Euan A. Ashley

Also affiliated with Stanford Health Care, Stanford Medicine, Center for Inherited Blood Disorders, Stanford University

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 1%percentile

12.4Author DataRank

Indexed papers

10in 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 10 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.

Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction

Circulation(2020)10.1161/circulationaha.119.044366

Top 4%

5.4DataRank

Top 4%216 citations

Larry Han, Sharlene M. Day, Iacopo Olivotto, Euan A. Ashley, Michelle Michels +13 more

Papers

Driven by 140 papers — median percentile 68. Top paper: “Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence”.

Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence

PLoS Genetics(2011)10.1371/journal.pgen.1002280

N/A

7.5DataRank · unranked

148 citations

Rong Chen, Sergio P. Cordero, Kelly E. Ormond, Colleen Caleshu, Konrad J. Karczewski +33 more

Hypertrophic Cardiomyopathy With Left Ventricular Systolic Dysfunction

Circulation(2020)10.1161/circulationaha.119.044366

Top 4%

5.4DataRank

Top 4%216 citations

Larry Han, Sharlene M. Day, Iacopo Olivotto, Euan A. Ashley, Michelle Michels +13 more

Multi-task deep learning for cardiac rhythm detection in wearable devices

npj Digital Medicine(2020)10.1038/s41746-020-00320-4

N/A

5.0DataRank · unranked

138 citations

Euan A. Ashley, Jessica Torres Soto

Temporal dynamics of the multi-omic response to endurance exercise training

Nature(2024)10.1038/s41586-023-06877-w

Top 7%

3.4DataRank

Top 7%248 citations

Primary authors, Lead Analysts, David Amar, Nicole R. Gay, Pierre M. Jean Beltran +95 more

Drug Discovery in a Multidimensional World: Systems, Patterns, and Networks

Journal of Cardiovascular Translational Research(2010)10.1007/s12265-010-9214-6

N/A

3.1DataRank · unranked

61 citations

Marina Sirota, Atul Janardhan Butte, Eric E. Schadt, Euan A. Ashley, Joel T. Dudley

Whole-Exome Sequencing Reveals TopBP1 as a Novel Gene in Idiopathic Pulmonary Arterial Hypertension

American Journal of Respiratory and Critical Care Medicine(2014)10.1164/rccm.201310-1749oc

N/A

3.1DataRank · unranked

77 citations

Ke Yuan, Maria A. Lyuksyutova, Mark E. Orcholski, Eric M. Shuffle, Luke Yancy +16 more

Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study

Frontiers in Cardiovascular Medicine(2017)10.3389/fcvm.2017.00053

N/A

2.8DataRank · unranked

56 citations

Shirin Zarafshar, Aleksandra Pavlovic, Benjamin A. Goldstein, Sandra Tsai, Jin Li +8 more

Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk

Nature Genetics(2022)10.1038/s41588-022-01069-0

N/A

2.5DataRank · unranked

159 citations

Shengen Shawn Hu, José Verdezoto Mosquera, Wei Feng, Chani J. Hodonsky, Doris Wong +19 more

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009

N/A

2.2DataRank · unranked

123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 more

Race, Sex, and Age Disparities in the Performance of ECG Deep Learning Models Predicting Heart Failure

Circulation Heart Failure(2023)10.1161/circheartfailure.123.010879

N/A

1.9DataRank · unranked

49 citations

J. Weston Hughes, Albert J. Rogers, Guson Kang, Sanjiv M. Narayan, Euan A. Ashley +2 more

Randomized Trial of Personal Genomics for Preventive Cardiology

Circulation: Cardiovascular Genetics(2012)10.1161/circgenetics.112.962746

N/A

1.6DataRank · unranked

30 citations

Themistocles L. Assimes, Michaela Kiernan, Aleksandra Pavlovic, Benjamin A. Goldstein, Veronica Yank +7 more

Left Ventricular Systolic Dysfunction in Patients Diagnosed With Hypertrophic Cardiomyopathy During Childhood: Insights From the SHaRe Registry

Circulation(2023)10.1161/circulationaha.122.062517

Top 17%

1.2DataRank

Top 17%21 citations

Thomas M. Roston, Peter Marstrand, Brian Claggett, Victoria N. Parikh, Adam Helms +20 more

Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

Cell(2012)10.1016/j.cell.2012.02.009

N/A

1.1DataRank · unranked

1301 citations

George I. Mias, Jennifer Li-Pook-Than, Lihua Jiang, Rong Chen, Elana Miriami +42 more

