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SY-YEU CHERN, MD
MD
Anesthesiology Physician
NPI: 1790002343IndividualAccepts Medicare
Specialties, Licenses & Credentials
Anesthesiology PhysicianPrimary
Anesthesiology
Code: 207L00000X
MT196581(PA)25MA09661900(NJ)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
MT196581(PA)
CMS Specialties
PrimaryANESTHESIOLOGY
Education
VANDERBILT UNIVERSITY SCHOOL OF MEDICINE
Class of 2010
Research & Publications (20)
Conformity of LINAC-based stereotactic radiosurgery using dynamic conformal arcs and micro-multileaf collimator.
PMID 18565688·Int J Radiat Oncol Biol Phys·2009
8-other
Prenatal diagnosis of 46,XX,DER(13;21)(Q10;Q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites.
PMID 19346201·Taiwan J Obstet Gynecol·2009
5-case
Structural organization of WrbA in apo- and holoprotein crystals.
PMID 19665595·Biochim Biophys Acta·2009
8-other
Methicillin-resistant Staphylococcus aureus retropharyngeal abscess complicated by a cervical spinal subdural empyema.
PMID 19013810·J Clin Neurosci·2009
5-case
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
PMID 18395879·Prenat Diagn·2008
5-case
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings.
PMID 18619002·Genet Couns·2008
5-case
Novalis intensity-modulated radiosurgery: methods for pretreatment planning.
PMID 18580777·Neurosurgery·2008
8-other
Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13.
PMID 18400592·Taiwan J Obstet Gynecol·2008
5-case
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
PMID 17953951·Fertil Steril·2008
5-case
High proportion of single CYP2D6 gene deletion in Chinese attention-deficit-hyperactivity disorder children and its risk in oppositional defiant disorder.
PMID 19068017·Psychiatry Clin Neurosci·2008
8-other
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.
PMID 18400591·Taiwan J Obstet Gynecol·2008
5-case
NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
PMID 18383001·Prenat Diagn·2008
5-case
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
PMID 18304539·Fertil Steril·2008
5-case
Sensitive and broadly reactive reverse transcription-PCR assays to detect novel paramyxoviruses.
PMID 18579717·J Clin Microbiol·2008
8-other
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
PMID 18661486·Prenat Diagn·2008
5-case
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies.
PMID 18019377·Genet Couns·2007
5-case
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer.
PMID 18004080·Oncology·2007
8-other
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.
PMID 17962112·Taiwan J Obstet Gynecol·2007
5-case
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.
PMID 17962111·Taiwan J Obstet Gynecol·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
- 100 MADISON AVE
MORRISTOWN, NJ 07960 - Phone
- (973) 886-6784
Quick Facts
- NPI
- 1790002343
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 16
- Publications
- 20
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