Alikaşifoğlu M - Search Results

1

CYP1A1 polymorphism in adolescents with polycystic ovary syndrome.

Akgül S, Derman O, Alikaşifoğlu M, Aktaş D. Akgül S, et al. Among authors: alikasifoglu m. Int J Gynaecol Obstet. 2011 Jan;112(1):8-10. doi: 10.1016/j.ijgo.2010.07.032. Epub 2010 Oct 20. Int J Gynaecol Obstet. 2011. PMID: 20965504

2

CYP1A1 gene polymorphism and risk of epithelial ovarian neoplasm.

Aktas D, Guney I, Alikasifoglu M, Yüce K, Tuncbilek E, Ayhan A. Aktas D, et al. Among authors: alikasifoglu m. Gynecol Oncol. 2002 Aug;86(2):124-8. doi: 10.1006/gyno.2002.6720. Gynecol Oncol. 2002. PMID: 12144816

3

CYP1A1 gene polymorphism as a risk factor for cervical intraepithelial neoplasia and invasive cervical cancer.

Taskiran C, Aktas D, Yigit-Celik N, Alikasifoglu M, Yuce K, Tunçbilek E, Ayhan A. Taskiran C, et al. Among authors: alikasifoglu m. Gynecol Oncol. 2006 Jun;101(3):503-6. doi: 10.1016/j.ygyno.2005.11.018. Epub 2006 Jan 5. Gynecol Oncol. 2006. PMID: 16403567

4

CYP1A1 gene polymorphism and polycystic ovary syndrome.

Esinler I, Aktas D, Otegen U, Alikasifoglu M, Yarali H, Tuncbilek E. Esinler I, et al. Among authors: alikasifoglu m. Reprod Biomed Online. 2008 Mar;16(3):356-60. doi: 10.1016/s1472-6483(10)60596-2. Reprod Biomed Online. 2008. PMID: 18339256

5

CYP1A1 gene polymorphism and risk of endometrial hyperplasia and endometrial carcinoma.

Esinler I, Aktas D, Alikasifoglu M, Tuncbilek E, Ayhan A. Esinler I, et al. Among authors: alikasifoglu m. Int J Gynecol Cancer. 2006 May-Jun;16(3):1407-11. doi: 10.1111/j.1525-1438.2006.00605.x. Int J Gynecol Cancer. 2006. PMID: 16803538

6

Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population.

Boduroğlu K, Alanay Y, Alikaşifoğlu M, Aktaş D, Tunçbilek E. Boduroğlu K, et al. Among authors: alikasifoglu m. Turk J Pediatr. 2005 Oct-Dec;47(4):327-33. Turk J Pediatr. 2005. PMID: 16363341

7

Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population.

Kasım B, İrkeç M, Alikaşifoğlu M, Orhan M, Mocan MC, Aktaş D. Kasım B, et al. Among authors: alikasifoglu m. Mol Vis. 2013;19:114-20. Epub 2013 Jan 28. Mol Vis. 2013. PMID: 23378724 Free PMC article.

8

Prospective Turkish Cohort Study to Investigate the Frequency of Niemann-Pick Disease Type C Mutations in Consanguineous Families with at Least One Homozygous Family Member.

Topçu M, Aktas D, Öztoprak M, Mungan NÖ, Yuce A, Alikasifoglu M. Topçu M, et al. Among authors: alikasifoglu m. Mol Diagn Ther. 2017 Dec;21(6):643-651. doi: 10.1007/s40291-017-0293-9. Mol Diagn Ther. 2017. PMID: 28808920

9

Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry.

Utine GE, Şimşek-Kiper PÖ, Akgün-Doğan Ö, Ürel-Demir G, Alanay Y, Aktaş D, Boduroğlu K, Tunçbilek E, Alikaşifoğlu M. Utine GE, et al. Among authors: alikasifoglu m. Eur J Obstet Gynecol Reprod Biol. 2018 Feb;221:76-80. doi: 10.1016/j.ejogrb.2017.12.028. Epub 2017 Dec 16. Eur J Obstet Gynecol Reprod Biol. 2018. PMID: 29275276

10

Etiological yield of SNP microarrays in idiopathic intellectual disability.

Utine GE, Haliloğlu G, Volkan-Salancı B, Çetinkaya A, Kiper PÖ, Alanay Y, Aktaş D, Anlar B, Topçu M, Boduroğlu K, Alikaşifoğlu M. Utine GE, et al. Among authors: alikasifoglu m. Eur J Paediatr Neurol. 2014 May;18(3):327-37. doi: 10.1016/j.ejpn.2014.01.004. Epub 2014 Jan 25. Eur J Paediatr Neurol. 2014. PMID: 24508361

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