
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:
Clinical use of current polygenic risk scores may exacerbate health disparities
Alicia R. Martin, Masahiro Kanai, Yoichiro Kamatani, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 584-591
Open Access | Times Cited: 2211
Alicia R. Martin, Masahiro Kanai, Yoichiro Kamatani, et al.
Nature Genetics (2019) Vol. 51, Iss. 4, pp. 584-591
Open Access | Times Cited: 2211
Showing 1-25 of 2211 citing articles:
The mutational constraint spectrum quantified from variation in 141,456 humans
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 434-443
Open Access | Times Cited: 7949
Konrad J. Karczewski, Laurent C. Francioli, Grace Tiao, et al.
Nature (2020) Vol. 581, Iss. 7809, pp. 434-443
Open Access | Times Cited: 7949
A cross-population atlas of genetic associations for 220 human phenotypes
Saori Sakaue, Masahiro Kanai, Yosuke Tanigawa, et al.
Nature Genetics (2021) Vol. 53, Iss. 10, pp. 1415-1424
Open Access | Times Cited: 1420
Saori Sakaue, Masahiro Kanai, Yosuke Tanigawa, et al.
Nature Genetics (2021) Vol. 53, Iss. 10, pp. 1415-1424
Open Access | Times Cited: 1420
Mendelian randomization
Eleanor Sanderson, M. Maria Glymour, Michael V. Holmes, et al.
Nature Reviews Methods Primers (2022) Vol. 2, Iss. 1
Open Access | Times Cited: 1171
Eleanor Sanderson, M. Maria Glymour, Michael V. Holmes, et al.
Nature Reviews Methods Primers (2022) Vol. 2, Iss. 1
Open Access | Times Cited: 1171
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Niamh Mullins, Andreas J. Forstner, Kevin S. O’Connell, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 817-829
Open Access | Times Cited: 1092
Niamh Mullins, Andreas J. Forstner, Kevin S. O’Connell, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 817-829
Open Access | Times Cited: 1092
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: 1084
Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, et al.
Nature Reviews Methods Primers (2021) Vol. 1, Iss. 1
Open Access | Times Cited: 1084
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: 1025
Cathryn M. Lewis, Evangelos Vassos
Genome Medicine (2020) Vol. 12, Iss. 1
Open Access | Times Cited: 1025
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 990
Elliot Sollis, Abayomi Mosaku, Ala Abid, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D977-D985
Open Access | Times Cited: 990
Analysis of polygenic risk score usage and performance in diverse human populations
Laramie E. Duncan, Hanyang Shen, Bizu Gelaye, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 888
Laramie E. Duncan, Hanyang Shen, Bizu Gelaye, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 888
The genetic architecture of Parkinson's disease
Cornelis Blauwendraat, Mike A. Nalls, Andrew Singleton
The Lancet Neurology (2019) Vol. 19, Iss. 2, pp. 170-178
Open Access | Times Cited: 874
Cornelis Blauwendraat, Mike A. Nalls, Andrew Singleton
The Lancet Neurology (2019) Vol. 19, Iss. 2, pp. 170-178
Open Access | Times Cited: 874
The genetics of obesity: from discovery to biology
Ruth J. F. Loos, Giles S.H. Yeo
Nature Reviews Genetics (2021) Vol. 23, Iss. 2, pp. 120-133
Open Access | Times Cited: 836
Ruth J. F. Loos, Giles S.H. Yeo
Nature Reviews Genetics (2021) Vol. 23, Iss. 2, pp. 120-133
Open Access | Times Cited: 836
The power of genetic diversity in genome-wide association studies of lipids
Sarah E. Graham, Shoa L. Clarke, Kuan-Han Wu, et al.
Nature (2021) Vol. 600, Iss. 7890, pp. 675-679
Open Access | Times Cited: 630
Sarah E. Graham, Shoa L. Clarke, Kuan-Han Wu, et al.
