Associated Papers
Expansion of Phenotyping and Genotypic Spectra of KIF7 -Related Intellectual Disability: Case Report and Review of Literature.
Wongong R et al.
American Journal of Medical Genetics. Part A, 2026
40935806 (PubMed )
Supplement: supplement_1.docx
The ciliary kinesin KIF7 controls the development of the cerebral cortex by acting differentially on SHH signaling in dorsal and ventral forebrain.
Pedraza M et al.
Elife, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach.
Rai A et al.
American Journal of Human Genetics, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach.
Rai A et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Sequences in the stalk domain regulate auto-inhibition and ciliary tip localization of the immotile kinesin-4 KIF7.
Blasius TL et al.
Journal of Cell Science, 2021
Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors.
Akhavanfard S et al.
Nature Communications, 2020
32371905 (PubMed )
Supplement: 41467_2020_16067_MOESM19_ESM.xlsx › Supplementary_Data_16
Novel KIF7 missense substitutions in two patients presenting with multiple malformations and features of acrocallosal syndrome.
Tunovic S et al.
American Journal of Medical Genetics. Part A, 2015
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