GRANVIL: Rare Variant Analysis of Genome-Wide Association Studies

GRANVIL: Rare Variant Analysis of Genome-Wide Association Studies

Podrobná bibliografie
Hlavní autoři:	Magi, R, Morris, A
Médium:	Conference item
Vydáno:	2010

Podobné jednotky

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Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases
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Meta-analysis of sex-specific genome-wide association studies.
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Assessing the impact of missing genotype data in rare variant association analysis.
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Vydáno: (2011)

GWAMA: software for genome-wide association meta-analysis
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Rapid Testing of Gene-gene Interactions in Genome-wide Association Studies
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Rare variants create synthetic genome-wide associations.
Autor: Samuel P Dickson, a další
Vydáno: (2010-01-01)

Corrigendum: Genome-wide association study identifying variants related to performance and injury in high-performance athletes
Autor: Jay R. Ebert, a další
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SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes
Autor: Mägi, R, a další
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Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
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GWAMA: Software Tool for Meta-analysis and Visualization of Whole Genome Association Data
Autor: Magi, R, a další
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Exome‐based genome‐wide screening of rare variants associated with the risk of polycystic ovary syndrome
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An evaluation of statistical approaches to rare variant analysis in genetic association studies.
Autor: Morris, A, a další
Vydáno: (2010)

SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes
Autor: Mägi, Reedik, a další
Vydáno: (2017)

Large-scale integrated genome-wide RNA sequencing, miRNA array, and genomic analyses to unravel the functionality of genome-wide association results in endometriosis
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Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses
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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
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SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations
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A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.
Autor: Evangelou, E, a další
Vydáno: (2014)

Gearing up for genome-wide gene-association studies.
Autor: Farrall, M, a další
Vydáno: (2005)

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
Autor: Costin Leu, a další
Vydáno: (2015-09-01)

Model Selection Strategies in Genome-Wide Association Studies
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Vydáno: (2009)

Genome-wide association study of germline variants and breast cancer-specific mortality
Autor: Escala-Garcia, M, a další
Vydáno: (2019)

Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets.
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Vydáno: (2014)

A phenome-wide scan reveals convergence of common and rare variant associations
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Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
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Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
Autor: Chambers, J, a další
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Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population
Autor: Robert W. Read, a další
Vydáno: (2021-03-01)

Genome-wide association scan for variants associated with early-onset prostate cancer.
Autor: Ethan M Lange, a další
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Association of common genetic variants with brain microbleeds: a genome-wide association study
Autor: Knol, MJ, a další
Vydáno: (2020)

Genome-wide association study identifies 48 common genetic variants associated with handedness
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Vydáno: (2020)

Identification of disease-associate variants of aggressive periodontitis using genome-wide association studies
Autor: Chiharu Fujihara, a další
Vydáno: (2023-12-01)

Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution.
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Genome-wide association analysis of treatment resistant schizophrenia for variant discovery and polygenic assessment
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Genome-wide screening for DNA variants associated with reading and language traits.
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Vydáno: (2014)