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European Psychiatry : the Journal of the Association of European Psychiatrists
|
August 21, 2018
Is it time to revise the diagnostic criteria for apathy in brain disorders? The 2018 international consensus group
P Robert, K L Lanctôt, L Agüera-Ortiz, et al.
BMC Infectious Diseases
|
November 19, 2016
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies
Kathryn L Jackson, Michael Mbagwu, Jennifer A Pacheco, et al.
Journal of the American College of Cardiology
|
March 25, 2017
Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans
Girish N Nadkarni, Geneviève Galarneau, Stephen B Ellis, et al.
Biodata Mining
|
December 18, 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)
Rishika De, Shefali S Verma, Fotios Drenos, et al.
Genetic Epidemiology
|
April 26, 2018
Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans
Jacob M Keaton, Chuan Gao, Meijian Guan, et al.
Psychiatric Research and Clinical Practice
|
October 18, 2022
Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women
Gabrielle A Mesches, Jody D Ciolino, Catherine S Stika, et al.
Nature Communications
|
June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders
Xinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.
Circulation. Heart Failure
|
May 6, 2021
Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network
Sadiya S Khan, Christin Hoell, Lisa M Castillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
Mark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
The Journal of Molecular Diagnostics : JMD
|
May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study
Laura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
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of 53
Search research articles
Search
Showing results (441-450 of 527) with videos related to
Sort By:
Page
of 53
European Psychiatry : the Journal of the Association of European Psychiatrists
|
August 21, 2018
Is it time to revise the diagnostic criteria for apathy in brain disorders? The 2018 international consensus group
P Robert, K L Lanctôt, L Agüera-Ortiz, et al.
BMC Infectious Diseases
|
November 19, 2016
Performance of an electronic health record-based phenotype algorithm to identify community associated methicillin-resistant Staphylococcus aureus cases and controls for genetic association studies
Kathryn L Jackson, Michael Mbagwu, Jennifer A Pacheco, et al.
Journal of the American College of Cardiology
|
March 25, 2017
Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans
Girish N Nadkarni, Geneviève Galarneau, Stephen B Ellis, et al.
Biodata Mining
|
December 18, 2015
Identifying gene-gene interactions that are highly associated with Body Mass Index using Quantitative Multifactor Dimensionality Reduction (QMDR)
Rishika De, Shefali S Verma, Fotios Drenos, et al.
Genetic Epidemiology
|
April 26, 2018
Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans
Jacob M Keaton, Chuan Gao, Meijian Guan, et al.
Psychiatric Research and Clinical Practice
|
October 18, 2022
Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women
Gabrielle A Mesches, Jody D Ciolino, Catherine S Stika, et al.
Nature Communications
|
June 14, 2022
Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders
Xinyuan Zhang, Anastasia M Lucas, Yogasudha Veturi, et al.
Circulation. Heart Failure
|
May 6, 2021
Practice Patterns After Return of Rare Variants Associated With Cardiomyopathy in the Electronic Medical Records and Genomics Network
Sadiya S Khan, Christin Hoell, Lisa M Castillo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 4, 2018
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome
Mark Drost, Yvonne Tiersma, Bryony A Thompson, et al.
The Journal of Molecular Diagnostics : JMD
|
May 16, 2017
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study
Laura J Rasmussen-Torvik, Berta Almoguera, Kimberly F Doheny, et al.
Page
of 53