|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, 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, 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, 2011
|A common molecular basis for three inherited kidney stone diseases|
SE Lloyd, SHS Pearce, SE Fisher, K Steinmeyer, B Schwappach, ...
Nature 379 (6564), 445, 1996
|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
|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, 1998
|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
|FOXP2 as a molecular window into speech and language|
SE Fisher, C Scharff
Trends in Genetics 25 (4), 166-177, 2009
|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
|Developmental dyslexia: genetic dissection of a complex cognitive trait|
SE Fisher, JC DeFries
Nature Reviews Neuroscience 3 (10), 767, 2002
|Common genetic variants influence human subcortical brain structures|
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224, 2015
|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
|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
|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, 2007
|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
|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
|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, 2001
|A genomewide scan identifies two novel loci involved in specific language impairment|
The American Journal of Human Genetics 70 (2), 384-398, 2002
|FOXP2 is not a major susceptibility gene for autism or specific language impairment|
DF Newbury, E Bonora, JA Lamb, SE Fisher, CSL Lai, G Baird, L Jannoun, ...
The American Journal of Human Genetics 70 (5), 1318-1327, 2002
|Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism|
SL Smalley, V Kustanovich, SL Minassian, JL Stone, MN Ogdie, ...
The American Journal of Human Genetics 71 (4), 959-963, 2002