(Q36785968)

16 August 2017

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma (English)

1 reference

16 August 2017

1 reference

Dominique Stoppa-Lyonnet

50

Dominique Stoppa-Lyonnet

0 references

Marion Gauthier-Villars

27

Marion Gauthier-Villars

0 references

Tanguy Martin-Denavit

43

Tanguy Martin-Denavit

0 references

Fabienne Lesueur

F Lesueur

1

0 references

Eve Maubec

Eve Maubec

45

0 references

Pierre Vabres

Pierre Vabres

52

0 references

Christine Lasset

37

Christine Lasset

1 reference

16 August 2017

17

Olivier Caron

1 reference

16 August 2017

28

Paul Gesta

1 reference

16 August 2017

14

Pascaline Berthet

1 reference

16 August 2017

15

Valérie Bonadona

1 reference

16 August 2017

26

Jean-Pierre Fricker

1 reference

16 August 2017

29

Sophie Giraud

1 reference

16 August 2017

48

Pascal Pujol

1 reference

16 August 2017

40

Michel Longy

1 reference

16 August 2017

34

Nicolas Janin

1 reference

16 August 2017

42

Karine Marrou

1 reference

16 August 2017

22

Liliane Demange

1 reference

16 August 2017

55

Hélène Zattara

1 reference

16 August 2017

13

Bertrand Bachollet

1 reference

16 August 2017

Jacqueline Chevrant-Breton

18

Jacqueline Chevrant-Breton

1 reference

16 August 2017

M de Lichy

2

1 reference

16 August 2017

M Barrois

3

1 reference

16 August 2017

G Durand

4

1 reference

16 August 2017

J Bombled

5

1 reference

16 August 2017

M-F Avril

6

1 reference

16 August 2017

A Chompret

7

1 reference

16 August 2017

F Boitier

8

1 reference

16 August 2017

G M Lenoir

9

1 reference

16 August 2017

French Familial Melanoma Study Group

10

1 reference

16 August 2017

B Bressac-de Paillerets

11

1 reference

16 August 2017

Monique Baccard

12

1 reference

16 August 2017

Jean-Marie Bonnetblanc

16

1 reference

16 August 2017

Jean-François Cuny

19

1 reference

16 August 2017

Stéphane Dalle

20

1 reference

16 August 2017

Michèle Delaunay

21

1 reference

16 August 2017

Julie De Quatrebarbes

23

1 reference

16 August 2017

Jean-François Doré

24

1 reference

16 August 2017

Marc Frénay

25

1 reference

16 August 2017

Philippe Gorry

30

1 reference

16 August 2017

Florent Grange

31

1 reference

16 August 2017

Andrew Green

32

1 reference

16 August 2017

Laetitia Huiart

33

1 reference

16 August 2017

Pascal Joly

35

1 reference

16 August 2017

Delphine Kérob

36

1 reference

16 August 2017

Dominique Leroux

38

1 reference

16 August 2017

Jean-Marc Limacher

39

1 reference

16 August 2017

Sandrine Mansard

41

1 reference

16 August 2017

Tanguy Martin-Denavit

43

1 reference

16 August 2017

Christine Mateus

44

1 reference

16 August 2017

Laurence Olivier-Faivre

46

1 reference

16 August 2017

Vincent Orlandini

47

1 reference

16 August 2017

Bruno Sassolas

49

1 reference

16 August 2017

Luc Thomas

51

1 reference

16 August 2017

Laurence Venat

53

1 reference

16 August 2017

Ewa Wierzbicka

54

1 reference

16 August 2017

language of work or name

English

0 references

publication date

8 July 2008

1 reference

British Journal of Cancer

16 August 2017

1 reference

16 August 2017

99

1 reference

16 August 2017

2

1 reference

16 August 2017

364-370

1 reference

Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

A novel type of deletion in the CDKN2A gene identified in a melanoma-prone family

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of 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=2480975

A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Genetic alterations of the NRP/B gene are associated with human brain tumors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Localization of a novel melanoma susceptibility locus to 1p22

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

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=2480975

Rapid detection of novel BRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Hypermethylation-associated inactivation of p14(ARF) is independent of p16(INK4a) methylation and p53 mutational status

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

The kelch repeat superfamily of proteins: propellers of cell function

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Germ-line deletion involving the INK4 locus in familial proneness to melanoma and nervous system tumors.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Low frequency of p16/CDKN2A methylation in sporadic melanoma: comparative approaches for methylation analysis of primary tumors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Temperature-sensitive mutants of p16CDKN2 associated 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=2480975

Germline mutations in the p16INK4a binding domain of CDK4 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=2480975

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

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=2480975

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Prevalence of 9p21 deletions in UK melanoma families.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Germline epimutation of MLH1 in individuals with multiple cancers

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

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

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Comparison between familial and nonfamilial melanoma in France

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL

20 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

Cutaneous phenotype andMC1R variants as modifying factors for the development of melanoma inCDKN2A G101W mutation carriers from 4 countries

20 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

Increased Risk of Pancreatic Cancer in Melanoma-Prone Kindreds withp16INK4Mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

Germline Mutations of the CDKN2 Gene in UK Melanoma Families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

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]

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

CDKN2A germline splicing mutation affecting both p16ink4 and p14arf RNA processing in a melanoma/neurofibroma kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

Familial and attributable risks in cutaneous melanoma: effects of proband and age

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2480975

A melanoma-predisposing germline CDKN2A mutation with functional significance for both p16 and p14ARF

20 October 2018

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

Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

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

Homozygous deletion of the p16INK4a and the p15INK4b tumour suppressor genes in a subset of human sporadic cutaneous malignant melanoma

1 reference

12 December 2020

Retention of the CDKN2A locus and low frequency of point mutations in primary and metastatic cutaneous malignant melanoma

1 reference

12 December 2020

Identification and characterization of a novel kelch-like gene KLHL15 in silico

1 reference

12 December 2020

Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanoma

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

CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas

1 reference

12 December 2020

Retention of theCDKN2A locus and low frequency of point mutations in primary and metastasic cutaneous malignant melanoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6604470

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.BJC.6604470

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

18612309

1 reference