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JAYA GANESH, M.D.
M.D.
NPI: 1740202159IndividualAccepts Medicare
Specialties, Licenses & Credentials
Clinical Biochemical Genetics Physician
Medical Genetics — Clinical Biochemical Genetics
Code: 207SG0202X
MD417029(PA)
Pediatrics Physician
Pediatrics
Code: 208000000X
MD417029(PA)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
MD417029(PA)
Education
OTHER
Class of 1994
Research & Publications (20)
Donor cardiac troponin-I: a biochemical surrogate of heart function.
PMID 19394856·Eur J Cardiothorac Surg·2009
8-other
Partial splenic embolization in a child with Gaucher disease, massive splenomegaly and severe thrombocytopenia.
PMID 19471915·Pediatr Radiol·2009
5-case
Complex management of a patient with a contiguous Xp11.4 gene deletion involving ornithine transcarbamylase: a role for detailed molecular analysis in complex presentations of classical diseases.
PMID 18524659·Mol Genet Metab·2008
5-case
A false-positive newborn screening result: goat's milk acidopathy.
PMID 18596009·Pediatrics·2008
5-case
Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.
PMID 18504129·Neuromuscul Disord·2008
7-preclinical
Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations.
PMID 18695062·Arch Neurol·2008
5-case
Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
PMID 18546365·Hum Mutat·2008
8-other
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
PMID 18332249·Arch Neurol·2008
8-other
Does the method of lung preservation influence outcome after transplantation? An analysis of 681 consecutive procedures.
PMID 17976468·J Thorac Cardiovasc Surg·2007
8-other
Fasting c-peptide and insulin-like growth factor-binding protein-1 levels help to distinguish childhood type 1 and type 2 diabetes at diagnosis.
PMID 17448127·Pediatr Diabetes·2007
3-trial
What new information pediatric autopsies can provide: a retrospective evaluation of 100 consecutive autopsies using family-centered criteria.
PMID 18056565·Arch Pediatr Adolesc Med·2007
8-other
Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: a unique case of gamma-hydroxybutyric aciduria and Williams syndrome.
PMID 17471494·Am J Med Genet B Neuropsychiatr Genet·2007
5-case
Lewis acid-promoted rearrangement of 2,3-epoxy alcohol derivatives: stereochemical control and selective formation of two types of chiral quaternary carbon centers from the single carbon skeleton.
PMID 16808506·J Org Chem·2006
8-other
Two newborns with nutritional vitamin B12 deficiency: challenges in newborn screening for vitamin B12 deficiency.
PMID 16464760·Haematologica·2005
5-case
Donor cause of death and medium-term survival after heart transplantation: a United Kingdom national study.
PMID 15867793·J Thorac Cardiovasc Surg·2005
8-other
Cumulative risk adjusted monitoring of 30-day mortality after cardiothoracic transplantation: UK experience.
PMID 15896612·Eur J Cardiothorac Surg·2005
4-observational
Donor cause of death and mid-term survival in lung transplantation.
PMID 16210128·J Heart Lung Transplant·2005
8-other
Outcome of heart-lung and bilateral sequential lung transplantation for cystic fibrosis: a UK national study.
PMID 15929949·Eur Respir J·2005
4-observational
Control chart methods for monitoring cardiac surgical performance and their interpretation.
PMID 15573063·J Thorac Cardiovasc Surg·2004
8-other
Medical staff attitudes toward family presence during pediatric procedures.
PMID 15057176·Pediatr Emerg Care·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- GENETICS & GENOMIC SCIENCES, 1 GUSTAVE LEVY L. PLACE #1497
NEW YORK, NY 10029 - Phone
- (212) 241-6947
Quick Facts
- NPI
- 1740202159
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 32
- Publications
- 20
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