PubMed (RefSeq) for id: 2572895192

Year	Number of Results
1989	2
1993	3
1995	5
1996	2
1997	3
1998	3
1999	2
2000	2
2001	3
2002	1
2003	3
2005	4
2006	3
2007	4
2008	6
2009	6
2010	4
2011	5
2012	3
2013	3
2014	1
2015	2
2016	2
2017	3
2018	3
2019	1
2020	3
2021	1
2022	2
2023	5
2024	0

1

Autosomal recessive otospondylo-mega-epiphyseal dysplasia: comprehensive clinical review of a pediatric cohort.

Mutlu H, Elçioğlu N, Kiliç E. Mutlu H, et al. Clin Dysmorphol. 2023 Oct 1;32(4):151-155. doi: 10.1097/MCD.0000000000000467. Epub 2023 Jul 4. Clin Dysmorphol. 2023. PMID: 37646720

2

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis.

Rebello D, Wohler E, Erfani V, Li G, Aguilera AN, Santiago-Cornier A, Zhao S, Hwang SW, Steiner RD, Zhang TJ, Gurnett CA, Raggio C, Wu N, Sobreira N, Giampietro PF, Ciruna B. Rebello D, et al. Hum Mol Genet. 2023 Sep 16;32(19):2913-2928. doi: 10.1093/hmg/ddad117. Hum Mol Genet. 2023. PMID: 37462524

3

The Association of Variants within Types V and XI Collagen Genes with Knee Joint Laxity Measurements.

Beckley S, Dey R, Stinton S, van der Merwe W, Branch T, September AV, Posthumus M, Collins M. Beckley S, et al. Genes (Basel). 2022 Dec 14;13(12):2359. doi: 10.3390/genes13122359. Genes (Basel). 2022. PMID: 36553626 Free PMC article.

4

Physical and functional interactome atlas of human receptor tyrosine kinases.

Salokas K, Liu X, Öhman T, Chowdhury I, Gawriyski L, Keskitalo S, Varjosalo M. Salokas K, et al. EMBO Rep. 2022 Jun 7;23(6):e54041. doi: 10.15252/embr.202154041. Epub 2022 Apr 5. EMBO Rep. 2022. PMID: 35384245 Free PMC article.

5

Association Between COL5a1, COL11a1, and COL11a2 Gene Variations and Rotator Cuff Tendinopathy in Young Athletes.

Alakhdar Y, Cook J, Gallego D, Querol F, Chulvi-Medrano I, Alberola A, Hernández-Sánchez S. Alakhdar Y, et al. Clin J Sport Med. 2023 Sep 1;33(5):e152-e156. doi: 10.1097/JSM.0000000000000937. Epub 2021 May 7. Clin J Sport Med. 2023. PMID: 34009784

6

Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia.

Micale L, Morlino S, Schirizzi A, Agolini E, Nardella G, Fusco C, Castellana S, Guarnieri V, Villa R, Bedeschi MF, Grammatico P, Novelli A, Castori M. Micale L, et al. Genes (Basel). 2020 Dec 17;11(12):1513. doi: 10.3390/genes11121513. Genes (Basel). 2020. PMID: 33348901 Free PMC article.

7

RIG-I regulates myeloid differentiation by promoting TRIM25-mediated ISGylation.

Wu SF, Xia L, Shi XD, Dai YJ, Zhang WN, Zhao JM, Zhang W, Weng XQ, Lu J, Le HY, Tao SC, Zhu J, Chen Z, Wang YY, Chen S. Wu SF, et al. Proc Natl Acad Sci U S A. 2020 Jun 23;117(25):14395-14404. doi: 10.1073/pnas.1918596117. Epub 2020 Jun 8. Proc Natl Acad Sci U S A. 2020. PMID: 32513696 Free PMC article.

8

Genetic variant of COL11A2 gene is functionally associated with developmental dysplasia of the hip in Chinese Han population.

Xu R, Jiang X, Lu J, Wang K, Sun Y, Zhang Y. Xu R, et al. Aging (Albany NY). 2020 May 12;12(9):7694-7703. doi: 10.18632/aging.103040. Epub 2020 May 12. Aging (Albany NY). 2020. PMID: 32396528 Free PMC article.

9

Genetic variants in COL11A2 of lumbar disk degeneration among Chinese Han population.

Yang X, Jia H, Xing W, Li F, Li M, Sun K, Zhu Y. Yang X, et al. Mol Genet Genomic Med. 2019 Feb;7(2):e00524. doi: 10.1002/mgg3.524. Epub 2018 Dec 8. Mol Genet Genomic Med. 2019. PMID: 30548218 Free PMC article.

10

The uncommon occurrence of two common inherited disorders in a single patient: a mini case series.

Zuazo F, Dumitrescu AV. Zuazo F, et al. Ophthalmic Genet. 2018 Oct;39(5):631-636. doi: 10.1080/13816810.2018.1498530. Epub 2018 Aug 29. Ophthalmic Genet. 2018. PMID: 30156925

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