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:

10 Years of GWAS Discovery: Biology, Function, and Translation
Peter M. Visscher, Naomi R. Wray, Qian Zhang, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 1, pp. 5-22
Open Access | Times Cited: 3412

Showing 1-25 of 3412 citing articles:

The MR-Base platform supports systematic causal inference across the human phenome
Gibran Hemani, Jie Zheng, Benjamin Elsworth, et al.
eLife (2018) Vol. 7
Open Access | Times Cited: 6000

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry
Loïc Yengo, Julia Sidorenko, Kathryn E. Kemper, et al.
Human Molecular Genetics (2018) Vol. 27, Iss. 20, pp. 3641-3649
Open Access | Times Cited: 1970

Benefits and limitations of genome-wide association studies
Vivian Tam, Nikunj Patel, Michelle Turcotte, et al.
Nature Reviews Genetics (2019) Vol. 20, Iss. 8, pp. 467-484
Closed Access | Times Cited: 1692

Reproducible brain-wide association studies require thousands of individuals
Scott Marek, Brenden Tervo‐Clemmens, Finnegan J. Calabro, et al.
Nature (2022) Vol. 603, Iss. 7902, pp. 654-660
Open Access | Times Cited: 1483

Endometriosis
Krina T. Zondervan, Christian M. Becker, Stacey A. Missmer
New England Journal of Medicine (2020) Vol. 382, Iss. 13, pp. 1244-1256
Closed Access | Times Cited: 1427

The personal and clinical utility of polygenic risk scores
Ali Torkamani, Nathan E. Wineinger, Eric J. Topol
Nature Reviews Genetics (2018) Vol. 19, Iss. 9, pp. 581-590
Closed Access | Times Cited: 1380

Evaluating the potential role of pleiotropy in Mendelian randomization studies
Gibran Hemani, Jack Bowden, George Davey Smith
Human Molecular Genetics (2018) Vol. 27, Iss. R2, pp. R195-R208
Open Access | Times Cited: 1227

Genome-wide association studies
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1112

A global overview of pleiotropy and genetic architecture in complex traits
Kyoko Watanabe, Sven Stringer, Oleksandr Frei, et al.
Nature Genetics (2019) Vol. 51, Iss. 9, pp. 1339-1348
Open Access | Times Cited: 1094

Leveraging Polygenic Functional Enrichment to Improve GWAS Power
Gleb Kichaev, Gaurav Bhatia, Po−Ru Loh, et al.
The American Journal of Human Genetics (2018) Vol. 104, Iss. 1, pp. 65-75
Open Access | Times Cited: 884

The MRC IEU OpenGWAS data infrastructure
Ben Elsworth, Matthew Lyon, Tessa Alexander, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 757

rMVP: A Memory-Efficient, Visualization-Enhanced, and Parallel-Accelerated Tool for Genome-Wide Association Study
Lilin Yin, Haohao Zhang, Zhenshuang Tang, et al.
Genomics Proteomics & Bioinformatics (2021) Vol. 19, Iss. 4, pp. 619-628
Open Access | Times Cited: 732

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, et al.
Cell (2018) Vol. 173, Iss. 7, pp. 1705-1715.e16
Open Access | Times Cited: 725

An atlas of genetic influences on osteoporosis in humans and mice
John Morris, John P. Kemp, Scott E. Youlten, et al.
Nature Genetics (2018) Vol. 51, Iss. 2, pp. 258-266
Open Access | Times Cited: 688

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Gail Davies, Max Lam, Sarah E. Harris, et al.
Nature Communications (2018) Vol. 9, Iss. 1
Open Access | Times Cited: 614

Comparative genetic architectures of schizophrenia in East Asian and European populations
Max Lam, Chia‐Yen Chen, Zhiqiang Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1670-1678
Open Access | Times Cited: 580

The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, Parsa Akbari, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1214-1231.e11
Open Access | Times Cited: 560

Deep learning in biomedicine
Michael Wainberg, Daniele Merico, Andrew Delong, et al.
Nature Biotechnology (2018) Vol. 36, Iss. 9, pp. 829-838
Closed Access | Times Cited: 536

Towards clinical utility of polygenic risk scores
Samuel A. Lambert, Gad Abraham, Michael Inouye
Human Molecular Genetics (2019) Vol. 28, Iss. R2, pp. R133-R142
Open Access | Times Cited: 514

A saturated map of common genetic variants associated with human height
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, et al.
Nature (2022) Vol. 610, Iss. 7933, pp. 704-712
Open Access | Times Cited: 501

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

A resource-efficient tool for mixed model association analysis of large-scale data
Longda Jiang, Zhili Zheng, Ting Qi, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1749-1755
Open Access | Times Cited: 418

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

A scientometric review of genome-wide association studies
Melinda Mills, Charles Rahal
Communications Biology (2018) Vol. 2, Iss. 1
Open Access | Times Cited: 408

A Review of Feature Selection Methods for Machine Learning-Based Disease Risk Prediction
Nicholas Pudjihartono, Tayaza Fadason, Andreas W. Kempa-Liehr, et al.
Frontiers in Bioinformatics (2022) Vol. 2
Open Access | Times Cited: 406

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