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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:

Rare penetrant mutations confer severe risk of common diseases
Petko Fiziev, Jeremy F. McRae, Jacob C. Ulirsch, et al.
Science (2023) Vol. 380, Iss. 6648
Open Access | Times Cited: 36

Showing 1-25 of 36 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: 124
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 19
Identification of constrained sequence elements across 239 primate genomes
Lukas F. K. Kuderna, Jacob C. Ulirsch, Sabrina Mohd Rashid, et al.
Nature (2023) Vol. 625, Iss. 7996, pp. 735-742
Open Access | Times Cited: 36
Zero-shot prediction of mutation effects with multimodal deep representation learning guides protein engineering
Peng Cheng, Cong Mao, Jin Tang, et al.
Cell Research (2024) Vol. 34, Iss. 9, pp. 630-647
Open Access | Times Cited: 11
Genetic associations of protein-coding variants in venous thromboembolism
Xiao‐Yu He, Bang‐Sheng Wu, Yang Liu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 5
Genetic Variants Associated with Hypertension Risk: Progress and Implications
David Curtis
Pulse (2024) Vol. 12, Iss. 1, pp. 19-26
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
Genetics of Restless Legs Syndrome
Barbara Schormair
Sleep Medicine Clinics (2025)
Closed Access
Aberrant gene expression prediction across human tissues
Florian R. Hölzlwimmer, Jonas Lindner, George Tsitsiridis, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Enhancing prediction accuracy of coronary artery disease through machine learning-driven genomic variant selection
Z. Alireza, M. Maleeha, Minna U. Kaikkonen, et al.
Journal of Translational Medicine (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 3
G protein-coupled receptor (GPCR) pharmacogenomics
Miles D. Thompson, David Reiner‐Link, Alessandro Berghella, et al.
Critical Reviews in Clinical Laboratory Sciences (2024) Vol. 61, Iss. 8, pp. 641-684
Open Access | Times Cited: 2
Integration of variant annotations using deep set networks boosts rare variant association testing
Brian Clarke, Eva Holtkamp, Hakime Öztürk, et al.
Nature Genetics (2024) Vol. 56, Iss. 10, pp. 2271-2280
Open Access | Times Cited: 2
Exome-wide genetic risk score (ExGRS) to predict high myopia across multi-ancestry populations
Jian Yuan, Ruowen Qiu, Yuhan Wang, et al.
Communications Medicine (2024) Vol. 4, Iss. 1
Open Access | Times Cited: 2
The Metabolic Role of MAP3K15: Genetic and Phenotypic Insights from the 23andMe Research Database and Genetics-Driven Recruitment
Jennifer J. Brady, Kira Kalkus, Dominique T. Nguyen, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
PrimateAI-3D outperforms AlphaMissense in real-world cohorts
David Parry, Tom Bosc, Tobias Hamp, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Genome wide association study gateway—transitioning variants from association to causality in complex diseases
Chen Zhao
SLEEP (2024) Vol. 47, Iss. 7
Closed Access | Times Cited: 1
Rare variant effect estimation and polygenic risk prediction
Kisung Nam, Minjung Kho, Wei Zhou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Integration of variant annotations using deep set networks boosts rare variant association genetics
Brian Clarke, Eva Holtkamp, Hakime Öztürk, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Zero-shot prediction of mutation effects on protein function with multimodal deep representation learning
Wenjie Shu, Cheng Peng, Cong Mao, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3
The role of admixture in the rare variant contribution to inflammatory bowel disease
Courtney Astore, Shivam Sharma, Sini Nagpal, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 3
Next-generation primate genomics: New genome assemblies unlock new questions
Genevieve Housman, Jenny Tung
Cell (2023) Vol. 186, Iss. 25, pp. 5433-5437
Open Access | Times Cited: 3
Whole-Genome Sequencing Can Identify Clinically Relevant Variants from a Single Sub-Punch of a Dried Blood Spot Specimen
David J. McBride, Claire Fielding, Taksina Newington, et al.
International Journal of Neonatal Screening (2023) Vol. 9, Iss. 3, pp. 52-52
Open Access | Times Cited: 2
A multi-million-year natural experiment: comparative genomics on a massive scale and its implications for human health
Iker Rivas-González, Jenny Tung
Evolution Medicine and Public Health (2024) Vol. 12, Iss. 1, pp. 67-70
Open Access
ExGRS: exome-wide genetic risk score to predict high myopia across multi-ancestry populations
Jianzhong Su, Jian Yuan, Ruowen Qiu, et al.
Research Square (Research Square) (2024)
Open Access
Striking Departures from Polygenic Architecture in the Tails of Complex Traits
Tade Souaiaia, Hei Man Wu, Anil P. S. Ori, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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