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PHILIPPE STANIER, MD
MD
Emergency Medicine Physician
NPI: 1255891404IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
291022(MA)
CMS Specialties
PrimaryEMERGENCY MEDICINE
Education
LOMA LINDA UNIVERSITY SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossia.
PMID 19648124·J Med Genet·2009
8-other
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes.
PMID 19648291·Hum Mol Genet·2009
7-preclinical
Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects.
PMID 19533788·Am J Med Genet A·2009
8-other
Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression.
PMID 19487367·Hum Mol Genet·2009
8-other
Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing.
PMID 18480470·Genome Res·2008
4-observational
The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice.
PMID 18948418·Development·2008
7-preclinical
FGF signalling and SUMO modification: new players in the aetiology of cleft lip and/or palate.
PMID 17981355·Trends Genet·2007
6-review
Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight.
PMID 17180344·J Mol Med (Berl)·2007
8-other
STOX1 is not imprinted and is not likely to be involved in preeclampsia.
PMID 17325670·Nat Genet·2007
8-other
Abnormal folate metabolism in foetuses affected by neural tube defects.
PMID 17438019·Brain·2007
7-preclinical
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model.
PMID 17720888·Hum Mol Genet·2007
7-preclinical
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.
PMID 17846996·Am J Hum Genet·2007
7-preclinical
Limited evolutionary conservation of imprinting in the human placenta.
PMID 16614068·Proc Natl Acad Sci U S A·2006
7-preclinical
Imprinted genes and their role in human fetal growth.
PMID 16575189·Cytogenet Genome Res·2006
6-review
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.
PMID 17033962·Am J Hum Genet·2006
7-preclinical
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and human.
PMID 16531418·Hum Mol Genet·2006
7-preclinical
Neonatal buccal cell collection for DNA analysis.
PMID 15724057·Arch Dis Child Fetal Neonatal Ed·2005
8-other
Epithelial cell polarity genes are required for neural tube closure.
PMID 15800847·Am J Med Genet C Semin Med Genet·2005
6-review
Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients.
PMID 15952208·Am J Med Genet A·2005
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 300 Community Dr
Manhasset, NY 11030 - Phone
- (718) 470-8100
Quick Facts
- NPI
- 1255891404
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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