GRANVIL: Rare Variant Analysis of Genome-Wide Association Studies

GRANVIL: Rare Variant Analysis of Genome-Wide Association Studies

Detalhes bibliográficos
Principais autores:	Magi, R, Morris, A
Formato:	Conference item
Publicado em:	2010

Registros relacionados

Genome-Wide Association Analysis Of Rare Variants With Crohn's Disease
por: Magi, R, et al.
Publicado em: (2012)

Genome-Wide Association Analysis of Imputed Rare Variants: Application to Seven Common Complex Diseases
por: Mägi, R, et al.
Publicado em: (2012)

Genome-wide association analysis of imputed rare variants: application to seven common complex diseases.
por: Mägi, R, et al.
Publicado em: (2012)

Genome-wide association analysis of rare variants identifies potential novel susceptibility genes for type 1 diabetes and coronary artery disease
por: Magi, R, et al.
Publicado em: (2012)

Genome-wide Association Analysis of Rare Variants Identifies Potential Novel Susceptibility Genes for Type 1 Diabetes and Coronary Artery Disease
por: Morris, A, et al.
Publicado em: (2012)

GWAMA: software for genome-wide association meta-analysis
por: Mägi, R, et al.
Publicado em: (2010)

Genome-wide association analysis of rare variants with type 2 diabetes
por: Maegi, R, et al.
Publicado em: (2011)

Meta-analysis of sex-specific genome-wide association studies.
por: Magi, R, et al.
Publicado em: (2010)

Assessing the impact of missing genotype data in rare variant association analysis.
por: Mägi, R, et al.
Publicado em: (2011)

GWAMA: software for genome-wide association meta-analysis
por: Mägi Reedik, et al.
Publicado em: (2010-05-01)

Rapid Testing of Gene-gene Interactions in Genome-wide Association Studies
por: Bhattacharya, K, et al.
Publicado em: (2010)

Rare variants create synthetic genome-wide associations.
por: Samuel P Dickson, et al.
Publicado em: (2010-01-01)

Corrigendum: Genome-wide association study identifying variants related to performance and injury in high-performance athletes
por: Jay R. Ebert, et al.
Publicado em: (2024-09-01)

SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes
por: Mägi, R, et al.
Publicado em: (2017)

Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
por: Ada J. S. Chan, et al.
Publicado em: (2022-10-01)

GWAMA: Software Tool for Meta-analysis and Visualization of Whole Genome Association Data
por: Magi, R, et al.
Publicado em: (2009)

Exome‐based genome‐wide screening of rare variants associated with the risk of polycystic ovary syndrome
por: Satoshi Tamaoka, et al.
Publicado em: (2023-01-01)

An evaluation of statistical approaches to rare variant analysis in genetic association studies.
por: Morris, A, et al.
Publicado em: (2010)

SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes
por: Mägi, Reedik, et al.
Publicado em: (2017)

Large-scale integrated genome-wide RNA sequencing, miRNA array, and genomic analyses to unravel the functionality of genome-wide association results in endometriosis
por: Rahmioglu, N, et al.
Publicado em: (2017)

Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses
por: Michelle E. Penney, et al.
Publicado em: (2018-06-01)

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.
por: Harold, D, et al.
Publicado em: (2009)

SEAD reference panel with 22,134 haplotypes boosts rare variant imputation and genome-wide association analysis in Asian populations
por: Meng-Yuan Yang, et al.
Publicado em: (2024-12-01)

A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.
por: Evangelou, E, et al.
Publicado em: (2014)

Gearing up for genome-wide gene-association studies.
por: Farrall, M, et al.
Publicado em: (2005)

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
por: Costin Leu, et al.
Publicado em: (2015-09-01)

Model Selection Strategies in Genome-Wide Association Studies
por: Keildson, S, et al.
Publicado em: (2009)

Genome-wide association study of germline variants and breast cancer-specific mortality
por: Escala-Garcia, M, et al.
Publicado em: (2019)

Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets.
por: Rahmioglu, N, et al.
Publicado em: (2014)

A phenome-wide scan reveals convergence of common and rare variant associations
por: Dan Zhou, et al.
Publicado em: (2023-11-01)

Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
por: Elizabeth T. Cirulli, et al.
Publicado em: (2020-01-01)

Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.
por: Chambers, J, et al.
Publicado em: (2009)

Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population
por: Robert W. Read, et al.
Publicado em: (2021-03-01)

Genome-wide association scan for variants associated with early-onset prostate cancer.
por: Ethan M Lange, et al.
Publicado em: (2014-01-01)

Association of common genetic variants with brain microbleeds: a genome-wide association study
por: Knol, MJ, et al.
Publicado em: (2020)

Genome-wide association study identifies 48 common genetic variants associated with handedness
por: Cuellar-Partida, G, et al.
Publicado em: (2020)

Identification of disease-associate variants of aggressive periodontitis using genome-wide association studies
por: Chiharu Fujihara, et al.
Publicado em: (2023-12-01)

Trans-ethnic meta-regression of genome-wide association studies accounting for ancestry increases power for discovery and improves fine-mapping resolution.
por: Mägi, R, et al.
Publicado em: (2017)

Genome-wide association analysis of treatment resistant schizophrenia for variant discovery and polygenic assessment
por: Hasan Çağın Lenk, et al.
Publicado em: (2024-09-01)

Genome-wide screening for DNA variants associated with reading and language traits.
por: Gialluisi, A, et al.
Publicado em: (2014)