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PHILIP GIAMPIETRO, MD PHD
MD PHD
Pediatrics Physician
NPI: 1346340080IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
036-154133(IL)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
43529(WI)
CMS Specialties
PrimaryMEDICAL GENETICS AND GENOMICS
Additional
PEDIATRIC MEDICINE
Education
STATE UNIVERSITY OF NEW YORK AT STONY BROOK, SCHOOL OF MEDICINE
Class of 1987
Research & Publications (20)
The role of cigarette smoking and statins in the development of postmenopausal osteoporosis: a pilot study utilizing the Marshfield Clinic Personalized Medicine Cohort.
PMID 19506792·Osteoporos Int·2010
6-review
Progress in the understanding of the genetic etiology of vertebral segmentation disorders in humans.
PMID 19154516·Ann N Y Acad Sci·2009
6-review
Bone mineral density determinations by dual-energy x-ray absorptiometry in the management of patients with Marfan syndrome--some factors which affect the measurement.
PMID 18751776·HSS J·2007
8-other
Acute health events in adult patients with genetic disorders: the Marshfield Epidemiologic Study Area.
PMID 16912579·Genet Med·2006
8-other
Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome.
PMID 15875198·Childs Nerv Syst·2006
5-case
An analysis of PAX1 in the development of vertebral malformations.
PMID 16207213·Clin Genet·2005
8-other
New syndrome: focal dermal hypoplasia, morning glory anomaly, and polymicrogyria.
PMID 14699622·Am J Med Genet A·2004
5-case
Congenital and idiopathic scoliosis: clinical and genetic aspects.
PMID 15931299·Clin Med Res·2003
6-review
A novel locus for adolescent idiopathic scoliosis on chromosome 12p.
PMID 19340878·J Orthop Res·2009
8-other
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.
PMID 19129173·Hum Mol Genet·2009
7-preclinical
Ovarian failure and dilated cardiomyopathy due to a novel lamin mutation.
PMID 19283854·Am J Med Genet A·2009
5-case
A missense T (Brachyury) mutation contributes to vertebral malformations.
PMID 18466071·J Bone Miner Res·2008
8-other
Oral desensitization in children with immunoglobulin E-mediated cow's milk allergy--follow-up at 4 yr and 8 months.
PMID 18221476·Pediatr Allergy Immunol·2008
7-preclinical
Community consultation and communication for a population-based DNA biobank: the Marshfield clinic personalized medicine research project.
PMID 19006210·Am J Med Genet A·2008
8-other
Bile duct anomalies in a male child with Noonan syndrome: a case for ras and notch pathway synergism.
PMID 18080325·Am J Med Genet A·2008
5-case
Abnormal vertebral segmentation and the notch signaling pathway in man.
PMID 17497699·Dev Dyn·2007
6-review
A novel microdeletion at 16p11.2 harbors candidate genes for aortic valve development, seizure disorder, and mild mental retardation.
PMID 17568417·Am J Med Genet A·2007
4-observational
Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations.
PMID 17888180·Scoliosis·2007
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1500 HIGHLAND AVE
MADISON, WI 53705 - Phone
- (608) 829-5485
Quick Facts
- NPI
- 1346340080
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 39
- Publications
- 20
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