Ingrid A. Holm MD MPH
Clinical Genetics, Medical Biochemical Genetics
Assistant Professor of Pediatrics, Boston Children's Hospital
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300 Longwood AveBoston, MA 02115
Phone+1 617-355-7476
Fax+1 617-730-0245
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Summary
- Ingrid A. Holm, MD, MPH is a Pediatric Geneticist at Boston Children’s Hospital in Boston, MA. She completed her education at David Geffen School of Medicine at UCLA, and her Residency in Pediatrics and a dual fellowship in Medical Genetics and Pediatric Endocrinology at Boston Children’s Hospital. Dr. Holm has contributed extensively to the field with publications in Genetics in Medicine, Journal of Personalized Medicine, and Pediatrics. She primarily conducts research in the ethical, legal, and social implications (ELSI) of genomics, particularly in the pediatric setting. She has conducted clinical trials in integrating genomic sequencing into newborn sequencing and has been involved in large studies to understand the impact of returning genomic research results to individuals and health care providers. She also conducts rare disease research.
Education & Training
Boston Children’s Hospital/Boston Medical CenterFellowship, Pediatric Endocrinology, 1988 - 1992- Children's Hospital/Harvard Medical SchoolFellowship, Medical Biochemical Genetics, 1988 - 1992
- Boston Children’s Hospital/Boston Medical CenterResidency, Pediatrics, 1985 - 1988
David Geffen School of Medicine at UCLAClass of 1985
Certifications & Licensure
MA State Medical License 1990 - 2027
American Board of Pediatrics Pediatric Endocrinology
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Clinical Trials
- Genetic Contributions to Autism Spectrum Disorders Start of enrollment: 2007 Apr 01
- Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network Start of enrollment: 2015 Sep 16
Roles: Contact
Publications & Presentations
PubMed
- 1 citationsCovering medical care costs for participants in the eMERGE Network: Challenges for equity and implementation.Laura J Rasmussen-Torvik, Katherine E Bonini, Margaret H Harr, Mohammad Ali Abbass, Hana Bangash
Genetics in Medicine. 2025-08-01 - Growth Attenuation Therapy: Ongoing Ethical and Practical Challenges 20 Years Post Ashley.Stephen D Brown, Kerri O Kennedy, Faye F Holder-Niles, Irina A Anselm, Brian D Snyder
The American Journal of Bioethics. 2025-05-23 - 1 citationsPreferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns.Nina B Gold, Jacklyn O Omorodion, Maya C Del Rosario, Greysha Rivera-Cruz, Celeste Y Hsu
Journal of Genetic Counseling. 2025-04-01
Journal Articles
- Expanding the Phenotypic Spectrum Associated with OPHN1 VariantsJonathan D Picker, Ingrid A Holm, Monica H Wojcik, Pankaj B Agrawal, ScienceDirect
- Physicians’ Perspectives on Receiving Unsolicited Genomic ResultsGeorgia L Wiesner, Ingrid A Holm, Melanie F Myers, Kyle B Brothers, Ellen W Clayton, Nature
Press Mentions
Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill InfantsNovember 12th, 2024- Sudden, Unexplained Child Deaths Often Have a Genetic CauseMarch 8th, 2022
- Awards, Honors, and GrantsAugust 17th, 2021
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Grant Support
- Providing ethical guidance for the development of individualized genomic medicine as rare as n-of-1BOSTON CHILDREN'S HOSPITAL2022–2026
- Implementation of Whole Genome Sequencing as Screening in a Diverse Cohort of Healthy InfantsBRIGHAM AND WOMEN'S HOSPITAL2021–2025
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