PubMed for id: 934706

Year	Number of Results
1993	1
2018	3
2019	1
2020	3
2021	4
2022	7
2023	4
2024	1

1

A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the CSNK2A1 Gene in a Turkish Patient.

Zhuri D, Dusenkalkan F, Tunca Alparslan G, Gurkan H. Zhuri D, et al. Mol Syndromol. 2024 Feb;15(1):43-50. doi: 10.1159/000530585. Epub 2023 May 26. Mol Syndromol. 2024. PMID: 38357263

2

Exome sequencing in 16 patients with pituitary stalk interruption syndrome: A monocentric study.

Brauner R, Bignon-Topalovic J, Bashamboo A, McElreavey K. Brauner R, et al. PLoS One. 2023 Dec 14;18(12):e0292664. doi: 10.1371/journal.pone.0292664. eCollection 2023. PLoS One. 2023. PMID: 38096238 Free PMC article.

3

Inherited CSNK2A1 variants in families with Okur-Chung neurodevelopmental syndrome.

Belnap N, Price-Smith A, Ramsey K, Leka K, Abraham A, Lieberman E, Hassett K, Potu S, Rudy N, Smith K, Mikhail FM, Monaghan KG, Hendershot A, Mourmans J, Descartes M, Huentelman MJ, Sills J, Rangasamy S, Narayanan V. Belnap N, et al. Clin Genet. 2023 Nov;104(5):607-609. doi: 10.1111/cge.14408. Epub 2023 Jul 25. Clin Genet. 2023. PMID: 37491870

4

Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype.

Wafik M, Kuoppamaa H, Hirani P, Hignett J, Lillis S, Lascelles K, Sardesai S, Gomez K, Holder-Espinasse M. Wafik M, et al. Clin Dysmorphol. 2023 Jul 1;32(3):116-123. doi: 10.1097/MCD.0000000000000456. Epub 2023 May 1. Clin Dysmorphol. 2023. PMID: 37195306 No abstract available.

5

Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review.

Jafari Khamirani H, Zoghi S, Motealleh A, Dianatpour M, Tabei SMB, Mohammadi S, Dastgheib SA. Jafari Khamirani H, et al. Mol Syndromol. 2022 Dec;13(5):381-388. doi: 10.1159/000522353. Epub 2022 Mar 31. Mol Syndromol. 2022. PMID: 36588763 Free PMC article.

6

Predictive functional, statistical and structural analysis of CSNK2A1 and CSNK2B variants linked to neurodevelopmental diseases.

Unni P, Friend J, Weinberg J, Okur V, Hochscherf J, Dominguez I. Unni P, et al. Front Mol Biosci. 2022 Oct 13;9:851547. doi: 10.3389/fmolb.2022.851547. eCollection 2022. Front Mol Biosci. 2022. PMID: 36310603 Free PMC article.

7

Comparing Two Neurodevelopmental Disorders Linked to CK2: Okur-Chung Neurodevelopmental Syndrome and Poirier-Bienvenu Neurodevelopmental Syndrome-Two Sides of the Same Coin?

Ballardin D, Cruz-Gamero JM, Bienvenu T, Rebholz H. Ballardin D, et al. Front Mol Biosci. 2022 May 26;9:850559. doi: 10.3389/fmolb.2022.850559. eCollection 2022. Front Mol Biosci. 2022. PMID: 35693553 Free PMC article. Review.

8

Okur-Chung Neurodevelopmental Syndrome.

Chung W, Okur V. Chung W, et al. 2022 Jun 9. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2022 Jun 9. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 35679446 Free Books & Documents. Review.

9

The Okur-Chung Neurodevelopmental Syndrome Mutation CK2^K198R Leads to a Rewiring of Kinase Specificity.

Caefer DM, Phan NQ, Liddle JC, Balsbaugh JL, O'Shea JP, Tzingounis AV, Schwartz D. Caefer DM, et al. Front Mol Biosci. 2022 Apr 19;9:850661. doi: 10.3389/fmolb.2022.850661. eCollection 2022. Front Mol Biosci. 2022. PMID: 35517865 Free PMC article.

10

Structural and Enzymological Evidence for an Altered Substrate Specificity in Okur-Chung Neurodevelopmental Syndrome Mutant CK2α^Lys198Arg.

Werner C, Gast A, Lindenblatt D, Nickelsen A, Niefind K, Jose J, Hochscherf J. Werner C, et al. Front Mol Biosci. 2022 Apr 4;9:831693. doi: 10.3389/fmolb.2022.831693. eCollection 2022. Front Mol Biosci. 2022. PMID: 35445078 Free PMC article.

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