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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.

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Showing 1-25 of 215 citing articles:

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
Daniel Taliun, Daniel Harris, Michael D. Kessler, et al.
Nature (2021) Vol. 590, Iss. 7845, pp. 290-299
Open Access | Times Cited: 1641
Single-cell atlas reveals correlates of high cognitive function, dementia, and resilience to Alzheimer’s disease pathology
Hansruedi Mathys, Zhuyu Peng, Carles A. Boix, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4365-4385.e27
Open Access | Times Cited: 235
Multiple causal variants underlie genetic associations in humans
Nathan S. Abell, Marianne K. DeGorter, Michael J. Gloudemans, et al.
Science (2022) Vol. 375, Iss. 6586, pp. 1247-1254
Open Access | Times Cited: 136
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
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome
Hufeng Zhou, Theodore Arapoglou, Xihao Li, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D1300-D1311
Open Access | Times Cited: 82
Genetic variation across and within individuals
Zhi Yu, Tim H. H. Coorens, Md Mesbah Uddin, et al.
Nature Reviews Genetics (2024) Vol. 25, Iss. 8, pp. 548-562
Closed Access | Times Cited: 22
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Jinyoung Byun, Younghun Han, Yafang Li, et al.
Nature Genetics (2022) Vol. 54, Iss. 8, pp. 1167-1177
Open Access | Times Cited: 69
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Zilin Li, Xihao Li, Hufeng Zhou, et al.
Nature Methods (2022) Vol. 19, Iss. 12, pp. 1599-1611
Open Access | Times Cited: 65
Whole genome sequence analysis of blood lipid levels in >66,000 individuals
Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 52
Quantifying portable genetic effects and improving cross-ancestry genetic prediction with GWAS summary statistics
Jiacheng Miao, Hanmin Guo, Gefei Song, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 32
Penetrance of pathogenic genetic variants associated with premature ovarian insufficiency
Saleh Shekari, Stasa Stankovic, Eugene J. Gardner, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1692-1699
Open Access | Times Cited: 32
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
OTTERS: a powerful TWAS framework leveraging summary-level reference data
Qile Dai, Geyu Zhou, Hongyu Zhao, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 27
Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations
Elena V. Feofanova, Michael R. Brown, Taryn Alkis, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 27
Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesity
Lena R. Kaisinger, Katherine A. Kentistou, Stasa Stankovic, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100362-100362
Open Access | Times Cited: 26
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
A metabolomic profile of biological aging in 250,341 individuals from the UK Biobank
Shiyu Zhang, Zheng Wang, Yijing Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 10
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data
Yanbing Wang, Chloé Sarnowski, Honghuang Lin, et al.
Alzheimer s & Dementia (2024) Vol. 20, Iss. 5, pp. 3290-3304
Open Access | Times Cited: 9
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: 8
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 154-164
Open Access | Times Cited: 30
Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks
Rounak Dey, Wei Zhou, Tuomo Kiiskinen, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 28
Damaging missense variants in IGF1R implicate a role for IGF-1 resistance in the etiology of type 2 diabetes
Eugene J. Gardner, Katherine A. Kentistou, Stasa Stankovic, et al.
Cell Genomics (2022) Vol. 2, Iss. 12, pp. 100208-100208
Open Access | Times Cited: 28
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis
Younghun Han, Jinyoung Byun, Catherine Zhu, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 18
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
Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole‐genome sequencing from the Alzheimer's Disease Sequencing Project
Wan‐Ping Lee, Seung Hoan Choi, Margaret G. Shea, et al.
Alzheimer s & Dementia (2024)
Open Access | Times Cited: 7
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