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Human Genetics|October 10, 2006
Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndromeRosanna Weksberg, Andrea C Stachon, Jeremy A Squire, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 23, 2020
Gene coexpression patterns predict opiate-induced brain-state transitionsJulia K Brynildsen, Kyla D Mace, Eli J Cornblath, et al.
International Journal of Cardiology|December 15, 2015
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteriesGregory Costain, Anath C Lionel, Lucas Ogura, et al.
Plos One|October 11, 2017
Learning about learning: Mining human brain sub-network biomarkers from fMRI dataPetko Bogdanov, Nazli Dereli, Xuan-Hong Dang, et al.
Schizophrenia Bulletin|December 14, 2012
Evaluating genetic counseling for individuals with schizophrenia in the molecular ageGregory Costain, Mary Jane Esplen, Brenda Toner, et al.
Schizophrenia Research|January 26, 2017
Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal studyA M Fiksinski, E J Breetvelt, S N Duijff, et al.
International Journal of Neural Systems|May 18, 2018
Integrating EEG and MEG Signals to Improve Motor Imagery Classification in Brain-Computer InterfaceMarie-Constance Corsi, Mario Chavez, Denis Schwartz, et al.
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