(Q30662194)

19 August 2017

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project (English)

1 reference

19 August 2017

21

Loic Le Marchand

0 references

Charles Kooperberg

29

Charles Kooperberg

1 reference

19 August 2017

Goo Jun

6

0 references

Lisa W. Martin

Lisa W Martin

19

0 references

Steven Buyske

Steven Buyske

9

0 references

Dana Crawford

24

Dana C Crawford

1 reference

19 August 2017

27

Gerardo Heiss

1 reference

19 August 2017

Christopher A. Haiman

20

Christopher A Haiman

1 reference

19 August 2017

22

Tara C Matise

1 reference

19 August 2017

32

Kari E North

1 reference

19 August 2017

10

Nora Franceschini

1 reference

19 August 2017

23

Lucia A Hindorff

1 reference

19 August 2017

30

James G Wilson

1 reference

19 August 2017

14

Ulrike Peters

1 reference

19 August 2017

33

Deborah A Nickerson

1 reference

19 August 2017

34

Leslie A Lange

1 reference

19 August 2017

7

Chris Bizon

1 reference

19 August 2017

Themistocles L Assimes

25

Themistocles L Assimes

1 reference

19 August 2017

28

Rebecca D Jackson

1 reference

19 August 2017

Qing Duan

1

1 reference

19 August 2017

Eric Yi Liu

2

1 reference

19 August 2017

Paul L Auer

3

1 reference

19 August 2017

Guosheng Zhang

4

1 reference

19 August 2017

Ethan M Lange

5

1 reference

19 August 2017

Shuo Jiao

8

1 reference

19 August 2017

Chris S Carlson

11

1 reference

19 August 2017

Li Hsu

12

1 reference

19 August 2017

Alex P Reiner

13

1 reference

19 August 2017

Jeffrey Haessler

15

1 reference

19 August 2017

Keith Curtis

16

1 reference

19 August 2017

Christina L Wassel

17

1 reference

19 August 2017

Jennifer G Robinson

18

1 reference

19 August 2017

Hyun Min Kang

26

1 reference

19 August 2017

Gonçalo R Abecasis

31

1 reference

19 August 2017

Yun Li

35

1 reference

19 August 2017

language of work or name

English

0 references

publication date

16 August 2013

1 reference

19 August 2017

1 reference

19 August 2017

29

1 reference

19 August 2017

21

1 reference

19 August 2017

2744-2749

1 reference

AbCD: arbitrary coverage design for sequencing-based genetic studies

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Detecting rare variant effects using extreme phenotype sampling in sequencing association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

MaCH-admix: genotype imputation for admixed populations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Genotype imputation of Metabochip SNPs using a study-specific reference panel of ~4,000 haplotypes in African Americans from the Women's Health Initiative

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Evaluation of the metabochip genotyping array in African Americans and implications for fine mapping of GWAS-identified loci: the PAGE study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Low-coverage sequencing: implications for design of complex trait association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

A map of human genome variation from population-scale sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Biological, clinical and population relevance of 95 loci for blood lipids

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Utilizing genotype imputation for the augmentation of sequence data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Genotype imputation for genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Fast and accurate short read alignment with Burrows-Wheeler transform

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Power of deep, all-exon resequencing for discovery of human trait genes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

A note on exact tests of Hardy-Weinberg equilibrium

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Multi-Ethnic Study of Atherosclerosis: objectives and design

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Linkage disequilibrium in humans: models and data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

CARDIA: study design, recruitment, and some characteristics of the examined subjects

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Work organization and atherosclerosis: findings from the ARIC study. Atherosclerosis Risk in Communities

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT477

Design of the Women’s Health Initiative Clinical Trial and Observational Study

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTT477

Power in the phenotypic extremes: a simulation study of power in discovery and replication of rare variants

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3799474

Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23956302

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTT477

1 reference

journals/bioinformatics/DuanLA13

19 August 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

19 August 2017

PubMed publication ID

23956302

1 reference