Ingrid A. Holm

15.5k total citations · 2 hit papers
116 papers, 4.3k citations indexed

About

Ingrid A. Holm is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Ingrid A. Holm has authored 116 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Genetics, 34 papers in Pediatrics, Perinatology and Child Health and 27 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Ingrid A. Holm's work include Genomics and Rare Diseases (36 papers), BRCA gene mutations in cancer (24 papers) and Ethics in Clinical Research (23 papers). Ingrid A. Holm is often cited by papers focused on Genomics and Rare Diseases (36 papers), BRCA gene mutations in cancer (24 papers) and Ethics in Clinical Research (23 papers). Ingrid A. Holm collaborates with scholars based in United States, Canada and Australia. Ingrid A. Holm's co-authors include Thomas O. Carpenter, Suzanne M. Jan de Beur, Karl Insogna, Erik A. Imel, Robert C. Green, Benjamin S. Wilfond, Howard M. Saal, Jeffrey R. Botkin, Xiaoyan Huang and L M Kunkel and has published in prestigious journals such as Science, New England Journal of Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Ingrid A. Holm

111 papers receiving 4.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A clinician's guide to X-linked hypophosphatemia

2011 412 citations Ingrid A. Holm et al. profile →
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

2015 354 citations Ingrid A. Holm et al. The American Journal of Human Genetics profile →

Peers

Countries citing papers authored by Ingrid A. Holm

Since Specialization

Citations

This map shows the geographic impact of Ingrid A. Holm's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ingrid A. Holm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid A. Holm more than expected).

Fields of papers citing papers by Ingrid A. Holm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ingrid A. Holm. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ingrid A. Holm. The network helps show where Ingrid A. Holm may publish in the future.

