Associated Papers
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
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Cell Reports, 2025
41124077 (PubMed )
Supplement: NIHMS2125804-supplement-2.xlsx › TableS1B
A Comprehensive Study of De Novo Mutations on the Protein-Protein Interaction Interfaces Provides New Insights into Developmental Delay.
Maharjan DT et al.
Biomolecules, 2022
36358993 (PubMed )
Supplement: biomolecules-12-01643-s001.zip › Supplemental_Table_S2____PsychiPPI_in_developmental_delay.xlsx › Sheet1
Pathogenic missense mutation pattern of forkhead box genes in neurodevelopmental disorders.
Han L et al.
Molecular Genetics & Genomic Medicine, 2019
Prospective investigation of FOXP1 syndrome.
Siper PM et al.
Molecular Autism, 2017
29090079 (PubMed )
Supplement: 13229_2017_172_MOESM2_ESM.xlsx › Supplementary_Table_2
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