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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:

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: 28

Showing 1-25 of 28 citing articles:

Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traits
Chia‐Yen Chen, Tzu‐Ting Chen, Yen‐Chen Anne Feng, et al.
Cell Genomics (2023) Vol. 3, Iss. 12, pp. 100436-100436
Open Access | Times Cited: 33
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
An evolving understanding of multiple causal variants underlying genetic association signals
Erping Long, Jacob Williams, Haoyu Zhang, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
CXCL12 drives natural variation in coronary artery anatomy across diverse populations
Pamela E. Rios Coronado, Jiayan Zhou, Xiaochen Fan, et al.
Cell (2025)
Open Access | Times Cited: 1
Shared genetic architectures of educational attainment in East Asian and European populations
Tzu‐Ting Chen, Jaeyoung Kim, Max Lam, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 3, pp. 562-575
Open Access | Times Cited: 7
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height
Gareth Hawkes, Robin N. Beaumont, Zilin Li, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 7
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
Fine-mapping causal tissues and genes at disease-associated loci
Benjamin J. Strober, Martin Jinye Zhang, Tiffany Amariuta, et al.
Nature Genetics (2025)
Closed Access
Refining breast cancer genetic risk and biology through multi-ancestry fine-mapping analyses of 192 risk regions
Guochong Jia, Zhishan Chen, Jie Ping, et al.
Nature Genetics (2025) Vol. 57, Iss. 1, pp. 80-87
Closed Access
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
Global diversity in bipolar disorder: the role of cultural and social differences with a view to genomics
Janice M. Fullerton, Markos Tesfaye
Biological Psychiatry (2025)
Closed 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
Cross-ancestry genome-wide association study identifies new susceptibility genes for preeclampsia
Yuping Shan, Hong Hu, Yijing Chu
BMC Pregnancy and Childbirth (2025) Vol. 25, Iss. 1
Open Access
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Human height: a model common complex trait
Mitchell Conery, Struan F.A. Grant
Annals of Human Biology (2023) Vol. 50, Iss. 1, pp. 258-266
Open Access | Times Cited: 12
Improved multi-ancestry fine-mapping identifiescis-regulatory variants underlying molecular traits and disease risk
Zeyun Lu, Xinran Wang, Matthew Carr, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 4
The Farm Animal Genotype–Tissue Expression (FarmGTEx) Project
Lingzhao Fang, Jinyan Teng, Qing Lin, et al.
Nature Genetics (2025)
Closed Access
Fine-mapping genomic loci refines bipolar disorder risk genes
Maria Koromina, Ashvin Ravi, Georgia Panagiotaropoulou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 3
Biological Insights from Schizophrenia-associated Loci in Ancestral Populations
Tim B. Bigdeli, Chris Chatzinakos, Jaroslav Bendl, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Benjamin Meir Jacobs, Daniel Stow, Sam Hodgson, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Ancestry diversity in the genetic determinants of the human plasma proteome and associated new drug targets
Alfred Pozarickij, Saredo Said, Kuang Lin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Genome-wide association studies in a large Korean cohort identify novel quantitative trait loci for 36 traits and illuminates their genetic architectures
Yon Ho Jee, Ying Wang, Keum Ji Jung, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Genome-wide association study for circulating metabolites in 619,372 individuals
Ralf Tambets, Jaanika Kronberg, Erik Abner, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations
Sheng Fu, William Wheeler, Kevin Wang, et al.
PLoS Genetics (2024) Vol. 20, Iss. 10, pp. e1011322-e1011322
Open Access | Times Cited: 1
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