Nature (2021) Vol. 600, Iss. 7890, pp. 675-679
Open Access | Times Cited: 630
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations
Roseann E. Peterson, Karoline Kuchenbaecker, Raymond K. Walters, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 589-603
Open Access | Times Cited: 627
Roseann E. Peterson, Karoline Kuchenbaecker, Raymond K. Walters, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 589-603
Open Access | Times Cited: 627
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: 606
Melina Claussnitzer, Judy H. Cho, Rory Collins, et al.
Nature (2020) Vol. 577, Iss. 7789, pp. 179-189
Open Access | Times Cited: 606
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: 577
Max Lam, Chia‐Yen Chen, Zhiqiang Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1670-1678
Open Access | Times Cited: 577
Genetics of 35 blood and urine biomarkers in the UK Biobank
Nasa Sinnott-Armstrong, Yosuke Tanigawa, David Amar, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 185-194
Open Access | Times Cited: 569
Nasa Sinnott-Armstrong, Yosuke Tanigawa, David Amar, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 185-194
Open Access | Times Cited: 569
The trans-ancestral genomic architecture of glycemic traits
Jihua Chen, Cassandra N. Spracklen, Gaëlle Marenne, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 840-860
Open Access | Times Cited: 541
Jihua Chen, Cassandra N. Spracklen, Gaëlle Marenne, et al.
Nature Genetics (2021) Vol. 53, Iss. 6, pp. 840-860
Open Access | Times Cited: 541
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Ming‐Huei Chen, Laura M. Raffield, Abdou Mousas, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1198-1213.e14
Open Access | Times Cited: 523
Ming‐Huei Chen, Laura M. Raffield, Abdou Mousas, et al.
Cell (2020) Vol. 182, Iss. 5, pp. 1198-1213.e14
Open Access | Times Cited: 523
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: 508
Samuel A. Lambert, Gad Abraham, Michael Inouye
Human Molecular Genetics (2019) Vol. 28, Iss. R2, pp. R133-R142
Open Access | Times Cited: 508
Race and Genetic Ancestry in Medicine — A Time for Reckoning with Racism
Luisa N. Borrell, Jennifer R. Elhawary, Elena Fuentes‐Afflick, et al.
New England Journal of Medicine (2021) Vol. 384, Iss. 5, pp. 474-480
Open Access | Times Cited: 505
Luisa N. Borrell, Jennifer R. Elhawary, Elena Fuentes‐Afflick, et al.
New England Journal of Medicine (2021) Vol. 384, Iss. 5, pp. 474-480
Open Access | Times Cited: 505
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Anubha Mahajan, Cassandra N. Spracklen, Weihua Zhang, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 560-572
Open Access | Times Cited: 496
Anubha Mahajan, Cassandra N. Spracklen, Weihua Zhang, et al.
Nature Genetics (2022) Vol. 54, Iss. 5, pp. 560-572
Open Access | Times Cited: 496
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: 490
Loïc Yengo, Sailaja Vedantam, Eirini Marouli, et al.
Nature (2022) Vol. 610, Iss. 7933, pp. 704-712
Open Access | Times Cited: 490
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: 482
Samuel A. Lambert, Laurent Gil, Simon Jupp, et al.
Nature Genetics (2021) Vol. 53, Iss. 4, pp. 420-425
Open Access | Times Cited: 482
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: 478
Eddie Cano-Gamez, Gosia Trynka
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 478
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: 463
Aysu Okbay, Yeda Wu, Nancy Wang, et al.
Nature Genetics (2022) Vol. 54, Iss. 4, pp. 437-449
Open Access | Times Cited: 463
Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases
Kazuyoshi Ishigaki, Masato Akiyama, Masahiro Kanai, et al.
Nature Genetics (2020) Vol. 52, Iss. 7, pp. 669-679
Open Access | Times Cited: 449
Kazuyoshi Ishigaki, Masato Akiyama, Masahiro Kanai, et al.
Nature Genetics (2020) Vol. 52, Iss. 7, pp. 669-679
Open Access | Times Cited: 449