Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families.

[1]  David John Adams,et al.  Melanoma: a global perspective , 2017, Nature Reviews Cancer.

[2]  N. Gruis,et al.  The absence of multiple atypical nevi in germline CDKN2A mutations: Comment on "Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome". , 2016, Journal of the American Academy of Dermatology.

[3]  S. Puig,et al.  Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families. , 2016, The Journal of investigative dermatology.

[4]  H. Tsao,et al.  Hereditary melanoma: Update on syndromes and management: Genetics of familial atypical multiple mole melanoma syndrome. , 2016, Journal of the American Academy of Dermatology.

[5]  R. Dummer,et al.  The Genetic Evolution of Melanoma from Precursor Lesions. , 2015, The New England journal of medicine.

[6]  J. Malvehy,et al.  Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom , 2014, Hereditary cancer in clinical practice.

[7]  Jeffrey E. Lee,et al.  Genome-wide association study identifies three new melanoma susceptibility loci , 2011, Nature Genetics.

[8]  K. Nielsen,et al.  Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype , 2010, Melanoma research.

[9]  T. Spector,et al.  Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi , 2009, Nature Genetics.

[10]  E. Gillanders,et al.  Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families , 2008, European Journal of Human Genetics.

[11]  S. Puig,et al.  A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL). , 2008, European journal of cancer.

[12]  S. Puig,et al.  Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents , 2006, Journal of Medical Genetics.

[13]  J. Trent,et al.  A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions , 2007, European Journal of Human Genetics.

[14]  S. Puig,et al.  High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL. , 2006, Cancer research.

[15]  T. Spector,et al.  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. , 2006, Human molecular genetics.

[16]  L. Cannon-Albright,et al.  Longitudinal assessment of the nevus phenotype in a melanoma kindred. , 2004, The Journal of investigative dermatology.

[17]  H. Lynch,et al.  Characterization of the neoplastic phenotype in the familial atypical multiple‐mole melanoma–pancreatic carcinoma syndrome , 2003, Cancer.

[18]  J. Barrett,et al.  Linkage and association analysis of nevus density and the region containing the melanoma gene CDKN2A in UK twins , 2003, British Journal of Cancer.

[19]  J. Barrett,et al.  An assessment of the CDKN2A variant Ala148Thr as a nevus/melanoma susceptibility allele. , 2002, The Journal of investigative dermatology.

[20]  S. Kern,et al.  Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma–pancreatic carcinoma–prone families , 2002, Cancer.

[21]  M. Tucker,et al.  Genetic epidemiology of cutaneous melanoma: a global perspective. , 2001, Archives of dermatology.

[22]  J. Struewing,et al.  Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations. , 2000, Journal of the National Cancer Institute.

[23]  J. A. Bishop,et al.  Genotype/phenotype and penetrance studies in melanoma families with germline CDKN2A mutations. , 2000, The Journal of investigative dermatology.

[24]  M. Tucker,et al.  Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[25]  J F Aitken,et al.  A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. , 1999, American journal of human genetics.

[26]  L. Sandkuijl,et al.  Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds , 1995, Nature Genetics.

[27]  M. Skolnick,et al.  Penetrance and expressivity of the chromosome 9p melanoma susceptibility locus (MLM). , 1994, Cancer research.

[28]  W. Clark,et al.  Germline p16 mutations in familial melanoma , 1994, Nature Genetics.

[29]  D. Bishop,et al.  Family studies in melanoma: identification of the atypical mole syndrome (AMS) phenotype , 1994, Melanoma research.

[30]  H. Lynch,et al.  Familial atypical multiple mole-melanoma syndrome. , 1978, Journal of medical genetics.