OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
Krishna G. Aragam, Mark Chaffin, Rebecca T. Levinson, et al.
Circulation (2019) Vol. 139, Iss. 4, pp. 489-501
Open Access | Times Cited: 139

Showing 26-50 of 139 citing articles:

Leveraging Large-Scale Genetics of PTSD and Cardiovascular Disease to Demonstrate Robust Shared Risk and Improve Risk Prediction Accuracy
Antonia V. Seligowski, Burook Misganaw, Lucie Duffy, et al.
American Journal of Psychiatry (2022) Vol. 179, Iss. 11, pp. 814-823
Open Access | Times Cited: 26

Accelerometer-Measured Sedentary Behavior and Risk of Future Cardiovascular Disease
Ezimamaka Ajufo, Shinwan Kany, Joel Rämö, et al.
Journal of the American College of Cardiology (2024)
Closed Access | Times Cited: 5

Bone mineral density and cardiovascular diseases: a two-sample Mendelian randomization study
Ahmed Salih, Dorina-Gabriela Condurache, Stefania D’Angelo, et al.
JBMR Plus (2025) Vol. 9, Iss. 5
Open Access

The denitrosylase SCoR2 controls cardioprotective metabolic reprogramming
Zachary W. Grimmett, Rongli Zhang, Hua‐Lin Zhou, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Metastable Atrial State Underlies the Primary Genetic Substrate for MYL4 Mutation-Associated Atrial Fibrillation
Zaniar Ghazizadeh, Tuomas Kiviniemi, Sigurast Olafsson, et al.
Circulation (2019) Vol. 141, Iss. 4, pp. 301-312
Open Access | Times Cited: 35

The role of BAG3 in health and disease: A “Magic BAG of Tricks”
Heng Lin, Shon A. Koren, Gregor Cvetojevic, et al.
Journal of Cellular Biochemistry (2021) Vol. 123, Iss. 1, pp. 4-21
Open Access | Times Cited: 31

Contemporary and Future Approaches to Precision Medicine in Inherited Cardiomyopathies
Diane Fatkin, Hugh Calkins, Perry Elliott, et al.
Journal of the American College of Cardiology (2021) Vol. 77, Iss. 20, pp. 2551-2572
Open Access | Times Cited: 28

A lifecourse mendelian randomization study highlights the long-term influence of childhood body size on later life heart structure
Katie O’Nunain, Chloe Park, Helena Urquijo, et al.
PLoS Biology (2022) Vol. 20, Iss. 6, pp. e3001656-e3001656
Open Access | Times Cited: 21

Tissue-specific Grb10/Ddc insulator drives allelic architecture for cardiac development
Aimee M. Juan, Yee Hoon Foong, Joanne L. Thorvaldsen, et al.
Molecular Cell (2022) Vol. 82, Iss. 19, pp. 3613-3631.e7
Open Access | Times Cited: 21

The UK Biobank: A Shining Example of Genome-Wide Association Study Science with the Power to Detect the Murky Complications of Real-World Epidemiology
Vanessa Y. Tan, Nicholas J. Timpson
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 569-589
Open Access | Times Cited: 20

A genetically supported drug repurposing pipeline for diabetes treatment using electronic health records
Megan M. Shuey, Kyung Min Lee, Jacob M. Keaton, et al.
EBioMedicine (2023) Vol. 94, pp. 104674-104674
Open Access | Times Cited: 11

Integrating metabolomics and proteomics to identify novel drug targets for heart failure and atrial fibrillation
Marion van Vugt, Chris Finan, Sandesh Chopade, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 4

Titin-truncating mutations associated with dilated cardiomyopathy alter length-dependent activation and its modulation via phosphorylation
Petr G. Vikhorev, Natalia N. Vikhoreva, WaiChun Yeung, et al.
Cardiovascular Research (2020) Vol. 118, Iss. 1, pp. 241-253
Open Access | Times Cited: 28

Understanding the molecular basis of cardiomyopathy
Marie‐Louise Bang, Julius Bogomolovas, Ju Chen
AJP Heart and Circulatory Physiology (2021) Vol. 322, Iss. 2, pp. H181-H233
Open Access | Times Cited: 23

Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human
Julia E. Niskanen, Åsa Ohlsson, Ingrid Ljungvall, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 9

Shared genetic risk between anorexia nervosa and cardiovascular disease events: Evidence from genome‐wide association studies
Baiyu Qi, Mariaelisa Graff, Eating Disorders Working Group of the Psychiatric Genomics C, et al.
Brain and Behavior (2024) Vol. 14, Iss. 2
Open Access | Times Cited: 3

Association of Lifestyle With Incidence of Heart Failure According to Metabolic and Genetic Risk Status: A Population-Based Prospective Study
Zhengbao Zhu, Furong Li, Yiming Jia, et al.
Circulation Heart Failure (2022) Vol. 15, Iss. 9
Open Access | Times Cited: 14

Machine Learning to Understand Genetic and Clinical Factors Associated With the Pulse Waveform Dicrotic Notch
Jonathan W. Cunningham, Paolo Di Achille, Valerie N. Morrill, et al.
Circulation Genomic and Precision Medicine (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 14

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Rafik Tadros, Sean Zheng, Christopher Grace, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 8

Deep learning-enabled analysis of medical images identifies cardiac sphericity as an early marker of cardiomyopathy and related outcomes
Milos Vukadinovic, Alan C. Kwan, Victoria Yuan, et al.
Med (2023) Vol. 4, Iss. 4, pp. 252-262.e3
Open Access | Times Cited: 8

Integrated Multiomics Approach to Identify Genetic Underpinnings of Heart Failure and Its Echocardiographic Precursors
Charlotte Andersson, Honghuang Lin, Chunyu Liu, et al.
Circulation Genomic and Precision Medicine (2019) Vol. 12, Iss. 12
Open Access | Times Cited: 23

Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome‐wide analysis in African Americans
Laura M. Raffield, Ake T. Lu, Mindy D Szeto, et al.
Journal of Thrombosis and Haemostasis (2020) Vol. 18, Iss. 6, pp. 1335-1347
Open Access | Times Cited: 21

The impact of growth differentiation factor 15 on the risk of cardiovascular diseases: two-sample Mendelian randomization study
Zhuo Wang, Fangkun Yang, Menghuai Ma, et al.
BMC Cardiovascular Disorders (2020) Vol. 20, Iss. 1
Open Access | Times Cited: 21

The genomics of heart failure: design and rationale of the HERMES consortium
R. Thomas Lumbers, Sonia Shah, Honghuang Lin, et al.
ESC Heart Failure (2021) Vol. 8, Iss. 6, pp. 5531-5541
Open Access | Times Cited: 19

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