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American Journal of Human Genetics
|
March 5, 2016
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy
Tamar Harel, Gozde Yesil, Yavuz Bayram, et al.
Obesity (Silver Spring, Md.)
|
June 26, 2015
Epigenome-wide study identifies novel methylation loci associated with body mass index and waist circumference
Stella Aslibekyan, Ellen W Demerath, Michael Mendelson, et al.
Journal of the American Heart Association
|
March 11, 2018
Genome Wide Association Study Identifies the <i>HMGCS2</i> Locus to be Associated With Chlorthalidone Induced Glucose Increase in Hypertensive Patients
Sonal Singh, Caitrin W McDonough, Yan Gong, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2018
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease
Badri N Vardarajan, Sandra Barral, James Jaworski, et al.
Journal of the American Society of Nephrology : JASN
|
September 1, 2021
Proteins Associated with Risk of Kidney Function Decline in the General Population
Morgan E Grams, Aditya Surapaneni, Jingsha Chen, et al.
Circulation. Genomic and Precision Medicine
|
January 28, 2026
Genetic Architecture of N-Terminal Pro-B-Type Natriuretic Peptide in a Multiancestry Study Population
Naman S Shetty, Akhil Pampana, Mokshad Gaonkar, et al.
The Journal of Infectious Diseases
|
May 6, 2022
Antibody Duration After Infection From SARS-CoV-2 in the Texas Coronavirus Antibody Response Survey
Michael D Swartz, Stacia M DeSantis, Ashraf Yaseen, et al.
Genome Medicine
|
September 29, 2020
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs
Christina A Castellani, Ryan J Longchamps, Jason A Sumpter, et al.
BMC Medical Genomics
|
July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate
Wu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.
Plos Genetics
|
January 31, 2009
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
David Reich, Michael A Nalls, W H Linda Kao, et al.
Page
of 122
Search research articles
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Showing results (711-720 of 1,215) with videos related to
Sort By:
Page
of 122
American Journal of Human Genetics
|
March 5, 2016
Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy
Tamar Harel, Gozde Yesil, Yavuz Bayram, et al.
Obesity (Silver Spring, Md.)
|
June 26, 2015
Epigenome-wide study identifies novel methylation loci associated with body mass index and waist circumference
Stella Aslibekyan, Ellen W Demerath, Michael Mendelson, et al.
Journal of the American Heart Association
|
March 11, 2018
Genome Wide Association Study Identifies the <i>HMGCS2</i> Locus to be Associated With Chlorthalidone Induced Glucose Increase in Hypertensive Patients
Sonal Singh, Caitrin W McDonough, Yan Gong, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2018
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease
Badri N Vardarajan, Sandra Barral, James Jaworski, et al.
Journal of the American Society of Nephrology : JASN
|
September 1, 2021
Proteins Associated with Risk of Kidney Function Decline in the General Population
Morgan E Grams, Aditya Surapaneni, Jingsha Chen, et al.
Circulation. Genomic and Precision Medicine
|
January 28, 2026
Genetic Architecture of N-Terminal Pro-B-Type Natriuretic Peptide in a Multiancestry Study Population
Naman S Shetty, Akhil Pampana, Mokshad Gaonkar, et al.
The Journal of Infectious Diseases
|
May 6, 2022
Antibody Duration After Infection From SARS-CoV-2 in the Texas Coronavirus Antibody Response Survey
Michael D Swartz, Stacia M DeSantis, Ashraf Yaseen, et al.
Genome Medicine
|
September 29, 2020
Mitochondrial DNA copy number can influence mortality and cardiovascular disease via methylation of nuclear DNA CpGs
Christina A Castellani, Ryan J Longchamps, Jason A Sumpter, et al.
BMC Medical Genomics
|
July 21, 2016
Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate
Wu-Lin Charng, Ender Karaca, Zeynep Coban Akdemir, et al.
Plos Genetics
|
January 31, 2009
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
David Reich, Michael A Nalls, W H Linda Kao, et al.
Page
of 122