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:

Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy
Michael G. Ricos, Bree Hodgson, Tommaso Pippucci, et al.
Annals of Neurology (2015) Vol. 79, Iss. 1, pp. 120-131
Closed Access | Times Cited: 214

Showing 1-25 of 214 citing articles:

mTOR Signaling in Growth, Metabolism, and Disease
Robert A. Saxton, David M. Sabatini
Cell (2017) Vol. 168, Iss. 6, pp. 960-976
Open Access | Times Cited: 6337

Epilepsy in adults
Roland D. Thijs, Rainer Surges, Terence J. O’Brien, et al.
The Lancet (2019) Vol. 393, Iss. 10172, pp. 689-701
Closed Access | Times Cited: 1577

Epilepsy
Orrin Devinsky, Annamaria Vezzani, Terence J. O’Brien, et al.
Nature Reviews Disease Primers (2018) Vol. 4, Iss. 1
Closed Access | Times Cited: 722

Sudden unexpected death in epilepsy: epidemiology, mechanisms, and prevention
Orrin Devinsky, Dale C. Hesdorffer, David J. Thurman, et al.
The Lancet Neurology (2016) Vol. 15, Iss. 10, pp. 1075-1088
Closed Access | Times Cited: 604

The mTOR signalling cascade: paving new roads to cure neurological disease
Peter B. Crino
Nature Reviews Neurology (2016) Vol. 12, Iss. 7, pp. 379-392
Closed Access | Times Cited: 312

Translation deregulation in human disease
Soroush Tahmasebi, Arkady Khoutorsky, Michael B. Mathews, et al.
Nature Reviews Molecular Cell Biology (2018) Vol. 19, Iss. 12, pp. 791-807
Open Access | Times Cited: 210

The landscape of epilepsy-related GATOR1 variants
Sara Baldassari, Fabienne Picard, Nienke E. Verbeek, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 2, pp. 398-408
Open Access | Times Cited: 202

The Genetics of Epilepsy
Piero Perucca, Melanie Bahlo, Samuel F. Berkovic
Annual Review of Genomics and Human Genetics (2020) Vol. 21, Iss. 1, pp. 205-230
Open Access | Times Cited: 169

The molecular basis of nutrient sensing and signalling by mTORC1 in metabolism regulation and disease
Claire Goul, Roberta Peruzzo, Roberto Zoncu
Nature Reviews Molecular Cell Biology (2023) Vol. 24, Iss. 12, pp. 857-875
Closed Access | Times Cited: 81

The Genetics of Tuberous Sclerosis Complex and Related mTORopathies: Current Understanding and Future Directions
Alice Man, Matteo Di Scipio, Shan Grewal, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 332-332
Open Access | Times Cited: 18

Review: Mechanistic target of rapamycin (mTOR) pathway, focal cortical dysplasia and epilepsy
Elise Marsan, Stéphanie Baulac
Neuropathology and Applied Neurobiology (2018) Vol. 44, Iss. 1, pp. 6-17
Open Access | Times Cited: 161

Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Epilepsia (2016) Vol. 57, Iss. 6, pp. 994-1003
Open Access | Times Cited: 156

Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy
Rikke S. Møller, Sarah Weckhuysen, Mathilde Chipaux, et al.
Neurology Genetics (2016) Vol. 2, Iss. 6
Open Access | Times Cited: 143

Circadian rhythm and epilepsy
Sofia Khan, Lino Nobili, Ramin Khatami, et al.
The Lancet Neurology (2018) Vol. 17, Iss. 12, pp. 1098-1108
Closed Access | Times Cited: 142

Pharmacogenomics in epilepsy
Simona Balestrini, Sanjay M. Sisodiya
Neuroscience Letters (2017) Vol. 667, pp. 27-39
Open Access | Times Cited: 134

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy
Melodie R. Winawer, Nicole G. Griffin, Jorge Samanamud, et al.
Annals of Neurology (2018) Vol. 83, Iss. 6, pp. 1133-1146
Open Access | Times Cited: 116

Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort
Anne Rochtus, Heather E. Olson, Lacey Smith, et al.
Epilepsia (2020) Vol. 61, Iss. 2, pp. 249-258
Open Access | Times Cited: 109

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

A mouse model of DEPDC5-related epilepsy: Neuronal loss of Depdc5 causes dysplastic and ectopic neurons, increased mTOR signaling, and seizure susceptibility
Christopher J. Yuskaitis, Brandon Jones, Rachel L. Wolfson, et al.
Neurobiology of Disease (2017) Vol. 111, pp. 91-101
Open Access | Times Cited: 102

Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsy
Piero Perucca, Ingrid E. Scheffer, A. Simon Harvey, et al.
Epilepsy Research (2017) Vol. 131, pp. 1-8
Closed Access | Times Cited: 99

Advances in epilepsy gene discovery and implications for epilepsy diagnosis and treatment
Joseph D. Symonds, Sameer M. Zuberi, Michael R. Johnson
Current Opinion in Neurology (2017) Vol. 30, Iss. 2, pp. 193-199
Closed Access | Times Cited: 96

Depdc5 knockout rat: A novel model of mTORopathy
Elise Marsan, Saeko Ishida, Adrien E. Schramm, et al.
Neurobiology of Disease (2016) Vol. 89, pp. 180-189
Open Access | Times Cited: 88

Genome-wide CRISPR-KO Screen Uncovers mTORC1-Mediated Gsk3 Regulation in Naive Pluripotency Maintenance and Dissolution
Meng Li, Jason Yu, Katarzyna Tilgner, et al.
Cell Reports (2018) Vol. 24, Iss. 2, pp. 489-502
Open Access | Times Cited: 87

Epilepsy in the mTORopathies: opportunities for precision medicine
Patrick B. Moloney, Gianpiero L. Cavalleri, Norman Delanty
Brain Communications (2021) Vol. 3, Iss. 4
Open Access | Times Cited: 87

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