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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:

Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS
Lisa Bastarache
Annual Review of Biomedical Data Science (2021) Vol. 4, Iss. 1, pp. 1-19
Open Access | Times Cited: 132

Showing 1-25 of 132 citing articles:

Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects
Konrad J. Karczewski, Rahul Gupta, Masahiro Kanai, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 63
Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Anurag Verma, Jennifer E. Huffman, Alex A Rodriguez, et al.
Science (2024) Vol. 385, Iss. 6706
Open Access | Times Cited: 49
Leveraging electronic health records and knowledge networks for Alzheimer’s disease prediction and sex-specific biological insights
Alice Tang, Katherine P. Rankin, Gabriel Cerono, et al.
Nature Aging (2024) Vol. 4, Iss. 3, pp. 379-395
Open Access | Times Cited: 25
Comparison of phenomic profiles in the All of Us Research Program against the US general population and the UK Biobank
Chenjie Zeng, David J. Schlueter, Tam C Tran, et al.
Journal of the American Medical Informatics Association (2024) Vol. 31, Iss. 4, pp. 846-854
Open Access | Times Cited: 13
Developing real‐world evidence from real‐world data: Transforming raw data into analytical datasets
Lisa Bastarache, Jeffrey S. Brown, James J. Cimino, et al.
Learning Health Systems (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 43
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases
Chenjie Zeng, Lisa A. Bastarache, Ran Tao, et al.
JAMA Oncology (2022) Vol. 8, Iss. 6, pp. 835-835
Open Access | Times Cited: 35
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program
Anurag Verma, Jennifer E. Huffman, Álex Rodríguez, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 20
New Insights into Clinical and Mechanistic Heterogeneity of the Acute Respiratory Distress Syndrome: Summary of the Aspen Lung Conference 2021
Thomas R. Martin, Rachel L. Zemans, Lorraine B. Ware, et al.
American Journal of Respiratory Cell and Molecular Biology (2022) Vol. 67, Iss. 3, pp. 284-308
Open Access | Times Cited: 23
Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discovery
David Lewis‐Smith, Shridhar Parthasarathy, Julie Xian, et al.
Human Mutation (2022) Vol. 43, Iss. 11, pp. 1642-1658
Open Access | Times Cited: 22
Medications and conditions associated with weight loss in patients prescribed semaglutide based on real‐world data
William C. Powell, Xing Song, Yahia Mohamed, et al.
Obesity (2023) Vol. 31, Iss. 10, pp. 2482-2492
Open Access | Times Cited: 14
Disease-associated Kv1.3 variants are energy compromised with impaired nascent chain folding.
Audrey Sykes, Lannawill Caruth, Shefali S. Verma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Closed Access
Modeling diagnostic code dropout of schizophrenia in electronic health records improves phenotypic data quality and cross-ancestry transferability of polygenic scores
David E. Burstein, Simone Tomasi, Sanan Venkatesh, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Gene and phenome-based analysis of the shared genetic architecture of eye diseases
Alexandra Scalici, Tyne W. Miller‐Fleming, Megan M. Shuey, et al.
The American Journal of Human Genetics (2025)
Closed Access
Prevalence and disease risks for male and female sex chromosome trisomies: a registry-based phenome-wide association study in 1.5 million participants of MVP, FinnGen, and UK Biobank
Shanlee Davis, Aoxing Liu, Craig C. Teerlink, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Organizing COVID-19 research papers using text clustering
Tarq Abd-Alameer Shani, Suhad Malallah Kadhem
AIP conference proceedings (2025) Vol. 3224, pp. 030001-030001
Closed Access
Genetic association studies using disease liabilities from deep neural networks
Lu Yang, Marie C. Sadler, Russ B. Altman
The American Journal of Human Genetics (2025)
Open Access
Exploration of Genetic Liability to Insomnia and Substance Use Disorders in Patients With Bipolar Disorder
Lindsay Melhuish Beaupre, Brandon J. Coombes, Anthony Batzler, et al.
Bipolar Disorders (2025)
Closed Access
Sepsis in silico: definition, development and application of an electronic phenotype for sepsis
Zahraa Al-Sultani, Timothy J. J. Inglis, Benjamin McFadden, et al.
Journal of Medical Microbiology (2025) Vol. 74, Iss. 3
Closed Access
Automating the Addiction Behaviors Checklist for Problematic Opioid Use Identification
Angus H. Chatham, Eli D. Bradley, Vanessa Troiani, et al.
JAMA Psychiatry (2025)
Closed Access
Federated learning with multi‐cohort real‐world data for predicting the progression from mild cognitive impairment to Alzheimer's disease
Jinqian Pan, Zhengkang Fan, Glenn E. Smith, et al.
Alzheimer s & Dementia (2025) Vol. 21, Iss. 4
Open Access
Deep learning-based identification of patients at increased risk of cancer using routine laboratory markers
Vivek Singh, Shikha Chaganti, Matthias Siebert, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
MixEHR-Guided: A guided multi-modal topic modeling approach for large-scale automatic phenotyping using the electronic health record
Yuri Ahuja, Yuesong Zou, Aman Verma, et al.
Journal of Biomedical Informatics (2022) Vol. 134, pp. 104190-104190
Open Access | Times Cited: 21
Drug‐Induced Liver Injury with Commonly Used Antibiotics in the All of Us Research Program
Shaopeng Gu, Govarthanan Rajendiran, Kennedy Forest, et al.
Clinical Pharmacology & Therapeutics (2023) Vol. 114, Iss. 2, pp. 404-412
Open Access | Times Cited: 12
ADRA2A and IRX1 are putative risk genes for Raynaud’s phenomenon
Sylvia Hartmann, Summaira Yasmeen, Benjamin Meir Jacobs, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 11
Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease
Ruth Johnson, Alexis V. Stephens, Rachel Mester, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 745
Open Access | Times Cited: 4
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