Kendrah Kidd

Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

Nikhita Bolar, Christelle Golzio, Martina Živná et al. · The American Journal of Human Genetics · 2016 · 159 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1

Eric Olinger, Patrick Hofmann, Kendrah Kidd et al. · Kidney International · 2020 · 146 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Variable Clinical Presentation of an MUC1 Mutation Causing Medullary Cystic Kidney Disease Type 1

Anthony J. Bleyer, Stanislav Kmoch, Corinne Antignac et al. · Clinical Journal of the American Society of Nephrology · 2014 · 85 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6

Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová et al. · Human Molecular Genetics · 2016 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Elevated urinary CRELD2 is associated with endoplasmic reticulum stress–mediated kidney disease

Yeawon Kim, Sun-Ji Park, Scott R. Manson et al. · JCI Insight · 2017 · 72 citations · Full text

Medicine, Nephrology, Pathobiology +17