(Q35566206)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574160%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

review article

1 reference

title

Familial melanoma: a complex disorder leading to controversy on DNA testing (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574160%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference

3

1 reference

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20 December 2019

author name string

Femke A de Snoo

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574160%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

Wilma Bergman

series ordinal

2

1 reference

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20 December 2019

publication date

1 January 2003

1 reference

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20 December 2019

1 reference

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20 December 2019

volume

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574160%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574160%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

page(s)

109-116

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Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16INK4A, P14ARF or cdk4 genes

20 December 2019

cites work

1 reference

12 December 2020

Systemic cancer and the FAMMM syndrome

1 reference

12 December 2020

Localization of a novel melanoma susceptibility locus to 1p22

1 reference

12 December 2020

High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families

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12 December 2020

Psychological studies in Huntington's disease: making up the balance

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12 December 2020

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families

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12 December 2020

Melanoma in adolescents: a case-control study of risk factors in Queensland, Australia.

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12 December 2020

Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996

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12 December 2020

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion ofp16 (p16-Leiden)

1 reference

12 December 2020

Biallelic mutations in p16(INK4a) confer resistance to Ras- and Ets-induced senescence in human diploid fibroblasts

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12 December 2020

The Atypical-Mole Syndrome and Predisposition to Melanoma

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12 December 2020

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

1 reference

12 December 2020

Exclusion of the familial melanoma locus (MLM) from the PND/D1S47 and MYCL1 regions of chromosome arm 1p in 7 Australian pedigrees.

1 reference

12 December 2020

Further evidence for a locus for cutaneous malignant melanoma-dysplastic nevus (CMM/DN) on chromosome 1p, and evidence for genetic heterogeneity.

1 reference

12 December 2020

A melanoma-associated germline mutation in exon 1beta inactivates p14ARF.

1 reference

12 December 2020

A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families

1 reference

12 December 2020

Recent Trends in Cutaneous Melanoma Incidence Among Whites in the United States

1 reference

12 December 2020

Promoter hypermethylation: a common cause of reduced p16(INK4a) expression in uveal melanoma.

1 reference

12 December 2020

Risk of cutaneous melanoma in relation to the numbers, types and sites of naevi: a case-control study

1 reference

12 December 2020

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

1 reference

12 December 2020

Independence of dysplastic nevi from total nevi in determining risk for nonfamilial melanoma

1 reference

12 December 2020

Genetic susceptibility to naevi – a twin study

1 reference

12 December 2020

Hereditary melanoma in Australia variable association with dysplastic nevi and

1 reference

12 December 2020

Germline mutations in the p16INK4a binding domain of CDK4 in familial melanoma

1 reference

12 December 2020

Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group [published erratum appears in Hum Mol Genet 1998 May;7(5):941]

1 reference

12 December 2020

Familial tumor syndrome associated with a germline nonfunctional p16INK4a allele

1 reference

12 December 2020

Novel germline p16 mutation in familial malignant melanoma in southern Sweden

1 reference

12 December 2020

Familial atypical multiple mole-melanoma syndrome

1 reference

12 December 2020

Counseling and DNA testing for individuals perceived to be genetically predisposed to melanoma: A consensus statement of the Melanoma Genetics Consortium

1 reference

12 December 2020

Risk of cutaneous melanoma associated with pigmentation characteristics and freckling: systematic overview of 10 case-control studies. The International Melanoma Analysis Group (IMAGE).

1 reference

12 December 2020

Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22

1 reference

12 December 2020

Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36.

1 reference

12 December 2020

Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice

1 reference

12 December 2020

Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.

1 reference

12 December 2020

p16INK4A and p14ARF tumour suppressors in melanoma: lessons from the mouse

1 reference

12 December 2020

Tumour spectrum in the FAMMM syndrome

1 reference

12 December 2020

A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family

1 reference

12 December 2020

Family studies in melanoma: identification of the atypical mole syndrome (AMS) phenotype

1 reference

12 December 2020

Childhood sun exposure as a risk factor for melanoma: a systematic review of epidemiologic studies

1 reference

12 December 2020

Trends in the incidence of cutaneous malignant melanoma in New South Wales, 1983-1996.

1 reference

12 December 2020

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

1 reference

12 December 2020

Cancer prevalence in European registry areas

1 reference

12 December 2020

Genetic epidemiology of familial melanoma

1 reference

12 December 2020

Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to 1994.

1 reference

12 December 2020

Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study.

1 reference

12 December 2020

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

1 reference

12 December 2020

Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans

1 reference

12 December 2020

Linkage of cutaneous malignant melanoma/dysplastic nevi to chromosome 9p, and evidence for genetic heterogeneity.

1 reference

12 December 2020

The inheritance pattern of dysplastic naevi in families of dysplastic naevus patients

1 reference

12 December 2020

Confirmation of chromosome 9p linkage in familial melanoma.

1 reference

12 December 2020

Germline mutation of ARF in a melanoma kindred

1 reference

12 December 2020

New developments in melanoma genetics

1 reference

12 December 2020

Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families

1 reference

12 December 2020

Benign melanocytic naevi as a risk factor for malignant melanoma

1 reference

12 December 2020

Germline p16 mutations in familial melanoma

1 reference

12 December 2020

Genetic heterogeneity in familial malignant melanoma

1 reference

12 December 2020

Dysplastic nevi as risk markers of sporadic (nonfamilial) melanoma. A case-control study

1 reference

12 December 2020

A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4

1 reference

12 December 2020

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: evidence for common founders and independent mutations

1 reference

12 December 2020

Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.

1 reference

12 December 2020

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

1 reference

12 December 2020

Use of host factors to identify people at high risk for cutaneous malignant melanoma

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA-testing for Huntington's disease in The Netherlands: a retrospective study on psychosocial effects.

1 reference

12 December 2020

Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A ( P16INK4A ) gene

1 reference

12 December 2020

Familial cutaneous malignant melanoma: autosomal dominant trait possibly linked to the Rh locus

1 reference

12 December 2020

A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigrees.

1 reference

12 December 2020

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma

1 reference

12 December 2020

Count of benign melanocytic nevi as a major indicator of risk for nonfamilial nodular and superficial spreading melanoma

1 reference

12 December 2020

Genetic aspects of uveal melanoma: a brief review.

1 reference

12 December 2020

Genotype/phenotype and penetrance studies in melanoma families with germline CDKN2A mutations.

1 reference

12 December 2020

Defining the molecular basis of Arf and Hdm2 interactions

1 reference

12 December 2020

Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene

1 reference

12 December 2020

The genetics of cutaneous melanoma

1 reference

12 December 2020

Tumor suppression at the mouse INK4a locus mediated by the alternative reading frame product p19ARF

1 reference

12 December 2020

Geographical variation in the penetrance of CDKN2A mutations for melanoma

1 reference

12 December 2020

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families

1 reference

12 December 2020

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

1 reference

12 December 2020

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

1 reference

12 December 2020

Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of naevus count

1 reference

12 December 2020

A cell cycle regulator potentially involved in genesis of many tumor types

1 reference

12 December 2020

Influence of sun exposures during childhood and during adulthood on melanoma risk. EPIMEL and EORTC Melanoma Cooperative Group. European Organisation for Research and Treatment of Cancer

1 reference

12 December 2020

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma

1 reference

12 December 2020

Melanin offers protection against induction of cyclobutane pyrimidine dimers and 6-4 photoproducts by UVB in cultured human melanocytes

1 reference

12 December 2020