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Michael P Epstein

Showing results (41-50 of 140) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 21, 2007
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptorsMika Nakamoto, Vijayalaxmi Nalavadi, Michael P Epstein, et al.
American Journal of Human Genetics|July 24, 2012
A permutation procedure to correct for confounders in case-control studies, including tests of rare variationMichael P Epstein, Richard Duncan, Yunxuan Jiang, et al.
Genetic Epidemiology|June 21, 2012
Stratification-score matching improves correction for confounding by population stratification in case-control association studiesMichael P Epstein, Richard Duncan, K Alaine Broadaway, et al.
Statistics in Biosciences|May 4, 2010
A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical OutcomesMichael P Epstein, Jessica E Hunter, Emily G Allen, et al.
Plos Genetics|April 2, 2021
Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer's dementiaShizhen Tang, Aron S Buchman, Philip L De Jager, et al.
Biorxiv : the Preprint Server for Biology|September 25, 2023
Identifying latent genetic interactions in genome-wide association studies using multiple traitsAndrew J Bass, Shijia Bian, Aliza P Wingo, et al.
Genome Medicine|April 25, 2024
Identifying latent genetic interactions in genome-wide association studies using multiple traitsAndrew J Bass, Shijia Bian, Aliza P Wingo, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
SCAMPI: A scalable statistical framework for genome-wide interaction testing harnessing cross-trait correlationsShijia Bian, Andrew J Bass, Yue Liu, et al.
Journal of Inherited Metabolic Disease|January 16, 2013
Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemiaEmily L Ryan, Mary Ellen Lynch, Elles Taddeo, et al.
Genetics|June 24, 2017
Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured TraitsXiang Zhan, Ni Zhao, Anna Plantinga, et al.
Pageof 14

Showing results (41-50 of 140) with videos related to

Sort By:
Pageof 14
Proceedings of the National Academy of Sciences of the United States of America|September 21, 2007
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptorsMika Nakamoto, Vijayalaxmi Nalavadi, Michael P Epstein, et al.
American Journal of Human Genetics|July 24, 2012
A permutation procedure to correct for confounders in case-control studies, including tests of rare variationMichael P Epstein, Richard Duncan, Yunxuan Jiang, et al.
Genetic Epidemiology|June 21, 2012
Stratification-score matching improves correction for confounding by population stratification in case-control association studiesMichael P Epstein, Richard Duncan, K Alaine Broadaway, et al.
Statistics in Biosciences|May 4, 2010
A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical OutcomesMichael P Epstein, Jessica E Hunter, Emily G Allen, et al.
Plos Genetics|April 2, 2021
Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer's dementiaShizhen Tang, Aron S Buchman, Philip L De Jager, et al.
Biorxiv : the Preprint Server for Biology|September 25, 2023
Identifying latent genetic interactions in genome-wide association studies using multiple traitsAndrew J Bass, Shijia Bian, Aliza P Wingo, et al.
Genome Medicine|April 25, 2024
Identifying latent genetic interactions in genome-wide association studies using multiple traitsAndrew J Bass, Shijia Bian, Aliza P Wingo, et al.
Biorxiv : the Preprint Server for Biology|September 24, 2024
SCAMPI: A scalable statistical framework for genome-wide interaction testing harnessing cross-trait correlationsShijia Bian, Andrew J Bass, Yue Liu, et al.
Journal of Inherited Metabolic Disease|January 16, 2013
Cryptic residual GALT activity is a potential modifier of scholastic outcome in school age children with classic galactosemiaEmily L Ryan, Mary Ellen Lynch, Elles Taddeo, et al.
Genetics|June 24, 2017
Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured TraitsXiang Zhan, Ni Zhao, Anna Plantinga, et al.
Pageof 14