(Q36901270)

17 August 2017

Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma (English)

1 reference

17 August 2017

1

David L Duffy

1 reference

17 August 2017

Richard A Sturm

3

0 references

Grant W. Montgomery

object named as

Grant W Montgomery

6

0 references

Nick Martin

object named as

Nicholas G Martin

5

0 references

author name string

Zhen Z Zhao

2

1 reference

17 August 2017

Nicholas K Hayward

4

1 reference

17 August 2017

language of work or name

English

0 references

publication date

27 August 2009

1 reference

Journal of Investigative Dermatology

17 August 2017

1 reference

17 August 2017

130

1 reference

17 August 2017

2

1 reference

17 August 2017

520-528

1 reference

https://scigraph.springernature.com/pub.10.1038/jid.2009.258

17 August 2017

0 references

cites work

Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Two newly identified genetic determinants of pigmentation in Europeans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Common sequence variants on 20q11.22 confer melanoma susceptibility

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

The Queensland Study of Melanoma: environmental and genetic associations (Q-MEGA); study design, baseline characteristics, and repeatability of phenotype and sun exposure measures

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

A comprehensive genetic study of autosomal recessive ocular albinism in Caucasian patients

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Natural selection has driven population differentiation in modern humans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Genetic determinants of hair, eye and skin pigmentation in Europeans

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Haploview: analysis and visualization of LD and haplotype maps

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Genetic association and cellular function of MC1R variant alleles in human pigmentation

29 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

29 September 2017

https://api.crossref.org/works/10.1038%2FJID.2009.258

7 January 2021

inferred from DOI database lookup

MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphism

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Linkage strategies for genetically complex traits. I. Multilocus models

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Analysis of melanoma onset: assessing familial aggregation by using estimating equations and fitting variance components via Bayesian random effects models

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Frequency in relatives for an all‐or‐none trait

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

A polymorphism of the human tyrosinase gene is associated with temperature-sensitive enzymatic activity

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

SLC45A2: a novel malignant melanoma-associated gene

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3672059

Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder-Haplotype Analysis

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19710684

12 December 2020

inferred from PubMed ID database lookup

Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19710684

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FJID.2009.258

7 January 2021

inferred from DOI database lookup

A note on a general definition of the coefficient of determination

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FJID.2009.258

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/JID.2009.258

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

19710684

1 reference