
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:
Improved polygenic prediction by Bayesian multiple regression on summary statistics
Luke R. Lloyd‐Jones, Jian Zeng, Julia Sidorenko, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 420
Luke R. Lloyd‐Jones, Jian Zeng, Julia Sidorenko, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 420
Showing 1-25 of 420 citing articles:
Polygenic prediction via Bayesian regression and continuous shrinkage priors
Tian Ge, Chia‐Yen Chen, Yang Ni, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 1315
Tian Ge, Chia‐Yen Chen, Yang Ni, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 1315
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
Polygenic risk scores: from research tools to clinical instruments
Cathryn M. Lewis, Evangelos Vassos
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 1038
Cathryn M. Lewis, Evangelos Vassos
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 1038
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
LDpred2: better, faster, stronger
Florian Privé, Julyan Arbel, Bjarni J. Vilhjálmsson
Bioinformatics (2020) Vol. 36, Iss. 22-23, pp. 5424-5431
Open Access | Times Cited: 497
Florian Privé, Julyan Arbel, Bjarni J. Vilhjálmsson
Bioinformatics (2020) Vol. 36, Iss. 22-23, pp. 5424-5431
Open Access | Times Cited: 497
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Aysu Okbay, Yeda Wu, Nancy Wang, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 437-449
Open Access | Times Cited: 468
Aysu Okbay, Yeda Wu, Nancy Wang, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 437-449
Open Access | Times Cited: 468
Improving polygenic prediction in ancestrally diverse populations
Yunfeng Ruan, Kuang Lin, Yen‐Chen Anne Feng, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 573-580
Open Access | Times Cited: 440
Yunfeng Ruan, Kuang Lin, Yen‐Chen Anne Feng, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 573-580
Open Access | Times Cited: 440
A generalized linear mixed model association tool for biobank-scale data
Longda Jiang, Zhili Zheng, Hailing Fang, et al.
Nature Genetics (2021) Vol. 53, Iss. 11, pp. 1616-1621
Open Access | Times Cited: 419
Longda Jiang, Zhili Zheng, Hailing Fang, et al.
Nature Genetics (2021) Vol. 53, Iss. 11, pp. 1616-1621
Open Access | Times Cited: 419
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 388
Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, et al.
Nature Genetics (2021) Vol. 53, Iss. 12, pp. 1636-1648
Open Access | Times Cited: 388
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: 308
Joana Revez, Tian Lin, Zhen Qiao, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 308
Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association
Jack W. O’Sullivan, Sridharan Raghavan, Carla Márquez‐Luna, et al.
Circulation (2022) Vol. 146, Iss. 8
Open Access | Times Cited: 258
Jack W. O’Sullivan, Sridharan Raghavan, Carla Márquez‐Luna, et al.
Circulation (2022) Vol. 146, Iss. 8
Open Access | Times Cited: 258
Autism-related dietary preferences mediate autism-gut microbiome associations
Chloe X. Yap, Anjali K. Henders, Gail A. Alvares, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5916-5931.e17
Open Access | Times Cited: 254
Chloe X. Yap, Anjali K. Henders, Gail A. Alvares, et al.
Cell (2021) Vol. 184, Iss. 24, pp. 5916-5931.e17
Open Access | Times Cited: 254
Risk prediction of late-onset Alzheimer’s disease implies an oligogenic architecture
Qian Zhang, Julia Sidorenko, Baptiste Couvy‐Duchesne, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 251
Qian Zhang, Julia Sidorenko, Baptiste Couvy‐Duchesne, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 251
Leveraging fine-mapping and multipopulation training data to improve cross-population polygenic risk scores
Omer Weissbrod, Masahiro Kanai, Huwenbo Shi, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 450-458
Open Access | Times Cited: 201
Omer Weissbrod, Masahiro Kanai, Huwenbo Shi, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 450-458
Open Access | Times Cited: 201
Theoretical and empirical quantification of the accuracy of polygenic scores in ancestry divergent populations
Ying Wang, Jing Guo, Guiyan Ni, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 197
Ying Wang, Jing Guo, Guiyan Ni, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 197
Making the Most of Clumping and Thresholding for Polygenic Scores
Florian Privé, Bjarni J. Vilhjálmsson, Hugues Aschard, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 6, pp. 1213-1221
Open Access | Times Cited: 171
Florian Privé, Bjarni J. Vilhjálmsson, Hugues Aschard, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 6, pp. 1213-1221
Open Access | Times Cited: 171
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts
Guiyan Ni, Jian Zeng, Joana Revez, et al.
