Sandra Davenport is a Rare/Genetic physician affiliated with Saint Louis University. OpenAlex indexes 43 publications with 2,896 citations (h-index 22).
Overview
Scholarship
indexed output and impact (OpenAlex)Distinct works indexed by OpenAlex.
Total citations across indexed works.
Hirsch index, productivity × impact (OpenAlex).
Contact
The practice address and phone this provider lists in the federal NPPES (CMS) registry.
Practice address
Telephone
Practice address and telephone from the federal NPPES registry.
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Matched to this physician's OpenAlex author record; most-cited works shown first.
- An intragenic deletion of the gene <i>MNAT1</i> in a family with pectus deformities
American Journal of Medical Genetics Part A
2014 - Understanding obstructive sleep apnea in children with CHARGE syndrome
International Journal of Pediatric Otorhinolaryngology
2012 - Figure 1. [Ears1a. Clipped-off helix, prominent antihelix...].2012
- Figure 3. [Typical CHARGE hand: square hand, short fingers, finger-like thumb, hockey-stick palmar crease].2012
- Table 3. [Summary of Molecular Genetic Testing Used in CHARGE Syndrome].2012
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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.”