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OpenAlex Citation Counts

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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:

Okur-Chung neurodevelopmental syndrome-linked CK2α variants have reduced kinase activity
Isabel Domínguez, J. M. Cruz-Gamero, Victor Corasolla, et al.
Human Genetics (2021) Vol. 140, Iss. 7, pp. 1077-1096
Closed Access | Times Cited: 19

Showing 19 citing articles:

Okur‐Chung neurodevelopmental syndrome: Implications for phenotype and genotype expansion
Haitian Nan, Min Kyung Chu, Jing Zhang, et al.
Molecular Genetics & Genomic Medicine (2024) Vol. 12, Iss. 3
Open Access | Times Cited: 4
The Okur-Chung Neurodevelopmental Syndrome Mutation CK2K198R Leads to a Rewiring of Kinase Specificity
Danielle M. Caefer, Nhat Q. Phan, Jennifer Liddle, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 11
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
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
Structural and Enzymological Evidence for an Altered Substrate Specificity in Okur-Chung Neurodevelopmental Syndrome Mutant CK2αLys198Arg
Christian Werner, Alexander Gast, Dirk Lindenblatt, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 10
Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype–phenotype association
Maria Chiara Pelleri, Chiara Locatelli, Teresa Mattina, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 10
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
Diacerein reduces inflammasome activation and SARS-CoV-2 virus replication: a proof-of-concept translational study
Helison Rafael Pereira do Carmo, Alejandro Rossel Castillo, Isabella Bonilha, et al.
Frontiers in Pharmacology (2024) Vol. 15
Open Access | Times Cited: 1
Mechanism of CK2 Inhibition by a Ruthenium-Based Polyoxometalate
Simone Fabbian, Gabriele Giachin, Massimo Bellanda, et al.
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 7
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
Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype
Mohamed Wafik, Heidi Kuoppamaa, Priyal Hirani, et al.
Clinical Dysmorphology (2023) Vol. 32, Iss. 3, pp. 116-123
Closed Access | Times Cited: 2
Characterizing CSNK2A1 Mutant-Induced Morphological Phenotypes in Zebrafish (Danio rerio): Insights into Okur-Chung Neurodevelopmental Syndrome (OCNDS)
Katie Hassett, Sai Srihaas Potu, Sankaramoorthy Aravind, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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
Inherited loss of function variant in CSNK2A1: the oldest reported cases of Okur–Chung syndrome in a single family
Himanshu Goel, Sheridan O’Donnell
Clinical Dysmorphology (2024) Vol. 33, Iss. 3, pp. 121-124
Closed Access
Subtelomeric microdeletion in chromosome 20p13 associated with short stature
Jiao Liu, Y. Li, Hans C. Andersson, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 6
Open Access
Patient organization perspective: a research roadmap for Okur-Chung Neurodevelopmental Syndrome
Gabrielle V. Rushing, Jennifer Sills
Therapeutic Advances in Rare Disease (2024) Vol. 5
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
Report of an Asian–Indian patient with Okur–Chung Syndrome and comparison of the clinical phenotype in different ethnic groups
Priya Ranganath, Prajnya Ranganath, Venugopal Satidevi Vineeth, et al.
Clinical Dysmorphology (2021) Vol. 30, Iss. 4, pp. 209-212
Closed Access | Times Cited: 3
Partial trisomy 21 with or without highly restricted-Down syndrome critical region (HR- DSCR). Report of two new cases and reanalysis of the genotype-phenotype association
Maria Chiara Pelleri, Chiara Locatelli, Teresa Mattina, et al.
Research Square (Research Square) (2022)
Open Access | Times Cited: 1
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