PubMed for id: 80781

Year	Number of Results
1994	3
1996	2
1997	2
1998	3
2000	3
2001	7
2002	13
2003	12
2004	17
2005	12
2006	8
2007	13
2008	13
2009	22
2010	18
2011	12
2012	11
2013	15
2014	15
2015	13
2016	7
2017	10
2018	10
2019	4
2020	8
2021	10
2022	6
2023	4
2024	1

1

Knobloch Syndrome Associated with Novel COL18A1 Variants in Chinese Population.

Li S, Wang Y, Sun L, Yan W, Huang L, Zhang Z, Zhang T, Ding X. Li S, et al. Genes (Basel). 2021 Sep 26;12(10):1512. doi: 10.3390/genes12101512. Genes (Basel). 2021. PMID: 34680907 Free PMC article.

2

Collagen type XVIII alpha 1 chain (COL18A1) variants affect the risk of anti-tuberculosis drug-induced hepatotoxicity: A prospective study.

Cheng Y, Jiao L, Li W, Wang J, Lin Z, Lai H, Ying B. Cheng Y, et al. J Clin Lab Anal. 2021 Feb;35(2):e23630. doi: 10.1002/jcla.23630. Epub 2020 Dec 9. J Clin Lab Anal. 2021. PMID: 33296124 Free PMC article.

3

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children.

Levinger N, Hendler K, Banin E, Hanany M, Kimchi A, Mechoulam H, Meiner V, Parag Y, Sharon D, Macarov M, Yahalom C. Levinger N, et al. Eur J Ophthalmol. 2021 Nov;31(6):3349-3354. doi: 10.1177/1120672120977343. Epub 2020 Nov 25. Eur J Ophthalmol. 2021. PMID: 33238767

4

Knobloch syndrome in a patient from Chile.

Nakousi-Capurro N, Huserman J, Castillo S, Herrera L, Romero P, Pizarro F, Quezada C, Cea F. Nakousi-Capurro N, et al. Am J Med Genet A. 2020 Oct;182(10):2239-2242. doi: 10.1002/ajmg.a.61760. Epub 2020 Jul 22. Am J Med Genet A. 2020. PMID: 32700429

5

Three cases of molecularly confirmed Knobloch syndrome.

Balikova I, Sanak NS, Fanny D, Smits G, Soblet J, de Baere E, Cordonnier M. Balikova I, et al. Ophthalmic Genet. 2020 Feb;41(1):83-87. doi: 10.1080/13816810.2020.1737948. Epub 2020 Mar 17. Ophthalmic Genet. 2020. PMID: 32178553

6

Serum Endostatin Is a Novel Marker for COPD Associated with Lower Lung Function, Exacerbation and Systemic Inflammation.

Wu Y, Qin J, He J, Shen Y, Wang H, Li Y, Zeng Q, Dong J, An Y, Xiong S, Feng M, Wen F. Wu Y, et al. Int J Chron Obstruct Pulmon Dis. 2020 Feb 25;15:397-407. doi: 10.2147/COPD.S234760. eCollection 2020. Int J Chron Obstruct Pulmon Dis. 2020. PMID: 32158205 Free PMC article.

7

Functional Impact of Human Genetic Variants of COL18A1/Endostatin on Pulmonary Endothelium.

Goyanes AM, Moldobaeva A, Marimoutou M, Varela LC, Wang L, Johnston LF, Aladdin MM, Peloquin GL, Kim BS, Damarla M, Suresh K, Sato T, Kolb TM, Hassoun PM, Damico RL. Goyanes AM, et al. Am J Respir Cell Mol Biol. 2020 Apr;62(4):524-534. doi: 10.1165/rcmb.2019-0056OC. Am J Respir Cell Mol Biol. 2020. PMID: 31922883 Free PMC article.

8

Type XVIII Collagen Modulates Keratohyalin Granule Formation and Keratinization in Oral Mucosa.

Nguyen HTT, Ono M, Hara ES, Komori T, Edamatsu M, Yonezawa T, Kimura-Ono A, Maekawa K, Kuboki T, Oohashi T. Nguyen HTT, et al. Int J Mol Sci. 2019 Sep 24;20(19):4739. doi: 10.3390/ijms20194739. Int J Mol Sci. 2019. PMID: 31554264 Free PMC article.

9

The association between circulating endostatin levels and incident myocardial infarction.

Ruge T, Carlsson AC, Jansson JH, Söderberg S, Larsson A, Ärnlöv J. Ruge T, et al. Scand Cardiovasc J. 2018 Dec;52(6):315-319. doi: 10.1080/14017431.2018.1547839. Epub 2019 Feb 14. Scand Cardiovasc J. 2018. PMID: 30474426

10

COL18A1 is a candidate eye iridocorneal angle-closure gene in humans.

Suri F, Yazdani S, Chapi M, Safari I, Rasooli P, Daftarian N, Jafarinasab MR, Ghasemi Firouzabadi S, Alehabib E, Darvish H, Klotzle B, Fan JB, Turk C, Elahi E. Suri F, et al. Hum Mol Genet. 2018 Nov 1;27(21):3772-3786. doi: 10.1093/hmg/ddy256. Hum Mol Genet. 2018. PMID: 30007336

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