Expertise in
1
conditions
Expertise in
1
conditions
841 E Fayette St, 
Syracuse, NY 

Overview

Neeru Gandotra is a Medical Genetics provider in Syracuse, New York. Dr. Gandotra is highly rated in 1 condition, according to our data. Her top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia.

Her clinical research consists of co-authoring 24 peer reviewed articles. MediFind looks at clinical research from the past 15 years.

Specialties

Medical Genetics

Licenses

Medical Genetics, Ph.D. Medical Genetics in NY

Languages Spoken

English

Gender

Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Locations

841 E Fayette St, Syracuse, NY 13210

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.


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Frequently Asked Questions about Dr. Neeru Gandotra

How do I make an appointment with Dr. Neeru Gandotra?

You can book an appointment with Dr. Neeru Gandotra by calling their office at 203-980-5518. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.

Is Dr. Neeru Gandotra a top-rated expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency?

MediFind is an objective health platform that identifies experts based on real-world data. Dr. Neeru Gandotra is classified as an Advanced expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, 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. Neeru Gandotra specialize in?

While Dr. Neeru Gandotra is a Medical Genetics, they have specific expertise in Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Urea Cycle Disorders (UCD), and Methylmalonic Acidemia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.

Does Dr. Neeru Gandotra participate in research or clinical trials?

Yes. Dr. Neeru Gandotra has published 24 articles and abstracts on conditions like Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. You can view a list of Dr. Neeru Gandotra's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.

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

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