Med Genet 2011;48:856-9.
-
(2011)
J Med Genet
, vol.48
, pp. 856-859
-
-
Abdel-Rahman, M.H.1
Pilarski, R.2
Cebulla, C.M.3
-
53
-
-
84865461263
-
BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs
-
Carbone M, Ferris LK, Baumann F, et al. BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs. J Transl Med 2012;10:179.
-
(2012)
J Transl Med
, vol.10
, pp. 179
-
-
Carbone, M.1
Ferris, L.K.2
Baumann, F.3
-
55
-
-
84860142904
-
Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families
-
Njauw CN, Kim I, Piris A, et al. Germline BAP1 inactivation is preferentially associated with metastatic ocular melanoma and cutaneous-ocular melanoma families. PLoS One 2012;7:e35295.
-
(2012)
PLoS One
, vol.7
-
-
Njauw, C.N.1
Kim, I.2
Piris, A.3
-
56
-
-
84878846119
-
Germline BAP1 Mutations Predispose to Renal Cell Carcinomas
-
Popova T, Hebert L, Jacquemin V, et al. Germline BAP1 Mutations Predispose to Renal Cell Carcinomas. Am J Hum Genet 2013;92:974-80.
-
(2013)
Am J Hum Genet
, vol.92
, pp. 974-980
-
-
Popova, T.1
Hebert, L.2
Jacquemin, V.3
-
57
-
-
80053386896
-
Germline mutations in BAP1 predispose to melanocytic tumors
-
Wiesner T, Obenauf AC, Murali R, et al. Germline mutations in BAP1 predispose to melanocytic tumors. Nat Genet 2011;43:1018-21.
-
(2011)
Nat Genet
, vol.43
, pp. 1018-1021
-
-
Wiesner, T.1
Obenauf, A.C.2
Murali, R.3
-
58
-
-
84938844516
-
A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma
-
Wadt KA, Aoude LG, Johansson P, et al. A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma. Clin Genet 2015;88:267-72.
-
(2015)
Clin Genet
, vol.88
, pp. 267-272
-
-
Wadt, K.A.1
Aoude, L.G.2
Johansson, P.3
-
59
-
-
84938877109
-
Germline BAP1 mutations predispose also to multiple basal cell carcinomas
-
de la Fouchardière A, Cabaret O, Savin L, et al. Germline BAP1 mutations predispose also to multiple basal cell carcinomas. Clin Genet 2015;88:273-7.
-
(2015)
Clin Genet
, vol.88
, pp. 273-277
-
-
de la Fouchardière, A.1
Cabaret, O.2
Savin, L.3
-
60
-
-
84873725170
-
Hereditary uveal melanoma: a report of a germline mutation in BAP1
-
Höiom V, Edsgärd D, Helgadottir H, et al. Hereditary uveal melanoma: a report of a germline mutation in BAP1. Genes Chromosomes Cancer 2013;52:378-84.
-
(2013)
Genes Chromosomes Cancer
, vol.52
, pp. 378-384
-
-
Höiom, V.1
Edsgärd, D.2
Helgadottir, H.3
-
61
-
-
78649700287
-
Frequent mutation of BAP1 in metastasizing uveal melanomas
-
Harbour JW, Onken MD, Roberson ED, et al. Frequent mutation of BAP1 in metastasizing uveal melanomas. Science 2010;330:1410-3.
-
(2010)
Science
, vol.330
, pp. 1410-1413
-
-
Harbour, J.W.1
Onken, M.D.2
Roberson, E.D.3
-
62
-
-
84892601745
-
BAP1 germline mutation in two first grade family members with uveal melanoma
-
Maerker DA, Zeschnigk M, Nelles J, et al. BAP1 germline mutation in two first grade family members with uveal melanoma. Br J Ophthalmol 2014;98:224-7.
