Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents (Q37004819)

17 August 2017

Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents (English)

1 reference

17 August 2017

6

D Timothy Bishop

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Mitchell S. Stark

Mitchell Stark

35

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William Bruno

William Bruno

10

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Nelleke A Gruis

Nelleke A Gruis

19

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Florence Demenais

Florence Demenais

5

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Graham J Mann

Graham J Mann

30

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Susana Puig

Susana Puig

33

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Richard F. Kefford

Richard F Kefford

24

0 references

Julia A Newton Bishop

31

Julia Newton Bishop

1 reference

17 August 2017

25

Maria Teresa Landi

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17 August 2017

Giovanna Bianchi-Scarrà

9

Giovanna Bianchi-Scarra

1 reference

17 August 2017

Alisa M Goldstein

1

1 reference

17 August 2017

May Chan

2

1 reference

17 August 2017

Mark Harland

3

1 reference

17 August 2017

Nicholas K Hayward

4

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17 August 2017

Esther Azizi

7

1 reference

17 August 2017

Wilma Bergman

8

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17 August 2017

Donato Calista

11

1 reference

17 August 2017

Lisa A Cannon Albright

12

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17 August 2017

Valerie Chaudru

13

1 reference

17 August 2017

Agnes Chompret

14

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17 August 2017

Francisco Cuellar

15

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17 August 2017

David E Elder

16

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17 August 2017

Paola Ghiorzo

17

1 reference

17 August 2017

Elizabeth M Gillanders

18

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17 August 2017

Johan Hansson

20

1 reference

17 August 2017

David Hogg

21

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17 August 2017

Elizabeth A Holland

22

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17 August 2017

Peter A Kanetsky

23

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17 August 2017

Julie Lang

26

1 reference

17 August 2017

Sancy A Leachman

27

1 reference

17 August 2017

Rona M MacKie

28

1 reference

17 August 2017

Veronica Magnusson

29

1 reference

17 August 2017

Jane M Palmer

32

1 reference

17 August 2017

Joan A Puig-Butille

34

1 reference

17 August 2017

Hensin Tsao

36

1 reference

17 August 2017

Margaret A Tucker

37

1 reference

17 August 2017

Linda Whitaker

38

1 reference

17 August 2017

Emanuel Yakobson

39

1 reference

17 August 2017

Lund Melanoma Study Group

40

1 reference

17 August 2017

Melanoma Genetics Consortium (GenoMEL)

41

1 reference

17 August 2017

language of work or name

English

0 references

publication date

11 August 2006

1 reference

Journal of Medical Genetics

17 August 2017

1 reference

17 August 2017

44

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17 August 2017

2

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17 August 2017

99-106

1 reference

Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

MELPREDICT: a logistic regression model to estimate CDKN2A carrier probability

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Role of the CDKN2A locus in patients with multiple primary melanomas

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Pancreatic carcinoma surveillance in patients with familial melanoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Genetics of melanoma predisposition

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Mutation testing in melanoma families: INK4A, CDK4 and INK4D

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Germline p16 mutations in familial melanoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Systemic cancer and the FAMMM syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

The Dutch FAMMM family material: Clinical and genetic data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Differential expression of p16INK4a and p16beta transcripts in B-lymphoblastoid cells from members of hereditary melanoma families without CDKN2A exon mutations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

A novel methionine-53-valine mutation of p16 in a hereditary melanoma kindred

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Genetic susceptibility in familial melanoma from northeastern Italy.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Mutation screening of the CDKN2A promoter in melanoma families.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Analysis of the CDKN2A, CDKN2B and CDK4 genes in 48 Australian melanoma kindreds

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Familial melanoma and pancreatic cancer

20 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families

20 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

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

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

4 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2598064

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

4 December 2018

1 reference

12 December 2020

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

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

CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas

1 reference

12 December 2020

Characterization of ligurian melanoma families and risk of occurrence of other neoplasia

1 reference

12 December 2020

A piece of the melanoma puzzle

1 reference

12 December 2020

CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families

1 reference

12 December 2020

Population-Based Prevalence of CDKN2A Mutations in Utah Melanoma Families

1 reference

12 December 2020

CDKN2A as a uveal and cutaneous melanoma susceptibility gene

1 reference

12 December 2020

Familial melanoma, pancreatic cancer and germline CDKN2A mutations

1 reference

12 December 2020

Influence of Genes, Nevi, and Sun Sensitivity on Melanoma Risk in a Family Sample Unselected by Family History and in Melanoma-Prone Families

1 reference

12 December 2020

Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds

1 reference

12 December 2020

Novel germline p16 mutation in familial malignant melanoma in southern Sweden

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

Germline CDKN2A mutations in childhood 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

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

CDKN2A mutations in multiple primary melanomas

1 reference

12 December 2020

Screening of germline mutations in the CDK4, CDKN2C and TP53 genes in familial melanoma: a clinic-based population study

1 reference

12 December 2020

CDKN2A Variants in a Population-Based Sample of Queensland Families With Melanoma

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.2006.043802

1 reference

17 August 2017

1 reference

17 August 2017

1 reference