| Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ... Nature 515 (7526), 209-215, 2014 | 2761 | 2014 |
| The contribution of de novo coding mutations to autism spectrum disorder I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ... Nature 515 (7526), 216-221, 2014 | 2604 | 2014 |
| Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013 | 2346 | 2013 |
| De novo mutations revealed by whole-exome sequencing are strongly associated with autism SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ... Nature 485 (7397), 237-241, 2012 | 2345 | 2012 |
| 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 | 1757 | 2020 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1654 | 2007 |
| Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ... Neuron 70 (5), 863-885, 2011 | 1484 | 2011 |
| Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ... Neuron 87 (6), 1215-1233, 2015 | 1482 | 2015 |
| Autism spectrum disorder C Lord, TS Brugha, T Charman, J Cusack, G Dumas, T Frazier, EJH Jones, ... Nature reviews Disease primers 6 (1), 1-23, 2020 | 1345 | 2020 |
| Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ... Science 310 (5746), 317-320, 2005 | 1226 | 2005 |
| Common genetic variants on 5p14. 1 associate with autism spectrum disorders K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ... Nature 459 (7246), 528-533, 2009 | 1134 | 2009 |
| Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ... Cell 155 (5), 997-1007, 2013 | 965 | 2013 |
| De novo mutations in histone-modifying genes in congenital heart disease S Zaidi, M Choi, H Wakimoto, L Ma, J Jiang, JD Overton, ... Nature 498 (7453), 220-223, 2013 | 949 | 2013 |
| Rare independent mutations in renal salt handling genes contribute to blood pressure variation W Ji, JN Foo, BJ O'Roak, H Zhao, MG Larson, DB Simon, C Newton-Cheh, ... Nature genetics 40 (5), 592-599, 2008 | 945 | 2008 |
| Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ... Science 339 (6123), 1077-1080, 2013 | 853 | 2013 |
| Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder F Volkmar, M Siegel, M Woodbury-Smith, B King, J McCracken, M State Journal of the American Academy of Child & Adolescent Psychiatry 53 (2), 237-257, 2014 | 744 | 2014 |
| Functional and evolutionary insights into human brain development through global transcriptome analysis MB Johnson, YI Kawasawa, CE Mason, Ž Krsnik, G Coppola, ... Neuron 62 (4), 494-509, 2009 | 660 | 2009 |
| Integrative functional genomic analysis of human brain development and neuropsychiatric risks M Li, G Santpere, Y Imamura Kawasawa, OV Evgrafov, FO Gulden, ... Science 362 (6420), eaat7615, 2018 | 650 | 2018 |
| Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations K Bilgüvar, AK Öztürk, A Louvi, KY Kwan, M Choi, B Tatlı, D Yalnızoğlu, ... Nature 467 (7312), 207-210, 2010 | 622 | 2010 |
| Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders B Bakkaloglu, BJ O'Roak, A Louvi, AR Gupta, JF Abelson, TM Morgan, ... The American Journal of Human Genetics 82 (1), 165-173, 2008 | 614 | 2008 |
Stephan J. SandersProfessor, Oxford and UCSF在 ucsf.edu 的电子邮件经过验证
