Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects (Q37693580)

22 August 2017

Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects (English)

1 reference

genome-wide association study

22 August 2017

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author

Caroline M Nievergelt

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22 August 2017

Nicholas J Schork

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22 August 2017

Nathan E Wineinger

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22 August 2017

Ondrej Libiger

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22 August 2017

Phillip Pham

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22 August 2017

Guangfa Zhang

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22 August 2017

Dewleen G Baker

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22 August 2017

Marine Resiliency Study Investigators

1 reference

22 August 2017

language of work or name

English

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publication date

9 February 2014

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22 August 2017

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22 August 2017

540

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22 August 2017

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22 August 2017

104-109

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A Method for Inferring an Individual's Genetic Ancestry and Degree of Admixture Associated with Six Major Continental Populations

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1 reference

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Clinical implications of human population differences in genome-wide rates of functional genotypes

23 August 2017

1 reference

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Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

23 August 2017

1 reference

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Efficiency and power as a function of sequence coverage, SNP array density, and imputation

23 August 2017

1 reference

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Predictors of risk and resilience for posttraumatic stress disorder among ground combat Marines: methods of the Marine Resiliency Study.

23 August 2017

1 reference

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CNVs: harbingers of a rare variant revolution in psychiatric genetics

23 August 2017

1 reference

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Genotype imputation with thousands of genomes

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980715

Capability of common SNPs to tag rare variants.

23 August 2017

1 reference

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Rare and common variants: twenty arguments

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1 reference

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Five years of GWAS discovery

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1 reference

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Genome partitioning of genetic variation for complex traits using common SNPs

23 August 2017

1 reference

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The UCSC Genome Browser database: update 2011

23 August 2017

1 reference

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Integrating common and rare genetic variation in diverse human populations

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1 reference

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Genotype imputation for genome-wide association studies

23 August 2017

1 reference

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Human allelic variation: perspective from protein function, structure, and evolution

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1 reference

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Finding the missing heritability of complex diseases

23 August 2017

1 reference

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Fast model-based estimation of ancestry in unrelated individuals

23 August 2017

1 reference

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

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3980715

Common vs. rare allele hypotheses for complex diseases

23 August 2017

1 reference

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Fine-scaled human genetic structure revealed by SNP microarrays

23 August 2017

1 reference

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Human genetic variation and its contribution to complex traits

23 August 2017

1 reference

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The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research

23 August 2017

1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

23 August 2017

1 reference

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

23 August 2017

1 reference

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Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

23 August 2017

1 reference

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A human genome diversity cell line panel

23 August 2017

1 reference

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Inferring causality and functional significance of human coding DNA variants

23 August 2017

1 reference

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Statistical analysis strategies for association studies involving rare variants

6 September 2017

1 reference

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Evolutionary evidence of the effect of rare variants on disease etiology

6 September 2017

1 reference

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

6 September 2017

1 reference

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Post-traumatic stress disorder, depression, and health-related quality of life in OEF/OIF veterans

23 June 2018

1 reference

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To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

1 September 2018

1 reference

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10.1016/J.GENE.2014.01.069

3 December 2018

Identifiers

DOI

1 reference

22 August 2017

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22 August 2017

PubMed publication ID

24521671

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