Similar articles for PMID: 22942166

Year	Number of Results
1961	1
1979	1
1987	1
1997	1
1998	3
1999	2
2000	4
2001	5
2002	6
2003	11
2004	11
2005	6
2006	16
2007	11
2008	13
2009	16
2010	9
2011	10
2012	7
2013	15
2014	9
2015	11
2016	12
2017	9
2018	11
2019	9
2020	4
2021	11
2022	6
2023	6
2024	0

1

A clinical and molecular genetics study of primary congenital glaucoma in South Korea.

Suh W, Kee C. Suh W, et al. Br J Ophthalmol. 2012 Nov;96(11):1372-7. doi: 10.1136/bjophthalmol-2012-301517. Epub 2012 Sep 1. Br J Ophthalmol. 2012. PMID: 22942166

2

Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma.

Kim HJ, Suh W, Park SC, Kim CY, Park KH, Kook MS, Kim YY, Kim CS, Park CK, Ki CS, Kee C. Kim HJ, et al. Mol Vis. 2011;17:2093-101. Epub 2011 Aug 9. Mol Vis. 2011. PMID: 21850185 Free PMC article.

3

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

El-Ashry MF, Abd El-Aziz MM, Bhattacharya SS. El-Ashry MF, et al. J Glaucoma. 2007 Jan;16(1):104-11. doi: 10.1097/01.ijg.0000212288.00917.e1. J Glaucoma. 2007. PMID: 17224759

4

Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations.

Bagiyeva S, Marfany G, Gonzalez-Angulo O, Gonzalez-Duarte R. Bagiyeva S, et al. Mol Vis. 2007 Aug 27;13:1458-68. Mol Vis. 2007. PMID: 17893647

5

Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.

Hilal L, Boutayeb S, Serrou A, Refass-Buret L, Shisseh H, Bencherifa F, El Mzibri M, Benazzouz B, Berraho A. Hilal L, et al. Mol Vis. 2010 Jul 2;16:1215-26. Mol Vis. 2010. PMID: 20664688 Free PMC article.

6

Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population.

Geyer O, Wolf A, Levinger E, Harari-Shacham A, Walton DS, Shochat C, Korem S, Bercovich D. Geyer O, et al. Am J Ophthalmol. 2011 Feb;151(2):263-71.e1. doi: 10.1016/j.ajo.2010.08.038. Epub 2010 Dec 18. Am J Ophthalmol. 2011. PMID: 21168818

7

Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.

Al-Haddad C, Abdulaal M, Badra R, Barikian A, Noureddine B, Farra C. Al-Haddad C, et al. Ophthalmic Genet. 2016;37(1):31-6. doi: 10.3109/13816810.2014.924015. Epub 2014 Jun 18. Ophthalmic Genet. 2016. PMID: 24940937

8

Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.

Millá E, Mañé B, Duch S, Hernan I, Borràs E, Planas E, Dias Mde S, Carballo M, Gamundi MJ; Spanish Multicenter Glaucoma Group-Estudio Multicéntrico Español de Investigación Genética del Glaucoma, EMEIGG. Millá E, et al. Mol Vis. 2013 Aug 4;19:1707-22. Print 2013. Mol Vis. 2013. PMID: 23922489 Free PMC article.

9

Myocilin gene implicated in primary congenital glaucoma.

Kaur K, Reddy AB, Mukhopadhyay A, Mandal AK, Hasnain SE, Ray K, Thomas R, Balasubramanian D, Chakrabarti S. Kaur K, et al. Clin Genet. 2005 Apr;67(4):335-40. doi: 10.1111/j.1399-0004.2005.00411.x. Clin Genet. 2005. PMID: 15733270

10

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Vincent AL, et al. Am J Hum Genet. 2002 Feb;70(2):448-60. doi: 10.1086/338709. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774072 Free PMC article.

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