
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:
Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting
Alina Esterhuizen, Nicki Tiffin, Gillian Riordan, et al.
Genetics in Medicine (2022) Vol. 25, Iss. 2, pp. 100333-100333
Open Access | Times Cited: 8
Alina Esterhuizen, Nicki Tiffin, Gillian Riordan, et al.
Genetics in Medicine (2022) Vol. 25, Iss. 2, pp. 100333-100333
Open Access | Times Cited: 8
Showing 8 citing articles:
Is Precision Therapy in Infantile-Onset Epileptic Encephalopathies Still Too Far to Call Upon?
Raffaele Falsaperla, Vincenzo Sortino, Piero Pavone
Applied Sciences (2025) Vol. 15, Iss. 5, pp. 2372-2372
Open Access
Raffaele Falsaperla, Vincenzo Sortino, Piero Pavone
Applied Sciences (2025) Vol. 15, Iss. 5, pp. 2372-2372
Open Access
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B. Howell, Susan M. White, Amy McTague, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Katherine B. Howell, Susan M. White, Amy McTague, et al.
npj Genomic Medicine (2025) Vol. 10, Iss. 1
Open Access
Comprehensive Genetic Diagnosis and Therapeutic Perspectives in 155 Children with Developmental and Epileptic Encephalopathy.
Roxane Van Heurck, Eva Hammar, Dorothée Ville, et al.
European Journal of Paediatric Neurology (2025)
Closed Access
Roxane Van Heurck, Eva Hammar, Dorothée Ville, et al.
European Journal of Paediatric Neurology (2025)
Closed Access
Precision medicine approaches in epilepsy: A systematic review of genetic markers and personalized treatment strategies
Aman Agarwal, Ravneet Kaur, Faiza Ashfaque, et al.
Precision Medical Sciences (2024) Vol. 13, Iss. 2, pp. 72-83
Open Access | Times Cited: 1
Aman Agarwal, Ravneet Kaur, Faiza Ashfaque, et al.
Precision Medical Sciences (2024) Vol. 13, Iss. 2, pp. 72-83
Open Access | Times Cited: 1
Exome sequencing in Nigerian children with early‐onset epilepsy syndromes
Ibitayo Abigail Ademuwagun, Yagoub Adam, Solomon O. Rotimi, et al.
Epilepsia Open (2024) Vol. 10, Iss. 1, pp. 222-232
Open Access | Times Cited: 1
Ibitayo Abigail Ademuwagun, Yagoub Adam, Solomon O. Rotimi, et al.
Epilepsia Open (2024) Vol. 10, Iss. 1, pp. 222-232
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
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
Diagnosis and Classification of Pediatric Epilepsy in Sub-Saharan Africa: A Comprehensive Review
Sofia Di Noia, Linda Bonezzi, Ilaria Accorinti, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 21, pp. 6396-6396
Open Access
Sofia Di Noia, Linda Bonezzi, Ilaria Accorinti, et al.
Journal of Clinical Medicine (2024) Vol. 13, Iss. 21, pp. 6396-6396
Open Access
Examples of diseases where appropriate therapies were discovered
Moyra Smith
Elsevier eBooks (2024), pp. 209-262
Closed Access
Moyra Smith
Elsevier eBooks (2024), pp. 209-262
Closed Access
Case report: Novel variants cause developmental and epileptic encephalopathy in three unrelated families from Mali
S. Bamba, L. N. Sidibé, Seybou Hassane Diallo, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access
S. Bamba, L. N. Sidibé, Seybou Hassane Diallo, et al.
Frontiers in Genetics (2024) Vol. 15
Open Access