Dan M. Roden

MedicineImmunology and Microbiology

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 1%percentile

34.5Author DataRank

Indexed papers

16in 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 16 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.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 139 papers — median percentile 86. Top paper: “A global reference for human genetic variation”.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update

Clinical Pharmacology & Therapeutics(2022)10.1002/cpt.2526

N/A

8.6DataRank · unranked

473 citations

Jasmine A. Luzum, Katrin Sangkuhl, Roseann S. Gammal, Marc S. Sabatine, Charles Michael Stein +12 more

The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin‐Associated Musculoskeletal Symptoms

Clinical Pharmacology & Therapeutics(2022)10.1002/cpt.2557

N/A

7.7DataRank · unranked

336 citations

Mikko Niemi, Laura B. Ramsey, Jasmine A. Luzum, E. Katriina Tarkiainen, Robert J. Straka +16 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Association of step counts over time with the risk of chronic disease in the All of Us Research Program

Nature Medicine(2022)10.1038/s41591-022-02012-w

N/A

5.5DataRank · unranked

223 citations

Jeffrey Annis, Shi Huang, Joshua A. Beckman, Francis Ratsimbazafy, Kayla Marginean +7 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

Human Genetics(2014)10.1007/s00439-013-1355-7

N/A

5.1DataRank · unranked

148 citations

Joshua C. Denny, Keyue Ding, Hayan Jouni, David R. Crosslin, Mariza de Andrade +15 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records

Genetics in Medicine(2010)10.1097/gim.0b013e3181efe2df

N/A

3.3DataRank · unranked

106 citations

Marylyn D. Ritchie, Kristin Brown-Gentry, Jill M. Pulley, Melissa Basford, Joshua C. Denny +5 more

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

Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance study

European Heart Journal(2021)10.1093/eurheartj/ehab362

Top 9%

2.4DataRank

Top 9%78 citations

Lee S. Nguyen, Javid J. Moslehi, Stéphane Éderhy, Bénédicte Lebrun‐Vignes, Dan M. Roden +3 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Nature(2023)10.1038/s41586-023-05806-1

N/A

2.1DataRank · unranked

107 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel KV11.1

Heart Rhythm(2020)10.1016/j.hrthm.2020.05.041

N/A

1.8DataRank · unranked

66 citations

Andrew M. Glazer, Chai‐Ann Ng, Daniel J. Blackwell, Christian Egly, Loren Vanags +9 more

PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records

Journal of the American Medical Informatics Association(2020)10.1093/jamia/ocaa104

Top 12%

1.8DataRank

Top 12%54 citations

Qiping Feng, V. Eric Kerchberger, Juan Zhao, Todd L. Edwards, Nancy J. Cox +5 more

Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.008

N/A

1.7DataRank · unranked

56 citations

Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson +64 more

Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1911

N/A

1.6DataRank · unranked

56 citations

Thomas O. Bergmeijer, Li Gong, Jean‐Luc Reny, Joshua P. Lewis, Braxton D. Mitchell +44 more

The All of Us Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research

Annual Review of Biomedical Data Science(2023)10.1146/annurev-biodatasci-122120-104825

Top 14%

1.5DataRank

Top 14%60 citations

Melissa Basford, Robert J. Carroll, Moira Rose Dillon, Heather Fullen, Jesse Leung +30 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

An International Multicenter Evaluation of Type 5 Long QT Syndrome

Circulation(2020)10.1161/circulationaha.119.043114

Top 15%

1.4DataRank

Top 15%60 citations

S. Yukiko Asaki, Andrea Mazzanti, J. Martijn Bos, Izabela Tuleta, Alison Muir +54 more

Proteomic and genetic analyses of influenza A viruses identify pan-viral host targets

Nature Communications(2023)10.1038/s41467-023-41442-z

N/A

1.2DataRank · unranked

62 citations

Michael McGregor, Mehdi Bouhaddou, Benjamin J. Polacco, Eun‐Young Kim, Thông Nguyen +50 more

