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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:

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
Sean J. Jurgens, Seung Hoan Choi, Valerie N. Morrill, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 240-250
Open Access | Times Cited: 125

Showing 1-25 of 125 citing articles:

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao, et al.
Cell Genomics (2022) Vol. 2, Iss. 9, pp. 100168-100168
Open Access | Times Cited: 190
Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature
Seyedeh M. Zekavat, Vineet K. Raghu, Mark Trinder, et al.
Circulation (2021) Vol. 145, Iss. 2, pp. 134-150
Open Access | Times Cited: 111
Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots
Saaket Agrawal, Minxian Wang, Marcus D. R. Klarqvist, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 89
Genome-wide association studies of cardiovascular disease
Roddy Walsh, Sean J. Jurgens, Jeanette Erdmann, et al.
Physiological Reviews (2023) Vol. 103, Iss. 3, pp. 2039-2055
Closed Access | Times Cited: 44
Atrial fibrillation: age at diagnosis, incident cardiovascular events, and mortality
Christian Paludan‐Müller, Oliver Bundgaard Vad, Niels Kjær Stampe, et al.
European Heart Journal (2024) Vol. 45, Iss. 24, pp. 2119-2129
Open Access | Times Cited: 15
Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank
Kiran J. Biddinger, Sean J. Jurgens, Dimitri J. Maamari, et al.
JAMA Cardiology (2022) Vol. 7, Iss. 7, pp. 715-715
Open Access | Times Cited: 42
The impact of rare protein coding genetic variation on adult cognitive function
Chia‐Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 927-938
Open Access | Times Cited: 40
Adjusting for common variant polygenic scores improves yield in rare variant association analyses
Sean J. Jurgens, James P. Pirruccello, Seung Hoan Choi, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 544-548
Open Access | Times Cited: 29
Clonal haematopoiesis of indeterminate potential predicts incident cardiac arrhythmias
Art Schuermans, Caitlyn Vlasschaert, Victor Nauffal, et al.
European Heart Journal (2023) Vol. 45, Iss. 10, pp. 791-805
Open Access | Times Cited: 29
Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass
Shaan Khurshid, Julieta Lazarte, James P. Pirruccello, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 28
NK2R control of energy expenditure and feeding to treat metabolic diseases
Frederike Sass, Tao Ma, Jeppe H. Ekberg, et al.
Nature (2024) Vol. 635, Iss. 8040, pp. 987-1000
Open Access | Times Cited: 9
Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults
Yang Liu, Ya‐Nan Ou, Bang‐Sheng Wu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
The impact of common and rare genetic variants on bradyarrhythmia development
Lu‐Chen Weng, Joel Rämö, Sean J. Jurgens, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings
Sean L. Zheng, Sean J. Jurgens, Kathryn A. McGurk, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Population-Scale Studies of Protein S Abnormalities and Thrombosis
Sharjeel A. Chaudhry, Amelia K. Haj, Justine Ryu, et al.
JAMA (2025)
Closed Access | Times Cited: 1
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Seung Hoan Choi, Sean J. Jurgens, Ling Xiao, et al.
Nature Genetics (2025)
Closed Access | Times Cited: 1
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
Shweta Ramdas, Jonathan Judd, Sarah E. Graham, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 8, pp. 1366-1387
Open Access | Times Cited: 34
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 154-164
Open Access | Times Cited: 30
Damaging missense variants in IGF1R implicate a role for IGF-1 resistance in the etiology of type 2 diabetes
Eugene J. Gardner, Katherine A. Kentistou, Stasa Stankovic, et al.
Cell Genomics (2022) Vol. 2, Iss. 12, pp. 100208-100208
Open Access | Times Cited: 28
Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation
Kelly M. Schiabor Barrett, Elizabeth T. Cirulli, Alexandre Bolze, et al.
Genetics in Medicine (2023) Vol. 25, Iss. 4, pp. 100012-100012
Closed Access | Times Cited: 21
Genetic and epigenetic background of diabetic kidney disease
Niina Sandholm, Emma H. Dahlström, Per‐Henrik Groop
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 16
Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing
Xiaoxi Liu, Satoshi Koyama, Kohei Tomizuka, et al.
Science Advances (2024) Vol. 10, Iss. 16
Open Access | Times Cited: 7
TAD boundary deletion causes PITX2-related cardiac electrical and structural defects
Manon Baudic, Hiroshige Murata, Fernanda M. Bosada, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 7
Exome sequencing identifies genes associated with sleep-related traits
Chen-Jie Fei, Ze-Yu Li, Jing Ning, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 3, pp. 576-589
Closed Access | Times Cited: 6
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
Justine Ryu, Joel Rämö, Sean J. Jurgens, et al.
Blood (2024) Vol. 143, Iss. 23, pp. 2425-2432
Closed Access | Times Cited: 6
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