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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:

Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits
Nicholas Mancuso, Huwenbo Shi, Pagé C. Goddard, et al.
The American Journal of Human Genetics (2017) Vol. 100, Iss. 3, pp. 473-487
Open Access | Times Cited: 297

Showing 1-25 of 297 citing articles:

Orienting the causal relationship between imprecisely measured traits using GWAS summary data
Gibran Hemani, Kate Tilling, George Davey Smith
PLoS Genetics (2017) Vol. 13, Iss. 11, pp. e1007081-e1007081
Open Access | Times Cited: 1876
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
Hilary K. Finucane, Yakir Reshef, Verneri Anttila, et al.
Nature Genetics (2018) Vol. 50, Iss. 4, pp. 621-629
Open Access | Times Cited: 985
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics
Alvaro Barbeira, Scott Dickinson, Rodrigo Bonazzola, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 970
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
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Derek Klarin, Scott M. Damrauer, Kelly Cho, et al.
Nature Genetics (2018) Vol. 50, Iss. 11, pp. 1514-1523
Open Access | Times Cited: 595
Genetic architecture: the shape of the genetic contribution to human traits and disease
Nicholas J. Timpson, Celia M.T. Greenwood, Nicole Soranzo, et al.
Nature Reviews Genetics (2017) Vol. 19, Iss. 2, pp. 110-124
Open Access | Times Cited: 416
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
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
Single-cell RNA-seq reveals cell type–specific molecular and genetic associations to lupus
Richard K. Perez, M. Grace Gordon, Meena Subramaniam, et al.
Science (2022) Vol. 376, Iss. 6589
Open Access | Times Cited: 317
Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits
Huwenbo Shi, Nicholas Mancuso, Sarah Spendlove, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 5, pp. 737-751
Open Access | Times Cited: 300
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: 270
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
An integrative multi-omics analysis to identify candidate DNA methylation biomarkers related to prostate cancer risk
Lang Wu, Yaohua Yang, Xingyi Guo, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 237
Plasma proteome analyses in individuals of European and African ancestry identify cis-pQTLs and models for proteome-wide association studies
Jingning Zhang, Diptavo Dutta, Anna Köttgen, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 593-602
Open Access | Times Cited: 234
Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders
Chengran Yang, Fabiana Farias, Laura Ibáñez, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 9, pp. 1302-1312
Open Access | Times Cited: 207
Leveraging molecular quantitative trait loci to understand the genetic architecture of diseases and complex traits
Farhad Hormozdiari, Steven Gazal, Bryce van de Geijn, et al.
Nature Genetics (2018) Vol. 50, Iss. 7, pp. 1041-1047
Open Access | Times Cited: 189
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
Laura M. Huckins, Amanda Dobbyn, Douglas M. Ruderfer, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 659-674
Open Access | Times Cited: 179
The polygenic architecture of schizophrenia — rethinking pathogenesis and nosology
Olav B. Smeland, Oleksandr Frei, Anders M. Dale, et al.
Nature Reviews Neurology (2020) Vol. 16, Iss. 7, pp. 366-379
Closed Access | Times Cited: 163
Genomics of hypertension: the road to precision medicine
Sandosh Padmanabhan, Anna F. Dominiczak
Nature Reviews Cardiology (2020) Vol. 18, Iss. 4, pp. 235-250
Open Access | Times Cited: 158
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
Discovery of target genes and pathways at GWAS loci by pooled single-cell CRISPR screens
John Morris, Christina M. Caragine, Zharko Daniloski, et al.
Science (2023) Vol. 380, Iss. 6646
Open Access | Times Cited: 112
The missing link between genetic association and regulatory function
Noah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
eLife (2022) Vol. 11
Open Access | Times Cited: 102
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function
Johann S. Hawe, Rory Wilson, Katharina T. Schmid, et al.
Nature Genetics (2022) Vol. 54, Iss. 1, pp. 18-29
Closed Access | Times Cited: 97
Decoding the genetic and epigenetic basis of asthma
Bernard Stikker, Rudi W. Hendriks, Ralph Stadhouders
Allergy (2023) Vol. 78, Iss. 4, pp. 940-956
Open Access | Times Cited: 47
Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits
Eilís Hannon, T.J. Gorrie-Stone, Melissa Smart, et al.
The American Journal of Human Genetics (2018) Vol. 103, Iss. 5, pp. 654-665
Open Access | Times Cited: 150
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