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Heritability in the genome-wide association era
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scholarly article
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PubMed
title
Heritability in the genome-wide association era
(English)
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main subject
genome-wide association study
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heritability
1 reference
based on heuristic
inferred from title
author
Noah Zaitlen
series ordinal
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object named as
Noah Zaitlen
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stated in
Crossref
author name string
Peter Kraft
series ordinal
2
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Crossref
language of work or name
English
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stated in
PubMed
publication date
October 2012
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stated in
PubMed
published in
Human Genetics
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stated in
PubMed
volume
131
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PubMed
issue
10
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PubMed
page(s)
1655-64
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PubMed
cites work
Five years of GWAS discovery
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=3432754
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21 March 2017
Hundreds of variants clustered in genomic loci and biological pathways affect human height
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stated in
PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
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=3432754
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21 March 2017
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
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=3432754
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21 March 2017
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=3432754
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21 March 2017
Why Most Discovered True Associations Are Inflated
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=3432754
retrieved
21 March 2017
Heritability in the genomics era — concepts and misconceptions
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=3432754
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21 March 2017
Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings
1 reference
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PubMed Central
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21 March 2017
Principal components analysis corrects for stratification in genome-wide association studies
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
Merlin--rapid analysis of dense genetic maps using sparse gene flow trees
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
The mystery of missing heritability: Genetic interactions create phantom heritability
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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21 March 2017
Heritability of Threshold Characters.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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7 April 2017
GCTA: a tool for genome-wide complex trait analysis
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=3432754
retrieved
7 April 2017
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=3432754
retrieved
7 April 2017
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=3432754
retrieved
7 April 2017
Rare variants create synthetic genome-wide associations
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=3432754
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7 April 2017
Personal genomes: The case of the missing heritability
1 reference
stated in
PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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7 April 2017
Genetic contributions to stability and change in intelligence from childhood to old age.
1 reference
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PubMed Central
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28 September 2017
Rare and common variants: twenty arguments
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants
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=3432754
retrieved
28 September 2017
Genome partitioning of genetic variation for complex traits using common SNPs
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=3432754
retrieved
28 September 2017
Genomic inflation factors under polygenic inheritance
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=3432754
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28 September 2017
Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individuals
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=3432754
retrieved
28 September 2017
Estimating missing heritability for disease from genome-wide association studies
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=3432754
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28 September 2017
Synthetic associations created by rare variants do not explain most GWAS results
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=3432754
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28 September 2017
A commentary on 'common SNPs explain a large proportion of the heritability for human height' by Yang et al. (2010).
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=3432754
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28 September 2017
Predicting genetic predisposition in humans: the promise of whole-genome markers
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Reconciling the analysis of IBD and IBS in complex trait studies
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Variance component model to account for sample structure in genome-wide association studies
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Multi-locus models of genetic risk of disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk
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=3432754
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28 September 2017
Accuracy of predicting the genetic risk of disease using a genome-wide approach
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Curses--winner's and otherwise--in genetic epidemiology
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Genome partitioning of genetic variation for height from 11,214 sibling pairs
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Non-replication and inconsistency in the genome-wide association setting
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3432754
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28 September 2017
Population structure can inflate SNP-based heritability estimates
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PubMed Central
reference URL
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31 May 2018
Univariate and bivariate analyses of cholesterol and triglyceride levels in pedigrees.
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31 May 2018
The Correlation between Relatives on the Supposition of Mendelian Inheritance
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21 January 2018
FaST linear mixed models for genome-wide association studies
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21 January 2018
Bias, precision and heritability of self-reported and clinically measured height in Australian twins
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21 January 2018
Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases
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21 January 2018
Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study
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28 November 2018
Systems of Mating. I. the Biometric Relations between Parent and Offspring
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28 November 2018
Polygenic susceptibility to breast cancer and implications for prevention
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Polygenes, risk prediction, and targeted prevention of breast cancer
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MAXIMUM-LIKELIHOOD APPROACHES APPLIED TO QUANTITATIVE GENETICS OF NATURAL POPULATIONS.
1 reference
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Extensions to pedigree analysis. IV. Covariance components models for multivariate traits
1 reference
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1007/S00439-012-1199-6
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1595034
Dimensions Publication ID
1008951585
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Fatcat ID
release_ycn2gk2okrhtxnd4kzmw7p3xim
0 references
OpenCitations bibliographic resource ID
1595034
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1595034
PMC publication ID
3432754
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1595034
PubMed publication ID
22821350
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1595034
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