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 | 1822 | 2012 |
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ... Nature genetics 45 (9), 984, 2013 | 1724 | 2013 |
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 | 1707 | 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 | 1526 | 2014 |
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 | 837 | 2015 |
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 | 666 | 2013 |
Common genetic variants, acting additively, are a major source of risk for autism L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ... Molecular autism 3 (1), 1-13, 2012 | 359 | 2012 |
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways T Network, C O'Dushlaine, L Rossin, PH Lee, L Duncan, NN Parikshak, ... Nature neuroscience 18 (2), 199-209, 2015 | 286 | 2015 |
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 | 273 | 2020 |
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ... Nature genetics 49 (7), 978-985, 2017 | 238 | 2017 |
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment J Cotney, RA Muhle, SJ Sanders, L Liu, AJ Willsey, W Niu, W Liu, L Klei, ... Nature communications 6 (1), 1-11, 2015 | 227 | 2015 |
The psychencode project S Akbarian, C Liu, JA Knowles, FM Vaccarino, PJ Farnham, GE Crawford, ... Nature neuroscience 18 (12), 1707, 2015 | 175 | 2015 |
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data JT Glessner, AG Bick, K Ito, JG Homsy, L Rodriguez-Murillo, M Fromer, ... Circulation research 115 (10), 884-896, 2014 | 172 | 2014 |
Complete haplotype sequence of the human immunoglobulin heavy-chain variable, diversity, and joining genes and characterization of allelic and copy-number variation CT Watson, KM Steinberg, J Huddleston, RL Warren, M Malig, J Schein, ... The American Journal of Human Genetics 92 (4), 530-546, 2013 | 168 | 2013 |
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ... Cell 179 (7), 1469-1482. e11, 2019 | 166* | 2019 |
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ... The American Journal of Human Genetics 96 (2), 283-294, 2015 | 144 | 2015 |
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia Molecular autism 8, 1-17, 2017 | 132 | 2017 |
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? P Chaste, L Klei, SJ Sanders, V Hus, MT Murtha, JK Lowe, AJ Willsey, ... Biological psychiatry 77 (9), 775-784, 2015 | 128 | 2015 |
Autism spectrum disorders: from genes to neurobiology AJ Willsey, MW State Current opinion in neurobiology 30, 92-99, 2015 | 126 | 2015 |
Using large clinical data sets to infer pathogenicity for rare copy number variants in autism cohorts D Moreno-De-Luca, SJ Sanders, AJ Willsey, JG Mulle, JK Lowe, ... Molecular psychiatry 18 (10), 1090-1095, 2013 | 125 | 2013 |