(Q41677741)

7 October 2017

VEGAS2: Software for More Flexible Gene-Based Testing (English)

1 reference

7 October 2017

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1

Aniket Mishra

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Stuart Macgregor

object named as

Stuart Macgregor

series ordinal

2

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language of work or name

English

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publication date

18 December 2014

1 reference

Twin Research and Human Genetics

7 October 2017

1 reference

7 October 2017

18

1 reference

7 October 2017

86-91

1 reference

7 October 2017

1

1 reference

An integrated map of genetic variation from 1,092 human genomes

7 October 2017

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

The variant call format and VCFtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Testing for association on the X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Linkage-disequilibrium-based binning affects the interpretation of GWASs

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Genome-wide association study identifies novel loci predisposing to cutaneous melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Testing association for markers on the X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

A versatile gene-based test for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

X chromosome-wide association study of follicular lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FTHG.2014.79

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1017/THG.2014.79

1 reference

7 October 2017

1 reference

PubMed ID

25518859