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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:

Integrate GWAS, eQTL, and mQTL Data to Identify Alzheimer’s Disease-Related Genes
Tianyi Zhao, Yang Hu, Tianyi Zang, et al.
Frontiers in Genetics (2019) Vol. 10
Open Access | Times Cited: 50

Showing 1-25 of 50 citing articles:

DNA methylation QTL mapping across diverse human tissues provides molecular links between genetic variation and complex traits
Meritxell Oliva, Kathryn Demanelis, Yihao Lu, et al.
Nature Genetics (2022) Vol. 55, Iss. 1, pp. 112-122
Open Access | Times Cited: 115
Guidelines for bioinformatics of single-cell sequencing data analysis in Alzheimer’s disease: review, recommendation, implementation and application
Minghui Wang, Won‐Min Song, Ming Chen, et al.
Molecular Neurodegeneration (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 68
Genetic impacts on DNA methylation help elucidate regulatory genomic processes
Sergio Villicaña, Juan Castillo‐Fernandez, Eilís Hannon, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 29
Genetic approaches for increasing fitness in endangered species
Tiffany A. Kosch, Anthony W. Waddle, Caitlin Cooper, et al.
Trends in Ecology & Evolution (2022) Vol. 37, Iss. 4, pp. 332-345
Closed Access | Times Cited: 37
Identification of novel proteins for lacunar stroke by integrating genome-wide association data and human brain proteomes
Chengcheng Zhang, Fengqin Qin, Xiaojing Li, et al.
BMC Medicine (2022) Vol. 20, Iss. 1
Open Access | Times Cited: 35
Prediction of Chinese energy structure based on Convolutional Neural Network‐Long Short‐Term Memory (CNN‐LSTM)
Yan Li, Yaoyu He, Meizhen Zhang
Energy Science & Engineering (2020) Vol. 8, Iss. 8, pp. 2680-2689
Open Access | Times Cited: 33
Interaction of genetic variants and methylation in transcript-level expression regulation in Alzheimer’s disease by multi-omics data analysis
Seonggyun Han, Soo-ah Cho, Woojae Choi, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access
Identification of novel proteins associated with intelligence by integrating genome-wide association data and human brain proteomics
Zhang Zheng, Yousong Zhu, Junlong Zhang, et al.
PLoS ONE (2025) Vol. 20, Iss. 2, pp. e0319278-e0319278
Open Access
Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer’s disease, providing new insights into its disease mechanisms
Zhen Wang, Quanwei Zhang, Jhih‐Rong Lin, et al.
Scientific Reports (2021) Vol. 11, Iss. 1
Open Access | Times Cited: 24
Quantitative trait locus (xQTL) approaches identify risk genes and drug targets from human non-coding genomes
M. Bykova, Yuan Hou, Charis Eng, et al.
Human Molecular Genetics (2022) Vol. 31, Iss. R1, pp. R105-R113
Open Access | Times Cited: 17
Golgi apparatus, endoplasmic reticulum and mitochondrial function implicated in Alzheimer’s disease through polygenic risk and RNA sequencing
Karen Crawford, Ganna Leonenko, Emily Baker, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 3, pp. 1327-1336
Open Access | Times Cited: 16
Interval estimate of causal effect in summary data based Mendelian randomization in the presence of winner's curse
Kai Wang
Genetic Epidemiology (2024) Vol. 48, Iss. 2, pp. 74-84
Open Access | Times Cited: 3
Identifying diseases that cause psychological trauma and social avoidance by GCN-Xgboost
Huijuan Xu, Hairong Wang, Chenshan Yuan, et al.
BMC Bioinformatics (2020) Vol. 21, Iss. S16
Open Access | Times Cited: 21
Recent innovations and in-depth aspects of post-genome wide association study (Post-GWAS) to understand the genetic basis of complex phenotypes
Zahra Mortezaei, Mahmood Tavallaei
Heredity (2021) Vol. 127, Iss. 6, pp. 485-497
Open Access | Times Cited: 19
Identification of gene biomarkers for brain diseases via multi-network topological semantics extraction and graph convolutional network
Ping Zhang, Weihan Zhang, Weicheng Sun, et al.
BMC Genomics (2024) Vol. 25, Iss. 1
Open Access | Times Cited: 2
DRACP: a novel method for identification of anticancer peptides
Tianyi Zhao, Yang Hu, Tianyi Zang
BMC Bioinformatics (2020) Vol. 21, Iss. S16
Open Access | Times Cited: 14
Pursuit of precision medicine: Systems biology approaches in Alzheimer's disease mouse models
Brianna Gurdon, Catherine C. Kaczorowski
Neurobiology of Disease (2021) Vol. 161, pp. 105558-105558
Open Access | Times Cited: 12
Summary-Based Methylome-Wide Association Analyses Suggest Potential Genetically Driven Epigenetic Heterogeneity of Alzheimer’s Disease
Alireza Nazarian, Anatoliy I. Yashin, Alexander M. Kulminski
Journal of Clinical Medicine (2020) Vol. 9, Iss. 5, pp. 1489-1489
Open Access | Times Cited: 12
Convergent lines of evidence support BIN1 as a risk gene of Alzheimer’s disease
Jin Zhu, Xia Liu, Hongtao Yin, et al.
Human Genomics (2021) Vol. 15, Iss. 1
Open Access | Times Cited: 11
Genetic impacts on DNA methylation help elucidate regulatory genomic processes
Sergio Villicaña, Juan Castillo‐Fernandez, Eilís Hannon, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 4
Employing Informatics Strategies in Alzheimer's Disease Research: A Review from Genetics, Multiomics, and Biomarkers to Clinical Outcomes
Jingxuan Bao, Brian N. Lee, Junhao Wen, et al.
Annual Review of Biomedical Data Science (2024) Vol. 7, Iss. 1, pp. 391-418
Closed Access | Times Cited: 1
Translation of genome-wide association study: from genomic signals to biological insights
Winter S Bruner, Struan F.A. Grant
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 1
DNA Methylation in Alzheimer’s Disease
Luke Weymouth, Adam R. Smith, Katie Lunnon
Current topics in behavioral neurosciences (2024)
Closed Access | Times Cited: 1
Integrating Multi-Omics Data to Identify Novel Disease Genes and Single-Neucleotide Polymorphisms
Sheng Zhao, Huijie Jiang, Zonghui Liang, et al.
Frontiers in Genetics (2020) Vol. 10
Open Access | Times Cited: 9
Disease-associated genetic variants in the regulatory regions of human genes: mechanisms of action on transcription and genomic resources for dissecting these mechanisms
E. V. Ignatieva, E. A. Matrosova
Vavilov Journal of Genetics and Breeding (2021) Vol. 25, Iss. 1, pp. 18-29
Open Access | Times Cited: 9
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