Özçelik H - Search Results

1

The distinct genetic pattern of ALS in Turkey and novel mutations.

Özoğuz A, Uyan Ö, Birdal G, Iskender C, Kartal E, Lahut S, Ömür Ö, Agim ZS, Eken AG, Sen NE, Kavak P, Saygı C, Sapp PC, Keagle P, Parman Y, Tan E, Koç F, Deymeer F, Oflazer P, Hanağası H, Gürvit H, Bilgiç B, Durmuş H, Ertaş M, Kotan D, Akalın MA, Güllüoğlu H, Zarifoğlu M, Aysal F, Döşoğlu N, Bilguvar K, Günel M, Keskin Ö, Akgün T, Özçelik H, Landers JE, Brown RH, Başak AN. Özoğuz A, et al. Among authors: ozcelik h. Neurobiol Aging. 2015 Apr;36(4):1764.e9-1764.e18. doi: 10.1016/j.neurobiolaging.2014.12.032. Epub 2015 Jan 10. Neurobiol Aging. 2015. PMID: 25681989 Free PMC article.

2

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, Özoğuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, Başak AN. Lahut S, et al. Among authors: ozcelik h. PLoS One. 2012;7(8):e42956. doi: 10.1371/journal.pone.0042956. Epub 2012 Aug 20. PLoS One. 2012. PMID: 22916186 Free PMC article.

3

Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.

Uyan Ö, Ömür Ö, Ağım ZS, Özoğuz A, Li H, Parman Y, Deymeer F, Oflazer P, Koç F, Tan E, Özçelik H, Başak AN. Uyan Ö, et al. Among authors: ozcelik h. PLoS One. 2013 Aug 26;8(8):e72381. doi: 10.1371/journal.pone.0072381. eCollection 2013. PLoS One. 2013. PMID: 23991104 Free PMC article.

4

Molecular and population genetic analyses of beta-thalassemia in Turkey.

Tadmouri GO, Tüzmen S, Ozçelik H, Ozer A, Baig SM, Senga EB, Başak AN. Tadmouri GO, et al. Among authors: ozcelik h. Am J Hematol. 1998 Mar;57(3):215-20. doi: 10.1002/(sici)1096-8652(199803)57:3<215::aid-ajh6>3.0.co;2-y. Am J Hematol. 1998. PMID: 9495372 Free article.

5

Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.

Agim ZS, Esendal M, Briollais L, Uyan O, Meschian M, Martinez LA, Ding Y, Basak AN, Ozcelik H. Agim ZS, et al. Among authors: ozcelik h. PLoS One. 2013;8(1):e53042. doi: 10.1371/journal.pone.0053042. Epub 2013 Jan 3. PLoS One. 2013. PMID: 23301017 Free PMC article.

6

Prenatal diagnosis of beta-thalassaemia and sickle cell anaemia in Turkey.

Tüzmen S, Tadmouri GO, Ozer A, Baig SM, Ozçelik H, Başaran S, Başak AN. Tüzmen S, et al. Among authors: ozcelik h. Prenat Diagn. 1996 Mar;16(3):252-8. doi: 10.1002/(SICI)1097-0223(199603)16:3<252::AID-PD839>3.0.CO;2-W. Prenat Diagn. 1996. PMID: 8710780

7

The molecular basis of beta-thalassemia in Turkey.

Başak AN, Ozçelik H, Ozer A, Tolun A, Aksoy M, Ağaoğlu L, Ridolfi F, Ulukutlu L, Akar N, Gürgey A, et al. Başak AN, et al. Among authors: ozcelik h. Hum Genet. 1992 May;89(3):315-8. doi: 10.1007/BF00220549. Hum Genet. 1992. PMID: 1351036

8

A novel frameshift mutation: deletion of C in codons 74/75 of the beta-globin gene causes beta zero-thalassemia in a Turkish patient.

Başak AN, Ozer A, Ozçelik H, Kirdar B, Gürgey A. Başak AN, et al. Among authors: ozcelik h. Hemoglobin. 1992;16(4):309-12. doi: 10.3109/03630269208998874. Hemoglobin. 1992. PMID: 1517110 No abstract available.

9

A novel deletion in a Turkish beta-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp).

Ozçelik H, Başak AN, Tüzmen S, Kirdar B, Akar N. Ozçelik H, et al. Hemoglobin. 1993 Aug;17(4):387-91. doi: 10.3109/03630269308997492. Hemoglobin. 1993. PMID: 8226099 No abstract available.

10

BRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast cancer patients.

Yazici H, Bitisik O, Akisik E, Cabioglu N, Saip P, Muslumanoglu M, Glendon G, Bengisu E, Ozbilen S, Dincer M, Turkmen S, Andrulis IL, Dalay N, Ozcelik H. Yazici H, et al. Among authors: ozcelik h. Br J Cancer. 2000 Sep;83(6):737-42. doi: 10.1054/bjoc.2000.1332. Br J Cancer. 2000. PMID: 10952777 Free PMC article.

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