-
1
-
-
77953370205
-
-
SEER Database
-
SEER Database [http://seer.cancer.gov/statfacts/html/skin.html]
-
-
-
-
2
-
-
67650874081
-
Cancer statistics
-
Jemal A, Siegel R, Ward E, Hao Y, Xu J,Thun MJ: Cancer statistics, 2009. CA Cancer J Clin 2009, 59:225-249.
-
(2009)
2009. CA Cancer J Clin
, vol.59
, pp. 225-249
-
-
Jemal, A.1
Siegel, R.2
Ward, E.3
Hao, Y.4
Xu, J.5
Thun, M.J.6
-
3
-
-
77953376319
-
A history of melanoma: From Hunter to Clark
-
Cutaneous Melanoma. 4th edition. Edited by Balch CM, Houghton AN, Sober AJ, Soong S-j.
-
Roderick McLeod G, Davis NC, Sober AJ: A history of melanoma: From Hunter to Clark. In Cutaneous Melanoma. 4th edition. Edited by Balch CM, Houghton AN, Sober AJ, Soong S-j. St Louis: Quality Medical Publishing, Inc.; 2003:2-12.
-
(2003)
St Louis: Quality Medical Publishing, Inc.
, pp. 2-12
-
-
Roderick McLeod, G.1
Davis, N.C.2
Sober, A.J.3
-
4
-
-
0017970363
-
Origin of familial malignant melanomas from heritable melanocytic lesions
-
Clark WH Jr, Reimer RR, Greene M, Ainsworth AM, Mastrangelo MJ: Origin of familial malignant melanomas from heritable melanocytic lesions. 'The B-K mole syndrome'. Arch Dermatol 1978, 114:732-738.
-
(1978)
'The B-K mole syndrome'. Arch Dermatol
, vol.114
, pp. 732-738
-
-
Clark, W.H.1
Reimer, R.R.2
Greene, M.3
Ainsworth, A.M.4
Mastrangelo, M.J.5
-
5
-
-
0018123909
-
Familial atypical multiple mole-melanoma syndrome
-
Lynch HT, Frichot BC 3rd, Lynch JF: Familial atypical multiple mole-melanoma syndrome. J Med Genet 1978, 15:352-356.
-
(1978)
J Med Genet
, vol.15
, pp. 352-356
-
-
Lynch, H.T.1
Frichot, B.C.2
Lynch, J.F.3
-
6
-
-
0028048660
-
Familial melanoma and p16 - a hung jury
-
Wainwright B: Familial melanoma and p16 - a hung jury. Nat Genet 1994, 8:3-5.
-
(1994)
Nat Genet
, vol.8
, pp. 3-5
-
-
Wainwright, B.1
-
7
-
-
0029664339
-
Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma
-
Zuo L, Weger J, Yang Q, Goldstein AM, Tucker MA, Walker GJ, Hayward N, Dracopoli NC: Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma. Nat Genet 1996, 12:97-99.
-
(1996)
Nat Genet
, vol.12
, pp. 97-99
-
-
Zuo, L.1
Weger, J.2
Yang, Q.3
Goldstein, A.M.4
Tucker, M.A.5
Walker, G.J.6
Hayward, N.7
Dracopoli, N.C.8
-
8
-
-
65649118981
-
Melanoma genetics: an update on risk-associated genes
-
vii
-
Udayakumar D, Tsao H: Melanoma genetics: an update on risk-associated genes. Hematol Oncol Clin North Am 2009, 23: 415-429, vii.
-
(2009)
Hematol Oncol Clin North Am
, vol.23
, pp. 415-429
-
-
Udayakumar, D.1
Tsao, H.2
-
10
-
-
33747332544
-
Malignant melanoma: genetics and therapeutics in the genomic era
-
Chin L, Garraway LA, Fisher DE: Malignant melanoma: genetics and therapeutics in the genomic era. Genes Dev 2006, 20:2149-2182.
