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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:

Novel and de novo mutations in pediatric refractory epilepsy
Jing Liu, Lili Tong, Shuangshuang Song, et al.
Molecular Brain (2018) Vol. 11, Iss. 1
Open Access | Times Cited: 86

Showing 26-50 of 86 citing articles:

Assorted dysfunctions of endosomal alkali cation/proton exchanger SLC9A6 variants linked to Christianson syndrome
Alina Ilie, Annie Boucher, Jae-Ok Park, et al.
Journal of Biological Chemistry (2020) Vol. 295, Iss. 20, pp. 7075-7095
Open Access | Times Cited: 16
Structural mapping of GABRB3 variants reveals genotype–phenotype correlations
Katrine M. Johannesen, Sumaiya Iqbal, Milena Guazzi, et al.
Genetics in Medicine (2021) Vol. 24, Iss. 3, pp. 681-693
Open Access | Times Cited: 15
Use of perampanel in children with refractory epilepsy of genetic aetiology
Rui Qu, Yuanyuan Dai, Xiangju Qu, et al.
Epileptic Disorders (2022) Vol. 24, Iss. 4, pp. 687-695
Closed Access | Times Cited: 10
The role of ATP1A3 gene in epilepsy: We need to know more
Shuang Zou, Yu‐Long Lan, Yiwei Gong, et al.
Frontiers in Cellular Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6
Neonatal Seizures Revisited
Konrad Kaminiów, Sylwia Kozak, Justyna Paprocka
Children (2021) Vol. 8, Iss. 2, pp. 155-155
Open Access | Times Cited: 14
Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogenetics
Astrid J. Rodriguez‐Acevedo, Louisa G. Gordon, Nicola Waddell, et al.
Pharmacogenomics (2021) Vol. 22, Iss. 4, pp. 225-234
Closed Access | Times Cited: 14
Molecular dynamic approach to predict thermo-mechanical properties of poly(butylene terephthalate)/CaCO3 nanocomposites
Mirsadegh Seyedzavvar, Cem Boğa, Samet Akar, et al.
Materials Today Communications (2021) Vol. 28, pp. 102602-102602
Closed Access | Times Cited: 14
GABRB3-related epilepsy: novel variants, clinical features and therapeutic implications
Ying Yang, Qi Zeng, Miaomiao Cheng, et al.
Journal of Neurology (2021) Vol. 269, Iss. 5, pp. 2649-2665
Closed Access | Times Cited: 14
A novel CACNA1A variant in a child with early stroke and intractable epilepsy
Franciska J. Gudenkauf, Mahshid S. Azamian, Jill V. Hunter, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 10
Open Access | Times Cited: 14
Clinical phenotype and genotype of children with GABAA receptor α1 subunit gene-related epilepsy
Linlin Zhang, Xinjie Liu
Frontiers in Neurology (2022) Vol. 13
Open Access | Times Cited: 8
Temperature instability of a mutation at a multidomain junction in Na,K-ATPase isoform ATP1A3 (p.Arg756His) produces a fever-induced neurological syndrome
Elena Arystarkhova, Mads S. Toustrup-Jensen, Rikke Holm, et al.
Journal of Biological Chemistry (2022) Vol. 299, Iss. 1, pp. 102758-102758
Open Access | Times Cited: 8
Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting
Alina Esterhuizen, Nicki Tiffin, Gillian Riordan, et al.
Genetics in Medicine (2022) Vol. 25, Iss. 2, pp. 100333-100333
Open Access | Times Cited: 8
Clinical and genetic characteristics of patients with Doose syndrome
Nodoka Hinokuma, Mitsuko Nakashima, Hideyuki Asai, et al.
Epilepsia Open (2020) Vol. 5, Iss. 3, pp. 442-450
Open Access | Times Cited: 12
High genetic burden in 163 Chinese children with status epilepticus
Tianqi Wang, Ji Wang, Yu Ma, et al.
Seizure (2020) Vol. 84, pp. 40-46
Open Access | Times Cited: 11
Clinical and Functional Features of Epilepsy-Associated In-Frame Deletion Variants in SCN1A
Jingyang Wang, Bin Tang, Wen-Xiang Sheng, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 7
Customized multigene panels in epilepsy: the best things come in small packages
Simona Pellacani, Claudia Dosi, Giulia Valvo, et al.
Neurogenetics (2019) Vol. 21, Iss. 1, pp. 1-18
Closed Access | Times Cited: 10
Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration
Tao Su, Meng-Long Chen, Lihong Liu, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 14
Open Access | Times Cited: 6
Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies—Data from a Romanian Cohort
Anca‐Lelia Riza, Ioana Streață, Eugenia Roza, et al.
Genes (2022) Vol. 13, Iss. 7, pp. 1253-1253
Open Access | Times Cited: 6
New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies
Pedro H.M. Magalhães, Helena Tadiello de Moraes, Maria Carolina Pedro Athié, et al.
Epilepsy & Behavior (2019) Vol. 121, pp. 106428-106428
Open Access | Times Cited: 9
Epilepsy panels in clinical practice: Yield, variants of uncertain significance, and treatment implications
Dylan Brock, Megan Abbott, L Reed, et al.
Epilepsy Research (2023) Vol. 193, pp. 107167-107167
Closed Access | Times Cited: 3
Glutamatergic Fate of Neural Progenitor Cells of Rats with Inherited Audiogenic Epilepsy
А. А. Naumova, E. A. Oleynik, E. V. Chernigovskaya, et al.
Brain Sciences (2020) Vol. 10, Iss. 5, pp. 311-311
Open Access | Times Cited: 8
Genetic Etiologies of Neonatal Seizures
Shagun Kaur, Kara Pappas
NeoReviews (2020) Vol. 21, Iss. 10, pp. e663-e672
Closed Access | Times Cited: 8
Genotype and phenotype spectrum of 10 children with STXBP1 gene-related encephalopathy and epilepsy
Meng Dong, Tianyu Zhang, Ruimei Hu, et al.
Frontiers in Pediatrics (2022) Vol. 10
Open Access | Times Cited: 5
Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients
Matías Juanes, Gabriel Veneruzzo, Mariana Loos, et al.
Epilepsy & Behavior (2020) Vol. 111, pp. 107322-107322
Closed Access | Times Cited: 7
Gene therapy as an emerging treatment for Scn2a mutation-induced autism spectrum disorders
Arkadeep Ghosh, Nitin Nadella, A Paula Monaghan-Nichols, et al.
Fundamental Research (2023) Vol. 4, Iss. 6, pp. 1401-1404
Open Access | Times Cited: 2

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