George Feldman
Thomas Jefferson University(US)
Publications by Year
Research Areas
Heterotopic Ossification and Related Conditions, Hip disorders and treatments, Medical Imaging and Pathology Studies, Orthopaedic implants and arthroplasty, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva(2006)1,212 cited
- → Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22(1997)368 cited
- → Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome(1995)232 cited
- → Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2(1995)123 cited
- → The Genetics of Fibrodysplasia Ossificans Progressiva(2005)122 cited
- → Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31(2000)96 cited
- → Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain(1998)69 cited
- → Developmental Dysplasia of the Hip: Linkage Mapping and Whole Exome Sequencing Identify a Shared Variant in CX 3 CR 1 in All Affected Members of a Large Multigeneration Family(2013)66 cited
- → REPORTS(1994)59 cited
- → Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)(2000)59 cited