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STEPHANIE CHEUNG, M.D.
M.D.
Psychiatry Physician
NPI: 1548309990IndividualAccepts Medicare
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
A90940(CA)253852(NY)
CMS Specialties
PrimaryPSYCHIATRY
Education
OTHER
Class of 2003
Research & Publications (20)
Insights of prognostication of Davies disease: what could we learn from serial magnetic resonance imaging studies?
PMID 19144428·Int J Cardiol·2010
5-case
The natural history of untreated sporadic vestibular schwannomas: a comprehensive review of hearing outcomes.
PMID 19538047·J Neurosurg·2010
6-review
Use of computational fluid dynamics to study forces exerted on prey by aquatic suction feeders.
PMID 19674998·J R Soc Interface·2010
7-preclinical
Novel PRPF31 and PRPH2 mutations and co-occurrence of PRPF31 and RHO mutations in Chinese patients with retinitis pigmentosa.
PMID 19506198·Arch Ophthalmol·2009
8-other
Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.
PMID 19606479·Am J Med Genet A·2009
5-case
Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
PMID 19584063·J Med Genet·2009
8-other
Laparoscopic hernia repair in children by the hook method: a single-center series of 433 consecutive patients.
PMID 19635295·J Pediatr Surg·2009
8-other
Identification of critical regions for clinical features of distal 10q deletion syndrome.
PMID 19558528·Clin Genet·2009
5-case
Realignment of interaural cortical maps in asymmetric hearing loss.
PMID 19474333·J Neurosci·2009
7-preclinical
Quantifying spatial heterogeneity in dynamic contrast-enhanced MRI parameter maps.
PMID 19466747·Magn Reson Med·2009
8-other
Expression and subcellular targeting of human insulin-like growth factor binding protein-3 in transgenic tobacco plants.
PMID 19504171·Transgenic Res·2009
8-other
Genomic and genic deletions of the FOX gene cluster on 16q24.1 and inactivating mutations of FOXF1 cause alveolar capillary dysplasia and other malformations.
PMID 19500772·Am J Hum Genet·2009
8-other
Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder.
PMID 19471977·Neurogenetics·2009
5-case
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
PMID 19578123·Hum Mol Genet·2009
8-other
A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder.
PMID 19606485·Am J Med Genet A·2009
5-case
Facial nerve preservation after vestibular schwannoma Gamma Knife radiosurgery.
PMID 19430881·J Neurooncol·2009
1-meta
Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping.
PMID 19557438·Hum Genet·2009
5-case
Pharmacokinetics of plasma efavirenz and CYP2B6 polymorphism in southern Chinese.
PMID 19531981·Ther Drug Monit·2009
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
- 622 W 168TH ST
NEW YORK, NY 10032 - Phone
- (212) 305-9985
Quick Facts
- NPI
- 1548309990
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 23
- Publications
- 20
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