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European Child & Adolescent Psychiatry|May 7, 2014
The increasing prevalence of reported diagnoses of childhood psychiatric disorders: a descriptive multinational comparisonHjördis O Atladottir, David Gyllenberg, Amanda Langridge, et al.
Social Psychiatry and Psychiatric Epidemiology|January 8, 2020
Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS)Behrang Mahjani, Karin Dellenvall, Anna-Carin Säll Grahnat, et al.
Molecular Psychiatry|August 14, 2013
Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sampleJ P Szatkiewicz, B M Neale, C O'Dushlaine, et al.
Molecular Psychiatry|September 21, 2011
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophreniaE S Lips, L N Cornelisse, R F Toonen, et al.
Molecular Autism|October 7, 2021
How rare and common risk variation jointly affect liability for autism spectrum disorderLambertus Klei, Lora Lee McClain, Behrang Mahjani, et al.
Human Molecular Genetics|October 19, 2013
A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjectsJoseph L McClay, Karolina A Aberg, Shaunna L Clark, et al.
Epigenomics|December 19, 2012
MBD-seq as a cost-effective approach for methylome-wide association studies: demonstration in 1500 case--control samplesKarolina A Aberg, Joseph L McClay, Srilaxmi Nerella, et al.
Molecular Autism|October 7, 2021
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorderBehrang Mahjani, Silvia De Rubeis, Christina Gustavsson Mahjani, et al.
American Journal of Human Genetics|October 9, 2012
Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depthMenachem Fromer, Jennifer L Moran, Kimberly Chambert, et al.
The Lancet. Psychiatry|February 27, 2016
Polygenic overlap between schizophrenia risk and antipsychotic response: a genomic medicine approachDouglas M Ruderfer, Alexander W Charney, Ben Readhead, et al.
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