Rolf Morhart
Garmisch-Partenkirchen Medical Center(DE)
Publications by Year
Research Areas
Heterotopic Ossification and Related Conditions, Medical Imaging and Pathology Studies, Parathyroid Disorders and Treatments, Autoimmune and Inflammatory Disorders Research, Genetic Syndromes and Imprinting
Most-Cited Works
- → A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva(2006)1,212 cited
- → Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1(2008)444 cited
- → The Phenotype of Fibrodysplasia Ossificans Progressiva(2005)115 cited
- → Neurological symptoms in individuals with fibrodysplasia ossificans progressiva(2012)54 cited
- → Special considerations for clinical trials in fibrodysplasia ossificans progressiva (FOP)(2018)47 cited
- → Self-reported baseline phenotypes from the International Fibrodysplasia Ossificans Progressiva (FOP) Association Global Registry(2020)35 cited
- → The FOP Connection Registry: Design of an international patient-sponsored registry for Fibrodysplasia Ossificans Progressiva(2017)32 cited
- → Fibrodysplasia Ossificans Progressiva: What Have We Achieved and Where Are We Now? Follow-up to the 2015 Lorentz Workshop(2021)26 cited
- → Five year follow-up of a prospective cohort of juvenile chronic arthritis with recent onset(1987)24 cited
- → International physician survey on management of FOP: a modified Delphi study(2017)21 cited