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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:

Genomic Prediction of 16 Complex Disease Risks Including Heart Attack, Diabetes, Breast and Prostate Cancer
Louis Lello, Timothy G. Raben, Soke Yuen Yong, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 78

Showing 1-25 of 78 citing articles:

Calculating Polygenic Risk Scores (PRS) in UK Biobank: A Practical Guide for Epidemiologists
Jennifer A. Collister, Xiaonan Liu, Lei Clifton
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 100
Assessing Lung Cancer Absolute Risk Trajectory Based on a Polygenic Risk Model
Rayjean J. Hung, Matthew T. Warkentin, Yonathan Brhane, et al.
Cancer Research (2021) Vol. 81, Iss. 6, pp. 1607-1615
Open Access | Times Cited: 75
Utility and First Clinical Application of Screening Embryos for Polygenic Disease Risk Reduction
Nathan R. Treff, Jennifer Eccles, Lou Lello, et al.
Frontiers in Endocrinology (2019) Vol. 10
Open Access | Times Cited: 68
Complex-Trait Prediction in the Era of Big Data
Gustavo de los Campos, Ana I. Vázquez, Stephen Hsu, et al.
Trends in Genetics (2018) Vol. 34, Iss. 10, pp. 746-754
Open Access | Times Cited: 61
Risk‐stratified strategies in population screening for colorectal cancer
Iris Lansdorp‐Vogelaar, Reinier Meester, Lucie de Jonge, et al.
International Journal of Cancer (2021) Vol. 150, Iss. 3, pp. 397-405
Open Access | Times Cited: 41
Efficacy of federated learning on genomic data: a study on the UK Biobank and the 1000 Genomes Project
Dmitry Kolobkov, Satyarth Mishra Sharma, Aleksandr Medvedev, et al.
Frontiers in Big Data (2024) Vol. 7
Open Access | Times Cited: 7
Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs
Nathan R. Treff, Jennifer Eccles, Diego Marin, et al.
Genes (2020) Vol. 11, Iss. 6, pp. 648-648
Open Access | Times Cited: 48
Efficient blockLASSO for polygenic scores with applications to all of us and UK Biobank
Timothy G. Raben, Louis Lello, Erik Widén, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access
Sibling validation of polygenic risk scores and complex trait prediction
Louis Lello, Timothy G. Raben, Stephen Hsu
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 36
Polygenic risk scores in atrial fibrillation: Associations and clinical utility in disease prediction
Joel T. Gibson, James H.F. Rudd
Heart Rhythm (2024) Vol. 21, Iss. 6, pp. 913-918
Open Access | Times Cited: 4
Machine Learning Prediction of Biomarkers from SNPs and of Disease Risk from Biomarkers in the UK Biobank
Erik Widén, Timothy G. Raben, Louis Lello, et al.
Genes (2021) Vol. 12, Iss. 7, pp. 991-991
Open Access | Times Cited: 24
Embryo Screening for Polygenic Disease Risk: Recent Advances and Ethical Considerations
Laurent C. A. M. Tellier, Jennifer Eccles, Nathan R. Treff, et al.
Genes (2021) Vol. 12, Iss. 8, pp. 1105-1105
Open Access | Times Cited: 23
IVF and human evolution
Hans Ivar Hanevik, Dag O. Hessen
Human Reproduction Update (2022) Vol. 28, Iss. 4, pp. 457-479
Open Access | Times Cited: 16
Importance of Genetic Studies of Cardiometabolic Disease in Diverse Populations
Lindsay Fernández‐Rhodes, Kristin L. Young, Adam G. Lilly, et al.
Circulation Research (2020) Vol. 126, Iss. 12, pp. 1816-1840
Open Access | Times Cited: 26
Human genotype-to-phenotype predictions: Boosting accuracy with nonlinear models
Aleksandr Medvedev, Satyarth Mishra Sharma, Evgenii Tsatsorin, et al.
PLoS ONE (2022) Vol. 17, Iss. 8, pp. e0273293-e0273293
Open Access | Times Cited: 14
Genetic architecture of complex traits and disease risk predictors
Soke Yuen Yong, Timothy G. Raben, Louis Lello, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 23
PREIMPLANTATION GENETIC TESTING: Preimplantation genetic testing for polygenic disease risk
Nathan R. Treff, Diego Marin, Louis Lello, et al.
Reproduction (2020) Vol. 160, Iss. 5, pp. A13-A17
Open Access | Times Cited: 21
Polygenic Health Index, General Health, and Pleiotropy: Sibling Analysis and Disease Risk Reduction
Erik Widén, Louis Lello, Timothy G. Raben, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 13
Molecular Evaluation of the Impact of Polymorphic Variants in Apoptotic (Bcl-2/Bax) and Proinflammatory Cytokine (TNF-α/IL-8) Genes on the Susceptibility and Progression of Myeloproliferative Neoplasms: A Case-Control Biomarker Study
Mamdoh S. Moawadh, Rashid Mir, Faris J. Tayeb, et al.
Current Issues in Molecular Biology (2023) Vol. 45, Iss. 5, pp. 3933-3952
Open Access | Times Cited: 7
Preimplantation Genetic Testing for Polygenetic Conditions: A Legal, Ethical, and Scientific Challenge
Perrine Ginod, Michael H. Dahan
Seminars in Reproductive Medicine (2024) Vol. 42, Iss. 01, pp. 060-068
Closed Access | Times Cited: 2
Haplotype Analysis of Genomic Prediction Using Structural and Functional Genomic Information for Seven Human Phenotypes
Zuoxiang Liang, Cheng Tan, Dzianis Prakapenka, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 18
Should preimplantation genetic testing for polygenic disease be offered to all – or none?
Nathan R. Treff, Julian Savulescu, Inmaculada de Melo‐Martín, et al.
Fertility and Sterility (2022) Vol. 117, Iss. 6, pp. 1162-1167
Open Access | Times Cited: 12
Using a Polygenic Score to Predict the Risk of Developing Primary Osteoporosis
Bulat I. Yalaev, Anton Tyurin, Inga Prokopenko, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 17, pp. 10021-10021
Open Access | Times Cited: 11
Artificial Intelligence-Assisted Identification of Genetic Factors Predisposing High-Risk Individuals to Asymptomatic Heart Failure
Ning-I Yang, Chi‐Hsiao Yeh, Tsung‐Hsien Tsai, et al.
Cells (2021) Vol. 10, Iss. 9, pp. 2430-2430
Open Access | Times Cited: 14
Breaking bad news in the era of artificial intelligence and algorithmic medicine: an exploration of disclosure and its ethical justification using the hedonic calculus
Benjamin Post, Cosmin Badea, A. Aldo Faisal, et al.
AI and Ethics (2022) Vol. 3, Iss. 4, pp. 1215-1228
Open Access | Times Cited: 10
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