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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:

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Εvangelos Εvangelou, Helen R. Warren, David Mosén-Ansorena, et al.
Nature Genetics (2018) Vol. 50, Iss. 10, pp. 1412-1425
Open Access | Times Cited: 1172

Showing 1-25 of 1172 citing articles:

Heart Disease and Stroke Statistics—2021 Update
Salim S. Virani, Álvaro Alonso, Hugo J. Aparicio, et al.
Circulation (2021) Vol. 143, Iss. 8
Open Access | Times Cited: 4643
Heart Disease and Stroke Statistics—2022 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2022) Vol. 145, Iss. 8
Open Access | Times Cited: 4155
Heart Disease and Stroke Statistics—2023 Update: A Report From the American Heart Association
Connie W. Tsao, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2023) Vol. 147, Iss. 8
Open Access | Times Cited: 4073
2024 Heart Disease and Stroke Statistics: A Report of US and Global Data From the American Heart Association
Seth S. Martin, Aaron W. Aday, Zaid Almarzooq, et al.
Circulation (2024) Vol. 149, Iss. 8
Open Access | Times Cited: 782
Diretrizes Brasileiras de Hipertensão Arterial – 2020
Weimar Kunz Sebba Barroso, Cibele Isaac Saad Rodrigues, Luiz Aparecido Bortolotto, et al.
Arquivos Brasileiros de Cardiologia (2021) Vol. 116, Iss. 3, pp. 516-658
Open Access | Times Cited: 769
Genetic determinants of daytime napping and effects on cardiometabolic health
Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 481
Variable prediction accuracy of polygenic scores within an ancestry group
Hakhamanesh Mostafavi, Arbel Harpak, Ipsita Agarwal, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 387
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 379
Genetic drug target validation using Mendelian randomisation
Amand F. Schmidt, Chris Finan, María Gordillo‐Marañón, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 340
Stroke genetics informs drug discovery and risk prediction across ancestries
Aniket Mishra, Rainer Malik, Tsuyoshi Hachiya, et al.
Nature (2022) Vol. 611, Iss. 7934, pp. 115-123
Open Access | Times Cited: 322
Personalized Medicine and the Power of Electronic Health Records
Noura S. Abul‐Husn, Eimear E. Kenny
Cell (2019) Vol. 177, Iss. 1, pp. 58-69
Open Access | Times Cited: 291
15 years of GWAS discovery: Realizing the promise
Abdel Abdellaoui, Loïc Yengo, Karin J. H. Verweij, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 179-194
Open Access | Times Cited: 282
Mendelian randomization for cardiovascular diseases: principles and applications
Susanna C. Larsson, Adam S. Butterworth, Stephen Burgess
European Heart Journal (2023) Vol. 44, Iss. 47, pp. 4913-4924
Open Access | Times Cited: 274
Causal association between periodontitis and hypertension: evidence from Mendelian randomization and a randomized controlled trial of non-surgical periodontal therapy
Marta Cześnikiewicz‐Guzik, Grzegorz Osmenda, Mateusz Siedliński, et al.
European Heart Journal (2019) Vol. 40, Iss. 42, pp. 3459-3470
Open Access | Times Cited: 258
A single-nucleus RNA-sequencing pipeline to decipher the molecular anatomy and pathophysiology of human kidneys
Blue B. Lake, Song Chen, Masato Hoshi, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 257
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Mark K. Bakker, Rick A. A. van der Spek, Wouter van Rheenen, et al.
Nature Genetics (2020) Vol. 52, Iss. 12, pp. 1303-1313
Open Access | Times Cited: 252
Understanding the consequences of education inequality on cardiovascular disease: mendelian randomisation study
Alice R Carter, Dipender Gill, Neil M Davies, et al.
BMJ (2019), pp. l1855-l1855
Open Access | Times Cited: 250
Constrained maximum likelihood-based Mendelian randomization robust to both correlated and uncorrelated pleiotropic effects
Haoran Xue, Xiaotong Shen, Wei Pan
The American Journal of Human Genetics (2021) Vol. 108, Iss. 7, pp. 1251-1269
Open Access | Times Cited: 245
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Andrew R. Harper, Anuj Goel, Christopher Grace, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 135-142
Open Access | Times Cited: 238
Role of m6A RNA methylation in cardiovascular disease (Review)
Yuhan Qin, Linqing Li, Erfei Luo, et al.
International Journal of Molecular Medicine (2020) Vol. 46, Iss. 6, pp. 1958-1972
Open Access | Times Cited: 223
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits
Doruk Beyter, Helga Ingimundardóttir, Ásmundur Oddsson, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 779-786
Open Access | Times Cited: 219
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, et al.
Nature Medicine (2022) Vol. 28, Iss. 8, pp. 1679-1692
Open Access | Times Cited: 218
Advancing the use of genome-wide association studies for drug repurposing
William R. Reay, Murray J. Cairns
Nature Reviews Genetics (2021) Vol. 22, Iss. 10, pp. 658-671
Closed Access | Times Cited: 206
Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
Zhaotong Lin, Yangqing Deng, Wei Pan
PLoS Genetics (2021) Vol. 17, Iss. 11, pp. e1009922-e1009922
Open Access | Times Cited: 182
Arterial hypertension
Sofie Brouwers, Isabella Sudano, Yoshihiro Kokubo, et al.
The Lancet (2021) Vol. 398, Iss. 10296, pp. 249-261
Closed Access | Times Cited: 180
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