-
(2006)
Genes Dev
, vol.20
, pp. 2149-2182
-
-
Chin, L.1
Garraway, L.A.2
Fisher, D.E.3
-
11
-
-
33847282821
-
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
-
Goldstein AM, Chan M, Harland M, Hayward NK, Demenais F, Bishop DT, Azizi E, Bergman W, Bianchi-Scarra G, Bruno W,Calista D, Albright LA, Chaudru V, Chompret A, Cuellar F, Elder DE, Ghiorzo P, Gillanders EM, Gruis NA, Hansson J, Hogg D, Holland EA, Kanetsky PA, Kefford RF, Landi MT, Lang J, Leachman SA, MacKie RM, Magnusson V, Mann GJ, 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
Hayward, N.K.4
Demenais, F.5
Bishop, D.T.6
Azizi, E.7
Bergman, W.8
Bianchi-Scarra, G.9
Bruno, W.10
Calista, D.11
Albright, L.A.12
Chaudru, V.13
Chompret, A.14
Cuellar, F.15
Elder, D.E.16
Ghiorzo, P.17
Gillanders, E.M.18
Gruis, N.A.19
Hansson, J.20
Hogg, D.21
Holland, E.A.22
Kanetsky, P.A.23
Kefford, R.F.24
Landi, M.T.25
Lang, J.26
Leachman, S.A.27
MacKie, R.M.28
Magnusson, V.29
Mann, G.J.30
more..
-
12
-
-
68149170036
-
New common variants affecting susceptibility to basal cell carcinoma
-
Stacey S.N., Sulem P., Masson G, Gudjonsson S.A., Thorleifsson G., Jakobsdottir M, Sigurdsson A., Gudbjartsson D.F., Sigurgeirsson B., Benediktsdottir K.R., Thorisdottir K., Ragnarsson R, Scherer D., Hemminki K, Rudnai P., Gurzau E, Koppova K., Botella-Estrada R, Soriano V., Juberias P, Saez B., Gilaberte Y, Fuentelsaz V., Corredera C, Grasa M., Hoiom V, Lindblom A.Bonenkamp J.J., van Rossum MM, Aben KK, et al.: New common variants affecting susceptibility to basal cell carcinoma. Nat Genet 2009, 41:909-914.
-
(2009)
Nat Genet
, vol.41
, pp. 909-914
-
-
Stacey, S.N.1
Sulem, P.2
Masson, G.3
Gudjonsson, S.A.4
Thorleifsson, G.5
Jakobsdottir, M.6
Sigurdsson, A.7
Gudbjartsson, D.F.8
Sigurgeirsson, B.9
Benediktsdottir, K.R.10
Thorisdottir, K.11
Ragnarsson, R.12
Scherer, D.13
Hemminki, K.14
Rudnai, P.15
Gurzau, E.16
Koppova, K.17
Botella-Estrada, R.18
Soriano, V.19
Juberias, P.20
Saez, B.21
Gilaberte, Y.22
Fuentelsaz, V.23
Corredera, C.24
Grasa, M.25
Hoiom, V.26
Lindblom, A.27
Bonenkamp, J.J.28
Van Rossum, M.M.29
Aben, K.K.30
more..
-
13
-
-
25144506469
-
Meta-analysis of risk factors for cutaneous melanoma: III
-
Gandini S, Sera F, Cattaruzza MS, Pasquini P, Zanetti R, Masini C, Boyle P, Melchi CF: Meta-analysis of risk factors for cutaneous melanoma: III. Family history, actinic damage and phenotypic factors. Eur J Cancer 2005, 41: 2040-2059.
-
(2005)
Family history, actinic damage and phenotypic factors. Eur J Cancer
, vol.41
, pp. 2040-2059
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
Pasquini, P.4
Zanetti, R.5
Masini, C.6
Boyle, P.7
Melchi, C.F.8
-
14
-
-
47549118838
-
Genetics of melanoma predisposition
-
Lin J, Hocker TL, Singh M, Tsao H: Genetics of melanoma predisposition. Br J Dermatol 2008, 159:286-291.
-
(2008)
Br J Dermatol
, vol.159
, pp. 286-291
-
-
Lin, J.1
Hocker, T.L.2
Singh, M.3
Tsao, H.4
-
15
-
-
14644429805
-
MC1R and the response of melanocytes to ultraviolet radiation
-
Rouzaud F, Kadekaro AL, Abdel-Malek ZA, Hearing VJ: MC1R and the response of melanocytes to ultraviolet radiation. Mutat Res 2005, 571:133-152.
-
(2005)
Mutat Res
, vol.571
, pp. 133-152
-
-
Rouzaud, F.1
Kadekaro, A.L.2
Abdel-Malek, Z.A.3
Hearing, V.J.4
-
17
-
-
0042837972
-
Rate limiting factors in melanocortin 1 receptor signalling through the cAMP pathway
-
Mas JS, Gerritsen I, Hahmann C, Jimenez-Cervantes C, Garcia-Borron JC: Rate limiting factors in melanocortin 1 receptor signalling through the cAMP pathway. Pigment Cell Res 2003, 16:540-547.
