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E. Armagan, Almacıoglu, M. L., Yakut, T., Köse, A., Karkucak, M., Köksal, O., and Gorukmez, O., Cathecol-O-methyl transferase Val158Met genotype is not a risk factor for conversion disorder, vol. 12, pp. 852-858, 2013.
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Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype. Am. J. Med. Genet. 88: 497-502.<497::AID-AJMG12>3.0.CO;2-F   Glatt SJ, Faraone SV and Tsuang MT (2003). Association between a functional catechol O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies. Am. J. Psychiatry 160: 469-476. PMid:12611827   Gogos JA, Morgan M, Luine V, Santha M, et al. (1998). Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. Proc. Natl. Acad. Sci. U. S. A. 95: 9991-9996. PMid:9707588 PMCid:21449   Gutierrez B, Bertranpetit J, Guillamat R, Valles V, et al. (1997). Association analysis of the catechol O-methyltransferase gene and bipolar affective disorder. Am. J. Psychiatry 154: 113-115. 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Emerg. Med. Clin. North Am. 9: 137-159. PMid:2001663   Sadock BJ and Sadock VA (2000). Kaplan and Sadock's Comprehensive Textbook of Psychiatry. 7th edn. Lippincott Williams & Wilkins, Baltimore.   Sengupta S, Grizenko N, Schmitz N, Schwartz G, et al. (2008). COMT Val108/158Met polymorphism and the modulation of task-oriented behavior in children with ADHD. Neuropsychopharmacology 33: 3069-3077. PMid:18580877 PMCid:2885152   Shifman S, Bronstein M, Sternfeld M, Pisante A, et al. (2004). COMT: a common susceptibility gene in bipolar disorder and schizophrenia. Am. J. Med. Genet. B Neuropsychiatr. Genet. 128B: 61-64. PMid:15211633   Stonnington CM, Barry JJ and Fisher RS (2006). Conversion disorder. Am. J. Psychiatry 163: 1510-1517. PMid:16946174   Tunbridge EM, Bannerman DM, Sharp T and Harrison PJ (2004). Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex. J. Neurosci. 24: 5331- 5335. PMid:15190105   Weinshilboum RM, Otterness DM and Szumlanski CL (1999). Methylation pharmacogenetics: catechol O-methyltransferase, thiopurine methyltransferase, and histamine N-methyltransferase. Annu. Rev. Pharmacol. Toxicol. 39: 19-52. PMid:10331075   Wirgenes KV, Djurovic S, Sundet K, Agartz I, et al. (2010). Catechol O-methyltransferase variants and cognitive performance in schizophrenia and bipolar disorder versus controls. Schizophr. Res. 122: 31-37. PMid:20605701
T. Yakut, Karkucak, M., Ursavas, A., Gulten, T., Burgazlioglu, B., Gorukmez, O., and Karadag, M., Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients, vol. 9, pp. 734-738, 2010.
Agerholm-Larsen B, Nordestgaard BG and Tybjaerg-Hansen A (2000). ACE gene polymorphism in cardiovascular disease: meta-analyses of small and large studies in whites. Arterioscler. Thromb. Vasc. Biol. 20: 484-492. PMid:10669647   Ahmadi N, Shapiro GK, Chung SA and Shapiro CM (2009). Clinical diagnosis of sleep apnea based on single night of polysomnography vs. two nights of polysomnography. Sleep Breath. 13: 221-226. PMid:19067010   Barceló A, Elorza MA, Barbé F, Santos C, et al. (2001). Angiotensin converting enzyme in patients with sleep apnoea syndrome: plasma activity and gene polymorphisms. Eur. Respir. J. 17: 728-732. PMid:11401071   Bengtsson K, Orho-Melander M, Lindblad U, Melander O, et al. (1999). Polymorphism in the angiotensin converting enzyme but not in the angiotensinogen gene is associated with hypertension and type 2 diabetes: the Skaraborg Hypertension and Diabetes Project. J. Hypertens. 