Bayazit YA - Search Results

1

Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.

Shearer AE, Eppsteiner RW, Booth KT, Ephraim SS, Gurrola J 2nd, Simpson A, Black-Ziegelbein EA, Joshi S, Ravi H, Giuffre AC, Happe S, Hildebrand MS, Azaiez H, Bayazit YA, Erdal ME, Lopez-Escamez JA, Gazquez I, Tamayo ML, Gelvez NY, Leal GL, Jalas C, Ekstein J, Yang T, Usami S, Kahrizi K, Bazazzadegan N, Najmabadi H, Scheetz TE, Braun TA, Casavant TL, LeProust EM, Smith RJ. Shearer AE, et al. Among authors: bayazit ya. Am J Hum Genet. 2014 Oct 2;95(4):445-53. doi: 10.1016/j.ajhg.2014.09.001. Epub 2014 Sep 25. Am J Hum Genet. 2014. PMID: 25262649 Free PMC article.

2

Association of the T102C polymorphism of 5-HT2A receptor gene with aura in migraine.

Erdal ME, Herken H, Yilmaz M, Bayazit YA. Erdal ME, et al. Among authors: bayazit ya. J Neurol Sci. 2001 Jul 15;188(1-2):99-101. doi: 10.1016/s0022-510x(01)00556-1. J Neurol Sci. 2001. PMID: 11489292

3

GJB2 gene mutations causing familial hereditary deafness in Turkey.

Bayazit YA, Cable BB, Cataloluk O, Kara C, Chamberlin P, Smith RJ, Kanlikama M, Ozer E, Cakmak EA, Mumbuc S, Arslan A. Bayazit YA, et al. Int J Pediatr Otorhinolaryngol. 2003 Dec;67(12):1331-5. doi: 10.1016/j.ijporl.2003.08.003. Int J Pediatr Otorhinolaryngol. 2003. PMID: 14643477

4

Two novel missense mutations in the connexin 26 gene in Turkish patients with nonsyndromic hearing loss.

Yilmaz A, Menevse S, Bayazit Y, Karamert R, Ergin V, Menevse A. Yilmaz A, et al. Biochem Genet. 2010 Apr;48(3-4):248-56. doi: 10.1007/s10528-009-9314-7. Epub 2009 Nov 26. Biochem Genet. 2010. PMID: 19941053

5

Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndrome.

Ylmaz M, Bayazit YA, Ciftci TU, Erdal ME, Urhan M, Kokturk O, Kemaloglu YK, Inal E. Ylmaz M, et al. Among authors: bayazit ya. Laryngoscope. 2005 May;115(5):832-6. doi: 10.1097/01.MLG.0000157334.88700.E6. Laryngoscope. 2005. PMID: 15867649

6

GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.

Baysal E, Bayazit YA, Ceylaner S, Alatas N, Donmez B, Ceylaner G, San I, Korkmaz B, Yilmaz A, Menevse A, Altunyay S, Gunduz B, Goksu N, Arslan A, Ekmekci A. Baysal E, et al. Among authors: bayazit ya. J Genet. 2008 Apr;87(1):53-7. doi: 10.1007/s12041-008-0007-5. J Genet. 2008. PMID: 18560174 Free article.

7

T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction.

Mutlu N, Erdal ME, Herken H, Oz G, Bayazit YA. Mutlu N, et al. Among authors: bayazit ya. Oral Dis. 2004 Nov;10(6):349-52. doi: 10.1111/j.1601-0825.2004.01037.x. Oral Dis. 2004. PMID: 15533210

8

Association of GABA(B)R1 receptor gene polymorphism with obstructive sleep apnea syndrome.

Bayazit YA, Yilmaz M, Kokturk O, Erdal ME, Ciftci T, Gokdogan T, Kemaloglu Y, Ileri F. Bayazit YA, et al. ORL J Otorhinolaryngol Relat Spec. 2007;69(3):190-7. doi: 10.1159/000099230. Epub 2007 Jan 30. ORL J Otorhinolaryngol Relat Spec. 2007. PMID: 17264536

9

Insulin receptor substrate gene polymorphism is associated with obstructive sleep apnea syndrome in men.

Bayazit YA, Erdal ME, Yilmaz M, Ciftci TU, Soylemez F, Gokdoğan T, Kokturk O, Kemaloglu YK, Koybasioglu A. Bayazit YA, et al. Laryngoscope. 2006 Nov;116(11):1962-5. doi: 10.1097/01.mlg.0000235933.74319.80. Laryngoscope. 2006. PMID: 17075427

10

Significance of serotonin transporter gene polymorphism in migraine.

Yilmaz M, Erdal ME, Herken H, Cataloluk O, Barlas O, Bayazit YA. Yilmaz M, et al. Among authors: bayazit ya. J Neurol Sci. 2001 May 1;186(1-2):27-30. doi: 10.1016/s0022-510x(01)00491-9. J Neurol Sci. 2001. PMID: 11412868

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