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:

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: 127

Showing 26-50 of 127 citing articles:

Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease Endophenotypes
Nathaniel B. Gunter, Robel K Gebre, Jonathan Graff‐Radford, et al.
Neurology Genetics (2024) Vol. 10, Iss. 1
Open Access | Times Cited: 4

Idiopathic pulmonary fibrosis-specific Bayesian network integrating extracellular vesicle proteome and clinical information
Mei Tomoto, Yohei Mineharu, Noriaki Sato, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4

The association of GNB5 with Alzheimer disease revealed by genomic analysis restricted to variants impacting gene function
Jianhua Zhang, Mritunjay Pandey, Adam M. Awe, et al.
The American Journal of Human Genetics (2024) Vol. 111, Iss. 3, pp. 473-486
Open Access | Times Cited: 4

Shaping immunity: The influence of natural selection on population immune diversity
Haley E. Randolph, Katherine A Aracena, Yen‐Lung Lin, et al.
Immunological Reviews (2024) Vol. 323, Iss. 1, pp. 227-240
Open Access | Times Cited: 4

Predicting gene disease associations with knowledge graph embeddings for diseases with curtailed information
Francesco Gualdi, Baldomero Oliva, Janet Piñero
NAR Genomics and Bioinformatics (2024) Vol. 6, Iss. 2
Open Access | Times Cited: 4

Methodologies underpinning polygenic risk scores estimation: a comprehensive overview
Carene Anne Alene Ndong Sima, Kathryn Step, Yolandi Swart, et al.
Human Genetics (2024) Vol. 143, Iss. 11, pp. 1265-1280
Open Access | Times Cited: 4

Bayesian Effect Size Ranking to Prioritise Genetic Risk Variants in Common Diseases for Follow‐Up Studies
D. Crouch, Jamie Inshaw, Catherine C. Robertson, et al.
Genetic Epidemiology (2025) Vol. 49, Iss. 1
Open Access

Genetic Variants Associated with Suspected Neonatal Hypoxic Ischaemic Encephalopathy: A Study in a South African Context
C. L. Foden, Kevin Durant, Juanita Mellet, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 5, pp. 2075-2075
Open Access

Relatively independent and complementary roles of family history and polygenic risk score in age at onset and incident cases of 12 common diseases
Wenyan Hou, Y. Liu, Xingjie Hao, et al.
Social Science & Medicine (2025) Vol. 371, pp. 117942-117942
Closed Access

Novel ABCD1 and MTHFSD Variants in Taiwanese Bipolar Disorder: A Genetic Association Study
Yiguang Wang, Chih-Chung Huang, Ta‐Chuan Yeh, et al.
Medicina (2025) Vol. 61, Iss. 3, pp. 486-486
Open Access

What clinicians should know about the contribution of modern behavioral genetics to psychiatric problems
Robert Plomin, Evangelos Vassos
Psychological Medicine (2025) Vol. 55
Closed Access

Genetics of Restless Legs Syndrome
Barbara Schormair
Sleep Medicine Clinics (2025)
Closed Access

Gene-based therapeutics for rare genetic neurodevelopmental psychiatric disorders
Beverly L. Davidson, Guangping Gao, Elizabeth Berry‐Kravis, et al.
Molecular Therapy (2022) Vol. 30, Iss. 7, pp. 2416-2428
Open Access | Times Cited: 18

Hypertension, a dementia polygenic risk score, APOE genotype, and incident dementia
Thomas J. Littlejohns, Jennifer A. Collister, Xiaonan Liu, et al.
Alzheimer s & Dementia (2022) Vol. 19, Iss. 2, pp. 467-476
Open Access | Times Cited: 17

Genetics and Epigenetics: Implications for the Life Course of Gestational Diabetes
William L. Lowe
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6047-6047
Open Access | Times Cited: 10

Comparing Pruning and Thresholding with Continuous Shrinkage Polygenic Score Methods in a Large Sample of Ancestrally Diverse Adolescents from the ABCD Study®
Jonathan Ahern, Wesley K. Thompson, Chun Chieh Fan, et al.
Behavior Genetics (2023) Vol. 53, Iss. 3, pp. 292-309
Open Access | Times Cited: 10

A Systematic Review on the Genetic Contribution to Tinnitus
Patricia Perez‐Carpena, José A. López‐Escámez, Álvaro Gallego-Martinez
Journal of the Association for Research in Otolaryngology (2024) Vol. 25, Iss. 1, pp. 13-33
Open Access | Times Cited: 3

Low genetic diversity and high inbreeding in one of the last chlamydia-free strongholds for New South Wales koalas
Elspeth A. McLennan, Lachlan Wilmott, Kiersten M. Madden, et al.
Conservation Genetics (2025)
Open Access

Associations of Maternal Smoking During Pregnancy and Genetic Susceptibility with Incident Asthma from a Cohort Study
Shuo Zhang, Ting Wang, Ping Zeng
Prevention Science (2025) Vol. 26, Iss. 3, pp. 343-354
Closed Access

Genetically Transitional Disease and the Road to Personalized Medicine
Qingping Yao, Peter D. Gorevic, Greg Gibson
Genes (2025) Vol. 16, Iss. 4, pp. 401-401
Open Access

New Cardiovascular Risk Assessment Techniques for Primary Prevention
Kunal Verma, Michael Inouye, Peter J. Meikle, et al.
Journal of the American College of Cardiology (2022) Vol. 80, Iss. 4, pp. 373-387
Open Access | Times Cited: 16

Translating osteoarthritis genetics research: challenging times ahead
John Loughlin
Trends in Molecular Medicine (2022) Vol. 28, Iss. 3, pp. 176-182
Open Access | Times Cited: 15

Nutrigenomics in the context of evolution
Carsten Carlberg
Redox Biology (2023) Vol. 62, pp. 102656-102656
Open Access | Times Cited: 9

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