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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:

Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons
Siming Zhang, Xianglong Zhang, Carolin Purmann, et al.
Biological Psychiatry (2020) Vol. 89, Iss. 5, pp. 497-509
Open Access | Times Cited: 21

Showing 21 citing articles:

Multi-omics data integration methods and their applications in psychiatric disorders
Anita Sathyanarayanan, Tamara T. Mueller, Mohammad Ali Moni, et al.
European Neuropsychopharmacology (2023) Vol. 69, pp. 26-46
Open Access | Times Cited: 48
Integrative omics of schizophrenia: from genetic determinants to clinical classification and risk prediction
Fanglin Guan, Tong Ni, Weili Zhu, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 113-126
Open Access | Times Cited: 57
Role of sperm DNA damage in creating de-novo mutations in human offspring: the ‘post-meiotic oocyte collusion’ hypothesis
R. John Aitken
Reproductive BioMedicine Online (2022) Vol. 45, Iss. 1, pp. 109-124
Open Access | Times Cited: 37
Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome
Brianna K. Unda, Leon Chalil, Sehyoun Yoon, et al.
Molecular Psychiatry (2023)
Open Access | Times Cited: 11
Redox-Driven Epigenetic Modifications in Sperm: Unraveling Paternal Influences on Embryo Development and Transgenerational Health
Aron Moazamian, Fabrice Saez, Joël R. Drevet, et al.
Antioxidants (2025) Vol. 14, Iss. 5, pp. 570-570
Open Access
Cell-type specific global reprogramming of the transcriptome and epigenome in induced neurons with the 16p11.2 neuropsychiatric CNVs
Thomas Ward, Pingping Qu, Louis C. Leung, et al.
European Journal of Human Genetics (2025)
Closed Access
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons
Alena Kozlova, Siwei Zhang, Alex Kotlar, et al.
The American Journal of Human Genetics (2022) Vol. 109, Iss. 8, pp. 1500-1519
Open Access | Times Cited: 16
Meta-analyses of genome wide association studies in lines of laying hens divergently selected for feather pecking using imputed sequence level genotypes
Clemens Falker‐Gieske, Hanna Iffland, Siegfried Preuß, et al.
BMC Genomic Data (2020) Vol. 21, Iss. 1
Open Access | Times Cited: 18
Modeling common and rare genetic risk factors of neuropsychiatric disorders in human induced pluripotent stem cells
Abdurrahman W. Muhtaseb, Jubao Duan
Schizophrenia Research (2022)
Open Access | Times Cited: 9
Bioinformatic Evaluation of KLF13 Genetic Variant: Implications for Neurodevelopmental and Psychiatric Symptoms
Mirella Vinci, Donatella Greco, Simone Treccarichi, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1056-1056
Open Access | Times Cited: 1
Gene Editing in Pluripotent Stem Cells and Their Derived Organoids
Hang Zhou, Yun Wang, Li‐Ping Liu, et al.
Stem Cells International (2021) Vol. 2021, pp. 1-14
Open Access | Times Cited: 9
Shedding light on latent pathogenesis and pathophysiology of mental disorders: The potential of iPS cell technology
Yuko Arioka, Hiroki Okumura, Hideya Sakaguchi, et al.
Psychiatry and Clinical Neurosciences (2023) Vol. 77, Iss. 6, pp. 308-314
Open Access | Times Cited: 3
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
Marek B. Körner, Akhil Velluva, Linnaeus Bundalian, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 5
Duplication Versus Deletion Through the Lens of 15q13.3: Clinical and Research Implications of Studying Copy Number Variants Associated with Neuropsychiatric Disorders in Induced Pluripotent Stem Cell-Derived Neurons
Irene Antony, Mishka Narasimhan, Renata Shen, et al.
Stem Cell Reviews and Reports (2022) Vol. 19, Iss. 3, pp. 639-650
Closed Access | Times Cited: 5
Modeling schizophrenia with iPS cell technology and disease mouse models
Takanobu Nakazawa
Neuroscience Research (2021) Vol. 175, pp. 46-52
Open Access | Times Cited: 6
Deepening the understanding of CNVs on chromosome 15q11–13 by using hiPSCs: An overview
Angela Maria Giada Giovenale, Giorgia Ruotolo, Amata Amy Soriano, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 10
Open Access | Times Cited: 1
Exploring 15q13.3 copy number variants in iPSCs
Madelyn A. Gillentine
Elsevier eBooks (2022), pp. 333-360
Closed Access | Times Cited: 2
Cell-type specific global reprogramming of the transcriptome and epigenome in induced neurons with the 16p11.2 neuropsychiatric CNVs
Xianglong Zhang, Thomas Ward, Louis C. Leung, et al.
Research Square (Research Square) (2023)
Open Access
Loss-of-function of OTUD7A in the schizophrenia-associated 15q13.3 deletion impairs synapse development and function in human neurons
Alena Kozlova, Siwei Zhang, Alex Kotlar, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
Marek B. Körner, Akhil Velluva, Linnaeus Bundalian, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Cross-Platform Validation of 15q13.3 Microdeletion Network Effects in Human Neurons
Michael B. Fernando
Biological Psychiatry (2021) Vol. 89, Iss. 5, pp. e25-e27
Closed Access
Functional genomics of psychiatric disease risk using genome engineering
Meilín Fernández García, Samuel K. Powell, Elizabeth A. LaMarca, et al.
Elsevier eBooks (2021), pp. 711-734
Closed Access
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