A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation (Q33335147)

25 July 2017

title

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

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genome-wide association study

25 July 2017

main subject

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9

David L Duffy

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25 July 2017

Grant W Montgomery

12

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Nick Martin

object named as

Nicholas G Martin

11

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Hongmei Nan

3

object named as

Hongmei Nan

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25 July 2017

8

Frank B Hu

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16

Stephen Chanock

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17

David J Hunter

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7

Susan E Hankinson

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6

Abrar Qureshi

1 reference

25 July 2017

Yuan Yi Constance Chen

5

object named as

Constance Chen

1 reference

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2

Peter Kraft

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15

Robert N Hoover

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Jiali Han

1

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25 July 2017

Qun Guo

4

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Zhen Zhen Zhao

10

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Nicholas K Hayward

13

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Gilles Thomas

14

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25 July 2017

publication date

16 May 2008

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25 July 2017

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25 July 2017

volume

4

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25 July 2017

issue

5

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25 July 2017

page(s)

e1000074

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Creative Commons Attribution 4.0 International

25 July 2017

copyright license

start time

16 May 2008

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

genome-wide association study

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Natural selection has driven population differentiation in modern humans

inferred from title

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Genetic determinants of hair, eye and skin pigmentation in Europeans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A second generation human haplotype map of over 3.1 million SNPs

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Population structure and eigenanalysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Risk factors for skin cancers: a nested case-control study within the Nurses' Health Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A golden age of human pigmentation genetics

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Melanocortin 1 receptor variants and skin cancer risk

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

The genetics of sun sensitivity in humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Expression of the B-cell proliferation marker MUM1 by melanocytic lesions and comparison with S100, gp100 (HMB45), and MelanA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Identification of Aim-1 as the underwhite mouse mutant and its transcriptional regulation by MITF

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

The evolution of human skin coloration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Cloning of human lymphocyte-specific interferon regulatory factor (hLSIRF/hIRF4) and mapping of the gene to 6p23-p25

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A novel interferon regulatory factor family transcription factor, ICSAT/Pip/LSIRF, that negatively regulates the activity of interferon-regulated genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Pip, a novel IRF family member, is a lymphoid-specific, PU.1-dependent transcriptional activator

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

Molecular cloning of LSIRF, a lymphoid-specific member of the interferon regulatory factor family that binds the interferon-stimulated response element (ISRE).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2367449

A prospective study of plasma prolactin concentrations and risk of premenopausal and postmenopausal breast cancer.

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000074

Genetic variation in IL6 gene and type 2 diabetes: tagging-SNP haplotype analysis in large-scale case-control study and meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000074

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000074

Demonstrating stratification in a European American population

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1000074

Heritability and components of phenotypic expression in skin reflectance of Mestizos from the Peruvian lowlands

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18483556

12 December 2020

inferred from PubMed ID database lookup

A twin study of skin reflectance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18483556

12 December 2020

inferred from PubMed ID database lookup

STUDIES ON THE INHERITANCE OF HUMAN SKIN COLOUR

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18483556

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1371/JOURNAL.PGEN.1000074

1 reference

25 July 2017

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25 July 2017

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