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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:

Malformations of cortical development
Rahul S. Desikan, A. James Barkovich
Annals of Neurology (2016) Vol. 80, Iss. 6, pp. 797-810
Open Access | Times Cited: 115

Showing 1-25 of 115 citing articles:

Definitions and classification of malformations of cortical development: practical guidelines
Mariasavina Severino, Ana Filipa Geraldo, Norbert Utz, et al.
Brain (2020) Vol. 143, Iss. 10, pp. 2874-2894
Open Access | Times Cited: 227
Positive Controls in Adults and Children Support That Very Few, If Any, New Neurons Are Born in the Adult Human Hippocampus
Shawn F. Sorrells, Mercedes F. Paredes, Zhuangzhi Zhang, et al.
Journal of Neuroscience (2021) Vol. 41, Iss. 12, pp. 2554-2565
Open Access | Times Cited: 125
Mechanisms of radial glia progenitor cell lineage progression
Robert Beattie, Simon Hippenmeyer
FEBS Letters (2017) Vol. 591, Iss. 24, pp. 3993-4008
Open Access | Times Cited: 119
Malformations of Cerebral Cortex Development: Molecules and Mechanisms
Gordana Juric‐Sekhar, Robert F. Hevner
Annual Review of Pathology Mechanisms of Disease (2019) Vol. 14, Iss. 1, pp. 293-318
Open Access | Times Cited: 103
Genes and Mechanisms Involved in the Generation and Amplification of Basal Radial Glial Cells
Maxime Penisson, Julia Ladewig, Richard Belvindrah, et al.
Frontiers in Cellular Neuroscience (2019) Vol. 13
Open Access | Times Cited: 89
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene
Jean Chemin, Karine Siquier-Pernet, Michaël Nicouleau, et al.
Brain (2018) Vol. 141, Iss. 7, pp. 1998-2013
Open Access | Times Cited: 87
New insights into a spectrum of developmental malformations related tomTORdysregulations: challenges and perspectives
Angelika Mühlebner, Anika Bongaarts, Harvey B. Sarnat, et al.
Journal of Anatomy (2019) Vol. 235, Iss. 3, pp. 521-542
Open Access | Times Cited: 80
Fetal Brain Development: Regulating Processes and Related Malformations
Z. Leibovitz, Tally Lerman‐Sagie, Leila Haddad
Life (2022) Vol. 12, Iss. 6, pp. 809-809
Open Access | Times Cited: 39
Synaptic Dysregulation Drives Hyperexcitability in Pyramidal Neurons Surrounding Freeze-Induced Neocortical Malformations in Rats
Sergey L. Malkin, Dmitry V. Amakhin, Elena B. Soboleva, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1423-1423
Open Access | Times Cited: 1
mTOR dysregulation and tuberous sclerosis-related epilepsy
Paolo Curatolo, Romina Moavero, Jackelien van Scheppingen, et al.
Expert Review of Neurotherapeutics (2018) Vol. 18, Iss. 3, pp. 185-201
Closed Access | Times Cited: 81
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis
Pamela Magini, Daphne J. Smits, Laura Vandervore, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 4, pp. 689-705
Open Access | Times Cited: 64
Cellular and Molecular Mechanisms Linking Human Cortical Development and Evolution
Baptiste Libé‐Philippot, Pierre Vanderhaeghen
Annual Review of Genetics (2021) Vol. 55, Iss. 1, pp. 555-581
Closed Access | Times Cited: 55
Dysregulation of Neurite Outgrowth and Cell Migration in Autism and Other Neurodevelopmental Disorders
Smrithi Prem, James H. Millonig, Emanuel DiCicco‐Bloom
Advances in neurobiology (2020), pp. 109-153
Closed Access | Times Cited: 51
Mechanisms of Development
Hans J. ten Donkelaar, Bernd Fritzsch
Springer eBooks (2023), pp. 77-169
Closed Access | Times Cited: 20
Stereoelectroencephalography and surgical outcome in polymicrogyria‐related epilepsy: A multicentric study
Louis Maillard, Laura Tassi, Fabricē Bartolomei, et al.
Annals of Neurology (2017) Vol. 82, Iss. 5, pp. 781-794
Open Access | Times Cited: 55
Usp11 controls cortical neurogenesis and neuronal migration through Sox11 stabilization
Shang-Yin Chiang, Hsin-Chieh Wu, Shu‐Yu Lin, et al.
Science Advances (2021) Vol. 7, Iss. 7
Open Access | Times Cited: 34
Using cortical organoids to understand the pathogenesis of malformations of cortical development
Kellen D. Winden, Isabel Gisser, Mustafa Şahin
Frontiers in Neuroscience (2025) Vol. 18
Open Access
Clonal lineage tracing and transcriptomics of cortical progenitor populations reveal maintenance of differentiation potential
Danyon Harkins, Shawar Ali, Teodora Tockovska, et al.
Stem Cell Reports (2025), pp. 102418-102418
Open Access
Behavioral Impairments in Rats with Focal Cortical Dysplasia Following Febrile Seizures
O. E. Zubareva, D. S. Sinyak, M. R. Subkhankulov, et al.
Journal of Evolutionary Biochemistry and Physiology (2025) Vol. 61, Iss. 1, pp. 285-297
Closed Access
Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
Meng‐Han Tsai, Haw-Yuan Cheng, Fang-Shin Nian, et al.
Acta Neuropathologica Communications (2020) Vol. 8, Iss. 1
Open Access | Times Cited: 33
Mutations in TP73 cause impaired mucociliary clearance and lissencephaly
Julia Wallmeier, Diana Bracht, Hessa S. Alsaif, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 7, pp. 1318-1329
Open Access | Times Cited: 27
Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis
Gillian V. Blayney, Eoghan Laffan, Preethi A. Jacob, et al.
Prenatal Diagnosis (2023) Vol. 44, Iss. 4, pp. 422-431
Open Access | Times Cited: 11
Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development
Loïc Broix, Laure Asselin, Carla G. Silva, et al.
Human Molecular Genetics (2017) Vol. 27, Iss. 2, pp. 224-238
Open Access | Times Cited: 36
DEPDC5 and NPRL3 modulate cell size, filopodial outgrowth, and localization of mTOR in neural progenitor cells and neurons
Philip H. Iffland, Marianna Baybis, Allan E. Barnes, et al.
Neurobiology of Disease (2018) Vol. 114, pp. 184-193
Open Access | Times Cited: 34
Roots of the Malformations of Cortical Development in the Cell Biology of Neural Progenitor Cells
Chiara Ossola, Nereo Kalebic
Frontiers in Neuroscience (2022) Vol. 15
Open Access | Times Cited: 16
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