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Print Staff CV |
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Print Staff CV |
Sinem Yalcintepe, Drenushe Zhuri, Hazal Sezginer Guler, Engin Atli, Selma Demir, Emine Ikbal Atli, Cisem Mail, Hakan Gurkan. Jacobsen Syndrome Firstly Reported with Dextrocardia Diagnosed with del(11) (q24q25). Molecular syndromology. https://doi.org/10.1159/000519149 (May 2022) |
Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes (August 2021) |
Drenushe Zhuri , Hakan Gurkan , Damla Eker , Yasemin Karal , Sinem Yalcintepe , Engin Atli , Selma Demir , Emine Ikbal Atli Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype Glob Med Genet 2022; 09(03): 226-236 DOI: 10.1055/s-0042-1751302 (September 2022) |
Sinem Yalcintepe, Hazal Sezginer Guler, Drenushe Zhuri, Damla Eker, Hakan Gurkan. Identification of a Novel KIF11 Variant p.(Leu804Thrfs Ter13) in a Case with Isolated Microcephaly.Journal of Head & Neck Physicians and Surgeons.DOI: 10.4103/jhnps.j hnps_14_22 (June 2022) |
Sinem Yalcintepe, Hakan Gurkan, Fatma Nur Korkmaz, Selma Demir, Engin Atli, Damla Eker, Hazal Sezginer Guler, Drenusha Zhuri, Emine Ikbal Atli, Semra Ayturk Salt, Mustafa Sahin, Sibel Guldiken. Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma. Journal of Kidney Cancer and VHL doi: 10.15586/jkcvhl.v8i1.171 (March 2021) |
Drenushe Zhuri, Hazal Sezginer Guler, Damla Eker, Fulya Dusenkalkan, Engin Atli, Sinem Yalcintepe, Selma Demir, Hakan Gurkan. Investigation of genetic etiology in gastrointestinal cancer patients with next generation sequencing method.6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi (16-18 september) Sözlü sunum (September 2021) |
Hazal Sezginer Guler, Drenushe Zhuri, Damla Eker, Fulya Dusenkalkan, Engin Atli, Sinem Yalcintepe, Selma Demir, Hakan Gurkan. Investigation of hereditary breast and ovarian cancer variants by targeted high-throughput sequencing method: single center experience. 6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi (16-18 september) Sözlü sunum (September 2021) |
Drenushë Zhuri, Hakan Gürkan, Damla Eker, Sinem Yalçıntepe, Engin Atlı, Selma Demir, Emine İkbal Atlı. Spinal müsküler atrofi fenotipinde modifiye edici genlerin etkilerinin araştırılması. 14 Ulusal Tıbbi Genetik Kongresi, e-kongre, 20-22 Kasım 2020. (Sözlü sunum) (December 2020) |
Damla EKER, Hakan GÜRKAN, Sinem YALÇINTEPE, Emine İkbal ATLI, Selma DEMİR, Engin ATLI, Drenushë ZHURİ, Nihan Alişya ERMAN, Hilmi TOZKIR. FARKLI KLİNİK ÖN TANILI HASTALARDA FMR 1 GENİ (CGG) TEKRAR SAYILARININ ARAŞTIRILMASI. 13 Ulusal Tıbbi Genetik Kongresi, Poster (7-11 Kasım) (November 2018) |