William Gahl is a Rare/Genetic physician affiliated with National Institutes of Health. OpenAlex indexes 1,393 publications with 43,581 citations (h-index 103); ClinicalTrials.gov lists 13 registered studies matched to this name.
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 fundingClinical trials
- An Open-Label Phase 2 Study of N-Acetyl-D-Mannosamine (ManNAc) in Subjects With Primary Focal Segmental Glomerulosclerosis
Sponsor: National Human Genome Research Institute (NHGRI)
- Reverse Transcriptase Inhibitors in Aicardi Goutières Syndrome
Sponsor: Children's Hospital of Philadelphia
- Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
Sponsor: National Human Genome Research Institute (NHGRI)
Registered studies on ClinicalTrials.gov where the overall official or a site investigator name-matches this physician, confirmed against known institution/geography. Latest few shown; the full list is part of the full profile.
Similar KOLs
Other experts from the same institution or the same specialty.
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Steven Pavletic, MD
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Ronald Wapner, MD
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Virginia Kimonis, MD
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Robert Hopkin, MD
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Joel Charrow, MD
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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.”