-
(2003)
Pigment Cell Res
, vol.16
, pp. 540-547
-
-
Mas, J.S.1
Gerritsen, I.2
Hahmann, C.3
Jimenez-Cervantes, C.4
Garcia-Borron, J.C.5
-
18
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
Valverde P, Healy E, Jackson I, Rees JL,Thody AJ: Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet 1995, 11:328-330.
-
(1995)
Nat Genet
, vol.11
, pp. 328-330
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
Rees, J.L.4
Thody, A.J.5
-
19
-
-
43049148341
-
MC1R variants
-
Raimondi S, Sera F, Gandini S, Iodice S, Caini S, Maisonneuve P,Fargnoli MC: MC1R variants, melanoma and red hair color phenotype: a meta-analysis. Int J Cancer 2008, 122:2753-2760.
-
(2008)
melanoma and red hair color phenotype: a meta-analysis. Int J Cancer
, vol.122
, 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
-
20
-
-
0034837773
-
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
-
Box NF, Duffy DL, Chen W, Stark M, Martin NG, Sturm RA, Hayward NK: MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. Am J Hum Genet 2001, 69:765-773.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 765-773
-
-
Box, N.F.1
Duffy, D.L.2
Chen, W.3
Stark, M.4
Martin, N.G.5
Sturm, R.A.6
Hayward, N.K.7
-
21
-
-
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
-
Kennedy C, ter Huurne J, Berkhout M, Gruis N, Bastiaens M, Bergman W, Willemze R, Bavinck JN: 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. J Invest Dermatol 2001, 117:294-300.
-
(2001)
J Invest Dermatol
, vol.117
, 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
Bavinck, J.N.8
-
22
-
-
51749099797
-
MC1R variants increase risk of melanomas harboring BRAF mutations
-
Fargnoli MC, Pike K, Pfeiffer RM, Tsang S, Rozenblum E, Munroe DJ, Golubeva Y, Calista D, Seidenari S, Massi D, Carli P, Bauer J, Elder DE, Bastian BC, Peris K, Landi MT: MC1R variants increase risk of melanomas harboring BRAF mutations. J Invest Dermatol 2008, 128:2485-2490.
-
(2008)
J Invest Dermatol
, vol.128
, pp. 2485-2490
-
-
Fargnoli, M.C.1
Pike, K.2
Pfeiffer, R.M.3
Tsang, S.4
Rozenblum, E.5
Munroe, D.J.6
Golubeva, Y.7
Calista, D.8
Seidenari, S.9
Massi, D.10
Carli, P.11
Bauer, J.12
Elder, D.E.13
Bastian, B.C.14
Peris, K.15
Landi, M.T.16
-
23
-
-
33746589029
-
MC1R germline variants confer risk for BRAF-mutant melanoma
-
Landi MT, Bauer J, Pfeiffer RM, Elder DE, Hulley B, Minghetti P, Calista D, Kanetsky PA, Pinkel D, Bastian BC: MC1R germline variants confer risk for BRAF-mutant melanoma. Science 2006, 313:521-522.
-
(2006)
Science
, vol.313
, pp. 521-522
-
-
Landi, M.T.1
Bauer, J.2
Pfeiffer, R.M.3
Elder, D.E.4
Hulley, B.5
Minghetti, P.6
Calista, D.7
Kanetsky, P.A.8
Pinkel, D.9
Bastian, B.C.10
-
24
-
-
36549071998
-
Genetic determinants of hair
-
Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Magnusson KP, Manolescu A, Karason A, Palsson A, Thorleifsson G, Jakobsdottir M, Steinberg S, Palsson S, Jonasson F, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Kiemeney LA, Olafsson JH, Gulcher J, Kong A, Thorsteinsdottir, U,Stefansson, K: Genetic determinants of hair, eye and skin pigmentation in Europeans. Nat Genet 2007, 39:1443-1452.
