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:
Phenotypic and Genotypic Characterization of NPRL2-Related Epilepsy: Two Case Reports and Literature Review
Yulin Sun, Lin Wan, Huimin Yan, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 6
Yulin Sun, Lin Wan, Huimin Yan, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 6
Showing 6 citing articles:
GATOR1 Mutations Impair PI3 Kinase-Dependent Growth Factor Signaling Regulation of mTORC1
Maéline Muller, Jasmine Bélanger, Imane Hadj-Aissa, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2068-2068
Open Access | Times Cited: 3
Maéline Muller, Jasmine Bélanger, Imane Hadj-Aissa, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 4, pp. 2068-2068
Open Access | Times Cited: 3
Clinical phenotypic and genotypic characterization of NPRL3-related epilepsy
Hongwei Zhang, Jie Deng, Xiaohui Wang, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 5
Hongwei Zhang, Jie Deng, Xiaohui Wang, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 5
Differential amino acid transporter expression in adult
Ymani Wright, Alissa Richmond Armstrong
PubMed (2024) Vol. 2024
Closed Access | Times Cited: 1
Ymani Wright, Alissa Richmond Armstrong
PubMed (2024) Vol. 2024
Closed Access | Times Cited: 1
Precision Medicine in Epilepsy Management; GET Application (Gene, Epilepsy, Treatment)
Ali A. Asadi‐Pooya
Clinical Neuropharmacology (2023)
Closed Access | Times Cited: 2
Ali A. Asadi‐Pooya
Clinical Neuropharmacology (2023)
Closed Access | Times Cited: 2
Clinical phenotype and genotype of NPRL2-related epilepsy: Four cases reports and literature review
Hongwei Zhang, Jie Deng, Zaifen Gao, et al.
Seizure (2023) Vol. 116, pp. 100-106
Closed Access | Times Cited: 2
Hongwei Zhang, Jie Deng, Zaifen Gao, et al.
Seizure (2023) Vol. 116, pp. 100-106
Closed Access | Times Cited: 2
Nitrogen Permease Regulator Like-2 (NPRL2) truncating mutation causes Ohtahara syndrome with incomplete penetrance: expanding the genotype-phenotype correlations
Xing Zhou, Fengying Chen, Xingguang Ye, et al.
Clinical Dysmorphology (2022)
Open Access | Times Cited: 1
Xing Zhou, Fengying Chen, Xingguang Ye, et al.
Clinical Dysmorphology (2022)
Open Access | Times Cited: 1
