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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 1-25 of 169 citing articles:

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, et al.
Nature Medicine (2022) Vol. 28, Iss. 8, pp. 1679-1692
Open Access | Times Cited: 230
Actionable druggable genome-wide Mendelian randomization identifies repurposing opportunities for COVID-19
Liam Gaziano, Claudia Giambartolomei, Alexandre C. Pereira, et al.
Nature Medicine (2021) Vol. 27, Iss. 4, pp. 668-676
Open Access | Times Cited: 194
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease
Aniruddh P. Patel, Minxian Wang, Yunfeng Ruan, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1793-1803
Open Access | Times Cited: 125
Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19
Jennifer E. Huffman, Guillaume Butler‐Laporte, Atlas Khan, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 125-127
Open Access | Times Cited: 99
Genomics and phenomics of body mass index reveals a complex disease network
Jie Huang, Jennifer E. Huffman, Yunfeng Huang, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 80
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Hang Zhou, Rachel L. Kember, Joseph D. Deak, et al.
Nature Medicine (2023) Vol. 29, Iss. 12, pp. 3184-3192
Open Access | Times Cited: 74
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, et al.
Nature Genetics (2024) Vol. 56, Iss. 2, pp. 222-233
Open Access | Times Cited: 64
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: 50
Rare copy-number variants as modulators of common disease susceptibility
Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 23
A review of UMAP in population genetics
Alex Diaz-Papkovich, Luke Anderson-Trocmé, Simon Gravel
Journal of Human Genetics (2020) Vol. 66, Iss. 1, pp. 85-91
Open Access | Times Cited: 125
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Derek Klarin, Shefali S. Verma, Renae Judy, et al.
Circulation (2020) Vol. 142, Iss. 17, pp. 1633-1646
Open Access | Times Cited: 104
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
Jacqueline Saw, Min‐Lee Yang, Mark Trinder, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 85
APOL1 risk variants in individuals of African genetic ancestry drive endothelial cell defects that exacerbate sepsis
Junnan Wu, Ziyuan Ma, Archana Raman, et al.
Immunity (2021) Vol. 54, Iss. 11, pp. 2632-2649.e6
Open Access | Times Cited: 73
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits
Roshni Patel, Shaila Musharoff, Jeffrey P. Spence, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 7, pp. 1286-1297
Open Access | Times Cited: 58
A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci
Nathan A. Kimbrel, Allison E. Ashley‐Koch, Xuejun Qin, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 4, pp. 2264-2272
Open Access | Times Cited: 51
African ancestry GWAS of dementia in a large military cohort identifies significant risk loci
Richard Sherva, Rui Zhang, Nathan Sahelijo, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 3, pp. 1293-1302
Open Access | Times Cited: 45
APOL1 Risk Variants, Acute Kidney Injury, and Death in Participants With African Ancestry Hospitalized With COVID-19 From the Million Veteran Program
Adriana M. Hung, Shailja C. Shah, Alexander G. Bick, et al.
JAMA Internal Medicine (2022) Vol. 182, Iss. 4, pp. 386-386
Open Access | Times Cited: 43
From pharmacogenetics to pharmaco-omics: Milestones and future directions
Chiara Auwerx, Marie C. Sadler, Alexandre Reymond, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 2, pp. 100100-100100
Open Access | Times Cited: 43
Genetic architecture of heart failure with preserved versus reduced ejection fraction
Jacob Joseph, Chang Liu, Qin Hui, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 39
Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex
Tamar Sofer, Nuzulul Kurniansyah, Michael Murray, et al.
EBioMedicine (2023) Vol. 90, pp. 104536-104536
Open Access | Times Cited: 32
Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease
Adriana M. Hung, Victoria A. Assimon, Hua‐Chang Chen, et al.
Journal of the American Society of Nephrology (2023) Vol. 34, Iss. 11, pp. 1889-1899
Open Access | Times Cited: 30
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity
Veera M. Rajagopal, Andrea Ganna, Jonathan R. I. Coleman, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 23
Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program
Jason L. Vassy, Daniel Posner, Yuk‐Lam Ho, et al.
JAMA Cardiology (2023) Vol. 8, Iss. 6, pp. 564-564
Closed Access | Times Cited: 23
The Association between Circulating Lipids and Female Infertility Risk: A Univariable and Multivariable Mendelian Randomization Analysis
Xiaoqi Zhu, Xiang Hong, Jingying Wu, et al.
Nutrients (2023) Vol. 15, Iss. 14, pp. 3130-3130
Open Access | Times Cited: 23
A multi-ancestry genetic study of pain intensity in 598,339 veterans
Sylvanus Toikumo, Rachel Vickers‐Smith, Zeal Jinwala, et al.
Nature Medicine (2024) Vol. 30, Iss. 4, pp. 1075-1084
Open Access | Times Cited: 14
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