-
(2014)
Br J Ophthalmol
, vol.98
, pp. 224-227
-
-
Maerker, D.A.1
Zeschnigk, M.2
Nelles, J.3
-
63
-
-
84890127613
-
Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases
-
Pilarski R, Cebulla CM, Massengill JB, et al. Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases. Genes Chromosomes Cancer 2014;53:177-82.
-
(2014)
Genes Chromosomes Cancer
, vol.53
, pp. 177-182
-
-
Pilarski, R.1
Cebulla, C.M.2
Massengill, J.B.3
-
64
-
-
84884497841
-
A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma
-
Farley MN, Schmidt LS, Mester JL, et al. A novel germline mutation in BAP1 predisposes to familial clear-cell renal cell carcinoma. Mol Cancer Res 2013;11:1061-71.
-
(2013)
Mol Cancer Res
, vol.11
, pp. 1061-1071
-
-
Farley, M.N.1
Schmidt, L.S.2
Mester, J.L.3
-
65
-
-
84867918271
-
A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma
-
Wadt K, Choi J, Chung JY, et al. A cryptic BAP1 splice mutation in a family with uveal and cutaneous melanoma, and paraganglioma. Pigment Cell Melanoma Res 2012;25:815-8.
-
(2012)
Pigment Cell Melanoma Res
, vol.25
, pp. 815-818
-
-
Wadt, K.1
Choi, J.2
Chung, J.Y.3
-
66
-
-
84862777919
-
Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family
-
Yang XR, Brown K, Landi MT, et al. Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family. Pigment Cell Melanoma Res 2012;25:243-7.
-
(2012)
Pigment Cell Melanoma Res
, vol.25
, pp. 243-247
-
-
Yang, X.R.1
Brown, K.2
Landi, M.T.3
-
67
-
-
77649180958
-
Telomeres: protecting chromosomes against genome instability
-
O'Sullivan RJ, Karlseder J. Telomeres: protecting chromosomes against genome instability. Nat Rev Mol Cell Biol 2010;11:171-81.
-
(2010)
Nat Rev Mol Cell Biol
, vol.11
, pp. 171-181
-
-
O'Sullivan, R.J.1
Karlseder, J.2
-
68
-
-
23844517498
-
Obesity, cigarette smoking, and telomere length in women
-
Valdes AM, Andrew T, Gardner JP, et al. Obesity, cigarette smoking, and telomere length in women. Lancet 2005;366:662-4.
-
(2005)
Lancet
, vol.366
, pp. 662-664
-
-
Valdes, A.M.1
Andrew, T.2
Gardner, J.P.3
-
69
-
-
58549092034
-
A prospective study of telomere length and the risk of skin cancer
-
Han J, Qureshi AA, Prescott J, et al. A prospective study of telomere length and the risk of skin cancer. J Invest Dermatol 2009;129:415-21.
-
(2009)
J Invest Dermatol
, vol.129
, pp. 415-421
-
-
Han, J.1
Qureshi, A.A.2
Prescott, J.3
-
70
-
-
84930397756
-
The effect on melanoma risk of genes previously associated with telomere length
-
Iles MM, Bishop DT, Taylor JC, et al. The effect on melanoma risk of genes previously associated with telomere length. J Natl Cancer Inst 2014;106.
-
(2014)
J Natl Cancer Inst
, pp. 106
-
-
Iles, M.M.1
Bishop, D.T.2
Taylor, J.C.3
-
71
-
-
84874191269
-
TERT promoter mutations in familial and sporadic melanoma
-
Horn S, Figl A, Rachakonda PS, et al. TERT promoter mutations in familial and sporadic melanoma. Science 2013;339:959-61.
-
(2013)
Science
, vol.339
, pp. 959-961
-
-
Horn, S.1
Figl, A.2
Rachakonda, P.S.3
-
72
-
-
84899624984
-
POT1 loss-of-function variants predispose to familial melanoma
-
Robles-Espinoza CD, Harland M, Ramsay AJ, et al. POT1 loss-of-function variants predispose to familial melanoma. Nat Genet 2014;46:478-81.
