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| The polygenic and monogenic basis of blood traits and diseases D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ... Cell 182 (5), 1214-1231. e11, 2020 | 468 | 2020 |
| Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants FK Satterstrom, RK Walters, T Singh, EM Wigdor, F Lescai, D Demontis, ... Nature neuroscience 22 (12), 1961-1965, 2019 | 209 | 2019 |
| Paternal-age-related de novo mutations and risk for five disorders JL Taylor, JCPG Debost, SU Morton, EM Wigdor, HO Heyne, D Lal, ... Nature Communications 10 (1), 3043, 2019 | 83 | 2019 |
| Pregnancy outcomes in women with spinal cord lesions L Sterling, J Keunen, E Wigdor, M Sermer, C Maxwell Journal of Obstetrics and Gynaecology Canada 35 (1), 39-43, 2013 | 77 | 2013 |
| The female protective effect against autism spectrum disorder EM Wigdor, DJ Weiner, J Grove, JM Fu, WK Thompson, CE Carey, ... Cell Genomics 2 (6), 2022 | 59 | 2022 |
| Analysis of genetic dominance in the UK Biobank DS Palmer, W Zhou, L Abbott, EM Wigdor, N Baya, C Churchhouse, ... Science 379 (6639), 1341-1348, 2023 | 27 | 2023 |
| Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes V Warrier, EM Stauffer, QQ Huang, EM Wigdor, EAW Slob, J Seidlitz, ... Nature genetics 55 (9), 1483-1493, 2023 | 26* | 2023 |
| AlphaMissense is better correlated with functional assays of missense impact than earlier prediction algorithms A Ljungdahl, S Kohani, NF Page, ES Wells, EM Wigdor, S Dong, ... BioRxiv, 2023 | 6 | 2023 |
| Thalamocortical organoids enable in vitro modeling of 22q11. 2 microdeletion associated with neuropsychiatric disorders D Shin, CN Kim, J Ross, KM Hennick, SR Wu, N Paranjape, R Leonard, ... Cell Stem Cell 31 (3), 421-432. e8, 2024 | 3 | 2024 |
| Investigating the role of common cis-regulatory variants in modifying penetrance of putatively damaging, inherited variants in severe neurodevelopmental disorders EM Wigdor, KE Samocha, RY Eberhardt, VK Chundru, HV Firth, CF Wright, ... Scientific Reports 14 (1), 8708, 2024 | 2 | 2024 |
| Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populations VK Chundru, Z Zhang, K Walter, S Lindsay, P Danecek, RY Eberhardt, ... medRxiv, 2023.07. 24.23293070, 2023 | 1 | 2023 |
| Genome-wide association meta-analysis of age at onset of walking A Gui, A Hollowell, EM Wigdor, MJ Morgan, LJ Hannigan, EC Corfield, ... medRxiv, 2024.05. 07.24306845, 2024 | | 2024 |
| Dissecting the contribution of common variants to risk of rare neurodevelopmental conditions QQ Huang, EM Wigdor, P Campbell, DS Malawsky, KE Samocha, ... medRxiv, 2024.03. 05.24303772, 2024 | | 2024 |
| Common genetic variation and spliceosome variants in rare developmental disorders E Wigdor | | 2022 |
