Philip F. Giampietro, MD Print Friendly PageFaculty, 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.
UW School of Medicine and Public Health
|Department of Pediatrics|
Professional Certifications and Education
Weill Medical College of Cornell University
State University of New York Stony Brook University Hospital
Long Island Jewish Medical Center
State University of New York, Stony Brook, NY, 1986
|Medical interpreters are available to help patients communicate with hospital and clinic staff. For more information, please contact interpreter services at (608) 262-9000.|
Giampietro PF .
SNPping away at the genetic basis of adolescent idiopathic scoliosis. Ann Transl Med. 2015 May;3(Suppl 1):S26
[PubMed ID: 26046072]
Giampietro PF Armstrong L Stoddard A Blank RD Livingston J Raggio CL Rasmussen K Pickart M Lorier R Turner A Sund S Sobrera N Neptune E Sweetser D Santiago-Cornier A Broeckel U .
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes. Am J Med Genet A. 2015 Jan;167A(1):95-102
[PubMed ID: 25348728]
Liu S Wu N Liu J Ming X Chen J Pavelec D Su X Qiu G Tian Y Giampietro P Wu Z .
Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis. J Child Neurol. 2014 Oct 14;
[PubMed ID: 25316729]
Giampietro PF .
CORR Insights ®: Are copy number variants associated with adolescent idiopathic scoliosis? Clin Orthop Relat Res. 2014 Oct;472(10):3226-7
[PubMed ID: 25070916]
Giampietro PF Raggio CL Blank RD .
Heterozygous mutations in the T (brachyury) gene. J Med Genet. 2014 May;51(5):354
[PubMed ID: 24556085]
Scott Schwoerer J Laffin J Haun J Raca G Friez MJ Giampietro PF .
MECP2 duplication: possible cause of severe phenotype in females. Am J Med Genet A. 2014 Apr;164A(4):1029-34
[PubMed ID: 24458799]
Solomon BD Baker LA Bear KA Cunningham BK Giampietro PF Hadigan C Hadley DW Harrison S Levitt MA Niforatos N Paul SM Raggio C Reutter H Warren-Mora N .
An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association. J Pediatr. 2014 Mar;164(3):451-7.e1
[PubMed ID: 24332453]
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 Jun;161A(6):1432-5
[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]
Giampietro PF .
Genetic aspects of congenital and idiopathic scoliosis. Scientifica (Cairo). 2012;2012:152365
[PubMed ID: 24278672]
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]