
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:
An atlas of polygenic risk score associations to highlight putative causal relationships across the human phenome
Tom G. Richardson, Sean Harrison, Gibran Hemani, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 195
Tom G. Richardson, Sean Harrison, Gibran Hemani, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 195
Showing 1-25 of 195 citing articles:
A brief history of human disease genetics
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 600
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 600
Mendelian Randomization: Concepts and Scope
Rebecca C. Richmond, George Davey Smith
Cold Spring Harbor Perspectives in Medicine (2021) Vol. 12, Iss. 1, pp. a040501-a040501
Open Access | Times Cited: 492
Rebecca C. Richmond, George Davey Smith
Cold Spring Harbor Perspectives in Medicine (2021) Vol. 12, Iss. 1, pp. a040501-a040501
Open Access | Times Cited: 492
The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation
Samuel A. Lambert, Laurent Gil, Simon Jupp, et al.
Nature Genetics (2021) Vol. 53, Iss. 4, pp. 420-425
Open Access | Times Cited: 478
Samuel A. Lambert, Laurent Gil, Simon Jupp, et al.
Nature Genetics (2021) Vol. 53, Iss. 4, pp. 420-425
Open Access | Times Cited: 478
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: 477
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 477
Genetics meets proteomics: perspectives for large population-based studies
Karsten Suhre, Mark I. McCarthy, Jochen M. Schwenk
Nature Reviews Genetics (2020) Vol. 22, Iss. 1, pp. 19-37
Closed Access | Times Cited: 329
Karsten Suhre, Mark I. McCarthy, Jochen M. Schwenk
Nature Reviews Genetics (2020) Vol. 22, Iss. 1, pp. 19-37
Closed Access | Times Cited: 329
Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes
Irene Miguel-Escalada, Sílvia Bonàs‐Guarch, Inês Cebola, et al.
Nature Genetics (2019) Vol. 51, Iss. 7, pp. 1137-1148
Open Access | Times Cited: 254
Irene Miguel-Escalada, Sílvia Bonàs‐Guarch, Inês Cebola, et al.
Nature Genetics (2019) Vol. 51, Iss. 7, pp. 1137-1148
Open Access | Times Cited: 254
Systems biology in cardiovascular disease: a multiomics approach
Abhishek Joshi, Marieke Rienks, Konstantinos Theofilatos, et al.
Nature Reviews Cardiology (2020) Vol. 18, Iss. 5, pp. 313-330
Closed Access | Times Cited: 198
Abhishek Joshi, Marieke Rienks, Konstantinos Theofilatos, et al.
Nature Reviews Cardiology (2020) Vol. 18, Iss. 5, pp. 313-330
Closed Access | Times Cited: 198
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
Daniel L. McCartney, Josine L. Min, Rebecca C. Richmond, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 184
Daniel L. McCartney, Josine L. Min, Rebecca C. Richmond, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 184
The variant call format provides efficient and robust storage of GWAS summary statistics
Matthew Lyon, Shea J. Andrews, Benjamin Elsworth, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 166
Matthew Lyon, Shea J. Andrews, Benjamin Elsworth, et al.
Genome biology (2021) Vol. 22, Iss. 1
Open Access | Times Cited: 166
UK Biobank release and systematic evaluation of optimised polygenic risk scores for 53 diseases and quantitative traits
Deborah J. Thompson, Daniel Wells, Saskia Selzam, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 164
Deborah J. Thompson, Daniel Wells, Saskia Selzam, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 164
Significant sparse polygenic risk scores across 813 traits in UK Biobank
Yosuke Tanigawa, Junyang Qian, Guhan Venkataraman, et al.
PLoS Genetics (2022) Vol. 18, Iss. 3, pp. e1010105-e1010105
Open Access | Times Cited: 79
Yosuke Tanigawa, Junyang Qian, Guhan Venkataraman, et al.
PLoS Genetics (2022) Vol. 18, Iss. 3, pp. e1010105-e1010105
Open Access | Times Cited: 79
Prospective study design and data analysis in UK Biobank
Naomi E. Allen, Ben Lacey, Debbie A. Lawlor, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 729
Open Access | Times Cited: 40
Naomi E. Allen, Ben Lacey, Debbie A. Lawlor, et al.
Science Translational Medicine (2024) Vol. 16, Iss. 729
Open Access | Times Cited: 40
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
A systematic evaluation of the performance and properties of the UK Biobank Polygenic Risk Score (PRS) Release
Deborah J. Thompson, Daniel Wells, Saskia Selzam, et al.
