Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney diseaseLaura R. Claus, F. Maleady-Crowe, Chloe Mighton et al.|Kidney International|2023Cited by 38
Characterization of the Cystic Phenotype Associated with Monoallelic ALG8 and ALG9 Pathogenic VariantsTabinda Jawaid, Peter C. Harris, Doaa E. Elbarougy et al.|Journal of the American Society of Nephrology|2025Cited by 12
FC044: Heterozygous Variants in Kinase Domain of NEK8 cause an Autosomal-Dominant CiliopathyLaura R. Claus, Richard Steet, Jennifer L. Stallworth et al.|Nephrology Dialysis Transplantation|2022Cited by 2
Cover ImageTabinda Jawaid, Peter C. Harris, Doaa E. Elbarougy et al.|Journal of the American Society of Nephrology|2025Cited by 0
Clinical Characterization of Monoallelic-PKHD1 SubjectsTabinda Jawaid, Peter C. Harris, Christian Hanna et al.|Journal of the American Society of Nephrology|2022Cited by 0