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562

N/A

1.2DataRank · unranked

49 citations

Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger +46 more

Genetic testing in early-onset atrial fibrillation

European Heart Journal(2024)10.1093/eurheartj/ehae298

N/A

1.1DataRank · unranked

39 citations

Sean J. Jurgens, Joel Rämö, Ingrid E. Christophersen, Michiel Rienstra, Mina K. Chung +14 more

Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics

Bioinformatics(2023)10.1093/bioinformatics/btad655

Top 19%

1.1DataRank

Top 19%59 citations

William W. Stead, Ida Aka, April Barnado, Julie A. Bastarache, Elly Brokamp +22 more

Demonstrating paths for unlocking the value of cloud genomics through cross cohort analysis

Nature Communications(2023)10.1038/s41467-023-41185-x

N/A

1.0DataRank · unranked

22 citations

Margaret Sunitha Selvaraj, Henry Robert Condon, Kelsey Mayo, Sara Haidermota, Melissa Basford +12 more

The All of Us Research Program: Data quality, utility, and diversity

Patterns(2022)10.1016/j.patter.2022.100570

N/A

0.874DataRank · unranked

339 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +81 more

Atropine-induced sinus tachycardia protects against exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia

EP Europace(2020)10.1093/europace/euaa029

N/A

0.826DataRank · unranked

18 citations

M. Benjamin Shoemaker, Kathryn A. Gayle, Darlene Fountain, Dan M. Roden, Björn C. Knollmann +1 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics(2022)10.1038/s41588-021-01007-6

N/A

0.747DataRank · unranked

144 citations

Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet +95 more

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Science Translational Medicine(2017)10.1126/scitranslmed.aai8708

N/A

0.740DataRank · unranked

138 citations

Lisa Bastarache, Christian M. Shaffer, Silvana Gaudieri, Yaomin Xu, Andrew M. Glazer +12 more

Antipsychotics and the QTc Interval During Delirium in the Intensive Care Unit

JAMA Network Open(2024)10.1001/jamanetworkopen.2023.52034

N/A

0.734DataRank · unranked

18 citations

Christina Boncyk, Caroline I. Birdrow, Wencong Chen, Rameela Chandrasekhar, Deepak Gupta +9 more

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

The Journal of Pediatrics(2020)10.1016/j.jpeds.2020.03.064

N/A

0.727DataRank · unranked

17 citations

Lynn A. Sleeper, Bruce D. Gelb, Shaine A. Morris, Harry C. Dietz, Geoffrey A. Forbus +19 more

2-Hydroxybenzylamine (2-HOBA) to prevent early recurrence of atrial fibrillation after catheter ablation: protocol for a randomized controlled trial including detection of AF using a wearable device

Trials(2021)10.1186/s13063-021-05553-6

N/A

0.638DataRank · unranked

11 citations

Zachary T. Yoneda, Diane M. Crawford, Fei Ye, Mingfang Ao, Lisa M. Pitchford +7 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer’s disease with real-world clinical validation

npj Digital Medicine(2024)10.1038/s41746-024-01038-3

N/A

0.626DataRank · unranked

64 citations

Monika E. Grabowska, Alyson L. Dickson, Bingshan Li, Zhexing Wen, Dan M. Roden +7 more

Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension

Nature Communications(2022)10.1038/s41467-021-27751-1

N/A

0.621DataRank · unranked

62 citations

Qiping Feng, V. Eric Kerchberger, Scott D. Nelson, Qingxia Chen, Bingshan Li +8 more

Shared Decision Making in Cardiac Electrophysiology Procedures and Arrhythmia Management

Circulation Arrhythmia and Electrophysiology(2021)10.1161/circep.121.007958

N/A

0.614DataRank · unranked

59 citations

Angela Fagerlin, Paul J. Wang, Tinuola B. Ajayi, Larry A. Allen, Tina Baykaner +37 more

