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:
Identification of five novel SCN1A variants
Baitao Zeng, Haoyi Zhang, Qing Lu, et al.
Frontiers in Behavioral Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Baitao Zeng, Haoyi Zhang, Qing Lu, et al.
Frontiers in Behavioral Neuroscience (2023) Vol. 17
Open Access | Times Cited: 7
Showing 7 citing articles:
Mate-pair sequencing assisted prenatal counseling for a rare complex chromosomal rearrangement carrier
Lu Wan, Zeng Baitao, Tan Yuxin, et al.
Human Molecular Genetics (2025)
Open Access
Lu Wan, Zeng Baitao, Tan Yuxin, et al.
Human Molecular Genetics (2025)
Open Access
Evaluation of burden of SCN1A pathogenicity in North Indian children with Dravet syndrome
Sandeep Negi, Prateek Bhatia, Anupriya Kaur, et al.
Seizure (2024) Vol. 122, pp. 10-18
Closed Access | Times Cited: 1
Sandeep Negi, Prateek Bhatia, Anupriya Kaur, et al.
Seizure (2024) Vol. 122, pp. 10-18
Closed Access | Times Cited: 1
Association of SCN1A Polymorphisms rs3812718 and rs2298771 with Epilepsy
Martha-Spyridoula Katsarou, Anna Siatouni, Danae Tsikrika, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1224-1224
Open Access | Times Cited: 1
Martha-Spyridoula Katsarou, Anna Siatouni, Danae Tsikrika, et al.
Genes (2024) Vol. 15, Iss. 9, pp. 1224-1224
Open Access | Times Cited: 1
SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations
Danai Veltra, Virginia Theodorou, Marina Katsalouli, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 11, pp. 5644-5644
Open Access
Danai Veltra, Virginia Theodorou, Marina Katsalouli, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 11, pp. 5644-5644
Open Access
Lethal Complications and Complex Genotypes in Shwachman Diamond Syndrome: Report of a Family with Recurrent Neonatal Deaths and a Case-Based Brief Review of the Literature
Danai Veltra, Nikolaos M. Marinakis, Ioannis Kotsios, et al.
Children (2024) Vol. 11, Iss. 6, pp. 705-705
Open Access
Danai Veltra, Nikolaos M. Marinakis, Ioannis Kotsios, et al.
Children (2024) Vol. 11, Iss. 6, pp. 705-705
Open Access
SCN1A rs6732655A/T polymorphism: Diagnostic and therapeutic insights for drug-resistant epilepsy
Aroop Viswas, Pradeep Kumar Dabla, Dharmsheel Shrivastav, et al.
World Journal of Experimental Medicine (2024) Vol. 14, Iss. 3
Open Access
Aroop Viswas, Pradeep Kumar Dabla, Dharmsheel Shrivastav, et al.
World Journal of Experimental Medicine (2024) Vol. 14, Iss. 3
Open Access
Genes to therapy: a comprehensive literature review of whole-exome sequencing in neurology and neurosurgery
Joecelyn Kirani Tan, Wireko Andrew Awuah, Arjun Ahluwalia, et al.
European journal of medical research (2024) Vol. 29, Iss. 1
Open Access
Joecelyn Kirani Tan, Wireko Andrew Awuah, Arjun Ahluwalia, et al.
European journal of medical research (2024) Vol. 29, Iss. 1
Open Access
