(Q37083452)

18 August 2017

0 references

Meta-analysis of gene-level associations for rare variants based on single-variant statistics (English)

1 reference

18 August 2017

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0 references

Andrea Ganna

4

0 references

Erik Ingelsson

series ordinal

8

object named as

Erik Ingelsson

1 reference

18 August 2017

3

Stefan Gustafsson

1 reference

18 August 2017

7

Kari E North

1 reference

18 August 2017

2

Sonja I Berndt

1 reference

18 August 2017

6

Joel Hirschhorn

1 reference

18 August 2017

Yi-Juan Hu

1

1 reference

18 August 2017

Genetic Investigation of ANthropometric Traits (GIANT) Consortium

series ordinal

5

1 reference

18 August 2017

Dan-Yu Lin

series ordinal

9

1 reference

18 August 2017

language of work or name

English

0 references

publication date

25 July 2013

1 reference

American Journal of Human Genetics

18 August 2017

1 reference

18 August 2017

93

1 reference

18 August 2017

2

1 reference

18 August 2017

236-248

1 reference

Quantitative trait analysis in sequencing studies under trait-dependent sampling

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

An integrated map of genetic variation from 1,092 human genomes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

On the relative efficiency of using summary statistics versus individual-level data in meta-analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

A general framework for detecting disease associations with rare variants in sequencing studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Rare-variant association testing for sequencing data with the sequence kernel association test

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Testing for an unusual distribution of rare variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Hundreds of variants clustered in genomic loci and biological pathways affect human height

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Pooled association tests for rare variants in exon-resequencing studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Prioritizing GWAS results: A review of statistical methods and recommendations for their application

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Meta-analysis of genome-wide association studies: no efficiency gain in using individual participant data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

An evaluation of statistical approaches to rare variant analysis in genetic association studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Common vs. rare allele hypotheses for complex diseases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

A groupwise association test for rare mutations using a weighted sum statistic

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Meta-analysis in genome-wide association studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

A second generation human haplotype map of over 3.1 million SNPs

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

Haplotype-based association analysis via variance-components score test.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3738834

GWAsimulator: a rapid whole-genome simulation program

29 September 2017

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23891470

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2013.06.011

1 reference

18 August 2017

1 reference

18 August 2017

PubMed publication ID

23891470

1 reference