Münch J - Search Results

1

Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation.

Lehmann C, Pehnke S, Weimann A, Bachmann A, Dittrich K, Petzold F, Fürst D, de Fallois J, Landgraf R, Henschler R, Lindner TH, Halbritter J, Doxiadis I, Popp B, Münch J. Lehmann C, et al. Among authors: munch j. Front Immunol. 2023 Jan 27;14:1094862. doi: 10.3389/fimmu.2023.1094862. eCollection 2023. Front Immunol. 2023. PMID: 36776892 Free PMC article.

2

Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown origin.

Münch J, Grohmann M, Lindner TH, Bergmann C, Halbritter J. Münch J, et al. BMC Med Genet. 2016 Oct 12;17(1):73. doi: 10.1186/s12881-016-0336-9. BMC Med Genet. 2016. PMID: 27733133 Free PMC article.

3

Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of CFHR1/CFHR3 and the presence of CFH antibodies.

Münch J, Bachmann A, Grohmann M, Mayer C, Kirschfink M, Lindner TH, Bergmann C, Halbritter J. Münch J, et al. Clin Kidney J. 2017 Dec;10(6):742-746. doi: 10.1093/ckj/sfx053. Epub 2017 Jul 10. Clin Kidney J. 2017. PMID: 29225802 Free PMC article.

4

Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease.

Ottlewski I, Münch J, Wagner T, Schönauer R, Bachmann A, Weimann A, Hentschel J, Lindner TH, Seehofer D, Bergmann C, Jamra RA, Halbritter J. Ottlewski I, et al. Among authors: munch j. Kidney Int. 2019 Jul;96(1):222-230. doi: 10.1016/j.kint.2019.01.038. Epub 2019 Mar 15. Kidney Int. 2019. PMID: 31027891 Free article.

5

Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1.

Münch J, Kirschner KM, Schlee H, Kraus C, Schönauer R, Jin W, Le Duc D, Scholz H, Halbritter J. Münch J, et al. J Med Genet. 2020 May 7:jmedgenet-2019-106633. doi: 10.1136/jmedgenet-2019-106633. Online ahead of print. J Med Genet. 2020. PMID: 32381729

6

Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes.

Schönauer R, Baatz S, Nemitz-Kliemchen M, Frank V, Petzold F, Sewerin S, Popp B, Münch J, Neuber S, Bergmann C, Halbritter J. Schönauer R, et al. Among authors: munch j. Genet Med. 2020 Aug;22(8):1374-1383. doi: 10.1038/s41436-020-0816-3. Epub 2020 May 13. Genet Med. 2020. PMID: 32398770 Free PMC article.

7

Posttransplant nephrotic syndrome resulting from NELL1-positive membranous nephropathy.

Münch J, Krüger BM, Weimann A, Wiech T, Reinhard L, Hoxha E, Pfister F, Halbritter J. Münch J, et al. Am J Transplant. 2021 Sep;21(9):3175-3179. doi: 10.1111/ajt.16610. Epub 2021 May 8. Am J Transplant. 2021. PMID: 33866674 Free article.

8

Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics.

de Fallois J, Schönauer R, Münch J, Nagel M, Popp B, Halbritter J. de Fallois J, et al. Among authors: munch j. Front Genet. 2021 Jun 25;12:682565. doi: 10.3389/fgene.2021.682565. eCollection 2021. Front Genet. 2021. PMID: 34249099 Free PMC article.

9

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.

Münch J, Engesser M, Schönauer R, Hamm JA, Hartig C, Hantmann E, Akay G, Pehlivan D, Mitani T, Coban Akdemir Z, Tüysüz B, Shirakawa T, Dateki S, Claus LR, van Eerde AM; Genomics England Research Consortium; Smol T, Devisme L, Franquet H, Attié-Bitach T, Wagner T, Bergmann C, Höhn AK, Shril S, Pollack A, Wenger T, Scott AA, Paolucci S, Buchan J, Gabriel GC, Posey JE, Lupski JR, Petit F, McCarthy AA, Pazour GJ, Lo CW, Popp B, Halbritter J. Münch J, et al. Kidney Int. 2022 May;101(5):1039-1053. doi: 10.1016/j.kint.2022.01.028. Epub 2022 Feb 26. Kidney Int. 2022. PMID: 35227688 Free PMC article.

10

The diagnostic value of native kidney biopsy in low grade, subnephrotic, and nephrotic range proteinuria: A retrospective cohort study.

de Fallois J, Schenk S, Kowald J, Lindner TH, Engesser M, Münch J, Meigen C, Halbritter J. de Fallois J, et al. Among authors: munch j. PLoS One. 2022 Sep 2;17(9):e0273671. doi: 10.1371/journal.pone.0273671. eCollection 2022. PLoS One. 2022. PMID: 36054109 Free PMC article.

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