
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:
Developmental outcome of electroencephalographic findings in SYNGAP1 encephalopathy
Juliana Ribeiro‐Constante, Alba Tristán‐Noguero, Fernando Francisco Martínez Calvo, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 3
Juliana Ribeiro‐Constante, Alba Tristán‐Noguero, Fernando Francisco Martínez Calvo, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 3
Showing 3 citing articles:
Key roles of C2/GAP domains in SYNGAP1-related pathophysiology
Danai Katsanevaki, Sally M. Till, Ingrid Buller‐Peralta, et al.
Cell Reports (2024) Vol. 43, Iss. 9, pp. 114733-114733
Open Access | Times Cited: 9
Danai Katsanevaki, Sally M. Till, Ingrid Buller‐Peralta, et al.
Cell Reports (2024) Vol. 43, Iss. 9, pp. 114733-114733
Open Access | Times Cited: 9
Unveiling a de novo SYNGAP1 variant: Clinical progression and management challenges in a case of developmental and epileptic encephalopathy – A case report
Norma Elena de León Ojeda, Fridha V. Villalpando-Vargas, Fabrizio A Mortola, et al.
SAGE Open Medical Case Reports (2024) Vol. 12
Open Access
Norma Elena de León Ojeda, Fridha V. Villalpando-Vargas, Fabrizio A Mortola, et al.
SAGE Open Medical Case Reports (2024) Vol. 12
Open Access
Genotype–Phenotype Correlations in SYNGAP1‐Related Mental Retardation Type 5
L. Elliot Hong, Qifeng Yuan
Clinical Genetics (2024) Vol. 107, Iss. 2, pp. 136-146
Closed Access
L. Elliot Hong, Qifeng Yuan
Clinical Genetics (2024) Vol. 107, Iss. 2, pp. 136-146
Closed Access