PubMed for id: 23562

Year	Number of Results
1993	1
1995	1
1999	1
2000	2
2001	3
2002	2
2003	3
2004	1
2005	2
2006	1
2007	1
2008	1
2009	3
2010	3
2011	1
2012	3
2013	6
2014	1
2015	1
2016	5
2017	5
2018	2
2019	1
2020	1
2022	1
2023	1
2024	0

1

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.

Kitano T, Kitajiri SI, Nishio SY, Usami SI. Kitano T, et al. Int J Mol Sci. 2019 Sep 16;20(18):4579. doi: 10.3390/ijms20184579. Int J Mol Sci. 2019. PMID: 31527509 Free PMC article.

2

Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss.

Lu Y, Yao J, Wei Q, Xu J, Xing G, Cao X. Lu Y, et al. Int J Pediatr Otorhinolaryngol. 2018 Feb;105:6-11. doi: 10.1016/j.ijporl.2017.11.016. Epub 2017 Nov 22. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29447821

3

A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

Pater JA, Benteau T, Griffin A, Penney C, Stanton SG, Predham S, Kielley B, Squires J, Zhou J, Li Q, Abdelfatah N, O'Rielly DD, Young TL. Pater JA, et al. Hum Genet. 2017 Jan;136(1):107-118. doi: 10.1007/s00439-016-1746-7. Epub 2016 Nov 12. Hum Genet. 2017. PMID: 27838790 Free PMC article.

4

A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density.

Tang R, Wei Y, Li Z, Chen H, Miao Q, Bian Z, Zhang H, Wang Q, Wang Z, Lian M, Yang F, Jiang X, Yang Y, Li E, Seldin MF, Gershwin ME, Liao W, Shi Y, Ma X. Tang R, et al. Sci Rep. 2016 Feb 4;6:19877. doi: 10.1038/srep19877. Sci Rep. 2016. PMID: 26842849 Free PMC article.

5

Frequency of rare allelic variation in candidate genes among individuals with low and high urinary calcium excretion.

Toka HR, Genovese G, Mount DB, Pollak MR, Curhan GC. Toka HR, et al. PLoS One. 2013 Aug 26;8(8):e71885. doi: 10.1371/journal.pone.0071885. eCollection 2013. PLoS One. 2013. PMID: 23991001 Free PMC article.

6

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A. Charif M, et al. Gene. 2013 Jul 1;523(1):103-5. doi: 10.1016/j.gene.2013.03.123. Epub 2013 Apr 13. Gene. 2013. PMID: 23590985 Free article.

7

Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.

Bashir ZE, Latief N, Belyantseva IA, Iqbal F, Riazuddin SA, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Bashir ZE, et al. J Hum Genet. 2013 Feb;58(2):102-8. doi: 10.1038/jhg.2012.143. Epub 2012 Dec 13. J Hum Genet. 2013. PMID: 23235333 Free PMC article.

8

Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss.

Lee K, Ansar M, Andrade PB, Khan B, Santos-Cortez RL, Ahmad W, Leal SM. Lee K, et al. Am J Med Genet A. 2012 Feb;158A(2):315-21. doi: 10.1002/ajmg.a.34407. Epub 2012 Jan 13. Am J Med Genet A. 2012. PMID: 22246673 Free PMC article.

9

Mutations in CLDN14 are associated with different hearing thresholds.

Bashir R, Fatima A, Naz S. Bashir R, et al. J Hum Genet. 2010 Nov;55(11):767-70. doi: 10.1038/jhg.2010.104. Epub 2010 Sep 2. J Hum Genet. 2010. PMID: 20811388 Free PMC article.

10

Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.

Thorleifsson G, Holm H, Edvardsson V, Walters GB, Styrkarsdottir U, Gudbjartsson DF, Sulem P, Halldorsson BV, de Vegt F, d'Ancona FC, den Heijer M, Franzson L, Christiansen C, Alexandersen P, Rafnar T, Kristjansson K, Sigurdsson G, Kiemeney LA, Bodvarsson M, Indridason OS, Palsson R, Kong A, Thorsteinsdottir U, Stefansson K. Thorleifsson G, et al. Nat Genet. 2009 Aug;41(8):926-30. doi: 10.1038/ng.404. Epub 2009 Jun 28. Nat Genet. 2009. PMID: 19561606

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