Research
Autism Spectrum Disorder, Autism Spectrum Disorders
Adhd
Ocd
Statistical Genetics
Genome Wide Association Studies, Genome Wide Association Study
Obsessive Compulsive Disorder
Neurodevelopmental Disorder, Neurodevelopmental Disorders
Copy Number Variants
Meta Analysis
Anxiety Disorders, Anxiety Disorder
Lower Urinary Tract Symptoms
Genetic Architecture
Systematic Review, Systematic Reviews
Machine Learning
Perinatal Depression
Early Life Exposures
Familial Risk
Genetic Risk
Genomic Architecture
Mental Health
Monte Carlo Method, Monte Carlo Methods
Polygenic Risk Score
Postpartum Psychosis
Tourette Syndrome
Risk Gene, Risk Genes
Urinary Symptoms
Population Characteristics
Symptom Dimensions
Complex Traits
Genetic Analysis
Computational Challenges
Psychiatric Disorders
Quantitative Trait Loci
Statistical Computing
Population Models
List of Publications (65)
In 2024
65
Genome-wide association study identifies new loci associated with OCD. NI Strom, MW Halvorsen, C Tian, C Ru ck, G Kvale, B Hansen, ... MedRxiv, 2024.
Found on Publication Page
64
CLINICAL AND COGNITIVE PHENOTYPING OF COPY NUMBER VARIANTS PATHOGENIC FOR NEURODEVELOPMENTAL DISORDERS FROM A MULTI-ANCESTRY BIOBANK. N Zaks, B Mahjani, A Reichenberg, R Birnbaum medRxiv, 2024.07. 16.24310489, 2024.
Found on Publication Page
63
Identification of moderate effect size genes in autism spectrum disorder through a novel gene pairing approach. M Caballero, FK Satterstrom, JD Buxbaum, B Mahjani medRxiv, 2024.
Found on Publication Page
62
Genome-wide association study identifies 30 obsessive-compulsive disorder associated loci. NI Strom, ZF Gerring, M Galimberti, D Yu, MW Halvorsen, A Abdellaoui, ... medRxiv, 2024.
Found on Publication Page
61
Interactions of perinatal depression versus anxiety and infants' early temperament trajectories. F So rensen, MC Kimmel, V Brenner, I Kra geloh Mann, A Skalkidou, ... Child Development 95 (3), 721-733, 2024.
Found on Publication Page
In 2023
60
Direct additive genetics and maternal effect contribute to the risk of Tourette disorder. B Mahjani, L Klei, ASB Grice, H Larsson, CM Hultman, S Sandin, B Devlin, ... Journal of Neurology, Neurosurgery & Psychiatry 94 (8), 638-642, 2023.
Found on Publication Page
59
Association between mental health and reproductive system disorders in women: A systematic review and meta-analysis. N Zaks, A Batuure, E Lin, AS Rommel, A Reichenberg, D Grice, V Bergink, ... JAMA network open 6 (4), e238685-e238685, 2023.
Found on Publication Page
58
Quasi-monte carlo methods for binary event models with complex family data. B Christoffersen, B Mahjani, M Clements, H Kjellstro m, K Humphreys Journal of Computational and Graphical Statistics 32 (4), 1393-1401, 2023.
Found on Publication Page
57
F36. FAMILIAL RISK OF POSTPARTUM PSYCHOSIS. A Kepinska, T Robakis, K Humphreys, R Kahn, T Munk-Olsen, V Bergink, ... European Neuropsychopharmacology 75, S239-S240, 2023.
Found on Publication Page
56
Comorbidities in autism spectrum disorder and their etiologies. V Khachadourian, B Mahjani, S Sandin, A Kolevzon, JD Buxbaum, ... Translational Psychiatry 13 (1), 71, 2023.
Found on Publication Page
55
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome. P Jain, T Miller-Fleming, A Topaloudi, D Yu, P Drineas, M Georgitsi, ... Translational psychiatry 13 (1), 69, 2023.
Found on Publication Page
54
Prenatal Mood and Anxiety Disorders and Risk of Neurodevelopmental Disorders in Children. AP Kepinska, L Cohen, JD Buxbaum, DE Grice, B Mahjani INSAR 2023, 2023.
