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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:

GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background
Nasa Sinnott-Armstrong, Sahin Naqvi, Manuel A. Rivas, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 131

Showing 1-25 of 131 citing articles:

Genome-wide association studies
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1084
Discovery and implications of polygenicity of common diseases
Peter M. Visscher, Loïc Yengo, Nancy J. Cox, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1468-1473
Open Access | Times Cited: 127
Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways
Kyoko Watanabe, Philip R. Jansen, Jeanne E. Savage, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1125-1132
Open Access | Times Cited: 122
From variant to function in human disease genetics
Tuuli Lappalainen, Daniel G. MacArthur
Science (2021) Vol. 373, Iss. 6562, pp. 1464-1468
Closed Access | Times Cited: 121
Limited overlap of eQTLs and GWAS hits due to systematic differences in discovery
Hakhamanesh Mostafavi, Jeffrey P. Spence, Sahin Naqvi, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 91
Amplification is the primary mode of gene-by-sex interaction in complex human traits
Carrie Zhu, Matthew J. Ming, Jared M. Cole, et al.
Cell Genomics (2023) Vol. 3, Iss. 5, pp. 100297-100297
Open Access | Times Cited: 64
Genetic effects on the timing of parturition and links to fetal birth weight
Pol Solé-Navais, Christopher Flatley, Valgerður Steinthórsdóttir, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 559-567
Open Access | Times Cited: 48
A single gene orchestrates androgen variation underlying male mating morphs in ruffs
Jasmine L. Loveland, Alex Zemella, Vladimir Jovanović, et al.
Science (2025) Vol. 387, Iss. 6732, pp. 406-412
Closed Access | Times Cited: 4
Reviewing the genetics of heterogeneity in depression: operationalizations, manifestations and etiologies
Na Cai, Karmel W. Choi, Eiko I. Fried
Human Molecular Genetics (2020) Vol. 29, Iss. R1, pp. R10-R18
Open Access | Times Cited: 133
The omnigenic model and polygenic prediction of complex traits
Iain Mathieson
The American Journal of Human Genetics (2021) Vol. 108, Iss. 9, pp. 1558-1563
Open Access | Times Cited: 86
Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases
Scott C. Ritchie, Samuel A. Lambert, Matthew Arnold, et al.
Nature Metabolism (2021) Vol. 3, Iss. 11, pp. 1476-1483
Open Access | Times Cited: 67
MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies
Arjun Bhattacharya, Yun Li, Michael I. Love
PLoS Genetics (2021) Vol. 17, Iss. 3, pp. e1009398-e1009398
Open Access | Times Cited: 66
Prospective analyses of testosterone and sex hormone‐binding globulin with the risk of 19 types of cancer in men and postmenopausal women in UK Biobank
Eleanor L. Watts, Aurora Perez‐Cornago, Anika Knüppel, et al.
International Journal of Cancer (2021) Vol. 149, Iss. 3, pp. 573-584
Open Access | Times Cited: 57
The pathogenesis of gout: molecular insights from genetic, epigenomic and transcriptomic studies
Megan Leask, Tania O. Crişan, Aichang Ji, et al.
Nature Reviews Rheumatology (2024) Vol. 20, Iss. 8, pp. 510-523
Closed Access | Times Cited: 14
Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics
Juulia Partanen, Paavo Häppölä, Wei Zhou, et al.
Cell Genomics (2022) Vol. 2, Iss. 10, pp. 100181-100181
Open Access | Times Cited: 34
A flexible modeling and inference framework for estimating variant effect sizes from GWAS summary statistics
Jeffrey P. Spence, Nasa Sinnott-Armstrong, Themistocles L. Assimes, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 31
Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation
Courtney J. Smith, Nasa Sinnott-Armstrong, Anna Cichońska, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 29
Genetic Risk, Adherence to a Healthy Lifestyle, and Hyperuricemia: The TCLSIH Cohort Study
Tingjing Zhang, Yeqing Gu, Ge Meng, et al.
The American Journal of Medicine (2023) Vol. 136, Iss. 5, pp. 476-483.e5
Open Access | Times Cited: 21
A genome-wide genetic screen uncovers determinants of human pigmentation
Vivek K. Bajpai, Tomek Swigut, Jaaved Mohammed, et al.
Science (2023) Vol. 381, Iss. 6658
Open Access | Times Cited: 21
Probabilistic integration of transcriptome-wide association studies and colocalization analysis identifies key molecular pathways of complex traits
Jeffrey Okamoto, Lijia Wang, Xianyong Yin, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 1, pp. 44-57
Open Access | Times Cited: 17
Genetic analyses implicate complex links between adult testosterone levels and health and disease
Jaakko T. Leinonen, Nina Mars, Leevi E. Lehtonen, et al.
Communications Medicine (2023) Vol. 3, Iss. 1
Open Access | Times Cited: 16
Insulin‐like growth factor‐1 and site‐specific cancers: A Mendelian randomization study
Susanna C. Larsson, Paul Carter, Mathew Vithayathil, et al.
Cancer Medicine (2020) Vol. 9, Iss. 18, pp. 6836-6842
Open Access | Times Cited: 43
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
MRLocus: Identifying causal genes mediating a trait through Bayesian estimation of allelic heterogeneity
Anqi Zhu, Nana Matoba, Emmaleigh Wilson, et al.
PLoS Genetics (2021) Vol. 17, Iss. 4, pp. e1009455-e1009455
Open Access | Times Cited: 36
Simple scaling laws control the genetic architectures of human complex traits
Yuval B. Simons, Hakhamanesh Mostafavi, Courtney J. Smith, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 27
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