A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats TV de Jong, Y Pan, P Rastas, D Munro, M Tutaj, H Akil, C Benner, D Chen, ... Cell Genomics 4 (4), 2024 | 3 | 2024 |
Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypes AX Maihofer, A Ratanatharathorn, SMJ Hemmings, KH Costenbader, ... Translational Psychiatry 14 (1), 172, 2024 | | 2024 |
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes G Huguet, T Renne, C Poulain, A Dubuc, K Kumar, S Kazem, ... bioRxiv, 2024.04. 16.589618, 2024 | | 2024 |
Interactions of rare copy number variations with polygenic risk scores in psychiatric disorders and quantitative traits M Klein, O Shanta, O Hong, J MacDonald, B Thiruvahindrapuram, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 489-490, 2024 | | 2024 |
Neurocognitive Profiles of 22q11. 2 and 16p11. 2 Deletions and Duplications R Gur, C Bearden, S Jacquemont, K Jizi, M van den Bree, J Vorstman, ... | | 2023 |
W56. UNRAVELING THE IMPACT OF GENOMIC VARIATIONS ON COGNITIVE ABILITY ACROSS THE HUMAN CORTEX: INSIGHTS FROM GENE EXPRESSION AND COPY NUMBER VARIANTS K Kumar, S Kazem, G Huguet, T Renne, B Engchuan, O Shanta, ... European Neuropsychopharmacology 75, S133, 2023 | | 2023 |
70. GENE-BASED ANALYSIS OF RARE CNVS ACROSS SIX PSYCHIATRIC DISORDERS IDENTIFIES COMMON BIOLOGICAL COMPONENTS BUT DISTINCTLY DIFFERENT GENETIC EFFECTS IN AUTISM AND SCHIZOPHRENIA W Engchuan, B Thiruvahindrapuram, JR MacDonald, O Shanta, K Kumar, ... European Neuropsychopharmacology 75, S93-S94, 2023 | | 2023 |
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions EA Maury, MA Sherman, G Genovese, TG Gilgenast, T Kamath, SJ Burris, ... Cell Genomics 3 (8), 2023 | 7 | 2023 |
Control-independent mosaic single nucleotide variant detection with DeepMosaic X Yang, X Xu, MW Breuss, D Antaki, LL Ball, C Chung, J Shen, C Li, ... Nature biotechnology 41 (6), 870-877, 2023 | 14 | 2023 |
The relationship of attention-deficit/hyperactivity disorder with posttraumatic stress disorder: a two-sample mendelian randomization and population-based sibling comparison study FR Wendt, M Garcia-Argibay, B Cabrera-Mendoza, UA Valdimarsdóttir, ... Biological psychiatry 93 (4), 362-369, 2023 | 17 | 2023 |
Genome-wide association of copy number variants across six major psychiatric disorders reveals genotype-phenotype relationships of rare variants O Shanta University of California, San Diego, 2023 | | 2023 |
Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism R Corominas, X Yang, GN Lin, S Kang, Y Shen, L Ghamsari, M Broly, ... Nature communications 14, 2023 | | 2023 |
Rare copy number variation in posttraumatic stress disorder AX Maihofer, W Engchuan, G Huguet, M Klein, JR MacDonald, O Shanta, ... Molecular psychiatry 27 (12), 5062-5069, 2022 | 4 | 2022 |
Genomic architecture of autism from comprehensive whole-genome sequence annotation B Trost, B Thiruvahindrapuram, AJS Chan, W Engchuan, ... Cell 185 (23), 4409-4427. e18, 2022 | 94 | 2022 |
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p DJ Weiner, E Ling, S Erdin, DJC Tai, R Yadav, J Grove, JM Fu, A Nadig, ... Nature genetics 54 (11), 1630-1639, 2022 | 18 | 2022 |
Characterization of the combined effects of rare variants and polygenic risk by whole genome analysis of psychiatric disorders and quantitative traits J Sebat European Neuropsychopharmacology 63, e315, 2022 | 1 | 2022 |
34. A GENOME-WIDE ASSOCIATION STUDY OF COPY NUMBER VARIATION ACROSS MAJOR PSYCHIATRIC DISORDERS IN 500,000 INDIVIDUALS O Shanta, M Klein, W Engchuan, J MacDonald, B Thiruvahindrapuram, ... European Neuropsychopharmacology 63, e63-e64, 2022 | | 2022 |
INTERACTIONS OF RARE CNVS WITH POLYGENIC RISK SCORES IN PSYCHIATRIC DISORDERS AND QUANTITATIVE TRAITS M Klein, O Shanta, O Hong, J MacDonald, B Thiruvahindrapuram, ... European Neuropsychopharmacology 63, e43, 2022 | | 2022 |
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex D Antaki, J Guevara, AX Maihofer, M Klein, M Gujral, J Grove, CE Carey, ... Nature genetics 54 (9), 1284-1292, 2022 | 105 | 2022 |
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex D Antaki, J Guevara, AX Maihofer, M Klein, M Gujral, J Grove, CE Carey, ... Nature genetics 54 (8), 1259, 2022 | 2 | 2022 |