Clinical assessment incorporating a personal genome

The Lancet(2010)10.1016/s0140-6736(10)60452-7

N/A

0.978DataRank · unranked

676 citations

Atul Janardhan Butte, Matthew T. Wheeler, Rong Chen, Teri E. Klein, Frederick E. Dewey +28 more

Long-Term Outcomes After Septal Reduction Therapies in Obstructive Hypertrophic Cardiomyopathy: Insights From the SHARE Registry

Circulation(2024)10.1161/circulationaha.124.069378

Top 21%

0.961DataRank

Top 21%47 citations

Panagiotis Antiochos, Anjali Owens, Neal Lakdwala, Sara Saberi, Mark W. Russell +24 more

Molecular Choreography of Acute Exercise

Cell(2020)10.1016/j.cell.2020.04.043

N/A

0.929DataRank · unranked

488 citations

Si Wu, Kegan Moneghetti, Daniel Hornburg, Sara Ahadi, Ming‐Shian Tsai +27 more

Molecular adaptations in response to exercise training are associated with tissue-specific transcriptomic and epigenomic signatures

Cell Genomics(2024)10.1016/j.xgen.2023.100421

N/A

0.928DataRank · unranked

38 citations

Hanna Pinças, Gregory R. Smith, Elena Zaslavsky, Yongchao Ge, Mary Anne S. Amper +75 more

Clinical Interpretation and Implications of Whole-Genome Sequencing

JAMA(2014)10.1001/jama.2014.1717

N/A

0.919DataRank · unranked

456 citations

Megan E. Grove, Cuiping Pan, Benjamin A. Goldstein, Jonathan A. Bernstein, Hassan Chaib +26 more

A guide for the diagnosis of rare and undiagnosed disease: beyond the exome

Genome Medicine(2022)10.1186/s13073-022-01026-w

N/A

0.894DataRank · unranked

387 citations

Joshua W. Knowles, Euan A. Ashley, Shruti Marwaha

Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks

Nature Communications(2021)10.1038/s41467-020-20516-2

N/A

0.870DataRank · unranked

24 citations

Nicholas A. Sinnott-Armstrong, Euan A. Ashley, Manuel A. Rivas, David Amar

Performance comparison of whole-genome sequencing platforms

Nature Biotechnology(2011)10.1038/nbt.2065

N/A

0.865DataRank · unranked

319 citations

Michael J. Clark, Rui Chen, Rong Chen, Georges Natsoulis, Maeve O'Huallachain +9 more

Challenges in the clinical application of whole-genome sequencing

The Lancet(2010)10.1016/s0140-6736(10)60599-5

N/A

0.818DataRank · unranked

232 citations

Matthew T. Wheeler, Louanne Hudgins, Teri E. Klein, Atul Janardhan Butte, Russ B. Altman +3 more

High-throughput SARS-CoV-2 and host genome sequencing from single nasopharyngeal swabs

medRxiv(2020)10.1101/2020.07.27.20163147

Top 25%

0.801DataRank

Top 25%9 citations

Hannah N. De Jong, David Amar, Craig D. Hughes, Alexander G. Ioannidis, Rob Bierman +37 more

Erratum: Corrigendum: Performance comparison of whole-genome sequencing platforms

Nature Biotechnology(2012)10.1038/nbt0612-562e

N/A

0.771DataRank · unranked

9 citations

Michael J. Clark, Rui Chen, Rong Chen, Georges Natsoulis, Maeve O'Huallachain +10 more

Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic Cardiomyopathy

Circulation(2024)10.1161/circulationaha.124.069398

N/A

0.724DataRank · unranked

22 citations

Aaron Renberg, Eric D. Smith, Yao-Chang Tsan, Brynn Elder, Abbey Bullard +27 more

Time trajectories in the transcriptomic response to exercise - a meta-analysis

Nature Communications(2021)10.1038/s41467-021-23579-x

N/A

0.719DataRank · unranked

120 citations

Maléne E. Lindholm, Jessica Norrbom, Matthew T. Wheeler, Manuel A. Rivas, Euan A. Ashley +1 more

The mitochondrial multi-omic response to exercise training across rat tissues

Cell Metabolism(2024)10.1016/j.cmet.2023.12.021

N/A

0.650DataRank · unranked

75 citations

Nicole R. Gay, David Jimenez‐Morales, Pierre M. Jean Beltran, Megan E. Ramaker, Archana N. Raja +95 more

Accuracy of Smartphone Camera Applications for Detecting Atrial Fibrillation

JAMA Network Open(2020)10.1001/jamanetworkopen.2020.2064

N/A

0.648DataRank · unranked

74 citations

Sam Grigg, William Crawford, Mintu P. Turakhia, Marco Perez, Erik Ingelsson +5 more

