SCHOLARLY PUBLICATION ✓ Open Access

Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

Alkes L. Price, Gregory V. Kryukov, Paul I.W. de Bakker, Shaun Purcell, Jeff Staples, Lee‐Jen Wei, Shamil R. Sunyaev

📖 The American Journal of Human Genetics → 📅 2010-05-14 🔗 DOI: 10.1016/j.ajhg.2010.04.005

View Journal Profile → ⬇ Download PDF View Official Paper ↗

📄 Abstract

The abstract has not yet been added. Use the official source link for the complete publication record.

ℹ️ Publication Details

Journal: The American Journal of Human Genetics
Published: 2010-05-14
DOI: 10.1016/j.ajhg.2010.04.005
OpenAlex: W2070984858
Access: ✓ Open Access

📋 Cite This Paper

Alkes L. Price, Gregory V. Kryukov, Paul I.W. de Bakker, Shaun Purcell, Jeff Staples, Lee‐Jen Wei, Shamil R. Sunyaev (2010). Pooled Association Tests for Rare Variants in Exon-Resequencing Studies. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2010.04.005

🔬 Related Research Papers

The American Journal of Human Genetics

The Dawn of Human Matrilineal Diversity

Doron M. Behar, Richard Villems et al. 2008-04-25 · Read paper → The American Journal of Human Genetics

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

Yong‐hui Jiang, Ryan K. C. Yuen et al. 2013-07-11 · Read paper → The American Journal of Human Genetics

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

Mariem Ben Khelifa, Charles Coutton et al. 2013-12-19 · Read paper → The American Journal of Human Genetics

Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

Katherine R. Smith, John A. Damiano et al. 2012-05-17 · Read paper → The American Journal of Human Genetics

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

Gabriela López‐Herrera, Giacomo Tampella et al. 2012-05-17 · Read paper → The American Journal of Human Genetics

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Paweł Stankiewicz, Partha Sen et al. 2009-06-01 · Read paper → The American Journal of Human Genetics

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

Vikas Rao Pejaver, Alicia B. Byrne et al. 2022-11-21 · Read paper → The American Journal of Human Genetics

📄 Abstract

🔬 Related Research Papers

The Dawn of Human Matrilineal Diversity

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

Strikingly Different Clinicopathological Phenotypes Determined by Progranulin-Mutation Dosage

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

The Genetic Ancestry of African Americans, Latinos, and European Americans across the United States

NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

Mendelian Inheritance in Man and Its Online Version, OMIM

Random-Effects Model Aimed at Discovering Associations in Meta-Analysis of Genome-wide Association Studies