Behrang Mahjani
Behrang Mahjani
Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY
Verified email at - Homepage
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Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Association of genetic and environmental factors with autism in a 5-country cohort
D Bai, BHK Yip, GC Windham, A Sourander, R Francis, R Yoffe, ...
JAMA psychiatry 76 (10), 1035-1043, 2019
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
Genetics of obsessive-compulsive disorder
B Mahjani, K Bey, J Boberg, C Burton
Psychological medicine 51 (13), 2247-2259, 2021
Heritable variation, with little or no maternal effect, accounts for recurrence risk to autism spectrum disorder in Sweden
BHK Yip, D Bai, B Mahjani, L Klei, Y Pawitan, CM Hultman, DE Grice, ...
Biological psychiatry 83 (7), 589-597, 2018
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, SD Rubeis, JY An, ...
BioRxiv, 484113, 2018
MW State, AE Cicek, ME Talkowski, DJ Cutler, B. Devlin, SJ Sanders, K. Roeder, MJ Daly, JD Buxbaum, Large-scale exome sequencing study implicates both developmental and …
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (568-584), e23, 2020
Comorbidities in autism spectrum disorder and their etiologies
V Khachadourian, B Mahjani, S Sandin, A Kolevzon, JD Buxbaum, ...
Translational Psychiatry 13 (1), 71, 2023
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, L Klei, ...
MedRxiv, 2021.12. 20.21267194, 2021
How rare and common risk variation jointly affect liability for autism spectrum disorder
KRBD Lambertus Klei, Lora Lee McClain, Behrang Mahjani, Klea Panayidou ...
Molecular Autism 12, 2021
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder
B Mahjani, S De Rubeis, C Gustavsson Mahjani, M Mulhern, X Xu, L Klei, ...
Molecular autism 12, 1-12, 2021
Sequential Markov coalescent algorithms for population models with demographic structure
A Eriksson, B Mahjani, B Mehlig
Theoretical population biology 76 (2), 84-91, 2009
Maternal effects as causes of risk for obsessive-compulsive disorder
B Mahjani, L Klei, CM Hultman, H Larsson, B Devlin, JD Buxbaum, ...
Biological Psychiatry 87 (12), 1045-1051, 2020
Systematic review and meta-analysis: Relationships between attention-deficit/hyperactivity disorder and urinary symptoms in children
B Mahjani, LR Koskela, CG Mahjani, M Janecka, A Batuure, CM Hultman, ...
European child & adolescent psychiatry, 1-8, 2021
Clinical characterization of copy number variants associated with neurodevelopmental disorders in a large-scale multiancestry biobank
R Birnbaum, B Mahjani, RJF Loos, AJ Sharp
JAMA psychiatry 79 (3), 250-259, 2022
The genetic architecture of obsessive-compulsive disorder: contribution of liability to OCD from alleles across the frequency spectrum
B Mahjani, L Klei, M Mattheisen, MW Halvorsen, A Reichenberg, ...
American Journal of Psychiatry 179 (3), 216-225, 2022
Cohort profile: Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden (EGOS)
B Mahjani, K Dellenvall, ACS Grahnat, G Karlsson, A Tuuliainen, ...
Social psychiatry and psychiatric epidemiology 55, 1383-1393, 2020
Genome-wide association study identifies new locus associated with OCD
NI Strom, D Yu, ZF Gerring, MW Halvorsen, A Abdellaoui, ...
Medrxiv, 2021.10. 13.21261078, 2021
Systematic review and meta‐analysis identify significant relationships between clinical anxiety and lower urinary tract symptoms
B Mahjani, LR Koskela, A Batuure, C Gustavsson Mahjani, M Janecka, ...
Brain and Behavior 11 (9), e2268, 2021
Phenotypic Impact of Rare Potentially Damaging Copy Number Variation in Obsessive-Compulsive Disorder and Chronic Tic Disorders
B Mahjani, R Birnbaum, A Buxbaum Grice, C Cappi, S Jung, MN Avila, ...
Genes 13 (10), 1796, 2022
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