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Genes|October 27, 2022
Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic DisordersBehrang Mahjani, Rebecca Birnbaum, Ariela Buxbaum Grice, et al.
European Child & Adolescent Psychiatry|February 26, 2021
Systematic review and meta-analysis: relationships between attention-deficit/hyperactivity disorder and urinary symptoms in childrenBehrang Mahjani, Lotta Renström Koskela, Christina Gustavsson Mahjani, et al.
Brain and Behavior|August 17, 2021
Systematic review and meta-analysis identify significant relationships between clinical anxiety and lower urinary tract symptomsBehrang Mahjani, Lotta Renström Koskela, Anita Batuure, et al.
Biological Psychiatry|November 5, 2017
Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in SwedenBenjamin Hon Kei Yip, Dan Bai, Behrang Mahjani, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorderF Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani, 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 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.
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.
Biological Psychiatry|October 24, 2025
Postpartum Psychosis and Bipolar Disorder: Review of Neurobiology and Expert Consensus Statement on ClassificationVeerle Bergink, Schahram Akbarian, Nancy Byatt, et al.
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