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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:

Machine learning approaches to explore digenic inheritance
Atsuko Okazaki, Jürg Ott
Trends in Genetics (2022) Vol. 38, Iss. 10, pp. 1013-1018
Open Access | Times Cited: 29

Showing 1-25 of 29 citing articles:

Genetically transitional disease: a new concept in genomic medicine
Qingping Yao, Peter D. Gorevic, Bo Shen, et al.
Trends in Genetics (2022) Vol. 39, Iss. 2, pp. 98-108
Closed Access | Times Cited: 28
Genetics of inherited peripheral neuropathies and the next frontier: looking backwards to progress forwards
Jevin Parmar, Nigel G. Laing, Marina Kennerson, et al.
Journal of Neurology Neurosurgery & Psychiatry (2024) Vol. 95, Iss. 11, pp. 992-1001
Open Access | Times Cited: 5
Faster and more accurate pathogenic combination predictions with VarCoPP2.0
Nassim Versbraegen, Barbara Gravel, Charlotte Nachtegael, et al.
BMC Bioinformatics (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 11
Targeting Liposome-Driven Inflammation in Gestational Diabetes Mellitus: Insights from Multiomics and Molecular Docking
Yanyan Hu, Dan Wang, Jizheng Wang, et al.
(2025)
Closed Access
Digenic variant interpretation with hypothesis-driven explainable AI
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
NAR Genomics and Bioinformatics (2025) Vol. 7, Iss. 2
Open Access
Benchmark of computational methods to detect digenism in sequencing data
Marie‐Sophie C. Ogloblinsky, Donald F. Conrad, Anaı̈s Baudot, et al.
European Journal of Human Genetics (2025)
Closed Access
Personalized Prophylactic Antiemetic Regimens for Control of Chemotherapy-Induced Nausea and Vomiting by Pharmacogenetic Analysis of Three Receptor Genes: HTR3A , HTR3B , TACR1
Winnie Yeo, Frankie Mo, Jinghan Huang, et al.
JCO Precision Oncology (2025), Iss. 9
Closed Access
Exploring the relationship between urban residents' emotional changes and built environment before and during the COVID-19 pandemic from the perspective of resilience
Donghui Dai, Wen Dong, Yaowu Wang, et al.
Cities (2023) Vol. 141, pp. 104510-104510
Closed Access | Times Cited: 10
Nuclear Receptor Gene Variants Underlying Disorders/Differences of Sex Development through Abnormal Testicular Development
Atsushi Hattori, Maki Fukami
Biomolecules (2023) Vol. 13, Iss. 4, pp. 691-691
Open Access | Times Cited: 7
Digenic Inheritance in Rare Disorders and Mitochondrial Disease—Crossing the Frontier to a More Comprehensive Understanding of Etiology
Christiane Neuhofer, Holger Prokisch
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 9, pp. 4602-4602
Open Access | Times Cited: 2
Digenic or oligogenic mutations in presumed monogenic disorders: A review
Afif Ben‐Mahmoud, Vijay Gupta, Cheol‐Hee Kim, et al.
Journal of Genetic Medicine (2023) Vol. 20, Iss. 1, pp. 15-24
Open Access | Times Cited: 4
Digenic variant interpretation with hypothesis-driven explainable AI
Federica De Paoli, Giovanna Nicora, Silvia Berardelli, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
GDF9His209GlnfsTer6/S428T and GDF9Q321X/S428T bi-allelic variants caused female subfertility with defective follicle enlargement
Yuwei Duan, Bing Cai, Jing Guo, et al.
Cell Communication and Signaling (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
A comprehensive benchmarking with interpretation and operational guidance for the hierarchy of topologically associating domains
Jingxuan Xu, Xiang Xu, Dandan Huang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 1
Overview of frequent pattern mining
Jürg Ott, Taesung Park
Genomics & Informatics (2022) Vol. 20, Iss. 4, pp. e39-e39
Open Access | Times Cited: 6
A multi-threaded approach to genotype pattern mining for detecting digenic disease genes
Qingrun Zhang, Muskan Bhatia, Taesung Park, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 2
Genome‐wide exploration of genetic interactions for bladder cancer risk
Evan Y. Yu, Qiu‐Yi Tang, Ya‐Ting Chen, et al.
International Journal of Cancer (2023) Vol. 154, Iss. 1, pp. 81-93
Open Access | Times Cited: 2
Unveiling Digenic Pathogenic Variants and Mutation Susceptibility in Chinese Patients with Suspected Retinitis Pigmentosa
Ziwei Wang, Dongming Han, Jiankang Li
Research Square (Research Square) (2024)
Open Access
Machine learning methods applied to classify complex diseases using genomic data
Magdalena Arnal, Giorgio Bini, Anastasia Krithara, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Pseudodominant inheritance of retinitis pigmentosa in a family with mutations in the Eyes Shut Homolog (EYS) gene
Enzo Di Iorio, Ginevra Adamo, Ugo Sorrentino, et al.
Research Square (Research Square) (2024)
Closed Access
s Generalization of Gene Network Representation on the Hypercube
Pabel Shahrear, Ummey Habiba, Shajedul Karim, et al.
Engineered Science (2024)
Closed Access
Complex Disease Prediction Using Systems Biology Approach
H. R. Meghashree, Saravanan Yuvaraj, Sunitha C. Mesta, et al.
(2024), pp. 415-435
Closed Access
Determination of reinforcement diameters of reinforced concrete deep beams with genetic algorithms
Mustafa Kaya
Global Journal of Computer Sciences Theory and Research (2024) Vol. 14, Iss. 1, pp. 1-14
Open Access
Pseudodominant inheritance of retinitis pigmentosa in a family with mutations in the Eyes Shut Homolog (EYS) gene
Enzo Di Iorio, Ginevra Adamo, Ugo Sorrentino, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access
The co-occurrence of genetic variants in the TYR and OCA2 genes confers susceptibility to albinism
David J. Green, Vincent Michaud, Eulalie Lasseaux, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
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