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Shedding new light on genetic dark matter
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
editorial
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title
Shedding new light on genetic dark matter
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
main subject
dark matter
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author name string
Nadine Melhem
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
Bernie Devlin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
publication date
21 October 2010
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
published in
Genome Medicine
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
volume
2
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
page(s)
79
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stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
issue
10
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
exact match
https://scigraph.springernature.com/pub.10.1186/gm200
0 references
cites work
Genome-Wide Significance Levels and Weighted Hypothesis Testing
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=3092108
retrieved
8 July 2018
Common SNPs explain a large proportion of the heritability for human height
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=3092108
retrieved
8 July 2018
Estimation of effect size distribution from genome-wide association studies and implications for future discoveries
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=3092108
retrieved
8 July 2018
Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes
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=3092108
retrieved
8 July 2018
Missing heritability and strategies for finding the underlying causes of complex disease
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=3092108
retrieved
8 July 2018
Genotype-by-diet interactions drive metabolic phenotype variation in Drosophila melanogaster.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092108
retrieved
8 July 2018
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS
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=3092108
retrieved
8 July 2018
Genome-wide association study of CNVs in 16,000 cases of eight 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=3092108
retrieved
8 July 2018
Genome-wide association identifies multiple ulcerative colitis susceptibility 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=3092108
retrieved
8 July 2018
Understanding mechanisms underlying human gene expression variation with RNA sequencing
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=3092108
retrieved
8 July 2018
Parental origin of sequence variants associated with 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=3092108
retrieved
8 July 2018
Common variants at five new loci associated with early-onset inflammatory bowel disease
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092108
retrieved
8 July 2018
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=3092108
retrieved
8 July 2018
Transgenerational genetic effects on phenotypic variation and disease risk
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=3092108
retrieved
8 July 2018
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
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=3092108
retrieved
8 July 2018
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
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=3092108
retrieved
8 July 2018
Pathway-based approaches for analysis of genomewide 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=3092108
retrieved
8 July 2018
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
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=3092108
retrieved
8 July 2018
Factor XIII Val34Leu variant is protective against venous thromboembolism: a HuGE review and meta-analysis
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=3092108
retrieved
8 July 2018
Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol
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=3092108
retrieved
8 July 2018
Linkage strategies for genetically complex traits. I. Multilocus models
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=3092108
retrieved
8 July 2018
Identifiers
DOI
10.1186/GM200
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
Dimensions Publication ID
1044608837
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PMCID
3092108
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
PubMed ID
21067556
1 reference
stated in
Europe PubMed Central
PubMed ID
21067556
retrieved
5 August 2017
ResearchGate publication ID
47741812
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