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English
GWAS: heritability missing in action?
scientific article published on 17 March 2010
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
title
GWAS: heritability missing in action?
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
main subject
genome-wide association study
0 references
heritability
1 reference
based on heuristic
inferred from title
author
David N. Cooper
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
author name string
Angus J Clarke
series ordinal
1
1 reference
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Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
publication date
17 March 2010
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
volume
18
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stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
issue
8
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
page(s)
859-861
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
exact match
https://scigraph.springernature.com/pub.10.1038/ejhg.2010.35
0 references
cites work
Finding the missing heritability of complex diseases
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=2987389
retrieved
29 May 2018
Origins and functional impact of copy number variation in the human genome
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=2987389
retrieved
29 May 2018
Epistasis and its implications for personal genetics.
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=2987389
retrieved
29 May 2018
Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
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=2987389
retrieved
29 May 2018
From genotypes to genometypes: putting the genome back in genome-wide 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=2987389
retrieved
29 May 2018
Using biological networks to search for interacting loci in genome-wide 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=2987389
retrieved
29 May 2018
Personal genomes: The case of the missing heritability
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=2987389
retrieved
29 May 2018
Extending genome-wide association studies to copy-number variation
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=2987389
retrieved
29 May 2018
Tilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causation
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=2987389
retrieved
29 May 2018
Large recurrent microdeletions associated with schizophrenia
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=2987389
retrieved
29 May 2018
Rare chromosomal deletions and duplications increase risk of schizophrenia
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=2987389
retrieved
29 May 2018
Strong association of de novo copy number mutations with sporadic schizophrenia
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=2987389
retrieved
29 May 2018
Common and rare variants in multifactorial susceptibility to common diseases
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=2987389
retrieved
29 May 2018
Positive selection in the human genome: from genome scans to biological significance
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=2987389
retrieved
29 May 2018
The success of the genome-wide association approach: a brief story of a long struggle
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=2987389
retrieved
29 May 2018
Association between microdeletion and microduplication at 16p11.2 and autism
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=2987389
retrieved
29 May 2018
Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide 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=2987389
retrieved
29 May 2018
Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA
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=2987389
retrieved
29 May 2018
Scan of human genome reveals no new Loci under ancient balancing selection
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=2987389
retrieved
29 May 2018
The genetic architecture of quantitative traits: lessons from Drosophila
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=2987389
retrieved
29 May 2018
Popper revisited: GWAS here, last year.
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=2987389
retrieved
17 August 2018
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEJHG.2010.35
retrieved
21 January 2018
A limited role for balancing selection
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20234388
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hypotheses in genome-wide association scans
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/20234388
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/EJHG.2010.35
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
Dimensions Publication ID
1016362535
0 references
PMCID
2987389
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
PubMed ID
20234388
1 reference
stated in
Europe PubMed Central
PMCID
2987389
retrieved
27 October 2017
ResearchGate publication ID
42109454
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