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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:

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution
Masahiro Kanai, Roy Elzur, Wei Zhou, et al.
Cell Genomics (2022) Vol. 2, Iss. 12, pp. 100210-100210
Open Access | Times Cited: 57

Showing 1-25 of 57 citing articles:

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Wei Zhou, Masahiro Kanai, Kuan-Han Wu, et al.
Cell Genomics (2022) Vol. 2, Iss. 10, pp. 100192-100192
Open Access | Times Cited: 231
Fine-mapping from summary data with the “Sum of Single Effects” model
Yuxin Zou, Peter Carbonetto, Gao Wang, et al.
PLoS Genetics (2022) Vol. 18, Iss. 7, pp. e1010299-e1010299
Open Access | Times Cited: 208
Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries
Zhanju Liu, Ruize Liu, Han Gao, et al.
Nature Genetics (2023) Vol. 55, Iss. 5, pp. 796-806
Open Access | Times Cited: 98
Nuclear genetic control of mtDNA copy number and heteroplasmy in humans
Rahul Gupta, Masahiro Kanai, Timothy Durham, et al.
Nature (2023) Vol. 620, Iss. 7975, pp. 839-848
Open Access | Times Cited: 74
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Xiangrui Meng, Georgina Navoly, Olga Giannakopoulou, et al.
Nature Genetics (2024) Vol. 56, Iss. 2, pp. 222-233
Open Access | Times Cited: 61
Molecular quantitative trait loci
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 50
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1841-1850
Closed Access | Times Cited: 27
CARMA is a new Bayesian model for fine-mapping in genome-wide association meta-analyses
Zikun Yang, Chen Wang, Linxi Liu, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 1057-1065
Closed Access | Times Cited: 35
Loci for insulin processing and secretion provide insight into type 2 diabetes risk
K. Alaine Broadaway, Xianyong Yin, Alice Williamson, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 284-299
Open Access | Times Cited: 27
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
Nana Liu, Long Jiang Zhang, Tian Tian, et al.
Nature Genetics (2023) Vol. 55, Iss. 7, pp. 1126-1137
Open Access | Times Cited: 24
Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Kai Yuan, Ryan J. Longchamps, Antonio F. Pardiñas, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 23
Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology
Ying Wang, Masahiro Kanai, Taotao Tan, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100408-100408
Open Access | Times Cited: 23
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 9
Multi-omics approaches for understanding gene-environment interactions in noncommunicable diseases: techniques, translation, and equity issues
Robel Alemu, Nigussie Tadesse Sharew, Yodit Y. Arsano, et al.
Human Genomics (2025) Vol. 19, Iss. 1
Open Access | Times Cited: 1
A large-scale genome-wide association study on female genital tract polyps highlights role of DNA repair, cell proliferation, and cell growth
Amruta D. S. Pathare, Jelisaveta Džigurski, Natàlia Pujol‐Gualdo, et al.
Human Reproduction (2025)
Closed Access | Times Cited: 1
Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies
Pouria Salehi Nowbandegani, Anthony Wilder Wohns, Jenna L. Ballard, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1494-1502
Open Access | Times Cited: 20
Improving fine-mapping by modeling infinitesimal effects
Ran Cui, Roy Elzur, Masahiro Kanai, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 162-169
Open Access | Times Cited: 20
A genome-wide association analysis reveals new pathogenic pathways in gout*
Tanya J. Major, Riku Takei, Hirotaka Matsuo, et al.
Nature Genetics (2024) Vol. 56, Iss. 11, pp. 2392-2406
Closed Access | Times Cited: 7
Fast and accurate Bayesian polygenic risk modeling with variational inference
Shadi Zabad, Simon Gravel, Yue Li
The American Journal of Human Genetics (2023) Vol. 110, Iss. 5, pp. 741-761
Open Access | Times Cited: 14
Fast and flexible joint fine-mapping of multiple traits via the Sum of Single Effects model
Yuxin Zou, Peter Carbonetto, Dongyue Xie, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 14
XMAP: Cross-population fine-mapping by leveraging genetic diversity and accounting for confounding bias
Mingxuan Cai, Zhiwei Wang, Jiashun Xiao, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 14
Using omics data and genome editing methods to decipher GWAS loci associated with coronary artery disease
Arnaud Chignon, Guillaume Lettre
Atherosclerosis (2025) Vol. 401, pp. 118621-118621
Open Access
Secure and federated genome-wide association studies for biobank-scale datasets
Hyunghoon Cho, David Froelicher, Jeffrey Chen, et al.
Nature Genetics (2025)
Open Access
Fine-mapping in admixed populations using CARMA-X, with applications to Latin American studies
Zikun Yang, Chen Wang, Yuridia S. Posadas‐García, et al.
The American Journal of Human Genetics (2025)
Closed Access
Single-cell genomics improves the discovery of risk variants and genes of atrial fibrillation
Alan Selewa, Kaixuan Luo, Michael Wasney, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 11
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