Co-authorship network of co-authors of Ingrid A. Holm

This figure shows the co-authorship network connecting the top 25 collaborators of Ingrid A. Holm. A scholar is included among the top collaborators of Ingrid A. Holm based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ingrid A. Holm. Ingrid A. Holm is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Plasma proteomic markers of pain and emotional dysfunction in fibrous dysplasia/McCune-Albright syndrome 2025 ·Bone ·(unknown), (unknown), (unknown), (unknown), Edin T. Randall, (unknown), (unknown), S R O'Donnell, Boyu Ren, Ingrid A. Holm, Alison M. Boyce, Zachary S. Peacock, Navil F. Sethna, Michael Mannstadt, Pui Y. Lee, Jaymin Upadhyay	0
2	Family genetic risk communication and reverse cascade testing in the BabySeq project 2024 ·Genetics in Medicine ·Melissa Kurtz Uveges, Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs, Robert C. Green, Ingrid A. Holm, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	0
3	P491: Enrollment of a diverse population into a trial of newborn genomic sequencing: Preliminary data from the BabySeq Project 2024 ·SHILAP Revista de lepidopterología ·Kurt D. Christensen, Hadley Stevens Smith, (unknown), (unknown), Stacey Pereira, Bruce R. Korf, Bruce D. Gelb, Carol R. Horowitz, Ramin Homayouni, Amy L. McGuire, Ingrid A. Holm, Robert C. Green	1
4	Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study 2023 ·Journal of the American Medical Informatics Association ·(unknown), (unknown), (unknown), Suzanne Bakken, John Lynch, Wendy K. Chung, Kathleen F. Mittendorf, Eta S. Berner, John J. Connolly, Chunhua Weng, Ingrid A. Holm, Atlas Khan, Krzysztof Kiryluk, Nita A. Limdi, Lynn Petukhova, Maya Sabatello, Julia Wynn	2
5	NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders 2023 ·International Journal of Neonatal Screening ·Kee Chan, Zhanzhi Hu, (unknown), Heidi Cope, Ingrid A. Holm, Stephen F. Kingsmore, (unknown), Curt Scharfe, Amy Brower	6
6	Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project 2023 ·The American Journal of Human Genetics ·Robert C. Green, Nidhi Shah, Casie A. Genetti, Timothy W. Yu, (unknown), Melissa Kurtz Uveges, Ozge Ceyhan‐Birsoy, Matthew S. Lebo, Stacey Pereira, Pankaj B. Agrawal, Richard B. Parad, Amy L. McGuire, Kurt D. Christensen, Talia S. Schwartz, Heidi L. Rehm, Ingrid A. Holm, Alan H. Beggs	25
7	Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression 2021 ·Journal of Genetic Counseling ·Talia S. Schwartz, Kurt D. Christensen, Melissa Kurtz Uveges, Susan E. Waisbren, Amy L. McGuire, Stacey Pereira, Jill O. Robinson, Alan H. Beggs, Robert C. Green, (unknown), Gloria Bachmann, Arnold B. Rabson, Ingrid A. Holm	7
8	Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study 2021 ·Journal of Medical Internet Research ·Jianqiao Li, Margaret A. Hojlo, (unknown), (unknown), (unknown), Kent Shefchek, Casie A. Genetti, Emily Cohn, Kara Sewalk, (unknown), Elizabeth D. Buttermore, (unknown), Alan H. Beggs, Pankaj B. Agrawal, John S. Brownstein, Melissa Haendel, Ingrid A. Holm, Joseph Gonzalez–Heydrich, Catherine A. Brownstein	3
9	Retrospective study of patterns of vitamin D testing and status at a single institution paediatric orthopaedics and sports clinics 2021 ·BMJ Open ·Susan T. Mahan, Kathryn E. Ackerman, Rachel L. DiFazio, Patricia E. Miller, (unknown), Nicholas J. Sullivan, Michael P. Glotzbecker, Ingrid A. Holm	1
10	Participant choices for return of genomic results in the eMERGE Network 2020 ·Genetics in Medicine ·Christin Hoell, Julia Wynn, Luke V. Rasmussen, Keith Marsolo, Sharon Aufox, Wendy K. Chung, John J. Connolly, Robert R. Freimuth, (unknown), Håkon Håkonarson, Margaret Harr, Ingrid A. Holm, Iftikhar J. Kullo, Philip E. Lammers, Kathleen A. Leppig, Nancy D. Leslie, Melanie F. Myers, Richard R. Sharp, Maureen E. Smith, Cynthia A. Prows	24
11	Placebo‐controlled crossover assessment of mecasermin for the treatment of Rett syndrome 2018 ·Annals of Clinical and Translational Neurology ·Heather M. O’Leary, Walter E. Kaufmann, (unknown), (unknown), Kush Kapur, Daniel Tarquinio, Nicole G. Cantwell, (unknown), Suzanne Rose, (unknown), (unknown), (unknown), Ingrid A. Holm, Mark E. Alexander, Lindsay C. Swanson, (unknown), (unknown), Charles A. Nelson, Mustafa Şahin	58
12	Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing? 2018 ·Journal of Empirical Research on Human Research Ethics ·(unknown), Sonja I. Ziniel, Sarah Savage, Kurt D. Christensen, Elissa R. Weitzman, Robert C. Green, Noelle Huntington, Debra Mathews, Ingrid A. Holm	5
13	From Sequence Data to Returnable Results: Ethical Issues in Variant Calling and Interpretation 2017 ·Genetic Testing and Molecular Biomarkers ·Ingrid A. Holm, Timothy W. Yu, Steven Joffe	3
14	Pediatric Issues in Return of Results and Incidental Findings: Weighing Autonomy and Best Interests 2017 ·Genetic Testing and Molecular Biomarkers ·Ingrid A. Holm	9
15	Family health history reporting is sensitive to small changes in wording 2016 ·Genetics in Medicine ·(unknown), Kurt D. Christensen, Sarah Savage, Noelle Huntington, Elissa R. Weitzman, Sonja I. Ziniel, (unknown), (unknown), Robert C. Green, Ingrid A. Holm	6
16	Practical considerations for implementing genomic information resources 2016 ·Applied Clinical Informatics ·Casey Lynnette Overby, John J. Connolly, Christopher G. Chute, Joshua C. Denny, Robert R. Freimuth, Andrea L. Hartzler, Ingrid A. Holm, Shannon Manzi, Jyotishman Pathak, Peggy Peissig, Maureen E. Smith, Marc S. Williams, Brian H. Shirts, Elena M. Stoffel, Peter Tarczy‐Hornoch, Carolyn R. Rohrer Vitek, Wendy A. Wolf, Justin Starren, Luke V. Rasmussen	22
17	Diagnostic Imaging of Child Abuse 2015 ·Cambridge University Press eBooks ·Paul K. Kleinman, (unknown), (unknown), John A. Kirkpatrick, Andrew E. Rosenberg, Ingrid A. Holm, Deborah Krakow, Christopher S. Greeley, Lori D. Frasier	50
18	Return of results in the genomic medicine projects of the eMERGE network 2014 ·Frontiers in Genetics ·Iftikhar J. Kullo, Raad A. Haddad, Cynthia A. Prows, Ingrid A. Holm, Saskia C. Sanderson, Nanibaa’ A. Garrison, Richard R. Sharp, Maureen E. Smith, Helena Kuivaniemi, Erwin P. Böttinger, John J. Connolly, Brendan J. Keating, Catherine A. McCarty, Marc S. Williams, Gail P. Jarvik	36
19	Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children’s Hospital Gene Partnership Informed Cohort Oversight Board 2014 ·Genetics in Medicine ·Ingrid A. Holm, Sarah Savage, Robert C. Green, Eric T. Juengst, Amy L. McGuire, Susan Kornetsky, Stephanie J. Brewster, Steven Joffe, Patrick Taylor	46
20	Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia 2009 ·The American Journal of Human Genetics ·Deborah Krakow, Joris Vriens, Natalia Camacho, Phi Luong, (unknown), Tara Funari, Carlos A. Bacino, Mira Irons, Ingrid A. Holm, Laurie S. Sadler, Ericka Okenfuss, Annelies Janssens, Thomas Voets, David L. Rimoin, Ralph S. Lachman, Bernd Nilius, Daniel H. Cohn	148

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact