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Plos One
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November 17, 2015
Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)
Ana Maria Fernandez-Pujals, Mark James Adams, Pippa Thomson, et al.
Addiction Biology
|
April 14, 2015
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort
Toni-Kim Clarke, Andrew H Smith, Joel Gelernter, et al.
Critical Care Medicine
|
December 4, 2024
Adjunctive Midodrine Therapy for Vasopressor-Dependent Shock in the ICU: A Systematic Review and Meta-Analysis
Sebastian J Kilcommons, Fadi Hammal, Mostafa Kamaleldin, et al.
Ebiomedicine
|
November 14, 2016
Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression
Yanni Zeng, Pau Navarro, Charley Xia, et al.
International Journal of Epidemiology
|
July 13, 2012
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness
Blair H Smith, Archie Campbell, Pamela Linksted, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 11, 2016
Multicenter Experience With Catheter Ablation for Ventricular Tachycardia in Lamin A/C Cardiomyopathy
Saurabh Kumar, Alexander F A Androulakis, Jean-Marc Sellal, et al.
Journal of the American College of Cardiology
|
November 26, 2016
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers
Saurabh Kumar, Samuel H Baldinger, Estelle Gandjbakhch, et al.
American Journal of Human Genetics
|
December 1, 2009
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
Helen M Knight, Benjamin S Pickard, Alan Maclean, et al.
Molecular Psychiatry
|
March 11, 2015
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population
T-K Clarke, M K Lupton, A M Fernandez-Pujals, et al.
Acta Crystallographica. Section E, Structure Reports Online
|
May 18, 2011
2-Acetyl-pyridinium bromanilate
Lynne H Thomas, Bryan Boyle, Lesley A Clive, et al.
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of 24
Search research articles
Search
Showing results (211-220 of 240) with videos related to
Sort By:
Page
of 24
Plos One
|
November 17, 2015
Epidemiology and Heritability of Major Depressive Disorder, Stratified by Age of Onset, Sex, and Illness Course in Generation Scotland: Scottish Family Health Study (GS:SFHS)
Ana Maria Fernandez-Pujals, Mark James Adams, Pippa Thomson, et al.
Addiction Biology
|
April 14, 2015
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort
Toni-Kim Clarke, Andrew H Smith, Joel Gelernter, et al.
Critical Care Medicine
|
December 4, 2024
Adjunctive Midodrine Therapy for Vasopressor-Dependent Shock in the ICU: A Systematic Review and Meta-Analysis
Sebastian J Kilcommons, Fadi Hammal, Mostafa Kamaleldin, et al.
Ebiomedicine
|
November 14, 2016
Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression
Yanni Zeng, Pau Navarro, Charley Xia, et al.
International Journal of Epidemiology
|
July 13, 2012
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness
Blair H Smith, Archie Campbell, Pamela Linksted, et al.
Circulation. Arrhythmia and Electrophysiology
|
August 11, 2016
Multicenter Experience With Catheter Ablation for Ventricular Tachycardia in Lamin A/C Cardiomyopathy
Saurabh Kumar, Alexander F A Androulakis, Jean-Marc Sellal, et al.
Journal of the American College of Cardiology
|
November 26, 2016
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers
Saurabh Kumar, Samuel H Baldinger, Estelle Gandjbakhch, et al.
American Journal of Human Genetics
|
December 1, 2009
A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression
Helen M Knight, Benjamin S Pickard, Alan Maclean, et al.
Molecular Psychiatry
|
March 11, 2015
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population
T-K Clarke, M K Lupton, A M Fernandez-Pujals, et al.
Acta Crystallographica. Section E, Structure Reports Online
|
May 18, 2011
2-Acetyl-pyridinium bromanilate
Lynne H Thomas, Bryan Boyle, Lesley A Clive, et al.
Page
of 24