Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
B Peter, WH Raskind, M Matsushita, M Lisowski… - Journal of …, 2011 - Springer
Two functionally related genes, FOXP2 and CNTNAP2, influence language abilities in
families with rare syndromic and common nonsyndromic forms of impaired language …
families with rare syndromic and common nonsyndromic forms of impaired language …
Convergent genetic linkage and associations to language, speech and reading measures in families of probands with specific language impairment
ML Rice, SD Smith, J Gayán - Journal of neurodevelopmental disorders, 2009 - Springer
We analyzed genetic linkage and association of measures of language, speech and reading
phenotypes to candidate regions in a single set of families ascertained for SLI. Sib-pair and …
phenotypes to candidate regions in a single set of families ascertained for SLI. Sib-pair and …
The songbird as a model for the generation and learning of complex sequential behaviors
Over the past four decades songbirds have become a widely used model organism for
neuroscientists studying complex sequential behaviors and sensory-guided motor learning …
neuroscientists studying complex sequential behaviors and sensory-guided motor learning …
Understanding language from a genomic perspective
SA Graham, SE Fisher - Annual review of genetics, 2015 - annualreviews.org
Language is a defining characteristic of the human species, but its foundations remain
mysterious. Heritable disorders offer a gateway into biological underpinnings, as illustrated …
mysterious. Heritable disorders offer a gateway into biological underpinnings, as illustrated …
Prospective investigation of FOXP1 syndrome
PM Siper, S De Rubeis, MP Trelles, A Durkin… - Molecular autism, 2017 - Springer
Background Haploinsufficiency of the forkhead-box protein P1 (FOXP1) gene leads to a
neurodevelopmental disorder termed FOXP1 syndrome. Previous studies in individuals …
neurodevelopmental disorder termed FOXP1 syndrome. Previous studies in individuals …
Recent advances in the genetics of language impairment
Specific language impairment (SLI) is defined as an unexpected and persistent impairment
in language ability despite adequate opportunity and intelligence and in the absence of any …
in language ability despite adequate opportunity and intelligence and in the absence of any …
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
J Den Hoed, E de Boer, N Voisin… - The American Journal of …, 2021 - cell.com
Whereas large-scale statistical analyses can robustly identify disease-gene relationships,
they do not accurately capture genotype-phenotype correlations or disease mechanisms …
they do not accurately capture genotype-phenotype correlations or disease mechanisms …
Atypically rightward cerebral asymmetry in male adults with autism stratifies individuals with and without language delay
In humans, both language and fine motor skills are associated with left‐hemisphere
specialization, whereas visuospatial skills are associated with right‐hemisphere …
specialization, whereas visuospatial skills are associated with right‐hemisphere …
Speech and language: Translating the genome
P Deriziotis, SE Fisher - Trends in Genetics, 2017 - cell.com
Investigation of the biological basis of human speech and language is being transformed by
developments in molecular technologies, including high-throughput genotyping and next …
developments in molecular technologies, including high-throughput genotyping and next …