Showing results (1-10 of 29) with videos related to
Sort By:
Pageof 3
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 17, 2024
Lymphoblast transcriptome analysis in 22q11.2 deletion syndrome individuals with schizophrenia-spectrum disorderElena Michaelovsky, Miri Carmel, Doron Gothelf, et al.Journal of Mental Health Research in Intellectual Disabilities|January 30, 2010
Velo-Cardio-Facial SyndromeDoron Gothelf, Amos Frisch, Elena Michaelovsky, et al.Human Genetics|January 17, 2004
Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesisAmos Frisch, Roberto Colombo, Elena Michaelovsky, et al.The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 28, 2020
Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disordersMiri Carmel, Elena Michaelovsky, Ronnie Weinberger, et al.Translational Psychiatry|February 3, 2019
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approachElena Michaelovsky, Miri Carmel, Amos Frisch, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|October 13, 2006
Association of the serotonin transporter promotor polymorphism with suicide attempters with a high medical damageDanuta Wasserman, Thomas Geijer, Marcus Sokolowski, et al.Journal of Psychiatric Research|May 24, 2014
Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjectsMiri Carmel, Omer Zarchi, Elena Michaelovsky, et al.Neuroscience Letters|July 27, 2005
COMT Val158Met polymorphism in schizophrenia with obsessive-compulsive disorder: a case-control studyMichael Poyurovsky, Elena Michaelovsky, Amos Frisch, et al.Psychophysiology|January 22, 2015
Hyperactive auditory processing in Williams syndrome: Evidence from auditory evoked potentialsOmer Zarchi, Chen Avni, Josef Attias, et al.BMC Medical Genetics|December 19, 2012
Genotype-phenotype correlation in 22q11.2 deletion syndromeElena Michaelovsky, Amos Frisch, Miri Carmel, et al.Pageof 3