117 papers found
The genetics of situs inversus without primary ciliary dyskinesia
Altered structural brain asymmetry in autism spectrum disorder in a study of 54 datasets
Genetic architecture of subcortical brain structures in 38,851 individuals
Rare variants in axonogenesis genes connect three families with sound–color synesthesia
Loss of Intercalated Cells (ITCs) in the Mouse Amygdala ofTshz1Mutants Correlates with Fear, Depression, and Social Interaction Phenotypes
Polygenic selection underlies evolution of human brain structure and behavioral traits
Novel genetic loci associated with hippocampal volume
Novel genetic loci underlying human intracranial volume identified through genome-wide association
Lack of replication for the myosin-18B association with mathematical ability in independent cohorts
Genome-wide screening for DNA variants associated with reading and language traits
Culture, Genes, and the Human Revolution
FOXP2 Targets Show Evidence of Positive Selection in European Populations
Persistence and transmission of recessive deafness and sign language: new insights from village sign languages
Absolute pitch exhibits phenotypic and genetic overlap with synesthesia
Is synaesthesia more common in autism?
Neurogenomics of speech and language disorders: the road ahead
Decoding the genetics of speech and language
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
The DISC1 promoter: characterization and regulation by FOXP2
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