Simon E. Fisher

Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.

A genomewide linkage screen for relative hand skill in sibling pairs.

Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.

A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.

Molecular evolution of FOXP2, a gene involved in speech and language.

Developmental dyslexia: genetic dissection of a complex cognitive trait.

Deciphering the genetic basis of speech and language disorders.

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

Confirmatory evidence for linkage of relative hand skill to 2p12-q11.

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.

FOXP2 in focus: what can genes tell us about speech and language?

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.

Familial and genetic effects on motor coordination, laterality, and reading-related cognition.

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

On genes, speech, and language.

The eloquent ape: genes, brains and the evolution of language.

Genes, cognition and dyslexia: learning to read the genome.

Tangled webs: tracing the connections between genes and cognition.

Functional genetic analysis of mutations implicated in a human speech and language disorder.

Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.

Molecular windows into speech and language disorders.

Generation of mice with a conditional Foxp2 null allele.

Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.

A functional genetic link between distinct developmental language disorders.

FOXP2 as a molecular window into speech and language.

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.

Modified sound-evoked brainstem potentials in Foxp2 mutant mice.

CMIP and ATP2C2 modulate phonological short-term memory in language impairment.

Unravelling neurogenetic networks implicated in developmental language disorders.

Genetic susceptibility to stuttering.

Recent advances in the genetics of language impairment.

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.

Foxp2 mutations impair auditory-motor association learning.

The DISC1 promoter: characterization and regulation by FOXP2.

Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.

Decoding the genetics of speech and language.

Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.

Absolute pitch exhibits phenotypic and genetic overlap with synesthesia.

Neurogenomics of speech and language disorders: the road ahead.

FOXP2 targets show evidence of positive selection in European populations.

Evolution. Culture, genes, and the human revolution.

Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Molecular genetics of dyslexia: an overview.

Is synaesthesia more common in autism?

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.

Associations of HLA alleles with specific language impairment.

On the other hand: including left-handers in cognitive neuroscience and neurogenetics.

Differences in cerebral cortical anatomy of left- and right-handers.

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.

Measurement and genetics of human subcortical and hippocampal asymmetries in large datasets.