
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:
Widespread signatures of natural selection across human complex traits and functional genomic categories
Jian Zeng, Angli Xue, Longda Jiang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 102
Jian Zeng, Angli Xue, Longda Jiang, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 102
Showing 1-25 of 102 citing articles:
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 502-508
Open Access | Times Cited: 1791
Vassily Trubetskoy, Antonio F. Pardiñas, Ting Qi, et al.
Nature (2022) Vol. 604, Iss. 7906, pp. 502-508
Open Access | Times Cited: 1791
Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 303
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 303
15 years of GWAS discovery: Realizing the promise
Abdel Abdellaoui, Loïc Yengo, Karin J. H. Verweij, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 179-194
Open Access | Times Cited: 292
Abdel Abdellaoui, Loïc Yengo, Karin J. H. Verweij, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 179-194
Open Access | Times Cited: 292
Discovery and implications of polygenicity of common diseases
Peter M. Visscher, Loïc Yengo, Nancy J. Cox, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1468-1473
Open Access | Times Cited: 127
Peter M. Visscher, Loïc Yengo, Nancy J. Cox, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1468-1473
Open Access | Times Cited: 127
From variant to function in human disease genetics
Tuuli Lappalainen, Daniel G. MacArthur
Science (2021) Vol. 373, Iss. 6562, pp. 1464-1468
Closed Access | Times Cited: 121
Tuuli Lappalainen, Daniel G. MacArthur
Science (2021) Vol. 373, Iss. 6562, pp. 1464-1468
Closed Access | Times Cited: 121
Challenges and Opportunities for Developing More Generalizable Polygenic Risk Scores
Ying Wang, Kristin Tsuo, Masahiro Kanai, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 293-320
Open Access | Times Cited: 101
Ying Wang, Kristin Tsuo, Masahiro Kanai, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 293-320
Open Access | Times Cited: 101
Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts
Ying Wang, Shinichi Namba, Esteban A. Lopera-Maya, et al.
Cell Genomics (2023) Vol. 3, Iss. 1, pp. 100241-100241
Open Access | Times Cited: 69
Ying Wang, Shinichi Namba, Esteban A. Lopera-Maya, et al.
Cell Genomics (2023) Vol. 3, Iss. 1, pp. 100241-100241
Open Access | Times Cited: 69
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1483-1493
Open Access | Times Cited: 44
Varun Warrier, Eva-Maria Stauffer, Qin Qin Huang, et al.
Nature Genetics (2023) Vol. 55, Iss. 9, pp. 1483-1493
Open Access | Times Cited: 44
Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 31
Zhili Zheng, Shouye Liu, Julia Sidorenko, et al.
Nature Genetics (2024) Vol. 56, Iss. 5, pp. 767-777
Open Access | Times Cited: 31
Genetic architecture of the structural connectome
Michael Wainberg, Natalie J. Forde, Salim Mansour, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 20
Michael Wainberg, Natalie J. Forde, Salim Mansour, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 20
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
Mark J. Adams, Fabian Streit, Xiangrui Meng, et al.
Cell (2025)
Open Access | Times Cited: 5
Mark J. Adams, Fabian Streit, Xiangrui Meng, et al.
Cell (2025)
Open Access | Times Cited: 5
Scientists' warning against the society of waste
Isabel Marín, Federico Demaria, Claudia Ofelio, et al.
The Science of The Total Environment (2021) Vol. 811, pp. 151359-151359
Open Access | Times Cited: 76
Isabel Marín, Federico Demaria, Claudia Ofelio, et al.
The Science of The Total Environment (2021) Vol. 811, pp. 151359-151359
Open Access | Times Cited: 76
Polygenic adaptation after a sudden change in environment
Laura K. Hayward, Guy Sella
eLife (2022) Vol. 11
Open Access | Times Cited: 60
Laura K. Hayward, Guy Sella
eLife (2022) Vol. 11
Open Access | Times Cited: 60
Utility of polygenic embryo screening for disease depends on the selection strategy
Todd Lencz, Daniel Backenroth, Einat Granot‐Hershkovitz, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 58
Todd Lencz, Daniel Backenroth, Einat Granot‐Hershkovitz, et al.
eLife (2021) Vol. 10
Open Access | Times Cited: 58
Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes
Yang Wu, Ting Qi, Naomi R. Wray, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100344-100344
Open Access | Times Cited: 32
Yang Wu, Ting Qi, Naomi R. Wray, et al.
