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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:

Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits
Eleonora Porcu, Sina Rüeger, Kaido Lepik, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 269

Showing 1-25 of 269 citing articles:

Guidelines for performing Mendelian randomization investigations
Stephen Burgess, George Davey Smith, Neil M Davies, et al.
Wellcome Open Research (2019) Vol. 4, pp. 186-186
Open Access | Times Cited: 1431
Guidelines for performing Mendelian randomization investigations
Stephen Burgess, George Davey Smith, Neil M Davies, et al.
Wellcome Open Research (2020) Vol. 4, pp. 186-186
Open Access | Times Cited: 1151
Guidelines for performing Mendelian randomization investigations: update for summer 2023
Stephen Burgess, George Davey Smith, Neil M Davies, et al.
Wellcome Open Research (2023) Vol. 4, pp. 186-186
Open Access | Times Cited: 351
A compendium of uniformly processed human gene expression and splicing quantitative trait loci
Nurlan Kerimov, James Hayhurst, Kateryna Peikova, et al.
Nature Genetics (2021) Vol. 53, Iss. 9, pp. 1290-1299
Open Access | Times Cited: 313
Interpretation of risk loci from genome-wide association studies of Alzheimer's disease
Shea J. Andrews, Brian Fulton‐Howard, Alison Goate
The Lancet Neurology (2020) Vol. 19, Iss. 4, pp. 326-335
Open Access | Times Cited: 286
Quantifying genetic effects on disease mediated by assayed gene expression levels
Douglas Yao, Luke J. O’Connor, Alkes L. Price, et al.
Nature Genetics (2020) Vol. 52, Iss. 6, pp. 626-633
Open Access | Times Cited: 274
An integrated framework for local genetic correlation analysis
Josefin Werme, Sophie van der Sluis, Daniëlle Posthuma, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 274-282
Open Access | Times Cited: 243
Persistent inflammatory and non-inflammatory mechanisms in refractory rheumatoid arthritis
Maya H Buch, Stephen Eyre, Dennis McGonagle
Nature Reviews Rheumatology (2020) Vol. 17, Iss. 1, pp. 17-33
Closed Access | Times Cited: 191
The single-cell eQTLGen consortium
Monique G.P. van der Wijst, DH de Vries, Hilde E. Groot, et al.
eLife (2020) Vol. 9
Open Access | Times Cited: 190
Integrating genomics with biomarkers and therapeutic targets to invigorate cardiovascular drug development
Michael V. Holmes, Tom G. Richardson, Brian A. Ference, et al.
Nature Reviews Cardiology (2021) Vol. 18, Iss. 6, pp. 435-453
Open Access | Times Cited: 144
Genetic control of RNA splicing and its distinct role in complex trait variation
Ting Qi, Yang Wu, Hailing Fang, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1355-1363
Open Access | Times Cited: 126
Combining SNP-to-gene linking strategies to identify disease genes and assess disease omnigenicity
Steven Gazal, Omer Weissbrod, Farhad Hormozdiari, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 827-836
Open Access | Times Cited: 125
Mendelian randomization for studying the effects of perturbing drug targets
Dipender Gill, Marios K. Georgakis, Venexia Walker, et al.
Wellcome Open Research (2021) Vol. 6, pp. 16-16
Open Access | Times Cited: 108
Using genetic association data to guide drug discovery and development: Review of methods and applications
Stephen Burgess, Amy M. Mason, Andrew J. Grant, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 195-214
Open Access | Times Cited: 102
Association between frailty and depression: A bidirectional Mendelian randomization study
Ming‐Gang Deng, Fang Liu, Yuehui Liang, et al.
Science Advances (2023) Vol. 9, Iss. 38
Open Access | Times Cited: 89
Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture
Linda Kachuri, Angel C. Y. Mak, Donglei Hu, et al.
Nature Genetics (2023) Vol. 55, Iss. 6, pp. 952-963
Open Access | Times Cited: 58
Adjusting for genetic confounders in transcriptome-wide association studies improves discovery of risk genes of complex traits
Siming Zhao, Wesley L. Crouse, Sheng Qian, et al.
Nature Genetics (2024)
Open Access | Times Cited: 36
A practical view of fine-mapping and gene prioritization in the post-genome-wide association era
Roeland Broekema, Olivier B. Bakker, Iris H. Jonkers
Open Biology (2020) Vol. 10, Iss. 1, pp. 190221-190221
Open Access | Times Cited: 113
The association between depression and metabolic syndrome and its components: a bidirectional two-sample Mendelian randomization study
Min Zhang, Jing Chen, Zhiqun Yin, et al.
Translational Psychiatry (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 101
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome
Eleonora Porcu, Marie C. Sadler, Kaido Lepik, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 98
The individual and global impact of copy-number variants on complex human traits
Chiara Auwerx, Maarja Lepamets, Marie C. Sadler, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 4, pp. 647-668
Open Access | Times Cited: 60
Sex- and age-dependent genetics of longevity in a heterogeneous mouse population
Maroun Bou Sleiman, Suheeta Roy, Arwen W. Gao, et al.
Science (2022) Vol. 377, Iss. 6614
Open Access | Times Cited: 52
Tissue-specific impacts of aging and genetics on gene expression patterns in humans
Ryō Yamamoto, Ryan Chung, Juan Manuel Vázquez, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 47
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases
Kousik Kundu, Manuel Tardáguila, Alice Mann, et al.
Nature Genetics (2022) Vol. 54, Iss. 3, pp. 251-262
Closed Access | Times Cited: 44
From pharmacogenetics to pharmaco-omics: Milestones and future directions
Chiara Auwerx, Marie C. Sadler, Alexandre Reymond, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 2, pp. 100100-100100
Open Access | Times Cited: 43
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