(Q36109132)

12 August 2017

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (English)

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12 August 2017

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Jana V van Vliet-Ostaptchouk

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Andres Metspalu

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10

Jana V van Vliet-Ostaptchouk

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Andrew Bakshi

Andrew Bakshi

2

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Matthew R Robinson

Matthew R Robinson

7

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Jian Yang

Jian Yang

1

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Sang Hong Lee

Sang Hong Lee

6

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Lili Milani

Lili Milani

14

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Patrik K E Magnusson

Patrik K E Magnusson

18

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Zhihong Zhu

Zhihong Zhu

3

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Michael Goddard

Michael E Goddard

24

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Gibran Hemani

Gibran Hemani

4

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Erik Ingelsson

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Erik Ingelsson

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12 August 2017

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Anders Hamsten

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12 August 2017

23

Naomi R Wray

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12 August 2017

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Nancy L Pedersen

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12 August 2017

11

Harold Snieder

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12 August 2017

Anna A E Vinkhuyzen

5

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12 August 2017

John R B Perry

8

1 reference

12 August 2017

Ilja M Nolte

9

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12 August 2017

LifeLines Cohort Study

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12 August 2017

Matthew C Keller

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12 August 2017

language of work or name

English

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publication date

31 August 2015

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12 August 2017

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12 August 2017

47

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10

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12 August 2017

1114-1120

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https://scigraph.springernature.com/pub.10.1038/ng.3390

12 August 2017

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cites work

The UK10K project identifies rare variants in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Genetic studies of body mass index yield new insights for obesity biology

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Leveraging population admixture to characterize the heritability of complex traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Defining the role of common variation in the genomic and biological architecture of adult human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Biological insights from 108 schizophrenia-associated genetic loci

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

The deleterious mutation load is insensitive to recent population history

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Sequencing depth and coverage: key considerations in genomic analyses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Quantifying missing heritability at known GWAS loci

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Whole-genome sequence-based analysis of high-density lipoprotein cholesterol

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Improved heritability estimation from genome-wide SNPs

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Repetitive DNA and next-generation sequencing: computational challenges and solutions

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

From Galton to GWAS: quantitative genetics of human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Estimating missing heritability for disease from genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

GCTA: a tool for genome-wide complex trait analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

A map of human genome variation from population-scale sequencing

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Common SNPs explain a large proportion of the heritability for human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Finding the missing heritability of complex diseases

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Genotype-imputation accuracy across worldwide human populations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Principal components analysis corrects for stratification in genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Estimation of SNP heritability from dense genotype data

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4589513

Selection and explosive growth alter genetic architecture and hamper the detection of causal rare variants

2 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26323059

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Recovery of inter-block information when block sizes are unequal

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3390

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.3390

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12 August 2017

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12 August 2017

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