1. Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Issue 14 (18th February 2022) Authors: Brunet, Theresa; Berutti, Riccardo; Dill, Veronika; Hecker, Judith S; Choukair, Daniela; Andres, Stephanie; Deschauer, Marcus; Diehl-Schmid, Janine; Krenn, Martin; Eckstein, Gertrud; Graf, Elisabeth; Gasser, Thomas; Strom, Tim M; Hoefele, Julia; Götze, Katharina S; Meitinger, Thomas; Wagner, Matias Journal: Human molecular genetics Issue: Volume 31:Issue 14(2022) Page Start: 2386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. First replication that biallelic variants in FITM2 cause a complex deafness‐dystonia syndrome. Issue 10 (4th October 2018) Authors: Riedhammer, Korbinian Maria; Leszinski, Gloria Sarah; Andres, Stephanie; Strobl‐Wildemann, Gertrud; Wagner, Matias Journal: Movement disorders Issue: Volume 33:Issue 10(2018) Page Start: 1665 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. FP548CONTINUOUS SALINE INFUSION VERSUS INTERMITTENT SALINE FLUSHING IN PREVENTING CLOT FORMATION DURING HEPARIN-FREE HEMODIALYSIS. (13th June 2019) Authors: Vega-Alava, Kristine Mae; Andres, Stephanie Journal: Nephrology dialysis transplantation Issue: Volume 34(2019)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Maffucci syndrome and neoplasms: a case report and review of the literature. (December 2016) Authors: Prokopchuk, Olga; Andres, Stephanie; Becker, Karen; Holzapfel, Konstantin; Hartmann, Daniel; Friess, Helmut Journal: BMC research notes Issue: Volume 9:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