-
(2007)
eye and skin pigmentation in Europeans. Nat Genet
, vol.39
, pp. 1443-1452
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.N.3
Helgason, A.4
Rafnar, T.5
Magnusson, K.P.6
Manolescu, A.7
Karason, A.8
Palsson, A.9
Thorleifsson, G.10
Jakobsdottir, M.11
Steinberg, S.12
Palsson, S.13
Jonasson, F.14
igurgeirsson, B.15
Thorisdottir, K.16
Ragnarsson, R.17
Benediktsdottir, K.R.18
Aben, K.K.19
Kiemeney, L.A.20
Olafsson, J.H.21
Gulcher, J.22
Kong, A.23
Thorsteinsdottir, U.24
Stefansson, K.25
more..
-
25
-
-
45549095745
-
Two newly identified genetic determinants of pigmentation in Europeans
-
Sulem P, Gudbjartsson DF, Stacey SN, Helgason A, Rafnar T, Jakobsdottir M, Steinberg S, Gudjonsson SA, Palsson A, Thorleifsson G, Palsson S, Sigurgeirsson B, Thorisdottir K, Ragnarsson R, Benediktsdottir KR, Aben KK, Vermeulen SH, Goldstein AM, Tucker MA, Kiemeney LA, Olafsson JH, GulcherJ, Kong A, Thorsteinsdottir U,Stefansson K: Two newly identified genetic determinants of pigmentation in Europeans. Nat Genet 2008, 40:835-837.
-
(2008)
Nat Genet
, vol.40
, pp. 835-837
-
-
Sulem, P.1
Gudbjartsson, D.F.2
Stacey, S.N.3
Helgason, A.4
Rafnar, T.5
Jakobsdottir, M.6
Steinberg, S.7
Gudjonsson, S.A.8
Palsson, A.9
Thorleifsson, G.10
Palsson, S.11
Sigurgeirsson, B.12
Thorisdottir, K.13
Ragnarsson, R.14
Benediktsdottir, K.R.15
Aben, K.K.16
Vermeulen, S.H.17
Goldstein, A.M.18
Tucker, M.A.19
Kiemeney, L.A.20
Olafsson, J.H.21
Gulcher, J.22
Kong, A.23
Thorsteinsdottir, U.24
Stefansson, K.25
more..
-
26
-
-
45549097424
-
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
-
Gudbjartsson DF, Sulem P, Stacey SN, Goldstein AM, Rafnar T, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Sveinsdottir SG, Magnusson V, Lindblom A, Kostulas K, Botella-Estrada R, Soriano V, Juberias P, Grasa M, Saez B, Andres R, Scherer D, Rudnai P, Gurzau E, Koppova K, Kiemeney LA, Jakobsdottir M, Steinberg S, Helgason A, Gretarsdottir S, Tucker MA, Mayordomo JI, et al.: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nat Genet 2008, 40: 886-891.
-
(2008)
Nat Genet
, vol.40
, pp. 886-891
-
-
Gudbjartsson, D.F.1
Sulem, P.2
Stacey, S.N.3
Goldstein, A.M.4
Rafnar, T.5
Sigurgeirsson, B.6
Benediktsdottir, K.R.7
Thorisdottir, K.8
Ragnarsson, R.9
Sveinsdottir, S.G.10
Magnusson, V.11
Lindblom, A.12
Kostulas, K.13
Botella-Estrada, R.14
Soriano, V.15
Juberias, P.16
Grasa, M.17
Saez, B.18
Andres, R.19
Scherer, D.20
Rudnai, P.21
Gurzau, E.22
Koppova, K.23
Kiemeney, L.A.24
Jakobsdottir, M.25
Steinberg, S.26
Helgason, A.27
Gretarsdottir, S.28
Tucker, M.A.29
Mayordomo, J.I.30
more..
-
27
-
-
45549095449
-
Common sequence variants on 20q11.22 confer melanoma susceptibility
-
Brown KM, Macgregor S, Montgomery GW, Craig DW, Zhao ZZ, Iyadurai K, Henders AK, Homer N, Campbell MJ, Stark M, Thomas S, Schmid H, Holland EA, Gillanders EM, Duffy DL, Maskiell JA, Jetann J, Ferguson M, Stephan DA, Cust AE, Whiteman D, Green A, Olsson H, Puig S, Ghiorzo P, Hansson J, Demenais F, Goldstein AM, Gruis NA, Elder DE, et al.: Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet 2008, 40:838-840.