-
(2014)
Nat Genet
, vol.46
, pp. 478-481
-
-
Robles-Espinoza, C.D.1
Harland, M.2
Ramsay, A.J.3
-
73
-
-
84899648964
-
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma
-
Shi J, Yang XR, Ballew B, et al. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. Nat Genet 2014;46:482-6.
-
(2014)
Nat Genet
, vol.46
, pp. 482-486
-
-
Shi, J.1
Yang, X.R.2
Ballew, B.3
-
74
-
-
46249125488
-
How shelterin protects mammalian telomeres
-
Palm W, de Lange T. How shelterin protects mammalian telomeres. Annu Rev Genet 2008;42:301-34.
-
(2008)
Annu Rev Genet
, vol.42
, pp. 301-334
-
-
Palm, W.1
de Lange, T.2
-
75
-
-
84925547048
-
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma
-
Aoude LG, Pritchard AL, Robles-Espinoza CD, et al. Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma. J Natl Cancer Inst 2014;107.
-
(2014)
J Natl Cancer Inst
, pp. 107
-
-
Aoude, L.G.1
Pritchard, A.L.2
Robles-Espinoza, C.D.3
-
76
-
-
80052397478
-
Melanocortin 1 receptor variants: functional role and pigmentary associations
-
Dessinioti C, Antoniou C, Katsambas A, et al. Melanocortin 1 receptor variants: functional role and pigmentary associations. Photochem Photobiol 2011;87:978-87.
-
(2011)
Photochem Photobiol
, vol.87
, pp. 978-987
-
-
Dessinioti, C.1
Antoniou, C.2
Katsambas, A.3
-
77
-
-
79960912284
-
Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden
-
Williams PF, Olsen CM, Hayward NK, et al. Melanocortin 1 receptor and risk of cutaneous melanoma: a meta-analysis and estimates of population burden. Int J Cancer 2011;129:1730-40.
-
(2011)
Int J Cancer
, vol.129
, pp. 1730-1740
-
-
Williams, P.F.1
Olsen, C.M.2
Hayward, N.K.3
-
78
-
-
0034641860
-
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation
-
Flanagan N, Healy E, Ray A, et al. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation. Hum Mol Genet 2000;9:2531-7.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2531-2537
-
-
Flanagan, N.1
Healy, E.2
Ray, A.3
-
79
-
-
43049148341
-
MC1R variants, melanoma and red hair color phenotype: a meta-analysis
-
Raimondi S, Sera F, Gandini S, et al. MC1R variants, melanoma and red hair color phenotype: a meta-analysis. Int J Cancer 2008;122:2753-60.
-
(2008)
Int J Cancer
, vol.122
, pp. 2753-2760
-
-
Raimondi, S.1
Sera, F.2
Gandini, S.3
-
80
-
-
77951667623
-
MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis
-
Fargnoli MC, Gandini S, Peris K, et al. MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis. Eur J Cancer 2010;46:1413-20.
-
(2010)
Eur J Cancer
, vol.46
, pp. 1413-1420
-
-
Fargnoli, M.C.1
Gandini, S.2
Peris, K.3
-
81
-
-
84891859589
-
MC1R gene variants and sporadic malignant melanoma susceptibility in the Canary Islands population
-
Córdoba-Lanús E, Hernández-Jiménez JG, Medina-Coello C, et al. MC1R gene variants and sporadic malignant melanoma susceptibility in the Canary Islands population. Arch Dermatol Res 2014;306:51-8.
-
(2014)
Arch Dermatol Res
, vol.306
, pp. 51-58
-
-
Córdoba-Lanús, E.1
Hernández-Jiménez, J.G.2
Medina-Coello, C.3
-
82
-
-
84885587653
-
Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population
-
Puig-Butillé JA, Carrera C, Kumar R, et al. Distribution of MC1R variants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population. Br J Dermatol 2013;169:804-11.
