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[S10]: High‐resolution analysis of genome copy number variation in autism J Sebat, B Lakshmi, J Troge, C Martin, S Spence, D Ledbetter, TC Gilliam, ... International Journal of Developmental Neuroscience 24 (8), 474-474, 2006 | | 2006 |
11,364 Whole-Genome Sequences in the Cloud for Autism Spectrum Disorder Research B Trost, D Hartley, B Thiruvahindrapuram, J Whitney, R Patel, J Howe, ... INSAR 2020 Virtual Meeting, 0 | | |
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 |
48. A PHENOTYPIC SPECTRUM OF AUTISM IS ATTRIBUTABLE TO THE COMBINED EFFECTS OF RARE VARIANTS, POLYGENIC RISK AND SEX J Sebat, D Antaki, AX Maihofer, M Klein, J Guevara, J Grove, C Carey, ... European Neuropsychopharmacology 51, e66, 2021 | | 2021 |
6. CONTRIBUTION OF COPY NUMBER VARIANTS TO SCHIZOPHRENIA IN EAST ASIAN POPULATIONS Q Feng, B Thiruvahindrapuram, D Howrigan, J Sebat, T Ge, H Huang European Neuropsychopharmacology 51, e42-e43, 2021 | | 2021 |
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 |
84 16P11. 2 Patient-derived cerebral organoids show migration and synaptic defects J Urresti, PM Losada, P Zhang, PD Negraes, N Kyung-Yu, C Trujillo, ... European Neuropsychopharmacology 29, S106, 2019 | 2 | 2019 |
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics … CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ... bioRxiv, 040493, 2016 | | 2016 |
A CONTRIBUTION OF RARE COPY NUMBER VARIATIONS TO THE DEVELOPMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER: GENOME-WIDE META-ANALYSES IN 12548 INDIVIDUALS T Zayats, J Martin, B Thiruvahindrapuram, Z Wang, D Howrigan, O Shanta, ... European Neuropsychopharmacology 29, S1042, 2019 | | 2019 |
A framework for the investigation of rare genetic disorders in neuropsychiatry SJ Sanders, M Sahin, J Hostyk, A Thurm, S Jacquemont, P Avillach, ... Nature medicine 25 (10), 1477-1487, 2019 | 120 | 2019 |
A map of human genome variation from population scale sequencing 1000 Genomes Project Consortium Nature 467 (7319), 1061, 2010 | 8805 | 2010 |
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 |
A Pseudomonas stutzeri gene cluster encoding the biosynthesis of the CCI-dechlorination agent pyridine-2, 6-bis (thiocarboxylic acid) JL Sebat, TL Green, CH Lee Environmental Microbiology 2 (4), 407-416, 2000 | | 2000 |
A Pseudomonas stutzeri gene cluster encoding the biosynthesis of the CCl4‐dechlorination agent pyridine‐2,6‐bis(thiocarboxylic acid) TA Lewis, MS Cortese, JL Sebat, TL Green, CH Lee, RL Crawford Environmental Microbiology 2 (4), 407-416, 2000 | 83 | 2000 |
A rare deletion at distal 16p11. 2 is implicated in schizophrenia S Guha, E Rees, A Darvasi, D Ivanov, M Ikeda, SE Bergen, ... JAMA psychiatry (Chicago, Ill.) 70 (3), 253, 2013 | 3 | 2013 |
A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ... Nature genetics 42 (3), 203-209, 2010 | 662 | 2010 |
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 |
A systems biology approach to unravel the underlying functional modules involved in autism R Corominas, S Kang, GN Lin, X Yang, Y Shen, P Braun, J Sebat, DE Hill, ... Department of Bioengineering and Bioinformatics of MV Lomonosov Moscow State …, 2011 | | 2011 |
A unified genetic theory for sporadic and inherited autism X Zhao, A Leotta, V Kustanovich, C Lajonchere, DH Geschwind, K Law, ... Proceedings of the National Academy of Sciences 104 (31), 12831-12836, 2007 | 378 | 2007 |