Max C. Liebau

Universitätsklinikum Aachen — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

33h-index4.2kcitations184works6.02yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(97), Renal and related cancers(83), Biomedical Research and Pathophysiology(36), Renal Diseases and Glomerulopathies(32), Pediatric Urology and Nephrology Studies(27)

Publications180 total

Improving precision diagnosis in unexplained CKD
Clinical Kidney Journal·2026Open Access
KDIGO 2025 ADPKD guideline through pediatric eyes
Pediatric Nephrology·2025Open Access
PAX2-Associated Kidney Dysplasia and Podocyte Injury: 2 Faces of a Monogenic Disorder
Kidney International Reports·2025Open Access
#2550 Targeted plasma proteomics links inflammation with progression of chronic kindey disease in a multi-national pediatric cohort
Nephrology Dialysis Transplantation·2025Open Access
#2593 The nephronophthisis protein GLIS2/NPHP7 is required for the DNA damage response in kidney tubular epithelial cells
Nephrology Dialysis Transplantation·2025Open Access
Qualitative Analysis and Comparison of Externally Led Patient-Focused Drug Development Concepts for Autosomal Recessive Polycystic Kidney Disease Against SONG Initiatives
Kidney Medicine·2025Open Access
Transition of patients with hereditary nephropathies from paediatric to adult care
Nephrology Dialysis Transplantation·2025Open Access
The fibrocystin C-terminal domain inhibits Src/STAT3 signal induced cystogenesis of kidney epithelia
2025Open Access
The nephronophthisis protein <i>GLIS2</i> / <i>NPHP7</i> is required for the DNA damage response in kidney tubular epithelial cells
American Journal of Physiology-Renal Physiology·2025Open Access
Growth hormone treatment associates with improved circulating anti-aging protein Klotho and reduced arterial stiffness in children with CKD
Clinical Kidney Journal·2025Open Access
Anti-nephrin antibodies guide living donor kidney transplantation in a pediatric patient with primary focal segmental glomerular sclerosis
Kidney International·2025· 8 citedOpen Access
Are we ACE-ing the early treatment of Alport syndrome?
Pediatric Nephrology·2025
Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet)
Pediatric Nephrology·2025Open Access
Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney disease
Clinical Kidney Journal·2025· 2 citedOpen Access
Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high- and middle-income countries
Kidney International·2025· 6 citedOpen Access
Polycystic Kidney Disease in Children: The Current Status and the Next Horizon
American Journal of Kidney Diseases·2025· 5 citedOpen Access
A risk score to predict kidney survival in patients with autosomal recessive polycystic kidney disease at the age of two months
Kidney International·2025· 3 citedOpen Access
Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndrome
Pediatric Nephrology·2025· 4 citedOpen Access
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summary
Kidney International·2025· 58 citedOpen Access
KDIGO 2025 Clinical Practice Guideline for the Evaluation, Management, and Treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD)
Kidney International·2025· 64 citedOpen Access
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Frequent Co-authors

Thomas Benzing(17), Franz Schaefer(17), Bernhard Schermer(16), Djalila Mekahli(15), Lutz T. Weber(15), Claudia Dafinger(10), Sandra Habbig(10), Jens König(9), Lars Pape(8), Carsten Bergmann(8), Jun Oh(8), Dieter Haffner(8), Jörg Dötsch(8), Bodo B. Beck(7), Matthias Galiano(7), Michaela Geßner(7), Kathrin Burgmaier(7), Rukshana Shroff(7), Augustina Jankauskienė(7), Ali Düzova(7)