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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.

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Showing 1-25 of 29 citing articles:

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations
Dulcie Lai, Meethila Gade, Edward Yang, et al.
Brain (2022) Vol. 145, Iss. 8, pp. 2704-2720
Open Access | Times Cited: 57
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes
Ming‐Feng He, Lihong Liu, Sheng Luo, et al.
Journal of Medical Genetics (2024) Vol. 61, Iss. 7, pp. 652-660
Open Access | Times Cited: 13
DEPDC5-related epilepsy: A comprehensive review
Debopam Samanta
Epilepsy & Behavior (2022) Vol. 130, pp. 108678-108678
Closed Access | Times Cited: 37
CCDC22 variants caused X-linked focal epilepsy and focal cortical dysplasia
Ye He, Yi-Chen Ye, Peng-Yu Wang, et al.
Seizure (2024) Vol. 123, pp. 1-8
Closed Access | Times Cited: 7
ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus
Yang Tian, Qiong‐Xiang Zhai, Xiaojing Li, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 20
CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications
Xuelian Li, Zongjun Li, Xiaoyu Liang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 18
SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation
Sheng Luo, Xingguang Ye, Liang Jin, et al.
Frontiers in Molecular Neuroscience (2023) Vol. 16
Open Access | Times Cited: 11
Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery
Hao Wang, Wenwei Liu, Yuehua Zhang, et al.
Epilepsia Open (2023) Vol. 8, Iss. 3, pp. 969-979
Open Access | Times Cited: 10
Genotypic and clinical phenotypic analysis of DEPDC5 gene mutations
Baoguang Li, Zhenzhen Qu, Wenjuan Wu, et al.
Neurogenetics (2025) Vol. 26, Iss. 1
Closed Access
Editorial: Sub-molecular mechanism of genetic epilepsy
Wei‐Ping Liao, Qian Chen, Yuwu Jiang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 12
AFF2 Is Associated With X-Linked Partial (Focal) Epilepsy With Antecedent Febrile Seizures
Dongfang Zou, Bing Qin, Jie Wang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 11
DEPDC5 plays a vital role in epilepsy: Genotypic and phenotypic features in cohort and literature
Chunyu Gu, Xinping Wei, Dandan Yan, et al.
Epileptic Disorders (2024) Vol. 26, Iss. 3, pp. 341-349
Closed Access | Times Cited: 2
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
Xiao‐Rong Liu, Ting‐Ting Ye, Wenjun Zhang, et al.
CNS Neuroscience & Therapeutics (2021) Vol. 27, Iss. 10, pp. 1146-1156
Open Access | Times Cited: 14
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy
Shiyue Du, Sheng Zeng, Song Li, et al.
Science China Life Sciences (2023) Vol. 66, Iss. 9, pp. 2152-2166
Closed Access | Times Cited: 5
SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges
Wen‐Jun Bian, Zongjun Li, Jie Wang, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 9
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyria
Athina Ververi, Sara Zagaglia, Lara Menzies, et al.
Human Molecular Genetics (2022) Vol. 32, Iss. 4, pp. 580-594
Open Access | Times Cited: 8
Reply: UNC13B and focal epilepsy
Jing‐Da Qiao, Xin Li, Jia Li, et al.
Brain (2021) Vol. 145, Iss. 3, pp. e13-e16
Open Access | Times Cited: 7
ZFHX3variants cause childhood partial epilepsy and infantile spasms with favorable outcomes
Ming‐Feng He, Lihong Liu, Sheng Luo, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Gene-disease association: pathogenic potential/pathogenic feature assessment
Wei‐Ping Liao, Wen‐Jun Bian, Jie Wang, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 2
Gene-disease association: pathogenic potential/pathogenic feature assessment
Wen‐Jun Bian, Jie Wang, Bin Li, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 2
Pharmacogenetics in Epilepsy and Refractory Epilepsy
Liliana Czornyj, Jerónimo Auzmendi, Alberto Lazarowski
Springer eBooks (2023), pp. 177-206
Closed Access | Times Cited: 1
Evaluating the efficacy of a ketogenic diet in managing drug resistant paediatric DEDPC5-related epilepsy
Anna Winczewska‐Wiktor, Małgorzata Braszka, Mia Harada‐Laszlo, et al.
Epilepsy & Behavior (2023) Vol. 150, pp. 109535-109535
Closed Access | Times Cited: 1
A novel variation in DEPDC5 causing familial focal epilepsy with variable foci
Yanchi Wang, Wenbin Niu, Hao Shi, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
Sibling cases of DEPDC5-related developmental and epileptic encephalopathy successfully treated with lacosamide
Chiho Tokorodani, Ritsuo Nishiuchi, Fuyuki Miya, et al.
Brain and Development Case Reports (2024) Vol. 2, Iss. 4, pp. 100044-100044
Open 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
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