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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 in a patient from Spain
Antonio Federico Martínez‐Monseny, Dídac Casas‐Alba, César Arjona, et al.
American Journal of Medical Genetics Part A (2019) Vol. 182, Iss. 1, pp. 20-24
Closed Access | Times Cited: 16

Showing 16 citing articles:

Protein kinase CK2: a potential therapeutic target for diverse human diseases
Christian Borgo, Claudio D’Amore, Stefania Sarno, et al.
Signal Transduction and Targeted Therapy (2021) Vol. 6, Iss. 1
Open Access | Times Cited: 246
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
Central precocious puberty associated with duplicated pituitary: a case report and literature review
Kun Yang, Yanmei Sang, Li Dai, et al.
Frontiers in Endocrinology (2025) Vol. 16
Open Access
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
Identification of novel CSNK2A1 variants and the genotype–phenotype relationship in patients with Okur–Chung neurodevelopmental syndrome: a case report and systematic literature review
Ruohao Wu, Wenting Tang, Kun‐yin Qiu, et al.
Journal of International Medical Research (2021) Vol. 49, Iss. 5
Open Access | Times Cited: 18
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
Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review
Hossein Jafari Khamirani, Sina Zoghi, Ali Motealleh, et al.
Molecular Syndromology (2022) Vol. 13, Iss. 5, pp. 381-388
Open Access | Times Cited: 8
Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome
A Blanc, Céline Bonnet, Marion Wandzel, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 9
Open Access | Times Cited: 1
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
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
A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the <i>CSNK2A1</i> Gene in a Turkish Patient
Drenushe Zhuri̇, Fulya Dusenkalkan, Guzin Tunca Alparslan, et al.
Molecular Syndromology (2023) Vol. 15, Iss. 1, pp. 43-50
Open Access | Times Cited: 2
Persistent Hyperplastic Primary Vitreous with Microphthalmia and Coloboma in a Patient with Okur-Chung Neurodevelopmental Syndrome
Hiroaki Murakami, Tomoko Uehara, Yumi Enomoto, et al.
Molecular Syndromology (2021) Vol. 13, Iss. 1, pp. 75-79
Open Access | Times Cited: 4
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
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
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