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Author Details

Ingrid A Holm
Harvard Medical School
1985
147
39
PMIDPaper TitleJournal TitlePublished Year
37860921Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.J Am Med Inform Assoc2024
37860921Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.J Am Med Inform Assoc2024
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37987476NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders.Int J Neonatal Screen2023
37883979Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.Am J Hum Genet2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37155167Perspectives of Rare Disease Experts on Newborn Genome Sequencing.JAMA Netw Open2023
37279760Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project.Am J Hum Genet2023
37332751The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths.Front Med (Lausanne)2023
37246632Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.Genet Med2023
36621880Returning integrated genomic risk and clinical recommendations: The eMERGE study.Genet Med2023
37517917Advancing Understanding of Inequities in Rare Disease Genomics.Clin Ther2023
37517917Advancing Understanding of Inequities in Rare Disease Genomics.Clin Ther2023
37883979Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.Am J Hum Genet2023
37987476NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders.Int J Neonatal Screen2023
37155167Perspectives of Rare Disease Experts on Newborn Genome Sequencing.JAMA Netw Open2023
37343562Studying the impact of translational genomic research: Lessons from eMERGE.Am J Hum Genet2023
37279760Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project.Am J Hum Genet2023
37246632Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.Genet Med2023
37332751The fundamental need for unifying phenotypes in sudden unexpected pediatric deaths.Front Med (Lausanne)2023
34309124Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression.J Genet Couns2022
35571041Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.Front Genet2022
35938011Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One).Front Genet2022
36443235Re: Technical Report for Updated 2022 Recommendations for Reducing Infant Deaths in the Sleep Environment.Pediatrics2022
36422086Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.J Pers Med2022
36910592Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age.Adv Genet (Hoboken)2022
36556166Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their Children.J Pers Med2022
34309124Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression.J Genet Couns2022
35341654Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.Genet Med2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35027292Genetic Determinants of Sudden Unexpected Death in Pediatrics.Genet Med2022
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
35571041Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.Front Genet2022
36443235Re: Technical Report for Updated 2022 Recommendations for Reducing Infant Deaths in the Sleep Environment.Pediatrics2022
36910592Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age.Adv Genet (Hoboken)2022
36422086Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.J Pers Med2022
36556166Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their Children.J Pers Med2022
35938011Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One).Front Genet2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
35027292Genetic Determinants of Sudden Unexpected Death in Pediatrics.Genet Med2022
35341654Impact of returning unsolicited genomic results to nongenetic health care providers in the eMERGE III Network.Genet Med2022
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
33005041Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI).Genet Med2021
36046768Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.Am J Med Genet A2021
33538495Current Trends in Genetics and Neonatal Care.Adv Neonatal Care2021
34065005Preferences for Updates on General Research Results: A Survey of Participants in Genomic Research from Two Institutions.J Pers Med2021
33623412Genetic Factors Underlying Sudden Infant Death Syndrome.Appl Clin Genet2021
33776893Nicotinic 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.Front Neurol2021
33724192Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study.J Med Internet Res2021
34314210The Unrecognized Mortality Burden of Genetic Disorders in Infancy.Am J Public Health2021
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Jennifer A Sullivan
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Cinnamon Bloss
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William Gregory Feero
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Anneke Lucassen
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William A Faucett
Genomic Medicine Institute
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Anne-Marie Laberge
UNIVERSITY OF MONTREAL
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Misha Angrist
Duke University.
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Barbara B Biesecker
and Translational Research Center
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Mildred K Cho
Center for Biomedical Ethics, Stanford University School of Medicine
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Joann Bodurtha
Johns Hopkins McKusick-Nathans Department of Genetic Medicine
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Collaborators

Robert C Green
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 28
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 22
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 21
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 20
Alan H Beggs
Broad Institute of MIT and Harvard
Co-authored papers 20
John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 20
Cynthia A Prows
Cincinnati Children's Hospital Medical Center
Co-authored papers 17
Janet L Williams
Genomic Medicine Institute
Co-authored papers 16
Amy L McGuire
Baylor College of Medicine.
Co-authored papers 16
Melanie F Myers
Cincinnati Children's Hospital Medical Center
Co-authored papers 15
Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 15
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 14
Marc S Williams
University of Washington Medical Center
Co-authored papers 14
Heidi L Rehm
The Broad Institute of MIT and Harvard
Co-authored papers 14
Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
Co-authored papers 12
Margaret Harr
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 12
Kurt D Christensen
Harvard Medical School, Harvard Pilgrim Health Care Institute
Co-authored papers 12
Catherine A Brownstein
Harvard Medical School.
Co-authored papers 12
Kathleen A Leppig
Kaiser Permanente Washington
Co-authored papers 11
Sharon Aufox
Northwestern University, Center for Genetic Medicine
Co-authored papers 11
Kyle B Brothers
Norton Children's Research Institute Affiliated with the University of Louisville
Co-authored papers 11
Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
Co-authored papers 11
Isaac S Kohane
Harvard Medical School
Co-authored papers 10
Pankaj B Agrawal
Broad Institute of MIT and Harvard
Co-authored papers 10
Hakon Hakonarson
The Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 10
Sarah K Savage
Invitae Corporation
Co-authored papers 10
Timothy W Yu
Harvard Medical School
Co-authored papers 10
Stacey Pereira
Baylor College of Medicine.
Co-authored papers 9
Cassandra L Perry
Boston Children's Hospital.
Co-authored papers 9
Casie A Genetti
Boston Children's Hospital
Co-authored papers 9
Release 1.2