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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:

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: 156

Showing 1-25 of 156 citing articles:

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: 133
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
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations
Niall J. Lennon, Leah C. Kottyan, Christopher Kachulis, et al.
Nature Medicine (2024) Vol. 30, Iss. 2, pp. 480-487
Open Access | Times Cited: 78
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: 67
A new method for multiancestry polygenic prediction improves performance across diverse populations
Haoyu Zhang, Jianan Zhan, Jin Jin, et al.
Nature Genetics (2023) Vol. 55, Iss. 10, pp. 1757-1768
Open Access | Times Cited: 49
Recent advances in polygenic scores: translation, equitability, methods and FAIR tools
Ruidong Xiang, Martin Kelemen, Yu Xu, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 30
An ensemble penalized regression method for multi-ancestry polygenic risk prediction
Jingning Zhang, Jianan Zhan, Jin Jin, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 25
Genetic and molecular architecture of complex traits
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 21
Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
Nature Genetics (2024) Vol. 56, Iss. 7, pp. 1386-1396
Open Access | Times Cited: 21
Multi-omics approaches for understanding gene-environment interactions in noncommunicable diseases: techniques, translation, and equity issues
Robel Alemu, Nigussie Tadesse Sharew, Yodit Y. Arsano, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 2
Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with an alcohol use disorder
Peter B. Barr, Zoë Neale, Chris Chatzinakos, et al.
Complex Psychiatry (2025) Vol. 11, Iss. 1, pp. 1-11
Closed Access | Times Cited: 2
Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility
Michelle N. Meyer, Paul S. Appelbaum, Daniel J. Benjamin, et al.
The Hastings Center Report (2023) Vol. 53, Iss. S1
Open Access | Times Cited: 41
Inferring disease architecture and predictive ability with LDpred2-auto
Florian Privé, Clara Albiñana, Julyan Arbel, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 2042-2055
Open Access | Times Cited: 27
Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology
Ying Wang, Masahiro Kanai, Taotao Tan, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100408-100408
Open Access | Times Cited: 24
Towards a Global View of Parkinson's Disease Genetics
Marzieh Khani, Catalina Cerquera‐Cleves, Mariam Kekenadze, et al.
Annals of Neurology (2024) Vol. 95, Iss. 5, pp. 831-842
Open Access | Times Cited: 15
Genotype × environment interactions in gene regulation and complex traits
Carly Boye, Shreya Nirmalan, Ali Ranjbaran, et al.
Nature Genetics (2024)
Closed Access | Times Cited: 14
Evaluation of polygenic scoring methods in five biobanks shows larger variation between biobanks than methods and finds benefits of ensemble learning
Remo Monti, Lisa Eick, Georgi Hudjashov, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 7, pp. 1431-1447
Closed Access | Times Cited: 14
Screening embryos for polygenic disease risk: a review of epidemiological, clinical, and ethical considerations
Antonio Capalbo, G. de Wert, Heidi Mertes, et al.
Human Reproduction Update (2024) Vol. 30, Iss. 5, pp. 529-557
Open Access | Times Cited: 11
Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores
Sarah Abramowitz, Kristin Boulier, Karl Keat, et al.
JAMA (2024)
Closed Access | Times Cited: 9
Leveraging haplotype information in heritability estimation and polygenic prediction
Jonas Meisner, Michael E. Benros, Simon Rasmussen
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 1
A Litmus Test for Confounding in Polygenic Scores
Samuel Pattillo Smith, Olivia S. Smith, Hakhamanesh Mostafavi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Polygenic scores for autism are associated with reduced neurite density in adults and children from the general population
Yuanjun Gu, Eva-Maria Stauffer, Saashi A. Bedford, et al.
Molecular Psychiatry (2025)
Open Access | Times Cited: 1
Multi-trait GWAS for diverse ancestries: mapping the knowledge gap
Lucie Troubat, Deniz Fettahoglu, Léo Henches, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 7
Rare coding variant analysis for human diseases across biobanks and ancestries
Sean J. Jurgens, Xin Wang, Seung Hoan Choi, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1811-1820
Closed Access | Times Cited: 7
Polygenic risk score portability for common diseases across genetically diverse populations
Sonia Moreno‐Grau, Manvi Vernekar, Arturo López Pineda, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 7
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