Overview
Jaya Ganesh is a Pediatrics provider practicing medicine in New York, New York.
Dr. Ganesh is highly rated in 27 conditions, according to our data. Her clinical expertise encompasses Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Fabry Disease.
She is actively involved in clinical research, co-authoring 42 peer reviewed articles and participating in 2 clinical trials.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-MEDICAID PLAN
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1428 Madison Ave, New York, NY 10029
1 Gustave L Levy Pl, New York, NY 10029
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
2 Clinical Trials
Weill Cornell Medicine Brain & Spine Center
Mark Souweidane is a Pediatrics specialist and a Neurosurgery provider practicing medicine in New York, New York. Dr. Souweidane is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Diffuse Midline Glioma H3 K27M-Mutant, Brain Tumor, Gliomatosis Cerebri, Medulloblastoma, and Osteotomy. Dr. Souweidane is board certified in American Board Of Pediatric Neurological Surgery and American Board Of Neurological Surgery. Dr. Souweidane is currently accepting new patients.
Robert Desnick is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Desnick is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Hereditary Coproporphyria, Fabry Disease, Aplasia Cutis Congenita, and Ectodermal Dysplasias.
CUIMC/NewYork-Presbyterian Morgan Stanley Children's Hospital
Joshua Milner is a leader in the field of discovery and immunopathogenesis of genetic diseases that lead to allergic symptoms. Among the disorders he has described and/or found major mechanistic insight are PLAID—an immune disorder that leads to lifelong cold urticaria, the glycosylation disorder PGM3 deficiency, ERBIN mutation, CARD11 dominant negative mutations, STAT3 gain-of-function, Hereditary Alpha Tryptasemia Syndrome, IL-6 receptor deficiency, and others. Dr. Milner graduated with an SB in biology from the Massachusetts Institute of Technology (MIT) in 1995 and an MD with distinction in immunology from the Albert Einstein College of Medicine. He completed his residency in pediatrics at the Children’s National Medical Center in Washington, DC, and, as the recipient of the Pediatric Scientist Development Program Fellowship, did his fellowship in allergy and immunology at NIAID. He completed a postdoctoral fellowship with Dr. William E. Paul, NIAID, examining issues of mouse T-cell receptor repertoires before beginning as an investigator in the Laboratory of Allergic Diseases in the NIAID, where he was eventually named chief.Dr. Milner's vision is to establish how genetic variation can help inform diagnosis and care of all patients with allergic disease—rare and common, severe and mild. This is achieved by performing genetic sequencing on samples from patients with allergic disease of all sorts, as well as performing functional studies on the same patient samples, which together help point to specific immune pathways that may be fundamentally causing disease. This comprehensive analysis, when performed in larger populations, will help personalize medicine so that patients can be better categorized for targeted care. Furthermore, this type of research and care requires a coordinated and comprehensive interdisciplinary approach, taking advantage of the expertise across the department of pediatrics and at multiple outpatient sites. Dr. Milner is highly rated in 11 conditions, according to our data. His clinical expertise encompasses Autosomal Dominant Hyper IgE Syndrome, Hyper IgE Syndrome, Multisystem Inflammatory Syndrome in Children (MIS-C), and Hereditary Alpha-Tryptasemia. Dr. Milner is board certified in Allergy And Immunology. Dr. Milner is currently accepting new patients.
Office
Morris Nejat is an Allergy and Immunologist and a Pediatrics provider practicing medicine in New York, New York. Dr. Nejat is highly rated in 12 conditions, according to our data. His clinical expertise encompasses Allergic Conjunctivitis, Conjunctivitis (Pink Eye), Sinusitis, and Allergic Rhinitis.
Icahn School Of Medicine At Mount Sinai
Margo Breilyn is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Breilyn is highly rated in 42 conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Phenylketonuria (PKU).
Elaine Pereira is a Medical Genetics specialist and a Pediatrics provider practicing medicine in New York, New York. Dr. Pereira is highly rated in 7 conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Deletion, Trisomy 13, Chromosome 13q Duplication, and Micrognathia.
Frequently Asked Questions about Dr. Jaya B. Ganesh
How do I make an appointment with Dr. Jaya B. Ganesh?
You can book an appointment with Dr. Jaya B. Ganesh by calling their office at 212-241-6947. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Jaya B. Ganesh a top-rated expert for Acid Sphingomyelinase Deficiency (ASMD)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Jaya B. Ganesh is classified as an Elite expert for Acid Sphingomyelinase Deficiency (ASMD), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Jaya B. Ganesh specialize in?
