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Items: 1 to 20 of 36

1.

Nicotinamide-N-Methyltransferase gene rs694539 variant and migraine risk.

Sazci A, Sazci G, Sazci B, Ergul E, Idrisoglu HA.

J Headache Pain. 2016 Dec;17(1):93. Epub 2016 Oct 10.

2.

Transcription factor 4 gene rs9960767 polymorphism in bipolar disorder.

Ozel MD, Onder ME, Sazci A.

Biomed Rep. 2016 Oct;5(4):506-510. Epub 2016 Aug 23.

3.

Association of the nibrin gene (NBN) variants with breast cancer.

Uzunoglu H, Korak T, Ergul E, Uren N, Sazci A, Utkan NZ, Kargi E, Triyaki Ç, Yirmibesoglu O.

Biomed Rep. 2016 Mar;4(3):369-373. Epub 2016 Jan 25.

4.

Association of Nicotinamide-N-Methyltransferase Gene rs694539 Variant with Epilepsy.

Sazci G, Sazci B, Sazci A, Idrisoglu HA.

Mol Neurobiol. 2016 Aug;53(6):4197-200. doi: 10.1007/s12035-015-9364-2. Epub 2015 Jul 28.

PMID:
26215836
5.

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, Crosiers D, Corsmit E, Elinck E, Sharma M, Krüger R, Lesage S, Brice A, Chung SJ, Kim MJ, Kim YJ, Ross OA, Wszolek ZK, Rogaeva E, Xi Z, Lang AE, Klein C, Weissbach A, Mellick GD, Silburn PA, Hadjigeorgiou GM, Dardiotis E, Hattori N, Ogaki K, Tan EK, Zhao Y, Aasly J, Valente EM, Petrucci S, Annesi G, Quattrone A, Ferrarese C, Brighina L, Deutschländer A, Puschmann A, Nilsson C, Garraux G, LeDoux MS, Pfeiffer RF, Boczarska-Jedynak M, Opala G, Maraganore DM, Engelborghs S, De Deyn PP, Cras P, Cruts M, Van Broeckhoven C; GEO-PD Consortium..

Neurology. 2014 Nov 18;83(21):1906-13. doi: 10.1212/WNL.0000000000001012. Epub 2014 Oct 17.

6.

Association of rs62063857 variant of the saitohin gene with Parkinson's disease.

Sonmez E, Ozel MD, Islek EE, Sazci A, Idrisoglu HA.

Cell Mol Neurobiol. 2015 Jan;35(1):115-21. doi: 10.1007/s10571-014-0102-5. Epub 2014 Aug 29.

PMID:
25168738
7.

Genetic variants in the PNPLA3 gene are associated with nonalcoholic steatohepatitis.

Islek EE, Sazci A, Ozel MD, Aygun C.

Genet Test Mol Biomarkers. 2014 Jul;18(7):489-96. doi: 10.1089/gtmb.2014.0019. Epub 2014 May 15.

PMID:
24831885
8.

Association of nicotinamide-N-methyltransferase (NNMT) gene rs694539 variant with bipolar disorder.

Sazci A, Ozel MD, Ergul E, Onder ME.

Gene. 2013 Dec 15;532(2):272-5. doi: 10.1016/j.gene.2013.08.077. Epub 2013 Sep 1.

PMID:
24004542
9.

Association of nicotinamide-N-methyltransferase gene rs694539 variant with patients with nonalcoholic steatohepatitis.

Sazci A, Ozel MD, Ergul E, Aygun C.

Genet Test Mol Biomarkers. 2013 Nov;17(11):849-53. doi: 10.1089/gtmb.2013.0309. Epub 2013 Aug 21.

PMID:
23964925
10.

Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.

Heckman MG, Elbaz A, Soto-Ortolaza AI, Serie DJ, Aasly JO, Annesi G, Auburger G, Bacon JA, Boczarska-Jedynak M, Bozi M, Brighina L, Chartier-Harlin MC, Dardiotis E, Destée A, Ferrarese C, Ferraris A, Fiske B, Gispert S, Hadjigeorgiou GM, Hattori N, Ioannidis JP, Jasinska-Myga B, Jeon BS, Kim YJ, Klein C, Kruger R, Kyratzi E, Lin CH, Lohmann K, Loriot MA, Lynch T, Mellick GD, Mutez E, Opala G, Park SS, Petrucci S, Quattrone A, Sharma M, Silburn PA, Sohn YH, Stefanis L, Tadic V, Tomiyama H, Uitti RJ, Valente EM, Vassilatis DK, Vilariño-Güell C, White LR, Wirdefeldt K, Wszolek ZK, Wu RM, Xiromerisiou G, Maraganore DM, Farrer MJ, Ross OA; Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium..

