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Anzahl der Publikationen: 11
Zeitschriftenartikel
Chan, Henry L. Y.; Vogel, Arndt; Berg, Thomas; De Toni, Enrico N.; Kudo, Masatoshi; Trojan, Joerg; Eiblmaier, Anja; Klein, Hanns-Georg; Hegel, Johannes Kolja; Sharma, Ashish; Madin, Kairat; Rolny, Vinzent; Lisy, Marcus-Rene und Piratvisuth, Teerha
(2022):
Performance evaluation of the Elecsys PIVKA-II and Elecsys AFP assays for hepatocellular carcinoma diagnosis.
In: Clinical and Experimental Gastroenterology and Hepatology, Bd. 6, Nr. 5: S. 292-300
Willimsky, Eva-Katharina; Munzig, Anna; Mayer, Karin; Biskup, Saskia; Abicht, Angela; Hoertnagel, Konstanze; Voss, Hubertus von; Klein, Hanns-Georg; Rost, Imma; Larsen, Line H. G.; Dahl, Hanns Atli; Hoelz, Hannes; Stülpnagel, Celina von und Borggraefe, Ingo
(2020):
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.
In: Neuropediatrics, Bd. 52, Nr. 02: S. 92-97
Konstandin, Nikola P.; Pastore, Friederike; Herold, Tobias; Dufour, Annika; Rothenberg-Thurley, Maja; Hinrichsen, Tanja; Ksienzyk, Bianka; Tschuri, Sebastian; Schneider, Stephanie; Hoster, Eva; Berdel, Wolfgang E.; Wörmann, Bernhard J.; Sauerland, Maria C.; Braess, Jan; Bohlander, Stefan K.; Klein, Hanns-Georg; Hiddemann, Wolfgang; Metzeler, Klaus H. und Spiekermann, Karsten
(2018):
Genetic heterogeneity of cytogenetically normal AML with mutations of CEBPA.
In: Blood Advances, Bd. 2, Nr. 20: S. 2724-2731
Höfele, Julia; Kemper, Markus J.; Schönermarck, Ulf; Müller, Susanna; Klein, Hanns-Georg und Lemke, Anja
(2017):
Truncating Wilms Tumor Suppressor Gene 1 Mutation in an XX Female with Adult-Onset Focal Segmental Glomerulosclerosis and Streak Ovaries: A Case Report.
In: Nephron, Bd. 135, Nr. 1: S. 72-76
Rogenhofer, Nina; Markoff, Arseni; Wagner, Annett; Klein, Hanns-Georg; Petroff, David; Schleussner, Ekkehard und Thaler, Christian J.
(2017):
Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers.
In: Clinical and Applied Thrombosis-Hemostasis, Bd. 23, Nr. 1: S. 27-33
[PDF, 200kB]
Hoefele, Julia; Mayer, Karin; Marschall, Christoph; Alberer, Martin; Klein, Hanns-Georg und Kirschstein, Martin
(2016):
Rare co-occurrence of osteogenesis imperfecta type I and autosomal dominant polycystic kidney disease.
In: World Journal of Pediatrics, Bd. 12, Nr. 4: S. 501-503
Weber, Stefanie; Büscher, Anja K.; Hagmann, Henning; Liebau, Max C.; Heberle, Christian; Ludwig, Michael; Rath, Sabine; Alberer, Martin; Beissert, Antje; Zenker, Martin; Hoyer, Peter F.; Konrad, Martin; Klein, Hanns-Georg und Hoefele, Julia
(2016):
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
In: Pediatric Nephrology, Bd. 31, Nr. 1: S. 73-81
Weber, Stefanie; Strasser, Katja; Rath, Sabine; Kittke, Achim; Beicht, Sonja; Alberer, Martin; Lange-Sperandio, Bärbel; Hoyer, Peter F.; Benz, Marcus R.; Ponsel, Sabine; Weber, Lutz T.; Klein, Hanns-Georg und Hoefele, Julia
(2016):
Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy.
In: Pediatric Nephrology, Bd. 31, Nr. 6: S. 941-955
Pfeufer, Arne; Dockhorn-Dworniczak, Barbara; Findeisen, Peter; Hoffmann, Georg; Kiehntopf, Michael; Klein, Hanns-Georg und Teupser, Daniel
(2013):
12. Jahrestagung der Sektion Molekulare Diagnostik der DGKL am 6. und 7. Juni 2013 in der Evangelischen Akademie Tutzing / Report on the 12th Annual Meeting of the Section of Molecular Diagnostics of the DGKL on 6th/7th June 2013 in Tutzing.
In: Laboratoriumsmedizin - Journal of Laboratory Medicine, Bd. 37, Nr. 6: S. 337-343
[PDF, 368kB]
Vogl, Ina; Benet-Pagès, Anna; Eck, Sebastian H.; Kuhn, Marius; Vosberg, Sebastian; Greif, Philipp A.; Metzeler, Klaus H.; Biskup, Saskia; Müller-Reible, Clemens und Klein, Hanns-Georg
(2013):
Applications and data analysis of next-generation sequencing.
In: Laboratoriumsmedizin - Journal of Laboratory Medicine, Bd. 37, Nr. 6: S. 305-315
[PDF, 2MB]
Vogl, Ina; Eck, Sebastian H.; Benet-Pages, Anna; Greif, Philipp A.; Hirv, Kaimo; Kotschote, Stefan; Kuhn, Marius; Gehring, Andrea; Bergmann, Carsten; Bolz, Hanno Joern; Stuhrmann, Manfred; Biskup, Saskia; Metzeler, Klaus H. und Klein, Hanns-Georg
(2012):
Diagnostic applications of next generation sequencing: working towards quality standards.
In: Laboratoriumsmedizin - Journal of Laboratory Medicine, Bd. 36, Nr. 4: S. 227-239
[PDF, 647kB]