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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:

Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation
Shuquan Rao, Yao Yao, Daniel E. Bauer
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 56

Showing 1-25 of 56 citing articles:

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program
Anurag Verma, Jennifer E. Huffman, Alex A Rodriguez, et al.
Science (2024) Vol. 385, Iss. 6706
Open Access | Times Cited: 58
Decoding the genetic and epigenetic basis of asthma
Bernard Stikker, Rudi W. Hendriks, Ralph Stadhouders
Allergy (2023) Vol. 78, Iss. 4, pp. 940-956
Open Access | Times Cited: 47
The landscape of GWAS validation; systematic review identifying 309 validated non-coding variants across 130 human diseases
Ammar J. Alsheikh, Sabrina Wollenhaupt, Emily A. King, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 54
How data science and AI-based technologies impact genomics
Kee Yuan Ngiam, Lin Jing
Singapore Medical Journal (2023) Vol. 64, Iss. 1, pp. 59-66
Open Access | Times Cited: 33
Methods and Insights from Single-Cell Expression Quantitative Trait Loci
Joyce B. Kang, Alessandro Raveane, Aparna Nathan, et al.
Annual Review of Genomics and Human Genetics (2023) Vol. 24, Iss. 1, pp. 277-303
Open Access | Times Cited: 26
Genetic regulation of cell type–specific chromatin accessibility shapes brain disease etiology
Biao Zeng, Jaroslav Bendl, Chengyu Deng, et al.
Science (2024) Vol. 384, Iss. 6698
Closed Access | Times Cited: 14
Functional dissection of complex and molecular trait variants at single nucleotide resolution
Layla Siraj, Rodrigo Castro, Hannah B. Dewey, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 11
An evolving understanding of multiple causal variants underlying genetic association signals
Erping Long, Jacob Williams, Haoyu Zhang, et al.
The American Journal of Human Genetics (2025)
Closed Access | Times Cited: 1
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
William J. Young, Najim Lahrouchi, Aaron Isaacs, et al.
Nature Communications (2022) Vol. 13, Iss. 1
Open Access | Times Cited: 34
Diversity and Scale: Genetic Architecture of 2,068 Traits in the VA Million Veteran Program
Anurag Verma, Jennifer E. Huffman, Álex Rodríguez, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 21
Genetic insights into immune mechanisms of Alzheimer’s and Parkinson’s disease
Alexi Nott, Inge R. Holtman
Frontiers in Immunology (2023) Vol. 14
Open Access | Times Cited: 20
Establishing chromosomal design-build-test-learn through a synthetic chromosome and its combinatorial reconfiguration
Jee Loon Foo, Shohei Kitano, Adelia Vicanatalita Susanto, et al.
Cell Genomics (2023) Vol. 3, Iss. 11, pp. 100435-100435
Open Access | Times Cited: 17
Sensitivity ecology and evolution, toxicology organism assessment model in the use of chemical applications for the management of toxic substances
Great Iruoghene Edo, Princess Oghenekeno Samuel, Agatha Ngukuran Jikah, et al.
Deleted Journal (2024) Vol. 44, Iss. 5, pp. 890-908
Closed Access | Times Cited: 8
Functional studies of lung cancer GWAS beyond association
Erping Long, Harsh Patel, Jinyoung Byun, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. R1, pp. R22-R36
Open Access | Times Cited: 27
Metabolic disorders and risk of cardiovascular diseases: a two-sample mendelian randomization study
Zhe Wang, Jiawei Chen, Longyang Zhu, et al.
BMC Cardiovascular Disorders (2023) Vol. 23, Iss. 1
Open Access | Times Cited: 16
Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing
Lori L. Bonnycastle, Amy J. Swift, Erin C. Mansell, et al.
The CRISPR Journal (2024) Vol. 7, Iss. 1, pp. 53-67
Open Access | Times Cited: 6
Emerging insights into enhancer biology and function
Mirjam Arnold, Kristy R. Stengel
Transcription (2023) Vol. 14, Iss. 1-2, pp. 68-87
Closed Access | Times Cited: 12
A review of genetic risk in systemic lupus erythematosus
Suri Guga, Yuxuan Wang, Deborah Cunninghame Graham, et al.
Expert Review of Clinical Immunology (2023) Vol. 19, Iss. 10, pp. 1247-1258
Open Access | Times Cited: 12
Assigning function to SNPs: Considerations when interpreting genetic variation
Tayaza Fadason, Sophie Farrow, Sreemol Gokuladhas, et al.
Seminars in Cell and Developmental Biology (2021) Vol. 121, pp. 135-142
Closed Access | Times Cited: 26
ULK4 in Neurodevelopmental and Neuropsychiatric Disorders
Shilin Luo, Nanxi Zheng, Bing Lang
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 17
A Genetic Perspective on Ischemic Stroke: Recent Advances and Future Directions
Praveen Kumar Chandra Sekar, Ramakrishnan Veerabathiran
Annals of Clinical and Experimental Neurology (2025) Vol. 18, Iss. 4, pp. 55-67
Open Access
Identification of Pathogenic Regulatory Variants in Mendelian Diseases
Zainab Jan, Manoj K Balyan, Nismabi A Nisamudheen, et al.
Elsevier eBooks (2025), pp. 302-325
Closed Access
Multi‐Omic Insight Into the Molecular Networks in the Pathogenesis of Coronary Artery Disease
Qinghua Fang, Hong-Dan Fan, Qiaoqiao Li, et al.
Journal of the American Heart Association (2025)
Open Access
Enhanced diagnosis of multi-drug-resistant microbes using group association modeling and machine learning
Julian G. Saliba, Wenshu Zheng, Qingbo Shu, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Trans-ancestry transcriptome-wide association and functional studies to uncover novel susceptibility genes and therapeutic targets for colorectal cancer
Lijuan Wang, Lidan Hu, Jing Sun, et al.
npj Precision Oncology (2025) Vol. 9, Iss. 1
Open Access
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