Biological Psychiatry (2021) Vol. 90, Iss. 9, pp. 611-620
Open Access | Times Cited: 171
Guiyan Ni, Jian Zeng, Joana Revez, et al.
Biological Psychiatry (2021) Vol. 90, Iss. 9, pp. 611-620
Open Access | Times Cited: 171
Polygenic scoring accuracy varies across the genetic ancestry continuum
Yi Ding, Kangcheng Hou, Ziqi Xu, et al.
Nature (2023) Vol. 618, Iss. 7966, pp. 774-781
Open Access | Times Cited: 164
Yi Ding, Kangcheng Hou, Ziqi Xu, et al.
Nature (2023) Vol. 618, Iss. 7966, pp. 774-781
Open Access | Times Cited: 164
Improving the trans-ancestry portability of polygenic risk scores by prioritizing variants in predicted cell-type-specific regulatory elements
Tiffany Amariuta, Kazuyoshi Ishigaki, Hiroki Sugishita, et al.
Nature Genetics (2020) Vol. 52, Iss. 12, pp. 1346-1354
Open Access | Times Cited: 158
Tiffany Amariuta, Kazuyoshi Ishigaki, Hiroki Sugishita, et al.
Nature Genetics (2020) Vol. 52, Iss. 12, pp. 1346-1354
Open Access | Times Cited: 158
Evaluation of polygenic prediction methodology within a reference-standardized framework
Oliver Pain, Kylie P. Glanville, Saskia P. Hagenaars, et al.
PLoS Genetics (2021) Vol. 17, Iss. 5, pp. e1009021-e1009021
Open Access | Times Cited: 155
Oliver Pain, Kylie P. Glanville, Saskia P. Hagenaars, et al.
PLoS Genetics (2021) Vol. 17, Iss. 5, pp. e1009021-e1009021
Open Access | Times Cited: 155
Identifying individuals with high risk of Alzheimer’s disease using polygenic risk scores
Ganna Leonenko, Emily Baker, Joshua Stevenson‐Hoare, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 148
Ganna Leonenko, Emily Baker, Joshua Stevenson‐Hoare, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 148
Improved genetic prediction of complex traits from individual-level data or summary statistics
Qianqian Zhang, Florian Privé, Bjarni J. Vilhjálmsson, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 147
Qianqian Zhang, Florian Privé, Bjarni J. Vilhjálmsson, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 147
Principles and methods for transferring polygenic risk scores across global populations
Linda Kachuri, Nilanjan Chatterjee, Jibril Hirbo, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 8-25
Open Access | Times Cited: 140
Linda Kachuri, Nilanjan Chatterjee, Jibril Hirbo, et al.
Nature Reviews Genetics (2023) Vol. 25, Iss. 1, pp. 8-25
Open Access | Times Cited: 140
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex
Danny Antaki, James P. Guevara, Adam X. Maihofer, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1284-1292
Open Access | Times Cited: 139
Danny Antaki, James P. Guevara, Adam X. Maihofer, et al.
Nature Genetics (2022) Vol. 54, Iss. 9, pp. 1284-1292
Open Access | Times Cited: 139
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: 130
Peter M. Visscher, Loïc Yengo, Nancy J. Cox, et al.
Science (2021) Vol. 373, Iss. 6562, pp. 1468-1473
Open Access | Times Cited: 130