Amanda Barone Pritchard
Biochemistry, Genetics and Molecular Biology · University of Michigan
Publications
32
Citations
204
Est. group size
~4
Recurring co-author estimate
Active years
8
Publishing since 2019
Typically publishes in teams of ~8 · 21% small-team papers (≤3 authors) · across 13 venues
- Direct Oral Challenge for Penicillin Allergy: A Hospital Implementation Evaluation Via the International Network of Antibiotic Allergy Nations (iNAAN) Study
Clinical Infectious Diseases · 2026
- Direct Oral Challenge for Penicillin Allergy: The International Network of Antibiotic Allergy Nations (iNAAN) Study
Clinical Infectious Diseases · 2026
- A nurse-run, pharmacist-led outpatient penicillin allergy de-label clinic in the UK
JAC-Antimicrobial Resistance · 2026
- P431: Advancing genetics and genomics education: The role and impact of the Association of Professors of Human and Medical Genetics (APHMG)*
Genetics in Medicine Open · 2026
- P730: Actionable parental diagnoses from expanded carrier screening
Genetics in Medicine Open · 2026
- Complex Problem, Digital Cure? Rethinking Penicillin Allergy Relabeling Using Technology-Enabled Care
Clinical Infectious Diseases · 2026
- Genetic Evaluation of the Child With Intellectual Disability or Global Developmental Delay: Clinical Report
PEDIATRICS · 2025
- Health Supervision for Children With 22q11.2 Deletion Syndrome: Clinical Report
PEDIATRICS · 2025
- P29 A nurse-run, pharmacist-led outpatient penicillin allergy de-label clinic in Cornwall
JAC-Antimicrobial Resistance · 2025
- Trisomy 5p: Long Recognized, Rarely Published‐ Three New Cases and Review of the Literature
American Journal of Medical Genetics Part A · 2025
- P266: Trisomy 5p: Long recognized, rarely published
Genetics in Medicine Open · 2024
- Ode to Fiona: The Face of Fortitude in <scp>FBXL4</scp> Deficiency
American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2024
- <i>TELO2</i>‐related syndrome (<scp>You‐Hoover‐Fong</scp> syndrome): Description of 14 new affected individuals and review of the literature
American Journal of Medical Genetics Part A · 2023
- An atypically mild case of ethylmalonic encephalopathy with pathogenic <scp><i>ETHE1</i></scp> variant
American Journal of Medical Genetics Part A · 2023
- ATYPICALLY MILD ETHYLMALONIC ENCEPHALOPATHY EXPANDS PHENOTYPIC SPECTRUM
Molecular Genetics and Metabolism · 2023
- American Journal of Medical Genetics Part A×6
- Genetics in Medicine Open×6
- Clinical Infectious Diseases×3
- Genetics in Medicine×3
- PEDIATRICS×2
- Kristen Lee
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Melissa Lah
Biochemistry, Genetics and Molecular Biology · Indiana University
- Elizabeth G. Ames
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Ayesha Ahmad
Biochemistry, Genetics and Molecular Biology · University of Michigan
- Bruce A. Palfey
Biochemistry, Genetics and Molecular Biology · University of Michigan
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 25, 2026.
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