Education/Academic Info | ||
---|---|---|
Undergraduate Degree | Marmara University Tıp Fakültesi | 2003 |
Specialization in Medicine | Gazi University Tıp Fakültesi Tıbbi Genetik Anabilim Dalı | 2008 |
Assistant Professor | Dokuz Eylül University Tıp Fakültesi | 2018 |
Associate Professor | Turkish Inter-Universities Board Tıbbi Genetik | 2020 |
NO | NAME | YEAR |
1 | Late onset Bartter syndrome: Bartter syndrome type 2 presenting with isolated nephrocalcinosis and h... | 2022 |
2 | Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation seq... | 2022 |
3 | Selective bilateral vestibular neuropathy in a Turkish CMT1B family with a novel MPZ mutation... | 2021 |
4 | The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma pati... | 2020 |
5 | Could high levels of cell-free DNA in maternal blood be associated with maternal health and perinata... | 2020 |
6 | Warburg Micro Syndrome 1 due to Segmental Paternal Uniparental Isodisomy of Chromosome 2 Detected by... | 2020 |
7 | Can fetal fractions in the cell-free DNA test predict the onset of fetal growth restriction?... | 2020 |
8 | Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with p... | 2019 |
9 | Initial Next-Generation Sequencing (NGS) Results of Alport Syndrome... | 2019 |
10 | First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss.... | 2019 |
11 | Spinal Muscular Atrophy Results and Comparison of Commonly Used Methods.... | 2019 |
12 | Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes... | 2019 |
13 | A toddler with a novel LEPR mutation... | 2019 |
14 | The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15... | 2019 |
15 | New Insight of Tumor Microenvironment in Non-Small Cell Lung Cancer... | 2019 |
16 | Targeted fetal cell-free DNA screening for aneuploidies in 4,594 pregnancies: Single center study.... | 2019 |
17 | cfDNA in exhaled breath condensate (EBC) and contamination by ambient air: toward volatile biopsies... | 2019 |
18 | Targeted Next Generation Sequencing of MLH1, MSH2, and MSH6 Genes in Patients with Endometrial Carci... | 2019 |
19 | Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)... | 2018 |
20 | Fetal HLA-G Alleles and Their Effect on Miscarriage... | 2018 |
21 | An unusual cause of cavitating leukoencephalopathy: ethylmalonic encephalopathy.... | 2018 |
22 | Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum... | 2018 |
23 | Experiences in Microarray-based Evaluation of Developmental Disabilities and Congenital Anomalies.... | 2017 |
24 | QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey.... | 2017 |
25 | Determination of HER2 and p53 Mutations by Sequence Analysis Method and EGFR/Chromosome 7 Gene Statu... | 2015 |
26 | Chromosome abnormality incidence in fetuses with cerebral ventriculomegaly... | 2014 |
27 | Asn680ser polymorphism of the follicle-stimulating hormone receptor gene (FSHR) is not associated wi... | 2014 |
28 | Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syn... | 2014 |
29 | Chromosomal and structural anomalies in fetuses with open neural tube defects.... | 2014 |
30 | Prenatal diagnosis of an autosomal translocation with regular trisomy 21.... | 2013 |
31 | A case of dup(3q) syndrome. Genetic Counseling... | 2013 |
32 | New Phenotype with Generalized Platyspondyly, Large Mandible, Hypoplastic Teeth, Strabismus, Hyperop... | 2011 |
33 | The progeny of homozygous identical reciprocal translocation carrier mother.... | 2010 |
34 | The importance of systematic genetic approach to familial schizophrenia cases and discussion of cryp... | 2010 |
35 | The apolipoprotein E gene and Taq1A polymorphisms in childhood obesity.... | 2010 |
36 | Prenatal diagnosis of mosaic ring 22 duplication/deletion with terminal 22q13 deletion due to abnorm... | 2009 |
37 | Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity.... | 2009 |
38 | A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anem... | 2009 |
39 | CTLA4 gene polymorphisms in children and adolescents with autoimmune thyroid diseases.... | 2008 |
40 | A case with bilateral radio-ulnar synostosis... | 2008 |
