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:

Genetic associations of protein-coding variants in human disease
Benjamin B. Sun, Mitja Kurki, Christopher N. Foley, et al.
Nature (2022) Vol. 603, Iss. 7899, pp. 95-102
Open Access | Times Cited: 114

Showing 1-25 of 114 citing articles:

FinnGen provides genetic insights from a well-phenotyped isolated population
Mitja Kurki, Juha Karjalainen, Priit Palta, et al.
Nature (2023) Vol. 613, Iss. 7944, pp. 508-518
Open Access | Times Cited: 2231

TTD: Therapeutic Target Database describing target druggability information
Ying Zhou, Yintao Zhang, Donghai Zhao, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D1465-D1477
Open Access | Times Cited: 234

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes
Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao, et al.
Cell Genomics (2022) Vol. 2, Iss. 9, pp. 100168-100168
Open Access | Times Cited: 194

RNA editing underlies genetic risk of common inflammatory diseases
Qin Li, Michael J. Gloudemans, Jonathan M. Geisinger, et al.
Nature (2022) Vol. 608, Iss. 7923, pp. 569-577
Open Access | Times Cited: 119

Polygenic architecture of rare coding variation across 394,783 exomes
Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, et al.
Nature (2023) Vol. 614, Iss. 7948, pp. 492-499
Open Access | Times Cited: 112

Refining the impact of genetic evidence on clinical success
Eric Vallabh Minikel, Jeffery L. Painter, Coco Chengliang Dong, et al.
Nature (2024) Vol. 629, Iss. 8012, pp. 624-629
Open Access | Times Cited: 93

Polygenic prediction of preeclampsia and gestational hypertension
Michael C. Honigberg, Buu Truong, Raiyan R. Khan, et al.
Nature Medicine (2023) Vol. 29, Iss. 6, pp. 1540-1549
Open Access | Times Cited: 66

Whole genome sequencing in clinical practice
Frederik Otzen Bagger, Line Borgwardt, Andreas Sand Jespersen, et al.
BMC Medical Genomics (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 44

High-dimensional phenotyping to define the genetic basis of cellular morphology
Matthew Tegtmeyer, Jatin Arora, Samira Asgari, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 31

Atlas of the plasma proteome in health and disease in 53,026 adults
Yue‐Ting Deng, Jia You, Yu He, et al.
Cell (2024)
Open Access | Times Cited: 18

Estimating the number of diseases – the concept of rare, ultra-rare, and hyper-rare
Smith Rjh, Peter Bergman, Daniel W. Hagey
iScience (2022) Vol. 25, Iss. 8, pp. 104698-104698
Open Access | Times Cited: 46

The impact of rare protein coding genetic variation on adult cognitive function
Chia‐Yen Chen, Ruoyu Tian, Tian Ge, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 927-938
Open Access | Times Cited: 42

Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle
Ruidong Xiang, Lingzhao Fang, Shuli Liu, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100385-100385
Open Access | Times Cited: 27

Brain Lipids and Lipid Droplet Dysregulation in Alzheimer’s Disease and Neuropsychiatric Disorders
Xiaojie Zhao, Siwei Zhang, Alan R. Sanders, et al.
Complex Psychiatry (2023) Vol. 9, Iss. 1-4, pp. 154-171
Open Access | Times Cited: 26

Polygenic risk alters the penetrance of monogenic kidney disease
Atlas Khan, Ning Shang, Jordan G. Nestor, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 26

Refining the impact of genetic evidence on clinical success
Eric Vallabh Minikel, Jeffery L. Painter, Coco Chengliang Dong, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 23

ProtVar: mapping and contextualizing human missense variation
James Stephenson, Prabhat Totoo, David F. Burke, et al.
Nucleic Acids Research (2024) Vol. 52, Iss. W1, pp. W140-W147
Open Access | Times Cited: 14

Rare coding variant analysis for human diseases across biobanks and ancestries
Sean J. Jurgens, Xin Wang, Seung Hoan Choi, et al.
Nature Genetics (2024) Vol. 56, Iss. 9, pp. 1811-1820
Closed Access | Times Cited: 11

Potential Causal Association between Plasma Metabolites, Immunophenotypes, and Female Reproductive Disorders: A Two-Sample Mendelian Randomization Analysis
Hui‐Hui Shen, Yangyang Zhang, Xuan-Yu Wang, et al.
Biomolecules (2024) Vol. 14, Iss. 1, pp. 116-116
Open Access | Times Cited: 10

Biobanking with genetics shapes precision medicine and global health
C. Scott Gallagher, Geoffrey S. Ginsburg, Anjené Addington
Nature Reviews Genetics (2024)
Closed Access | Times Cited: 10

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: 9

Genes, Cognition, and Their Interplay in Methamphetamine Use Disorder
Raheela Khan, Alyna Turner, Michael Berk, et al.
Biomolecules (2025) Vol. 15, Iss. 2, pp. 306-306
Open Access | Times Cited: 1

Maximizing treatment efficacy through patient stratification in neuropathic pain trials
Ralf Baron, Anthony H. Dickenson, Margarita Calvo, et al.
Nature Reviews Neurology (2022) Vol. 19, Iss. 1, pp. 53-64
Closed Access | Times Cited: 36

Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations
Catherine Lovegrove, Jelena Bešević, Akira Wiberg, et al.
Journal of the American Society of Nephrology (2023) Vol. 34, Iss. 12, pp. 1991-2011
Open Access | Times Cited: 17

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