-
(2008)
Nat Genet
, vol.40
, pp. 838-840
-
-
Brown, K.M.1
Macgregor, S.2
Montgomery, G.W.3
Craig, D.W.4
Zhao, Z.Z.5
Iyadurai, K.6
Henders, A.K.7
Homer, N.8
Campbell, M.J.9
Stark, M.10
Thomas, S.11
Schmid, H.12
Holland, E.A.13
Gillanders, E.M.14
Duffy, D.L.15
Maskiell, J.A.16
Jetann, J.17
Ferguson, M.18
Stephan, D.A.19
Cust, A.E.20
Whiteman, D.21
Green, A.22
Olsson, H.23
Puig, S.24
Ghiorzo, P.25
Hansson, J.26
Demenais, F.27
Goldstein, A.M.28
Gruis, N.A.29
Elder, D.E.30
more..
-
28
-
-
68149179663
-
Genome-wide association study identifies three loci associated with melanoma risk
-
Bishop DT, Demenais F, Iles MM, Harland M, Taylor JC, Corda E, Randerson-Moor J, Aitken JF, Avril MF, Azizi E, Bakker B, Bianchi-Scarra G, Bressac-de Paillerets B, Calista D, Cannon-Albright LA, Chin AWT, Debniak T, Galore-Haskel G, Ghiorzo P, Gut I, Hansson J, Hocevar M, Hoiom V, Hopper JL, Ingvar C, Kanetsky PA, Kefford RF, Landi MT, Lang J, Lubinski J, et al.: Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet 2009, 41:920-925.
-
(2009)
Nat Genet
, vol.41
, pp. 920-925
-
-
Bishop, D.T.1
Demenais, F.2
Iles, M.M.3
Harland, M.4
Taylor, J.C.5
Corda, E.6
Randerson-Moor, J.7
Aitken, J.F.8
Avril, M.F.9
Azizi, E.10
Bakker, B.11
Bianchi-Scarra, G.12
Bressac-de Paillerets, B.13
Calista, D.14
Cannon-Albright, L.A.15
Chin, A.W.T.16
Debniak, T.17
Galore-Haskel, G.18
Ghiorzo, P.19
Gut, I.20
Hansson, J.21
Hocevar, M.22
Hoiom, V.23
Hopper, J.L.24
Ingvar, C.25
Kanetsky, P.A.26
Kefford, R.F.27
Landi, M.T.28
Lang, J.29
Lubinski, J.30
more..
-
29
-
-
44849091227
-
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation
-
Han J, Kraft P, Nan H, Guo Q, Chen C, Qureshi A, Hankinson SE, Hu FB, Duffy DL, Zhao ZZ, Martin NG, Montgomery GW, Hayward NK, Thomas G, Hoover RN, Chanock S, Hunter DJ: A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. PLoS Genet 2008, 4:e1000074.
-
(2008)
PLoS Genet
, vol.4
-
-
Han, J.1
Kraft, P.2
Nan, H.3
Guo, Q.4
Chen, C.5
Qureshi, A.6
Hankinson, S.E.7
Hu, F.B.8
Duffy, D.L.9
Zhao, Z.Z.10
Martin, N.G.11
Montgomery, G.W.12
Hayward, N.K.13
Thomas, G.14
Hoover, R.N.15
Chanock, S.16
Hunter, D.J.17
-
30
-
-
0031002840
-
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome
-
Kimonis VE, Goldstein AM, Pastakia B, Yang ML, Kase R, DiGiovanna JJ, Bale AE, Bale SJ: Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet 1997, 69:299-308.
-
(1997)
Am J Med Genet
, vol.69
, pp. 299-308
-
-
Kimonis, V.E.1
Goldstein, A.M.2
Pastakia, B.3
Yang, M.L.4
Kase, R.5
DiGiovanna, J.J.6
Bale, A.E.7
Bale, S.J.8
-
31
-
-
0028271569
-
Nevoid basal cell carcinoma syndrome: review of 118 affected individuals
-
Shanley S, Ratcliffe J, Hockey A, Haan E, Oley C, Ravine D, Martin N, Wicking C, Chenevix-Trench G: Nevoid basal cell carcinoma syndrome: review of 118 affected individuals. Am J Med Genet 1994, 50:282-290.
