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Jonathan Sebat
Jonathan Sebat
Professor of Psychiatry and Cellular & Molecular Medicine, UC San Diego
在 ucsd.edu 的电子邮件经过验证 - 首页
标题
引用次数
年份
" Gene mutations and cognitive delay": Response.
JM McClellan, T Wals, SE McCarthy, MC King, J Sebat
American Assn for the Advancement of Science, 2008
2008
[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
22019
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
1202019
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
88052010
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
1052022
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
832000
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
32013
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
6622010
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
32024
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
3782007
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