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Baris Sonmez

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Anthony J Aldave; V Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
V Yellore; Baris Sonmez; S A Rayner; Anthony J Aldave
A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.
Anthony J Aldave; V Yellore; Fei Yu; Nirit Bourla; Baris Sonmez; Andrew K Salem; Sylvia A Rayner; Kapil M Sampat; Charles M Krafchak; Julia E Richards
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.

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2008: Anthony J Aldave; V Yellore; Baris Sonmez; Nirit Bourla; Andrew K Salem; M Ali Khan; Sylvia A Rayner; Ben J Glasgow
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
Archives of ophthalmology 2008;126(3):371-7.
2008: V Yellore; Baris Sonmez; S A Rayner; Anthony J Aldave
A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.
The British journal of ophthalmology 2008;92(3):426-7.
2007: Anthony J Aldave; V Yellore; Fei Yu; Nirit Bourla; Baris Sonmez; Andrew K Salem; Sylvia A Rayner; Kapil M Sampat; Charles M Krafchak; Julia E Richards
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
American journal of medical genetics. Part A 2007;143A(21):2549-56.
2007: V Yellore; Baris Sonmez; Michael C Chen; Sylvia A Rayner; Eugene Thonar; Anthony J Aldave
An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.
Ophthalmic genetics 2007;28(3):169-74.
2007: Anthony J Aldave; Nirit Bourla; V Yellore; Sylvia A Rayner; M Ali Khan; Andrew K Salem; Baris Sonmez
Keratoconus is not associated with mutations in COL8A1 and COL8A2.
Cornea 2007;26(8):963-5.
2007: Anthony J Aldave; Baris Sonmez; Nirit Bourla; Gerald Schultz; Jeanette C Papp; Andrew K Salem; Sylvia A Rayner; V Yellore
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
Ophthalmic genetics 2007;28(2):57-67.
2007: Anthony J Aldave; Baris Sonmez; S Lance Forstot; Sylvia A Rayner; V Yellore; Ben J Glasgow
A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.
American journal of ophthalmology 2007;143(3):416-9.
2007: Baris Sonmez; Minh-Phuong Doan; David Rex Hamilton
Identification of scanning slit-beam topographic parameters important in distinguishing normal from keratoconic corneal morphologic features.
American journal of ophthalmology 2007;143(3):401-8.
2007: Baris Sonmez; Robert K Maloney
Central toxic keratopathy: description of a syndrome in laser refractive surgery.
American journal of ophthalmology 2007;143(3):420-7.
2007: Anthony J Aldave; Baris Sonmez
Elucidating the molecular genetic basis of the corneal dystrophies: are we there yet?
Archives of ophthalmology 2007;125(2):177-86.
2007: Baris Sonmez; Brian T Kim; Anthony J Aldave
Amniotic membrane transplantation with anterior stromal micropuncture for treatment of painful bullous keratopathy in eyes with poor visual potential.
Cornea 2007;26(2):227-9.
2007: V Yellore; M Ali Khan; Nirit Bourla; Sylvia A Rayner; Michael C Chen; Baris Sonmez; Rominder S Momi; Kapil M Sampat; Michael B Gorin; Anthony J Aldave
Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Molecular vision 2007;13():1777-82.
2006: Anthony J Aldave; Sylvia A Rayner; Andrew K Salem; Gina L Yoo; Brian T Kim; Monika Saeedian; Baris Sonmez; V Yellore
No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.
Investigative ophthalmology & visual science 2006;47(9):3787-90.