🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Daniel P. Judge

Brigham and Women's Hospital

ORCID: 0000-0002-3407-0248

Also affiliated with Medical University of South Carolina

MedicineBiochemistry, Genetics and Molecular Biology

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 3%percentile
1.1Author DataRank

Indexed papers

2in 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 2 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 →

Top data-sharing exemplar

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

Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study

Circulation(2023)10.1161/circulationaha.123.064847
Top 25%
0.805DataRank
Top 25%25 citations

Garrie J. Haas, Elizabeth Jordan, Jinwen Cao, E. Kransdorf, Gregory A. Ewald +25 more

Papers

Driven by 21 papers — median percentile 59. Top paper: “Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study”.

Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study

Circulation(2023)10.1161/circulationaha.123.064847
Top 25%
0.805DataRank
Top 25%25 citations

Garrie J. Haas, Elizabeth Jordan, Jinwen Cao, E. Kransdorf, Gregory A. Ewald +25 more

Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial

Circulation(2023)10.1161/circulationaha.122.062507
N/A
0.469DataRank · unranked
12 citations

Elizabeth Jordan, Garrie J. Haas, Mark Hofmeyer, E. Kransdorf, Gregory A. Ewald +28 more

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

medRxiv(2023)10.1101/2023.04.03.23287612
Top 56%
0.292DataRank
Top 56%6 citations

Angharad M. Roberts, Pantazis I. Theotokis, Roddy Walsh, Philip J. Ostrowski, Matthew Edwards +30 more

An Evidence-based Assessment of Genes in Dilated Cardiomyopathy

medRxiv(2020)10.1101/2020.12.10.20247197
N/A
0DataRank · unranked
41 citations

Laiken Peterson, Tomohiko Ai, Babken Asatryan, Lucas Bronicki, Emily Brown +29 more

International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003273
N/A
0DataRank · unranked
236 citations

Jan D.H. Jongbloed, Ray E. Hershberger, Ana Morales, Daniel P. Judge, Petros Syrris +15 more

Exercise triggers CAPN1-mediated AIF truncation, inducing myocyte cell death in arrhythmogenic cardiomyopathy

Science Translational Medicine(2021)10.1126/scitranslmed.abf0891
N/A
0DataRank · unranked
92 citations

Gizem Keceli, Andrea Carpi, Nunzianna Doti, Jacopo Agrimi, Angeliki Asimaki +21 more

Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives

Journal of the American College of Cardiology(2023)10.1016/j.jacc.2023.03.419
N/A
0DataRank · unranked
23 citations

Elizabeth Jordan, Daniel D. Kinnamon, Jinwen Cao, Garrie J. Haas, Mark Hofmeyer +26 more

A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

Journal of Cardiovascular Translational Research(2023)10.1007/s12265-023-10403-8
N/A
0DataRank · unranked
16 citations

Edgar T. Hoorntje, Wouter P. te Rijdt, Laurens P. Bosman, Petros Syrris, Alexandros Protonotarios +36 more

The farnesyl transferase inhibitor (FTI) lonafarnib improves nuclear morphology in ZMPSTE24-deficient fibroblasts from patients with the progeroid disorder MAD-B

Nucleus(2023)10.1080/19491034.2023.2288476
N/A
0DataRank · unranked
7 citations

Khurts Shilagardi, Kelsey Tuminelli, Daniel P. Judge, Leslie B. Gordon, Susan Michaelis +1 more

Anticipating adaptation: tracking the impact of planned and unplanned adaptations during the implementation of a complex population-based genomic screening program

Translational Behavioral Medicine(2023)10.1093/tbm/ibad006
N/A
0DataRank · unranked
5 citations

Daniel P. Judge, Paul J. Nietert, Kelly J. Hunt, Amy Jackson, Sam Gallegos +9 more

Applying the R = MC2 implementation science heuristic to assess the impact of readiness on reach and implementation of a population‐wide genomic screening program

Journal of Genetic Counseling(2023)10.1002/jgc4.1775
N/A
0DataRank · unranked
1 citations

Kelly J. Hunt, Amy Jackson, Joseph Baierl, Lori McMahon, Daniel P. Judge +1 more

Establishing an infrastructure to optimize the integration of genomics into research: Results from a precision health needs assessment

Translational Behavioral Medicine(2024)10.1093/tbm/ibae008
N/A
0DataRank · unranked
1 citations

Gwendolyn S. Bouchie, Daniel P. Judge, Emma Coen, Sarah English, Samantha Norman +6 more

Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome

Research Square(2024)10.21203/rs.3.rs-4547888/v1
N/A
0DataRank · unranked
4 citations

Tyler Beck, Lilong Guo, Taylor Petrucci, Jordan E. Morningstar, Isabelle Kornblau +51 more

Implementing Precision Medicine for Dilated Cardiomyopathy: Insights from The DCM Consortium

medRxiv(2024)10.1101/2024.11.22.24317816
N/A
0DataRank · unranked
0 citations

Hanyu Ni, P. Parker, Daniel D. Kinnamon, Anjali Owens, Brian D. Lowes +27 more

KLK15 alters connective tissues in hypermobile Ehlers-Danlos syndrome

iScience(2025)10.1016/j.isci.2025.113343
N/A
0DataRank · unranked
8 citations

Taylor Petrucci, Tyler Beck, Victoria Daylor, Molly Griggs, Charlotte Griggs +52 more

The contribution of RBM20 truncating variants to human cardiomyopathy

medRxiv(2025)10.1101/2025.07.26.25332081
N/A
0DataRank · unranked
3 citations

Joyce Njoroge, Vikki A. Krysov, Bruna Gomes, Ryan Murtha, Chiaka Aribeana +42 more

Evaluation of Women with Peripartum or Dilated Cardiomyopathy and Their First-Degree Relatives: The DCM Precision Medicine Study

medRxiv(2025)10.1101/2025.02.18.25322501
N/A
0DataRank · unranked
0 citations

Rashmi Jain, Jonathan O. Mead, Garrie J. Haas, Mark Hofmeyer, Gregory A. Ewald +26 more

Hypermobile Ehlers‐Danlos syndromes: Complex phenotypes, challenging diagnoses, and poorly understood causes

Developmental Dynamics(2020)10.1002/dvdy.220
N/A
0DataRank · unranked
145 citations

Randall Burks, Steven A. Kautz, Daniel P. Judge, Mark E. Lavallee, Russell A. Norris +1 more

From Uncertain to Actionable: Significant Reduction in Variants of Uncertain Significance in Hereditary Germline Testing via Multi-Institutional Real-World Evidence

medRxiv(2025)10.1101/2025.08.12.25333547
N/A
0DataRank · unranked
0 citations

Matthew J. Ferber, Sophie I. Candille, Ildiko Thibodeau, Daniela Iacoboni, Amy C. Sturm +15 more

Endomyocardial Biopsy Characterization of Heart Failure With Preserved Ejection Fraction and Prevalence of Cardiac Amyloidosis

JACC Heart Failure(2020)10.1016/j.jchf.2020.04.007
N/A
0DataRank · unranked
289 citations

Lisa R. Yanek, Joban Vaishnav, Wendy Ying, Dhananjay Vaidya, Yizhen J. Lee +16 more

The prevalent I686T human variant and loss-of-function mutations in the cardiomyocyte-specific kinase gene TNNI3K cause adverse contractility and concentric remodeling in mice

Human Molecular Genetics(2020)10.1093/hmg/ddaa234
N/A
0DataRank · unranked
12 citations

Catalin F. Baicu, Hirofumi Watanabe, Kristy Wang, Ge Tao, Daniel P. Judge +5 more