Associated Papers
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
King J et al.
Cell Reports, 2025
41124077 (PubMed )
Supplement: NIHMS2125804-supplement-2.xlsx › TableS1B
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
King J et al.
Biorxiv : the Preprint Server for Biology, 2025
40488133 (PubMed )
Supplement: media-2.xlsx › ClinVar
A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development.
Eising E et al.
Molecular Psychiatry, 2019
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders.
Estruch SB et al.
Human Molecular Genetics, 2018
Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.
Estruch SB et al.
Journal of Neurodevelopmental Disorders, 2016
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization.
Laffin JJ et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2012
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