The 3D mutational constraint on amino acid sites in the human proteome

Nature Communications(2022)10.1038/s41467-022-30936-x

N/A

0.571DataRank · unranked

44 citations

Dan M. Roden, John A. Capra, Bian Li

Comparing medical history data derived from electronic health records and survey answers in the All of Us Research Program

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac046

N/A

0.568DataRank · unranked

43 citations

Robert M. Cronin, Robert J. Carroll, Karthik Natarajan, Kayla Marginean, Brandy Mapes +4 more

ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variants

Nature Communications(2024)10.1038/s41467-024-52474-4

N/A

0.558DataRank · unranked

13 citations

Tao Yang, Julie Laudeman, Maria Calandranis, M. Lorena Harvey, Joseph F. Solus +3 more

Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2 -LQTS Variant Classification and Cardiac Event Risk Stratification

Circulation(2024)10.1161/circulationaha.124.069828

N/A

0.553DataRank · unranked

39 citations

Chai‐Ann Ng, Takanori Aizawa, Luca Sala, Sahej Bains, Annika Winbo +37 more

Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.3821

N/A

0.553DataRank · unranked

39 citations

Lide Han, Jeffrey Annis, Hiral Master, Andrew Hughes, Dan M. Roden +3 more

Development of a System for Postmarketing Population Pharmacokinetic and Pharmacodynamic Studies Using Real‐World Data From Electronic Health Records

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1787

N/A

0.524DataRank · unranked

32 citations

Cole Beck, Elizabeth McNeer, Hannah L. Weeks, Michael L. Williams, Nathan T. James +9 more

Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization

Circulation(2022)10.1161/circulationaha.122.062193

N/A

0.510DataRank · unranked

29 citations

Tao Yang, Jonathan D. Mosley, Andrew M. Glazer, Andrew T. Hale, Dmytro O. Kryshtal +29 more

Benchmarking computational variant effect predictors by their ability to infer human traits

Genome biology(2024)10.1186/s13059-024-03314-7

N/A

0.494DataRank · unranked

26 citations

Da Kuang, Megan Lancaster, Roujia Li, Karen Liu, Jochen Weile +6 more

A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19

Journal of Biomedical Informatics(2020)10.1016/j.jbi.2020.103657

N/A

0.494DataRank · unranked

26 citations

Jeremy L. Warner, Travis Osterman, Quinn S. Wells, Xiao‐Ou Shu, Stephen A. Deppen +10 more

Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries

Genetics(2021)10.1093/genetics/iyab044

N/A

0.489DataRank · unranked

25 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology

Scientific Reports(2020)10.1038/s41598-020-64525-z

N/A

0.442DataRank · unranked

18 citations

Rebecca T. Levinson, Eric Farber‐Eger, Todd L. Edwards, Jacklyn N. Hellwege, Adriana M. Hung +20 more

Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci

European Heart Journal(2022)10.1093/eurheartj/ehac322

N/A

0.434DataRank · unranked

17 citations

Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W. Skov, Dan M. Roden +22 more

Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis

Arthritis & Rheumatology(2020)10.1002/art.41291

N/A

0.434DataRank · unranked

17 citations

Mingjian Shi, Qiping Feng, Cecilia P. Chung, Ge Liu, Nancy J. Cox +13 more

Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes

JACC. Clinical electrophysiology(2024)10.1016/j.jacep.2024.06.035

N/A

0.430DataRank · unranked

7 citations

Zachary T. Yoneda, Katherine Anderson, Fei Ye, Joseph A. Quintana, Jose Roberto Martinez‐Parachini +35 more

DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions

Journal of the American Medical Informatics Association(2021)10.1093/jamia/ocab019

N/A

0.425DataRank · unranked

16 citations

Scott D. Nelson, Juan Zhao, Cosby A. Stone, Qiping Feng, Qingxia Chen +9 more

The All of Us Research Program: data quality, utility, and diversity

medRxiv(2020)10.1101/2020.05.29.20116905

N/A

0.416DataRank · unranked

15 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +42 more

Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.123.004320

N/A

0.413DataRank · unranked

10 citations

Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N. Morrill, Yan V. Sun +54 more

Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid

Human Genetics(2022)10.1007/s00439-022-02442-z

N/A

0.406DataRank · unranked

14 citations

Jacklyn N. Hellwege, Yanfei Zhang, Eric S. Torstenson, Gail P. Jarvik, Ozan Dikilitas +10 more

Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.122.003792

N/A

0.406DataRank · unranked

14 citations

Jochen Weile, Prince J. Kannankeril, Andrew M. Glazer, Chloe Reuter, Calum A. MacRae +5 more

Clinical Management of Brugada Syndrome: Commentary From the Experts

Circulation Arrhythmia and Electrophysiology(2023)10.1161/circep.123.012072

N/A

0.406DataRank · unranked

14 citations

Lee L. Eckhardt, Elizabeth S. Kaufman, Elena Arbelo, Elijah R. Behr, Pedro Brugada +23 more

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

Nature Aging(2024)10.1038/s43587-024-00647-7

N/A

0.406DataRank · unranked

14 citations

Michael A. Raddatz, Yash Pershad, Daniel Nachun, Kent D. Taylor, Xiuqing Guo +40 more

The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young

Genome Medicine(2024)10.1186/s13073-024-01284-w

N/A

0.406DataRank · unranked

14 citations

Lorenzo L. Pesce, Edgar J. Hernández, Gregory Webster, Lisa Dellefave‐Castillo, Mark W. Russell +18 more

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

Cecelia Laurie, Jai Broome, Kent D. Taylor, Xiuqing Guo, Alan R. Shuldiner +82 more

Phenotyping coronavirus disease 2019 during a global health pandemic: Lessons learned from the characterization of an early cohort

Journal of Biomedical Informatics(2021)10.1016/j.jbi.2021.103777

N/A

0.396DataRank · unranked

13 citations

Harris T. Bland, Melissa L McPheeters, Quinn S. Wells, Eric Farber‐Eger, Cosmin A. Bejan +8 more

Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height

The Journal of Clinical Endocrinology & Metabolism(2021)10.1210/clinem/dgab272

N/A

0.396DataRank · unranked

13 citations

Ali Manouchehri, Christian M. Shaffer, Nataraja Sarma Vaitinadin, Jacklyn N. Hellwege, Joe‐Elie Salem +7 more

High-throughput framework for genetic analyses of adverse drug reactions using electronic health records

PLoS Genetics(2021)10.1371/journal.pgen.1009593

N/A

0.385DataRank · unranked

12 citations

Cosby A. Stone, Lan Jiang, Christian M. Shaffer, V. Eric Kerchberger, Cecilia P. Chung +8 more

Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.124.004569

N/A

0.373DataRank · unranked

11 citations

Matthew J. O’Neill, Ebony Richardson, Kate Thomson, Jodie Ingles, Ayesha Muhammad +15 more

Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100131

N/A

0.373DataRank · unranked

11 citations

Thomas Cassini, Ningning Hu, Tao Yang, Bian Li, Wangzhen Shen +13 more

Clonal hematopoiesis is driven by aberrant activation of TCL1A

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.10.471810

N/A

0.360DataRank · unranked

10 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

Genetic evaluation of early-onset atrial fibrillation: impact on patient management

European Heart Journal(2025)10.1093/eurheartj/ehaf829

N/A

0.345DataRank · unranked

9 citations

Mahsima Shabani, Hollie L. Williams, Dakota Grauherr, Wendy M. Kilbourne, Diane M. Crawford +39 more

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac057

N/A

0.345DataRank · unranked

9 citations

Laura Findley, Madison P. Goldrich, Tejinder Rakhra-Burris, Ana Stevens, Pamela A. Williams +34 more

