Simon E. Fisher

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 26	2014

Other Publications

Article	Year
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature genetics\| PubMed ID: 11743577	2002
A genomewide linkage screen for relative hand skill in sibling pairs. American journal of human genetics\| PubMed ID: 11774074	2002
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric genetics\| PubMed ID: 11901358	2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American journal of human genetics\| PubMed ID: 11923911	2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American journal of human genetics\| PubMed ID: 12187510	2002
Molecular evolution of FOXP2, a gene involved in speech and language. Nature\| PubMed ID: 12192408	2002
Developmental dyslexia: genetic dissection of a complex cognitive trait. Nature reviews. Neuroscience\| PubMed ID: 12360321	2002
Deciphering the genetic basis of speech and language disorders. Annual review of neuroscience\| PubMed ID: 12524432	2003
Use of multivariate linkage analysis for dissection of a complex cognitive trait. American journal of human genetics\| PubMed ID: 12587094	2003
Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American journal of human genetics\| PubMed ID: 12596796	2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American journal of human genetics\| PubMed ID: 12687500	2003
FOXP2 in focus: what can genes tell us about speech and language? Trends in cognitive sciences\| PubMed ID: 12804692	2003
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a journal of neurology\| PubMed ID: 12876151	2003
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human molecular genetics\| PubMed ID: 14583442	2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American journal of psychiatry\| PubMed ID: 14594743	2003
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11. American journal of human genetics\| PubMed ID: 15297934	2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American journal of human genetics\| PubMed ID: 15514892	2004
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American journal of human genetics\| PubMed ID: 15877281	2005
On genes, speech, and language. The New England journal of medicine\| PubMed ID: 16236736	2005
The eloquent ape: genes, brains and the evolution of language. Nature reviews. Genetics\| PubMed ID: 16369568	2006
Genes, cognition and dyslexia: learning to read the genome. Trends in cognitive sciences\| PubMed ID: 16675285	2006
Tangled webs: tracing the connections between genes and cognition. Cognition\| PubMed ID: 16764847	2006
Functional genetic analysis of mutations implicated in a human speech and language disorder. Human molecular genetics\| PubMed ID: 16984964	2006
Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language. The Journal of neuroscience : the official journal of the Society for Neuroscience\| PubMed ID: 17035521	2006
Molecular windows into speech and language disorders. Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP)\| PubMed ID: 17556856	2007
Generation of mice with a conditional Foxp2 null allele. Genesis (New York, N.Y. : 2000)\| PubMed ID: 17619227	2007
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain. American journal of human genetics\| PubMed ID: 17999357	2007
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders. American journal of human genetics\| PubMed ID: 17999362	2007
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Current biology : CB\| PubMed ID: 18328704	2008
A functional genetic link between distinct developmental language disorders. The New England journal of medicine\| PubMed ID: 18987363	2008
FOXP2 as a molecular window into speech and language. Trends in genetics : TIG\| PubMed ID: 19304338	2009
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG\| PubMed ID: 19352412	2009
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell\| PubMed ID: 19490899	2009
Modified sound-evoked brainstem potentials in Foxp2 mutant mice. Brain research\| PubMed ID: 19596273	2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American journal of human genetics\| PubMed ID: 19646677	2009
Unravelling neurogenetic networks implicated in developmental language disorders. Biochemical Society transactions\| PubMed ID: 19909259	2009
Genetic susceptibility to stuttering. The New England journal of medicine\| PubMed ID: 20147708	2010
Recent advances in the genetics of language impairment. Genome medicine\| PubMed ID: 20193051	2010
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex. Human molecular genetics\| PubMed ID: 20858596	2010
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature genetics\| PubMed ID: 21572417	2011
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS genetics\| PubMed ID: 21765815	2011
Foxp2 mutations impair auditory-motor association learning. PloS one\| PubMed ID: 22412993	2012
The DISC1 promoter: characterization and regulation by FOXP2. Human molecular genetics\| PubMed ID: 22434823	2012
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder. European journal of human genetics : EJHG\| PubMed ID: 22909776	2013
Decoding the genetics of speech and language. Current opinion in neurobiology\| PubMed ID: 23228431	2013
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages. European journal of human genetics : EJHG\| PubMed ID: 23321624	2013
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia. Human molecular genetics\| PubMed ID: 23406871	2013
Neurogenomics of speech and language disorders: the road ahead. Genome biology\| PubMed ID: 23597266	2013
FOXP2 targets show evidence of positive selection in European populations. American journal of human genetics\| PubMed ID: 23602712	2013
Evolution. Culture, genes, and the human revolution. Science (New York, N.Y.)\| PubMed ID: 23704558	2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. PLoS genetics\| PubMed ID: 24068947	2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental medicine and child neurology\| PubMed ID: 24117048	2014
Molecular genetics of dyslexia: an overview. Dyslexia (Chichester, England)\| PubMed ID: 24133036	2013
Is synaesthesia more common in autism? Molecular autism\| PubMed ID: 24252644	2013
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain imaging and behavior\| PubMed ID: 24399358	2014
Associations of HLA alleles with specific language impairment. Journal of neurodevelopmental disorders\| PubMed ID: 24433325	2014
On the other hand: including left-handers in cognitive neuroscience and neurogenetics. Nature reviews. Neuroscience\| PubMed ID: 24518415	2014
Differences in cerebral cortical anatomy of left- and right-handers. Frontiers in psychology\| PubMed ID: 24734025	2014
A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. PloS one\| PubMed ID: 24801482	2014
Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets. Human brain mapping\| PubMed ID: 24827550	2013