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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:

SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests
Wei Zhou, Wenjian Bi, Zhangchen Zhao, et al.
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1466-1469
Open Access | Times Cited: 89

Showing 1-25 of 89 citing articles:

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: 76
Adjusting for common variant polygenic scores improves yield in rare variant association analyses
Sean J. Jurgens, James P. Pirruccello, Seung Hoan Choi, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 544-548
Open Access | Times Cited: 29
Genetic drivers and cellular selection of female mosaic X chromosome loss
Aoxing Liu, Giulio Genovese, Yajie Zhao, et al.
Nature (2024) Vol. 631, Iss. 8019, pp. 134-141
Closed Access | Times Cited: 11
Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults
Yang Liu, Ya‐Nan Ou, Bang‐Sheng Wu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
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
Addressing overfitting bias due to sample overlap in polygenic risk scoring
Seokho Jeong, Manu Shivakumar, Sang‐Hyuk Jung, et al.
Alzheimer s & Dementia (2025) Vol. 21, Iss. 4
Open Access | Times Cited: 1
Association of biological age with health outcomes and its modifiable factors
Wei‐Shi Liu, Jia You, Yi‐Jun Ge, et al.
Aging Cell (2023) Vol. 22, Iss. 12
Open Access | Times Cited: 18
Exome sequencing identifies genes associated with sleep-related traits
Chen-Jie Fei, Ze-Yu Li, Jing Ning, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 3, pp. 576-589
Closed Access | Times Cited: 6
The genetic architecture of the human hypothalamus and its involvement in neuropsychiatric behaviours and disorders
Shi-Dong Chen, Jia You, Wei Zhang, et al.
Nature Human Behaviour (2024) Vol. 8, Iss. 4, pp. 779-793
Closed Access | Times Cited: 5
Identification of prospective aging drug targets via Mendelian randomization analysis
Rui Mao, Ji Li, Wenqin Xiao
Aging Cell (2024) Vol. 23, Iss. 7
Open Access | Times Cited: 5
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank
Frederik H. Lassen, Samvida S. Venkatesh, Nikolas Baya, et al.
Cell Genomics (2024) Vol. 4, Iss. 7, pp. 100602-100602
Open Access | Times Cited: 5
RAVAR: a curated repository for rare variant–trait associations
Chen Cao, Mengting Shao, Chunman Zuo, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D990-D997
Open Access | Times Cited: 11
HLA allele-calling using multi-ancestry whole-exome sequencing from the UK Biobank identifies 129 novel associations in 11 autoimmune diseases
Guillaume Butler‐Laporte, Yossi Farjoun, Tomoko Nakanishi, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 11
Whole-exome sequencing identifies protein-coding variants associated with brain iron in 29,828 individuals
Weikang Gong, Yan Fu, Bang‐Sheng Wu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Exome sequencing identifies genes for socioeconomic status in 350,770 individuals
Xinrui Wu, Yang Liu, Bang‐Sheng Wu, et al.
Proceedings of the National Academy of Sciences (2025) Vol. 122, Iss. 2
Open Access
NERINE reveals rare variant associations in gene networks across multiple phenotypes and implicates an SNCA-PRL-LRRK2 subnetwork in Parkinson's disease
Sumaiya Nazeen, Xinyuan Wang, Autumn Morrow, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Exome sequencing identifies protein-coding variants associated with loneliness and social isolation
Yixuan Wang, Chen-Jie Fei, Chun Shen, et al.
Journal of Affective Disorders (2025)
Closed Access
Investigating the contribution of coding variants in alcohol use disorder using whole-exome sequencing across ancestries
Lu Wang, Henry R. Kranzler, Joel Gelernter, et al.
Biological Psychiatry (2025)
Open Access
Meta-analysis of Germline Whole-exome Sequencing in 1435 Cases of Testicular Germ Cell Tumour to Evaluate Disruptive Mutations Under Dominant, Recessive, and X-linked Inheritance Models
Zeid Kuzbari, Charlie F Rowlands, Isaac Wade, et al.
European Urology Open Science (2025) Vol. 73, pp. 51-59
Open Access
High-dimensional mediation analysis reveals the mediating role of physical activity patterns in genetic pathways leading to AD-like brain atrophy
Hanxiang Xu, Shizhuo Mu, Jingxuan Bao, et al.
BioData Mining (2025) Vol. 18, Iss. 1
Open Access
Aberrant gene expression prediction across human tissues
Florian R. Hölzlwimmer, Jonas Lindner, George Tsitsiridis, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum
David S.M. Lee, Kathleen M. Cardone, David Zhang, et al.
Nature Genetics (2025)
Closed Access
An allelic-series rare-variant association test for candidate-gene discovery
Zachary R. McCaw, Colm O’Dushlaine, Hari Somineni, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 8, pp. 1330-1342
Open Access | Times Cited: 9
Genetic architectures of cerebral ventricles and their overlap with neuropsychiatric traits
Yi‐Jun Ge, Bang‐Sheng Wu, Yi Zhang, et al.
Nature Human Behaviour (2023) Vol. 8, Iss. 1, pp. 164-180
Open Access | Times Cited: 9
A phenome-wide scan reveals convergence of common and rare variant associations
Dan Zhou, Yuan Zhou, Yue Xu, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 9
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