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:
DLG3 variants caused X-linked epilepsy with/without neurodevelopmental disorders and the genotype-phenotype correlation
Yunyan He, Sheng Luo, Liang Jin, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 16
Open Access | Times Cited: 8
Yunyan He, Sheng Luo, Liang Jin, et al.
Frontiers in Molecular Neuroscience (2024) Vol. 16
Open Access | Times Cited: 8
Showing 8 citing articles:
Variants in EP400, encoding a chromatin remodeler, cause epilepsy with neurodevelopmental disorders
Sheng Luo, Pengyu Wang, Peng Zhou, et al.
The American Journal of Human Genetics (2024) Vol. 112, Iss. 1, pp. 87-105
Closed Access | Times Cited: 8
Sheng Luo, Pengyu Wang, Peng Zhou, et al.
The American Journal of Human Genetics (2024) Vol. 112, Iss. 1, pp. 87-105
Closed Access | Times Cited: 8
De Novo ACTB Variant Associated With Juvenile‐Onset Temporal Lobe Epilepsy With Favorable Outcomes
Hong-Jun Yan, Peng-Yu Wang, Wenhui Liu, et al.
Human Mutation (2025) Vol. 2025, Iss. 1
Open Access | Times Cited: 1
Hong-Jun Yan, Peng-Yu Wang, Wenhui Liu, et al.
Human Mutation (2025) Vol. 2025, Iss. 1
Open Access | Times Cited: 1
MDN1 variants cause susceptibility to epilepsy
Q. G. Wen, Dongming Zhang, Yan Ding, et al.
Acta Epileptologica (2025) Vol. 7, Iss. 1
Open Access | Times Cited: 1
Q. G. Wen, Dongming Zhang, Yan Ding, et al.
Acta Epileptologica (2025) Vol. 7, Iss. 1
Open Access | Times Cited: 1
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
Ye He, Yi-Chen Ye, Peng-Yu Wang, et al.
Seizure (2024) Vol. 123, pp. 1-8
Closed Access | Times Cited: 7
De novo TANC2 variants caused developmental and epileptic encephalopathy and epilepsy
Sheng Luo, Wenjun Zhang, Mi Jiang, et al.
Epilepsia (2025)
Closed Access
Sheng Luo, Wenjun Zhang, Mi Jiang, et al.
Epilepsia (2025)
Closed Access
De novo KCNK4 variant caused epilepsy with febrile seizures plus, neurodevelopmental abnormalities, and hypertrichosis
Hong-Jun Yan, Wenhui Liu, Min Xu, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Hong-Jun Yan, Wenhui Liu, Min Xu, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
De novo heterozygous missense variants inATP11Aare associated with refractory focal epilepsy
Zi-Long Ye, Nan-Xiang Shen, Xiang-Yun Luo, et al.
Journal of Medical Genetics (2025), pp. jmg-110540
Closed Access
Zi-Long Ye, Nan-Xiang Shen, Xiang-Yun Luo, et al.
Journal of Medical Genetics (2025), pp. jmg-110540
Closed Access
The P38MAPK Pathway Mediates the Destruction of the Blood–Brain Barrier in Anti-NMDAR Encephalitis Mice
Dayuan Lao, Zhuowei Gong, Taiyan Li, et al.
Neurochemical Research (2024) Vol. 50, Iss. 1
Open Access
Dayuan Lao, Zhuowei Gong, Taiyan Li, et al.
Neurochemical Research (2024) Vol. 50, Iss. 1
Open Access