PLoS ONE (2024) Vol. 19, Iss. 9, pp. e0307270-e0307270
Open Access | Times Cited: 22
Deborah J. Thompson, Daniel Wells, Saskia Selzam, et al.
PLoS ONE (2024) Vol. 19, Iss. 9, pp. e0307270-e0307270
Open Access | Times Cited: 22
Genome-wide rare variant analysis for thousands of phenotypes in over 70,000 exomes from two cohorts
Elizabeth T. Cirulli, Simon White, Robert W. Read, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 128
Elizabeth T. Cirulli, Simon White, Robert W. Read, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 128
Causal Associations Between Modifiable Risk Factors and the Alzheimer's Phenome
Shea J. Andrews, Brian Fulton‐Howard, Paul F. O’Reilly, et al.
Annals of Neurology (2020) Vol. 89, Iss. 1, pp. 54-65
Open Access | Times Cited: 121
Shea J. Andrews, Brian Fulton‐Howard, Paul F. O’Reilly, et al.
Annals of Neurology (2020) Vol. 89, Iss. 1, pp. 54-65
Open Access | Times Cited: 121
Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders
Phil H. Lee, Yen‐Chen Anne Feng, Jordan W. Smoller
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 20-31
Open Access | Times Cited: 121
Phil H. Lee, Yen‐Chen Anne Feng, Jordan W. Smoller
Biological Psychiatry (2020) Vol. 89, Iss. 1, pp. 20-31
Open Access | Times Cited: 121
Accurate and Scalable Construction of Polygenic Scores in Large Biobank Data Sets
Sheng Yang, Xiang Zhou
The American Journal of Human Genetics (2020) Vol. 106, Iss. 5, pp. 679-693
Open Access | Times Cited: 110
Sheng Yang, Xiang Zhou
The American Journal of Human Genetics (2020) Vol. 106, Iss. 5, pp. 679-693
Open Access | Times Cited: 110
Trans-biobank analysis with 676,000 individuals elucidates the association of polygenic risk scores of complex traits with human lifespan
Saori Sakaue, Masahiro Kanai, Juha Karjalainen, et al.
Nature Medicine (2020) Vol. 26, Iss. 4, pp. 542-548
Open Access | Times Cited: 104
Saori Sakaue, Masahiro Kanai, Juha Karjalainen, et al.
Nature Medicine (2020) Vol. 26, Iss. 4, pp. 542-548
Open Access | Times Cited: 104
Genetic prediction of complex traits with polygenic scores: a statistical review
Ying Ma, Xiang Zhou
Trends in Genetics (2021) Vol. 37, Iss. 11, pp. 995-1011
Open Access | Times Cited: 94
Ying Ma, Xiang Zhou
Trends in Genetics (2021) Vol. 37, Iss. 11, pp. 995-1011
Open Access | Times Cited: 94
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
Julian R. Homburger, Cynthia L. Neben, Gilad Mishne, et al.
Genome Medicine (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 88
Julian R. Homburger, Cynthia L. Neben, Gilad Mishne, et al.
Genome Medicine (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 88
Genomic Prediction of 16 Complex Disease Risks Including Heart Attack, Diabetes, Breast and Prostate Cancer
Louis Lello, Timothy G. Raben, Soke Yuen Yong, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 78
Louis Lello, Timothy G. Raben, Soke Yuen Yong, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 78
A principal component approach to improve association testing with polygenic risk scores
Brandon J. Coombes, Alexander Ploner, Sarah E. Bergen, et al.
Genetic Epidemiology (2020) Vol. 44, Iss. 7, pp. 676-686
Open Access | Times Cited: 77
Brandon J. Coombes, Alexander Ploner, Sarah E. Bergen, et al.
Genetic Epidemiology (2020) Vol. 44, Iss. 7, pp. 676-686
Open Access | Times Cited: 77
Genetics and Gene-Environment Interactions in Childhood and Adult Onset Asthma
Eva Morales, David L. Duffy
Frontiers in Pediatrics (2019) Vol. 7
Open Access | Times Cited: 76
Eva Morales, David L. Duffy
Frontiers in Pediatrics (2019) Vol. 7
Open Access | Times Cited: 76
Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans
Hengameh Shams, Xiaorong Shao, Adam Santaniello, et al.
Brain (2022) Vol. 146, Iss. 2, pp. 645-656
Open Access | Times Cited: 39
Hengameh Shams, Xiaorong Shao, Adam Santaniello, et al.
Brain (2022) Vol. 146, Iss. 2, pp. 645-656
Open Access | Times Cited: 39