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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:

Abundant associations with gene expression complicate GWAS follow-up
Boxiang Liu, Michael J. Gloudemans, Abhiram Rao, et al.
Nature Genetics (2019) Vol. 51, Iss. 5, pp. 768-769
Open Access | Times Cited: 312

Showing 1-25 of 312 citing articles:

The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Shankara Anand, Kristin Ardlie, et al.
Science (2020) Vol. 369, Iss. 6509, pp. 1318-1330
Open Access | Times Cited: 3798
From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 480
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
Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes
Catherine C. Robertson, Jamie Inshaw, Suna Önengüt-Gümüşcü, et al.
Nature Genetics (2021) Vol. 53, Iss. 7, pp. 962-971
Open Access | Times Cited: 214
The GTEx Consortium atlas of genetic regulatory effects across human tissues
François Aguet, Alvaro Barbeira, Rodrigo Bonazzola, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 207
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
Derek Klarin, Emma Busenkell, Renae Judy, et al.
Nature Genetics (2019) Vol. 51, Iss. 11, pp. 1574-1579
Open Access | Times Cited: 201
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, et al.
Brain (2019) Vol. 143, Iss. 1, pp. 234-248
Open Access | Times Cited: 200
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
A genome-wide association study of serum proteins reveals shared loci with common diseases
Alexander Guðjónsson, Valborg Guðmundsdóttir, G. Axelsson, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 170
Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease
Nooshin Ghodsian, Erik Abner, Connor A. Emdin, et al.
Cell Reports Medicine (2021) Vol. 2, Iss. 11, pp. 100437-100437
Open Access | Times Cited: 151
Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank
Kim Valette, Zhonglin Li, Valentin Bon-Baret, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 127
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
Features and applications of haplotypes in crop breeding
Javaid Akhter Bhat, Deyue Yu, Abhishek Bohra, et al.
Communications Biology (2021) Vol. 4, Iss. 1
Open Access | Times Cited: 106
GPNMB confers risk for Parkinson’s disease through interaction with α-synuclein
Maria E. Diaz‐Ortiz, Yunji Seo, Marijan Posavi, et al.
Science (2022) Vol. 377, Iss. 6608
Open Access | Times Cited: 101
Single-nucleus chromatin accessibility profiling highlights regulatory mechanisms of coronary artery disease risk
Adam W. Turner, Shengen Hu, José Verdezoto Mosquera, et al.
Nature Genetics (2022) Vol. 54, Iss. 6, pp. 804-816
Open Access | Times Cited: 94
Identification of novel protein biomarkers and drug targets for colorectal cancer by integrating human plasma proteome with genome
Jing Sun, Jianhui Zhao, Fangyuan Jiang, et al.
Genome Medicine (2023) Vol. 15, Iss. 1
Open Access | Times Cited: 92
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Jonggeol Jeffrey Kim, Dan Vitale, Diego Véliz Otani, et al.
Nature Genetics (2023) Vol. 56, Iss. 1, pp. 27-36
Open Access | Times Cited: 83
Leveraging base-pair mammalian constraint to understand genetic variation and human disease
Patrick F. Sullivan, Jennifer R. S. Meadows, Steven Gazal, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 72
Molecular quantitative trait loci
François Aguet, Kaur Alasoo, Yang Li, et al.
Nature Reviews Methods Primers (2023) Vol. 3, Iss. 1
Closed Access | Times Cited: 52
Multi-ancestry meta-analysis and fine-mapping in Alzheimer’s disease
Julie Lake, Caroline Warly Solsberg, Jonggeol Jeffrey Kim, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 7, pp. 3121-3132
Open Access | Times Cited: 47
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
Insights Into Causal Effects of Genetically Proxied Lipids and Lipid‐Modifying Drug Targets on Cardiometabolic Diseases
Liwan Fu, Qin Liu, Hong Cheng, et al.
Journal of the American Heart Association (2025)
Open Access | Times Cited: 2
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D
Ana Viñuela, Arushi Varshney, Martijn van de Bunt, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 120
The GTEx Consortium atlas of genetic regulatory effects across human tissues The Genotype Tissue Expression Consortium
François Aguet, Alvaro Barbeira, Rodrigo Bonazzola, et al.
(2019)
Open Access | Times Cited: 99
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