-
(1994)
Am J Med Genet
, vol.50
, pp. 282-290
-
-
Shanley, S.1
Ratcliffe, J.2
Hockey, A.3
Haan, E.4
Oley, C.5
Ravine, D.6
Martin, N.7
Wicking, C.8
Chenevix-Trench, G.9
-
32
-
-
55049127580
-
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
-
Stacey SN, Gudbjartsson DF, Sulem P, Bergthorsson JT, Kumar R, Thorleifsson G, Sigurdsson A, Jakobsdottir M, Sigurgeirsson B, Benediktsdottir KR, Thorisdottir K, Ragnarsson R, Scherer D, Rudnai P, Gurzau E, Koppova K, Hoiom V, Botella-Estrada R, Soriano V, Juberias P, Grasa M, Carapeto FJ, Tabuenca P, Gilaberte Y, Gudmundsson J, Thorlacius S, Helgason A, Thorlacius T, Jonasdottir A, Blondal T, et al.: Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. Nat Genet 2008, 40:1313-1318.
-
(2008)
Nat Genet
, vol.40
, pp. 1313-1318
-
-
Stacey, S.N.1
Gudbjartsson, D.F.2
Sulem, P.3
Bergthorsson, J.T.4
Kumar, R.5
Thorleifsson, G.6
Sigurdsson, A.7
Jakobsdottir, M.8
Sigurgeirsson, B.9
Benediktsdottir, K.R.10
Thorisdottir, K.11
Ragnarsson, R.12
Scherer, D.13
Rudnai, P.14
Gurzau, E.15
Koppova, K.16
Hoiom, V.17
Botella-Estrada, R.18
Soriano, V.19
Juberias, P.20
Grasa, M.21
Carapeto, F.J.22
Tabuenca, P.23
Gilaberte, Y.24
Gudmundsson, J.25
Thorlacius, S.26
Helgason, A.27
Thorlacius, T.28
Jonasdottir, A.29
Blondal, T.30
more..
-
33
-
-
11144298761
-
Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi
-
34
-
Gandini S, Sera F, Cattaruzza MS, Pasquini P, Abeni D, Boyle P, Melchi CF: Meta-analysis of risk factors for cutaneous melanoma: I. Common and atypical naevi. Eur J Cancer 2005, 41:28-44. 34.
-
(2005)
Eur J Cancer
, vol.41
, pp. 28-44
-
-
Gandini, S.1
Sera, F.2
Cattaruzza, M.S.3
Pasquini, P.4
Abeni, D.5
Boyle, P.6
Melchi, C.F.7
-
34
-
-
0027153535
-
Accelerated detection with prospective surveillance for cutaneous malignant melanoma in high-risk groups
-
MacKie RM, McHenry P, Hole D: Accelerated detection with prospective surveillance for cutaneous malignant melanoma in high-risk groups. Lancet 1993, 341:1618-1620.
-
(1993)
Lancet
, vol.341
, pp. 1618-1620
-
-
MacKie, R.M.1
McHenry, P.2
Hole, D.3
-
35
-
-
33749579172
-
Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort
-
Falchi M, Spector TD, Perks U, Kato BS, Bataille V: Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort. Hum Mol Genet 2006, 15: 2975-2979.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2975-2979
-
-
Falchi, M.1
Spector, T.D.2
Perks, U.3
Kato, B.S.4
Bataille, V.5
-
36
-
-
33845520278
-
A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions
-
Zhu G, Montgomery GW, James MR, Trent JM, Hayward NK, Martin NG, Duffy DL: A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions. Eur J Hum Genet 2007, 15:94-102.
-
(2007)
Eur J Hum Genet
, vol.15
, pp. 94-102
-
-
Zhu, G.1
Montgomery, G.W.2
James, M.R.3
Trent, J.M.4
Hayward, N.K.5
Martin, N.G.6
Duffy, D.L.7
-
37
-
-
68149100807
-
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
-
Falchi M, Bataille V, Hayward NK, Duffy DL, Bishop JA, Pastinen T, Cervino A, Zhao ZZ, Deloukas P, Soranzo N, Elder DE, Barrett JH, Martin NG, Bishop DT, Montgomery GW, Spector TD: Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nat Genet 2009, 41:915-919.
-
(2009)
Nat Genet
, vol.41
, pp. 915-919
-
-
Falchi, M.1
Bataille, V.2
Hayward, N.K.3
Duffy, D.L.4
Bishop, J.A.5
Pastinen, T.6
Cervino, A.7
Zhao, Z.Z.8
Deloukas, P.9
Soranzo, N.10
Elder, D.E.11
Barrett, J.H.12
Martin, N.G.13
Bishop, D.T.14
Montgomery, G.W.15
Spector, T.D.16
|