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.02.016

N/A

0.639DataRank · unranked

70 citations

Chloe Reuter, Maura Ruzhnikov, Anita E. Beck, Emily Farrow, Lisa Emrick +91 more

Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis

American Journal of Epidemiology(2017)10.1093/aje/kww224

N/A

0.621DataRank · unranked

62 citations

Dennis P. Wall, Muin J. Khoury, John P. A. Ioannidis, Euan A. Ashley, Rachel L. Goldfeder

Bi-allelic ATG4D variants are associated with a neurodevelopmental disorder characterized by speech and motor impairment

npj Genomic Medicine(2023)10.1038/s41525-022-00343-8

N/A

0.605DataRank · unranked

18 citations

Vikas Bhambhani, Nour Gazzaz, Mariska Davids, Paalini Sathiyaseelan, Ellen F. Macnamara +95 more

Stretch-Induced Biased Signaling in Angiotensin II Type 1 and Apelin Receptors for the Mediation of Cardiac Contractility and Hypertrophy

Frontiers in Physiology(2020)10.3389/fphys.2020.00181

N/A

0.529DataRank · unranked

33 citations

Victoria N. Parikh, Euan A. Ashley, Kinya Seo

Molecular Transducers of Physical Activity Consortium (MoTrPAC): human studies design and protocol

Journal of Applied Physiology(2024)10.1152/japplphysiol.00102.2024

Top 40%

0.483DataRank

Top 40%21 citations

John M. Jakicic, Wendy M. Kohrt, Joseph A. Houmard, Michael E. Miller, Shlomit Radom‐Aizik +89 more

Mono- and Biallelic Protein-Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.121.003419

N/A

0.477DataRank · unranked

23 citations

David Jimenez‐Morales, Han Zhu, Kinya Seo, David Amar, Chunli Zhao +13 more

Learning epistatic polygenic phenotypes with Boolean interactions

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.24.396846

N/A

0.460DataRank · unranked

5 citations

Karl Kumbier, Aldo Cordova-Palomera, Matthew Aguire, Omer Ronen, Chengzhong Ye +8 more

Local read haplotagging enables accurate long-read small variant calling

Nature Communications(2024)10.1038/s41467-024-50079-5

N/A

0.457DataRank · unranked

20 citations

Daniel E. Cook, Maria Nattestad, Lucas Brambrink, Brandy McNulty, John E. Gorzynski +9 more

Temporal dynamics of the multi-omic response to endurance exercise training across tissues

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.21.508770

N/A

0.457DataRank · unranked

20 citations

David Amar, Nicole R. Gay, Pierre M. Jean Beltran, Joshua Adkins, José Juan Almagro Armenteros +95 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

Genome Research(2025)10.1101/gr.279323.124

N/A

0.425DataRank · unranked

11 citations

Bohan Ni, Chloe Reuter, John E. Gorzynski, Sarah Fazal, Devon Bonner +13 more

Interactions of physical activity, muscular fitness, adiposity, and genetic risk for NAFLD

Hepatology Communications(2022)10.1002/hep4.1932

N/A

0.406DataRank · unranked

14 citations

Sophia Figueroa Katz, Johanne Marie Justesen, Jack W. O’Sullivan, Peter Saliba‐Gustafsson, Themistocles L. Assimes +6 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

Kosmos: An AI Scientist for Autonomous Discovery

arXiv (Cornell University)(2025)10.48550/arxiv.2511.02824

N/A

0.396DataRank · unranked

13 citations

Angela Yiu, Benjamin Chang, Mathieu Bourdenx, Tyler Nadolski, Arvis Sulovari +32 more

Disruption of protein quality control of the human ether-à-go-go related gene K+ channel results in profound long QT syndrome

Heart Rhythm(2021)10.1016/j.hrthm.2021.10.005

N/A

0.385DataRank · unranked

12 citations

Lu Ren, Phung N. Thai, Seojin Park, Valeriy Timofeyev, Padmini Sirish +10 more

The Clinical Trajectory of NYHA Functional Class I Patients With Obstructive Hypertrophic Cardiomyopathy

JACC Heart Failure(2024)10.1016/j.jchf.2024.09.008

N/A

0.373DataRank · unranked

11 citations

Jiankang Liu, Iacopo Olivotto, Victoria N. Parikh, Euan A. Ashley, Michelle Michels +17 more

De novo variants in DENND5B cause a neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.001

