Beck, Bodo | Erger, Florian - assoc. RG 03
Rare and herediatry kidney diseases
PD Dr. Bodo Beck
Institute of Human Genetics - CMMC Research Building
CMMC - PI - assoc. RG 03
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Institute of Human Genetics - CMMC Research Building
Robert-Koch-Str. 21
50931 Cologne
Dr. Florian Erger
Institute of Human Genetics - CMMC Research Building
CMMC - Co-PI - assoc. RG 03
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Institute of Human Genetics - CMMC Research Building
Robert-Koch-Str. 21
50931 Cologne
Introduction
The working group for rare and hereditary kidney diseases, led by Dr. Bodo Beck, has been researching the genetic basis of kidney dysfunction at the Institute of Human Genetics since 2010. This work primarily benefits people affected by rare and hereditary kidney diseases and their families and is carried out in close cooperation with the treating physicians at the children's clinic and other biomedical disciplines. Our working group is an integral part of the Cologne Center for Rare Diseases.
Lab Website
For information about Dr. Beck's and Dr. Erger's research and work, please visit the following page: Institut for Human Genetics
Publications generated during 1/2023-12/2025 with CMMC affiliation
2024 (up to June)
- Kaufeld JK, Kuhne L, Schonermarck U, Brasen JH, von Kaisenberg C, Beck BB, Erger F, Bergmann C, von Bergwelt-Baildon A, Brinkkotter PT, Volker LA, and Menne J (2024). Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition. Kidney Int Rep9, 919-928. doi:10.1016/j.ekir.2024.01.035.
- Kolbuc M, Kolek MF, Motyka R, Bienias B, Habbig S, Burgmaier K, Prikhodina L, Papizh S, Tasic V, Okorn C, Szczepanska M, Kilis-Pstrusinska K, Wasilewska A, Adamczyk P, Tkaczyk M, Panczyk-Tomaszewska M, Miklaszewska M, Pawlaczyk K, Bukowska-Olech E, Jamsheer A, Jankauskiene A, Konig J, Cheong HI, Ahn YH, Kaspar S, Sikora P, Beck BB, and Zaniew M (2024). Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract. Pediatr Nephrol. doi:10.1007/s00467-023-06262-9.
- Lamot L, Vuković Brinar I, Fištrek Prlić M, Beck B. Editorial: Cystic kidney diseases in children and adults: from diagnosis to etiology and back. Front Pediatr. 2024 Apr 10;12:1401593. doi: 10.3389/fped.2024.1401593. PMID: 38659695; PMCID: PMC11040088.
- Martin-Higueras C, Borghese L, Torres A, Fraga-Bilbao F, Santana-Estupinan R, Stefanidis CJ, Tory K, Walli A, Gondra L, Kempf C, Gessner M, Habbig S, Eifler L, Schmitt CP, Rudel B, Bartram MP, Beck BB, and Hoppe B (2024). Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1. Kidney Int Rep9, 114-133. doi:10.1016/j.ekir.2023.10.004.