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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:

A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia
Ashley Pacheco, Ralph Berger, Robert Freedman, et al.
Scientific Reports (2019) Vol. 9, Iss. 1
Open Access | Times Cited: 25

Showing 25 citing articles:

Translational genomics and beyond in bipolar disorder
Chen Zhang, Xiao Xiao, Tao Li, et al.
Molecular Psychiatry (2020) Vol. 26, Iss. 1, pp. 186-202
Closed Access | Times Cited: 43
Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans
Kohei Hamanaka, Daisuke Yamauchi, Eriko Koshimizu, et al.
Genome Research (2023) Vol. 33, Iss. 3, pp. 435-447
Open Access | Times Cited: 16
miR-137: A Novel Therapeutic Target for Human Glioma
Yajun Wang, Riling Chen, Xia Zhou, et al.
Molecular Therapy — Nucleic Acids (2020) Vol. 21, pp. 614-622
Open Access | Times Cited: 31
Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences
Marzieh Eslami Rasekh, Yözen Hernández, Samantha D. Drinan, et al.
Nucleic Acids Research (2021) Vol. 49, Iss. 8, pp. 4308-4324
Open Access | Times Cited: 24
Multifaceted Regulation of MicroRNA Biogenesis: Essential Roles and Functional Integration in Neuronal and Glial Development
Izabela Suster, Yue Feng
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 13, pp. 6765-6765
Open Access | Times Cited: 24
Association of the VNTR Polymorphism in the MIR137 Gene with Cognitive Functions in Schizophrenia Patients and Healthy Individuals
M. V. Alfimova, Г. И. Коровайцева, V. V. Plakunova, et al.
Russian Journal of Genetics (2025) Vol. 61, Iss. 1, pp. 124-128
Closed Access
Neurodevelopmental concepts of schizophrenia in the genome-wide association era: AKT/mTOR signaling as a pathological mediator of genetic and environmental programming during development
Kristy R. Howell, Amanda J. Law
Schizophrenia Research (2019) Vol. 217, pp. 95-104
Open Access | Times Cited: 25
Variable number tandem repeats – Their emerging role in sickness and health
Jack N.G. Marshall, Ana Illera Lopez, Abigail L. Pfaff, et al.
Experimental Biology and Medicine (2021) Vol. 246, Iss. 12, pp. 1368-1376
Open Access | Times Cited: 19
Revisiting tandem repeats in psychiatric disorders from perspectives of genetics, physiology, and brain evolution
Xiao Xiao, Chuyi Zhang, Zhuohua Zhang, et al.
Molecular Psychiatry (2021) Vol. 27, Iss. 1, pp. 466-475
Closed Access | Times Cited: 16
An Insight into the microRNAs Associated with Arteriovenous and Cavernous Malformations of the Brain
Ioan Alexandru Florian, Andrei Buruiană, Teodora Larisa Timiș, et al.
Cells (2021) Vol. 10, Iss. 6, pp. 1373-1373
Open Access | Times Cited: 15
The MIR137 VNTR rs58335419 Is Associated With Cognitive Impairment in Schizophrenia and Altered Cortical Morphology
Ebrahim Mahmoudi, Joshua Atkins, Yann Quidé, et al.
Schizophrenia Bulletin (2020) Vol. 47, Iss. 2, pp. 495-504
Open Access | Times Cited: 13
MicroRNA binding site variation is enriched in psychiatric disorders
Michael P. Geaghan, William R. Reay, Murray J. Cairns
Human Mutation (2022) Vol. 43, Iss. 12, pp. 2153-2169
Open Access | Times Cited: 8
A Study of Association of the MIR137 VNTR rs58335419 with Schizophrenia
Г. И. Коровайцева, И. В. Олейчик, Т. В. Лежейко, et al.
Russian Journal of Genetics (2024) Vol. 60, Iss. 2, pp. 192-198
Closed Access | Times Cited: 1
Schizophrenia risk-associated SNPs affect expression of microRNA 137 host gene: a postmortem study
Ningping Feng, Ajeet Mandal, Ananya Jambhale, et al.
Human Molecular Genetics (2024)
Closed Access | Times Cited: 1
A single-nucleotide polymorphism induced alternative splicing in Tacr3 involves in hypoxic-ischemic brain damage
Lu‐Lu Xue, Fang Wang, Liu‐Lin Xiong, et al.
Brain Research Bulletin (2019) Vol. 154, pp. 106-115
Open Access | Times Cited: 7
Enhancer Function of MicroRNA-3681 Derived from Long Terminal Repeats Represses the Activity of Variable Number Tandem Repeats in the 3' UTR of
Hee-Eun Lee, Sang-Je Park, Jae‐Won Huh, et al.
Molecules and Cells (2020) Vol. 43, Iss. 7, pp. 607-618
Closed Access | Times Cited: 7
Significant Association of Variable Number Tandem Repeat Polymorphism rs58335419 in the MIR137 Gene With the Risk of Gastric and Colon Cancers
Pegah Jafari, Sedighe Baghernia, Mehdi Moghanibashi, et al.
British Journal of Biomedical Science (2022) Vol. 79
Open Access | Times Cited: 5
Downregulating EVA1C exerts the potential to promote neuron growth after neonatal hypoxic‐ischemic encephalopathy injury associated with alternative splicing
Yue Hu, Rong Rong, Yi Wang, et al.
Ibrain (2022) Vol. 8, Iss. 4, pp. 481-491
Open Access | Times Cited: 4
RNA epitranscriptomics dysregulation: A major determinant for significantly increased risk of ASD pathogenesis
Athanasios Beopoulos, Manuel Géa, Alessio Fasano, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 2
Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences
Marzieh Eslami Rasekh, Yözen Hernández, Samantha D. Drinan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 3
Rediscovering tandem repeat variation in schizophrenia: challenges and opportunities
Rebecca Birnbaum
Translational Psychiatry (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 1
A study of association of the VNTR MIR-137 rs58335419 with schizophrenia
Г. И. Коровайцева, И. В. Олейчик, Т. В. Лежейко, et al.
Генетика (2024) Vol. 60, Iss. 2, pp. 63-69
Closed Access
Genetic Variation in Microrna-423 and Microrna 137 Genes among Patients with Breast Cancer
Nahidah Kzar Madhloom
Journal of Prevention Diagnosis and Management of Human Diseases (2024), Iss. 51, pp. 20-31
Closed Access
A polymorphic transcriptional regulatory domain in the amyotrophic lateral sclerosis risk gene CFAP410 correlates with differential isoform expression
Jack N.G. Marshall, Alexander Fröhlich, Li Li, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 2
MicroRNA binding site variation is enriched in psychiatric disorders
Michael P. Geaghan, William R. Reay, Murray J. Cairns
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access
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