N/A

0.345DataRank · unranked

9 citations

Valeria Tomati, Matteo P. Ferla, Mariateresa Lena, Julie S. Cohen, Ali Fatemi +94 more

Deconvoluting complex correlates of COVID-19 severity with a multi-omic pandemic tracking strategy

Nature Communications(2022)10.1038/s41467-022-32397-8

N/A

0.345DataRank · unranked

9 citations

Alexander G. Ioannidis, David Jimenez‐Morales, John E. Gorzynski, Hannah N. De Jong, Xiran Liu +65 more

Continuing a search for a diagnosis: the impact of adolescence and family dynamics

Orphanet Journal of Rare Diseases(2023)10.1186/s13023-022-02598-x

N/A

0.292DataRank · unranked

6 citations

Beverly M. Yashar, Undiagnosed Disease Network, Maria T. Acosta, Margaret P Adam, David R. Adams +95 more

Epistasis regulates genetic control of cardiac hypertrophy

Nature Cardiovascular Research(2025)10.1038/s44161-025-00656-8

N/A

0.288DataRank · unranked

5 citations

Tiffany M. Tang, Michelle Youlton, Chad S. Weldy, Omer Ronen, J. Weston Hughes +19 more

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

N/A

0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

Epistasis regulates genetic control of cardiac hypertrophy

Research Square(2023)10.21203/rs.3.rs-3509208/v1

N/A

0.256DataRank · unranked

4 citations

Nathan Youlton, Ana Kenney, Omer Ronen, Elizabeth Chin, Shirley Sutton +21 more

Mono- and bi-allelic protein truncating variants in alpha-actinin 2 cause cardiomyopathy through distinct mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.19.389064

N/A

0.241DataRank · unranked

4 citations

David Jimenez‐Morales, Han Zhu, Kinya Seo, David Amar, Chunli Zhao +12 more

A Just Genomics Needs an ELSI of Translation

The Hastings Center Report(2024)10.1002/hast.4938

N/A

0.241DataRank · unranked

4 citations

Nate Olson, Euan A. Ashley, Aaron J. Goldenberg, Holly K. Tabor, Meghan C. Halley

Cell-specific chromatin landscape of human coronary artery resolves regulatory mechanisms of disease risk

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.07.447388

N/A

0.241DataRank · unranked

4 citations

Shengen Shawn Hu, José Verdezoto Mosquera, Wei Feng, Chani J. Hodonsky, Doris Wong +18 more

Local read haplotagging enables accurate long-read small variant calling

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.556731

N/A

0.241DataRank · unranked

4 citations

Daniel E. Cook, Maria Nattestad, Brandy McNulty, John E. Gorzynski, Sneha D. Goenka +8 more

Clinical assessment incorporating a personal genome – Authors' reply

The Lancet(2010)10.1016/s0140-6736(10)61405-5

N/A

0.224DataRank · unranked

2 citations

Rong Chen, Atul Janardhan Butte, Euan A. Ashley, Alexander A. Morgan

Deep Learning–Based Continuous QT Monitoring to Identify High-Risk Prolongation Events After Class III Antiarrhythmic Initiation

Circulation(2025)10.1161/circulationaha.125.077494

N/A

0.215DataRank · unranked

3 citations

Sabyasachi Bandyopadhyay, Rishi Trivedi, Kelly Brennan, Xichong Liu, Prasanth Ganesan +10 more

Cardiac imaging of aortic valve area from 26,142 UK Biobank participants reveal novel genetic associations and shared genetic comorbidity with multiple disease phenotypes

medRxiv(2020)10.1101/2020.04.09.20060012

N/A

0.208DataRank · unranked

3 citations

Catherine Tcheandjieu, Jason Fries, Paroma Varma, Vincent S. Chen, Madalina Fiterau +11 more

Deciphering epistatic genetic regulation of cardiac hypertrophy

medRxiv(2023)10.1101/2023.11.06.23297858

N/A

0.208DataRank · unranked

3 citations

Tiffany M. Tang, Michelle Youlton, Chad S. Weldy, Omer Ronen, J. Weston Hughes +20 more

The contribution of RBM20 truncating variants to human cardiomyopathy

medRxiv(2025)10.1101/2025.07.26.25332081

N/A

0.208DataRank · unranked

3 citations

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

Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.121.003563

N/A

0.208DataRank · unranked

3 citations

Frederick E. Dewey, Pablo Cordero, Andreas A. Werdich, Anna Kirillova, Yong Huang +23 more

