OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Functional screening of GATOR1 complex variants reveals a role for mTORC1 deregulation in FCD and focal epilepsy
Ruby Dawson, Alvaro F. Nieto Guil, Louise J. Robertson, et al.
Neurobiology of Disease (2019) Vol. 134, pp. 104640-104640
Open Access | Times Cited: 41

Showing 26-50 of 41 citing articles:

Clinical phenotype and genotype of NPRL2-related epilepsy: Four cases reports and literature review
Hongwei Zhang, Jie Deng, Zaifen Gao, et al.
Seizure (2023) Vol. 116, pp. 100-106
Closed Access | Times Cited: 2

Neuroimaging and genetic characteristics of malformation of cortical development due to mTOR pathway dysregulation: clues for the epileptogenic lesions and indications for epilepsy surgery
Nicola Specchio, Chiara Pepi, Luca De Palma, et al.
Expert Review of Neurotherapeutics (2021) Vol. 21, Iss. 11, pp. 1333-1345
Closed Access | Times Cited: 5

Neurophysiological assessment of cortical activity in DEPDC5- and NPRL3-related epileptic mTORopathies
Madora Mabika, Kristian Agbogba, Samantha Côté, et al.
Orphanet Journal of Rare Diseases (2023) Vol. 18, Iss. 1
Open Access | Times Cited: 1

Modeling genetic mosaicism of the mammalian target of rapamycin pathway in the cerebral cortex
David M. Feliciano
Frontiers in Mammal Science (2023) Vol. 2
Open Access | Times Cited: 1

Functional analysis of the epilepsy gene Pcdh19 using a novel GFP-reporter mouse model
Stefka Mincheva-Tasheva, Michaela Scherer, Louise J. Robertson, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access

Pathogenic genes implicated in sleep-related hypermotor epilepsy: a research progress update
Yufang Yang, Jinmei Tuo, Jun Zhang, et al.
Frontiers in Neurology (2024) Vol. 15
Open Access

From Alpha-Thalassemia Trait to NPRL3-Related Epilepsy: A Genomic Diagnostic Odyssey
Maryam Nabavi Nouri, Lama Alandijani, Kalene van Engelen, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 836-836
Open Access

Brain Mosaicism in Epileptogenic Cortical Malformations
Théo Ribierre, Stéphanie Baulac
Oxford University Press eBooks (2024), pp. 874-880
Closed Access

mTOR in Acquired and Genetic Models of Epilepsy
Michael Y. Wong, Angélique Bordey, Steve C. Danzer
Oxford University Press eBooks (2024), pp. 65-74
Closed Access

Neuropathology and epilepsy surgery
Lucas Hoffmann, Ingmar Blümcke
Current Opinion in Neurology (2022) Vol. 35, Iss. 2, pp. 202-207
Closed Access | Times Cited: 2

Epilepsy and movement disorders
Moyra Smith
Elsevier eBooks (2021), pp. 195-224
Closed Access | Times Cited: 1

Clinical and genetic features of GATOR1 complex-associated epilepsy
Kaili Yin, Xingxing Lei, Zhaofen Yan, et al.
Journal of Medical Genetics (2023) Vol. 60, Iss. 8, pp. 784-790
Closed Access

Malformación del desarrollo cortical hemisférico
José Ángel Romero Figueroa, Jorge Alderete Berzabá, Ernesto Ramírez Navarrete
Anales Médicos de la Asociación Médica del Centro Médico ABC (2020) Vol. 65, Iss. 3, pp. 239-245
Open Access

Previous Page - Page 2

Scroll to top