Michael Gambello is a Rare/Genetic physician affiliated with Emory University. OpenAlex indexes 128 publications with 10,151 citations (h-index 48).
Overview
Scholarship
indexed output and impact (OpenAlex)Distinct works indexed by OpenAlex, matched via ORCID.
Total citations across indexed works.
Hirsch index, productivity × impact (OpenAlex).
Clinical & industry
trials, payments and federal fundingContact
The practice address and phone this provider lists in the federal NPPES (CMS) registry.
Practice address
2165 N Decatur Rd
Decatur, GA 300335307
Telephone
404-778-8570Registry record last updated 24 Apr 2014.
Medicare prescribing footprint (2022)
The drugs this prescriber writes for Medicare patients, grouped by drug class and therapeutic area. Every percentage is a share of their total prescribing, so you can see what they prescribe most. These are proportions, not patient counts or dollar amounts. No condition is inferred: the claims record what was prescribed, never why.
Metabolism & gastrointestinal
100%Phenylalanine Hydroxylase Activator100%Kuvan100%Part D<11 patients
Drug classes come from the WHO ATC and U.S. National Library of Medicine (RxClass) classifications; prescribing counts come from the CMS Medicare Part D Prescribers file. Each drug is counted once, under its primary class. Medicare fee-for-service only, so no Medicare Advantage, commercial, or pediatric prescribing is included. CMS publishes this data about 17 months after the fact.
NIH funding
1 NIH research award on record, funded 2017–2018 per NIH RePORTER. The latest:
- The Role of Polyamines in the Neuropathology of Tuberous Sclerosis Complex
Emory University
FY2018$195,000R21NS104410 - The Role of Polyamines in the Neuropathology of Tuberous Sclerosis Complex
Emory University
FY2017$234,000R21NS104410
Awards in the NIH RePORTER records where a principal investigator name matches this physician at an organization in their practice state. Latest award years shown; each row links to the project record on RePORTER.
Publications
Matched to this physician's OpenAlex author record; most-cited works shown first.
- Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
Genetics in Medicine
2021 - Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7
Genetics in Medicine
2020 - Rare <i>SUZ12</i> variants commonly cause an overgrowth phenotype
American Journal of Medical Genetics Part C Seminars in Medical Genetics
2019 - Natural history and genotype‐phenotype correlations in 72 individuals with <i>SATB2</i>‐associated syndrome
American Journal of Medical Genetics Part A
2018
Similar KOLs
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Robert Guyton, MD
Emory University
Keith Delman, MD
Emory University
Paolo Raggi, MD
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Monica Farley, MD
Emory University
A basic profile from our physician directory: identity and practice contact from the federal NPPES registry, research from OpenAlex, trials from ClinicalTrials.gov, payments from CMS Open Payments — shown itemized where we have matched records, as a count where we only have a total. This person hasn't been through our full identity-adjudication pipeline yet, so funding, congress activity and public presence aren't shown. Absence of a section means “not yet looked,” never “none found.”