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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:

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

Showing 12 citing articles:

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Madelyn A. Gillentine, Tianyun Wang, Kendra Hoekzema, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 82
SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis
Jiangwei Ding, Xinxiao Li, Haiyan Tian, et al.
Frontiers in Neurology (2021) Vol. 12
Open Access | Times Cited: 70
Epilepsy with myoclonic-atonic seizures: an update on genetic causes, nosological limits, and treatment strategies
Renzo Guerrini, Ingrid E. Scheffer, Simona Balestrini
The Lancet Neurology (2025) Vol. 24, Iss. 4, pp. 348-360
Closed Access
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder
Francesca Semino, Julian Schröter, Marjolein H. Willemsen, et al.
Human Mutation (2021) Vol. 42, Iss. 9, pp. 1094-1100
Open Access | Times Cited: 17
A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation
Tatsuo Mori, Masamune Sakamoto, Takahiro Tayama, et al.
Brain and Development (2023) Vol. 45, Iss. 7, pp. 395-400
Open Access | Times Cited: 6
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy
Se Hee Kim, Jieun Seo, Soon Sung Kwon, et al.
Epilepsia (2023) Vol. 65, Iss. 3, pp. 766-778
Closed Access | Times Cited: 6
Genetic Epilepsy Syndromes
Kenneth A. Myers
CONTINUUM Lifelong Learning in Neurology (2022) Vol. 28, Iss. 2, pp. 339-362
Closed Access | Times Cited: 9
Epilepsy with myoclonic-atonic seizures, also known as Doose syndrome: Modification of the diagnostic criteria
Hirokazu Oguni
European Journal of Paediatric Neurology (2021) Vol. 36, pp. 37-50
Closed Access | Times Cited: 8
Genetic mechanisms in generalized epilepsies
Xiaoqian Wang, Xueyi Rao, Jia Zhang, et al.
Acta Epileptologica (2023) Vol. 5, Iss. 1
Open Access | Times Cited: 2
Parent-Reported Sleep Profile of Children With Early-Life Epilepsies
Gita Gupta, Louis T. Dang, Louise M. O’Brien, et al.
Pediatric Neurology (2021) Vol. 128, pp. 9-15
Open Access | Times Cited: 4
Recurrent Bilateral Pleural and Pericardial Effusions due to Tuberculosis in a Child With Doose Syndrome: A Case Report
Carla Melisa Leon-Viveros, Julio Cesar Ramirez-Reyes, Daniel Juárez-Rebollar, et al.
International Journal of Clinical Pediatrics (2022) Vol. 11, Iss. 1, pp. 14-19
Open Access | Times Cited: 1
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