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:
Clinical phenotypic spectrum of CTNNB1 neurodevelopmental disorder
Khemika K. Sudnawa, Alison Garber, Ryan Cohen, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 523-532
Closed Access | Times Cited: 8
Khemika K. Sudnawa, Alison Garber, Ryan Cohen, et al.
Clinical Genetics (2024) Vol. 105, Iss. 5, pp. 523-532
Closed Access | Times Cited: 8
Showing 8 citing articles:
A Systematic Review of Cognitive and Behavioural Symptoms in CTNNB1 Syndrome
Mercè Pallarès‐Sastre, Imanol Amayra, Mónika Salgueiro, et al.
Neuropsychology Review (2025)
Open Access | Times Cited: 1
Mercè Pallarès‐Sastre, Imanol Amayra, Mónika Salgueiro, et al.
Neuropsychology Review (2025)
Open Access | Times Cited: 1
Use of poly adenosine tail mimetics to enhance mRNA expression from genes associated with haploinsufficiency disorders
Bahareh Torkzaban, Yining Zhu, Christian Lopez, et al.
Molecular Therapy — Nucleic Acids (2025) Vol. 36, Iss. 1, pp. 102453-102453
Open Access
Bahareh Torkzaban, Yining Zhu, Christian Lopez, et al.
Molecular Therapy — Nucleic Acids (2025) Vol. 36, Iss. 1, pp. 102453-102453
Open Access
CTNNB1 syndrome mouse models
Duško Lainšček, Vida Forstnerič, Špela Miroševič
Mammalian Genome (2025)
Open Access
Duško Lainšček, Vida Forstnerič, Špela Miroševič
Mammalian Genome (2025)
Open Access
Paving the way toward treatment solutions for CTNNB1 syndrome: a patient organization perspective
Špela Miroševič, Shivang Khandelwal, Emily Amerson, et al.
Therapeutic Advances in Rare Disease (2025) Vol. 6
Open Access
Špela Miroševič, Shivang Khandelwal, Emily Amerson, et al.
Therapeutic Advances in Rare Disease (2025) Vol. 6
Open Access
Cognitive and Adaptive Functioning of CTNNB1 Syndrome Patients: A Comparison With Autism Spectrum Disorder and Cerebral Palsy
Mercè Pallarès‐Sastre, Imanol Amayra, Rafael Pulido, et al.
Journal of Intellectual Disability Research (2025)
Open Access
Mercè Pallarès‐Sastre, Imanol Amayra, Rafael Pulido, et al.
Journal of Intellectual Disability Research (2025)
Open Access
Inhibition of GSK3α,β rescues cognitive phenotypes in a preclinical mouse model of CTNNB1 syndrome
Jonathan Alexander, Leeanne Vazquez-Ramirez, Crystal Lin, et al.
EMBO Molecular Medicine (2024) Vol. 16, Iss. 9, pp. 2109-2131
Closed Access | Times Cited: 2
Jonathan Alexander, Leeanne Vazquez-Ramirez, Crystal Lin, et al.
EMBO Molecular Medicine (2024) Vol. 16, Iss. 9, pp. 2109-2131
Closed Access | Times Cited: 2
Clinical characteristics, longitudinal adaptive functioning, and association with electroencephalogram activity in PPP2R5D‐related neurodevelopmental disorder
Khemika K. Sudnawa, Nicolò Pini, Wenxing Li, et al.
Clinical Genetics (2024) Vol. 107, Iss. 1, pp. 34-43
Open Access | Times Cited: 2
Khemika K. Sudnawa, Nicolò Pini, Wenxing Li, et al.
Clinical Genetics (2024) Vol. 107, Iss. 1, pp. 34-43
Open Access | Times Cited: 2
Clinical Response of Levodopa in CTNNB1-Related Dystonia
Anna Revert Barberà, Loreto Martorell, Cristina Martínez Boix, et al.
Journal of Pediatric Neurology (2024) Vol. 22, Iss. 06, pp. 466-469
Closed Access
Anna Revert Barberà, Loreto Martorell, Cristina Martínez Boix, et al.
Journal of Pediatric Neurology (2024) Vol. 22, Iss. 06, pp. 466-469
Closed Access
