Ingrid A. Holm

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile

0.405Author DataRank

Indexed papers

3in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 3 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

Advanced Genetics(2022)10.1002/ggn2.202200012

Top 57%

0.281DataRank

Top 57%4 citations

Élise Douard, Robin L. Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan +10 more

Papers

Driven by 42 papers — median percentile 36. Top paper: “Returning integrated genomic risk and clinical recommendations: The eMERGE study”.

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Frontiers in Genetics(2022)10.3389/fgene.2022.867371

N/A

2.6DataRank · unranked

70 citations

Kurt D. Christensen, Casie A. Genetti, Richard B. Parad, Jill O. Robinson, Carrie L. Blout Zawatsky +9 more

Children’s rare disease cohorts: an integrative research and clinical genomics initiative

npj Genomic Medicine(2020)10.1038/s41525-020-0137-0

N/A

1.4DataRank · unranked

69 citations

Nicholas LeCompte, Mary M. Carmack, Andrew Quitadamo, Lily Wang, Meredith Park +16 more

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia

Brain(2023)10.1093/brain/awac460

N/A

0.992DataRank · unranked

35 citations

Hagar Mor Shaked, Kenneth Gable, Sita D. Gupta, Xueyang Pan, Niranjanakumari Somashekarappa +93 more

Perspectives of Rare Disease Experts on Newborn Genome Sequencing

JAMA Network Open(2023)10.1001/jamanetworkopen.2023.12231

N/A

0.596DataRank · unranked

52 citations

Sophia Adelson, Nidhi Shah, Shardae Williams, Sarah L. Bick, Emilie S. Zoltick +17 more

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Genetics in Medicine(2020)10.1038/s41436-020-01027-3

N/A

0.587DataRank · unranked

49 citations

Kirsty McWalter, Heleen te Brinke, Lodewijk IJlst, Petra M. Mooijer, Jos P.N. Ruiter +95 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

N/A

0.564DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression

Journal of Genetic Counseling(2021)10.1002/jgc4.1475

N/A

0.542DataRank · unranked

10 citations

Kurt D. Christensen, Melissa Kurtz Uveges, Susan E. Waisbren, Amy L. McGuire, Stacey Pereira +8 more

Adrenal Insufficiency in Mitochondrial Disease

Journal of Child Neurology(2016)10.1177/0883073815587327

N/A

0.505DataRank · unranked

28 citations

Ingrid A. Holm, Lisa A. Teot, Irina Anselm, Laurel Calderwood

A de novo BRPF1 variant in a case of Sudden Unexplained Death in Childhood

European Journal of Medical Genetics(2020)10.1016/j.ejmg.2020.104002

N/A

0.449DataRank · unranked

19 citations

Ingrid A. Holm, Annapurna Poduri, Catherine A. Brownstein, Sanda Alexandrescu, Jennifer Chen +3 more

Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

Value in Health(2020)10.1016/j.jval.2020.01.017

N/A

0.416DataRank · unranked

15 citations

Dmitry Dukhovny, Kathryn A. Phillips, Alan H. Beggs, Robert C. Green, Richard B. Parad +27 more

Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

Genetics in Medicine(2024)10.1016/j.gim.2024.101115

N/A

0.292DataRank · unranked

6 citations

Lauren C. Briere, Chloe Reuter, Perman Gochyyev, Maria T. Acosta, David R. Adams +94 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121

N/A

0.292DataRank · unranked

6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

Advanced Genetics(2022)10.1002/ggn2.202200012

Top 57%

0.281DataRank

Top 57%4 citations

Élise Douard, Robin L. Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan +10 more

Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad207

N/A

0.241DataRank · unranked

4 citations

Michelle E. Florido, Jamie Galarza-Cornejo, Suzanne Bakken, John Lynch, Wendy K. Chung +12 more

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

medRxiv(2022)10.1101/2022.03.18.22272284

N/A

0.241DataRank · unranked

4 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Talia S. Schwartz +13 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174

N/A

0.241DataRank · unranked

4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

Family genetic risk communication and reverse cascade testing in the BabySeq project

Genetics in Medicine(2024)10.1016/j.gim.2024.101350

N/A

0.208DataRank · unranked

3 citations

Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs +38 more

Diverse Participant Recruitment for Infant Sequencing in the BabySeq Project

medRxiv(2024)10.1101/2024.10.01.24314717

N/A

0.165DataRank · unranked

2 citations

Sheyenne A. Walmsley, Barbara W. Harrison, Crystal T. Stephens, Bethany Zettler, Greysha Rivera-Cruz +17 more

Development of self-phenotyping tools to empower patients and improve diagnostics

EBioMedicine(2025)10.1016/j.ebiom.2025.105965

Top 71%

0.124DataRank

Top 71%1 citations

Sonja I. Ziniel, Julie A. McMurry, Catherine A. Brownstein, John S. Brownstein, Erin Rooney Riggs +10 more

Insights from the largest diverse ancestry sex-specific disease map for genetically predicted height

npj Genomic Medicine(2025)10.1038/s41525-025-00464-w

N/A

0.104DataRank · unranked

1 citations

Elizabeth Litkowski, Mariaelisa Graff, Zhe Wang, Roelof A. J. Smit, Geetha Chittoor +34 more

Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patients

BioData Mining(2025)10.1186/s13040-024-00418-5

N/A

0.104DataRank · unranked

1 citations

Undiagnosed Diseases Network, Maria T. Acosta, David R. Adams, Ben Afzali, Ali Al-Beshri +95 more

Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia

medRxiv(2023)10.1101/2023.02.09.23285734

N/A

0DataRank · unranked

0 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

Prospective phenotyping of long-term survivors of generalized arterial calcification of infancy (GACI)

Genetics in Medicine(2020)10.1038/s41436-020-00983-0

N/A

0DataRank · unranked

90 citations

Mary E. Hackbarth, Shira G. Ziegler, Kristen S. Pan, Mary Scott Roberts, Douglas R. Rosing +18 more

Concurrent prenatal drinking and smoking increases risk for SIDS: Safe Passage Study report

EClinicalMedicine(2020)10.1016/j.eclinm.2019.100247

N/A

0DataRank · unranked

79 citations

Hannah C. Kinney, Robin L. Haynes, Johan Dempers, Colleen A. Wright, William P. Fifer +27 more

Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants

PEDIATRICS(2024)10.1542/peds.2024-068197

N/A

0DataRank · unranked

3 citations

Maya C. del Rosario, Henry A. Feldman, Hadley Stevens Smith, Ingrid A. Holm, Monica H. Wojcik

Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.008

N/A

0DataRank · unranked

3 citations

Eunjin Ryu, Benjamin Steger, Abhijit Dixit, Yoshihiko Saito, Juyeong Yoo +36 more

Genetic predictors of blood pressure traits are associated with preeclampsia

Scientific Reports(2024)10.1038/s41598-024-68469-6

N/A

0DataRank · unranked

2 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

LUSTR: a new customizable tool for calling genome-wide germline and somatic short tandem repeat variants

BMC Genomics(2024)10.1186/s12864-023-09935-9

N/A

0DataRank · unranked

0 citations

Camilo Toro, David R. Adams, Undiagnosed Diseases Network, Maria T. Acosta, Margaret P Adam +95 more

Multidimensional and Longitudinal Impact of a Genetic Diagnosis for Critically Ill Infants

medRxiv(2024)10.1101/2024.06.29.24309646

N/A

0DataRank · unranked

0 citations

Maya C. del Rosario, Henry A. Feldman, Hadley Stevens Smith, Ingrid A. Holm, Monica H. Wojcik

Rare and resilient: Longer-term experiences of families after genetic evaluation in the neonatal intensive care unit

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103490

N/A

0DataRank · unranked

1 citations

Maya del Rosario, Ingrid A. Holm, Monica H. Wojcik, Siwaar Abouhala

Parental Anxiety in Differences of Sex Development and Hypospadias: A Psychosocial Characterization

medRxiv(2025)10.1101/2025.08.07.25332342

N/A

0DataRank · unranked

0 citations

Jessica Kremen, Alayna Dutcher, Stacey Pereira, Ingrid A. Holm, Yee-Ming Chan +1 more

Population-Based Screening of Newborns: Findings From the NBS Expansion Study (Part One)

Frontiers in Genetics(2022)10.3389/fgene.2022.867337

N/A

0DataRank · unranked

21 citations

Kee Chan, Marc S. Williams, Susan A. Berry, Robert J. Currier, Piero Rinaldo +22 more

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

Genetics in Medicine(2022)10.1016/j.gim.2022.100002

N/A

0DataRank · unranked

24 citations

Amanda M. Gutierrez, Jill O. Robinson, Kurt D. Christensen, Casie A. Genetti, Carrie L. Blout Zawatsky +9 more

Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study

Journal of Medical Internet Research(2021)10.2196/21023

N/A

0DataRank · unranked

13 citations

Margaret A. Hojlo, Sampath Chennuri, Nitin Gujral, Heather Paterson, Kent A Shefchek +14 more

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.007

N/A

0DataRank · unranked

55 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Melissa Kurtz Uveges +12 more

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

UNC Libraries(2020)10.17615/rpzn-a165

N/A

0DataRank · unranked

0 citations

Gail P. Jarvik, Nanibaa’ A. Garrison, Wylie Burke, Jonathan S. Berg, John F. Connolly +27 more

Newborn Sequencing in Genomic Medicine and Public Health

UNC Libraries(2020)10.17615/p3y4-3s09

N/A

0DataRank · unranked

0 citations

Stacey Pereira, Sean D. Mooney, Anastasia L. Wise, Jennifer M. Puck, Timothy W. Yu +37 more

Returning Individual Research Results from Digital Phenotyping in Psychiatry

The American Journal of Bioethics(2023)10.1080/15265161.2023.2180109

N/A

0DataRank · unranked

32 citations

Matthew L. Baum, Nicole Martinez‐Martin, Adam S. Miner, Melissa Abraham, Catherine A. Brownstein +23 more

Advancing Understanding of Inequities in Rare Disease Genomics

Clinical Therapeutics(2023)10.1016/j.clinthera.2023.06.010

N/A

0DataRank · unranked

22 citations

Melanie O’Leary, Grace E. VanNoy, Brian Mangilog, Ingrid A. Holm, Yarden S. Fraiman +4 more

NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders

International Journal of Neonatal Screening(2023)10.3390/ijns9040063

N/A

0DataRank · unranked

13 citations

Zhanzhi Hu, Lynn Bush, Heidi Cope, Ingrid A. Holm, Stephen F. Kingsmore +4 more

NBSTRN Tools to Advance Newborn Screening Research and Support Newborn Screening Stakeholders

Preprints.org(2023)10.20944/preprints202309.2039.v1

N/A

0DataRank · unranked

10 citations

Zhanzhi Hu, Lynn Bush, Heidi Cope, Ingrid A. Holm, Stephen F. Kingsmore +4 more

Ingrid A. Holm

Indexed papers

Top data-sharing exemplar

Papers