Mind the Gap: The Complete Human Genome Unlocks Benefits for Clinical Genomics

Clinical Chemistry(2022)10.1093/clinchem/hvac133

Top 66%

0.187DataRank

Top 66%2 citations

Laurens Wiel, Euan A. Ashley, Daniel Seung Kim

Molecular Choreography of Acute Exercise

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.13.905349

N/A

0.165DataRank · unranked

2 citations

Si Wu, Kegan Moneghetti, Daniel Hornburg, Sara Ahadi, Ming‐Shian Tsai +27 more

Learning epistatic polygenic phenotypes with Boolean interactions

PLOS ONE(2024)10.1371/journal.pone.0298906

N/A

0.165DataRank · unranked

2 citations

Karl Kumbier, Aldo Cordova-Palomera, Matthew Aguirre, Omer Ronen, Chengzhong Ye +8 more

The Accuracy of Smartphone Camera Apps to Detect Atrial Fibrillation: A Systematic Review, Meta-Analysis, Meta-Regression and Modeling Study

SSRN Electronic Journal(2019)10.2139/ssrn.3478118

N/A

0.104DataRank · unranked

1 citations

Sam Grigg, William Crawford, Marco Perez, Erik Ingelsson, Matthew T. Wheeler +5 more

Personalized Medicine and Cardiovascular Disease: From Genome to Bedside

Current Cardiovascular Risk Reports(2011)10.1007/s12170-011-0202-4

N/A

0.104DataRank · unranked

1 citations

Frederick E. Dewey, Juan Manuel Peralta, Joshua W. Knowles, Rong Chen, Atul Janardhan Butte +3 more

Generation of two human iPSC lines with Exon 3 mutations in BCL2-Associated Athanogene 3 (BAG3) from dilated cardiomyopathy patients

Stem Cell Research(2023)10.1016/j.scr.2023.103019

N/A

0.104DataRank · unranked

1 citations

Yang Zhou, Audrey Li, Euan A. Ashley, Matthew T. Wheeler, Joseph C. Wu +1 more

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

Genetics in Medicine(2025)10.1016/j.gim.2025.101369

N/A

0DataRank · unranked

4 citations

Lindsay C. Burrage, Sharayu Jangam, Jill A. Rosenfeld, Sandra von Hardenberg, Anke K. Bergmann +92 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

0DataRank · unranked

1 citations

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

Fine-tuning Large Language Models in Behavioral Psychology for Scalable Physical Activity Coaching

medRxiv(2025)10.1101/2025.02.19.25322559

N/A

0DataRank · unranked

6 citations

Anders Johnson, Marily Oppezzo, Narayan Schütz, Alexander Tolas, Ritu Doijad +9 more

Sustainability in translational genomics research with undiagnosed patients: What is it, why do we need it, and how do we do it?

Genetics in Medicine(2025)10.1016/j.gim.2025.101458

N/A

0DataRank · unranked

0 citations

Charis Tang, Lily Liang, Euan A. Ashley, Holly K. Tabor, Meghan C. Halley +1 more

Nucleosome-mediated conformational switches in micro-eccDNAs

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.14.659616

N/A

0DataRank · unranked

0 citations

Victor Velasco-Berrelleza, William Sandel, Thana Sutthibutpong, Victoria N. Parikh, Euan A. Ashley +5 more

Developing therapeutics for rare cardiovascular diseases

American Heart Journal(2025)10.1016/j.ahj.2025.09.004

N/A

0DataRank · unranked

0 citations

Dwight D. Koeberl, Shilpi Epstein, Lothar Roessig, Rodica Stan, Meghan C. Halley +10 more

Deep Learning-Based Approach to Emergency Department Chest Pain Risk Stratification by ECG

EMJ Cardiology(2025)10.33590/emjcardiol/kkid8224

N/A

0DataRank · unranked

0 citations

J. Weston Hughes, Guson Kang, James Zou, Albert J. Rogers, Sanjiv M. Narayan +3 more

Mapping the Functional Landscape of KCNQ1 to Define Ion Channel Mechanisms and Arrhythmia Risk

medRxiv(2025)10.64898/2025.12.15.25341924

N/A

0DataRank · unranked

0 citations

Ellen M Osborn, Megan Lancaster, Joseh J. Smith, Qianyi Shen, Temidayo Abe +24 more

Multiparametric Assessment of TNNI3 Variant Phenotypes in Human iPSC-Cardiomyocytes Correlates with Disease Severity in Patients

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.64898/2025.12.13.691658

N/A

0DataRank · unranked

0 citations

Peter PQ Tran, Brendan J. Floyd, Kyla Dunn, Dongju Han, Xiomara Carhuamaca +7 more

