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OpenAlex Citation Counts

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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:

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power
Elizabeth G. Atkinson, Adam X. Maihofer, Masahiro Kanai, et al.
Nature Genetics (2021) Vol. 53, Iss. 2, pp. 195-204
Open Access | Times Cited: 183

Showing 1-25 of 183 citing articles:

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: 431
A roadmap to increase diversity in genomic studies
Segun Fatumo, Tinashe Chikowore, Ananyo Choudhury, et al.
Nature Medicine (2022) Vol. 28, Iss. 2, pp. 243-250
Open Access | Times Cited: 416
Ancestry-inclusive dog genomics challenges popular breed stereotypes
Kathleen M. Morrill, Jessica P. Hekman, Xue Li, et al.
Science (2022) Vol. 376, Iss. 6592
Open Access | Times Cited: 135
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: 133
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
Recommendations on the use and reporting of race, ethnicity, and ancestry in genetic research: Experiences from the NHLBI TOPMed program
Alyna Khan, Stephanie M. Gogarten, Caitlin McHugh, et al.
Cell Genomics (2022) Vol. 2, Iss. 8, pp. 100155-100155
Open Access | Times Cited: 82
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals
Kangcheng Hou, Yi Ding, Ziqi Xu, et al.
Nature Genetics (2023) Vol. 55, Iss. 4, pp. 549-558
Closed Access | Times Cited: 75
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
Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects
Konrad J. Karczewski, Rahul Gupta, Masahiro Kanai, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 66
The Singapore National Precision Medicine Strategy
Eleanor Wong, Nicolas Bertin, Maxime Hebrard, et al.
Nature Genetics (2023) Vol. 55, Iss. 2, pp. 178-186
Closed Access | Times Cited: 51
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI
Quan Sun, Bryce Rowland, Jiawen Chen, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 26
Genomewide Association Studies in Pharmacogenomics
Gregory McInnes, Sook Wah Yee, Yash Pershad, et al.
Clinical Pharmacology & Therapeutics (2021) Vol. 110, Iss. 3, pp. 637-648
Open Access | Times Cited: 71
Fast, accurate local ancestry inference with FLARE
Sharon R. Browning, Ryan K. Waples, Brian L. Browning
The American Journal of Human Genetics (2023) Vol. 110, Iss. 2, pp. 326-335
Open Access | Times Cited: 41
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Yask Gupta, David J. Friedman, Michelle Mcnulty, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 35
Quantifying portable genetic effects and improving cross-ancestry genetic prediction with GWAS summary statistics
Jiacheng Miao, Hanmin Guo, Gefei Song, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 33
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
Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization
Johanna L. Smith, Catherine Tcheandjieu, Ozan Dikilitas, et al.
Circulation Genomic and Precision Medicine (2024) Vol. 17, Iss. 3
Open Access | Times Cited: 11
Genetic architecture distinguishes tinnitus from hearing loss
Royce E. Clifford, Adam X. Maihofer, Chris Chatzinakos, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 8
Characterizing features affecting local ancestry inference performance in admixed populations
Jessica Honorato‐Mauer, Nirav N. Shah, Adam X. Maihofer, et al.
The American Journal of Human Genetics (2025)
Open Access | Times Cited: 1
A novel genome-wide association study method for detecting quantitative trait loci interacting with complex population structures in plant genetics
Kosuke Hamazaki, Hiroyoshi Iwata, Tristan Mary‐Huard
Genetics (2025)
Closed Access | Times Cited: 1
Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information
Adam X. Maihofer, Karmel W. Choi, Jonathan R. I. Coleman, et al.
Biological Psychiatry (2021) Vol. 91, Iss. 7, pp. 626-636
Open Access | Times Cited: 45
Importance of Including Non-European Populations in Large Human Genetic Studies to Enhance Precision Medicine
Dan Ju, Daniel Hui, Dorothy A. Hammond, et al.
Annual Review of Biomedical Data Science (2022) Vol. 5, Iss. 1, pp. 321-339
Open Access | Times Cited: 37
Stability of polygenic scores across discovery genome-wide association studies
Laura M. Schultz, Alison Merikangas, Kosha Ruparel, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 2, pp. 100091-100091
Open Access | Times Cited: 31
Ten challenges for clinical translation in psychiatric genetics
Eske M. Derks, Jackson G. Thorp, Zachary F. Gerring
Nature Genetics (2022) Vol. 54, Iss. 10, pp. 1457-1465
Closed Access | Times Cited: 31
Decoding the Human Face: Progress and Challenges in Understanding the Genetics of Craniofacial Morphology
Sahin Naqvi, Hanne Hoskens, Franziska Wilke, et al.
Annual Review of Genomics and Human Genetics (2022) Vol. 23, Iss. 1, pp. 383-412
Open Access | Times Cited: 29
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