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Clinical Kidney Journal|July 3, 2026
Primary hyperoxaluria type 1-current practice in the siRNA era: an ERA Genes & Kidney Working Group surveyMalte P Bartram, Giovambattista Capasso, Emilie Cornec-Le Gall, et al.
Kidney International Reports|February 23, 2023
Modeling of <i>ACTN4</i>-Based Podocytopathy Using <i>Drosophila</i> NephrocytesJohanna Odenthal, Sebastian Dittrich, Vivian Ludwig, et al.
Genome Medicine|August 23, 2023
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletionsNikolai Tschernoster, Florian Erger, Stefan Kohl, et al.
Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.
Kidney International|December 8, 2018
The proteome microenvironment determines the protective effect of preconditioning in cisplatin-induced acute kidney injuryMartin R Späth, Malte P Bartram, Nicolàs Palacio-Escat, et al.
Npj Aging|May 28, 2026
An in-depth analysis of the molecular changes induced by short-term calorie restriction before living kidney donationMartin R Späth, Sita Arjune, Katrin Bohl, et al.
The EMBO Journal|August 23, 2012
AATF/Che-1 acts as a phosphorylation-dependent molecular modulator to repress p53-driven apoptosisKatja Höpker, Henning Hagmann, Safiya Khurshid, et al.
Human Mutation|July 22, 2014
Mutation of POC1B in a severe syndromic retinal ciliopathyBodo B Beck, Jennifer B Phillips, Malte P Bartram, et al.
The New England Journal of Medicine|April 28, 2016
Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 MutationsKamel Laghmani, Bodo B Beck, Sung-Sen Yang, et al.
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