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Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
Diaz-Horta O, Duman D, Foster J 2nd, Sırmacı A, Gonzalez M, Mahdieh N, Fotouhi N, Bonyadi M, Cengiz FB, Menendez I, Ulloa RH, Edwards YJ, Züchner S, Blanton S, Tekin M. Diaz-Horta O, et al. Among authors: fotouhi n. PLoS One. 2012;7(11):e50628. doi: 10.1371/journal.pone.0050628. Epub 2012 Nov 30. PLoS One. 2012. PMID: 23226338 Free PMC article.
Evaluation of CC-cytokine ligand 2 and complementary factor H Y402H polymorphisms and their interactional association with age-related macular degeneration.
Bonyadi M, Foruzandeh Z, Mohammadian T, Fotouhi N, Soheilian M, Jabbarpoor Bonyadi MH, Javadzadeh A, Moein H, Yaseri M. Bonyadi M, et al. Among authors: fotouhi n. Acta Ophthalmol. 2016 Dec;94(8):e779-e785. doi: 10.1111/aos.13143. Epub 2016 Jun 18. Acta Ophthalmol. 2016. PMID: 27316788 Free article.
Association between proto-oncogene mutations and clinicopathologic characteristics and overall survival in colorectal cancer in East Azerbaijan, Iran.
Dolatkhah R, Somi MH, Asvadi Kermani I, Bonyadi M, Sepehri B, Boostani K, Azadbakht S, Fotouhi N, Farassati F, Dastgiri S. Dolatkhah R, et al. Among authors: fotouhi n. Onco Targets Ther. 2016 Dec 7;9:7385-7395. doi: 10.2147/OTT.S116373. eCollection 2016. Onco Targets Ther. 2016. PMID: 27994469 Free PMC article.
64 results