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Journal Article
Erger, Florian 
ORCID: 0000-0002-2768-1702, Noerling, Deborah, Borchert, Domenica, Leenen, Esther, Habbig, Sandra, Wiesener, Michael S., Bartram, Malte P., Wenzel, Andrea, Becker, Christian, Toliat, Mohammad R., Nuernberg, Peter, Beck, Bodo B. and Altmueller, Janine
(2020).
cfNOMe- A single assay for comprehensive epigenetic analyses of cell-free DNA.
Genome Med., 12 (1).
LONDON:
BMC.
ISSN 1756-994X
Leenen, Esther, Beck, Bodo, Joerres, Achim and Weidemann, Alexander (2020). Rare genetic Diseases with adult onset - Investigations of a Transplant Centre in Cologne. Internist, 61 (SUPPL 1). S. S53 - 1. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-1289
Leenen, Esther, Erger, Florian, Altmuller, Janine ORCID: 0000-0003-4372-1521, Wenzel, Andrea, Thiele, Holger, Harth, Ana ORCID: 0000-0002-1551-9214, Tschernoster, Nikolai ORCID: 0000-0002-6058-9342, Lokhande, Shanti, Joerres, Achim, Becker, Jan-Ulrich, Ekici, Arif, Huettel, Bruno, Beck, Bodo and Weidemann, Alexander
(2022).
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis.
Nephrol. Dial. Transplant., 37 (10).
S. 1895 - 1906.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385