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Inhalt
(Geteilter) Erst- & Letztautor
Schamarek I., Pasieka B., Stumvoll M., Ebert T., Sandner B., Münch J. – Recognizing the gap: A case series of euglycemic and hyperglycemic SGLT2 inhibitor associated diabetic ketoacidosis. Diabetes Case Rep
. (2024); 10.35841/2572-5629.24.09.204.
Münch J., Goodyer P.R., Wagner C.A. – Tubular diseases and stones seen from pediatric and adult nephrology perspective. Semin Nephrol (2023); 10.1016/j.semnephrol.2023.151437
Lehmann C., Pehnke, S., Weimann A., Bachmann A., Dittrich K., Petzold F., Fürst D., de Fallois J., Landgraf R., Henschler R., Lindner T., Halbritter J., Doxiadis I., Popp B., Münch J. - Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation. Frontiers Immunol (2023); 10.3389/fimmu.2023.1094862
Münch J., Engesser E, Schönauer R., Hamm J.A., Hartitg C., Hantmann E., Akay G., Phelivan D., Mitani T., Akdemir Z.C., Tüysüz B., Shirakawa T., Dateki S., Claus. L.R., von Eerde A., Wagner T., Bergmann. C., Höhn A.K., Shril S., Pollack A., Wegner T., Scott A, Paolucci S., Buchan J, Gabriel G.C., Posey J.E., Lupski J.R., McCarthy A.A., Pazour J.P., Lo C.W., Popp B., Halbritter J. - Biallelic pathogenic variants in ROBO1 associate with syndromic CAKUT. Kidney Int (2022); 10.1016/j.kint.2022.01.028
Münch J., Krüger B., Weimann A., Wiech T., Reinhard L., Hoxha E., Pfister F., Halbritter J. - Post‐transplant nephrotic syndrome resulting from NELL1‐positive membranous nephropathy. Am J Transpl (2021); 10.1111/ajt.16610
Münch J., Kirschner K., Schlee H., Schönauer R., Le Duc G.D., Scholz H., Halbritter J. – ADPKD in absence of renal cyst formation illustrates genetic interaction between WT1 und PKD1. J Med Genet (2019); jmedgenet-2019-106633.
Ottlewski I.*, Münch J.*, Wagner T., Schönauer R., Bachmann A., Weimann A., Hentschel J., Lindner T.H., Seehofer, D., Bergmann C., Jamra R.A., Halbritter J. - Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease. Kidney Int (2019) ii: S0085-2538(19)30187-5 (*contributed equally)
Münch J., Bachmann A., Grohmann M., Mayer C., Kirschfink M., Lindner T. H., Bergmann C., Halbritter J. - 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. Clin Kidney J (2017) 10(6):742-746
Münch J., Grohmann M., Lindner T. H., Bergmann C., Halbritter J. - Diagnosing FSGS without kidney biopsy – a novel INF2-mutation in a family with ESRD. BMC Medical Genetics
(2016); 10.1186/s12881-016-0336-9.
Ko-Autor
de Fallois J., Sieckmann T., Schönauer R., Petzold F., Münch J., Pauly M., Vasileiou G., Findeisen C., Kampmeier A., Kuechler A., Reis A., Decker E., Bergmann C., Platzer K., Tasic V., Kirschner KM., Shril S., Hildebrandt F., Chung WK., Halbritter J. – Kidney Int Rep (2024);
Hoerschelmann E.v., Münch J., Gao L., Lücht C., Naik M., Schmidt D., Pitzinger P., Michel D., Avaniadi P., Schrezenmeier E., Choi M., Halleck F., Budde K. - Letermovir Rescue Therapy in Kidney Transplant Recipients with Refractory/Resistant CMV Disease. J Clin Med
(2023); doi.org/10.3390/jcm13010100
Schönauer R., Jin W., Findeisen C., Valenzuela I., Devlin LA., Murrell J., Bedoukian EC., Pöschla L., Hantmann E., Riedhammer KM., Hoefele J., Platzer K., Biemann R., Campeau PM, Münch J., Heyne H., Hoffmann A., Ghosh A., Sun W., Dong H., Noé F., Wolfrum C., Woods E., Parker MJ., Neatu R., Le Guyader G., Bruel AL., Perrin L., Spiewak H.; Genomics England Research Consortium; Missotte I., Fourgeaud M., Michaud V., Lacombe D., Paolucci SA., Buchan JG., Glissmeyer M., Popp B., Blüher M., Sayer JA., Halbritter J. - Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene's candidacy in 6q16.1 deletions. Am J Hum Genet
(2023); doi.org/10.1016/j.ajhg.2023.04.010
Schenk S., Kowald J., Lindner T. H., Engesser M., Münch J., Meigen C., Halbritter J., De Fallois J. - The diagnostic value of native kidney biopsy in low grade, subnephrotic, and nephrotic range proteinuria: a retrospective cohort study. PLOS One (2022)
de Fallois J., Schönauer R., Münch J., Nagel M., Popp B., Halbritter J. – Challenging disease ontology by instances of atypical PKHD1 and PKD1 genetics. Front Genet
(2021); doi.org/10.3389/fgene.2021.682565
Schönauer R., Baatz S., Nemitz-Kliemchen M., Frank V., Petzold F., Sewerin S., Popp B., Münch J., Neuber S., Bergmann C., Halbritter J. - Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes. Genet Med (2020), Aug;22(8):1374-1383
Pietsch C., Michalski D., Münch J., Petros S., Bergs S., Trawinski H., Lübbert C., Liebert U. G. - Autochthonous West Nile virus infection outbreak in humans, Leipzig, Germany, August to September 2020. Eurosurveillance (2020)
Buchkapitel
Münch J., Lindner T. - Präeklampsie - Diagnostik und Klinisches Management; Thema: „Genetik der Präeklampsie“; ISBN 9783110611908 (2022)
Scharlemann-Mönks D., Münch J. - Medikationsmanagement im Krankenhaus - Ein Arbeitsbuch für Stationsapotheker; Thema: „Akutes Nierenversagen - hypochlorämische metabolische Alkalose; Chronische Niereninsuffizienz mit Hypocalcämie und Hypomagnesiämie“, ISBN 978-3-7692-7521-6 (2021)