Additional file 8: of Achieving high-sensitivity for clinical applications using augmented exome sequencing

Figshare(2015)10.6084/m9.figshare.c.3641885_d12

Top 100%

0DataRank

Top 100%0 citations

Jason Harris, Nan Leng, Gábor Bartha, Deanna M. Church, Shujun Luo +20 more

Long-term, ambulatory 12-lead ECG from a single non-standard lead using perceptual reconstruction

medRxiv(2025)10.64898/2025.12.17.25342224

N/A

0DataRank · unranked

0 citations

I-Min Chiu, Rayan Ansari, Sheng Liu, J. Weston Hughes, Alexander C. Perino +8 more

Additional file 9: of Achieving high-sensitivity for clinical applications using augmented exome sequencing

Figshare(2015)10.6084/m9.figshare.c.3641885_d7

Top 100%

0DataRank

Top 100%0 citations

Jason Harris, Nan Leng, Gábor Bartha, Deanna M. Church, Shujun Luo +20 more

Additional file 2: of Achieving high-sensitivity for clinical applications using augmented exome sequencing

Figshare(2015)10.6084/m9.figshare.c.3641885_d11

Top 100%

0DataRank

Top 100%0 citations

Jason Harris, Nan Leng, Gábor Bartha, Deanna M. Church, Shujun Luo +20 more

Video-based AI for beat-to-beat assessment of cardiac function

Nature(2020)10.1038/s41586-020-2145-8

N/A

0DataRank · unranked

1051 citations

Bryan He, Amirata Ghorbani, Neal Yuan, Joseph E. Ebinger, Curtis P. Langlotz +6 more

Deep learning interpretation of echocardiograms

npj Digital Medicine(2020)10.1038/s41746-019-0216-8

N/A

0DataRank · unranked

480 citations

David Ouyang, Abubakar Abid, Bryan He, Jonathan H. Chen, Robert A. Harrington +4 more

Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy

Circulation(2020)10.1161/circulationaha.119.042339

N/A

0DataRank · unranked

332 citations

Amanda C. Garfinkel, Gabriela Venturini, Hiroko Wakimoto, Giuliana G. Repetti, Lorenzo Álamo +23 more

Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.120.002929

N/A

0DataRank · unranked

100 citations

Andrea D. Thompson, Amelia A. Glazier, Neha Hafeez, Samat Kabani, Juliani Rodriguez +18 more

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Brain(2020)10.1093/brain/awaa204

N/A

0DataRank · unranked

59 citations

Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy +95 more

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Physiological Genomics(2020)10.1152/physiolgenomics.00021.2020

N/A

0DataRank · unranked

52 citations

Kathia Zaleta-Rivera, Alexandre J. S. Ribeiro, Andrew Chia Hao Chang, Ching Shang, Feng Lan +8 more

Digital Health Applications for Pharmacogenetic Clinical Trials

Genes(2020)10.3390/genes11111261

N/A

0DataRank · unranked

12 citations

Latha Palaniappan, Euan A. Ashley, Stuart A. Scott, Hetanshi Naik

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Biophysical Journal(2020)10.1016/j.bpj.2020.01.012

N/A

0DataRank · unranked

36 citations

Kinya Seo, Euan A. Ashley, Ellen Kuhl, Francisco Sahli Costabal

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medRxiv(2020)10.1101/2020.06.17.20134163

N/A

0DataRank · unranked

14 citations

Anna Shcherbina, Johanne Marie Justesen, Mintu P. Turakhia, Marco Pérez, Hannah Wand +6 more

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.29.402974

N/A

0DataRank · unranked

0 citations

Adam Helms, Anamika Kannan, Jaime Yob, Neal K. Lakdawala, Samuel G. Wittekind +15 more

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The Journal of Experimental Medicine(2021)10.1084/jem.20210582

N/A

0DataRank · unranked

230 citations

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Clinical Infectious Diseases(2021)10.1093/cid/ciab394

N/A

0DataRank · unranked

70 citations

David Kim, Elizabeth J. Zudock, Marjan Hashemi, Kristel C. Tjandra, Angela J Rogers +55 more

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European Heart Journal(2021)10.1093/eurheartj/ehab598

N/A

0DataRank · unranked

65 citations

Peter Marstrand, Larry Han, Victoria N. Parikh, Adam Helms, Jodie Ingles +16 more

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EBioMedicine(2021)10.1016/j.ebiom.2021.103613

N/A

0DataRank · unranked

63 citations

Neal Yuan, Bryan He, Jiahong Ouyang, Joseph E. Ebinger, Patrick Botting +13 more

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Genetics in Medicine(2021)10.1038/s41436-020-01084-8

