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:

A systematic review of adults with Dravet syndrome
Arunan Selvarajah, Quratulain Zulfiqar Ali, Paula Marques, et al.
Seizure (2021) Vol. 87, pp. 39-45
Open Access | Times Cited: 52

Showing 26-50 of 52 citing articles:

Persistent ∆FosB expression limits recurrent seizure activity and provides neuroprotection in the dentate gyrus of APP mice
Gabriel S. Stephens, Jin Park, Andrew L. Eagle, et al.
Progress in Neurobiology (2024) Vol. 237, pp. 102612-102612
Closed Access | Times Cited: 2

Stiripentol Enteric Solid Dispersion-Loaded Effervescent Tablets: Enhanced Dissolution, Stability, and Absorption
Ying Wang, Siyuan Xu, Ziyue Xiao, et al.
AAPS PharmSciTech (2022) Vol. 23, Iss. 5
Closed Access | Times Cited: 9

Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox–Gastaut syndrome
Farah Qaiser, Tara Sadoway, Yue Yin, et al.
Brain Communications (2021) Vol. 3, Iss. 3
Open Access | Times Cited: 11

Comorbidities in Dravet Syndrome and Lennox–Gastaut Syndrome
Francesca Marchese, Simona Cappelletti, M. Filippini, et al.
SN Comprehensive Clinical Medicine (2021) Vol. 3, Iss. 10, pp. 2167-2179
Open Access | Times Cited: 10

Managing patients with intellectual disability and epilepsy in the acute medical setting
Shanika Samarasekera
Clinical Medicine (2024) Vol. 24, Iss. 2, pp. 100039-100039
Open Access | Times Cited: 1

A high seizure burden increases several prostaglandin species in the hippocampus of a Scn1a mouse model of Dravet syndrome
Cilla Zhou, Vaishali Satpute, Ka Lai Yip, et al.
Prostaglandins & Other Lipid Mediators (2024) Vol. 172, pp. 106836-106836
Closed Access | Times Cited: 1

Epilepsies
Amy McTague, Ingrid E. Scheffer, Dimitri M. Kullmann, et al.
Handbook of clinical neurology (2024), pp. 157-184
Closed Access | Times Cited: 1

Caregiver burden and therapeutic needs in Dravet syndrome - a national UK cross-sectional questionnaire study
Erin Freeman-Jones, Galia Wilson, Claire Eldred, et al.
European Journal of Paediatric Neurology (2024) Vol. 53, pp. 138-143
Closed 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

Personalization of SUDEP risk: A survey of transient subclinical comorbid changes
Kristina A. Simeone, Dawn M. Martenz, Shruthi H. Iyer, et al.
Epilepsy Research (2023) Vol. 199, pp. 107259-107259
Closed Access | Times Cited: 3

Inherited SCN1A missense mutation in a Dravet Syndrome family: Neuropathological correlation, family screening and implications for adult carriers
Alba Sierra‐Marcos, Roser Ribosa‐Nogué, Nuria Vidal‐Robau, et al.
Epilepsy Research (2023) Vol. 199, pp. 107266-107266
Closed Access | Times Cited: 3

Prevalence and healthcare resource utilization of patients with Dravet syndrome: Retrospective linkage cohort study
William Owen Pickrell, F Guelfucci, Monique Martin, et al.
Seizure (2022) Vol. 99, pp. 159-163
Open Access | Times Cited: 4

Evaluating adult care in Dravet syndrome upon transferring from pediatrics in the U.S.: A caregiver-based survey study
Fábio A. Nascimento, Veronica Hood, Samantha V. Yap, et al.
Epilepsy & Behavior (2023) Vol. 147, pp. 109368-109368
Open Access | Times Cited: 2

Developmental and Epileptic Encephalopathies in Adults
Carolina Gorodetsky, Alfonso Fasano
Neurology (2022) Vol. 99, Iss. 3, pp. 89-91
Closed Access | Times Cited: 3

EEG band power and phase‐amplitude coupling in patients with Dravet syndrome
Joanne Hall, Shahid Bashir, Melissa Tsuboyama, et al.
Annals of the Child Neurology Society (2024) Vol. 2, Iss. 2, pp. 92-105
Open Access

Are We Doing Enough to Prevent SUDEP?
Danielle M. Andrade
Epiliepsy currents/Epilepsy currents (2024) Vol. 24, Iss. 4, pp. 242-244
Open Access

Eficácia do canabidiol no manejo da Síndrome de Dravet em pacientes pediátricos: uma revisão integrativa
Martha de Araujo Medeiros Pereira, Maria Clara Leite dos Santos, Maria Luísa Vieira Cuyabano Leite, et al.
Contribuciones a las Ciencias Sociales (2024) Vol. 17, Iss. 8, pp. e9083-e9083
Open Access

The profile of social communication in Dravet syndrome
Borja Laña, Nerea Crespo-Eguílaz, Rocío Sánchez‐Carpintero
Epilepsy & Behavior (2024) Vol. 159, pp. 110007-110007
Open Access

Antiepileptic Stiripentol May Influence Bones
Agnieszka Matuszewska, Beata Nowak, Anna Nikodem, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 13, pp. 7162-7162
Open Access | Times Cited: 3

SCN1A and Dravet syndrome
Richard Rosch, Ethan M. Goldberg
Elsevier eBooks (2022), pp. 43-63
Open Access | Times Cited: 2

Broadening Neurologic Manifestations in Adult Patients With Dravet Syndrome
Shoji Tsuji
Neurology (2022) Vol. 98, Iss. 22, pp. 913-914
Closed Access | Times Cited: 1

Tratamientos empleados para el síndrome de Dravet
María Cielo Duran Guerrero, Juan Carlos Pozo Palacios
Revista Vive (2023) Vol. 6, Iss. 16, pp. 172-182
Open Access

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