(Q31060192)

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

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Europe PubMed Central

PMC publication ID

11 August 2017

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

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11 August 2017

genome-wide association study

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Eric Boerwinkle

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Eric Boerwinkle

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Loic Le Marchand

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Loic Le Marchand

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Charles Kooperberg

21

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Charles Kooperberg

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11 August 2017

Jose Luis Ambite

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Jose Luis Ambite

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Steven Buyske

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31

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Karen L Mohlke

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34

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Dana C Crawford

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Christopher A. Haiman

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Christopher A Haiman

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Teri A Manolio

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Benjamin F. Voight

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Benjamin F Voight

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Tara C Matise

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Kari E North

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Nora Franceschini

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Nora Franceschini

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Lucia A Hindorff

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Lucia A Hindorff

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33

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Ulrike Peters

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Megan Fesinmeyer

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Megan D Fesinmeyer

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Themistocles L Assimes

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Themistocles L Assimes

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Charles B Eaton

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Charles B Eaton

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11 August 2017

author name string

Ying Wu

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Cara L Carty

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Iona Cheng

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Logan Dumitrescu

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Sabrina Mitchell

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Petra Buzkova

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Chris S Carlson

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Barbara Cochran

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David Duggan

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Jeffrey Haessler

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Nancy Jenny

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11 August 2017

Hyun Min Kang

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11 August 2017

Yi Lin

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Jennifer G Robinson

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Carlos Rodriguez

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Fredrick R Schumacher

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Alicia Young

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publication date

23 April 2012

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11 August 2017

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4

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11 August 2017

e35651

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11 August 2017

copyright license

Creative Commons CC0 License

23 April 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

0 references

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Performance of genotype imputations using data from the 1000 Genomes Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

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14 July 2018

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips

1 reference

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14 July 2018

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

1 reference

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14 July 2018

Promise and pitfalls of the Immunochip

1 reference

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14 July 2018

A map of human genome variation from population-scale sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Integrating common and rare genetic variation in diverse human populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

LocusZoom: regional visualization of genome-wide association scan results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

METAL: fast and efficient meta-analysis of genomewide association scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Genotype imputation for genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Genome-wide association studies in diverse populations

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

A method and server for predicting damaging missense mutations

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14 July 2018

Quality control for genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Methodological challenges of genome-wide association analysis in Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

Common variants at 30 loci contribute to polygenic dyslipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

1 reference

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14 July 2018

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3335090

14 July 2018

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

1 reference

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14 July 2018

Population structure and eigenanalysis

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GENCODE: producing a reference annotation for ENCODE

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

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14 July 2018

Cholesteryl ester transfer protein promoter single-nucleotide polymorphisms in Sp1-binding sites affect transcription and are associated with high-density lipoprotein cholesterol

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14 July 2018

Measuring inconsistency in meta-analyses

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A multiethnic cohort in Hawaii and Los Angeles: baseline characteristics

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14 July 2018

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

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14 July 2018

Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge

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14 July 2018

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

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14 July 2018

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

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https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0035651

21 January 2018

GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population.

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12 December 2020

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10.1371/JOURNAL.PONE.0035651

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Europe PubMed Central

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11 August 2017

2012PLoSO...735651B

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PMC publication ID

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Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

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11 August 2017

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