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Sex chromosomes and genetic association studies
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Sex chromosomes and genetic association studies
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
author name string
David G Clayton
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
publication date
24 November 2009
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
published in
Genome Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
volume
1
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
issue
11
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
page(s)
110
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
exact match
https://scigraph.springernature.com/pub.10.1186/gm110
0 references
cites work
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Association test for X-linked QTL in family-based designs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Testing for association on the X chromosome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
EFBAT: exact family-based association tests
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
X-APL: an improved family-based test of association in the presence of linkage for the X chromosome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Monte Carlo pedigree disequilibrium test for markers on the X chromosome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
X chromosome-inactivation patterns of 1,005 phenotypically unaffected females
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Silencing of the mammalian X chromosome
1 reference
stated in
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reference URL
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retrieved
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Statistical aspects of the analysis of data from retrospective studies of disease
1 reference
stated in
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reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
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A test for linkage and association in general pedigrees: the pedigree disequilibrium test
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
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A general test of association for quantitative traits in nuclear families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
From genotypes to genes: doubling the sample size
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
General score tests for associations of genetic markers with disease using cases and their parents.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Genotype relative risks: methods for design and analysis of candidate-gene association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
21 June 2018
Testing association for markers on the X chromosome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
30 October 2018
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
30 October 2018
The transmission/disequilibrium test and parental-genotype reconstruction: the reconstruction-combined transmission/ disequilibrium test
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2808745
retrieved
30 October 2018
Statistical methods in cancer research. Volume I - The analysis of case-control studies.
1 reference
stated in
PubMed Central
reference URL
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retrieved
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On estimating HLA/disease association with application to a study of aplastic anemia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/19939292
retrieved
12 December 2020
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Identifiers
DOI
10.1186/GM110
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
Dimensions Publication ID
1045044702
0 references
PMCID
2808745
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
PubMed ID
19939292
1 reference
stated in
Europe PubMed Central
PubMed ID
19939292
retrieved
28 July 2017
ResearchGate publication ID
40032514
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