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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:

Genotyping Array Design and Data Quality Control in the Million Veteran Program
Haley Hunter-Zinck, Yunling Shi, Man Li, et al.
The American Journal of Human Genetics (2020) Vol. 106, Iss. 4, pp. 535-548
Open Access | Times Cited: 169

Showing 26-50 of 169 citing articles:

Long-Term Body Mass Index Variability and Adverse Cardiovascular Outcomes
Zakaria Almuwaqqat, Qin Hui, Chang Liu, et al.
JAMA Network Open (2024) Vol. 7, Iss. 3, pp. e243062-e243062
Open Access | Times Cited: 12
Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization
Johanna L. Smith, Catherine Tcheandjieu, Ozan Dikilitas, et al.
Circulation Genomic and Precision Medicine (2024) Vol. 17, Iss. 3
Open Access | Times Cited: 11
Genetic drivers and cellular selection of female mosaic X chromosome loss
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
Nature (2024) Vol. 631, Iss. 8019, pp. 134-141
Closed Access | Times Cited: 11
Role of the X Chromosome in Alzheimer Disease Genetics
Michaël E. Belloy, Yann Le Guen, Ilaria Stewart, et al.
JAMA Neurology (2024)
Closed Access | Times Cited: 11
Adaptive selection at G6PD and disparities in diabetes complications
Joseph H. Breeyear, Jacklyn N. Hellwege, Philip Schroeder, et al.
Nature Medicine (2024) Vol. 30, Iss. 9, pp. 2480-2488
Closed Access | Times Cited: 9
Utility of Candidate Genes From an Algorithm Designed to Predict Genetic Risk for Opioid Use Disorder
Christal N. Davis, Zeal Jinwala, Alexander S. Hatoum, et al.
JAMA Network Open (2025) Vol. 8, Iss. 1, pp. e2453913-e2453913
Open Access | Times Cited: 1
CXCL12 drives natural variation in coronary artery anatomy across diverse populations
Pamela E. Rios Coronado, Jiayan Zhou, Xiaochen Fan, et al.
Cell (2025)
Open Access | Times Cited: 1
Lipid traits and type 2 diabetes risk in African ancestry individuals: A Mendelian Randomization study
Opeyemi Soremekun, Ville Karhunen, Yiyan He, et al.
EBioMedicine (2022) Vol. 78, pp. 103953-103953
Open Access | Times Cited: 35
Mild-to-Moderate Kidney Dysfunction and Cardiovascular Disease: Observational and Mendelian Randomization Analyses
Liam Gaziano, Luanluan Sun, Matthew Arnold, et al.
Circulation (2022) Vol. 146, Iss. 20, pp. 1507-1517
Open Access | Times Cited: 35
Penetrance and Pleiotropy of Polygenic Risk Scores for Schizophrenia, Bipolar Disorder, and Depression Among Adults in the US Veterans Affairs Health Care System
Tim B. Bigdeli, Georgios Voloudakis, Peter B. Barr, et al.
JAMA Psychiatry (2022) Vol. 79, Iss. 11, pp. 1092-1092
Open Access | Times Cited: 31
Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure
Laura Balagué-Dobón, Alejandro Cáceres, Juan R. González
Briefings in Bioinformatics (2022) Vol. 23, Iss. 2
Open Access | Times Cited: 28
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
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation
Bryan R. Gorman, Michael Francis, Cari L. Nealon, et al.
Communications Biology (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 7
Biobanking with genetics shapes precision medicine and global health
C. Scott Gallagher, Geoffrey S. Ginsburg, Anjené Addington
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 7
Protein-truncating variant in APOL3 increases chronic kidney disease risk in epistasis with APOL1 risk alleles
David Zhang, Michael G. Levin, Jeffrey Duda, et al.
JCI Insight (2024) Vol. 9, Iss. 19
Open Access | Times Cited: 6
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm
Tanmoy Roychowdhury, Haocheng Lu, Whitney Hornsby, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 9, pp. 1578-1589
Open Access | Times Cited: 35
Measured Blood Pressure, Genetically Predicted Blood Pressure, and Cardiovascular Disease Risk in the UK Biobank
So Mi Jemma Cho, Satoshi Koyama, Yunfeng Ruan, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 11, pp. 1129-1129
Open Access | Times Cited: 28
Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans
Nathan A. Kimbrel, Allison E. Ashley‐Koch, Xuejun Qin, et al.
JAMA Psychiatry (2022) Vol. 80, Iss. 2, pp. 135-135
Open Access | Times Cited: 27
Validation of a multi-ancestry polygenic risk score and age-specific risks of prostate cancer: A meta-analysis within diverse populations
Fei Chen, Burcu F. Darst, Ravi Madduri, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 25
Polygenic risk of any, metastatic, and fatal prostate cancer in the Million Veteran Program
Meghana S. Pagadala, Julie A. Lynch, Roshan Karunamuni, et al.
JNCI Journal of the National Cancer Institute (2022) Vol. 115, Iss. 2, pp. 190-199
Open Access | Times Cited: 25
Genetics of Alzheimer’s Disease in the African American Population
Mark W. Logue, Shoumita Dasgupta, Lindsay A. Farrer
Journal of Clinical Medicine (2023) Vol. 12, Iss. 16, pp. 5189-5189
Open Access | Times Cited: 15
Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veteran Program
Allison E. Ashley‐Koch, Nathan A. Kimbrel, Xuejun Qin, et al.
PLoS Genetics (2023) Vol. 19, Iss. 3, pp. e1010623-e1010623
Open Access | Times Cited: 14
Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries
Ida Surakka, Kuan-Han Wu, Whitney Hornsby, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100345-100345
Open Access | Times Cited: 13
Mendelian randomization study of diabetes and dementia in the Million Veteran Program
Elizabeth Litkowski, Mark W. Logue, Rui Zhang, et al.
Alzheimer s & Dementia (2023) Vol. 19, Iss. 10, pp. 4367-4376
Open Access | Times Cited: 13
Characterising the genetic architecture of changes in adiposity during adulthood using electronic health records
Samvida S. Venkatesh, Habib Ganjgahi, Duncan S. Palmer, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5

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