
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:
Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy
Bin Mao, Na Lin, Danhua Guo, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6
Bin Mao, Na Lin, Danhua Guo, et al.
Frontiers in Neuroscience (2023) Vol. 17
Open Access | Times Cited: 6
Showing 6 citing articles:
Congenital muscular dystrophies and myopathies: the leading cause of genetic muscular disorders in eleven Chinese families
Bin Mao, Xiaoling Cai, Na Lin, et al.
BMC Musculoskeletal Disorders (2025) Vol. 26, Iss. 1
Open Access
Bin Mao, Xiaoling Cai, Na Lin, et al.
BMC Musculoskeletal Disorders (2025) Vol. 26, Iss. 1
Open Access
Setting the Stage for Treatment of Aminoacyl‐tRNA Synthetase (ARS )1‐Deficiencies: Phenotypic Characterization and a Review of Treatment Effects
Eva M. M. Hoytema van Konijnenburg, Joline Rohof, Gautam Kok, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Eva M. M. Hoytema van Konijnenburg, Joline Rohof, Gautam Kok, et al.
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Case Report: A 3’ splice site variation in RORB exon 3 associated with idiopathic generalized epilepsy in a child
Dandan Shi, Nannan Li, Cheng Yan Fan, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Dandan Shi, Nannan Li, Cheng Yan Fan, et al.
Frontiers in Genetics (2025) Vol. 15
Open Access
Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy: QARS1 new variants associated with a severe phenotype in a patient
Rania Sakka, Hayet Ben Hamida, Mabrouk Abdelali, et al.
(2024)
Closed Access
Rania Sakka, Hayet Ben Hamida, Mabrouk Abdelali, et al.
(2024)
Closed Access
Microcephaly, progressive, seizures, and cerebral and cerebellar atrophy: QARS1 variants associated with a severe phenotype in a patient
Rania Sakka, Hayet Ben Hamida, Mabrouk Abdelali, et al.
Deleted Journal (2024) Vol. 1, Iss. 1
Open Access
Rania Sakka, Hayet Ben Hamida, Mabrouk Abdelali, et al.
Deleted Journal (2024) Vol. 1, Iss. 1
Open Access
Childhood-onset focal epilepsy and acute para-infectious encephalopathy in a patient with biallelic QARS1 variants
Vidal Yahya, Edoardo Monfrini, Andrea Celato, et al.
Neurological Sciences (2024)
Closed Access
Vidal Yahya, Edoardo Monfrini, Andrea Celato, et al.
Neurological Sciences (2024)
Closed Access