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 26-50 of 156 citing articles:

Adopting Mechanistic Molecular Biology Approaches in Exposome Research for Causal Understanding
Amy Foreman, Benedikt Warth, Ellen V.S. Hessel, et al.
Environmental Science & Technology (2024) Vol. 58, Iss. 17, pp. 7256-7269
Open Access | Times Cited: 6

Managing differential performance of polygenic risk scores across groups: Real-world experience of the eMERGE Network
Anna Lewis, Rex L Chisholm, John J. Connolly, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 6, pp. 999-1005
Closed Access | Times Cited: 6

Social-Science Genomics: Progress, Challenges, and Future Directions
Daniel J. Benjamin, David Cesarini, Patrick Turley, et al.
(2024)
Open Access | Times Cited: 6

Pervasive findings of directional selection realize the promise of ancient DNA to elucidate human adaptation
Ali Akbari, Alison R. Barton, Steven Gazal, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 6

Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction
Kristia Yiangou, Nasim Mavaddat, Joe Dennis, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations
Kangcheng Hou, Stephanie M. Gogarten, Joohyun Kim, et al.
Bioinformatics (2024) Vol. 40, Iss. 4
Open Access | Times Cited: 5

Conditional frequency spectra as a tool for studying selection on complex traits in biobanks
Roshni Patel, Clemens L. Weiß, Huisheng Zhu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

The effect of long-range linkage disequilibrium on allele-frequency dynamics under stabilizing selection
Sherif Negm, Carl Veller
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 5

Integrated clinical risk prediction of type 2 diabetes with a multifactorial polygenic risk score
Scott C. Ritchie, Henry J. Taylor, Yujian Liang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 5

Iron and risk of dementia: Mendelian randomisation analysis in UK Biobank
Francesco Casanova, Qu Tian, Janice L. Atkins, et al.
Journal of Medical Genetics (2024), pp. jmg-109295
Open Access | Times Cited: 4

Highly parameterized polygenic scores tend to overfit to population stratification via random effects
Alan J. Aw, Jeremy F. McRae, Elior Rahmani, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

Improved multi-ancestry fine-mapping identifiescis-regulatory variants underlying molecular traits and disease risk
Zeyun Lu, Xinran Wang, Matthew Carr, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4

Genes with differential expression across ancestries are enriched in ancestry-specific disease effects likely due to gene-by-environment interactions
Juehan Wang, Zixuan Zhang, Zeyun Lu, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 10, pp. 2117-2128
Open Access | Times Cited: 4

Causal interpretations of family GWAS in the presence of heterogeneous effects
Carl Veller, Molly Przeworski, Graham Coop
Proceedings of the National Academy of Sciences (2024) Vol. 121, Iss. 38
Open Access | Times Cited: 4

Precision Medicine for Pulmonary Vascular Disease: The Future Is Now (2023 Grover Conference Series)
Lindsay M. Forbes, Natalie Bauer, Aritra Bhadra, et al.
Pulmonary Circulation (2025) Vol. 15, Iss. 1
Open Access

PennPRS: a centralized cloud computing platform for efficient polygenic risk score training in precision medicine
Jin Jin, Bingxuan Li, Xiyao Wang, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Assessment of polygenic risk score performance in East Asian populations for ten common diseases
Hae‐Un Jung, Hyein Jung, Eun Ju Baek, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access

Polygenic risk scores for incident dementia in the Multi-Ethnic Study of Atherosclerosis
Diane Xue, Elizabeth Blue, Tamar Sofer, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access

Evolution, genetic diversity, and health
María J. Palma-Martínez, Yuridia S. Posadas‐García, Amara Shaukat, et al.
Nature Medicine (2025)
Closed Access

Predicting Cardiometabolic Risk in American Indian Adults—Moving Away From Heritability Without Heritage
Daniel Felsky
JAMA Network Open (2025) Vol. 8, Iss. 3, pp. e250545-e250545
Closed Access

Direct-to-Consumer Genetic Testing for Cardiovascular Disease: A Scientific Statement From the American Heart Association
Leland E. Hull, Aaron W. Aday, Quan M. Bui, et al.
Circulation (2025)
Closed Access

The elusive associations of nucleotides with human success: evolutionary genetics in education and social policies
Diddahally R. Govindaraju, A. Goldstein
Evolution Education and Outreach (2025) Vol. 18, Iss. 1
Open Access

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