Jonathan Sebat
Jonathan Sebat
Professor of Psychiatry & Cellular and Molecular Medicine, UCSD
ucsd.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
74252010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
69972012
Strong association of de novo copy number mutations with autism
J Sebat, B Lakshmi, D Malhotra, J Troge, C Lese-Martin, T Walsh, ...
Science 316 (5823), 445-449, 2007
29762007
Large-scale copy number polymorphism in the human genome
J Sebat, B Lakshmi, J Troge, J Alexander, J Young, P Lundin, S Månér, ...
Science 305 (5683), 525-528, 2004
28862004
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
T Walsh, JM McClellan, SE McCarthy, AM Addington, SB Pierce, ...
science 320 (5875), 539-543, 2008
19032008
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
15082015
Modelling schizophrenia using human induced pluripotent stem cells
KJ Brennand, A Simone, J Jou, C Gelboin-Burkhart, N Tran, S Sangar, ...
Nature 473 (7346), 221-225, 2011
13172011
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
10762011
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
M Alarcón, BS Abrahams, JL Stone, JA Duvall, JV Perederiy, JM Bomar, ...
The American Journal of Human Genetics 82 (1), 150-159, 2008
8862008
CNVs: harbingers of a rare variant revolution in psychiatric genetics
D Malhotra, J Sebat
Cell 148 (6), 1223-1241, 2012
7842012
Recurrent rearrangements of chromosome 1q21. 1 and variable pediatric phenotypes
HC Mefford, AJ Sharp, C Baker, A Itsara, Z Jiang, K Buysse, S Huang, ...
New England Journal of Medicine 359 (16), 1685-1699, 2008
7442008
Microduplications of 16p11. 2 are associated with schizophrenia
SE McCarthy, V Makarov, G Kirov, AM Addington, J McClellan, S Yoon, ...
Nature genetics 41 (11), 1223-1227, 2009
7102009
Sensitive and accurate detection of copy number variants using read depth of coverage
S Yoon, Z Xuan, V Makarov, K Ye, J Sebat
Genome research 19 (9), 1586-1592, 2009
6232009
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
5712011
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
5682010
Whole-genome sequencing in autism identifies hot spots for de novo germline mutation
JJ Michaelson, Y Shi, M Gujral, H Zheng, D Malhotra, X Jin, M Jian, G Liu, ...
Cell 151 (7), 1431-1442, 2012
5452012
Genomewide association studies: history, rationale, and prospects for psychiatric disorders
Psychiatric GWAS Consortium Coordinating Committee
American Journal of Psychiatry 166 (5), 540-556, 2009
5372009
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation
R Lucito, J Healy, J Alexander, A Reiner, D Esposito, M Chi, L Rodgers, ...
Genome research 13 (10), 2291-2305, 2003
5182003
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
Nature genetics 49 (1), 27-35, 2017
4602017
Integrative annotation of variants from 1092 humans: application to cancer genomics
E Khurana, Y Fu, V Colonna, XJ Mu, HM Kang, T Lappalainen, A Sboner, ...
Science 342 (6154), 2013
3612013
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20