Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Journal of Psychopharmacology (Oxford, England)|February 28, 2019
Pharmaco-epidemiology of antidepressant exposure in a UK cohort record-linkage studyJonathan D Hafferty, Eleanor M Wigmore, David M Howard, et al.
Frontiers in Genetics|July 12, 2012
Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depressionAndrew M McIntosh, Arthur A Simen, Kathryn L Evans, et al.
Pediatric Research|October 12, 2021
Language function following preterm birth: prediction using machine learningEvdoxia Valavani, Manuel Blesa, Paola Galdi, et al.
Glia|January 7, 2021
A loss of mature microglial markers without immune activation in schizophreniaGijsje J L J Snijders, Welmoed van Zuiden, Marjolein A M Sneeboer, et al.
Biological Psychiatry|July 17, 2016
A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive DisorderYanni Zeng, Pau Navarro, Ana M Fernandez-Pujals, et al.
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 cohortToni-Kim Clarke, Andrew H Smith, Joel Gelernter, et al.
Ebiomedicine|November 14, 2016
Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared DepressionYanni 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 illnessBlair H Smith, Archie Campbell, Pamela Linksted, 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 depressionHelen M Knight, Benjamin S Pickard, Alan Maclean, et al.
Pageof 4