Detalhe da pesquisa
1.
Birth cohort-specific trends of sun-related behaviors among individuals from an international consortium of melanoma-prone families.
BMC Public Health
; 21(1): 692, 2021 04 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888076
2.
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT.
J Am Acad Dermatol
; 81(2): 386-394, 2019 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30731170
3.
A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma.
Nature
; 480(7375): 99-103, 2011 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-22080950
4.
Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom.
Hered Cancer Clin Pract
; 12(1): 20, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25780468
5.
MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study.
BMC Cancer
; 13: 406, 2013 Sep 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24134749
6.
Association of germline variants in telomere maintenance genes (POT1, TERF2IP, ACD, and TERT) with spitzoid morphology in familial melanoma: A multi-center case series.
JAAD Int
; 11: 43-51, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36876055
7.
MC1R genotypes and risk of melanoma before age 40 years: a population-based case-control-family study.
Int J Cancer
; 131(3): E269-81, 2012 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22095472
8.
Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK.
J Med Genet
; 48(4): 266-72, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21325014
9.
FRAMe: Familial Risk Assessment of Melanoma-a risk prediction tool to guide CDKN2A germline mutation testing in Australian familial melanoma.
Fam Cancer
; 20(3): 231-239, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32989607
10.
Population-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family Study.
Am J Epidemiol
; 170(12): 1541-54, 2009 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19887461
11.
Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma.
Melanoma Res
; 29(5): 483-490, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31464824
12.
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL).
Eur J Cancer
; 44(9): 1269-74, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18394881
13.
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
J Med Genet
; 44(2): 99-106, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16905682
14.
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
Cancer Res
; 66(20): 9818-28, 2006 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17047042
15.
Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.
J Natl Cancer Inst
; 109(12)2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29522175
16.
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
J Natl Cancer Inst
; 94(12): 894-903, 2002 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-12072543
17.
Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
J Natl Cancer Inst
; 107(2)2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25505254
18.
eMelanoBase: an online locus-specific variant database for familial melanoma.
Hum Mutat
; 21(1): 2-7, 2003 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-12497626
19.
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.
J Invest Dermatol
; 136(5): 1066-1069, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26827760
20.
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Nat Genet
; 43(11): 1114-8, 2011 Oct 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21983785