(Q41775611)

9 October 2017

Empirical power of very rare variants for common traits and disease: results from sanger sequencing 1998 individuals (English)

1 reference

9 October 2017

Martin Ladouceur

1

1 reference

9 October 2017

Hou-Feng Zheng

series ordinal

2

1 reference

9 October 2017

Celia M T Greenwood

series ordinal

3

1 reference

9 October 2017

J Brent Richards

series ordinal

4

1 reference

9 October 2017

16 January 2013

1 reference

European Journal of Human Genetics

9 October 2017

1 reference

9 October 2017

21

1 reference

9 October 2017

9

1 reference

9 October 2017

1027-1030

1 reference

https://scigraph.springernature.com/pub.10.1038/ejhg.2012.284

9 October 2017

0 references

cites work

Rare variant density across the genome and across populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Sequencing of Lp-PLA2-encoding PLA2G7 gene in 2000 Europeans reveals several rare loss-of-function mutations

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Replication strategies for rare variant complex trait association studies via next-generation sequencing

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Deep resequencing reveals excess rare recent variants consistent with explosive population growth

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Rare variant association analysis methods for complex traits

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Missing heritability and strategies for finding the underlying causes of complex disease

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Pooled association tests for rare variants in exon-resequencing studies

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Sequencing technologies - the next generation

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3746260

Effect of genome-wide genotyping and reference panels on rare variants imputation

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23321613

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2012.284

1 reference

Dimensions Publication ID

9 October 2017

0 references

1 reference

9 October 2017

PubMed publication ID

23321613

1 reference