| Identification and evaluation of children with autism spectrum disorders CP Johnson, SM Myers Pediatrics 120 (5), 1183-1215, 2007 | 3071 | 2007 |
| Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals JJ Lee, R Wedow, A Okbay, E Kong, O Maghzian, M Zacher, ... Nature genetics 50 (8), 1112-1121, 2018 | 2086 | 2018 |
| 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 | 1501 | 2015 |
| Genome-wide association study identifies 74 loci associated with educational attainment A Okbay, JP Beauchamp, MA Fontana, JJ Lee, TH Pers, CA Rietveld, ... Nature 533 (7604), 539-542, 2016 | 1415 | 2016 |
| Identification, evaluation, and management of children with autism spectrum disorder SL Hyman, SE Levy, SM Myers, DZ Kuo, S Apkon, LF Davidson, ... Pediatrics 145 (1), 2020 | 1155 | 2020 |
| Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics … ER Riggs, EF Andersen, AM Cherry, S Kantarci, H Kearney, A Patel, ... Genetics in Medicine 22 (2), 245-257, 2020 | 1144 | 2020 |
| Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders S Srivastava, JA Love-Nichols, KA Dies, DH Ledbetter, CL Martin, ... Genetics in Medicine 21 (11), 2413-2421, 2019 | 490 | 2019 |
| Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the clinical genome resource NT Strande, ER Riggs, AH Buchanan, O Ceyhan-Birsoy, M DiStefano, ... The American Journal of Human Genetics 100 (6), 895-906, 2017 | 478 | 2017 |
| Developmental brain dysfunction: revival and expansion of old concepts based on new genetic evidence A Moreno-De-Luca, SM Myers, TD Challman, D Moreno-De-Luca, ... The Lancet Neurology 12 (4), 406-414, 2013 | 358 | 2013 |
| The genetic architecture of economic and political preferences DJ Benjamin, D Cesarini, MJHM Van Der Loos, CT Dawes, PD Koellinger, ... Proceedings of the National Academy of Sciences 109 (21), 8026-8031, 2012 | 357 | 2012 |
| SPARK: a US cohort of 50,000 families to accelerate autism research P Feliciano, AM Daniels, LAG Snyder, A Beaumont, A Camba, A Esler, ... Neuron 97 (3), 488-493, 2018 | 346 | 2018 |
| A megastudy of text-based nudges encouraging patients to get vaccinated at an upcoming doctor’s appointment KL Milkman, MS Patel, L Gandhi, HN Graci, DM Gromet, H Ho, JS Kay, ... Proceedings of the National Academy of Sciences 118 (20), e2101165118, 2021 | 323 | 2021 |
| Progress in understanding and treating SCN2A-mediated disorders SJ Sanders, AJ Campbell, JR Cottrell, RS Moller, FF Wagner, ... Trends in neurosciences 41 (7), 442-456, 2018 | 271 | 2018 |
| The cognitive and behavioral phenotype of the 16p11. 2 deletion in a clinically ascertained population E Hanson, R Bernier, K Porche, FI Jackson, RP Goin-Kochel, LAG Snyder, ... Biological psychiatry 77 (9), 785-793, 2015 | 253 | 2015 |
| Defining the effect of the 16p11. 2 duplication on cognition, behavior, and medical comorbidities D D’Angelo, S Lebon, Q Chen, S Martin-Brevet, LAG Snyder, L Hippolyte, ... JAMA psychiatry 73 (1), 20-30, 2016 | 237 | 2016 |
| Genetic insights into the causes and classification of the cerebral palsies A Moreno-De-Luca, DH Ledbetter, CL Martin The lancet neurology 11 (3), 283-292, 2012 | 235 | 2012 |
| A review of fragile X premutation disorders: expanding the psychiatric perspective. JA Bourgeois, SM Coffey, SM Rivera, D Hessl, LW Gane, F Tassone, ... Journal of Clinical Psychiatry 70 (6), 852, 2009 | 221 | 2009 |
| The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species KA Shefchek, NL Harris, M Gargano, N Matentzoglu, D Unni, M Brush, ... Nucleic acids research 48 (D1), D704-D715, 2020 | 213 | 2020 |
| Exome sequencing–based screening for BRCA1/2 expected pathogenic variants among adult biobank participants K Manickam, AH Buchanan, MLB Schwartz, MLG Hallquist, JL Williams, ... JAMA Network Open 1 (5), e182140-e182140, 2018 | 204 | 2018 |
| Penetrance and pleiotropy of polygenic risk scores for schizophrenia in 106,160 patients across four health care systems AB Zheutlin, J Dennis, R Karlsson Linnér, A Moscati, N Restrepo, ... American Journal of Psychiatry 176 (10), 846-855, 2019 | 198 | 2019 |
Christa Lese MartinChief Scientific Officer, Geisinger; Professor and Director, Autism & DevelopmentalVerified email at geisinger.edu