PubMed for id: 23322

Year	Number of Results
1993	3
1996	1
1999	1
2002	2
2003	2
2004	1
2005	1
2006	1
2007	3
2008	6
2009	8
2010	6
2011	8
2012	4
2013	1
2014	1
2015	3
2016	6
2017	4
2018	9
2019	3
2020	3
2021	5
2022	3
2023	2
2024	0

1

Identification of Pathogenic Variants in RPGRIP1L with Meckel Syndrome and Preimplantation Genetic Testing in a Chinese Family.

Zhang P, Wu B, Wang Y, Ren Y, Li G, Qan Y, Lei C, Wang H. Zhang P, et al. Reprod Sci. 2022 Aug;29(8):2200-2207. doi: 10.1007/s43032-022-00898-y. Epub 2022 Mar 1. Reprod Sci. 2022. PMID: 35233738

2

A novel association of rs13334070 in the RPGRIP1L gene with adiposity factors discovered by joint linkage and linkage disequilibrium analysis in Iranian pedigrees: Tehran Cardiometabolic Genetic Study (TCGS).

Javanrouh N, Soltanian AR, Tapak L, Azizi F, Ott J, Daneshpour MS. Javanrouh N, et al. Genet Epidemiol. 2019 Apr;43(3):342-351. doi: 10.1002/gepi.22179. Epub 2018 Dec 30. Genet Epidemiol. 2019. PMID: 30597647

3

Rs3213758 in the RPGRIP1L Gene Associated with Susceptibility to Segmental Vitiligo in a Chinese Han Population.

Hu M, Wang TM, Dong YY, She QY, Gao S, Liu DX, Deng YH. Hu M, et al. Chin Med J (Engl). 2018 Dec 20;131(24):3022-3024. doi: 10.4103/0366-6999.247203. Chin Med J (Engl). 2018. PMID: 30539925 Free PMC article. No abstract available.

4

The basal body gene, RPGRIP1L, is a candidate tumour suppressor gene in human hepatocellular carcinoma.

Lin YW, Yan MD, Shih YL, Hsieh CB. Lin YW, et al. Eur J Cancer. 2009 Jul;45(11):2041-9. doi: 10.1016/j.ejca.2009.04.012. Epub 2009 May 4. Eur J Cancer. 2009. PMID: 19410446

5

RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.

Brancati F, Travaglini L, Zablocka D, Boltshauser E, Accorsi P, Montagna G, Silhavy JL, Barrano G, Bertini E, Emma F, Rigoli L; International JSRD Study Group; Dallapiccola B, Gleeson JG, Valente EM. Brancati F, et al. Clin Genet. 2008 Aug;74(2):164-70. doi: 10.1111/j.1399-0004.2008.01047.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18565097 Free PMC article.

6

Mutations in RPGRIP1L: extending the clinical spectrum of ciliopathies.

Devuyst O, Arnould VJ. Devuyst O, et al. Nephrol Dial Transplant. 2008 May;23(5):1500-3. doi: 10.1093/ndt/gfn033. Epub 2008 Feb 14. Nephrol Dial Transplant. 2008. PMID: 18281315 Review. No abstract available.

7

Association of fat mass and obesity-associated and retinitis pigmentosa guanosine triphosphatase (GTPase) regulator-interacting protein-1 like polymorphisms with body mass index in Chinese women.

Chen B, Li Z, Chen J, Ji J, Shen J, Xu Y, Zhao Y, Liu D, Shen Y, Zhang W, Shen J, Wang Y, Shi Y. Chen B, et al. Endocr J. 2018 Jul 28;65(7):783-791. doi: 10.1507/endocrj.EJ17-0554. Epub 2018 Apr 14. Endocr J. 2018. PMID: 29657248 Free article.

8

The molecular motor Myosin Va interacts with the cilia-centrosomal protein RPGRIP1L.

Assis LH, Silva-Junior RM, Dolce LG, Alborghetti MR, Honorato RV, Nascimento AF, Melo-Hanchuk TD, Trindade DM, Tonoli CC, Santos CT, Oliveira PS, Larson RE, Kobarg J, Espreafico EM, Giuseppe PO, Murakami MT. Assis LH, et al. Sci Rep. 2017 Mar 7;7:43692. doi: 10.1038/srep43692. Sci Rep. 2017. PMID: 28266547 Free PMC article.

9

Genetic association of the gene encoding RPGRIP1L with susceptibility to vascular dementia.

Woo J, Lee C. Woo J, et al. Gene. 2012 May 10;499(1):160-2. doi: 10.1016/j.gene.2012.03.010. Epub 2012 Mar 8. Gene. 2012. PMID: 22425971

10

Regulation of FTO and FTM expression during human preadipocyte differentiation.

Tews D, Fischer-Posovszky P, Wabitsch M. Tews D, et al. Horm Metab Res. 2011 Jan;43(1):17-21. doi: 10.1055/s-0030-1265130. Epub 2010 Sep 23. Horm Metab Res. 2011. PMID: 20865646

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