41 | An unexpected finding in a child with neurological problems: mosaic ring chromosome 18... | 2008 |
42 | A case with a ring chromosome 22... | 2008 |
43 | A boy with small supernumerary marker chromosome X identified by FISH.... | 2007 |
44 | A new case of hairy elbows syndrome (hypertrichosis cubiti)... | 2007 |
NO | NAME | DATE |
1 | Kawasaki hastalığının sıklık ve ÅŸiddeti ile MEFV mutasyonları arasındaki iliÅŸkinin araÅŸtÄ... | 23/03/2022 - 26/03/2022 |
2 | LATE-ONSET BARTTER SYNDROME TYPE 2 PRESENTING WITH ISOLATED NEPHROCALCINOSIS WITHOUT HYPOKALEMIC ALK... | 16/09/2021 - 19/09/2021 |
3 | A novel mutation of SGSH gene and clinical presentation of two patients with mucopolysaccharidosis t... | 20/11/2020 - 22/11/2020 |
4 | Genetic analyses in understanding of renal tubulopathies... | 20/02/2020 - 22/02/2020 |
5 | Pathogenic variations of MUTYH gene in hereditary cancer cases... | 20/02/2020 - 22/02/2020 |
6 | Kolon kanserinde alt tip transkriptom veri analizi... | 16/01/2020 - 18/01/2020 |
7 | NÖROFİBROMATOZİSTE OPTİK GLİOM: NOVEL MUTASYON VE LİTERATÜRÜN GÖZDEN GEÇİRİLMES... | 09/01/2020 - 11/01/2020 |
8 | Distrofinonopatili Ailelerde Genotip ve Fenotip İlişkisinin Ayrıntılandırılması.... | 01/11/2019 - 03/11/2019 |
9 | Küçük hücreli dışı akciğer kanseri (KHDAK) olgularına ait epidermal büyüme faktörü rese... | 05/10/2019 - 06/10/2019 |
10 | PKD1 geninde yeni mutasyon saptanan polikistik böbrek hastalığı ailesi... | 25/09/2019 - 27/09/2019 |
11 | Atipik bulgularla baÅŸvuran noonnan sendromlu, nadir bir patojenik deÄŸiÅŸime sahip olgu sunumu... | 25/09/2019 - 27/09/2019 |
12 | Prenatal Izlemde Genetiğin Tani Koyduğu En Net Örneklerden Biri Tuberoskleroz... | 25/09/2019 - 27/09/2019 |
13 | Retinitis Pigmentosali Olgularımızın Genetik Spektrumu... | 25/09/2019 - 27/09/2019 |
14 | PKD1 geninde yeni mutasyon saptanan polikistik böbrek hastalığı ailesi.... | 25/09/2019 - 27/09/2019 |
15 | Nörofibromatosis Olgularının Klinik Genetik Özellikleri ve 2 Yeni Varyantın Tanımlanması... | 25/09/2019 - 27/09/2019 |
16 | Alport Sendromlu Olgularımızın Genetik Sonuçları... | 25/09/2019 - 27/09/2019 |
17 | Investigation of Epidermal Growth Factor Receptor (EGFR) Pathway Related, Exosomal miRNAs in Non-sma... | 22/09/2019 - 24/09/2019 |
18 | CLINICAL ANALYSIS OF GERMLINE CELL AND SOMATIC VARIANTS... | 22/09/2019 - 24/09/2019 |
19 | Microarray Based Prenatal Diagnosis.... | 17/04/2019 - 20/04/2019 |
20 | Two Novel Variants of AGL and GBE1 Genes in Glycogen Storage Disease Patients... | 17/04/2019 - 20/04/2019 |
21 | DIFFERENT PRESENTATIONS OF LONG QT SYNDROME... | 17/04/2019 - 20/04/2019 |
22 | A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic feature... | 17/04/2019 - 20/04/2019 |
23 | Novel LEPR and MC4R gene mutations in two early onset obesity patients... | 17/04/2019 - 20/04/2019 |
24 | Tükürük Bezi Malignitelerinin Davranışında EGFR Gen Mutasyonunun Etkisi: Moleküler Gen Analiz... | 04/04/2019 - 07/04/2019 |
25 | A case with mutation in the TNFRSF1A gene.... | 21/02/2019 - 23/02/2019 |
26 | Investigation of cfDNA in volatile condensate.... | 21/02/2019 - 23/02/2019 |
27 | A novel pathogenic frameshift variant of ETFDH in a patient with myopathy.... | 29/11/2018 - 02/12/2018 |
28 | Liquid biopsy for EGFR mutations in non-small cell lung cancer cases by RTPCR... | 15/09/2018 - 19/09/2018 |
29 | Liquid Biopsy in Lung Cancer: Tepecik Experience... | 11/04/2018 - 18/04/2018 |
30 | Non fonksiyone, benign ve operasyon endikasyonu olmayan surrenal insidentalomalı hastalarda JAK-2 m... | 14/10/2015 - |
NO | NAME | DATE |
1 | Koroner Yoğun Bakım'a yatan hastalarda ilaçla-indüklenen QT uzaması prevalansı ve risk faktörleri... | 1/2021 - / |
2 | TÜSEB Ağ-tabanlı bir sistem biyolojisi yaklaşımı ile kolorektal kanseri gelişiminde ve karaciğer metastazında etkili olan yolakların ve biyo-belirteçlerin tespiti... | 4/2020 - / |
3 | Kawasaki Hastalığında MEFV gen mutasyonu sıklığının ve hastalık seyri ile ilişkisinin değerlendirilmesi.... | 12/2020 - / |
4 | Volatil Kondensatta cfDNA Varlığının Araştırılması... | 7/2017 - 7/2018 |
NO | NAME | DATE |
1 | TAILOR OF SCIENCE REWARDS... | 2019 |