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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:

Functional genetic variants can mediate their regulatory effects through alteration of transcription factor binding
Andrew D. Johnston, Cláudia A. Simões‐Pires, Taylor V. Thompson, et al.
Nature Communications (2019) Vol. 10, Iss. 1
Open Access | Times Cited: 60

Showing 1-25 of 60 citing articles:

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
A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis
Yuting Guan, Xiujie Liang, Ziyuan Ma, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 65
ANANSE: an enhancer network-based computational approach for predicting key transcription factors in cell fate determination
Quan Xu, Γεώργιος Γεωργίου, Siebren Frölich, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 14, pp. 7966-7985
Open Access | Times Cited: 62
Complex regulatory networks influence pluripotent cell state transitions in human iPSCs
Timothy D. Arthur, Jennifer Nguyen, Agnieszka D’Antonio‐Chronowska, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 13
Bioinformatics Applications in Chronic Diseases: A Comprehensive Review of Genomic, Transcriptomics, Proteomic, Metabolomics, and Machine Learning Approaches
Taiwo Temitope Ogunjobi, Precious Nkeiruka Ohaeri, Olamide Tayo Akintola, et al.
Deleted Journal (2024)
Open Access | Times Cited: 11
Polymorphisms in transcription factor binding sites and enhancer regions and pancreatic ductal adenocarcinoma risk
Pelin Gürkan Ünal, Ye Lu, Bas Bueno‐de‐Mesquita, et al.
Human Genomics (2024) Vol. 18, Iss. 1
Open Access | Times Cited: 5
Genetic Variants in Transcription Factor Binding Sites in Humans: Triggered by Natural Selection and Triggers of Diseases
Chia‐Chun Tseng, Man-Chun Wong, Wei‐Ting Liao, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 8, pp. 4187-4187
Open Access | Times Cited: 25
Epigenetic Impacts of Non‐Coding Mutations Deciphered Through Pre‐Trained DNA Language Model at Single‐Cell Resolution
Zhe Liu, An Gu, Yihang Bao, et al.
Advanced Science (2025)
Open Access
reg-eQTL: Integrating transcription factor effects to unveil regulatory variants
Rekha Mudappathi, Tatiana Patton, Hai Chen, et al.
The American Journal of Human Genetics (2025)
Closed Access
Cardiovascular Disease-Associated Non-Coding Variants Disrupt GATA4-DNA Binding and Regulatory Functions
Edwin G. Peña-Martínez, Jean L. Messon-Bird, Jessica Rodríguez‐Ríos, et al.
Human Genetics and Genomics Advances (2025) Vol. 6, Iss. 2, pp. 100415-100415
Open Access
Early Alzheimer’s brain atrophy in entorhinal cortex is associated with HSD11B1-cortisol axis in APOE4 carriers
Rai‐Hua Lai, Ren-Hua Chung, Paul Hsu, et al.
Research Square (Research Square) (2025)
Closed Access
The Role of AI-Based Chatbots in Public Health Emergencies: A Narrative Review
Francesco Branda, Massimo Stella, C. Ceccarelli, et al.
Future Internet (2025) Vol. 17, Iss. 4, pp. 145-145
Open Access
Genotype inference from aggregated chromatin accessibility data reveals genetic regulatory mechanisms
Brandon M. Wenz, Yuan He, Nae-Chyun Chen, et al.
Genome biology (2025) Vol. 26, Iss. 1
Open Access
CRISPR base editing of cis-regulatory elements enables the perturbation of neurodegeneration-linked genes
Colin K.W. Lim, Tristan X. McCallister, Christian Saporito-Magriñá, et al.
Molecular Therapy (2022) Vol. 30, Iss. 12, pp. 3619-3631
Open Access | Times Cited: 16
Methods for Functional Characterization of Genetic Polymorphisms of Non-Coding Regulatory Regions of the Human Genome
А. Н. Уварова, Е А Ткаченко, Ekaterina M. Stasevich, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 6, pp. 1002-1013
Open Access | Times Cited: 3
Importance of transcript variants in transcriptome analyses
Kevin D. Vo, Ryan Mohamadi, Yashica Sharma, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 3
Using epigenomics to understand cellular responses to environmental influences in diseases
Julia Wattacheril, Srilakshmi M. Raj, David A. Knowles, et al.
PLoS Genetics (2023) Vol. 19, Iss. 1, pp. e1010567-e1010567
Open Access | Times Cited: 8
Significant association of LXRβ (NR1H2) polymorphisms (rs28514894, rs2303044) with type 2 diabetes mellitus and laboratory characteristics
Mohammad Bagher Sadeghi, Alireza Nakhaee, Ramin Saravani, et al.
Journal of Diabetes & Metabolic Disorders (2021) Vol. 20, Iss. 1, pp. 261-270
Open Access | Times Cited: 18
Multiomics uncovers the epigenomic and transcriptomic response to viral and bacterial stimulation in turbot
Óscar Aramburu, Belén G. Pardo, Paula R. Villamayor, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
The rs2564978(T) Allele Associated with Severe Influenza A Disrupts the Binding Site for Myeloid Differentiation Factor PU.1 and Reduces CD55/DAF Gene Promoter Activity in Macrophages
А. Н. Уварова, E. A. Tkachenko, Ekaterina M. Stasevich, et al.
Molecular Biology (2024) Vol. 58, Iss. 2, pp. 255-265
Open Access | Times Cited: 2
Parkinson’s disease risk enhancers in microglia
Alix Booms, Steven Pierce, Edwin J. C. Van der Schans, et al.
iScience (2024) Vol. 27, Iss. 2, pp. 108921-108921
Open Access | Times Cited: 2
The SNP polymorphisms associated with WSSV-resistance of prophenoloxidase in red swamp crayfish (Procambarus clarkii) and its immune response against white spot syndrome virus (WSSV)
Long Zhang, Yanhe Li, Minglin Wu, et al.
Aquaculture (2020) Vol. 530, pp. 735787-735787
Closed Access | Times Cited: 16
High-altitude pulmonary edema is aggravated by risk loci and associated transcription factors in HIF-prolyl hydroxylases
Kavita Sharma, Aastha Mishra, Himanshu Narayan Singh, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 18, pp. 1734-1749
Closed Access | Times Cited: 14
The role of neurotrophin genes involved in the vulnerability to gambling disorder
Neus Solé‐Morata, Isabel Baenas, Mikel Etxandi, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 10
An integrated transcriptome mapping the regulatory network of coding and long non-coding RNAs provides a genomics resource in chickpea
Mukesh Jain, Juhi Bansal, Mohan Singh Rajkumar, et al.
Communications Biology (2022) Vol. 5, Iss. 1
Open Access | Times Cited: 10
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