Open Access Helper

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:

SCN1A‐related phenotypes: Epilepsy and beyond
Ingrid E. Scheffer, Rima Nabbout
Epilepsia (2019) Vol. 60, Iss. S3
Open Access | Times Cited: 195

Showing 26-50 of 195 citing articles:

Epilepsy Genetics and Precision Medicine in Adults: A New Landscape for Developmental and Epileptic Encephalopathies
Álvaro Beltrán‐Corbellini, Ángel Aledo‐Serrano, Rikke S. Møller, et al.
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 28
Epilepsy and Cognitive Impairment in Childhood and Adolescence: A Mini-Review
Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, Andrea Viggiano, et al.
Current Neuropharmacology (2022) Vol. 21, Iss. 8, pp. 1646-1665
Closed Access | Times Cited: 27
Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes
Amber Postma, Crista A. Minderhoud, Willem M. Otte, et al.
Epilepsy & Behavior (2024) Vol. 154, pp. 109726-109726
Open Access | Times Cited: 5
The Role of Glutamate and Blood–Brain Barrier Disruption as a Mechanistic Link between Epilepsy and Depression
Benjamin F. Gruenbaum, Antonia Schonwald, Matthew Boyko, et al.
Cells (2024) Vol. 13, Iss. 14, pp. 1228-1228
Open Access | Times Cited: 5
Dravet syndrome
Lieven Lagae
Current Opinion in Neurology (2020) Vol. 34, Iss. 2, pp. 213-218
Closed Access | Times Cited: 37
Impact of COVID-19 pandemic on pediatric patients with epilepsy – The caregiver perspective
Marina Trivisano, Nicola Specchio, Nicola Pietrafusa, et al.
Epilepsy & Behavior (2020) Vol. 113, pp. 107527-107527
Open Access | Times Cited: 33
Use of Zebrafish Models to Boost Research in Rare Genetic Diseases
Lucie Crouzier, Élodie M. Richard, Jo Sourbron, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 24, pp. 13356-13356
Open Access | Times Cited: 30
Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity
Stefania Scalise, Clara Zannino, Valeria Lucchino, et al.
Biomedicines (2022) Vol. 10, Iss. 5, pp. 1075-1075
Open Access | Times Cited: 20
Adenosine-A2A Receptor Signaling Plays a Crucial Role in Sudden Unexpected Death in Epilepsy
Hai‐Ying Shen, Sadie B. Baer, Raey Gesese, et al.
Frontiers in Pharmacology (2022) Vol. 13
Open Access | Times Cited: 20
Rare genetic brain disorders with overlapping neurological and psychiatric phenotypes
Kathryn J. Peall, Michael J. Owen, Jérémy Hall
Nature Reviews Neurology (2023) Vol. 20, Iss. 1, pp. 7-21
Closed Access | Times Cited: 13
SCN1A channelopathies: Navigating from genotype to neural circuit dysfunction
Alexander Bryson, Steven Petrou
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 12
ANK2 loss-of-function variants are associated with epilepsy, and lead to impaired axon initial segment plasticity and hyperactive network activity in hiPSC-derived neuronal networks
Maria W A Teunissen, Elly Lewerissa, Eline van Hugte, et al.
Human Molecular Genetics (2023) Vol. 32, Iss. 14, pp. 2373-2385
Open Access | Times Cited: 11
Vitamin B12 Ameliorates Pesticide-Induced Sociability Impairment in Zebrafish (Danio rerio): A Prospective Controlled Intervention Study
Madalina Andreea Robea, Ovidiu-Dumitru Ilie, Mircea Nicoară, et al.
Animals (2024) Vol. 14, Iss. 3, pp. 405-405
Open Access | Times Cited: 4
Integrative analysis of epilepsy-associated genes reveals expression-phenotype correlations
Wanhao Chi, Evangelos Kiskinis
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 4
Familial hemiplegic migraine
María Dolores Villar‐Martínez, David Moreno‐Ajona, Peter J. Goadsby
Handbook of clinical neurology (2024), pp. 135-144
Closed Access | Times Cited: 4
Autism and Migraine: An Unexplored Association?
Luigi Vetri
Brain Sciences (2020) Vol. 10, Iss. 9, pp. 615-615
Open Access | Times Cited: 31
Neurological Disorders and Risk of Arrhythmia
Joyce Bernardi, Kelly A. Aromolaran, Ademuyiwa S. Aromolaran
International Journal of Molecular Sciences (2020) Vol. 22, Iss. 1, pp. 188-188
Open Access | Times Cited: 30
Multi-omics in mesial temporal lobe epilepsy with hippocampal sclerosis: Clues into the underlying mechanisms leading to disease
Estela M. Bruxel, Danielle Bruno, Amanda M. do Canto, et al.
Seizure (2021) Vol. 90, pp. 34-50
Open Access | Times Cited: 27
Haploinsufficiency, Dominant Negative, and Gain-of-Function Mechanisms in Epilepsy: Matching Therapeutic Approach to the Pathophysiology
Gemma L. Carvill, Tyler Matheny, Jay R. Hesselberth, et al.
Neurotherapeutics (2021) Vol. 18, Iss. 3, pp. 1500-1514
Open Access | Times Cited: 27
Altered Expression of Ion Channels in White Matter Lesions of Progressive Multiple Sclerosis: What Do We Know About Their Function?
Francesca Boscia, Maria L. Elkjaer, Zsolt Illés, et al.
Frontiers in Cellular Neuroscience (2021) Vol. 15
Open Access | Times Cited: 25
Dravet Syndrome: Novel Approaches for the Most Common Genetic Epilepsy
Lori L. Isom, Kelly G. Knupp
Neurotherapeutics (2021) Vol. 18, Iss. 3, pp. 1524-1534
Open Access | Times Cited: 24
SCN1A gain‐of‐function mutation causing an early onset epileptic encephalopathy
Jérôme Clatot, Shridhar Parthasarathy, Stacey Cohen, et al.
Epilepsia (2022) Vol. 64, Iss. 5, pp. 1318-1330
Closed Access | Times Cited: 19
Epilepsy Characteristics in Neurodevelopmental Disorders: Research from Patient Cohorts and Animal Models Focusing on Autism Spectrum Disorder
Sukanya Chakraborty, Rrejusha Parayil, Shefali Mishra, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 18, pp. 10807-10807
Open Access | Times Cited: 17
Gastrointestinal and eating problems in SCN1A-related seizure disorders
Crista A. Minderhoud, Albert Postma, Floor E. Jansen, et al.
Epilepsy & Behavior (2023) Vol. 146, pp. 109361-109361
Open Access | Times Cited: 10
Caring for Children with Dravet Syndrome: Exploring the Daily Challenges of Family Caregivers
Jan Domaradzki, Dariusz Walkowiak
Children (2023) Vol. 10, Iss. 8, pp. 1410-1410
Open Access | Times Cited: 10

Scroll to top