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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 receptors
Mika 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 variation
Michael 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 studies
Michael 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 Outcomes
Michael 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 dementia
Shizhen 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 traits
Andrew 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 traits
Andrew 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 correlations
Shijia 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 galactosemia
Emily 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 Traits
Xiang Zhan, Ni Zhao, Anna Plantinga, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 140) with videos related to
Sort By:
Page
of 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 receptors
Mika 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 variation
Michael 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 studies
Michael 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 Outcomes
Michael 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 dementia
Shizhen 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 traits
Andrew 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 traits
Andrew 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 correlations
Shijia 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 galactosemia
Emily 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 Traits
Xiang Zhan, Ni Zhao, Anna Plantinga, et al.
Page
of 14