-
(2013)
Br J Dermatol
, vol.169
, pp. 804-811
-
-
Puig-Butillé, J.A.1
Carrera, C.2
Kumar, R.3
-
83
-
-
82555187007
-
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma
-
Yokoyama S, Woods SL, Boyle GM, et al. A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature 2011;480:99-103.
-
(2011)
Nature
, vol.480
, pp. 99-103
-
-
Yokoyama, S.1
Woods, S.L.2
Boyle, G.M.3
-
84
-
-
82555205202
-
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
-
Bertolotto C, Lesueur F, Giuliano S, et al. A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma. Nature 2011;480:94-8.
-
(2011)
Nature
, vol.480
, pp. 94-98
-
-
Bertolotto, C.1
Lesueur, F.2
Giuliano, S.3
-
85
-
-
33747882661
-
MITF: master regulator of melanocyte development and melanoma oncogene
-
Levy C, Khaled M, Fisher DE. MITF: master regulator of melanocyte development and melanoma oncogene. Trends Mol Med 2006;12:406-14.
-
(2006)
Trends Mol Med
, vol.12
, pp. 406-414
-
-
Levy, C.1
Khaled, M.2
Fisher, D.E.3
-
86
-
-
84874367669
-
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history
-
Ghiorzo P, Pastorino L, Queirolo P, et al. Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. Pigment Cell Melanoma Res 2013;26:259-62.
-
(2013)
Pigment Cell Melanoma Res
, vol.26
, pp. 259-262
-
-
Ghiorzo, P.1
Pastorino, L.2
Queirolo, P.3
-
87
-
-
84890994849
-
Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients
-
Sturm RA, Fox C, McClenahan P, et al. Phenotypic characterization of nevus and tumor patterns in MITF E318K mutation carrier melanoma patients. J Invest Dermatol 2014;134:141-9.
-
(2014)
J Invest Dermatol
, vol.134
, pp. 141-149
-
-
Sturm, R.A.1
Fox, C.2
McClenahan, P.3
-
88
-
-
84898917509
-
MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors
-
Berwick M, MacArthur J, Orlow I, et al. MITF E318K's effect on melanoma risk independent of, but modified by, other risk factors. Pigment Cell Melanoma Res 2014;27:485-8.
-
(2014)
Pigment Cell Melanoma Res
, vol.27
, pp. 485-488
-
-
Berwick, M.1
MacArthur, J.2
Orlow, I.3
-
89
-
-
84872679543
-
Germline melanoma susceptibility and prognostic genes: a review of the literature
-
Ward KA, Lazovich D, Hordinsky MK. Germline melanoma susceptibility and prognostic genes: a review of the literature. J Am Acad Dermatol 2012;67:1055-67.
-
(2012)
J Am Acad Dermatol
, vol.67
, pp. 1055-1067
-
-
Ward, K.A.1
Lazovich, D.2
Hordinsky, M.K.3
-
90
-
-
66949130735
-
Pigmentation-related genes and their implication in malignant melanoma susceptibility
-
Fernandez LP, Milne RL, Pita G, et al. Pigmentation-related genes and their implication in malignant melanoma susceptibility. Exp Dermatol 2009;18:634-42.
-
(2009)
Exp Dermatol
, vol.18
, pp. 634-642
-
-
Fernandez, L.P.1
Milne, R.L.2
Pita, G.3
-
92
-
-
33644893065
-
HLA class II polymorphisms in Spanish melanoma patients: homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor
-
Planelles D, Nagore E, Moret A, et al. HLA class II polymorphisms in Spanish melanoma patients: homozygosity for HLA-DQA1 locus can be a potential melanoma risk factor. Br J Dermatol 2006;154:261-6.
-
(2006)
Br J Dermatol
, vol.154
, pp. 261-266
-
-
Planelles, D.1
Nagore, E.2
Moret, A.3
-
93
-
-
84875332980
-
Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population
-
Peña-Chilet M, Blanquer-Maceiras M, Ibarrola-Villava M, et al. Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population. BMC Cancer 2013;13:160.