Found on Publication Page
53
Genomic Architecture and Genetic Risk for Autism Spectrum Disorder in Individuals of Latin American Ancestry. JD Buxbaum, MP Trelles, C Lattig, MA Pericak-Vance, A Kolevzon, ... INSAR 2023, 2023.
Found on Publication Page
52
W57. AUTISM HETEROGENEITY RELATED TO EARLY-LIFE EXPOSURES: MULTI-ANCESTRY RESULTS FROM THE SPARK SAMPLE. C Chatzigeorgiou, B Mahjani, MN Avila, P O'Reilly, N Mullins, M Janecka European Neuropsychopharmacology 75, S133-S134, 2023.
Found on Publication Page
In 2022
51
Psychometric properties of the Swedish translation of the Obsessive-Compulsive Inventory-Revised and the population characteristics of the symptom dimensions of OCD. B Mahjani, C Gustavsson Mahjani, A Reichenberg, S Sandin, ... Social psychiatry and psychiatric epidemiology 57 (10), 2147-2155, 2022.
Found on Publication Page
50
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.
Found on Publication Page
49
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.
Found on Publication Page
48
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.
Found on Publication Page
47
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.
Found on Publication Page
46
The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD. B Mahjani, L Klei, M Mattheisen, MW Halvorsen, A Reichenberg, ... The American journal of psychiatry 179 (3), 216, 2022.
Found on Publication Page
45
Family history of breast cancer is associated with elevated risk of prostate cancer: Evidence for shared genetic risks. A Calvo Chozas, B Mahjani, L Ro nnega rd Human Heredity 87 (1), 12-20, 2022.
Found on Publication Page
44
Recent Advances in the Genetic Architecture of OCD: Genetic Maternal Effect, Ultrarare, Rare, and Common Variation Contribute to Risk. B Mahjani, S Jung, C Cappi, MN Avila, L Cohen, J Crowley, K Roeder, ... NEUROPSYCHOPHARMACOLOGY 47, 306-306, 2022.
Found on Publication Page
43
De Novo Mutations in Conserved Genes Contribute to OCD Risk. S Jung, C Cappi, MN Avila, K Roeder, J Crowley, B Mahjani, J Buxbaum, ... NEUROPSYCHOPHARMACOLOGY 47 (SUPPL 1), 306-307, 2022.
Found on Publication Page
42
13.1 Genetic Maternal Effect, Ultra-Rare, Rare, and Common Variation Contribute to the Genetic Risk Architecture of OCD. B Mahjani Journal of the American Academy of Child & Adolescent Psychiatry 61 (10), S296, 2022.
Found on Publication Page
In 2021
41
Genetics of obsessive-compulsive disorder. B Mahjani, K Bey, J Boberg, C Burton Psychological Medicine 51 (13), 2247-2259, 2021.
Found on Publication Page
40
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.
Found on Publication Page
39
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.
Found on Publication Page
38
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.
Found on Publication Page
37
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.
Found on Publication Page
36
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.
Found on Publication Page
35
OCD symptom severity and comorbid psychiatric diagnoses in a Swedish genetic epidemiological obsessive-compulsive disorder cohort. B Mahjani, CG Mahjani, A Reichenberg, S Sandin, CM Hultman, ... medRxiv, 2021.06. 28.21259652, 2021.
Found on Publication Page
34
A Survey of Copy Number Variants Associated with Neurodevelopmental Disorders in a Large-Scale, Multi-Ancestry Biobank. R Birnbaum, B Mahjani, RJF Loos, AJ Sharp medRxiv, 2021.06. 09.21258554, 2021.
Found on Publication Page
In 2020
33
Epidemiology and genetics of obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS). B Mahjani, K Dellenvall, ACS Grahnat, G Karlsson, A Tuuliainen, ... .
Found on Publication Page
32
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.
Found on Publication Page
31
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.
Found on Publication Page
30
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.
Found on Publication Page
29
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.
Found on Publication Page
28
Genetic maternal effects contributes to the risk of Tourette's disorder. B Mahjani, L Klei, CM Hultman, H Larsson, S Sandin, B Devlin, ... medRxiv, 2020.11. 30.20240598, 2020.
Found on Publication Page
27
Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum Disorder. B Mahjani, S De Rubeis, CG Mahjani, M Mulhern, X Xu, L Klei, ... .