While Dr. Jaya B. Ganesh is a Pediatrics, they have specific expertise in Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, and Pompe Disease. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Jaya B. Ganesh participate in research or clinical trials?
Yes. Dr. Jaya B. Ganesh has published 42 articles and abstracts on conditions like Acid Sphingomyelinase Deficiency (ASMD). You can view a list of Dr. Jaya B. Ganesh's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Jaya B. Ganesh accept my insurance?
Dr. Jaya B. Ganesh accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 212-241-6947 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Elite
- Acid Sphingomyelinase Deficiency (ASMD)
- Distinguished
- Fabry DiseaseDr. Ganesh isDistinguished. Learn about Fabry Disease.
- Gaucher DiseaseDr. Ganesh isDistinguished. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Ganesh isDistinguished. Learn about Gaucher Disease Type 1.
- Niemann-Pick DiseaseDr. Ganesh isDistinguished. Learn about Niemann-Pick Disease.
- Pompe DiseaseDr. Ganesh isDistinguished. Learn about Pompe Disease.
- Advanced
- Autosomal Recessive Congenital Methemoglobinemia
- Beta-Ketothiolase DeficiencyDr. Ganesh isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Dihydrolipoamide Dehydrogenase Deficiency
- Gaucher Disease Type 2Dr. Ganesh isAdvanced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Ganesh isAdvanced. Learn about Gaucher Disease Type 3.
- Glutaric Acidemia Type 2Dr. Ganesh isAdvanced. Learn about Glutaric Acidemia Type 2.
- HyperlysinemiaDr. Ganesh isAdvanced. Learn about Hyperlysinemia.
- Leigh SyndromeDr. Ganesh isAdvanced. Learn about Leigh Syndrome.
- Mucopolysaccharidoses (MPS)Dr. Ganesh isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- PEPCK 1 DeficiencyDr. Ganesh isAdvanced. Learn about PEPCK 1 Deficiency.
- Phenylketonuria (PKU)Dr. Ganesh isAdvanced. Learn about Phenylketonuria (PKU).
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy
- Pyruvate Carboxylase DeficiencyDr. Ganesh isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Thymidine Kinase 2 Deficiency (TK2d)
- Urea Cycle Disorders (UCD)Dr. Ganesh isAdvanced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Von Gierke DiseaseDr. Ganesh isAdvanced. Learn about Von Gierke Disease.
- Experienced
- Acromicric DysplasiaDr. Ganesh isExperienced. Learn about Acromicric Dysplasia.
- Activated PI3K Delta Syndrome (APDS)Dr. Ganesh isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- AnemiaDr. Ganesh isExperienced. Learn about Anemia.
- Atrial TachycardiaDr. Ganesh isExperienced. Learn about Atrial Tachycardia.
- Delayed GrowthDr. Ganesh isExperienced. Learn about Delayed Growth.
- Glycogen Storage Disease Type 0Dr. Ganesh isExperienced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 13Dr. Ganesh isExperienced. Learn about Glycogen Storage Disease Type 13.
- Glycogen Storage Disease Type 7Dr. Ganesh isExperienced. Learn about Glycogen Storage Disease Type 7.
- Glycogen Storage Disease Type 9Dr. Ganesh isExperienced. Learn about Glycogen Storage Disease Type 9.
- HypotoniaDr. Ganesh isExperienced. Learn about Hypotonia.
- Infantile NeutropeniaDr. Ganesh isExperienced. Learn about Infantile Neutropenia.
- Isovaleric AcidemiaDr. Ganesh isExperienced. Learn about Isovaleric Acidemia.
- Kearns-Sayre SyndromeDr. Ganesh isExperienced. Learn about Kearns-Sayre Syndrome.
- Maternally Inherited Leigh SyndromeDr. Ganesh isExperienced. Learn about Maternally Inherited Leigh Syndrome.
- MosaicismDr. Ganesh isExperienced. Learn about Mosaicism.
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Phosphoglycerate Kinase DeficiencyDr. Ganesh isExperienced. Learn about Phosphoglycerate Kinase Deficiency.
- Phosphoglycerate Mutase DeficiencyDr. Ganesh isExperienced. Learn about Phosphoglycerate Mutase Deficiency.
- RASopathiesDr. Ganesh isExperienced. Learn about RASopathies.
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
