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:
Comparing Two Neurodevelopmental Disorders Linked to CK2: Okur-Chung Neurodevelopmental Syndrome and Poirier-Bienvenu Neurodevelopmental Syndrome—Two Sides of the Same Coin?
Demetra Ballardin, J. M. Cruz-Gamero, Thierry Bienvenu, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
Demetra Ballardin, J. M. Cruz-Gamero, Thierry Bienvenu, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
Showing 11 citing articles:
Protein Kinase CK2 and SARS-CoV-2: An Expected Interplay Story
Camila Paz Quezada Meza, Maria Ruzzene
Kinases and Phosphatases (2023) Vol. 1, Iss. 2, pp. 141-150
Open Access | Times Cited: 14
Camila Paz Quezada Meza, Maria Ruzzene
Kinases and Phosphatases (2023) Vol. 1, Iss. 2, pp. 141-150
Open Access | Times Cited: 14
A CK2α′ mutant indicating why CK2α and CK2α′, the isoforms of the catalytic subunit of human protein kinase CK2, deviate in affinity to CK2β
Christian Werner, Sophia Eimermacher, Hugo Harasimowicz, et al.
Biological Chemistry (2025)
Closed Access
Christian Werner, Sophia Eimermacher, Hugo Harasimowicz, et al.
Biological Chemistry (2025)
Closed Access
Predictive functional, statistical and structural analysis of CSNK2A1 and CSNK2B variants linked to neurodevelopmental diseases
P. Ambili Unni, Jack Friend, Janice Weinberg, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
P. Ambili Unni, Jack Friend, Janice Weinberg, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
Missense mutation in the activation segment of the kinase CK2 models Okur-Chung neurodevelopmental disorder and alters the hippocampal glutamatergic synapse
J. M. Cruz-Gamero, Demetra Ballardin, Barbara Lecis, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 1
J. M. Cruz-Gamero, Demetra Ballardin, Barbara Lecis, et al.
Molecular Psychiatry (2024)
Closed Access | Times Cited: 1
Exploring Protein Kinase CK2 Substrate Recognition and the Dynamic Response of Substrate Phosphorylation to Kinase Modulation
Luca Cesaro, Angelica Maria Zuliani, Valentina Bosello-Travain, et al.
Kinases and Phosphatases (2023) Vol. 1, Iss. 4, pp. 251-264
Open Access | Times Cited: 3
Luca Cesaro, Angelica Maria Zuliani, Valentina Bosello-Travain, et al.
Kinases and Phosphatases (2023) Vol. 1, Iss. 4, pp. 251-264
Open Access | Times Cited: 3
Genetic analysis and literature review of a Poirier–Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B
D. Li, Bingbo Zhou, Xinyuan Tian, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 3
D. Li, Bingbo Zhou, Xinyuan Tian, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 12, Iss. 1
Open Access | Times Cited: 3
Missense mutation in the activation segment of the kinase CK2 models Okur Chung neurodevelopmental disorder and alters the hippocampal glutamatergic synapse
J. M. Cruz-Gamero, Demetra Ballardin, Barbara Lecis, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
J. M. Cruz-Gamero, Demetra Ballardin, Barbara Lecis, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
Case report: Novel deletions in the 6p21.33 involving the CSNK2B gene in patients with Poirier-Bienvenu neurodevelopmental syndrome and literature review
Xuan Zhang, Hongjuan Lu, Yichen Ji, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access
Xuan Zhang, Hongjuan Lu, Yichen Ji, et al.
Frontiers in Medicine (2024) Vol. 11
Open Access
Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndrome
Swetha Ramadesikan, Iftekhar A. Showpnil, Mohammad Marhabaie, et al.
Human Genetics and Genomics Advances (2024) Vol. 6, Iss. 1, pp. 100379-100379
Open Access
Swetha Ramadesikan, Iftekhar A. Showpnil, Mohammad Marhabaie, et al.
Human Genetics and Genomics Advances (2024) Vol. 6, Iss. 1, pp. 100379-100379
Open Access
CSNK2B Mutation: A Rare Cause of IGHD
Karine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Clinical Endocrinology (2024)
Closed Access
Karine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Clinical Endocrinology (2024)
Closed Access
Towards the CSNK2 phosphoproteome – With lessons from the COVID-19 pandemic to revealing the secrets of CSNK2 and its promise as a therapeutic target
David W. Litchfield, Laszlo Gyenis, Daniel Menyhart, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2023) Vol. 1867, Iss. 10, pp. 130441-130441
Closed Access | Times Cited: 1
David W. Litchfield, Laszlo Gyenis, Daniel Menyhart, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2023) Vol. 1867, Iss. 10, pp. 130441-130441
Closed Access | Times Cited: 1
