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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:

Interpreting type 1 diabetes risk with genetics and single-cell epigenomics
Joshua Chiou, Ryan J. Geusz, Mei-Lin Okino, et al.
Nature (2021) Vol. 594, Iss. 7863, pp. 398-402
Open Access | Times Cited: 294

Showing 26-50 of 294 citing articles:

Shared genetic risk factors and causal association between psoriasis and coronary artery disease
Matthew T. Patrick, Qinmengge Li, Rachael Wasikowski, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 50
High-throughput genetic clustering of type 2 diabetes loci reveals heterogeneous mechanistic pathways of metabolic disease
Hyunkyung Kim, Kenneth E. Westerman, Kirk Smith, et al.
Diabetologia (2022) Vol. 66, Iss. 3, pp. 495-507
Open Access | Times Cited: 46
Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8
Sevim Kahraman, Ercument Dirice, Giorgio Basile, et al.
Nature Metabolism (2022) Vol. 4, Iss. 1, pp. 76-89
Closed Access | Times Cited: 42
Interpreting non-coding disease-associated human variants using single-cell epigenomics
Kyle J. Gaulton, Sebastian Preißl, Bing Ren
Nature Reviews Genetics (2023) Vol. 24, Iss. 8, pp. 516-534
Open Access | Times Cited: 39
Single-nucleus multi-omics of human stem cell-derived islets identifies deficiencies in lineage specification
Punn Augsornworawat, Nathaniel J. Hogrebe, Matthew Ishahak, et al.
Nature Cell Biology (2023) Vol. 25, Iss. 6, pp. 904-916
Open Access | Times Cited: 38
Clinical utility of polygenic risk scores: a critical 2023 appraisal
Sebastian Koch, Jörg Schmidtke, Michael Krawczak, et al.
Journal of Community Genetics (2023) Vol. 14, Iss. 5, pp. 471-487
Open Access | Times Cited: 36
Genetics of diabetes-associated microvascular complications
Valeriya Lyssenko, Allan Vaag
Diabetologia (2023) Vol. 66, Iss. 9, pp. 1601-1613
Open Access | Times Cited: 36
An Integrated Map of Cell Type–Specific Gene Expression in Pancreatic Islets
Ruth M. Elgamal, Parul Kudtarkar, Rebecca L. Melton, et al.
Diabetes (2023) Vol. 72, Iss. 11, pp. 1719-1728
Open Access | Times Cited: 35
Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus
Chachrit Khunsriraksakul, Qinmengge Li, Havell Markus, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 34
From genetic associations to genes: methods, applications, and challenges
Ting Qi, Liyang Song, Yazhou Guo, et al.
Trends in Genetics (2024) Vol. 40, Iss. 8, pp. 642-667
Open Access | Times Cited: 15
Characterizing the impacts of dataset imbalance on single-cell data integration
Hassaan Maan, Lin Zhang, Chengxin Yu, et al.
Nature Biotechnology (2024)
Closed Access | Times Cited: 14
Identification of unique cell type responses in pancreatic islets to stress
Marlie M. Maestas, Matthew Ishahak, Punn Augsornworawat, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 11
A multi-ancestry genome-wide association study in type 1 diabetes
Dominika Michałek, Courtney Tern, Wei Zhou, et al.
Human Molecular Genetics (2024) Vol. 33, Iss. 11, pp. 958-968
Open Access | Times Cited: 9
Exploring potential causal associations between autoimmune diseases and colorectal cancer using bidirectional Mendelian randomization
Lu Chen, Feifan Wang, Hua Zhang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Immune dysregulation in bipolar disorder
Benney M.R. Argue, Lucas G. Casten, S.C. McCool, et al.
Journal of Affective Disorders (2025)
Closed Access | Times Cited: 1
TCL1A in naïve B cells as a therapeutic target for type 1 diabetes
Siweier Luo, Lína Zhang, Chunfang Wei, et al.
EBioMedicine (2025) Vol. 113, pp. 105593-105593
Closed Access | Times Cited: 1
Linking molecular pathways and islet cell dysfunction in human type 1 diabetes
Theodore dos Santos, Xiao Qing Dai, Robert C. Jones, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access | Times Cited: 1
Causal relationship between type I diabetes mellitus and atrial fibrillation: A Mendelian randomization study
Yongkai Li, Shasha Liu, Yiming Dong, et al.
IJC Heart & Vasculature (2025) Vol. 57, pp. 101643-101643
Open Access | Times Cited: 1
How dysregulation of the immune system promotes diabetes mellitus and cardiovascular risk complications
Diane Girard, Claire Vandiedonck
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 31
Advanced Glycation End Products and Inflammation in Type 1 Diabetes Development
Chenping Du, Rani Whiddett, Irina Buckle, et al.
Cells (2022) Vol. 11, Iss. 21, pp. 3503-3503
Open Access | Times Cited: 28
Innate and adaptive immune abnormalities underlying autoimmune diseases: the genetic connections
Xinxin Chi, Miaozhen Huang, Hailin Tu, et al.
Science China Life Sciences (2023) Vol. 66, Iss. 7, pp. 1482-1517
Open Access | Times Cited: 20
Integration of epigenetic and genetic profiles identifies multiple sclerosis disease-critical cell types and genes
Qin Ma, Hengameh Shams, Alessandro Didonna, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 18
Identification of genetic variants that impact gene co-expression relationships using large-scale single-cell data
Shuang Li, Katharina T. Schmid, Dylan H. de Vries, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 17
Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots
Clara Albiñana, Zhihong Zhu, Nis Borbye‐Lorenzen, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 16
Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes
Bergithe E Oftedal, Kristian Assing, Safa Barış, et al.
iScience (2023) Vol. 26, Iss. 6, pp. 106818-106818
Open Access | Times Cited: 16

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