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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:

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

Showing 11 citing articles:

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
Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders
Mariateresa Di Stazio, Caterina Zanus, Flavio Faletra, et al.
Genes (2023) Vol. 14, Iss. 2, pp. 250-250
Open Access | Times Cited: 4
Autism spectrum disorder and various mechanisms behind it
Parisa Rajabi, Ali Sabbah Noori, Javad Sargolzaei
Pharmacology Biochemistry and Behavior (2024) Vol. 245, pp. 173887-173887
Closed Access | Times Cited: 1
Refining of the electroclinical phenotype in familial and sporadic cases of CSNK2B-related Neurodevelopmental Syndrome
Marina Trivisano, Angela De Dominicis, Fabrizia Stregapede, et al.
Epilepsy & Behavior (2023) Vol. 147, pp. 109436-109436
Closed Access | Times Cited: 3
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
Subtelomeric Microdeletion in Chromosome 20p13 Associated with Short Stature
Jiao Liu, Yuwen Li, Hans C. Andersson, et al.
Authorea (Authorea) (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
Integrative analysis of senescence-related genes in endothelial cells of Cerebral Ischemic Stroke patients
Biao Li, Shuai Li, Yantao Jing, et al.
Research Square (Research Square) (2024)
Closed 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
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