Suri F - Search Results

1

Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma.

Suri F, Yazdani S, Narooie-Nejhad M, Zargar SJ, Paylakhi SH, Zeinali S, Pakravan M, Elahi E. Suri F, et al. Ophthalmology. 2009 Nov;116(11):2101-9. doi: 10.1016/j.ophtha.2009.04.045. Epub 2009 Sep 10. Ophthalmology. 2009. PMID: 19744731

2

Contributions of MYOC and CYP1B1 mutations to JOAG.

Bayat B, Yazdani S, Alavi A, Chiani M, Chitsazian F, Tusi BK, Suri F, Narooie-Nejhad M, Sanati MH, Elahi E. Bayat B, et al. Among authors: suri f. Mol Vis. 2008 Mar 13;14:508-17. Mol Vis. 2008. PMID: 18385784 Free PMC article.

3

Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.

Suri F, Kalhor R, Zargar SJ, Nilforooshan N, Yazdani S, Nezari H, Paylakhi SH, Narooie-Nejhad M, Bayat B, Sedaghati T, Ahmadian A, Elahi E. Suri F, et al. Mol Vis. 2008;14:2349-56. Epub 2008 Dec 18. Mol Vis. 2008. PMID: 19096718 Free PMC article.

4

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma.

Narooie-Nejad M, Paylakhi SH, Shojaee S, Fazlali Z, Rezaei Kanavi M, Nilforushan N, Yazdani S, Babrzadeh F, Suri F, Ronaghi M, Elahi E, Paisán-Ruiz C. Narooie-Nejad M, et al. Among authors: suri f. Hum Mol Genet. 2009 Oct 15;18(20):3969-77. doi: 10.1093/hmg/ddp338. Epub 2009 Aug 4. Hum Mol Genet. 2009. PMID: 19656777

5

Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients.

Elahi E, Narooie-Nejhad M, Suri F, Yazdani S. Elahi E, et al. Among authors: suri f. J Ophthalmic Vis Res. 2010 Apr;5(2):101-4. J Ophthalmic Vis Res. 2010. PMID: 22737338 Free PMC article.

6

Sex Bias in Primary Congenital Glaucoma Patients with and without CYP1B1 Mutations.

Suri F, Chitsazian F, Khoramian-Tusi B, Amini H, Yazdani S, Nilforooshan N, Zargar SJ, Elahi E. Suri F, et al. J Ophthalmic Vis Res. 2009 Apr;4(2):75-8. J Ophthalmic Vis Res. 2009. PMID: 23198051 Free PMC article.

7

Contribution of the latent transforming growth factor-β binding protein 2 gene to etiology of primary open angle glaucoma and pseudoexfoliation syndrome.

Jelodari-Mamaghani S, Haji-Seyed-Javadi R, Suri F, Nilforushan N, Yazdani S, Kamyab K, Elahi E. Jelodari-Mamaghani S, et al. Among authors: suri f. Mol Vis. 2013;19:333-47. Epub 2013 Feb 7. Mol Vis. 2013. PMID: 23401661 Free PMC article.

8

FOXC1 in human trabecular meshwork cells is involved in regulatory pathway that includes miR-204, MEIS2, and ITGβ1.

Paylakhi SH, Moazzeni H, Yazdani S, Rassouli P, Arefian E, Jaberi E, Arash EH, Gilani AS, Fan JB, April C, Amin S, Suri F, Elahi E. Paylakhi SH, et al. Among authors: suri f. Exp Eye Res. 2013 Jun;111:112-21. doi: 10.1016/j.exer.2013.03.009. Epub 2013 Mar 27. Exp Eye Res. 2013. PMID: 23541832

9

Diagnosis of cystathionine beta-synthase deficiency by genetic analysis.

Suri F, Narooie-Nejad M, Safari I, Moazzeni H, Rohani MR, Khajeh A, Klotzle B, Fan JB, Elahi E. Suri F, et al. J Neurol Sci. 2014 Dec 15;347(1-2):305-9. doi: 10.1016/j.jns.2014.10.031. Epub 2014 Oct 22. J Neurol Sci. 2014. PMID: 25455305

10

Glaucoma in iran and contributions of studies in iran to the understanding of the etiology of glaucoma.

Suri F, Yazdani S, Elahi E. Suri F, et al. J Ophthalmic Vis Res. 2015 Jan-Mar;10(1):68-76. doi: 10.4103/2008-322X.156120. J Ophthalmic Vis Res. 2015. PMID: 26005556 Free PMC article. Review.

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