Dr. Ingrid A Holm, MD

• Pediatric Endocrinology

*Healthgrades does not verify qualifications for medical specialties. Please verify your provider's specialty and qualifications directly with your provider and applicable medical board.

• Harvard School Of Public Health

  Medical School, 2003

• Harvard School Of Public Health|ucla School Of Medicine|university Of California School Of Medicine - Los Angeles

  Medical School, 2003

• Boston Children's Hospital, Genetics And Pediatric Endocrinology

  Fellowship Hospital, 2003

• University Of California, Los Angeles David Geffen School Of Medicine

  Medical School, 1989

• Boston Children's Hospital, Pediatrics

  Residency Hospital, 1989

• Boston Children's Hospital, Pediatrics

  Internship Hospital, 1986

• Brown University, Psychology

  Undergraduate School, 1979

• English

• Swedish

• Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically linksPLCL1to speech language development andIL5-IL13to Eosinophilic Esophagitis, 2014-11-18

• When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority, 2015-10-23

• The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths, 2023-06-02

• Clinical Management of Pediatric Genomic Testing, 2014-08-09

• Reconciling newborn screening and a novel splice variant inBTDassociated with partial biotinidase deficiency: a BabySeq Project case report BabySeq BTD case report, 2018-08-01

• A curated gene list for reporting results of newborn genomic sequencing, 2017-01-12

• Bone Disease in Thalassemia: A Frequent and Still Unresolved Problem, 2008-05-19

• Children's rare disease cohorts: an integrative research and clinical genomics initiative, 2020-07-06

• Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research, 2022-11-16

• A Systematic Literature Review of Individuals' Perspectives on Broad Consent and Data Sharing in the United States, 2015-11-19

• Suboptimal Clinical Documentation in Young Children with Severe Obesity at Tertiary Care Centers, 2016-09-06

• IgG Fc glycosylation as an axis of humoral immunity in childhood, 2019-10-24

• Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders, 2012-12-05

• Preferences for the return of individual results from research on pediatric biobank samples, 2016-09-13

• Participant choices for return of genomic results in the eMERGE Network, 2020-07-16

• Data sharing in the Undiagnosed Diseases Network, 2015-08-27

• EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children, 2013-12-03

• Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age, 2022-11-07

• Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project, 2019-03-17

• Perspectives of Rare Disease Experts on Newborn Genome Sequencing Perspectives of Rare Disease Experts on Newborn Genome Sequencing, 2023-05-08

• Loss-of-Function Mutations inPTPN11Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome, 2011-04-14

• Rethinking the "Open Future” Argument against Predictive Genetic Testing of Children, 2019-03-21

• Professional Responsibilities Regarding the Provision, Publication and Dissemination of Patient Phenotypes in the Context of Clinical Genetic and Genomic Testing: Points to Consider. A statement of the American College of Medical Genetics and Genomics (ACMG), 2018-01-11

• Association of Prenatal Exposure to Maternal Drinking and Smoking With the Risk of Stillbirth Association of Prenatal Exposure to Maternal Drinking and Smoking With Stillbirth, 2021-08-23

• Parental Perception of Self-Empowerment in Pediatric Pharmacogenetic Testing: The Reactions of Parents to the Communication of Actual and HypotheticalCYP2D6Test Results, 2016-08-30

• An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge, 2014-03-25

• Studying the impact of translational genomic research: Lessons from eMERGE, 2023-06-20

• The role of sodium channels in sudden unexpected death in pediatrics, 2020-05-25

• A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories, 2016-11-03

• Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One) NBS Expansion Study, 2022-07-22

• Participant satisfaction with a preference-setting tool for the return of individual research results in pediatric genomic research, 2019-07-17

• Preferences for Updates on General Research Results: A Survey of Participants in Genomic Research from Two Institutions, 2021-05-11

• Expanding the Phenotypic Spectrum Associated withOPHN1Variants, 2018-06-28

• Prospective phenotyping of long-term survivors of Generalized Arterial Calcification of Infancy (GACI), 2020-10-02

• Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network, 2022-03-24

• Physicians' Perspectives on Receiving Unsolicited Genomic Results, 2018-07-05

• Recommendations for returning genomic incidental findings? We need to talk!, 2013-08-01

• A GWAS Study on Liver Function Test Using eMERGE Network Participants, 2015-09-28

• Parents' Attitudes toward Consent and Data Sharing in Biobanks: A Multi-Site Experimental Survey, 2018-09-21

• Expectation versus Reality: The Impact of Utility on Emotional Outcomes after Returning Individualized Genetic Research Results in Pediatric Rare Disease Research, a Qualitative Interview Study, 2016-04-15

• Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing?, 2018-02-23

• Clinical Genetic Testing for Patients With Autism Spectrum Disorders, 2010-03-15

• Family Health History Reporting is Sensitive to Small Changes in Wording, 2016-05-05

• Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder, 2016-07-29

• Nicotinic Receptors in the Brainstem Ascending Arousal System in SIDS With Analysis of Pre-natal Exposures to Maternal Smoking and Alcohol in High-Risk Populations of the Safe Passage Study, 2021-03-10

• Do research participants share genomic screening results with family members?, 2021-10-19

• A CLINICIAN'S GUIDE TO X-LINKED HYPOPHOSPHATEMIA, 2011-05-02

• Parental Interest in Genomic Sequencing of Newborns: Enrollment Experience from the BabySeq Project, 2018-09-13

• The BabySeq project: implementing genomic sequencing in newborns, 2018-07-09

• In the Early Postpartum Period, Parents are Interested in Newborn Genomic Testing, 2014-12-04

• Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multi-Center Pilot for Pre-Emptive Pharmacogenomics in Electronic Health Record Systems, 2014-06-24

• The Informed Cohort Oversight Board: From Values to Architecture, 2012-08-27

• Ade novoBRPF1 variant in a case of Sudden Unexplained Death in Childhood, 2020-07-08

• The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network, 2022-02-23

• Discordant Results Between Conventional Newborn Screening and Genomic Sequencing in the BabySeq Project, 2021-03-26

• The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery, 2015-08-17

• Harmonizing Outcomes for Genomic Medicine: Comparison of eMERGE Outcomes to ClinGen Outcome/Intervention Pairs, 2018-07-13

• Impact of an electronic template on documentation of obesity in a primary care clinic, 2015-12-15

• Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network, 2018-03-01

• Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their Children, 2022-11-23

• Multiple juvenile idiopathic arthritis subtypes demonstrate pro-inflammatory IgG glycosylation, 2012-05-22

• Further Delineation of the Clinical Spectrum ofKAT6BDisorders and Allelic Series of Pathogenic Variants, 2020-05-19

• The Beliefs, Motivations, and Expectations of Parents Who Have Enrolled Their Children in a Genetic Biorepository, 2012-01-26

• Effects of Participation in a U.S. Trial of Newborn Genomic Sequencing on Parents at Risk for Depression, 2021-07-26

• Genetic Determinants of Sudden Unexpected Death in Pediatrics, 2022-01-10

• Plain-language medical vocabulary for precision diagnosis, 2018-11-14

• Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions, 2016-11-24

• FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation, 2019-12-10

• Inheritance of Febrile Seizures in Sudden Unexplained Death in Toddlers, 2014-04-23

• Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network, 2020-04-27

• Parents' Preferences for Return of Results in Pediatric Genomic Research, 2014-03-13

• Practical Guidance on Informed Consent for Pediatric Participants in a Biorepository, 2014-09-26

• SCN1AVariants Associated with Sudden Infant Death Syndrome, 2018-03-30

• Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network, 2020-05-13