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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:

Variable prediction accuracy of polygenic scores within an ancestry group
Hakhamanesh Mostafavi, Arbel Harpak, Ipsita Agarwal, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 390

Showing 1-25 of 390 citing articles:

Tutorial: a guide to performing polygenic risk score analyses
Shing Wan Choi, Timothy Shin Heng Mak, Paul F. O’Reilly
Nature Protocols (2020) Vol. 15, Iss. 9, pp. 2759-2772
Open Access | Times Cited: 1423
Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression
Urmo Võsa, Annique Claringbould, Harm-Jan Westra, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1300-1310
Open Access | Times Cited: 1177
Genome-wide association studies
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1112
The trans-ancestral genomic architecture of glycemic traits
Jihua Chen, Cassandra N. Spracklen, Gaëlle Marenne, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 840-860
Open Access | Times Cited: 550
Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps
Adebowale Adeyemo, Mary K. Balaconis, Deanna R. Darnes, et al.
Nature Medicine (2021) Vol. 27, Iss. 11, pp. 1876-1884
Open Access | Times Cited: 339
Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
Laurence J Howe, Michel G. Nivard, Tim Morris, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 581-592
Open Access | Times Cited: 276
Strategic vision for improving human health at The Forefront of Genomics
Eric D. Green, Chris Gunter, Leslie G. Biesecker, et al.
Nature (2020) Vol. 586, Iss. 7831, pp. 683-692
Open Access | Times Cited: 272
Deconstructing the sources of genotype-phenotype associations in humans
Alexander I. Young, Stefania Benónísdóttir, Molly Przeworski, et al.
Science (2019) Vol. 365, Iss. 6460, pp. 1396-1400
Open Access | Times Cited: 252
The influence of evolutionary history on human health and disease
Mary Lauren Benton, Abin Abraham, Abigail L. LaBella, et al.
Nature Reviews Genetics (2021) Vol. 22, Iss. 5, pp. 269-283
Open Access | Times Cited: 226
Solving the missing heritability problem
Alexander I. Young
PLoS Genetics (2019) Vol. 15, Iss. 6, pp. e1008222-e1008222
Open Access | Times Cited: 225
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
Omer Weissbrod, Masahiro Kanai, Huwenbo Shi, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 450-458
Open Access | Times Cited: 201
Evaluating the promise of inclusion of African ancestry populations in genomics
Amy R. Bentley, Shawneequa Callier, Charles N. Rotimi
npj Genomic Medicine (2020) Vol. 5, Iss. 1
Open Access | Times Cited: 164
Polygenic scoring accuracy varies across the genetic ancestry continuum
Yi Ding, Kangcheng Hou, Ziqi Xu, et al.
Nature (2023) Vol. 618, Iss. 7966, pp. 774-781
Open Access | Times Cited: 164
Using genetics for social science
K. Paige Harden, Philipp Koellinger
Nature Human Behaviour (2020) Vol. 4, Iss. 6, pp. 567-576
Open Access | Times Cited: 156
Polygenic risk scores in the clinic: new perspectives needed on familiar ethical issues
Anna Lewis, Robert C. Green
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 143
Principles and methods for transferring polygenic risk scores across global populations
Linda Kachuri, Nilanjan Chatterjee, Jibril Hirbo, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 8-25
Open Access | Times Cited: 138
Nurture might be nature: cautionary tales and proposed solutions
Sara A. Hart, Callie W. Little, Elsje van Bergen
npj Science of Learning (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 120
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Anna Köttgen, Émilie Cornec-Le Gall, Jan Halbritter, et al.
Kidney International (2022) Vol. 101, Iss. 6, pp. 1126-1141
Open Access | Times Cited: 113
Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores
Ying Wang, Kristin Tsuo, Masahiro Kanai, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 293-320
Open Access | Times Cited: 101
Mendelian imputation of parental genotypes improves estimates of direct genetic effects
Alexander I. Young, Seyed Moeen Nehzati, Stefania Benónísdóttir, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 897-905
Open Access | Times Cited: 78
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
Ying Wang, Shinichi Namba, Esteban A. Lopera-Maya, et al.
Cell Genomics (2023) Vol. 3, Iss. 1, pp. 100241-100241
Open Access | Times Cited: 73
Diagnosis and management of bipolar disorders
Fernando S. Goes
BMJ (2023), pp. e073591-e073591
Open Access | Times Cited: 64
Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe
Gaspard Kerner, Anna‐Lena Neehus, Quentin Philippot, et al.
Cell Genomics (2023) Vol. 3, Iss. 2, pp. 100248-100248
Open Access | Times Cited: 62
The Future of Social Determinants of Health: Looking Upstream to Structural Drivers
Tyson H. Brown, Patricia Homan
Milbank Quarterly (2023) Vol. 101, Iss. S1, pp. 36-60
Open Access | Times Cited: 47
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