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:

Probabilistic fine-mapping of transcriptome-wide association studies
Nicholas Mancuso, Malika Freund, Ruth Johnson, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 675-682
Open Access | Times Cited: 346

Showing 1-25 of 346 citing articles:

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Niamh Mullins, Andreas J. Forstner, Kevin S. O’Connell, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 817-829
Open Access | Times Cited: 1109

Opportunities and challenges for transcriptome-wide association studies
Michael Wainberg, Nasa Sinnott-Armstrong, Nicholas Mancuso, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 592-599
Open Access | Times Cited: 778

Stroke genetics informs drug discovery and risk prediction across ancestries
Aniket Mishra, Rainer Malik, Tsuyoshi Hachiya, et al.
Nature (2022) Vol. 611, Iss. 7934, pp. 115-123
Open Access | Times Cited: 344

webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study
Chen Cao, Jianhua Wang, Devin Kwok, et al.
Nucleic Acids Research (2021) Vol. 50, Iss. D1, pp. D1123-D1130
Open Access | Times Cited: 338

A statistical framework for cross-tissue transcriptome-wide association analysis
Yiming Hu, Mo Li, Qiongshi Lu, et al.
Nature Genetics (2019) Vol. 51, Iss. 3, pp. 568-576
Open Access | Times Cited: 332

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
Puya Gharahkhani, Eric Jorgenson, Pirro G. Hysi, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 297

Graph pangenome captures missing heritability and empowers tomato breeding
Yao Zhou, Zhiyang Zhang, Zhigui Bao, et al.
Nature (2022) Vol. 606, Iss. 7914, pp. 527-534
Open Access | Times Cited: 279

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

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Heidi Hautakangas, Bendik S. Winsvold, Sanni Ruotsalainen, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 152-160
Open Access | Times Cited: 258

Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms
Rebecca L. Walker, Gokul Ramaswami, Christopher Hartl, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 750-771.e22
Open Access | Times Cited: 243

Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease
Wei Zhou, Masahiro Kanai, Kuan-Han Wu, et al.
Cell Genomics (2022) Vol. 2, Iss. 10, pp. 100192-100192
Open Access | Times Cited: 239

A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis
Dan Zhou, Yi Jiang, Xue Zhong, et al.
Nature Genetics (2020) Vol. 52, Iss. 11, pp. 1239-1246
Open Access | Times Cited: 211

Advancing the use of genome-wide association studies for drug repurposing
William R. Reay, Murray J. Cairns
Nature Reviews Genetics (2021) Vol. 22, Iss. 10, pp. 658-671
Closed Access | Times Cited: 211

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

Genome-wide association analysis of plasma lipidome identifies 495 genetic associations
Linda Ottensmann, Rubina Tabassum, Sanni Ruotsalainen, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 136

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

Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals
Hang Zhou, Rachel L. Kember, Joseph D. Deak, et al.
Nature Medicine (2023) Vol. 29, Iss. 12, pp. 3184-3192
Open Access | Times Cited: 82

Multi-ancestry eQTL meta-analysis of human brain identifies candidate causal variants for brain-related traits
Biao Zeng, Jaroslav Bendl, Roman Kosoy, et al.
Nature Genetics (2022) Vol. 54, Iss. 2, pp. 161-169
Open Access | Times Cited: 74

Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications
Daniel F. Levey, Marco Galimberti, Joseph D. Deak, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2094-2103
Open Access | Times Cited: 60

Transcriptome-wide association studies: recent advances in methods, applications and available databases
Jialin Mai, Mingming Lu, Qianwen Gao, et al.
Communications Biology (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 59

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

Pleiotropy, epistasis and the genetic architecture of quantitative traits
Trudy F. C. Mackay, Robert R. H. Anholt
Nature Reviews Genetics (2024) Vol. 25, Iss. 9, pp. 639-657
Closed Access | Times Cited: 29

Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain
Cindy Wen, Michael Margolis, Rujia Dai, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 19

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