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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:

Impact of Genetic Testing on Therapeutic Decision-Making in Childhood-Onset Epilepsies—a Study in a Tertiary Epilepsy Center
Allan Bayat, Christina Fenger, Tanya Ramdal Techlo, et al.
Neurotherapeutics (2022) Vol. 19, Iss. 4, pp. 1353-1367
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Evaluation of the feasibility, diagnostic yield, and clinical utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): an international, multicentre, pilot cohort study
Alissa M. D’Gama, Sarah Mulhern, Beth Rosen Sheidley, et al.
The Lancet Neurology (2023) Vol. 22, Iss. 9, pp. 812-825
Open Access | Times Cited: 42
Epilepsies with onset during the first year of life: A prospective study on syndromes, etiologies, and outcomes
Henna Jonsson, Eija Gaily, Susanna Stjerna, et al.
Epilepsia Open (2024) Vol. 9, Iss. 4, pp. 1393-1405
Open Access | Times Cited: 4
Novel De Novo Intronic Variant of SYNGAP1 Associated With the Neurodevelopmental Disorders
Wuming Xie, Baoqiong Liao, Mei Shuai, et al.
Molecular Genetics & Genomic Medicine (2025) Vol. 13, Iss. 2
Open Access
Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals
Olivia J. Henry, Sofia Ygberg, Michela Barbaro, et al.
Epilepsia (2025)
Open Access
Genetic etiology of 283 Chinese individuals with epilepsy using copy number variation sequencing and whole exome sequencing: A single-center cohort study
Junji Hu, Xin Min, Jinxiu Liu, et al.
Research Square (Research Square) (2025)
Closed Access
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus
Danielle deCampo, Julie Xian, Alexis Karlin, et al.
Frontiers in Neurology (2023) Vol. 14
Open Access | Times Cited: 9
Solving the unsolved genetic epilepsies: Current and future perspectives
Katrine M. Johannesen, Zeynep Tümer, Sarah Weckhuysen, et al.
Epilepsia (2023) Vol. 64, Iss. 12, pp. 3143-3154
Open Access | Times Cited: 8
Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach
Barbara Castellotti, Francesca Ragona, Elena Freri, et al.
Epilepsia Open (2024)
Open Access | Times Cited: 3
From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practice
Matthias De Wachter, An‐Sofie Schoonjans, Sarah Weckhuysen, et al.
European Journal of Paediatric Neurology (2023) Vol. 48, pp. 46-60
Closed Access | Times Cited: 8
Pathogenic variants of human GABRA1 gene associated with epilepsy: A computational approach
Ayla Arslan
Heliyon (2023) Vol. 9, Iss. 9, pp. e20218-e20218
Open Access | Times Cited: 7
Genetic testing for unexplained epilepsy: A review of diagnostic approach, benefits, and referral algorithm
Alexis Karlin, Sarah Ruggiero, Mark P. Fitzgerald
Current problems in pediatric and adolescent health care (2024) Vol. 54, Iss. 8, pp. 101579-101579
Closed Access | Times Cited: 2
A retrospective review of reclassification of Variants of Uncertain Significance in a pediatric epilepsy cohort undergoing genetic panel testing.
Nitish Chourasia, Rohan Vaidya, Soham Sengupta, et al.
Pediatric Neurology (2024) Vol. 161, pp. 101-107
Closed Access | Times Cited: 2
Genetic testing in adults with neurologic disorders: indications, approach, and clinical impacts
Laynie Dratch, Meron Azage, Aaron F. Baldwin, et al.
Journal of Neurology (2023) Vol. 271, Iss. 2, pp. 733-747
Open Access | Times Cited: 6
From precision diagnosis to precision treatment in epilepsy
Katrine M. Johannesen
Nature Reviews Neurology (2022) Vol. 19, Iss. 2, pp. 69-70
Closed Access | Times Cited: 10
Hope in the uncertainties and certainty for parents of children with rare neurological disorders. Part I (of 3): Uncertainty
Elizabeth E. Palmer, Rani Sachdev, Erin Beavis, et al.
Journal of Paediatrics and Child Health (2022) Vol. 58, Iss. 10, pp. 1718-1721
Closed Access | Times Cited: 9
Pickering emulsion technology based on the concept of “the combination of medicine and adjuvant” to enhance the oxidation stability of volatile oils in solid preparations—taking Lingzhu Pulvis as an example
Lei Peng, Xiaofei Zhang, Dongyan Guo, et al.
RSC Advances (2022) Vol. 12, Iss. 42, pp. 27453-27462
Open Access | Times Cited: 7
Validation of targeted next-generation sequencing panels in a cohort of polish patients with epilepsy: assessing variable performance across clinical endophenotypes and uncovering novel genetic variants
Magdalena Badura‐Stronka, Katarzyna Wicher, Anna Winczewska‐Wiktor, et al.
Frontiers in Neurology (2024) Vol. 14
Open Access | Times Cited: 1
A retrospective study of the yield of next‐generation sequencing in the diagnosis of developmental and epileptic encephalopathies and epileptic encephalopathies in 0–12 years aged children at a single tertiary care hospital in South India
M Murthy, Bidisha Banerjee, Mitesh Shetty, et al.
Epileptic Disorders (2024) Vol. 26, Iss. 5, pp. 609-625
Closed Access | Times Cited: 1
ADGRL1 variants: From developmental and epileptic encephalopathy to genetic epilepsy with febrile seizures plus
Wenting Lei, Yu-Rong Xiong, Yongyuan Shi, et al.
Developmental Medicine & Child Neurology (2024)
Closed Access | Times Cited: 1
Predictive factors of genetic diagnosis and real‐life impact of next‐generation sequencing for children with epilepsy
Gustavo Moura da Mata Machado Ferreira Pinto, Solena Ziemer Kusma Fidalski, Mara Lúcia Schmitz Ferreira Santos, et al.
Epileptic Disorders (2023) Vol. 25, Iss. 5, pp. 724-730
Closed Access | Times Cited: 3
AGAP1-associated endolysosomal trafficking abnormalities link gene-environment interactions in a neurodevelopmental disorder
Sara A. Lewis, Somayeh Bakhtiari, Jacob Forstrom, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 2
Trends and hotspots in gene research of epilepsy in children: A review and bibliometric analysis from 2010 to 2022
Yu-Ling Tian, Xilian Zhang, Hanjiang Chen, et al.
Medicine (2023) Vol. 102, Iss. 30, pp. e34417-e34417
Open Access | Times Cited: 1
Utility of next generation sequencing in paediatric neurological disorders: experience from South Africa
Magriet van Niekerk, Shahida Moosa, Ronald van Toorn, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 10, pp. 1314-1318
Open Access
Navigating the Intersection of Technology and Depression Precision Medicine
M Burcu Irmak-Yazicioglu, Ayla Arslan
Advances in experimental medicine and biology (2024), pp. 401-426
Closed Access
Novel de novo intronic variant of SYNGAP1 associated with the neurodevelopmental disorders
Baoqiong Liao, Wuming Xie, Mei Shuai, et al.
Research Square (Research Square) (2024)
Closed Access
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