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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:

Exome sequencing of Finnish isolates enhances rare-variant association power
Adam E. Locke, Karyn Meltz Steinberg, Charleston W. K. Chiang, et al.
Nature (2019) Vol. 572, Iss. 7769, pp. 323-328
Open Access | Times Cited: 188

Showing 1-25 of 188 citing articles:

The GenomeAsia 100K Project enables genetic discoveries across Asia
Jeffrey D. Wall, Eric Stawiski, Aakrosh Ratan, et al.
Nature (2019) Vol. 576, Iss. 7785, pp. 106-111
Open Access | Times Cited: 367
Exploiting the GTEx resources to decipher the mechanisms at GWAS loci
Alvaro Barbeira, Rodrigo Bonazzola, Eric R. Gamazon, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 247
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
Alison R. Barton, Maxwell A. Sherman, Ronen E. Mukamel, et al.
Nature Genetics (2021) Vol. 53, Iss. 8, pp. 1260-1269
Open Access | Times Cited: 216
Host genetics and infectious disease: new tools, insights and translational opportunities
Andrew Kwok, Alexander J. Mentzer, Julian C. Knight
Nature Reviews Genetics (2020) Vol. 22, Iss. 3, pp. 137-153
Open Access | Times Cited: 178
A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease
Aniruddh P. Patel, Minxian Wang, Yunfeng Ruan, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1793-1803
Open Access | Times Cited: 130
Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci
Xianyong Yin, Lap Sum Chan, Debraj Bose, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 128
Genetic associations of protein-coding variants in human disease
Benjamin B. Sun, Mitja Kurki, Christopher N. Foley, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 95-102
Open Access | Times Cited: 114
Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Anna Köttgen, Émilie Cornec-Le Gall, Jan Halbritter, et al.
Kidney International (2022) Vol. 101, Iss. 6, pp. 1126-1141
Open Access | Times Cited: 113
Taxonomic signatures of cause-specific mortality risk in human gut microbiome
Aaro Salosensaari, Ville Laitinen, Aki S. Havulinna, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 111
From target discovery to clinical drug development with human genetics
Katerina Trajanoska, Claude Bhérer, Daniel Taliun, et al.
Nature (2023) Vol. 620, Iss. 7975, pp. 737-745
Closed Access | Times Cited: 103
Genome-wide characterization of circulating metabolic biomarkers
Minna K. Karjalainen, Savita Karthikeyan, Clare Oliver‐Williams, et al.
Nature (2024) Vol. 628, Iss. 8006, pp. 130-138
Open Access | Times Cited: 94
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Remi Stevelink, Ciarán Campbell, Siwei Chen, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1471-1482
Open Access | Times Cited: 89
Post-translational control of beige fat biogenesis by PRDM16 stabilization
Qiang Wang, Huixia Li, Kazuki Tajima, et al.
Nature (2022) Vol. 609, Iss. 7925, pp. 151-158
Open Access | Times Cited: 74
Mono- and biallelic variant effects on disease at biobank scale
Henrike Heyne, Juha Karjalainen, Konrad J. Karczewski, et al.
Nature (2023) Vol. 613, Iss. 7944, pp. 519-525
Open Access | Times Cited: 58
Accurate and Scalable Construction of Polygenic Scores in Large Biobank Data Sets
Sheng Yang, Xiang Zhou
The American Journal of Human Genetics (2020) Vol. 106, Iss. 5, pp. 679-693
Open Access | Times Cited: 112
Electronic health records and polygenic risk scores for predicting disease risk
Ruowang Li, Yong Chen, Marylyn D. Ritchie, et al.
Nature Reviews Genetics (2020) Vol. 21, Iss. 8, pp. 493-502
Closed Access | Times Cited: 99
Genetics of substance use disorders in the era of big data
Joel Gelernter, Renato Polimanti
Nature Reviews Genetics (2021) Vol. 22, Iss. 11, pp. 712-729
Open Access | Times Cited: 97
Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome
Jaakko Tyrmi, Riikka K. Arffman, Natàlia Pujol‐Gualdo, et al.
Human Reproduction (2021) Vol. 37, Iss. 2, pp. 352-365
Open Access | Times Cited: 57
Using human genetics to improve safety assessment of therapeutics
Keren Carss, Aimée M. Deaton, Alberto del Río-Espínola, et al.
Nature Reviews Drug Discovery (2022) Vol. 22, Iss. 2, pp. 145-162
Closed Access | Times Cited: 57
Identifying molecular mediators of the relationship between body mass index and endometrial cancer risk: a Mendelian randomization analysis
Emma Hazelwood, Eleanor Sanderson, Vanessa Y. Tan, et al.
BMC Medicine (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 47
High-throughput genetic clustering of type 2 diabetes loci reveals heterogeneous mechanistic pathways of metabolic disease
Hyunkyung Kim, Kenneth E. Westerman, Kirk Smith, et al.
Diabetologia (2022) Vol. 66, Iss. 3, pp. 495-507
Open Access | Times Cited: 47
Causal associations between type 1 diabetes mellitus and cardiovascular diseases: a Mendelian randomization study
Zirui Liu, Haocheng Wang, Zhengkai Yang, et al.
Cardiovascular Diabetology (2023) Vol. 22, Iss. 1
Open Access | Times Cited: 31
Drug-target Mendelian randomization analysis supports lowering plasma ANGPTL3, ANGPTL4, and APOC3 levels as strategies for reducing cardiovascular disease risk
Fredrik Landfors, Peter Henneman, Elin Chorell, et al.
European Heart Journal Open (2024) Vol. 4, Iss. 3
Open Access | Times Cited: 10
Practical guide for managing large-scale human genome data in research
Tomoya Tanjo, Yosuke Kawai, Katsushi Tokunaga, et al.
Journal of Human Genetics (2020) Vol. 66, Iss. 1, pp. 39-52
Open Access | Times Cited: 54
Increasing accuracy of HLA imputation by a population-specific reference panel in a FinnGen biobank cohort
Jarmo Ritari, Kati Hyvärinen, Jonna Clancy, et al.
NAR Genomics and Bioinformatics (2020) Vol. 2, Iss. 2
Open Access | Times Cited: 52
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