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BMC Nephrology|December 19, 2024
Eight-fold increased COVID-19 mortality in autosomal dominant tubulointerstitial kidney disease due to MUC1 mutations: an observational studyKendrah O Kidd, Adrienne H Williams, Abbigail Taylor, et al.
Plos One|December 17, 2014
Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageingLouiza Papazachariou, Panayiota Demosthenous, Myrtani Pieri, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
Eight-Fold Increased COVID-19 Mortality in Autosomal Dominant Tubulointerstitial Kidney Disease due to MUC1 Mutations: An Observational StudyKendrah O Kidd, Adrienne H Williams, Abbigail Taylor, et al.
Kidney International|December 14, 2020
Mild X-linked Alport syndrome due to the COL4A5 G624D variant originating in the Middle Ages is predominant in Central/East Europe and causes kidney failure in midlifeAleksandra M Żurowska, Olga Bielska, Patrycja Daca-Roszak, et al.
Genes|December 23, 2022
Novel and Founder Pathogenic Variants in X-Linked Alport Syndrome Families in GreeceDespina Hadjipanagi, Gregory Papagregoriou, Constantina Koutsofti, et al.
Kidney International|May 26, 2020
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1Eric Olinger, Patrick Hofmann, Kendrah Kidd, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 11, 2014
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1Anthony J Bleyer, Stanislav Kmoch, Corinne Antignac, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport SyndromeOliver Gross, Clifford E Kashtan, Michelle N Rheault, et al.
Journal of the American Society of Nephrology : JASN|April 10, 2026
Single-Molecule Real-Time Sequencing for MUC1 VNTR Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease DiagnosisAlena Vrbacká, Anna Přistoupilová, Kendrah O Kidd, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and ProgressionAlena Vrbacká, Anna Přistoupilová, Kendrah O Kidd, et al.
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