-
(2013)
BMC Cancer
, vol.13
, pp. 160
-
-
Peña-Chilet, M.1
Blanquer-Maceiras, M.2
Ibarrola-Villava, M.3
-
94
-
-
84861593805
-
Role of glutathione S-transferases in melanoma susceptibility: association with GSTP1 rs1695 polymorphism
-
Ibarrola-Villava M, Martin-Gonzalez M, Lazaro P, et al. Role of glutathione S-transferases in melanoma susceptibility: association with GSTP1 rs1695 polymorphism. Br J Dermatol 2012;166:1176-83.
-
(2012)
Br J Dermatol
, vol.166
, pp. 1176-1183
-
-
Ibarrola-Villava, M.1
Martin-Gonzalez, M.2
Lazaro, P.3
-
95
-
-
84875722359
-
A variant in FTO shows association with melanoma risk not due to BMI
-
Iles MM, Law MH, Stacey SN, et al. A variant in FTO shows association with melanoma risk not due to BMI. Nat Genet 2013;45:428-32, 432e1.
-
(2013)
Nat Genet
, vol.45
-
-
Iles, M.M.1
Law, M.H.2
Stacey, S.N.3
-
97
-
-
84863615237
-
Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors
-
Riley BD, Culver JO, Skrzynia C, et al. Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors. J Genet Couns 2012;21:151-61.
-
(2012)
J Genet Couns
, vol.21
, pp. 151-161
-
-
Riley, B.D.1
Culver, J.O.2
Skrzynia, C.3
-
98
-
-
65649118981
-
Melanoma genetics: an update on risk-associated genes
-
Udayakumar D, Tsao H. Melanoma genetics: an update on risk-associated genes. Hematol Oncol Clin North Am 2009;23:415-29, vii.
-
(2009)
Hematol Oncol Clin North Am
, vol.23
-
-
Udayakumar, D.1
Tsao, H.2
-
99
-
-
53349090631
-
CDKN2A/p16 genetic test reporting improves early detection intentions and practices in high-risk melanoma families
-
Aspinwall LG, Leaf SL, Dola ER, et al. CDKN2A/p16 genetic test reporting improves early detection intentions and practices in high-risk melanoma families. Cancer Epidemiol Biomarkers Prev 2008;17:1510-9.
-
(2008)
Cancer Epidemiol Biomarkers Prev
, vol.17
, pp. 1510-1519
-
-
Aspinwall, L.G.1
Leaf, S.L.2
Dola, E.R.3
-
100
-
-
2142645979
-
Clinical germline genetic testing for melanoma
-
Hansen CB, Wadge LM, Lowstuter K, et al. Clinical germline genetic testing for melanoma. Lancet Oncol 2004;5:314-9.
-
(2004)
Lancet Oncol
, vol.5
, pp. 314-319
-
-
Hansen, C.B.1
Wadge, L.M.2
Lowstuter, K.3
-
101
-
-
0033818195
-
Low prevalence of germline CDKN2A and CDK4 mutations in patients with early-onset melanoma
-
Tsao H, Zhang X, Kwitkiwski K, et al. Low prevalence of germline CDKN2A and CDK4 mutations in patients with early-onset melanoma. Arch Dermatol 2000;136:1118-22.
-
(2000)
Arch Dermatol
, vol.136
, pp. 1118-1122
-
-
Tsao, H.1
Zhang, X.2
Kwitkiwski, K.3
-
102
-
-
70249098475
-
Selection criteria for genetic assessment of patients with familial melanoma
-
Leachman SA, Carucci J, Kohlmann W, et al. Selection criteria for genetic assessment of patients with familial melanoma. J Am Acad Dermatol 2009;61:677.e1-14.
