Genome-wide association study identifies three loci associated with melanoma risk (Q37341178)

19 August 2017

Genome-wide association study identifies three loci associated with melanoma risk (English)

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genome-wide association study

19 August 2017

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42

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19 August 2017

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19 August 2017

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John Hopper

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Esther Azizi

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Donato Calista

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Srdjan Novakovic

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19 August 2017

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Gilli Galore-Haskel

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19 August 2017

Ivo Gut

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Marko Hocevar

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19 August 2017

Julie Lang

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19 August 2017

language of work or name

English

0 references

publication date

5 July 2009

1 reference

19 August 2017

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19 August 2017

41

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19 August 2017

8

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19 August 2017

920-925

1 reference

describes a project that uses

19 August 2017

genome-wide association study

1 reference

Prevalence of variations in melanoma susceptibility genes among Slovenian melanoma families

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1 reference

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A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes

6 September 2017

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Genes mirror geography within Europe

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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

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Common sequence variants on 20q11.22 confer melanoma susceptibility

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A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

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Testing for association on the X chromosome

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MC1R variants, melanoma and red hair color phenotype: a meta-analysis

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Common variants of DNA repair genes and malignant melanoma

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A new multipoint method for genome-wide association studies by imputation of genotypes

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6 September 2017

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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.

6 September 2017

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Population structure and eigenanalysis

6 September 2017

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

6 September 2017

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Principal components analysis corrects for stratification in genome-wide association studies

6 September 2017

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Pigmentary characteristics and moles in relation to melanoma risk

6 September 2017

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Haploview: analysis and visualization of LD and haplotype maps

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Mutation testing in melanoma families: INK4A, CDK4 and INK4D

6 September 2017

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

6 September 2017

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Role of the CDKN2A locus in patients with multiple primary melanomas

6 September 2017

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Cutaneous melanoma in women. I. Exposure to sunlight, ability to tan, and other risk factors related to ultraviolet light

14 September 2017

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14 September 2017

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CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.

26 June 2018

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2 September 2018

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Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma

2 September 2018

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The prevalence of CDKN2A germ-line mutations and relative risk for cutaneous malignant melanoma: an international population-based study

2 September 2018

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2 September 2018

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2 September 2018

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Cutaneous melanoma in women. II. Phenotypic characteristics and other host-related factors

2 September 2018

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

2 September 2018

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

20 October 2018

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Increased incidence of melanoma in renal transplantation recipients

3 December 2018

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https://pubmed.ncbi.nlm.nih.gov/19578364

12 December 2020

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

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12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/19578364

12 December 2020

Polygenic inheritance of breast cancer: Implications for design of association studies

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https://pubmed.ncbi.nlm.nih.gov/19578364

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

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https://pubmed.ncbi.nlm.nih.gov/19578364

12 December 2020

Genetic predisposition to cancer

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

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Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi

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Crossref

https://api.crossref.org/works/10.1038%2FNG.411

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.411

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

19578364

1 reference