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:
Phenotype and genotype analyses of Chinese patients with autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations
Yanxin Wang, Yuqiang Lv, Zilong Li, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 4
Yanxin Wang, Yuqiang Lv, Zilong Li, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 4
Showing 4 citing articles:
Roadmap to advance therapeutics for SYNGAP1-related disorder: a patient organization perspective from SynGAP Research Fund
J. Michael Graglia, Aaron J. Harding, Kathryn A. Helde
Therapeutic Advances in Rare Disease (2025) Vol. 6
Open Access
J. Michael Graglia, Aaron J. Harding, Kathryn A. Helde
Therapeutic Advances in Rare Disease (2025) Vol. 6
Open Access
[Autosomal dominant mental retardation type 5 caused by SYNGAP1 gene mutations: a report of 8 cases and literature review].
Xiaole Wang, Ya-Nan Tian, Chen Chen, et al.
PubMed (2023) Vol. 25, Iss. 5, pp. 489-496
Closed Access | Times Cited: 2
Xiaole Wang, Ya-Nan Tian, Chen Chen, et al.
PubMed (2023) Vol. 25, Iss. 5, pp. 489-496
Closed Access | Times Cited: 2
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
Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing
Giulia Rosti, Silvia Boeri, Maria Teresa Divizia, et al.
Molecular Syndromology (2023) Vol. 14, Iss. 5, pp. 433-438
Open Access
Giulia Rosti, Silvia Boeri, Maria Teresa Divizia, et al.
Molecular Syndromology (2023) Vol. 14, Iss. 5, pp. 433-438
Open Access
