
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Nicholas Pudjihartono, Tayaza Fadason, Andreas W. Kempa-Liehr, et al.
Frontiers in Bioinformatics (2022) Vol. 2
Open Access | Times Cited: 406