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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:

Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy
Mandy Ho‐Yin Tsang, Gordon Ka‐Chun Leung, Alvin Chi‐Chung Ho, et al.
Epilepsia Open (2018) Vol. 4, Iss. 1, pp. 63-72
Open Access | Times Cited: 28

Showing 1-25 of 28 citing articles:

Epilepsy-Related Voltage-Gated Sodium Channelopathies: A Review
Luis Felipe Santos Menezes, Elias Ferreira Sabiá Júnior, Diogo Vieira Tibery, et al.
Frontiers in Pharmacology (2020) Vol. 11
Open Access | Times Cited: 111
Genetic testing for the epilepsies: A systematic review
Beth Rosen Sheidley, Jennifer Malinowski, Amanda Bergner, et al.
Epilepsia (2021) Vol. 63, Iss. 2, pp. 375-387
Closed Access | Times Cited: 92
Genetic diagnosis of infantile‐onset epilepsy in the clinic: Application of whole‐exome sequencing following epilepsy gene panel testing
Soo Yeon Kim, Se Song Jang, Hunmin Kim, et al.
Clinical Genetics (2020) Vol. 99, Iss. 3, pp. 418-424
Closed Access | Times Cited: 30
Exome sequencing in paediatric patients with movement disorders
Anna Ka‐Yee Kwong, Mandy Ho‐Yin Tsang, Jasmine Lee‐Fong Fung, et al.
Orphanet Journal of Rare Diseases (2021) Vol. 16, Iss. 1
Open Access | Times Cited: 22
Rare versus common diseases: a false dichotomy in precision medicine
Brian Hon‐Yin Chung, Jeffrey Fong Ting Chau, Gane Ka‐Shu Wong
npj Genomic Medicine (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 22
Genetically guided precision medicine clinical decision support tools: a systematic review
Darren K. Johnson, Guilherme Del Fiol, Kensaku Kawamoto, et al.
Journal of the American Medical Informatics Association (2024) Vol. 31, Iss. 5, pp. 1183-1194
Open Access | Times Cited: 3
Expanding the genetic and phenotypic spectrum of CHD2‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy
Beatrice De Maria, Simona Balestrini, Davide Mei, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 522-533
Open Access | Times Cited: 20
Diagnostic value of whole‐exome sequencing in Chinese pediatric‐onset neuromuscular patients
Mandy Ho‐Yin Tsang, Annie Ting Gee Chiu, Bernard M. H. Kwong, et al.
Molecular Genetics & Genomic Medicine (2020) Vol. 8, Iss. 5
Open Access | Times Cited: 20
Molecular Insights of Drug Resistance in Epilepsy: Multi-omics Unveil
Maanvi Dhureja, Pragya Chaturvedi, Anita Choudhary, et al.
Molecular Neurobiology (2024)
Closed Access | Times Cited: 2
Genetic Testing In Pediatric Epilepsy: Tools, Tips And Navigating The Traps
Sayoni Roy Chowdhury, Robyn Whitney, Rajesh RamachandranNair, et al.
Pediatric Neurology (2024) Vol. 157, pp. 42-49
Closed Access | Times Cited: 2
High Diagnostic Yield and Clinical Utility of Next-Generation Sequencing in Children with Epilepsy and Neurodevelopmental Delays: A Retrospective Study
Daniel Charouf, D. Miller, Laith Haddad, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 17, pp. 9645-9645
Open Access | Times Cited: 2
Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogenetics
Astrid J. Rodriguez‐Acevedo, Louisa G. Gordon, Nicola Waddell, et al.
Pharmacogenomics (2021) Vol. 22, Iss. 4, pp. 225-234
Closed Access | Times Cited: 14
Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies
Dan Sun, Yan Liu, Wei Cai, et al.
Frontiers in Pediatrics (2021) Vol. 9
Open Access | Times Cited: 13
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population
Mandy Ho‐Yin Tsang, Anna Ka‐Yee Kwong, Kate Lok-San Chan, et al.
Human Genomics (2020) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Exploring the genetic etiology of drug-resistant epilepsy: incorporation of exome sequencing into practice
Mojdeh Mahdiannasser, Ali Rashidi‐Nezhad, Reza Shervin Badv, et al.
Acta Neurologica Belgica (2022) Vol. 122, Iss. 6, pp. 1457-1468
Closed Access | Times Cited: 8
Genetics in Epilepsy
Luis A. Martinez, Yi‐Chen Lai, J. Lloyd Holder, et al.
Neurologic Clinics (2021) Vol. 39, Iss. 3, pp. 743-777
Closed Access | Times Cited: 8
Functional Evaluation and Genetic Landscape of Children and Young Adults Referred for Assessment of Bronchiectasis
Jeffrey Fong Ting Chau, Mianne Lee, Martin Man Chun Chui, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 4
Genetic factors and the risk of drug-resistant epilepsy in young children with epilepsy and neurodevelopment disability
Chien‐Heng Lin, I‐Ching Chou, Syuan‐Yu Hong
Medicine (2021) Vol. 100, Iss. 12, pp. e25277-e25277
Open Access | Times Cited: 5
Synchronous heart rate reduction with suppression‐burst pattern in KCNT1‐related developmental and epileptic encephalopathies
Kaoru Yamamoto, Shimpei Baba, Takashi Saito, et al.
Epilepsia Open (2023) Vol. 8, Iss. 2, pp. 651-658
Open Access | Times Cited: 1
Genetically Guided Precision Medicine Clinical Decision Support Tools: A Systematic Review
Darren K. Johnson, Guilherme Del Fiol, Kensaku Kawamoto, et al.
medRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 1
Case report: Diagnosis of a patient with Sifrim–Hitz–Weiss syndrome, development and epileptic encephalopathy-14, and medium chain acyl-CoA dehydrogenase deficiency
Naim Zeka, Eris Zeka, Esra Zhubi, et al.
Frontiers in Pediatrics (2023) Vol. 11
Open Access | Times Cited: 1
Approaches for the discovery of drugs that target K Na 1.1 channels in KCNT1-associated epilepsy
Barbara Miziak, Stanisław J. Czuczwar
Expert Opinion on Drug Discovery (2022) Vol. 17, Iss. 12, pp. 1313-1328
Closed Access | Times Cited: 1
Genetics in epilepsy, Dravet and SUDEP: A systematic review
Paulo Henrique Pires de Aguiar, Mellina Stoianov Rocha, edro Henrique Avi, et al.
Journal of Neurology & Stroke (2019) Vol. 9, Iss. 5
Open Access
Febrile seizures, not so benign
Amit Vatkar, Saxena Amit, Pallavi Wadhawan, et al.
International Journal of Paediatrics and Geriatrics (2022) Vol. 5, Iss. 1, pp. 01-05
Open Access
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