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:

GWAS Central: an expanding resource for finding and visualising genotype and phenotype data from genome-wide association studies
Tim Beck, Thomas Rowlands, Tom Shorter, et al.
Nucleic Acids Research (2022) Vol. 51, Iss. D1, pp. D986-D993
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

The 2023 Nucleic Acids Research Database Issue and the online molecular biology database collection
Daniel J. Rigden, Xosé M. Fernández
Nucleic Acids Research (2023) Vol. 51, Iss. D1, pp. D1-D8
Open Access | Times Cited: 24

Synthetic biology advances towards a bio-based society in the era of artificial intelligence
Attia Iram, Yueming Dong, Codruţa Ignea
Current Opinion in Biotechnology (2024) Vol. 87, pp. 103143-103143
Open Access | Times Cited: 8

CropGS-Hub: a comprehensive database of genotype and phenotype resources for genomic prediction in major crops
Jiaxin Chen, Cong Tan, Min Zhu, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D1519-D1529
Open Access | Times Cited: 13

RAVAR: a curated repository for rare variant–trait associations
Chen Cao, Mengting Shao, Chunman Zuo, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D990-D997
Open Access | Times Cited: 11

Lipid Metabolism and Hepatic Growth Factors: A Mendelian Randomization Study
文卿 钟
Advances in Clinical Medicine (2025) Vol. 15, Iss. 04, pp. 1294-1301
Closed Access

Linking rare and common disease vocabularies by mapping between the human phenotype ontology and phecodes
Evonne McArthur, Lisa Bastarache, John A. Capra
JAMIA Open (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 9

The goldmine of GWAS summary statistics: a systematic review of methods and tools
Panagiota I. Kontou, Pantelis G. Bagos
BioData Mining (2024) Vol. 17, Iss. 1
Open Access | Times Cited: 2

Butyrophilin 2a2 (Btn2a2) expression on thymic epithelial cells promotes central T cell tolerance and prevents autoimmune disease
Michael Frech, Heike Danzer, Pooja Uchil, et al.
Journal of Autoimmunity (2023) Vol. 139, pp. 103071-103071
Open Access | Times Cited: 5

PGS-Depot: a comprehensive resource for polygenic scores constructed by summary statistics based methods
Chen Cao, Shuting Zhang, Jianhua Wang, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D963-D971
Open Access | Times Cited: 5

Personalized Medicine for Cardiovascular Disease Risk in Artificial Intelligence Framework
Manasvi Singh, Ashish Kumar, Narendra N. Khanna, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 4

Evaluation of Density-Based Spatial Clustering for Identifying Genomic Loci Associated with Ischemic Stroke in Genome-Wide Data
Gennady V. Khvorykh, Nikita A. Sapozhnikov, Limborskaia Sa, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 20, pp. 15355-15355
Open Access | Times Cited: 4

The causal effect of adipose tissue on Hodgkin’s lymphoma: two-sample Mendelian randomization study and validation
Lihua Wu, Fei Liao, Xiangli Guo, et al.
Frontiers in Immunology (2024) Vol. 15
Open Access | Times Cited: 1

Clinical Potential of Misshapen/NIKs-Related Kinase (MINK) 1—A Many-Sided Element of Cell Physiology and Pathology
Anna Kot, Dominika Koszewska, Błażej Ochman, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 12, pp. 13811-13845
Open Access | Times Cited: 1

The Hong Kong genome project: building genome sequencing capacity and capability for advancing genomic science in Hong Kong
Annie Chu, Amy H.Y. Tong, Desiree M. S. Tse, et al.
Journal of Translational Genetics and Genomics (2023) Vol. 7, Iss. 4, pp. 196-212
Open Access | Times Cited: 3

Candidate SNP Markers Significantly Altering the Affinity of TATA-Binding Protein for the Promoters of Human Hub Genes for Atherogenesis, Atherosclerosis and Atheroprotection
Anton Bogomolov, Sergey Filonov, И. В. Чадаева, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 10, pp. 9010-9010
Open Access | Times Cited: 2

Polymorphism of Estrogen Receptor Genes and Its Interactions With Neurodevelopmental Genes in Attention Deficit Hyperactivity Disorder Among Chinese Han Descent
Yiwei Lin, Haimei Li, Jing Zhang, et al.
Psychiatry Investigation (2023) Vol. 20, Iss. 8, pp. 775-785
Open Access | Times Cited: 2

A Dynamic Method and Program for Disease-Based Genetic Classification of Individuals
Onur ÇAKIRGÖZ, Süleyman Sevinç
Journal of Emerging Computer Technologies (2024) Vol. 3, Iss. 1, pp. 12-20
Open Access

Biological and Medical Ontologies: Disease Ontology (DO)
Ruba Al Khalaf, Anna Bernasconi, Marco Masseroli
Elsevier eBooks (2024)
Closed Access

Biological and Medical Ontologies: Human Phenotype Ontology (HPO)
Ruba Al Khalaf, Anna Bernasconi, Marco Masseroli
Elsevier eBooks (2024)
Closed Access

Association of asthma and bronchiectasis: Mendelian randomization analyses and observational study
Rui Fan, Hao Qian, Jiayan Xu, et al.
Respiratory Research (2024) Vol. 25, Iss. 1
Open Access

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