17: 1569-1575. PMid:10608470   Butler R, Morris AD and Struthers AD (1997). Angiotensin-converting enzyme gene polymorphism and cardiovascular disease. Clin. Sci. 93: 391-400. PMid:9486084   Candy GP, Skudicky D, Mueller UK, Woodiwiss AJ, et al. (1999). Association of left ventricular systolic performance and cavity size with angiotensin-converting enzyme genotype in idiopathic dilated cardiomyopathy. Am. J. Cardiol. 83: 740-744.   Lee YJ and Tsai JC (2002). ACE gene insertion/deletion polymorphism associated with 1998 World Health Organization definition of metabolic syndrome in Chinese type 2 diabetic patients. Diabetes Care 25: 1002-1008. PMid:12032106   Nakai K, Itoh C, Miura Y, Musya T, et al. (1994). Deletion polymorphism of the angiotensin I-converting enzyme gene associates with increased risk for ischemic heart diseases in the Japanese. Rinsho Byori 42: 689-694. PMid:8065033   O'Donnell CJ, Lindpaintner K, Larson MG, Rao VS, et al. (1998). Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study. Circulation 97: 1766-1772. PMid:9603529   Patel SR, Larkin EK, Mignot E, Lin L, et al. (2007). The association of angiotensin converting enzyme (ACE) polymorphisms with sleep apnea and hypertension. Sleep 30: 531-533. PMid:17520798   Piérola J, Barceló A, de la Pe-a M, Barbé F, et al. (2007). Beta3-adrenergic receptor Trp64Arg polymorphism and increased body mass index in sleep apnoea. Eur. Respir. J. 30: 743-747. PMid:17626108   Raynolds MV, Bristow MR, Bush EW, Abraham WT, et al. (1993). Angiotensin-converting enzyme DD genotype in patients with ischaemic or idiopathic dilated cardiomyopathy. Lancet 342: 1073-1075.   Rubinsztajn R, Kumor M, Byskiniewicz K and Chazan R (2004). Angiotensin-converting enzyme gene polymorphism in patients with obstructive sleep apnea. Pol. Arch. Med. Wewn. 112: 817-822. PMid:15526842   Sakai K, Takada T, Nakayama H, Kubota Y, et al. (2005). Serotonin-2A and 2C receptor gene polymorphisms in Japanese patients with obstructive sleep apnea. Intern. Med. 44: 928-933. PMid:16258205   Schunkert H, Hense HW, Holmer SR, Stender M, et al. (1994). Association between a deletion polymorphism of the angiotensin-converting-enzyme gene and left ventricular hypertrophy. N. Engl. J. Med. 330: 1634-1638. PMid:8177269   Seckin D, Ilhan N, Ilhan N and Ozbay Y (2006). The relationship between ACE insertion/deletion polymorphism and coronary artery disease with or without myocardial infarction. Clin. Biochem. 39: 50-54. PMid:16303122   Ursavaş A and Ege E (2003). Obstructive sleep apnea and cardiovascular diseases. Anadolu. Kardiyol. Derg. 3: 150-155. PMid:12826511   Xiao Y, Huang X, Qiu C, Zhu X, et al. (1999). Angiotensin I-converting enzyme gene polymorphism in Chinese patients with obstructive sleep apnea syndrome. Chin. Med. J. 112: 701-704.   Yaggi HK, Concato J, Kernan WN, Lichtman JH, et al. (2005). Obstructive sleep apnea as a risk factor for stroke and death. N. Engl. J. Med. 353: 2034-2041. PMid:16282178   Yavuz Z, Ursavas A, Ege E, Ozarda IY, et al. (2008). Homocysteine levels in patients with obstructive sleep apnea syndrome. Tuberk. Toraks 56: 37-42. PMid:18330753
M. Yildiz, Karkucak, M., Yakut, T., Gorukmez, O., and Ozmen, A., Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures, vol. 9, pp. 2131-2139, 2010.