Cell Genomics (2023) Vol. 3, Iss. 8, pp. 100344-100344
Open Access | Times Cited: 32
Inferring disease architecture and predictive ability with LDpred2-auto
Florian Privé, Clara Albiñana, Julyan Arbel, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 2042-2055
Open Access | Times Cited: 27
Florian Privé, Clara Albiñana, Julyan Arbel, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 12, pp. 2042-2055
Open Access | Times Cited: 27
mBAT-combo: A more powerful test to detect gene-trait associations from GWAS data
Ang Li, Shouye Liu, Andrew Bakshi, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 1, pp. 30-43
Open Access | Times Cited: 26
Ang Li, Shouye Liu, Andrew Bakshi, et al.
The American Journal of Human Genetics (2023) Vol. 110, Iss. 1, pp. 30-43
Open Access | Times Cited: 26
Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology
Ying Wang, Masahiro Kanai, Taotao Tan, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100408-100408
Open Access | Times Cited: 23
Ying Wang, Masahiro Kanai, Taotao Tan, et al.
Cell Genomics (2023) Vol. 3, Iss. 10, pp. 100408-100408
Open Access | Times Cited: 23
Genome-wide study of half a million individuals with major depression identifies 697 independent associations, infers causal neuronal subtypes and biological targets for novel pharmacotherapies
Andrew M. McIntosh, Cathryn M. Lewis
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
Andrew M. McIntosh, Cathryn M. Lewis
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
Distinct biological signature and modifiable risk factors underlie the comorbidity between major depressive disorder and cardiovascular disease
Jacob Bergstedt, Joëlle A. Pasman, Ziyan Ma, et al.
Nature Cardiovascular Research (2024) Vol. 3, Iss. 6, pp. 754-769
Open Access | Times Cited: 9
Jacob Bergstedt, Joëlle A. Pasman, Ziyan Ma, et al.
Nature Cardiovascular Research (2024) Vol. 3, Iss. 6, pp. 754-769
Open Access | Times Cited: 9
Genetic association data are broadly consistent with stabilizing selection shaping human common diseases and traits
Evan Koch, Noah J Connally, Nikolas Baya, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 8
Evan Koch, Noah J Connally, Nikolas Baya, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 8
Cross-species analysis of genetic architecture and polygenic risk scores for non-contact ACL rupture in dogs and humans
Mehdi Momen, Hannah K. Kearney, Margaret M. Patterson, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access | Times Cited: 1
Mehdi Momen, Hannah K. Kearney, Margaret M. Patterson, et al.
Communications Biology (2025) Vol. 8, Iss. 1
Open Access | Times Cited: 1
A scalable variational inference approach for increased mixed-model association power
Hrushikesh Loya, Georgios Kalantzis, Fergus Cooper, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
Hrushikesh Loya, Georgios Kalantzis, Fergus Cooper, et al.
Nature Genetics (2025)
Open Access | Times Cited: 1
A Gene-Set Enrichment and Protein–Protein Interaction Network-Based GWAS with Regulatory SNPs Identifies Candidate Genes and Pathways Associated with Carcass Traits in Hanwoo Cattle
Krishnamoorthy Srikanth, Seung Hwan Lee, Ki Yong Chung, et al.
Genes (2020) Vol. 11, Iss. 3, pp. 316-316
Open Access | Times Cited: 54
Krishnamoorthy Srikanth, Seung Hwan Lee, Ki Yong Chung, et al.
Genes (2020) Vol. 11, Iss. 3, pp. 316-316
Open Access | Times Cited: 54
A practical guideline of genomics-driven drug discovery in the era of global biobank meta-analysis
Shinichi Namba, Takahiro Konuma, Kuan-Han Wu, et al.
Cell Genomics (2022) Vol. 2, Iss. 10, pp. 100190-100190
Open Access | Times Cited: 33
Shinichi Namba, Takahiro Konuma, Kuan-Han Wu, et al.
Cell Genomics (2022) Vol. 2, Iss. 10, pp. 100190-100190
Open Access | Times Cited: 33