(Q28943349)

5

object named as

Constance Chen

1 reference

14 March 2017

12

Qingyi Wei

1 reference

14 March 2017

3

Peter Kraft

1 reference

14 March 2017

Mousheng Xu

2

1 reference

14 March 2017

Qun Guo

6

1 reference

14 March 2017

Li-E. Wang

10

1 reference

14 March 2017

Jeffrey E. Lee

11

1 reference

14 March 2017

Jiali Han

describes a project that uses

14

1 reference

14 March 2017

15 September 2011

1 reference

14 March 2017

Human Molecular Genetics

1 reference

14 March 2017

20

1 reference

14 March 2017

3718–3724

1 reference

14 March 2017

18

1 reference

14 March 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

New common variants affecting susceptibility to basal cell carcinoma

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Genetic determinants of hair, eye and skin pigmentation in Europeans

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Quantifying heterogeneity in a meta-analysis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Genome-wide association scans for secondary traits using case-control samples

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Genome-wide association study of tanning phenotype in a population of European ancestry

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Basal cell carcinomas: attack of the hedgehog

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Melanocortin 1 receptor variants and skin cancer risk

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Risk factors for basal cell carcinoma in a prospective cohort of women

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

3 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDR287

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDR287

Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FHMG%2FDDR287

Nonmelanoma skin cancer in the United States: incidence.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3159556

Validation of questionnaire information on risk factors and disease outcomes in a prospective cohort study of women

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21700618

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDR287

1 reference

3986846

3986846

1 reference

1 reference

1 reference