(Q33905176)

29 July 2017

Localization of a novel melanoma susceptibility locus to 1p22 (English)

1 reference

Brigitte Bressac-de Paillerets

29 July 2017

1 reference

16

Brigitte Bressac-de Paillerets

0 references

Derek Nancarrow

5

Derek Nancarrow

1 reference

29 July 2017

14

D Timothy Bishop

0 references

Nelleke A Gruis

Nelleke Gruis

19

0 references

Graham J Mann

Graham J Mann

23

0 references

Joan Bailey-Wilson

Joan E Bailey-Wilson

22

0 references

Richard F. Kefford

Richard F Kefford

11

0 references

Mitchell S. Stark

Mitchell Stark

18

0 references

Julia A Newton Bishop

20

Julia Newton Bishop

1 reference

29 July 2017

25

Jeffrey Trent

1 reference

29 July 2017

Elizabeth M Gillanders

1

Elizabeth Gillanders

1 reference

29 July 2017

6

Diana Freas-Lutz

1 reference

29 July 2017

10

Carol Markey

1 reference

29 July 2017

4

MaryPat Jones

1 reference

29 July 2017

Suh-Hang Hank Juo

2

1 reference

29 July 2017

Elizabeth A Holland

3

1 reference

29 July 2017

Raman Sood

7

1 reference

29 July 2017

Naeun Park

8

1 reference

29 July 2017

Mezbah Faruque

9

1 reference

29 July 2017

Jane Palmer

12

1 reference

29 July 2017

Wilma Bergman

13

1 reference

29 July 2017

Margaret A Tucker

15

1 reference

29 July 2017

Johan Hansson

17

1 reference

29 July 2017

Alisa M Goldstein

21

1 reference

29 July 2017

Nicholas Hayward

24

1 reference

29 July 2017

Lund Melanoma Study Group

26

1 reference

29 July 2017

Melanoma Genetics Consortium

27

1 reference

29 July 2017

language of work or name

English

0 references

publication date

3 July 2003

1 reference

American Journal of Human Genetics

29 July 2017

1 reference

29 July 2017

73

1 reference

29 July 2017

301-313

1 reference

29 July 2017

2

1 reference

The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type.

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Geographical variation in the penetrance of CDKN2A mutations for melanoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

TGF-beta signaling in tumor suppression and cancer progression

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Requirement of type III TGF-beta receptor for endocardial cell transformation in the heart

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Allele-sharing models: LOD scores and accurate linkage tests

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation of MCM subunits by a putative human homologue of Cdc7

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Parametric and nonparametric linkage analysis: a unified multipoint approach

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Germline p16 mutations in familial melanoma

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Effects of misspecifying genetic parameters in lod score analysis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Computer-simulation methods in human linkage analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Linkage of early-onset familial breast cancer to chromosome 17q21

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

The Dutch FAMMM family material: Clinical and genetic data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Linkage mapping of melanoma (MLM) using 172 microsatellite markers

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Mutation screening of the CDKN2A promoter in melanoma families.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180369

Genotype-Phenotype Relationships in U.S. Melanoma-Prone Families With CDKN2A and CDK4 Mutations

29 October 2018

1 reference

12 December 2020

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

1 reference

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

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

1 reference

12 December 2020

Hereditary melanoma in Australia variable association with dysplastic nevi and

1 reference

12 December 2020

Screening of germline mutations in the CDKN2A and CDKN2B genes in Swedish families with hereditary cutaneous 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

Melanoma development in relation to non-functional p16/INK4A protein and dysplastic naevus syndrome in Swedish melanoma kindreds

1 reference

12 December 2020

Identifiers

DOI

10.1086/377140

1 reference

29 July 2017

1 reference

29 July 2017

1 reference