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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:

Widespread genomic influences on phenotype in Dravet syndrome, a ‘monogenic’ condition
Helena Martins Custodio, Lisa M. Clayton, Ravishankara Bellampalli, et al.
Brain (2023) Vol. 146, Iss. 9, pp. 3885-3897
Open Access | Times Cited: 33

Showing 26-50 of 33 citing articles:

Italian report on RARE epilepsies (i‐RARE): A consensus on multidisciplinarity
Antonella Riva, Antonietta Coppola, Francesca Bisulli, et al.
Epilepsia Open (2024) Vol. 9, Iss. 5, pp. 1857-1867
Open Access | Times Cited: 1
Adult phenotypes of genetic developmental and epileptic encephalopathies
Angeliki Vakrinou, Susanna Pagni, James D. Mills, et al.
Brain Communications (2024) Vol. 7, Iss. 1
Open Access | Times Cited: 1
Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events
Henrike Heyne, Fanny‐Dhelia Pajuste, Julian Wanner, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 3
Response to Singh et al. 2023: It is premature for a unified hypothesis of sudden unexpected death in epilepsy: A great amount of research is still needed to understand the multisystem cascade
Carl L. Faingold, Huajun Feng
Epilepsia (2023) Vol. 64, Iss. 9, pp. 2256-2259
Open Access | Times Cited: 1
Clinical phenotypes of developmental and epileptic encephalopathy-related recurrent KCNH5 missense variant p.R327H in Chinese children
Sheng Huang, Chunhui Hu, Min Zhong, et al.
Epilepsy & Behavior Reports (2024) Vol. 26, pp. 100671-100671
Open Access
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
Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina
Roberto Caraballo, Gabriel Veneruzzo, Mariana Loos, et al.
Journal of Pediatric Epilepsy (2024) Vol. 13, Iss. 02, pp. 031-039
Closed Access
Big data research is everyone's research—Making epilepsy data science accessible to the global community: Report of the ILAE big data commission
Colin B. Josephson, Eleonora Aronica, Sándor Beniczky, et al.
Epileptic Disorders (2024)
Open Access
Co-Occurrence of Variants in 3 Genes in a Patient with Congenital Skeletal Dysplasia and Cardiac Anomalies: Diagnostic Challenge Posed by a Blended Phenotype
Pratibha Nair, Sami Bizzari, Cybel Mehawej, et al.
Molecular Syndromology (2024), pp. 1-10
Closed Access
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