-
(2009)
J Am Acad Dermatol
, vol.61
-
-
Leachman, S.A.1
Carucci, J.2
Kohlmann, W.3
-
103
-
-
0037954289
-
Dermatologist detection and skin self-examination are associated with thinner melanomas: results from a survey of the Italian Multidisciplinary Group on Melanoma
-
Carli P, De Giorgi V, Palli D, et al. Dermatologist detection and skin self-examination are associated with thinner melanomas: results from a survey of the Italian Multidisciplinary Group on Melanoma. Arch Dermatol 2003;139:607-12.
-
(2003)
Arch Dermatol
, vol.139
, pp. 607-612
-
-
Carli, P.1
De Giorgi, V.2
Palli, D.3
-
104
-
-
82955192301
-
Benefits of total body photography and digital dermatoscopy ("two-step method of digital follow-up") in the early diagnosis of melanoma in patients at high risk for melanoma
-
Salerni G, Carrera C, Lovatto L, et al. Benefits of total body photography and digital dermatoscopy ("two-step method of digital follow-up") in the early diagnosis of melanoma in patients at high risk for melanoma. J Am Acad Dermatol 2012;67:e17-27.
-
(2012)
J Am Acad Dermatol
, vol.67
, pp. e17-27
-
-
Salerni, G.1
Carrera, C.2
Lovatto, L.3
-
105
-
-
79956078755
-
Melanomas detected in a follow-up program compared with melanomas referred to a melanoma unit
-
Salerni G, Lovatto L, Carrera C, et al. Melanomas detected in a follow-up program compared with melanomas referred to a melanoma unit. Arch Dermatol 2011;147:549-55.
-
(2011)
Arch Dermatol
, vol.147
, pp. 549-555
-
-
Salerni, G.1
Lovatto, L.2
Carrera, C.3
-
106
-
-
84885587396
-
Melanoma genetic counseling and test reporting improve screening adherence among unaffected carriers 2 years later
-
Aspinwall LG, Taber JM, Leaf SL, et al. Melanoma genetic counseling and test reporting improve screening adherence among unaffected carriers 2 years later. Cancer Epidemiol Biomarkers Prev 2013;22:1687-97.
-
(2013)
Cancer Epidemiol Biomarkers Prev
, vol.22
, pp. 1687-1697
-
-
Aspinwall, L.G.1
Taber, J.M.2
Leaf, S.L.3
-
107
-
-
84908879271
-
Unaffected family members report improvements in daily routine sun protection 2 years following melanoma genetic testing
-
Aspinwall LG, Taber JM, Kohlmann W, et al. Unaffected family members report improvements in daily routine sun protection 2 years following melanoma genetic testing. Genet Med 2014;16:846-53.
-
(2014)
Genet Med
, vol.16
, pp. 846-853
-
-
Aspinwall, L.G.1
Taber, J.M.2
Kohlmann, W.3
-
108
-
-
58149229703
-
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families
-
de Snoo FA, Bishop DT, Bergman W, et al. Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families. Clin Cancer Res 2008;14:7151-7.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 7151-7157
-
-
de Snoo, F.A.1
Bishop, D.T.2
Bergman, W.3
-
109
-
-
79952316878
-
Magnetic resonance imaging surveillance detects early-stage pancreatic cancer in carriers of a p16-Leiden mutation
-
Vasen HF, Wasser M, van Mil A, et al. Magnetic resonance imaging surveillance detects early-stage pancreatic cancer in carriers of a p16-Leiden mutation. Gastroenterology 2011;140:850-6.
-
(2011)
Gastroenterology
, vol.140
, pp. 850-856
-
-
Vasen, H.F.1
Wasser, M.2
van Mil, A.3
-
110
-
-
84899711181
-
The Importance of Multidisciplinary Approach in Early Detection of BAP1 Tumor Predisposition Syndrome: Clinical Management and Risk Assessment
-
Battaglia A. The Importance of Multidisciplinary Approach in Early Detection of BAP1 Tumor Predisposition Syndrome: Clinical Management and Risk Assessment. Clin Med Insights Oncol 2014;8:37-47.
-
(2014)
Clin Med Insights Oncol
, vol.8
, pp. 37-47
-
-
Battaglia, A.1
|