Neurobiol Aging. 2014 Jan;35(1):266.e5-14. doi: 10.1016/j.neurobiolaging.2013.07.013. Epub 2013 Aug 17.

11.

Heteromorphic variants of chromosome 9.

Kosyakova N, Grigorian A, Liehr T, Manvelyan M, Simonyan I, Mkrtchyan H, Aroutiounian R, Polityko AD, Kulpanovich AI, Egorova T, Jaroshevich E, Frolova A, Shorokh N, Naumchik IV, Volleth M, Schreyer I, Nelle H, Stumm M, Wegner RD, Reising-Ackermann G, Merkas M, Brecevic L, Martin T, Rodríguez L, Bhatt S, Ziegler M, Kreskowski K, Weise A, Sazci A, Vorsanova S, Cioffi Mde B, Ergul E.

Mol Cytogenet. 2013 Apr 1;6(1):14. doi: 10.1186/1755-8166-6-14.

12.

ZNF804A rs1344706 variant and schizophrenia in a Romanian population from Cluj Napoca.

Zaharie A, Ergul E, Ozel MD, Miclutia IV, Stanculete MF, Sazci A.

Genet Test Mol Biomarkers. 2012 Sep;16(9):1135-7. doi: 10.1089/gtmb.2012.0066. Epub 2012 Jul 9.

PMID:
22775511
13.

Gender-specific association of methylenetetrahydrofolate reductase gene polymorphisms with sporadic amyotrophic lateral sclerosis.

Sazci A, Ozel MD, Emel E, Idrisoglu HA.

Genet Test Mol Biomarkers. 2012 Jul;16(7):716-21. doi: 10.1089/gtmb.2011.0313. Epub 2012 Mar 2.

PMID:
22385294
14.

A polymerase chain reaction-restriction fragment length polymorphism method for screening ZNF804A gene polymorphism (rs1344706) in patients with schizophrenia: a significant association.

Sazci A, Ozel MD, Ergul E, Yildiz M.

Genet Test Mol Biomarkers. 2012 Mar;16(3):157-61. doi: 10.1089/gtmb.2011.0142. Epub 2011 Oct 11.

PMID:
21988329
15.

Methylenetetrahydrofolate reductase gene polymorphisms in Turkish children with attention-deficit/hyperactivity disorder.

Ergul E, Sazci A, Kara I.

Genet Test Mol Biomarkers. 2012 Jan;16(1):67-9. doi: 10.1089/gtmb.2011.0062. Epub 2011 Aug 5.

PMID:
21819229
16.

TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis.

Ergul E, Ozel MD, Sazci A, Idrisoglu HA.

Neurobiol Aging. 2011 Nov;32(11):2107.e1-2. doi: 10.1016/j.neurobiolaging.2011.05.021. Epub 2011 Jul 7.

PMID:
21741128
17.

Evidence for the presence of full-length PARK2 mRNA and Parkin protein in human blood.

Kasap M, Akpinar G, Sazci A, Idrisoglu HA, Vahaboğlu H.

Neurosci Lett. 2009 Sep 4;460(3):196-200. doi: 10.1016/j.neulet.2009.05.079. Epub 2009 Jun 6.

PMID:
19501131
18.

A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.

Ergul E, Liehr T, Mrasek K, Sazci A.

Fertil Steril. 2009 Jul;92(1):391.e9-391.e12. doi: 10.1016/j.fertnstert.2009.02.042. Epub 2009 Apr 14.

PMID:
19368909
19.

Effect of the methylenetetrahydrofolate reductase gene polymorphisms on homocysteine, folate and vitamin B12 in patients with bipolar disorder and relatives.

Ozbek Z, Kucukali CI, Ozkok E, Orhan N, Aydin M, Kilic G, Sazci A, Kara I.

Prog Neuropsychopharmacol Biol Psychiatry. 2008 Jul 1;32(5):1331-7. doi: 10.1016/j.pnpbp.2008.04.016. Epub 2008 May 2.

PMID:
18513846
20.

The comparison of VEGFR-1-binding domain of VEGF-A with modelled VEGF-C sheds light on receptor specificity.

Kasap M, Sazci A.

J Theor Biol. 2008 Aug 7;253(3):446-51. doi: 10.1016/j.jtbi.2008.03.018. Epub 2008 Mar 26.

PMID:
18479712

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