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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.

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Showing 1-25 of 28 citing articles:

AI pitfalls and what not to do: mitigating bias in AI
Judy Wawira Gichoya, K.J. Thomas, Leo Anthony Celi, et al.
British Journal of Radiology (2023) Vol. 96, Iss. 1150
Open Access | Times Cited: 101
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
Michael G. Levin, Noah L. Tsao, Pankhuri Singhal, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 80
Identifying and correcting for misspecifications in GWAS summary statistics and polygenic scores
Florian Privé, Julyan Arbel, Hugues Aschard, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 4, pp. 100136-100136
Open Access | Times Cited: 53
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
Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery
J German, Mattia Cordioli, Veronica Tozzo, et al.
Nature Medicine (2025)
Open Access | Times Cited: 1
Neural ADMIXTURE for rapid genomic clustering
Albert Dominguez Mantes, Daniel Mas Montserrat, Carlos D. Bustamante, et al.
Nature Computational Science (2023) Vol. 3, Iss. 7, pp. 621-629
Open Access | Times Cited: 19
Biobanking with genetics shapes precision medicine and global health
C. Scott Gallagher, Geoffrey S. Ginsburg, Anjené Addington
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 7
Characterizing substructure via mixture modeling in large-scale genetic summary statistics
Hayley R Stoneman, Adelle Price, Nikole Scribner Trout, et al.
The American Journal of Human Genetics (2025)
Open Access
Polygenic Scores and Mood Disorder Onsets in the Context of Family History and Early Psychopathology
Kathryn Freeman, Alyson Zwicker, Janice M. Fullerton, et al.
JAMA Network Open (2025) Vol. 8, Iss. 4, pp. e255331-e255331
Open Access
Adjusting for principal components can induce spurious associations in genome-wide association studies in admixed populations
Kelsey Grinde, Brian L. Browning, Alexander P. Reiner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Diversity of cells and signals in the cardiovascular system
Eleonora Grandi, Manuel F. Navedo, Jeffrey J. Saucerman, et al.
The Journal of Physiology (2023) Vol. 601, Iss. 13, pp. 2547-2592
Open Access | Times Cited: 8
Hunter–gatherer genetics research: Importance and avenues
Cecilia Padilla‐Iglesias, Inez Derkx
Evolutionary Human Sciences (2024) Vol. 6
Open Access | Times Cited: 2
ADAMS project: a genetic Association study in individuals from Diverse Ancestral backgrounds with Multiple Sclerosis based in the UK
Benjamin Meir Jacobs, Luisa Schalk, Angie Dunne, et al.
BMJ Open (2023) Vol. 13, Iss. 5, pp. e071656-e071656
Open Access | Times Cited: 6
Characterizing substructure via mixture modeling of genetic similarity in large-scale summary statistics
Hayley R Stoneman, Adelle Price, Nikole Scribner Trout, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
On the effect heterogeneity of established disease susceptibility loci for Alzheimer's disease across different genetic ancestries
Sanghun Lee, Julian Hecker, Georg Hahn, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 5, pp. 3397-3405
Open Access | Times Cited: 1
Use of Estonian Biobank Data and Participant Recall to Improve Wilson’s Disease Management
Miriam Nurm, Anu Reigo, Tarmo Annilo, et al.
Research Square (Research Square) (2024)
Open Access | Times Cited: 1
Exploring the role of HLA variants in neuroblastoma susceptibility through whole exome sequencing
Ferdinando Bonfiglio, Vito Alessandro Lasorsa, Vincenzo Aievola, et al.
HLA (2024) Vol. 103, Iss. 5
Closed Access | Times Cited: 1
scAI-SNP: a method for inferring ancestry from single-cell data
Sung Chul Hong, Francesc Muyas, Isidro Cortés‐Ciriano, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Use of Estonian Biobank data and participant recall to improve Wilson’s disease management
Miriam Nurm, Anu Reigo, Tarmo Annilo, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 1
Adjusting for principal components can induce collider bias in genome-wide association studies
Kelsey Grinde, Brian L. Browning, Alex P. Reiner, et al.
PLoS Genetics (2024) Vol. 20, Iss. 12, pp. e1011242-e1011242
Open Access | Times Cited: 1
Assessing the impact of 20th century internal migrations on the genetic structure of Estonia
Ivan A. Kuznetsov, Mait Metspalu, Uku Vainik, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Inferring disease architecture and predictive ability with LDpred2-auto
Florian Privé, Clara Albiñana, Julyan Arbel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 5
Hunter-gatherer genetics research: Importance and avenues
Cecilia Padilla‐Iglesias, Inez Derkx
(2024)
Open Access
Multi-ancestry polygenic risk scores using phylogenetic regularization
Elliot Layne, Shadi Zabad, Yue Li, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
What’s UPDOG? A novel tool for trans-ancestral polygenic score prediction
David M. Howard, Oliver Pain, Alexandra C. Gillett, et al.
Wellcome Open Research (2024) Vol. 9, pp. 275-275
Open Access
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