FOXP2 as a molecular window into speech and languageFISHER, Simon E; SCHARFF, Constance.Trends in genetics (Regular ed.). 2009, Vol 25, Num 4, pp 166-177, issn 0168-9525, 12 p.Article

Tangled webs : Tracing the connections between genes and cognitionFISHER, Simon E.Cognition. 2006, Vol 101, Num 2, pp 270-297, issn 0010-0277, 28 p.Article

Genes, cognition and dyslexia : learning to read the genomeFISHER, Simon E; FRANCKS, Clyde.Trends in cognitive sciences (Regular ed.). 2006, Vol 10, Num 6, pp 250-257, issn 1364-6613, 8 p.Article

The eloquent ape : genes, brains and the evolution of languageFISHER, Simon E; MARCUS, Gary F.Nature reviews. Genetics (Print). 2006, Vol 7, Num 1, pp 9-20, issn 1471-0056, 12 p.Article

Le point sur FOXP2 : que peuvent nous enseigner les gènes sur la parole et le langage ?MARCUS, Gary F; FISHER, Simon E.Médecine & enfance. 2004, Vol 24, Num 5, pp 304-311, issn 0291-0233, 8 p.Article

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language ImpairmentNEWBURY, Dianne F; WINCHESTER, Laura; GOODYER, Ian M et al.American journal of human genetics. 2009, Vol 85, Num 2, pp 264-272, issn 0002-9297, 9 p.Article

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutationsO'ROAK, Brian J; DERIZIOTIS, Pelagia; RIEDER, Mark J et al.Nature genetics. 2011, Vol 43, Num 6, pp 585-589, issn 1061-4036, 5 p.Article

Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human BrainSPITERI, Elizabeth; KONOPKA, Genevieve; COPPOLA, Giovanni et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1144-1157, issn 0002-9297, 14 p.Article

Deciphering the genetic basis of speech and language disordersFISHER, Simon E; LAI, Cecilia S. L; MONACO, Anthony P et al.Annual review of neuroscience. 2003, Vol 26, pp 57-80, issn 0147-006X, 24 p.Article

Modified sound-evoked brainstem potentials in Foxp2 mutant miceKURT, Simone; GROSZER, Matthias; FISHER, Simon E et al.Brain research. 2009, Vol 1289, pp 30-36, issn 0006-8993, 7 p.Article

Measurement and Genetics of Human Subcortical and Hippocampal Asymmetries in Large DatasetsGUADALUPE, Tulio; ZWIERS, Marcel P; VÖLZKE, Henry et al.Human brain mapping. 2014, Vol 35, Num 7, pp 3277-3289, issn 1065-9471, 13 p.Article

A Functional Genetic Link between Distinct Developmental Language DisordersVERNES, Sonja C; NEWBURY, Dianne F; MONACO, Anthony P et al.The New England journal of medicine. 2008, Vol 359, Num 22, pp 2337-2345, issn 0028-4793, 9 p.Article

Attention deficit hyperactivity disorder: Fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11OGDIE, Matthew N; FISHER, Simon E; NELSON, Stanley F et al.American journal of human genetics. 2004, Vol 75, Num 4, pp 661-668, issn 0002-9297, 8 p.Article

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autismSMALLEY, Susan L; KUSTANOVICH, Vlad; CANTOR, Rita M et al.American journal of human genetics. 2002, Vol 71, Num 4, pp 959-963, issn 0002-9297, 5 p.Article

A forkhead-domain gene is mutated in a severe speech and language disorderLAI, Cecllia S. L; FISHER, Simon E; HURST, Jane A et al.Nature (London). 2001, Vol 413, Num 6855, pp 519-523, issn 0028-0836Article

The DISC1 promoter: characterization and regulation by FOXP2WALKER, Rosie M; HILL, Alison E; FISHER, Simon E et al.Human molecular genetics (Print). 2012, Vol 21, Num 13, pp 2862-2872, issn 0964-6906, 11 p.Article

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxiaVERNES, Sonja C; MACDERMOT, Kay D; MONACO, Anthony P et al.European journal of human genetics. 2009, Vol 17, Num 10, pp 1354-1358, issn 1018-4813, 5 p.Article

High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language DisordersVERNES, Sonja C; SPITERI, Elizabeth; NICOD, Jérome et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1232-1250, issn 0002-9297, 19 p.Article

Functional genetic analysis of mutations implicated in a human speech and language disorderVERNES, Sonja C; NICOD, Jérome; ELAHI, Fanny M et al.Human molecular genetics (Print). 2006, Vol 15, Num 21, pp 3154-3167, issn 0964-6906, 14 p.Article

Familial and genetic effects on motor coordination, laterality, and reading-related cognitionFRANCKS, Clyde; FISHER, Simon E; MARLOW, Angela J et al.The American journal of psychiatry. 2003, Vol 160, Num 11, pp 1970-1977, issn 0002-953X, 8 p.Article

Molecular evolution of FOXP2, a gene involved in speech and languageENARD, Wolfgang; PRZEWORSKI, Molly; FISHER, Simon E et al.Nature (London). 2002, Vol 418, Num 6900, pp 869-872, issn 0028-0836Article

No effect of schizophrenia risk genes MIR137, TCF4, and ZNF804A on macroscopic brain structureCOUSIJN, Helena; EISSING, Marc; FERNADEZ, Guillen et al.Schizophrenia research. 2014, Vol 159, Num 2-3, pp 329-332, issn 0920-9964, 4 p.Article

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complexROLL, Patrice; VERNES, Sonja C; SZEPETOWSKI, Pierre et al.Human molecular genetics (Print). 2010, Vol 19, Num 24, pp 4848-4860, issn 0964-6906, 13 p.Article

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficitsMACDERMOT, Kay D; BONORA, Elena; FISHER, Simon E et al.American journal of human genetics. 2005, Vol 76, Num 6, pp 1074-1080, issn 0002-9297, 7 p.Article

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11FRANCKS, Clyde; DELISI, Lynn E; SHAW, Sarah H et al.Human molecular genetics (Print). 2003, Vol 12, Num 24, pp 3225-3230, issn 0964-6906, 6 p.Article