Karl X. Knaup
Erlangen, BY, Germany
Last Updated: 09/26/2026
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Found 22 publications
Diagnosing Mendelian Kidney Disease: Hidden Niches in the (Kidney) Genome.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: December 22, 2025
Targeted VNTR long read sequencing resolves a diagnostic bottleneck in ADTKD and detects de novo ADTKD-MUC1.
Journal: Kidney international
Published: November 03, 2025
Alport Syndrome is a Partial Tubulointerstitial Disease of the Kidney.
Journal: Kidney international reports
Published: August 29, 2025
Progressive Kidney Failure by Angiotensinogen Inactivation in the Germline.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: July 15, 2024
Hypoxia controls expression of kidney-pathogenic MUC1 variants.
Journal: Life science alliance
Published: April 05, 2023
Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study.
Journal: European journal of human genetics : EJHG
Published: March 03, 2022
Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases.
Journal: Kidney international
Published: December 10, 2021
Biallelic ANKS6 mutations cause late-onset ciliopathy with chronic kidney disease through YAP dysregulation.
Journal: Human molecular genetics
Published: July 12, 2021
A noninvasive diagnostic approach to retrospective donor HLA typing in kidney transplant patients using urine.
Journal: Transplant international : official journal of the European Society for Organ Transplantation
Published: January 14, 2021
Molecular diagnosis of kidney transplant failure based on urine.
Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
Published: July 26, 2019
Last Updated: 09/26/2026