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George J. Feldman, PhD, DMD

Contact Dr. Feldman

1015 Walnut Street
Curtis Building, Room 501
Philadelphia, PA 19107

(215) 955-5480

Most Recent Peer-reviewed Publications

  1. A murine model for developmental dysplasia of the hip: Ablation of CX3CR1 affects acetabular morphology and gait
  2. Linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in a large multi-generation family
  3. Developmental biology of the hip
  4. Developmental dysplasia of the hip: Linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family
  5. Variable Expression and Incomplete Penetrance of Developmental Dysplasia of the Hip. Clinical Challenge in a 71-Member Multigeneration Family.
  6. The otto aufranc award: Identification of a 4 Mb region on chromosome 17q21 linked to developmental dysplasia of the hip in one 18-member, multigeneration family
  7. Response to "mutations of the Noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP)" by Lucotte et al
  8. Over-expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: A new syndrome
  9. Erratum: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva (Nature Genetics (2006) 38, (525-527))
  10. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva
  11. The genetics of fibrodysplasia ossificans progressiva
  12. Exoneration of NF-κB dysregulation in fibrodysplasia ossificans progressiva
  13. Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)
  14. Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31
  15. Opitz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain
  16. Erratum: Opiz G/BBB syndrome in Xp22: Mutations in the MID1 gene cluster in the carboxy-terminal domain (American Journal of Human Genetics (September 1998) 63 (703-710))
  17. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
  18. A novel phenotypic pattern in X-linked inheritance: Craniofrontonasal syndrome maps to Xp22
  19. Mutations in FGFR1 and FGFR2 cause familial and sporadic pfeiffer syndrome
  20. A gene for cleidocranial dysplasia maps to the short arm of chromosome 6