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| Synaptic, transcriptional and chromatin genes disrupted in autism S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ... Nature 515 (7526), 209-215, 2014 | 1797 | 2014 |
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| 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 | 1623 | 2014 |
| 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 | 1206 | 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 | 889 | 2015 |
| Most genetic risk for autism resides with common variation T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ... Nature genetics 46 (8), 881-885, 2014 | 866 | 2014 |
| A framework for the interpretation of de novo mutation in human disease KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ... Nature genetics 46 (9), 944-950, 2014 | 774 | 2014 |
| Combined results of searches for the standard model Higgs boson in pp collisions at s= 7 TeV S Chatrchyan, V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, ... Physics Letters B 710 (1), 26-48, 2012 | 707 | 2012 |
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| 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 | 687 | 2013 |
| Search for the standard model Higgs boson produced in association with a or a boson and decaying to bottom quarks S Chatrchyan, V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, ... Physical Review D 89 (1), 012003, 2014 | 666 | 2014 |
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| 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 | 520 | 2010 |
| De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies J Homsy, S Zaidi, Y Shen, JS Ware, KE Samocha, KJ Karczewski, ... Science 350 (6265), 1262-1266, 2015 | 418 | 2015 |
| Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority AK Halladay, S Bishop, JN Constantino, AM Daniels, K Koenig, K Palmer, ... Molecular autism 6 (1), 1-5, 2015 | 415 | 2015 |
| Search for physics beyond the standard model in dilepton mass spectra in proton-proton collisions at TeV V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, T Bergauer, ... Journal of High Energy Physics 2015 (4), 25, 2015 | 397 | 2015 |
| Using whole-exome sequencing to identify inherited causes of autism WY Timothy, MH Chahrour, ME Coulter, S Jiralerspong, K Okamura-Ikeda, ... Neuron 77 (2), 259-273, 2013 | 394 | 2013 |
| 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 | 377 | 2020 |
| Search for a light charged Higgs boson in top quark decays in pp collisions at S Chatrchyan, V Khachatryan, AM Sirunyan, A Tumasyan, W Adam, ... Journal of High Energy Physics 2012 (7), 1-38, 2012 | 374 | 2012 |
Matthew StateucsfVerified email at ucsf.edu