N/A

0DataRank · unranked

34 citations

Dustin Baldridge, Matt Velinder, Joel B. Krier, Kimberly LeBlanc, Cecilia Esteves +90 more

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Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.02.044

N/A

0DataRank · unranked

33 citations

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Genetics in Medicine(2021)10.1038/s41436-021-01152-7

N/A

0DataRank · unranked

30 citations

Georgi Stoyanov, Florian Erger, Constantine A. Stratakis, Nikolaos Settas, Edra London +95 more

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Genetics in Medicine(2021)10.1038/s41436-021-01216-8

N/A

0DataRank · unranked

26 citations

Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy Peirce, Jeremy Wegner +94 more

Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation

Genetics in Medicine(2021)10.1038/s41436-021-01134-9

N/A

0DataRank · unranked

18 citations

Adam Helms, Anamika Kannan, Jaime Yob, Neal K. Lakdawala, Samuel G. Wittekind +14 more

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Stem Cell Research(2021)10.1016/j.scr.2021.102284

N/A

0DataRank · unranked

4 citations

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Nature Biotechnology(2022)10.1038/s41587-022-01221-5

N/A

0DataRank · unranked

121 citations

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Annals of the Rheumatic Diseases(2022)10.1136/annrheumdis-2022-222629

N/A

0DataRank · unranked

70 citations

Shilpa Kodati, Laryssa A. Huryn, Hongying Wang, Blake M. Warner, Priyam Jani +95 more

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Human Molecular Genetics(2022)10.1093/hmg/ddac085

N/A

0DataRank · unranked

17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

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Brain(2022)10.1093/brain/awac223

N/A

0DataRank · unranked

16 citations

Aloran Mazumder, Daisuke Ogasawara, Rami Abou Jamra, Geneviève Bernard, Enrico Bertini +94 more

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Genetics in Medicine(2022)10.1016/j.gim.2022.03.014

N/A

0DataRank · unranked

16 citations

Kristin Grimsrud, Louise Lanoue, Alena Egense, Brandon Willis, Johanna Hörberg +95 more

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Nature Genetics(2022)10.1038/s41588-022-01150-8

N/A

0DataRank · unranked

8 citations

Euan A. Ashley, Holly K. Tabor, Meghan C. Halley

A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

Genetics in Medicine(2022)10.1016/j.gim.2022.12.001

N/A

0DataRank · unranked

1 citations

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npj Digital Medicine(2023)10.1038/s41746-023-00916-6

N/A

0DataRank · unranked

62 citations

James Tooley, Jessica Torres Soto, Anna Ostropolets, Tim Poterucha, Matthew Kai Christensen +12 more

Bi-allelic variants in INTS11 are associated with a complex neurological disorder

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.012

N/A

0DataRank · unranked

38 citations

Erica L. Macke, Marcello Niceta, Monika Weisz Hubshman, Oguz Kanca, Laura Schultz‐Rogers +95 more

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European Heart Journal(2023)10.1093/eurheartj/ehad561

N/A

0DataRank · unranked

20 citations

Petros Syrris, Alexandros Protonotarios, Athanasios Bakalakos, Jean-François Pruny, Raffaello Ditaranto +27 more

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897

N/A

0DataRank · unranked

10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.012

N/A

0DataRank · unranked

8 citations

Rossella Venditti, Evangelos A. Theodorou, Lauren C. Briere, Marion Rosello, Alfonsina Tirozzi +94 more

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The Journal of Pediatrics(2023)10.1016/j.jpeds.2023.113537

N/A

0DataRank · unranked

7 citations

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Journal of Community Genetics(2023)10.1007/s12687-023-00638-y

N/A

0DataRank · unranked

8 citations

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Genetics in Medicine(2023)10.1016/j.gim.2023.100833

N/A

0DataRank · unranked

6 citations

Jung-Wan Mok, Oguz Kanca, Sharayu Jangam, Cynthia J. Tifft, Ellen F. Macnamara +95 more

Macrocephaly and developmental delay caused by missense variants in RAB5C

Human Molecular Genetics(2023)10.1093/hmg/ddad130

N/A

0DataRank · unranked

4 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.13.523698

N/A

0DataRank · unranked

12 citations

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medRxiv(2023)10.1101/2023.07.06.23292312

N/A

0DataRank · unranked

11 citations

Yann Le Guen, Yi Zeng, John E. Gorzynski, Tanner Jensen, Chengran Yang +13 more

APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer’s Disease pathology

medRxiv(2023)10.1101/2023.07.20.23292771

N/A

0DataRank · unranked

5 citations

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Almanac — Retrieval-Augmented Language Models for Clinical Medicine