Abbas A, Delvinquiere K, Lechevrel M, Lebailly P, et al. (2004). GSTM1, GSTT1, GSTP1 and CYP1A1 genetic polymorphisms and susceptibility to esophageal cancer in a French population: different pattern of squamous cell carcinoma and adenocarcinoma. World J. Gastroenterol. 10: 3389-3393. PMid:15526353   Balogh A, Derzbach L, Vannay A and Vásárhelyi B (2006). Lack of association between insulin-like growth factor I receptor G (+3174)A polymorphism and retinopathy of prematurity. Graefes Arch. Clin. Exp. Ophthalmol. 244: 1035-1038. PMid:16362313   Bányász I, Bokodi G, Vannay A, Szebeni B, et al. (2006). Genetic polymorphisms of vascular endothelial growth factor and angiopoietin 2 in retinopathy of prematurity. Curr. Eye Res. 31: 685-690. PMid:16877277   Barceló A, Elorza MA, Barbé F, Santos C, et al. (2001). Angiotensin converting enzyme in patients with sleep apnoea syndrome: plasma activity and gene polymorphisms. Eur. Respir. J. 17: 728-732. 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The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity. Graefes Arch. Clin. Exp. Ophthalmol. 246: 1467-1475. PMid:18546007   Lee YJ and Tsai JC (2002). ACE gene insertion/deletion polymorphism associated with 1998 World Health Organization definition of metabolic syndrome in Chinese type 2 diabetic patients. Diabetes Care 25: 1002-1008. PMid:12032106   Ng YK, Fielder AR, Shaw DE and Levene MI (1988). Epidemiology of retinopathy of prematurity. Lancet 2: 1235-1238.   Nishimura H, Tsuji H, Masuda H, Kasahara T, et al. (1999). The effects of angiotensin metabolites on the regulation of coagulation and fibrinolysis in cultured rat aortic endothelial cells. Thromb. Haemost. 82: 1516-1521. PMid:10595647   Onaran I, Ozaydin A, Ozdas SB and Ulutin T (2000a). Inhibition of platelet function by GSTM1-null human peripheral lymphocytes exposed to benzo(a)pyrene-induced challenge. Cell Biol. Toxicol. 16: 313-323. PMid:11201055   Onaran I, Ozaydin A, Akbas F, Gultepe M, et al. (2000b). Are individuals with glutathione S-transferase GSTT1 null genotype more susceptible to in vitro oxidative damage? J. Toxicol. Environ. Health A 59: 15-26. PMid:10681096   Rusai K, Vannay A, Szebeni B, Borgulya G, et al. (2008). Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity. Mol. Vis. 14: 286-290. PMid:18334945 PMCid:2263012   Shah VA, Yeo CL, Ling YL and Ho LY (2005). Incidence, risk factors of retinopathy of prematurity among very low birth weight infants in Singapore. Ann. Acad. Med. Singapore 34: 169-178. PMid:15827664   Shastry BS (2007). Assessment of the contribution of insulin-like growth factor I receptor 3174 G→A polymorphism to the progression of advanced retinopathy of prematurity. Eur. J. Ophthalmol. 17: 950-953. PMid:18050122   Shastry BS (2009). Lack of association of VEGF (-2578 C→A) and ANG 2 (-35 G→C) gene polymorphisms with the progression of retinopathy of prematurity. Graefes Arch. Clin. Exp. Ophthalmol. 247: 859-860. PMid:19018553   Shastry BS and Qu X (2007). Lack of association of the VEGF gene promoter (-634 G→C and -460 C→T) polymorphism and the risk of advanced retinopathy of prematurity. Graefes Arch. Clin. Exp. Ophthalmol. 245: 741-743. PMid:17119993   Shastry BS, Pendergast SD, Hartzer MK, Liu X, et al. (1997). Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity. Arch. Ophthalmol. 115: 651-655. PMid:9152134   Smith LE (2002). Pathogenesis of retinopathy of prematurity. Acta Paediatr. 91: 26-28.   Strange RC, Spiteri MA, Ramachandran S and Fryer AA (2001). Glutathione-S-transferase family of enzymes. Mutat. Res. 482: 21-26.   Subhani M, Combs A, Weber P, Gerontis C, et al. (2001). Screening guidelines for retinopathy of prematurity: the need for revision in extremely low birth weight infants. Pediatrics 107: 656-659. PMid:11335739   Uzunoğlu S, Acar H, Okudan N, Gökbel H, et al. (2006). Evaluation of the association between null genotypes of glutathione-S-transferases and Behcet's disease. Arch. Dermatol. Res. 297: 289-293. PMid:16283344   Van der Hel OL, Peeters PH, Hein DW, Doll MA, et al. (2003). NAT2 slow acetylation and GSTM1 null genotypes may increase postmenopausal breast cancer risk in long-term smoking women. Pharmacogenetics 13: 399-407. PMid:12835615   Vaughan DE (1997). The renin-angiotensin system and fibrinolysis. Am. J. Cardiol. 79: 12-16.   Yaggi HK, Concato J, Kernan WN, Lichtman JH, et al. (2005). Obstructive sleep apnea as a risk factor for stroke and death. N. Engl. J. Med. 353: 2034-2041. PMid:16282178   Zhong SL, Zhou SF, Chen X, Chan SY, et al. (2006). Relationship between genotype and enzyme activity of glutathione S-transferases M1 and P1 in Chinese. Eur. J. Pharm. Sci. 28: 77-85. PMid:16488119