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Johannes Münch
Johannes Münch
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Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease
I Ottlewski, J Münch, T Wagner, R Schönauer, A Bachmann, A Weimann, ...
Kidney international 96 (1), 222-230, 2019
612019
Autochthonous West Nile virus infection outbreak in humans, Leipzig, Germany, August to September 2020
C Pietsch, D Michalski, J Münch, S Petros, S Bergs, H Trawinski, ...
Eurosurveillance 25 (46), 2001786, 2020
542020
Diagnosing FSGS without kidney biopsy – a novel INF2-mutation in a family with ESRD of unknown origin
J Münch, M Grohmann, TH Lindner, C Bergmann, J Halbritter
BMC medical genetics 17, 1-5, 2016
182016
Posttransplant nephrotic syndrome resulting from NELL1-positive membranous nephropathy
J Münch, BM Krüger, A Weimann, T Wiech, L Reinhard, E Hoxha, F Pfister, ...
American Journal of Transplantation 21 (9), 3175-3179, 2021
132021
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract
J Münch, M Engesser, R Schönauer, JA Hamm, C Hartig, E Hantmann, ...
Kidney international 101 (5), 1039-1053, 2022
112022
Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation
C Lehmann, S Pehnke, A Weimann, A Bachmann, K Dittrich, F Petzold, ...
Frontiers in Immunology 14, 1094862, 2023
82023
Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of CFHR1/CFHR3 and the …
J Münch, A Bachmann, M Grohmann, C Mayer, M Kirschfink, TH Lindner, ...
Clinical Kidney Journal 10 (6), 742-746, 2017
72017
Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16. 1 deletions
R Schönauer, W Jin, C Findeisen, I Valenzuela, LA Devlin, J Murrell, ...
The American Journal of Human Genetics 110 (6), 998-1007, 2023
32023
Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics
J de Fallois, R Schönauer, J Münch, M Nagel, B Popp, J Halbritter
Frontiers in Genetics 12, 682565, 2021
32021
Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1
J Münch, KM Kirschner, H Schlee, C Kraus, R Schönauer, W Jin, ...
Journal of Medical Genetics 58 (2), 140-144, 2021
22021
The diagnostic value of native kidney biopsy in low grade, subnephrotic, and nephrotic range proteinuria: A retrospective cohort study
J de Fallois, S Schenk, J Kowald, TH Lindner, M Engesser, J Münch, ...
Plos one 17 (9), e0273671, 2022
12022
Pathogenic PHIP variants are variably associated with CAKUT
J de Fallois, T Sieckmann, R Schönauer, F Petzold, J Münch, M Pauly, ...
Kidney International Reports, 2024
2024
Cracking the Code: Genetic Insights from the Swiss Kidney Stone Cohort
J Münch, JF da Silva, EC Ferrete, M Papik, I Ivanovski, D Fuster, H Seeger, ...
Utilizing Genetic Linkage and Rare Variant Association Studies to Unravel …, 2024
2024
Letermovir Rescue Therapy in Kidney Transplant Recipients with Refractory/Resistant CMV Disease
E von Hoerschelmann, J Münch, L Gao, C Lücht, MG Naik, D Schmidt, ...
Journal of Clinical Medicine 13 (1), 100, 2023
2023
Tubular Diseases and Stones Seen From Pediatric and Adult Nephrology Perspectives
J Münch, PR Goodyer, CA Wagner
Seminars in Nephrology, 151437, 2023
2023
Monogenic Disease Variants in the Swiss Kidney Stone Cohort and Stone-Free Controls: TH-PO460
J Muench, JF Silva, EM Cabello, I Rubio-Aliaga, DG Fuster, F Buchkremer, ...
Journal of the American Society of Nephrology 34 (11S), 218, 2023
2023
Navigating the Crossroads: Cytomegalovirus (CMV), Neutropenia, and Kidney Transplant Survival in High-Risk Patients: SA-PO1078
J Muench, E von Hoerschelmann, K Budde, F Halleck
Journal of the American Society of Nephrology 34 (11S), 1031, 2023
2023
NEXT-GENERATION SEQUENCING AND RISK STRATIFICATION IN LIVING KIDNEY TRANSPLANTATION
C Lehmann, J Muench, I Doxiadis
HLA 100, 10-10, 2022
2022
BIALLELIC PATHOGENIC VARIANTS IN ROBO1 ASSOCIATE WITH SYNDROMIC CAKUT
J Muench, M Engesser, R Schoenauer, JA Hamm, G Akay, B Tueysuez, ...
NEPHROLOGY DIALYSIS TRANSPLANTATION 37, I26-I28, 2022
2022
MO047: Biallelic pathogenic variants in ROBO1 associate with syndromic CAKUT
J Münch, M Engesser, R Schönauer, JA Hamm, G Akay, B Tüysüz, ...
Nephrology Dialysis Transplantation 37 (Supplement_3), gfac062. 028, 2022
2022
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