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Journal of Speech, Language, and Hearing Research : JSLHR
|
August 14, 2020
Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems
Courtney E Walters, Rachana Nitin, Katherine Margulis, 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.
Genes, Brain, and Behavior
|
February 12, 2025
Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report
Shirley Y Hill, Howard J Edenberg, Aiden Corvin, 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.
Plos One
|
November 17, 2015
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas
Eric L Brown, Jennifer E Below, Rebecca S B Fischer, et al.
Journal of the American Heart Association
|
May 15, 2025
Circulating Proteomics Identifies a Dynamic Profile of Hepatic Steatosis During Metabolic Intervention
Bassim El-Sabawi, Kahraman Tanriverdi, Priya Gajjar, et al.
Plos One
|
March 1, 2017
Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal
Esteban J Parra, Andrew Mazurek, Christopher R Gignoux, 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.
Diabetes
|
September 12, 2007
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies
M Geoffrey Hayes, Anna Pluzhnikov, Kazuaki Miyake, et al.
American Journal of Human Genetics
|
June 4, 2016
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L
Dong-Hui Chen, Jennifer E Below, Akiko Shimamura, et al.
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of 15
Search research articles
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Showing results (41-50 of 147) with videos related to
Sort By:
Page
of 15
Journal of Speech, Language, and Hearing Research : JSLHR
|
August 14, 2020
Automated Phenotyping Tool for Identifying Developmental Language Disorder Cases in Health Systems Data (APT-DLD): A New Research Algorithm for Deployment in Large-Scale Electronic Health Record Systems
Courtney E Walters, Rachana Nitin, Katherine Margulis, 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.
Genes, Brain, and Behavior
|
February 12, 2025
Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report
Shirley Y Hill, Howard J Edenberg, Aiden Corvin, 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.
Plos One
|
November 17, 2015
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas
Eric L Brown, Jennifer E Below, Rebecca S B Fischer, et al.
Journal of the American Heart Association
|
May 15, 2025
Circulating Proteomics Identifies a Dynamic Profile of Hepatic Steatosis During Metabolic Intervention
Bassim El-Sabawi, Kahraman Tanriverdi, Priya Gajjar, et al.
Plos One
|
March 1, 2017
Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal
Esteban J Parra, Andrew Mazurek, Christopher R Gignoux, 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.
Diabetes
|
September 12, 2007
Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies
M Geoffrey Hayes, Anna Pluzhnikov, Kazuaki Miyake, et al.
American Journal of Human Genetics
|
June 4, 2016
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L
Dong-Hui Chen, Jennifer E Below, Akiko Shimamura, et al.
Page
of 15