| A forkhead-domain gene is mutated in a severe speech and language disorder CSL Lai, SE Fisher, JA Hurst, F Vargha-Khadem, AP Monaco Nature 413 (6855), 519-523, 2001 | 2810 | 2001 |
| Molecular evolution of FOXP2, a gene involved in speech and language W Enard, M Przeworski, SE Fisher, CSL Lai, V Wiebe, T Kitano, ... Nature 418 (6900), 869-872, 2002 | 2194 | 2002 |
| Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz, S Girirajan, ... Nature genetics 43 (6), 585-589, 2011 | 1341 | 2011 |
| A functional genetic link between distinct developmental language disorders SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ... New England Journal of Medicine 359 (22), 2337-2345, 2008 | 823 | 2008 |
| Localisation of a gene implicated in a severe speech and language disorder SE Fisher, F Vargha-Khadem, KE Watkins, AP Monaco, ME Pembrey Nature genetics 18 (2), 168-170, 1998 | 796 | 1998 |
| A common molecular basis for three inherited kidney stone diseases SE Lloyd, SHS Pearce, SE Fisher, K Steinmeyer, B Schwappach, ... Nature 379 (6564), 445-449, 1996 | 786 | 1996 |
| Common genetic variants influence human subcortical brain structures DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ... Nature 520 (7546), 224-229, 2015 | 770 | 2015 |
| A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice W Enard, S Gehre, K Hammerschmidt, SM Hölter, T Blass, M Somel, ... Cell 137 (5), 961-971, 2009 | 641 | 2009 |
| FOXP2 as a molecular window into speech and language SE Fisher, C Scharff Trends in Genetics 25 (4), 166-177, 2009 | 622 | 2009 |
| The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data PM Thompson, JL Stein, SE Medland, DP Hibar, AA Vasquez, ... Brain imaging and behavior 8, 153-182, 2014 | 595 | 2014 |
| Developmental dyslexia: genetic dissection of a complex cognitive trait SE Fisher, JC DeFries Nature Reviews Neuroscience 3 (10), 767-780, 2002 | 565 | 2002 |
| Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits KD MacDermot, E Bonora, N Sykes, AM Coupe, CSL Lai, SC Vernes, ... The American Journal of Human Genetics 76 (6), 1074-1080, 2005 | 544 | 2005 |
| FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder CSL Lai, D Gerrelli, AP Monaco, SE Fisher, AJ Copp Brain 126 (11), 2455-2462, 2003 | 502 | 2003 |
| LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ... Molecular psychiatry 12 (12), 1129-1139, 2007 | 462 | 2007 |
| A genomewide scan for loci involved in attention-deficit/hyperactivity disorder SE Fisher, C Francks, JT McCracken, JJ McGough, AJ Marlow, ... The American Journal of Human Genetics 70 (5), 1183-1196, 2002 | 430 | 2002 |
| A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia SE Fisher, AJ Marlow, J Lamb, E Maestrini, DF Williams, AJ Richardson, ... The American journal of human genetics 64 (1), 146-156, 1999 | 407 | 1999 |
| The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 388 | 2020 |
| FOXP2 in focus: what can genes tell us about speech and language? GF Marcus, SE Fisher Trends in cognitive sciences 7 (6), 257-262, 2003 | 384 | 2003 |
| A genomewide scan identifies two novel loci involved in specific language impairment Sli Consortium The American Journal of Human Genetics 70 (2), 384-398, 2002 | 368 | 2002 |
| Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia SE Fisher, C Francks, AJ Marlow, IL MacPhie, DF Newbury, LR Cardon, ... Nature genetics 30 (1), 86-91, 2002 | 368 | 2002 |
Anthony P MonacoPresident, Tufts UniversityVerified email at tufts.edu