NEJM AI(2024)10.1056/aioa2300068

N/A

0DataRank · unranked

352 citations

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APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer’s disease pathology

Neuron(2024)10.1016/j.neuron.2024.01.008

N/A

0DataRank · unranked

41 citations

Yann Le Guen, Sunny Chen, Eun-Gyung Lee, Lesley Leong, John E. Gorzynski +23 more

Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humans

The Journal of Experimental Medicine(2024)10.1084/jem.20232005

N/A

0DataRank · unranked

37 citations

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Deep learning to detect left ventricular structural abnormalities in chest X-rays

European Heart Journal(2024)10.1093/eurheartj/ehad782

N/A

0DataRank · unranked

35 citations

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Physiological Adaptations to Progressive Endurance Exercise Training in Adult and Aged Rats: Insights from the Molecular Transducers of Physical Activity Consortium (MoTrPAC)

Function(2024)10.1093/function/zqae014

N/A

0DataRank · unranked

29 citations

Tyler J. Sagendorf, Gina M. Many, Ana K Lira, Luís Gustavo Oliveira de Sousa, Dam Bae +74 more

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Frontiers in Cardiovascular Medicine(2024)10.3389/fcvm.2024.1429230

N/A

0DataRank · unranked

16 citations

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The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.004

N/A

0DataRank · unranked

14 citations

Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill A. Rosenfeld +95 more

A 3′UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated With Increased Risk for FTLD-TDP

Neurology Genetics(2024)10.1212/nxg.0000000000200124

N/A

0DataRank · unranked

12 citations

Yann Le Guen, Yi Zeng, John E. Gorzynski, Tanner Jensen, Chengran Yang +13 more

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Acta Neuropathologica Communications(2024)10.1186/s40478-024-01853-5

N/A

0DataRank · unranked

12 citations

Jaume Forés-Martos, Claire Delpirou Nouh, Tanner Jensen, Kristen Vallejo, Romain Cayrol +5 more

Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

Genetics in Medicine(2024)10.1016/j.gim.2024.101166

N/A

0DataRank · unranked

11 citations

Nicole Legro, Dustin Baldridge, Jimann Shin, Angela Bowman, Berrak Uğur +89 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

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0DataRank · unranked

6 citations

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

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Genetics in Medicine(2024)10.1016/j.gim.2024.101218

N/A

0DataRank · unranked

4 citations

Kristy Jay, Alden Huang, Jijun Wan, Sharayu Jangam, Odelia Chorin +95 more

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Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.07.010

N/A

0DataRank · unranked

2 citations

Heena Patel, Siddharth Srivastava, Lindsay C. Swanson, Boris Keren, Sandra Whalen +95 more

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease

medRxiv(2024)10.1101/2024.03.22.24304565

N/A

0DataRank · unranked

5 citations

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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

The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

Genetics in Medicine(2024)10.1016/j.gim.2024.101203

N/A

0DataRank · unranked

0 citations

Laura Findley, Weihong Ni, Janet S. Sinsheimer, Francesca Cole, Cecilia Esteves +94 more

Prior vaccination prevents overactivation of innate immune responses during COVID-19 breakthrough infection

Science Translational Medicine(2025)10.1126/scitranslmed.adq1086

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0DataRank · unranked

20 citations

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Progress in Cardiovascular Diseases(2025)10.1016/j.pcad.2025.01.010

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0DataRank · unranked

9 citations

Narayan Schuetz, Anders Johnson, Alexander Tolas, Sriya Mantena, Jack W. O’Sullivan +12 more

Titin-related familial dilated cardiomyopathy: factors associated with disease onset

European Heart Journal(2025)10.1093/eurheartj/ehaf380

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0DataRank · unranked

9 citations

Robert A. Fletcher, Stacey Peters, Monique Ohanian, Magdalena Soka, Andrei Smolnikov +95 more

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npj Digital Medicine(2025)10.1038/s41746-024-01407-y

N/A

0DataRank · unranked

7 citations

Neal K. Bhatia, Sabyasachi Bandyopadhyay, James Tooley, Rayan Ansari, Vyom Thakkar +13 more

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npj Cardiovascular Health(2025)10.1038/s44325-025-00083-5

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0DataRank · unranked

5 citations

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Frontiers in Cardiovascular Medicine(2025)10.3389/fcvm.2025.1546493

N/A

0DataRank · unranked

2 citations

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N/A

0DataRank · unranked

4 citations

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