These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
277 related articles for article (PubMed ID: 18795926)
1. Dermoscopic features of melanomas associated with MC1R variants in Spanish CDKN2A mutation carriers. Cuéllar F; Puig S; Kolm I; Puig-Butille J; Zaballos P; Martí-Laborda R; Badenas C; Malvehy J Br J Dermatol; 2009 Jan; 160(1):48-53. PubMed ID: 18795926 [TBL] [Abstract][Full Text] [Related]
2. Dermoscopic features of cutaneous melanoma are associated with clinical characteristics of patients and tumours and with MC1R genotype. Fargnoli MC; Sera F; Suppa M; Piccolo D; Landi MT; Chiarugi A; Pellegrini C; Seidenari S; Peris K J Eur Acad Dermatol Venereol; 2014 Dec; 28(12):1768-75. PubMed ID: 24588892 [TBL] [Abstract][Full Text] [Related]
3. Melanocortin 1 receptor (MC1R) variants in high melanoma risk patients are associated with specific dermoscopic ABCD features. Quint KD; van der Rhee JI; Gruis NA; Ter Huurne JA; Wolterbeek R; van der Stoep N; Bergman W; Kukutsch NA Acta Derm Venereol; 2012 Nov; 92(6):587-92. PubMed ID: 22965007 [TBL] [Abstract][Full Text] [Related]
4. Influence of germline genetic variants on dermoscopic features of melanoma. Pozzobon FC; Tell-Marti G; Calbet-Llopart N; Barreiro A; Espinosa N; Potrony M; Alejo B; Podlipnik S; Combalia M; Puig-Butillé JA; Carrera C; Malvehy J; Puig S Pigment Cell Melanoma Res; 2021 May; 34(3):618-628. PubMed ID: 33342058 [TBL] [Abstract][Full Text] [Related]
5. Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. Demenais F; Mohamdi H; Chaudru V; Goldstein AM; Newton Bishop JA; Bishop DT; Kanetsky PA; Hayward NK; Gillanders E; Elder DE; Avril MF; Azizi E; van Belle P; Bergman W; Bianchi-Scarrà G; Bressac-de Paillerets B; Calista D; Carrera C; Hansson J; Harland M; Hogg D; Höiom V; Holland EA; Ingvar C; Landi MT; Lang JM; Mackie RM; Mann GJ; Ming ME; Njauw CJ; Olsson H; Palmer J; Pastorino L; Puig S; Randerson-Moor J; Stark M; Tsao H; Tucker MA; van der Velden P; Yang XR; Gruis N; J Natl Cancer Inst; 2010 Oct; 102(20):1568-83. PubMed ID: 20876876 [TBL] [Abstract][Full Text] [Related]
6. High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk. Duffy DL; Lee KJ; Jagirdar K; Pflugfelder A; Stark MS; McMeniman EK; Soyer HP; Sturm RA Br J Dermatol; 2019 Nov; 181(5):1009-1016. PubMed ID: 30820946 [TBL] [Abstract][Full Text] [Related]
7. Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries. Goldstein AM; Chaudru V; Ghiorzo P; Badenas C; Malvehy J; Pastorino L; Laud K; Hulley B; Avril MF; Puig-Butille JA; Miniere A; Marti R; Chompret A; Cuellar F; Kolm I; Mila M; Tucker MA; Demenais F; Bianchi-Scarra G; Puig S; de-Paillerets BB Int J Cancer; 2007 Aug; 121(4):825-31. PubMed ID: 17397031 [TBL] [Abstract][Full Text] [Related]
8. CDKN2A mutations could influence the dermoscopic pattern of presentation of multiple primary melanoma: a clinical dermoscopic genetic study. De Giorgi V; Savarese I; D'Errico A; Gori A; Papi F; Colombino M; Sini MC; Stanganelli I; Palmieri G; Massi D J Eur Acad Dermatol Venereol; 2015 Mar; 29(3):574-80. PubMed ID: 25200134 [TBL] [Abstract][Full Text] [Related]
9. CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma. Pastorino L; Bonelli L; Ghiorzo P; Queirolo P; Battistuzzi L; Balleari E; Nasti S; Gargiulo S; Gliori S; Savoia P; Abate Osella S; Bernengo MG; Bianchi Scarrà G Pigment Cell Melanoma Res; 2008 Dec; 21(6):700-9. PubMed ID: 18983535 [TBL] [Abstract][Full Text] [Related]
10. MC1R variants increase melanoma risk in families with CDKN2A mutations: a meta-analysis. Fargnoli MC; Gandini S; Peris K; Maisonneuve P; Raimondi S Eur J Cancer; 2010 May; 46(8):1413-20. PubMed ID: 20189796 [TBL] [Abstract][Full Text] [Related]
11. 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; Garcia-Casado Z; Badenas C; Aguilera P; Malvehy J; Nagore E; Puig S Br J Dermatol; 2013 Oct; 169(4):804-11. PubMed ID: 23647022 [TBL] [Abstract][Full Text] [Related]
12. Characteristics of Familial Melanoma in Valencia, Spain, Based on the Presence of CDKN2A Mutations and MC1R Variants. Huerta C; Garcia-Casado Z; Bañuls J; Moragon M; Oliver V; Unamuno B; Requena C; Kumar R; Nagore E Acta Derm Venereol; 2018 Apr; 98(5):512-516. PubMed ID: 29405243 [TBL] [Abstract][Full Text] [Related]
13. CDKN2A and MC1R variants influence dermoscopic and confocal features of benign melanocytic lesions in multiple melanoma patients. Bassoli S; Maurichi A; Rodolfo M; Casari A; Frigerio S; Pupelli G; Farnetani F; Pelosi G; Santinami M; Pellacani G Exp Dermatol; 2013 Jun; 22(6):411-6. PubMed ID: 23711066 [TBL] [Abstract][Full Text] [Related]
14. 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. Brudnik U; Branicki W; Wojas-Pelc A; Kanas P Exp Dermatol; 2009 Feb; 18(2):167-74. PubMed ID: 18637131 [TBL] [Abstract][Full Text] [Related]
16. Melanocortin 1 receptor (MC1R) polymorphisms' influence on size and dermoscopic features of nevi. Vallone MG; Tell-Marti G; Potrony M; Rebollo-Morell A; Badenas C; Puig-Butille JA; Gimenez-Xavier P; Carrera C; Malvehy J; Puig S Pigment Cell Melanoma Res; 2018 Jan; 31(1):39-50. PubMed ID: 28950052 [TBL] [Abstract][Full Text] [Related]
17. Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations. Goldstein AM; Landi MT; Tsang S; Fraser MC; Munroe DJ; Tucker MA Cancer Epidemiol Biomarkers Prev; 2005 Sep; 14(9):2208-12. PubMed ID: 16172233 [TBL] [Abstract][Full Text] [Related]
18. Melanocortin-1 receptor (MC1R) gene variants and dysplastic nevi modify penetrance of CDKN2A mutations in French melanoma-prone pedigrees. Chaudru V; Laud K; Avril MF; Minière A; Chompret A; Bressac-de Paillerets B; Demenais F Cancer Epidemiol Biomarkers Prev; 2005 Oct; 14(10):2384-90. PubMed ID: 16214921 [TBL] [Abstract][Full Text] [Related]
19. p53 codon 72 Pro homozygosity increases the risk of cutaneous melanoma in individuals with dark skin complexion and among noncarriers of melanocortin 1 receptor red hair variants. Stefanaki I; Stratigos AJ; Dimisianos G; Nikolaou V; Papadopoulos O; Polydorou D; Gogas H; Tsoutsos D; Panagiotou P; Kanavakis E; Antoniou C; Katsambas AD Br J Dermatol; 2007 Feb; 156(2):357-62. PubMed ID: 17223878 [TBL] [Abstract][Full Text] [Related]