Skip to Content
UW Health SMPH
Philip F. Giampietro, MD close
Philip F. Giampietro, MD
 

Philip F. Giampietro, MD Print Friendly Page

Faculty, University of Wisconsin School of Medicine and Public Health

Dr. Philip Giampietro earned his medical degree at the State University of New York - Stony Brook, and completed residencies at State University of New York - Stony Brook University Hospital and Long Island Jewish Medical Center. He also completed a fellowship at Weill Medical College of Cornell University.

Specialties

Pediatric Genetics and Metabolism

UW Health Clinics

Waisman Center
(608) 263-3301 | (800) 323-8942 | Map

Hospital Affiliation(s)

University of Wisconsin Hospital and Clinics (primary)
Meriter Hospital (secondary)

Languages Spoken

English
Medical interpreters are available to help patients communicate with hospital and clinic staff. For more information, please contact interpreter services at (608) 262-9000.

UW School of Medicine and Public Health

Department of Pediatrics

Professional Certifications and Education

Board Certification Clinical Genetics
Pediatrics
Fellowship Weill Medical College of Cornell University
Residency State University of New York Stony Brook University Hospital
Long Island Jewish Medical Center
Medical School State University of New York, Stony Brook, NY, 1986

PubMed Articles
Giampietro PF Baker MW Basehore MJ Jones JR Seroogy CM . Novel Mutation in TP63 Associated With Ectrodactyly Ectodermal Dysplasia and Clefting Syndrome and T Cell Lymphopenia. Am J Med Genet A. 2013 Apr 23;
[PubMed ID: 23613309]
Hesemann J Lauer E Ziska S Noonan K Nemeth B Scott-Schwoerer J McCarty C Rasmussen K Goldberg JM Sund S Eickhoff J Raggio CL Giampietro PF . Analysis of maternal risk factors associated with congenital vertebral malformations. Spine (Phila Pa 1976). 2013 Mar 1;38(5):E293-8
[PubMed ID: 23446706]
Ghebranious N Raggio CL Blank RD McPherson E Burmester JK Ivacic L Rasmussen K Kislow J Glurich I Jacobsen FS Faciszewski T Pauli RM Boachie-Adjei O Giampietro PF . Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations. Scoliosis. 2007 Sep 23;2:13
[PubMed ID: 17888180]