PubMed for id: 400917

Year	Number of Results
1976	1
1977	1
1978	1
1981	1
1990	3
1992	1
1994	3
1995	1
1996	2
1997	4
1998	1
1999	3
2000	9
2001	4
2002	3
2003	3
2004	4
2005	6
2006	3
2007	2
2008	5
2009	5
2011	1
2012	2
2013	5
2014	6
2015	7
2016	5
2017	1
2018	2
2019	1
2020	3
2021	5
2022	10
2023	3
2024	0

1

A Dutch family with progressive autosomal dominant non-syndromic sensorineural hearing impairment linked to DFNA13.

Ensink RJ, Huygen PL, Snoeckx RL, Caethoven G, Van Camp G, Cremers CW. Ensink RJ, et al. Clin Otolaryngol Allied Sci. 2001 Aug;26(4):310-6. doi: 10.1046/j.1365-2273.2001.00477.x. Clin Otolaryngol Allied Sci. 2001. PMID: 11559344

2

Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).

De Leenheer EM, Kunst HH, McGuirt WT, Prasad SD, Brown MR, Huygen PL, Smith RJ, Cremers CW. De Leenheer EM, et al. Arch Otolaryngol Head Neck Surg. 2001 Jan;127(1):13-7. doi: 10.1001/archotol.127.1.13. Arch Otolaryngol Head Neck Surg. 2001. PMID: 11177008

3

The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.

Kunst H, Huybrechts C, Marres H, Huygen P, Van Camp G, Cremers C. Kunst H, et al. Am J Otol. 2000 Mar;21(2):181-7. doi: 10.1016/s0196-0709(00)80006-x. Am J Otol. 2000. PMID: 10733181

4

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).

McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ. McGuirt WT, et al. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026

5

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.

Brown MR, Tomek MS, Van Laer L, Smith S, Kenyon JB, Van Camp G, Smith RJ. Brown MR, et al. Am J Hum Genet. 1997 Oct;61(4):924-7. doi: 10.1086/514892. Am J Hum Genet. 1997. PMID: 9382104 Free PMC article.

6

Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment.

van Beelen E, Oonk AM, Leijendeckers JM, Hoefsloot EH, Pennings RJ, Feenstra I, Dieker HJ, Huygen PL, Snik AF, Kremer H, Kunst HP. van Beelen E, et al. Ear Hear. 2016 Jan-Feb;37(1):103-11. doi: 10.1097/AUD.0000000000000217. Ear Hear. 2016. PMID: 26331839

7

Similar phenotypes caused by mutations in OTOG and OTOGL.

Oonk AM, Leijendeckers JM, Huygen PL, Schraders M, del Campo M, del Castillo I, Tekin M, Feenstra I, Beynon AJ, Kunst HP, Snik AF, Kremer H, Admiraal RJ, Pennings RJ. Oonk AM, et al. Ear Hear. 2014 May-Jun;35(3):e84-91. doi: 10.1097/AUD.0000000000000008. Ear Hear. 2014. PMID: 24378291 Free PMC article.

8

Audiometric characteristics of two Dutch families with non-ocular Stickler syndrome (COL11A2).

van Beelen E, Leijendeckers JM, Huygen PL, Admiraal RJ, Hoefsloot LH, Lichtenbelt KD, Stöbe L, Pennings RJ, Leuwer R, Snik AF, Kunst HP. van Beelen E, et al. Hear Res. 2012 Sep;291(1-2):15-23. doi: 10.1016/j.heares.2012.07.001. Epub 2012 Jul 14. Hear Res. 2012. PMID: 22796475

9

Audiometric characteristics of USH2a patients.

Leijendeckers JM, Pennings RJ, Snik AF, Bosman AJ, Cremers CW. Leijendeckers JM, et al. Audiol Neurootol. 2009;14(4):223-31. doi: 10.1159/000189265. Epub 2009 Jan 8. Audiol Neurootol. 2009. PMID: 19129697

10

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.

Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ. Plantinga RF, et al. J Assoc Res Otolaryngol. 2007 Mar;8(1):1-7. doi: 10.1007/s10162-006-0060-9. Epub 2006 Nov 30. J Assoc Res Otolaryngol. 2007. PMID: 17136632 Free PMC article.

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