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:
STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy
Mirella Vinci, Carola Costanza, Rosanna Galati Rando, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16436-16436
Open Access | Times Cited: 13
Mirella Vinci, Carola Costanza, Rosanna Galati Rando, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 22, pp. 16436-16436
Open Access | Times Cited: 13
Showing 13 citing articles:
Brain Plasticity and Cell Competition: Immediate Early Genes Are the Focus
П. П. Трегуб, Yulia K. Komleva, Maria V. Kukla, et al.
Cells (2025) Vol. 14, Iss. 2, pp. 143-143
Open Access | Times Cited: 1
П. П. Трегуб, Yulia K. Komleva, Maria V. Kukla, et al.
Cells (2025) Vol. 14, Iss. 2, pp. 143-143
Open Access | Times Cited: 1
Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies
Luigi Vetri, Francesco Calı̀, Salvatore Saccone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1146-1146
Open Access | Times Cited: 6
Luigi Vetri, Francesco Calı̀, Salvatore Saccone, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1146-1146
Open Access | Times Cited: 6
Implications of a De Novo Variant in the SOX12 Gene in a Patient with Generalized Epilepsy, Intellectual Disability, and Childhood Emotional Behavioral Disorders
Simone Treccarichi, Francesco Calı̀, Mirella Vinci, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 7, pp. 6407-6422
Open Access | Times Cited: 4
Simone Treccarichi, Francesco Calı̀, Mirella Vinci, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 7, pp. 6407-6422
Open Access | Times Cited: 4
Developmental and Epileptic Encephalopathy: Pathogenesis of Intellectual Disability Beyond Channelopathies
Alexandra D. Medyanik, Polina E. Anisimova, Angelina Kustova, et al.
Biomolecules (2025) Vol. 15, Iss. 1, pp. 133-133
Open Access
Alexandra D. Medyanik, Polina E. Anisimova, Angelina Kustova, et al.
Biomolecules (2025) Vol. 15, Iss. 1, pp. 133-133
Open Access
Non-Invasive Assessment of Neurogenesis Dysfunction in Fetuses with Early-Onset Growth Restriction Using Fetal Neuronal Exosomes Isolating from Maternal Blood: A Pilot Study
Vladislava Gusar, Н. Е. Кан, A.Y. Leonova, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1497-1497
Open Access
Vladislava Gusar, Н. Е. Кан, A.Y. Leonova, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 4, pp. 1497-1497
Open Access
“Trafficking Disorders: Phenotypical Similarities and Differences With Other IMDs ”
Àngels García‐Cazorla, Éva Morava, Jean‐Marie Saudubray
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Àngels García‐Cazorla, Éva Morava, Jean‐Marie Saudubray
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities
Francesco Calı̀, Mirella Vinci, Simone Treccarichi, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1096-1096
Open Access | Times Cited: 3
Francesco Calı̀, Mirella Vinci, Simone Treccarichi, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1096-1096
Open Access | Times Cited: 3
Bioinformatic Evaluation of KLF13 Genetic Variant: Implications for Neurodevelopmental and Psychiatric Symptoms
Mirella Vinci, Donatella Greco, Simone Treccarichi, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1056-1056
Open Access | Times Cited: 1
Mirella Vinci, Donatella Greco, Simone Treccarichi, et al.
Genes (2024) Vol. 15, Iss. 8, pp. 1056-1056
Open Access | Times Cited: 1
A genome-wide association study of Chinese and English language phenotypes in Hong Kong Chinese children
Yuping Lin, Yujia Shi, Ruoyu Zhang, et al.
npj Science of Learning (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 1
Yuping Lin, Yujia Shi, Ruoyu Zhang, et al.
npj Science of Learning (2024) Vol. 9, Iss. 1
Open Access | Times Cited: 1
PPP2R5E: New gene potentially involved in specific learning disorders and myopathy
Antonino Musumeci, Mirella Vinci, Iris Verbinnen, et al.
Gene (2024) Vol. 933, pp. 148945-148945
Closed Access | Times Cited: 1
Antonino Musumeci, Mirella Vinci, Iris Verbinnen, et al.
Gene (2024) Vol. 933, pp. 148945-148945
Closed Access | Times Cited: 1
The syntaxin-binding protein STXBP5 regulates progerin expression
Hongqian Qi, Yingying Wu, Weiyu Zhang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Hongqian Qi, Yingying Wu, Weiyu Zhang, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
A functional variant rs912304 for late-onset T1D risk contributes to islet dysfunction by regulating proinflammatory cytokine-responsive gene STXBP6 expression
Qian Yu, Shu Chen, Yan Wang, et al.
BMC Medicine (2024) Vol. 22, Iss. 1
Open Access
Qian Yu, Shu Chen, Yan Wang, et al.
BMC Medicine (2024) Vol. 22, Iss. 1
Open Access
Vesicles: New Advances in the Treatment of Neurodegenerative Diseases
Domenico Nuzzo, Antonella Girgenti, Laura Palumbo, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 12672-12672
Open Access
Domenico Nuzzo, Antonella Girgenti, Laura Palumbo, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 23, pp. 12672-12672
Open Access
