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Bioinformatics (Oxford, England)
|
November 22, 2022
IMMerge: merging imputation data at scale
Wanying Zhu, Hung-Hsin Chen, Alexander S Petty, et al.
Journal of Fluency Disorders
|
April 24, 2021
Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier
Dillon G Pruett, Douglas M Shaw, Hung-Hsin Chen, et al.
Frontiers in Psychology
|
March 13, 2026
A pilot study: virtual reality-based intervention to boost optimism and alleviate stress, anxiety, and depression in undergraduates
Yun-Ju Lai, Jiraporn Sangpara, Suppakorn Wankrathok, et al.
Translational Psychiatry
|
December 7, 2021
Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci
Hung-Hsin Chen, Lauren E Petty, Jin Sha, et al.
Genetic Epidemiology
|
June 27, 2026
DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data
James T Baker, Hung-Hsin Chen, Grahame F Evans, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 26, 2025
Neuroimaging PheWAS and molecular phenotyping implicate <i>PSMC3</i> in Alzheimer's Disease
Xavier Bledsoe, Ting-Chen Wang, Yiyang Wu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 24, 2026
Neuroimaging PheWAS and molecular phenotyping implicate PSMC3 in Alzheimer's disease
Xavier Bledsoe, Ting-Chen Wang, Yiyang Wu, et al.
American Journal of Human Genetics
|
December 3, 2021
Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering
Douglas M Shaw, Hannah P Polikowsky, Dillon G Pruett, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Research Square
|
October 4, 2023
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
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of 6
Search research articles
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Showing results (11-20 of 55) with videos related to
Sort By:
Page
of 6
Bioinformatics (Oxford, England)
|
November 22, 2022
IMMerge: merging imputation data at scale
Wanying Zhu, Hung-Hsin Chen, Alexander S Petty, et al.
Journal of Fluency Disorders
|
April 24, 2021
Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier
Dillon G Pruett, Douglas M Shaw, Hung-Hsin Chen, et al.
Frontiers in Psychology
|
March 13, 2026
A pilot study: virtual reality-based intervention to boost optimism and alleviate stress, anxiety, and depression in undergraduates
Yun-Ju Lai, Jiraporn Sangpara, Suppakorn Wankrathok, et al.
Translational Psychiatry
|
December 7, 2021
Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci
Hung-Hsin Chen, Lauren E Petty, Jin Sha, et al.
Genetic Epidemiology
|
June 27, 2026
DRIVE v3: Command Line Application for Identity-by-Descent Haplotype Clustering in Large Biobank Scale Data
James T Baker, Hung-Hsin Chen, Grahame F Evans, et al.
Medrxiv : the Preprint Server for Health Sciences
|
September 26, 2025
Neuroimaging PheWAS and molecular phenotyping implicate <i>PSMC3</i> in Alzheimer's Disease
Xavier Bledsoe, Ting-Chen Wang, Yiyang Wu, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 24, 2026
Neuroimaging PheWAS and molecular phenotyping implicate PSMC3 in Alzheimer's disease
Xavier Bledsoe, Ting-Chen Wang, Yiyang Wu, et al.
American Journal of Human Genetics
|
December 3, 2021
Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering
Douglas M Shaw, Hannah P Polikowsky, Dillon G Pruett, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 10, 2023
Detection of distant familial relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Research Square
|
October 4, 2023
Detection of distant relatedness in biobanks for identification of undiagnosed carriers of a Mendelian disease variant: application to Long QT Syndrome
Megan C Lancaster, Hung-Hsin Chen, M Benjamin Shoemaker, et al.
Page
of 6