Analysis of protein-coding genetic variation in 60,706 humans M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ... Nature 536 (7616), 285-291, 2016 | 7145 | 2016 |
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ... Nature genetics 51 (1), 63-75, 2019 | 721 | 2019 |
Identification of common genetic risk variants for autism spectrum disorder J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ... Nature genetics 51 (3), 431-444, 2019 | 455 | 2019 |
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 | 418 | 2017 |
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population EB Robinson, B St Pourcain, V Anttila, JA Kosmicki, B Bulik-Sullivan, ... Nature genetics 48 (5), 552-555, 2016 | 281 | 2016 |
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 |
Detecting autozygosity through runs of homozygosity: a comparison of three autozygosity detection algorithms DP Howrigan, MA Simonson, MC Keller BMC genomics 12 (1), 460, 2011 | 217 | 2011 |
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples JA Kosmicki, KE Samocha, DP Howrigan, SJ Sanders, K Slowikowski, ... Nature genetics 49 (4), 504, 2017 | 195 | 2017 |
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 |
Humor as a mental fitness indicator DP Howrigan, KB MacDonald Evolutionary Psychology 6 (4), 147470490800600411, 2008 | 113 | 2008 |
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor MC Keller, MA Simonson, S Ripke, BM Neale, PV Gejman, DP Howrigan, ... PLoS Genet 8 (4), e1002656, 2012 | 111 | 2012 |
Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation JC Bis, X Jian, BW Kunkle, Y Chen, KL Hamilton-Nelson, WS Bush, ... Molecular psychiatry 25 (8), 1859-1875, 2020 | 92 | 2020 |
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ... Biological psychiatry 83 (12), 1044-1053, 2018 | 89 | 2018 |
The psychometric assessment of human life history strategy: A meta-analytic construct validation. AJ Figueredo, PSA Wolf, SG Olderbak, PR Gladden, HBF Fernandes, ... Evolutionary Behavioral Sciences 8 (3), 148, 2014 | 88 | 2014 |
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population A Ganna, G Genovese, DP Howrigan, A Byrnes, MI Kurki, SM Zekavat, ... Nature neuroscience 19 (12), 1563-1565, 2016 | 80 | 2016 |
SynGO: an evidence-based, expert-curated knowledge base for the synapse F Koopmans, P van Nierop, M Andres-Alonso, A Byrnes, T Cijsouw, ... Neuron 103 (2), 217-234. e4, 2019 | 72 | 2019 |
Common risk variants identified in autism spectrum disorder J Grove, S Ripke, TD Als, M Mattheisen, R Walters, H Won, J Pallesen, ... BioRxiv, 224774, 2017 | 72 | 2017 |
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects AA Regier, Y Farjoun, DE Larson, O Krasheninina, HM Kang, ... Nature communications 9 (1), 1-8, 2018 | 66 | 2018 |
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 61 | 2019 |