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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:

Advances in genetic testing and optimization of clinical management in children and adults with epilepsy
Marcello Scala, Amedeo Bianchi, Francesca Bisulli, et al.
Expert Review of Neurotherapeutics (2020) Vol. 20, Iss. 3, pp. 251-269
Closed Access | Times Cited: 62

Showing 1-25 of 62 citing articles:

Unraveling the enigma of new‐onset refractory status epilepticus: a systematic review of aetiologies
Simona Lattanzi, Markus Leitinger, Chiara Rocchi, et al.
European Journal of Neurology (2021) Vol. 29, Iss. 2, pp. 626-647
Open Access | Times Cited: 58
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy
Dianalee McKnight, Sara L. Bristow, Rebecca Truty, et al.
Neurology Genetics (2021) Vol. 8, Iss. 1
Open Access | Times Cited: 40
Characterizing sensitivity and coverage of clinical WGS as a diagnostic test for genetic disorders
Yan Sun, Fengxia Liu, Chunna Fan, et al.
BMC Medical Genomics (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 33
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings.
Dianalee McKnight, Sara L. Bristow, Rebecca Truty, et al.
(2022) Vol. 8, Iss. 1, pp. e650-e650
Open Access | Times Cited: 26
The current benefit of genome sequencing compared to exome sequencing in patients with developmental or epileptic encephalopathies
Anna Grether, Ivan Ivanovski, Martina Russo, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 5
Open Access | Times Cited: 13
[Efficacy and safety of perampanel add-on therapy in children with epilepsy of genetic etiology].
Jia-Qin Yi, Dan Sun
PubMed (2025) Vol. 27, Iss. 2, pp. 171-175
Closed Access
Identification of Novel Epilepsy Genetics and Development of Advanced Diagnostic Approaches
Ramakrishnan Veerabathiran, B K Iyshwarya
Brain Disorders (2025) Vol. 17, pp. 100202-100202
Open Access
Unlocking Genetic Clues
Antonella Riva, Pasquale Striano
Neurology Genetics (2025) Vol. 11, Iss. 3
Closed Access
The improvement in diagnostic yield of developmental and epileptic encephalopathy by the multi-omics sequential testing method
Shiwei Yang, Jiatong Liu, Yuan Quan, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2025) Vol. 1871, Iss. 6, pp. 167854-167854
Closed Access
DAG1 haploinsufficiency is associated with sporadic and familial isolated or pauci-symptomatic hyperCKemia
Monica Traverso, Serena Baratto, Michele Iacomino, et al.
European Journal of Human Genetics (2024)
Open Access | Times Cited: 3
Retrospective study on neonatal seizures in a tertiary center of northern Italy after ILAE classification: Incidence, seizure type, EEG and etiology
Robertino Dilena, Maria Takeko Molisso, Agnese De Carli, et al.
Epilepsy & Behavior (2024) Vol. 159, pp. 109971-109971
Open Access | Times Cited: 3
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project
Elisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, et al.
˜The œItalian Journal of Pediatrics/Italian journal of pediatrics (2020) Vol. 46, Iss. 1
Open Access | Times Cited: 27
Developmental and epileptic encephalopathy: Personal utility of a genetic diagnosis for families
Jennifer S. Jeffrey, Janet Leathem, Chontelle King, et al.
Epilepsia Open (2020) Vol. 6, Iss. 1, pp. 149-159
Open Access | Times Cited: 25
Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice
Antonela Blažeković, Kristina Gotovac, Sarah Meglaj, et al.
Genes (2022) Vol. 13, Iss. 8, pp. 1466-1466
Open Access | Times Cited: 14
Efficacy of perampanel in pediatric epilepsy with known and presumed genetic etiology
Pu Miao, Xueying Zhu, Wenqin Jin, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 10, Iss. 8, pp. 1374-1382
Open Access | Times Cited: 7
ARV1 Gene: A Novel Cause of Autosomal Recessive Cerebellar Ataxia with Elevated Alpha Fetoprotein
Mahesh Kamate, Thanuja Basavanagowda
The Cerebellum (2023) Vol. 23, Iss. 3, pp. 1239-1244
Open Access | Times Cited: 7
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing
Antonietta Coppola, S. Krithika, Michele Iacomino, et al.
Epilepsia (2023) Vol. 65, Iss. 3, pp. 779-791
Open Access | Times Cited: 7
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children
Nour Elkhateeb, Mahmoud Y. Issa, Hasnaa M. Elbendary, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 510-522
Closed Access | Times Cited: 2
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: 2
Targeted re-sequencing in malformations of cortical development: genotype-phenotype correlations
Andrea Accogli, Mariasavina Severino, Antonella Riva, et al.
Seizure (2020) Vol. 80, pp. 145-152
Open Access | Times Cited: 18
Clinical next generation sequencing in developmental and epileptic encephalopathies: Diagnostic relevance of data re-analysis and variants re-interpretation
Valeria Salinas, Nerina Martínez, Josefina Pérez Maturo, et al.
European Journal of Medical Genetics (2021) Vol. 64, Iss. 12, pp. 104363-104363
Closed Access | Times Cited: 15
ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration
Haiyan Yang, Hongmei Liao, Siyi Gan, et al.
Molecular Genetics & Genomic Medicine (2022) Vol. 10, Iss. 7
Open Access | Times Cited: 10
Clinical Utility of Exome Sequencing and Reinterpreting Genetic Test Results in Children and Adults With Epilepsy
Yongli Jiang, Changgeng Song, Yuanyuan Wang, et al.
Frontiers in Genetics (2020) Vol. 11
Open Access | Times Cited: 13
A Multi-Disciplinary Team Approach to Genomic Testing for Drug-Resistant Epilepsy Patients—The GENIE Study
Lata Vadlamudi, Carmen Bennett, Melanie Tom, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 14, pp. 4238-4238
Open Access | Times Cited: 8
Genetic diagnoses in pediatric patients with epilepsy and comorbid intellectual disability
Mei Yang, Bocheng Xu, Jiamin Wang, et al.
Epilepsy Research (2021) Vol. 170, pp. 106552-106552
Closed Access | Times Cited: 11
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