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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:

Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies
Quan Sun, Misa Graff, Bryce Rowland, et al.
Journal of Human Genetics (2021) Vol. 67, Iss. 2, pp. 87-93
Open Access | Times Cited: 38

Showing 1-25 of 38 citing articles:

The sequences of 150,119 genomes in the UK Biobank
Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, et al.
Nature (2022) Vol. 607, Iss. 7920, pp. 732-740
Open Access | Times Cited: 333
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI
Quan Sun, Bryce Rowland, Jiawen Chen, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 26
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data
Le Huang, Jonathan D. Rosen, Quan Sun, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 6, pp. 1175-1181
Open Access | Times Cited: 60
Genetic Variants Associated With Hidradenitis Suppurativa
Quan Sun, K. Alaine Broadaway, Sharon N. Edmiston, et al.
JAMA Dermatology (2023) Vol. 159, Iss. 9, pp. 930-930
Open Access | Times Cited: 30
Polygenic Scores of Cardiometabolic Risk Factors in American Indian Adults
Quan Sun, Jiawen Du, Yihan Tang, et al.
JAMA Network Open (2025) Vol. 8, Iss. 3, pp. e250535-e250535
Open Access | Times Cited: 1
Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences
Justin E. Ideozu, Mengzhen Liu, Bridget Riley‐Gillis, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 8
Genetic architecture of alcohol consumption identified by a genotype-stratified GWAS and impact on esophageal cancer risk in Japanese people
Yuriko N. Koyanagi, Masahiro Nakatochi, Shinichi Namba, et al.
Science Advances (2024) Vol. 10, Iss. 4
Open Access | Times Cited: 7
Relative predictive value of sociodemographic factors for chronic diseases among All of Us participants: a descriptive analysis
Ansley J. Kunnath, Daniel Sack, Consuelo H. Wilkins
BMC Public Health (2024) Vol. 24, Iss. 1
Open Access | Times Cited: 7
Genetic Determinants of 25-Hydroxyvitamin D Concentrations and Their Relevance to Public Health
Elina Hyppönen, Karani S. Vimaleswaran, Ang Zhou
Nutrients (2022) Vol. 14, Iss. 20, pp. 4408-4408
Open Access | Times Cited: 27
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations
Gaurav Thareja, Aziz Belkadi, Matthias Arnold, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 6, pp. 907-916
Open Access | Times Cited: 26
The future of sickle cell disease therapeutics rests in genomics
Ambroise Wonkam
Disease Models & Mechanisms (2023) Vol. 16, Iss. 2
Open Access | Times Cited: 16
Improving polygenic risk prediction of renal function by removing biomarker-specific effects
Megan M. Shuey, Jiawen Du, Quan Sun, et al.
Research Square (Research Square) (2025)
Closed Access
EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints—A study in asthma
Elena Kharitonova, Quan Sun, Franklin Ockerman, et al.
The American Journal of Human Genetics (2025)
Closed Access
A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels
Paul S. de Vries, Paula Reventún, Michael R. Brown, et al.
Blood (2024) Vol. 143, Iss. 18, pp. 1845-1855
Open Access | Times Cited: 3
Opportunities and challenges of local ancestry in genetic association analyses
Quan Sun, Andréa R. V. R. Horimoto, Brian Chen, et al.
The American Journal of Human Genetics (2025) Vol. 112, Iss. 4, pp. 727-740
Closed Access
Leveraging TOPMed imputation server and constructing a cohort-specific imputation reference panel to enhance genotype imputation among cystic fibrosis patients
Quan Sun, Weifang Liu, Jonathan D. Rosen, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 2, pp. 100090-100090
Open Access | Times Cited: 15
MagicalRsq: Machine-learning-based genotype imputation quality calibration
Quan Sun, Yingxi Yang, Jonathan D. Rosen, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 11, pp. 1986-1997
Open Access | Times Cited: 14
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Amarise Little, Yao Hu, Quan Sun, et al.
Human Molecular Genetics (2021) Vol. 31, Iss. 3, pp. 347-361
Open Access | Times Cited: 16
The sequences of 150,119 genomes in the UK biobank
Bjarni V. Halldórsson, Hannes P. Eggertsson, Kristjan H. S. Moore, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 16
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric
Quan Sun, Yingxi Yang, Jonathan D. Rosen, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 990-995
Closed Access | Times Cited: 2
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Benjamin Meir Jacobs, Daniel Stow, Sam Hodgson, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes
Remo Monti, Pia Rautenstrauch, Mahsa Ghanbari, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 10
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI
Quan Sun, Bryce Rowland, Jiawen Chen, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 9
Under-Representation of Racial Groups in Genomics Studies of Gastroenteropancreatic Neuroendocrine Neoplasms
Brendon Herring, Andrew Bonner, Rachael Guenter, et al.
Cancer Research Communications (2022) Vol. 2, Iss. 10, pp. 1162-1173
Open Access | Times Cited: 8
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