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| 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 | 2366 | 2019 |
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| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium Science (New York, NY) 360 (6395), eaap8757, 2018 | 722 | 2018 |
| Examining and interpreting the female protective effect against autistic behavior EB Robinson, P Lichtenstein, H Anckarsäter, F Happé, A Ronald Proceedings of the National Academy of Sciences 110 (13), 5258-5262, 2013 | 604 | 2013 |
| 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 | 549 | 2017 |
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| 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 | 457 | 2016 |
| Evidence that autistic traits show the same etiology in the general population and at the quantitative extremes (5%, 2.5%, and 1%) EB Robinson, KC Koenen, MC McCormick, K Munir, V Hallett, F Happé, ... Archives of general psychiatry 68 (11), 1113-1121, 2011 | 392 | 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), 504-510, 2017 | 363 | 2017 |
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Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerified email at atgu.mgh.harvard.edu