Found on Publication Page
26
Systematic Review and Meta-Analysis Identifies Significant Relationships Between Anxiety Disorders and Daytime Lower Urinary Tract Symptoms. B Mahjani, LR Koskela, A Batuure, CG Mahjani, M Janecka, CM Hultman, ... medRxiv, 2020.08. 27.20183467, 2020.
Found on Publication Page
25
Association of Anxiety Disorders and Attention Deficit Hyperactivity Disorders With Lower Urinary Tract Symptoms. B Mahjani, LR Koskela, A Batuure, CG Mahjani, M Janecka, CM Hultman, ... Biological Psychiatry 87 (9), S254, 2020.
Found on Publication Page
24
Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum Disorder. https://www.researchsquare.com/article/rs-104532/v1, 2020.
Found on Publication Page
In 2019
23
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.
Found on Publication Page
22
Computer Intensive Methods in Statistics. S Zwanzig, B Mahjani https://www.routledge.com/Computer-Intensive-Methods-in-Statistics/Zwanzig ..., 2019.
Found on Publication Page
21
Meta-Analysis Identifies a Robust Association Between Anxiety Disorders and Lower Urinary Tract Symptoms (LUTS). D Grice, B Mahjani, LR Koskela, A Batuure, C Mahjani, M Janecka, ... NEUROPSYCHOPHARMACOLOGY 44 (SUPPL 1), 396-396, 2019.
Found on Publication Page
20
Recurrent and Large Copy Number Variation in OCD Risk: Results From the Egos Study. DE Grice, JD Buxbaum, B Devlin, S De Rubeis, CM Hultman, L Klei, ... 66th Annual Meeting, 2019.
Found on Publication Page
19
T63GENETIC AND ENVIRONMENTAL FACTORS AND RISK OF OBSESSIVE-COMPULSIVE DISORDER. B Mahjani, L Klei, C Hultman, H Larsson, B Devlin, J Buxbaum, S Sandin, ... European Neuropsychopharmacology 29, S249, 2019.
Found on Publication Page
In 2018
18
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.
Found on Publication Page
17
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.
Found on Publication Page
In 2016
16
A flexible computational framework using R and Map-Reduce for permutation tests of massive genetic analysis of complex traits. B Mahjani, S Toor, C Nettelblad, S Holmgren IEEE/ACM Transactions on Computational Biology and Bioinformatics 14 (2 ..., 2016.
Found on Publication Page
13
Methods from Statistical Computing for Genetic Analysis of Complex Traits. B Mahjani Uppsala University, 2016.
Found on Publication Page
12
Fitting linear mixed models using sparse matrix methods and Lanczos factorization. B Mahjani, L Ro nnega rd, L Elde n Computational Statistics & Data Analysis, 2016.
Found on Publication Page
11
QTL as a service: PruneDIRECT for multi-dimensional QTL scans in cloud settings. B Mahjani, S Toor, C Nettelblad, S Holmgren Bioinformatics, 2016.
Found on Publication Page
10
Computational challenges in modeling maternal effects in psychiatric disorders. B Mahjani, Y Pawitan, L Klei, B Devlin, J Buxbaum, D Grice, ... .
Found on Publication Page
In 2013
9
Fast and Accurate Detection of Multiple Quantitative Trait Loci. C Nettelblad, B Mahjani, S Holmgren Journal of Computational Biology 20 (9), 2013.
Found on Publication Page
In 2012
8
Fast and Accurate Detection of Multiple QTL. C Nettelblad, B Mahjani, S Holmgren arXiv preprint arXiv:1209.6245, 2012.
Found on Publication Page
7
Using peak shape to improve efficient and effective detection of multiple QTL in known crossings. SH Carl Nettelblad, Behrang Mahjani* 4th International Conference on Quantitative Genetics, 2012.
Found on Publication Page
In 2010
6
Exploring connectivity of random subgraphs of a graph. B Mahjani arXiv preprint arXiv:1008.4814, 2010.
Found on Publication Page
5
Exploring connectivity of random subgraphs of a graph: connectivity of random subgraphs of Cartesian products of K2, K3, and P3. A survey of uniformly most reliable networks. B Mahjani Chalmers University of Technology, 2010.
Found on Publication Page
In 2009
4
Sequential Markov coalescent algorithms for population models with demographic structure. A Eriksson, B Mahjani, B Mehlig Theoretical population biology 76 (2), 84-91, 2009.
Found on Publication Page
In 2008
Unspecified
