Gere Sunder–Plassmann
Researcher Next ID · RN-040283
Researcher · Medicine
Vienna, Austria
- Works count
- 470
- Citation count
- 14,399
- H-index
- 55
- i10-index
- 211
Research interests
Publications
A 12-gene pharmacogenetic panel to prevent adverse drug reactions: an open-label, multicentre, controlled, cluster-randomised crossover implementation study
The Lancet · 2023 · https://doi.org/10.1016/s0140-6736(22)01841-4
Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium
Clinical Pharmacology & Therapeutics · 2016 · 10.1002/cpt.602
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study
Journal of Medical Genetics · 2016 · https://doi.org/10.1136/jmedgenet-2016-104178
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document
Orphanet Journal of Rare Diseases · 2015 · https://doi.org/10.1186/s13023-015-0253-6
Sex-Specific Differences in Hemodialysis Prevalence and Practices and the Male-to-Female Mortality Rate: The Dialysis Outcomes and Practice Patterns Study (DOPPS)
PLoS Medicine · 2014 · 10.1371/journal.pmed.1001750
Dialysate Sodium Concentration and the Association with Interdialytic Weight Gain, Hospitalization, and Mortality
Clinical Journal of the American Society of Nephrology · 2011 · 10.2215/cjn.05440611
Predialysis Serum Sodium Level, Dialysate Sodium, and Mortality in Maintenance Hemodialysis Patients: The Dialysis Outcomes and Practice Patterns Study (DOPPS)
American Journal of Kidney Diseases · 2011 · 10.1053/j.ajkd.2011.07.013
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data
The Lancet · 2009 · https://doi.org/10.1016/s0140-6736(09)61493-8
Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey
Journal of Medical Genetics · 2009 · https://doi.org/10.1136/jmg.2008.065904
Molecular mimicry in pauci-immune focal necrotizing glomerulonephritis
Nature Medicine · 2008 · 10.1038/nm.1874
Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey
European Heart Journal · 2007 · https://doi.org/10.1093/eurheartj/ehm153
Fabry disease and the skin: data from FOS, the Fabry outcome survey
British Journal of Dermatology · 2007 · https://doi.org/10.1111/j.1365-2133.2007.08002.x
Fabry Disease: Perspectives from 5 Years of FOS
· 2006
Clinical manifestations of Fabry disease in children: Data from the Fabry Outcome Survey
Acta Paediatrica · 2005 · 10.1080/08035250500275022
Fabry disease: overall effects of agalsidase alfa treatment
European Journal of Clinical Investigation · 2004 · https://doi.org/10.1111/j.1365-2362.2004.01424.x
Results of a Nationwide Screening for Anderson-Fabry Disease among Dialysis Patients
Journal of the American Society of Nephrology · 2004 · 10.1097/01.asn.0000124671.61963.1e
Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey
European Journal of Clinical Investigation · 2004 · 10.1111/j.1365-2362.2004.01309.x
High prevalence of hyperhomocysteinemia in critically ill patients
Critical Care Medicine · 2000 · 10.1097/00003246-200004000-00013
Molecular biology of 5,10-methylenetetrahydrofolate reductase.
PubMed · 2000
Neutrophil impairment associated with iron therapy in hemodialysis patients with functional iron deficiency.
Journal of the American Society of Nephrology · 1998 · 10.1681/asn.v94655
Importance of iron supply for erythropoietin therapy
Nephrology Dialysis Transplantation · 1995 · 10.1093/ndt/10.11.2070
Current projects
No projects listed.