Similar articles for PMID: 9463332

Year	Number of Results
1994	1
1995	2
1996	3
1997	3
1998	6
1999	3
2000	5
2001	5
2002	5
2003	4
2004	6
2005	3
2006	7
2007	5
2008	5
2009	16
2010	8
2011	8
2012	2
2013	6
2014	6
2015	9
2016	5
2017	6
2018	8
2019	6
2020	5
2021	7
2022	9
2023	2
2024	0

1

Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia.

Bejjani BA, Lewis RA, Tomey KF, Anderson KL, Dueker DK, Jabak M, Astle WF, Otterud B, Leppert M, Lupski JR. Bejjani BA, et al. Am J Hum Genet. 1998 Feb;62(2):325-33. doi: 10.1086/301725. Am J Hum Genet. 1998. PMID: 9463332 Free PMC article.

2

Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.

Bejjani BA, Stockton DW, Lewis RA, Tomey KF, Dueker DK, Jabak M, Astle WF, Lupski JR. Bejjani BA, et al. Hum Mol Genet. 2000 Feb 12;9(3):367-74. doi: 10.1093/hmg/9.3.367. Hum Mol Genet. 2000. PMID: 10655546

3

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21.

Stoilov I, Akarsu AN, Sarfarazi M. Stoilov I, et al. Hum Mol Genet. 1997 Apr;6(4):641-7. doi: 10.1093/hmg/6.4.641. Hum Mol Genet. 1997. PMID: 9097971

4

Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.

Stoilov I, Akarsu AN, Alozie I, Child A, Barsoum-Homsy M, Turacli ME, Or M, Lewis RA, Ozdemir N, Brice G, Aktan SG, Chevrette L, Coca-Prados M, Sarfarazi M. Stoilov I, et al. Am J Hum Genet. 1998 Mar;62(3):573-84. doi: 10.1086/301764. Am J Hum Genet. 1998. PMID: 9497261 Free PMC article.

5

A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma.

Chakrabarti S, Ghanekar Y, Kaur K, Kaur I, Mandal AK, Rao KN, Parikh RS, Thomas R, Majumder PP. Chakrabarti S, et al. Hum Mol Genet. 2010 Oct 15;19(20):4083-90. doi: 10.1093/hmg/ddq309. Epub 2010 Jul 21. Hum Mol Genet. 2010. PMID: 20660114

6

Molecular basis of Peters anomaly in Saudi Arabia.

Edward D, Al Rajhi A, Lewis RA, Curry S, Wang Z, Bejjani B. Edward D, et al. Ophthalmic Genet. 2004 Dec;25(4):257-70. doi: 10.1080/13816810490902648. Ophthalmic Genet. 2004. PMID: 15621878

7

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma.

Plásilová M, Stoilov I, Sarfarazi M, Kádasi L, Feráková E, Ferák V. Plásilová M, et al. J Med Genet. 1999 Apr;36(4):290-4. J Med Genet. 1999. PMID: 10227395 Free PMC article.

8

Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.

Abu-Amero KK, Osman EA, Mousa A, Wheeler J, Whigham B, Allingham RR, Hauser MA, Al-Obeidan SA. Abu-Amero KK, et al. Mol Vis. 2011;17:2911-9. Epub 2011 Nov 12. Mol Vis. 2011. PMID: 22128238 Free PMC article.

9

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.

10

Linkage of autosomal recessive primary congenital glaucoma to the GLC3A locus in Roms (Gypsies) from Slovakia.

Plásilová M, Feráková E, Kádasi L, Poláková H, Gerinec A, Ott J, Ferák V. Plásilová M, et al. Hum Hered. 1998 Jan-Feb;48(1):30-3. doi: 10.1159/000022778. Hum Hered. 1998. PMID: 9463798

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