Sezerman OU - Search Results

1

Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms.

Ülgen E, Karacan S, Gerlevik U, Can Ö, Bilguvar K, Oktay Y, B Akyerli C, K Yüksel Ş, E Danyeli A, Tihan T, Sezerman OU, Yakıcıer MC, Pamir MN, Özduman K. Ülgen E, et al. Among authors: sezerman ou. Biomedicines. 2020 Dec 7;8(12):574. doi: 10.3390/biomedicines8120574. Biomedicines. 2020. PMID: 33297360 Free PMC article.

2

IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation.

Oktay Y, Ülgen E, Can Ö, Akyerli CB, Yüksel Ş, Erdemgil Y, Durası IM, Henegariu OI, Nanni EP, Selevsek N, Grossmann J, Erson-Omay EZ, Bai H, Gupta M, Lee W, Turcan Ş, Özpınar A, Huse JT, Sav MA, Flanagan A, Günel M, Sezerman OU, Yakıcıer MC, Pamir MN, Özduman K. Oktay Y, et al. Among authors: sezerman ou. Sci Rep. 2016 Jun 10;6:27569. doi: 10.1038/srep27569. Sci Rep. 2016. PMID: 27282637 Free PMC article.

3

Whole exome sequencing-based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas.

Ülgen E, Can Ö, Bilguvar K, Oktay Y, Akyerli CB, Danyeli AE, Yakıcıer MC, Sezerman OU, Pamir MN, Özduman K. Ülgen E, et al. Among authors: sezerman ou. J Neurosurg. 2019 Apr 5;132(5):1435-1446. doi: 10.3171/2019.1.JNS182938. J Neurosurg. 2019. PMID: 30952131

4

pathfindR: An R Package for Comprehensive Identification of Enriched Pathways in Omics Data Through Active Subnetworks.

Ulgen E, Ozisik O, Sezerman OU. Ulgen E, et al. Among authors: sezerman ou. Front Genet. 2019 Sep 25;10:858. doi: 10.3389/fgene.2019.00858. eCollection 2019. Front Genet. 2019. PMID: 31608109 Free PMC article.

5

Intraoperative Neuromonitoring of Blink Reflex During Posterior Fossa Surgeries and Its Correlation With Clinical Outcome.

Aydinlar EI, Kocak M, Soykam HO, Mat B, Dikmen PY, Sezerman OU, Elmaci İ, Pamir MN. Aydinlar EI, et al. Among authors: sezerman ou. J Clin Neurophysiol. 2022 May 1;39(4):299-306. doi: 10.1097/WNP.0000000000000777. Epub 2020 Sep 28. J Clin Neurophysiol. 2022. PMID: 33009043

6

Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma.

Ülgen E, Can Ö, Bilguvar K, Akyerli Boylu C, Kılıçturgay Yüksel Ş, Erşen Danyeli A, Sezerman OU, Yakıcıer MC, Pamir MN, Özduman K. Ülgen E, et al. Among authors: sezerman ou. BMC Med Genomics. 2021 Feb 23;14(1):54. doi: 10.1186/s12920-021-00904-3. BMC Med Genomics. 2021. PMID: 33622343 Free PMC article.

7

Identifying and elucidating the roles of Y198N and Y204F mutations in the PAH enzyme through molecular dynamic simulations.

Aslan T, Yenenler-Kutlu A, Gerlevik U, Aktuğlu Zeybek AÇ, Kıykım E, Sezerman OU, Birgul Iyison N. Aslan T, et al. Among authors: sezerman ou. J Biomol Struct Dyn. 2022;40(19):9018-9029. doi: 10.1080/07391102.2021.1921619. Epub 2021 May 10. J Biomol Struct Dyn. 2022. PMID: 33970801

8

driveR: a novel method for prioritizing cancer driver genes using somatic genomics data.

Ülgen E, Sezerman OU. Ülgen E, et al. Among authors: sezerman ou. BMC Bioinformatics. 2021 May 24;22(1):263. doi: 10.1186/s12859-021-04203-7. BMC Bioinformatics. 2021. PMID: 34030627 Free PMC article.

9

Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility.

Gerlevik U, Ergoren MC, Sezerman OU, Temel SG. Gerlevik U, et al. Among authors: sezerman ou. PeerJ. 2022 Mar 21;10:e12947. doi: 10.7717/peerj.12947. eCollection 2022. PeerJ. 2022. PMID: 35341049 Free PMC article.

10

Computational analysis of missense filamin-A variants, including the novel p.Arg484Gln variant of two brothers with periventricular nodular heterotopia.

Gerlevik U, Saygı C, Cangül H, Kutlu A, Çaralan EF, Topçu Y, Özören N, Sezerman OU. Gerlevik U, et al. Among authors: sezerman ou. PLoS One. 2022 May 25;17(5):e0265400. doi: 10.1371/journal.pone.0265400. eCollection 2022. PLoS One. 2022. PMID: 35613087 Free PMC article.

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