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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Philip F. Giampietro

Medical Genetic Services

Marshfield Clinic

1000 North Oak Avenue




Name/email consistency: high



  • Medical Genetic Services, Marshfield Clinic, 1000 North Oak Avenue, Marshfield, USA. 2003 - 2009
  • Division of Genetics, Department of Pediatrics, Weill Medical College of Cornell University, New York, USA. 2003


  1. Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans. Giampietro, P.F., Dunwoodie, S.L., Kusumi, K., Pourquié, O., Tassy, O., Offiah, A.C., Cornier, A.S., Alman, B.A., Blank, R.D., Raggio, C.L., Glurich, I., Turnpenny, P.D. Ann. N. Y. Acad. Sci. (2009) [Pubmed]
  2. Bone mineral density determinations by dual-energy x-ray absorptiometry in the management of patients with Marfan syndrome--some factors which affect the measurement. Giampietro, P.F., Peterson, M.G., Schneider, R., Davis, J.G., Burke, S.W., Boachie-Adjei, O., Mueller, C.M., Raggio, C.L. HSS. J (2007) [Pubmed]
  3. Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome. Giampietro, P.F., Schowalter, D.B., Merchant, S., Campbell, L.R., Swink, T., Roa, B.B. Childs. Nerv. Syst (2006) [Pubmed]
  4. DLL3 as a candidate gene for vertebral malformations. Giampietro, P.F., Raggio, C.L., Reynolds, C., Ghebranious, N., Burmester, J.K., Glurich, I., Rasmussen, K., McPherson, E., Pauli, R.M., Shukla, S.K., Merchant, S., Jacobsen, F.S., Faciszewski, T., Blank, R.D. Am. J. Med. Genet. A (2006) [Pubmed]
  5. An analysis of PAX1 in the development of vertebral malformations. Giampietro, P.F., Raggio, C.L., Reynolds, C.E., Shukla, S.K., McPherson, E., Ghebranious, N., Jacobsen, F.S., Kumar, V., Faciszewski, T., Pauli, R.M., Rasmussen, K., Burmester, J.K., Zaleski, C., Merchant, S., David, D., Weber, J.L., Glurich, I., Blank, R.D. Clin. Genet. (2005) [Pubmed]
  6. New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyria. Giampietro, P.F., Babu, D., Koehn, M.A., Jacobson, D.M., Mueller-Schrader, K.A., Moretti, C., Patten, S.F., Shaffer, L.G., Gorlin, R.J., Dobyns, W.B. Am. J. Med. Genet. A (2004) [Pubmed]
  7. Assessment of bone mineral density in adults and children with Marfan syndrome. Giampietro, P.F., Peterson, M., Schneider, R., Davis, J.G., Raggio, C., Myers, E., Burke, S.W., Boachie-Adjei, O., Mueller, C.M. Osteoporos. Int (2003) [Pubmed]
  8. Congenital and idiopathic scoliosis: clinical and genetic aspects. Giampietro, P.F., Blank, R.D., Raggio, C.L., Merchant, S., Jacobsen, F.S., Faciszewski, T., Shukla, S.K., Greenlee, A.R., Reynolds, C., Schowalter, D.B. Clin. Med. Res (2003) [Pubmed]
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