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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:

Comprehensive investigation of the phenotype of MEF2C‐related disorders in human patients: A systematic review
Jessica A. Cooley Coleman, Sara M. Sarasua, Luigi Boccuto, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 12, pp. 3884-3894
Closed Access | Times Cited: 17

Showing 17 citing articles:

Relating enhancer genetic variation across mammals to complex phenotypes using machine learning
Irene M. Kaplow, Alyssa J. Lawler, Daniel E. Schäffer, et al.
Science (2023) Vol. 380, Iss. 6643
Open Access | Times Cited: 43
Epigenetic genes and epilepsy — emerging mechanisms and clinical applications
Karen M. J. van Loo, Gemma L. Carvill, Albert J. Becker, et al.
Nature Reviews Neurology (2022) Vol. 18, Iss. 9, pp. 530-543
Open Access | Times Cited: 40
MEF2C regulates NK cell effector functions through control of lipid metabolism
Joey H. Li, Adalia Zhou, Cassidy D. Lee, et al.
Nature Immunology (2024) Vol. 25, Iss. 5, pp. 778-789
Closed Access | Times Cited: 12
Developmental Disruption of Mef2c in Medial Ganglionic Eminence–Derived Cortical Inhibitory Interneurons Impairs Cellular and Circuit Function
Claire Ward, Kaoutsar Nasrallah, Duy Tran, et al.
Biological Psychiatry (2024) Vol. 96, Iss. 10, pp. 804-814
Closed Access | Times Cited: 5
Fatal encephalopathy and congenital heart defects with MEF2C‐related disorder
Yoshitaka Asagai, Naoya Morisada, Yasunobu Miki, et al.
Pediatrics International (2025) Vol. 67, Iss. 1
Closed Access
Neuronal lineage tracing from progenitors in human cortical organoids reveals mechanisms of neuronal production, diversity, and disease
Luke A. D. Bury, Shuai Fu, Anthony Wynshaw‐Boris
Cell Reports (2024) Vol. 43, Iss. 10, pp. 114862-114862
Closed Access | Times Cited: 3
Fusion‐positive salivary gland carcinomas
Alena Skálová, Martin Hyrcza, Tomáš Vaněček, et al.
Genes Chromosomes and Cancer (2021) Vol. 61, Iss. 5, pp. 228-243
Closed Access | Times Cited: 16
Clinical findings from the landmark MEF2C‐related disorders natural history study
Jessica A. Cooley Coleman, Sara M. Sarasua, Hannah W. Moore, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 6
Open Access | Times Cited: 11
A postnatal molecular switch drives the activity-dependent maturation of parvalbumin interneurons
Monika Moissidis, Leyla Abbasova, Rafael Alis, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 2
The Cell Adhesion Molecule L1 Interacts with Methyl CpG Binding Protein 2 via Its Intracellular Domain
Gabriele Loers, Ralf Kleene, María Girbés Mínguez, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3554-3554
Open Access | Times Cited: 9
Peripheral Auditory Nerve Impairment in a Mouse Model of Syndromic Autism
Nathan McChesney, Jeremy L. Barth, Jeffrey A. Rumschlag, et al.
Journal of Neuroscience (2022) Vol. 42, Iss. 42, pp. 8002-8018
Open Access | Times Cited: 8
Breakpoint analysis for cytogenetically balanced translocation revealed unexpected complex structural abnormalities and suggested the position effect for MEF2C
Takeaki Tamura, Keiko Shimojima Yamamoto, Taichi Imaizumi, et al.
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 6, pp. 1632-1638
Closed Access | Times Cited: 4
Developmental disruption ofMef2cin Medial Ganglionic Eminence-derived cortical inhibitory interneurons impairs cellular and circuit function
Claire Ward, Kaoutsar Nasrallah, Duy Tran, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
The function of Mef2c toward the development of excitatory and inhibitory cortical neurons
Claire Ward, Lucas Sjulson, Renata Batista‐Brito
Frontiers in Cellular Neuroscience (2024) Vol. 18
Open Access | Times Cited: 1
CRISPR‐based approaches for studying inborn errors of immunity
Joey H. Li
Clinical and Translational Medicine (2024) Vol. 14, Iss. 10
Open Access | Times Cited: 1
EARLY PHYSICAL THERAPY MEF2C HAPLOID DEFICIENCY SYNDROME (5Q14.3 MICRODELETION)
Eliso Murvanidze
World Science (2023), Iss. 2(80)
Open Access
Peripheral Auditory Nerve Impairment in a Mouse Model of Syndromic Autism
Nathan McChesney, Jeremy L. Barth, Jeffrey A. Rumschlag, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
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