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:

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative
Ruth Johnson, Yi Ding, Vidhya Venkateswaran, et al.
Genome Medicine (2022) Vol. 14, Iss. 1
Open Access | Times Cited: 34

Showing 1-25 of 34 citing articles:

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: 152

Recent advances in polygenic scores: translation, equitability, methods and FAIR tools
Ruidong Xiang, Martin Kelemen, Yu Xu, et al.
Genome Medicine (2024) Vol. 16, Iss. 1
Open Access | Times Cited: 29

Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
Nature Genetics (2024) Vol. 56, Iss. 7, pp. 1386-1396
Open Access | Times Cited: 21

Genetic and molecular architecture of complex traits
Tuuli Lappalainen, Yang Li, Sohini Ramachandran, et al.
Cell (2024) Vol. 187, Iss. 5, pp. 1059-1075
Open Access | Times Cited: 20

Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder
Andrew Dahl, Michael Thompson, Ulzee An, et al.
Nature Genetics (2023) Vol. 55, Iss. 12, pp. 2082-2093
Open Access | Times Cited: 22

Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds
Ying Wang, Yixuan He, Yue Shi, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 5, pp. 809-824
Closed Access | Times Cited: 10

The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank
Ruth Johnson, Yi Ding, Arjun Bhattacharya, et al.
Cell Genomics (2023) Vol. 3, Iss. 1, pp. 100243-100243
Open Access | Times Cited: 21

Comparing methods for constructing and representing human pangenome graphs
Francesco Andreace, P Lechat, Yoann Dufresne, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 21

Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores
Sarah Abramowitz, Kristin Boulier, Karl Keat, et al.
JAMA (2024)
Closed Access | Times Cited: 4

Breaking research silos to achieve equitable precision medicine in rheumatology
Hannah C. Ainsworth, DeAnna Baker Frost, S. Sam Lim, et al.
Nature Reviews Rheumatology (2025)
Closed Access

Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 10

Disparities in Diagnosis, Access to Specialist Care, and Treatment for Inborn Errors of Immunity
Monica G. Lawrence, Nicholas L. Rider, Charlotte Cunningham‐Rundles, et al.
The Journal of Allergy and Clinical Immunology In Practice (2023) Vol. 12, Iss. 2, pp. 282-287
Closed Access | Times Cited: 8

Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer’s Disease
Mingzhou Fu, Thai Tran, Eleazar Eskin, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2

Cell-type deconvolution of bulk-blood RNA-seq reveals biological insights into neuropsychiatric disorders
Toni Boltz, Tommer Schwarz, Merel Bot, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 2, pp. 323-337
Open Access | Times Cited: 1

Improving genetic risk modeling of dementia from real-world data in underrepresented populations
Mingzhou Fu, Leopoldo Valiente‐Banuet, Satpal S. Wadhwa, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1

The Known and Unknown “Knowns” of Human Susceptibility to Coccidioidomycosis
Amy P. Hsu
Journal of Fungi (2024) Vol. 10, Iss. 4, pp. 256-256
Open Access | Times Cited: 1

Generalizability of PGS313 for breast cancer risk in a Los Angeles biobank
Helen H. Shang, Yi Ding, Vidhya Venkateswaran, et al.
Human Genetics and Genomics Advances (2024) Vol. 5, Iss. 3, pp. 100302-100302
Open Access | Times Cited: 1

Big data in sarcoidosis
Natalia V. Rivera
Current Opinion in Pulmonary Medicine (2024) Vol. 30, Iss. 5, pp. 561-569
Open Access | Times Cited: 1

Construction and representation of human pangenome graphs
Francesco Andreace, P Lechat, Yoann Dufresne, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4

Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region
Christa Caggiano, Arya Boudaie, Ruhollah Shemirani, et al.
Nature Medicine (2023) Vol. 29, Iss. 7, pp. 1845-1856
Open Access | Times Cited: 4

Calibrated prediction intervals for polygenic scores across diverse contexts
Kangcheng Hou, Ziqi Xu, Yi Ding, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 3

Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart disease
Sarah Spendlove, Leroy Bondhus, Gentian Lluri, et al.
Human Genetics and Genomics Advances (2022) Vol. 3, Iss. 3, pp. 100112-100112
Open Access | Times Cited: 5

Conducting Human Biology Research Using Invasive Clinical Samples: Methods, Strengths, and Limitations
Volney K. Friedrich, Morgan K. Hoke, Theodore G. Schurr
American Journal of Human Biology (2024)
Closed Access

Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles
Vidhya Venkateswaran, Kristin Boulier, Yi Ding, et al.
Translational Psychiatry (2024) Vol. 14, Iss. 1
Open Access

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