RenataCGallagherMDPhD(She/Her)
Medical Genetics • San Francisco, CAClinical Biochemical Genetics, Clinical Genetics
Professor of Clinical Pediatrics, University of California, San Francisco
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Office
1825 4th Street
San Francisco, CA 94143Phone+1 415-476-2757Fax+1 415-476-9976
Summary
- Dr. Renata Gallagher is a medical geneticist in San Francisco, CA and is affiliated with UCSF Medical Center. She received her medical degree from UCSF and has been in practice 20 years. She specializes in clinical biochemical genetics and clinical genetics.
Education & Training
University of WashingtonResidency, Pediatrics, 1998 - 2001
University of California San Francisco School of MedicineClass of 1997
Certifications & Licensure
CA State Medical License 2014 - 2026
CO State Medical License 2006 - 2015- American Board of Medical Genetics and Genomics Clinical Biochemical Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics
- American Board of Pediatrics Pediatrics
Clinical Trials
- Longitudinal Study of Urea Cycle Disorders Start of enrollment: 2006 Feb 01
- Oxidative Stress, Inflammation and Acute Decompensation in Urea Cycle Disorders Start of enrollment: 2012 Feb 01
- Long-term Outcome of N-Carbamylglutamate Treatment in Propionic Acidemia and Methylmalonic Acidemia Start of enrollment: 2012 Sep 01
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Publications & Presentations
PubMed
- 13 citationsFunctional genomics of OCTN2 variants informs protein-specific variant effect predictor for Carnitine Transporter Deficiency.Megan L Koleske, Gregory McInnes, Julia E H Brown, Neil Thomas, Keino Hutchinson
Proceedings of the National Academy of Sciences of the United States of America. 2022-11-16 - 35 citationsA randomized, placebo-controlled clinical trial evaluating olipudase alfa enzyme replacement therapy for chronic acid sphingomyelinase deficiency (ASMD) in adults: One...Melissa Wasserstein, Robin Lachmann, Carla Hollak, Laila Arash-Kaps, Antonio Barbato
Genetics in Medicine. 2022-07-01 - 9 citationsFetal therapies and trials for lysosomal storage diseases: a survey of attitudes of parents and patients.Marisa E Schwab, Julia E H Brown, Billie Lianoglou, Chengshi Jin, Patricia C Conroy
Orphanet Journal of Rare Diseases. 2022-01-29
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