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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:

Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans
Guihu Zhao, Kuokuo Li, Bin Li, et al.
Nucleic Acids Research (2019)
Open Access | Times Cited: 63

Showing 1-25 of 63 citing articles:

Integration of the Drug–Gene Interaction Database (DGIdb 4.0) with open crowdsource efforts
Sharon L. Freshour, Susanna Kiwala, Kelsy C. Cotto, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1144-D1151
Open Access | Times Cited: 718
Systematic discovery of protein interaction interfaces using AlphaFold and experimental validation
Chop Yan Lee, Dalmira Hubrich, Julia K. Varga, et al.
Molecular Systems Biology (2024)
Open Access | Times Cited: 31
Genetic evidence of gender difference in autism spectrum disorder supports the female-protective effect
Yi Zhang, Na Li, Chao Li, et al.
Translational Psychiatry (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 134
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
Leslie Matalonga, Carles Hernández-Ferrer, Davide Piscia, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 9, pp. 1337-1347
Open Access | Times Cited: 60
Signatures of TOP1 transcription-associated mutagenesis in cancer and germline
Martin A.M. Reijns, David Parry, Thomas Williams, et al.
Nature (2022) Vol. 602, Iss. 7898, pp. 623-631
Open Access | Times Cited: 59
Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder
Itaru Kushima, Masahiro Nakatochi, Branko Aleksić, et al.
Biological Psychiatry (2022) Vol. 92, Iss. 5, pp. 362-374
Open Access | Times Cited: 35
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects
Qun Li, Lin Zhao, Yang Zeng, et al.
Genome biology (2023) Vol. 24, Iss. 1
Open Access | Times Cited: 18
CircleBase: an integrated resource and analysis platform for human eccDNAs
Xiaolu Zhao, Leisheng Shi, Shasha Ruan, et al.
Nucleic Acids Research (2021) Vol. 50, Iss. D1, pp. D72-D82
Open Access | Times Cited: 34
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
Francesco Vetrini, Shane McKee, Jill A. Rosenfeld, et al.
Genome Medicine (2019) Vol. 11, Iss. 1
Open Access | Times Cited: 41
Integration of the Drug-Gene Interaction Database (DGIdb) with open crowdsource efforts
Sharon L. Freshour, Susanna Kiwala, Kelsy C. Cotto, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 38
Putative complement control protein CSMD3 dysfunction impairs synaptogenesis and induces neurodevelopmental disorders
Wei Song, Quan Li, Tao Wang, et al.
Brain Behavior and Immunity (2022) Vol. 102, pp. 237-250
Open Access | Times Cited: 20
DNA replication initiation shapes the mutational landscape and expression of the human genome
Pierre Murat, Consuelo Perez, Alastair Crisp, et al.
Science Advances (2022) Vol. 8, Iss. 45
Open Access | Times Cited: 19
Rare de novo damaging DNA variants are enriched in attention-deficit/hyperactivity disorder and implicate risk genes
Emily Olfson, Luís C. Farhat, Wenzhong Liu, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4
Genome-wide functional annotation of variants: a systematic review of state-of-the-art tools, techniques and resources
Eleftherios Pilalis, Dimitrios Zisis, Christina Andrinopoulou, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access
Characterizing Rare DNA Copy-Number Variants in Pediatric Obsessive-Compulsive Disorder
Sarah B. Abdallah, Emily Olfson, Carolina Cappi, et al.
Journal of the American Academy of Child & Adolescent Psychiatry (2025)
Closed Access
Gene4PD: A Comprehensive Genetic Database of Parkinson’s Disease
Bin Li, Guihu Zhao, Qiao Zhou, et al.
Frontiers in Neuroscience (2021) Vol. 15
Open Access | Times Cited: 24
Performance Comparison of Computational Methods for the Prediction of the Function and Pathogenicity of Non-Coding Variants
Zheng Wang, Guihu Zhao, Bin Li, et al.
Genomics Proteomics & Bioinformatics (2022) Vol. 21, Iss. 3, pp. 649-661
Open Access | Times Cited: 18
Identifying rare genetic variants in 21 highly multiplex autism families: the role of diagnosis and autistic traits
Ravi Prabhakar More, Varun Warrier, Héléna Brunel, et al.
Molecular Psychiatry (2023) Vol. 28, Iss. 5, pp. 2148-2157
Open Access | Times Cited: 9
An updated catalog of CTCF variants associated with neurodevelopmental disorder phenotypes
Emma Price, Liron M. Fedida, Elena M. Pugacheva, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 9
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders
Bo Zhou, Joseph G. Arthur, Hanmin Guo, et al.
Cell (2024) Vol. 187, Iss. 23, pp. 6687-6706.e25
Closed Access | Times Cited: 3
Performance evaluation of differential splicing analysis methods and splicing analytics platform construction
Kuokuo Li, Tengfei Luo, Yan Zhu, et al.
Nucleic Acids Research (2022) Vol. 50, Iss. 16, pp. 9115-9126
Open Access | Times Cited: 15
Integrative analysis prioritised oxytocin-related biomarkers associated with the aetiology of autism spectrum disorder
Tao Wang, Tingting Zhao, Liqiu Liu, et al.
EBioMedicine (2022) Vol. 81, pp. 104091-104091
Open Access | Times Cited: 14
Systematic discovery of protein interaction interfaces using AlphaFold and experimental validation
Chop Yan Lee, Dalmira Hubrich, Julia K. Varga, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 7
Research advances on neurite outgrowth inhibitor B receptor
Rui Zhang, Beisha Tang, Jifeng Guo
Journal of Cellular and Molecular Medicine (2020) Vol. 24, Iss. 14, pp. 7697-7705
Open Access | Times Cited: 17
VarCards2: an integrated genetic and clinical database for ACMG-AMP variant-interpretation guidelines in the human whole genome
Zheng Wang, Guihu Zhao, Zhaopo Zhu, et al.
Nucleic Acids Research (2023) Vol. 52, Iss. D1, pp. D1478-D1489
Open Access | Times Cited: 5
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