Determinants of mosaic chromosomal alteration fitness

Nature Communications(2024)10.1038/s41467-024-48190-8

N/A

0.345DataRank · unranked

9 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0.330DataRank · unranked

8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

Nature Communications(2024)10.1038/s41467-024-48394-y

N/A

0.330DataRank · unranked

8 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +95 more

Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors

PubMed(2022)10.1142/9789811270611_0039

N/A

0.330DataRank · unranked

8 citations

Chad Dorn, Marguerite R. Irvin, Nita A. Limdi, James J. Cimino, T. Mark Beasley +7 more

Clinical associations with a polygenic predisposition to benign lower white blood cell counts

Nature Communications(2024)10.1038/s41467-024-47804-5

N/A

0.312DataRank · unranked

7 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant

Heart Rhythm(2023)10.1016/j.hrthm.2023.05.006

N/A

0.312DataRank · unranked

7 citations

Suet Nee Chen, Lynne Rumping, Renée Johnson, Marjon van Slegtenhorst, Andrew M. Glazer +19 more

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Nature Communications(2024)10.1038/s41467-024-51977-4

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0.312DataRank · unranked

7 citations

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Nature Communications(2020)10.1038/s41467-020-15236-6

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0.275DataRank

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0.269DataRank · unranked

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0.269DataRank · unranked

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.23.167759

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0.269DataRank · unranked

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medRxiv(2024)10.1101/2024.03.28.24305045

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0.269DataRank · unranked

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European Heart Journal(2020)10.1093/ehjci/ehaa946.3625

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0.241DataRank · unranked

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medRxiv(2025)10.1101/2025.10.30.25338549

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0.241DataRank · unranked

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0.241DataRank · unranked

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Top 63%

0.217DataRank

Top 63%2 citations

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0.208DataRank · unranked

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0.208DataRank · unranked

3 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.22.461398

N/A

0.208DataRank · unranked

3 citations

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medRxiv(2022)10.1101/2022.02.01.21268115

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0.191DataRank · unranked

1 citations

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medRxiv(2022)10.1101/2022.07.07.22277385

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0.165DataRank · unranked

2 citations

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medRxiv(2023)10.1101/2023.07.23.23293047

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0.165DataRank · unranked

2 citations

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medRxiv(2023)10.1101/2023.08.21.23293271

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0.165DataRank · unranked

2 citations

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medRxiv(2023)10.1101/2023.12.19.23299592

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0.165DataRank · unranked

2 citations

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0.165DataRank · unranked

2 citations

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medRxiv(2025)10.1101/2025.08.17.25333868

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0.107DataRank · unranked

1 citations

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medRxiv(2023)10.1101/2023.10.20.23297280

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0.104DataRank · unranked

1 citations

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0.104DataRank · unranked

1 citations

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medRxiv(2023)10.1101/2023.03.27.23287711

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0.104DataRank · unranked

1 citations

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0.104DataRank · unranked

1 citations

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Cardiovascular Research(2024)10.1093/cvr/cvae042

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0DataRank · unranked

9 citations

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Blood(2022)10.1182/blood.2021014240

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0DataRank · unranked

18 citations

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International Journal of Molecular Sciences(2022)10.3390/ijms23042225

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0DataRank · unranked

12 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.17.952606

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0DataRank · unranked

0 citations

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0DataRank · unranked

7 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.14.484344

N/A

0DataRank · unranked

7 citations

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Preprints.org(2022)10.20944/preprints202201.0046.v1

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0DataRank · unranked

4 citations

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JAMA Network Open(2023)10.1001/jamanetworkopen.2023.3526

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0DataRank · unranked

26 citations

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0DataRank · unranked

0 citations

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0DataRank · unranked

0 citations

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0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/bjv3-ys88

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0DataRank

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0 citations

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medRxiv(2023)10.1101/2023.07.07.23292388

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0DataRank · unranked

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PLoS Genetics(2020)10.1371/journal.pgen.1008862

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24 citations

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4 citations

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The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.015

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ParSE-seq: A Calibrated Multiplexed Assay to Facilitate the Clinical Classification of Putative Splice-altering Variants

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The Journal of Clinical Endocrinology & Metabolism(2022)10.1210/clinem/dgac695

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