Cathleen L Raggio

Summary

Affiliation: Hospital for Special Surgery
Country: USA

Publications

  1. ncbi request reprint Sexual dimorphism in adolescent idiopathic scoliosis
    Cathleen L Raggio
    Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA
    Orthop Clin North Am 37:555-8. 2006
  2. pmc Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations
    Nader Ghebranious
    University of Wisconsin Medical School, Madison, Wisconsin, USA and Geriatrics Research, Education, and Clinical Center, William S, Middleton Veterans Administration Medical Center, Madison, Wisconsin, USA
    Scoliosis 2:13. 2007
  3. ncbi request reprint Advances in understanding etiology of achondroplasia and review of management
    Erin M Carter
    The Center for Skeletal Dysplasias, Hospital for Special Surgery, New York 10021, USA
    Curr Opin Pediatr 19:32-7. 2007
  4. ncbi request reprint Genetic and orthopedic aspects of collagen disorders
    Erin M Carter
    Kathryn O and Alan C Greenberg Center for Skeletal Dysplasias, Hospital for Special Surgery, New York, New York 11238, USA
    Curr Opin Pediatr 21:46-54. 2009
  5. pmc The kathryn o. And alan C. Greenberg center for skeletal dysplasias: an interdisciplinary approach
    Erin M Carter
    Kathryn O and Alan C Greenberg Center for Skeletal Dysplasias, Hospital for Special Surgery, 535 East 70th Street, New York, NY, 10021, USA
    HSS J 4:112-6. 2008
  6. ncbi request reprint Alendronate treatment for infants with osteogenesis imperfecta: demonstration of efficacy in a mouse model
    Edith A McCarthy
    Perinatology Division, The New York Presbyterian Hospital Cornell University, New York, USA
    Pediatr Res 52:660-70. 2002
  7. doi request reprint A novel locus for adolescent idiopathic scoliosis on chromosome 12p
    Cathleen L Raggio
    Department of Pediatric Orthopedics, Hospital for Special Surgery, 535 East 70th Street, New York, New York 10021, USA
    J Orthop Res 27:1366-72. 2009
  8. ncbi request reprint DLL3 as a candidate gene for vertebral malformations
    Philip F Giampietro
    Department of Medical Genetic Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA
    Am J Med Genet A 140:2447-53. 2006
  9. ncbi request reprint Evaluation of SLC35A3 as a candidate gene for human vertebral malformations
    Nader Ghebranious
    Molecular Diagnostics Genotyping Laboratory, Marshfield Clinic, Marshfield, Wisconsin, USA
    Am J Med Genet A 140:1346-8. 2006
  10. pmc Congenital and idiopathic scoliosis: clinical and genetic aspects
    Philip F Giampietro
    Medical Genetics Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA
    Clin Med Res 1:125-36. 2003

Research Grants

Collaborators

  • Adele L Boskey
  • Philip F Giampietro
  • Erin M Carter
  • Nader Ghebranious
  • Jessica G Davis
  • F Stig Jacobsen
  • Ingrid Glurich
  • Thomas Faciszewski
  • Jennifer Kislow
  • Elizabeth McPherson
  • Robert D Blank
  • James K Burmester
  • Kristen Rasmussen
  • Lynn Ivacic
  • Edith A McCarthy
  • Lorraine Montuori
  • Oheneba Boachie-Adjei
  • Richard M Pauli
  • James Womack
  • Vikram Kumar
  • Sargam Jain
  • Nancy P Camacho
  • Elizabeth A Miller
  • Michael D Hossack

Detail Information

Publications10

  1. ncbi request reprint Sexual dimorphism in adolescent idiopathic scoliosis
    Cathleen L Raggio
    Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021, USA
    Orthop Clin North Am 37:555-8. 2006
    ..There are important differences in male and female AIS that impact diagnosis, treatment, and outcomes...
  2. pmc Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations
    Nader Ghebranious
    University of Wisconsin Medical School, Madison, Wisconsin, USA and Geriatrics Research, Education, and Clinical Center, William S, Middleton Veterans Administration Medical Center, Madison, Wisconsin, USA
    Scoliosis 2:13. 2007
    ..We hypothesized that WNT3A mutations might account for a subset of congenital vertebral malformations...
  3. ncbi request reprint Advances in understanding etiology of achondroplasia and review of management
    Erin M Carter
    The Center for Skeletal Dysplasias, Hospital for Special Surgery, New York 10021, USA
    Curr Opin Pediatr 19:32-7. 2007
    ..Children commonly have recurrent ear infections, delayed motor milestones, and eventually develop bowed legs and lumbar lordosis. People with achondroplasia are generally of normal intelligence...
  4. ncbi request reprint Genetic and orthopedic aspects of collagen disorders
    Erin M Carter
    Kathryn O and Alan C Greenberg Center for Skeletal Dysplasias, Hospital for Special Surgery, New York, New York 11238, USA
    Curr Opin Pediatr 21:46-54. 2009
    ..Accordingly, abnormality in the various collagens produces a large category of diseases with heterogeneous symptoms. This review presents genetic and orthopedic aspects of type II, IX, and XI collagen disorders...
  5. pmc The kathryn o. And alan C. Greenberg center for skeletal dysplasias: an interdisciplinary approach
    Erin M Carter
    Kathryn O and Alan C Greenberg Center for Skeletal Dysplasias, Hospital for Special Surgery, 535 East 70th Street, New York, NY, 10021, USA
    HSS J 4:112-6. 2008
    ..Goals are achieved through a collaborative process that utilizes the expertise of the different professionals...
  6. ncbi request reprint Alendronate treatment for infants with osteogenesis imperfecta: demonstration of efficacy in a mouse model
    Edith A McCarthy
    Perinatology Division, The New York Presbyterian Hospital Cornell University, New York, USA
    Pediatr Res 52:660-70. 2002
    ..Based on the data from this study, ALN therapy in infants with OI should prove to be effective...
  7. doi request reprint A novel locus for adolescent idiopathic scoliosis on chromosome 12p
    Cathleen L Raggio
    Department of Pediatric Orthopedics, Hospital for Special Surgery, 535 East 70th Street, New York, New York 10021, USA
    J Orthop Res 27:1366-72. 2009
    ..This study is the first to find evidence of an AIS susceptibility locus on chromosome 12. Detection of AIS susceptibility QTLs on multiple chromosomes in this and other studies demonstrate that the condition is genetically heterogeneous...
  8. ncbi request reprint DLL3 as a candidate gene for vertebral malformations
    Philip F Giampietro
    Department of Medical Genetic Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA
    Am J Med Genet A 140:2447-53. 2006
    ....
  9. ncbi request reprint Evaluation of SLC35A3 as a candidate gene for human vertebral malformations
    Nader Ghebranious
    Molecular Diagnostics Genotyping Laboratory, Marshfield Clinic, Marshfield, Wisconsin, USA
    Am J Med Genet A 140:1346-8. 2006
  10. pmc Congenital and idiopathic scoliosis: clinical and genetic aspects
    Philip F Giampietro
    Medical Genetics Services, Marshfield Clinic, Marshfield, Wisconsin 54449, USA
    Clin Med Res 1:125-36. 2003
    ..Utilizing synteny analysis of the mouse and human genetic databases, likely candidate genes for human CS and IS were identified...

Research Grants1

  1. ALENDRONATE USE IN MODELS OF OSTEOGENESIS IMPERFECTA
    Cathleen Raggio; Fiscal Year: 2002
    ..Investigation of specific aspects of alendronate treatment will provide information critical to the determination of how to proceed with individualized treatment of infants and children with different types of O.I. ..