Academic Staff - Personal Page
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Professor Doctor AHMET OKAY ÇAĞLAYAN FACULTY OF MEDICINE INTERNAL MEDICINE DEPARTMENT OF MEDICAL GENETICS

  • Education/Academic Info
    Undergraduate Degree  Eskişehir Osmangazi University Tıp Fakültesi  2001
    Specialization in Medicine  Erciyes University Tıp Fakültesi Tıbbi Genetik Anabilim Dalı  2007
    Associate Professor  Tıbbi Genetik  2012
    Full Professor  Dokuz Eylül University Sağlık Bilimleri Enstitüsü  2019
  • NO NAME YEAR
    1  Dysregulation of mTOR signalling is a converging mechanism in lissencephaly....  2025
    2  Novel PIBF1 Pathogenic Variant in Three Siblings with Joubert Syndrome Type 33...  2024
    3  Exploring Molecular and Phenotypic Characteristics of NAGLU Arg234Gly and Asp312Asn Variants...  2024
    4  Investigation of genotype-phenotype and familial features of Turkish dystrophinopathy patients...  2024
    5  Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome....  2024
    6  Genetic, serological and clinical evaluation of childhood myasthenia syndromes- single center subgro...  2023
    7  Phenotypic comparison of a novel variant (p.P164R) and A founder mutation (c.748+1G>A) in Warburg Mi...  2023
    8  Clinical Heterogeneity in Patients with Long QT Syndrome and Segregation of Single Nucleotide Varian...  2023
    9  Investigation of different genomic variants in familial Mediterranean fever cases with monoallelic M...  2023
    10  Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a sin...  2023
    11  MIRAGE syndrome in a 10-year-old girl with a novel Lys1024Glu missense variant in SAMD9...  2023
    12  An investigation of the etiology and follow-up findings in 35 children with overgrowth syndromes, in...  2023
    13  Peripheral Expression of ADORA2A Is Increased and Is Correlated with Autism Spectrum Disorder Severi...  2023
    14  Unexpected finding in kidney biopsy of a child with nephrotic proteinuria: Questions...  2023
    15  Unexpected fnding in kidney biopsy of a child with nephrotic proteinuria: Answers...  2023
    16  Congenital Myasthenic Syndromes in Turkey: Clinical and Molecular Characterization of 16 Cases With ...  2022
    17  Hemoglobin A1C can differentiate subjects with GCK mutations among patients suspected to have MODY...  2022
    18  Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome....  2022
    19  Clinical and genetic studies of thiamine metabolism dysfunction syndrome-4: case series and review o...  2022
    20  Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the Na...  2022
    21  Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-re...  2022
    22  Importance of multigene panel test in patients with consanguineous marriage and family history of br...  2022
    23  Evaluation of hereditary/familial breast cancer patients with multigene targeted next generation seq...  2022
    24  Cerebral developmental venous anomalies in children with mismatch repair deficiency...  2022
    25  A novel homozygous frameshift mutation in the TUSC3 gene identified in siblings with intellectual di...  2022
    26  Familial clustering of nasopharyngeal carcinoma in the family of an adolescent with nasopharyngeal c...  2022
    27  Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes....  2021
    28  Peripheral Expression of MACROD2 Gene Is Reduced Among a Sample of Turkish Children with Autism Spec...  2021
    29  Nasopharyngeal carcinoma in a child with Kartagener`s syndrome....  2021
    30  Genetic alterations and pathways in patients with Hereditary Angioedema of Unknown Cause (U-HAE)...  2021
    31  Clinical Features, Treatment and Outcome of Childhood Glial Tumors....  2021
    32  Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atro...  2021
    33  METAP1 mutation is a novel candidate for autosomal recessive intellectual disability...  2021
    34  Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric ca...  2020
    35  COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration...  2019
    36  MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar,...  2019
    37  Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome....  2018
    38  Biallelic loss of human CTNNA2, encoding ?N-catenin, leads to ARP2/3 complex overactivity and disord...  2018
    39  Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families....  2018
    40  ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features...  2017
    41  Biallelic mutations in the 3' exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role i...  2017
    42  Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder...  2016
    43  Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblesto...  2016
    44  Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disab...  2016
    45  Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly...  2016
    46  Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population...  2016
    47  A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus ...  2015
    48  The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in ...  2015
    49  Clinical utility of next-generation sequencing in neurodevelopmental disorders: non-syndromic intell...  2015
    50  NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy...  2015
    51  Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spec...  2014
    52  Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: Expansion of the fa...  2014
    53  CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegenera...  2014
    54  Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders...  2014
    55  Whole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spec...  2013
    56  Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO...  2013
    57  Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalities...  2013
    58  A new patient with Andermann syndrome: an underdiagnosed clinical genetics entity?...  2013
    59  Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressiv...  2013
    60  A new syndrome of microtia with unilateral renal agenesis and short stature...  2012
    61  High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey...  2012
    62  Idiopathic hirsutism: local and peripheral expression of aromatase (CYP19A) and 5?-reductase genes (...  2011
    63  Recessive LAMC3 mutations cause malformations of occipital cortical development...  2011
    64  The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis...  2011
    65  Aniridia phenotype and myopia in a turkish boy with a PAX6 gene mutation...  2011
    66  A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 ge...  2011
    67  Magnetic resonance spectroscopy in two siblings with chorea-acanthocytosis...  2010
    68  Different aspects of atrial fibrillation genetics...  2010
    69  GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobb...  2010
    70  Maternal uniparental isodisomy is responsible for serious molybdenum cofactor deficiency...  2010
    71  Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations...  2010
    72  Are heterochromatin polymorphisms associated with recurrent miscarriage?...  2010
    73  MEFV gene compound heterozygous mutations in familial Mediterranean fever phenotype: a retrospective...  2010
    74  A very rare neurocutaneous disorder in 2 siblings: Sjögren-Larsson syndrome...  2010
    75  Two female siblings with West syndrome: Familial idiopathic West syndrome with genetic susceptibilit...  2010
    76  Genetic causes of syndromic and non-syndromic autism...  2010
    77  Expression of WT1 gene in multiple myeloma patients at diagnosis: is WT1 gene expression a useful ma...  2010
    78  A case with a rare chromosomal abnormality: isochromosome 18p...  2010
    79  Autism with del15p.11.1: case report with a new cytogenetic finding...  2010
    80  A unique case of a patient with partial trisomy 22 and lipodystrophy: is it a new syndrome due to an...  2010
    81  The Deletion Polymorphism of the Angiotensin-Converting Enzyme Gene Is Associated with Acute Aortic ...  2009
    82  Detection of p16 promotor hypermethylation in "Maras powder" and tobacco users...  2009
    83  Frank-ter Haar syndrome with unusual clinical features...  2009
    84  Lack of association between the Glu298Asp polymorphism of endothelial nitric oxide synthase and slow...  2009
    85  Inherited diseases and syndromes leading to aortic aneurysms and dissections...  2009
    86  The relationship between slow coronary flow and angiotensin converting enzyme and ATIIR1 gene polymo...  2009
    87  Can heterochromatin polymorphism of chromosome 6 affect fertility?...  2009
    88  Fluorescence in situ hybridization and single nucleotide polymorphism of a new case with inv dup del...  2009
    89  A provisionally unique syndrome with features including "molar tooth" sign and "femoral hypoplasia"...  2009
    90  Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype...  2009
    91  Apolipoprotein E3/E3 genotype decreases the risk of pituitary dysfunction after traumatic brain inju...  2008
    92  The effect of maras powder on DNA methylation and micronucleus formation in human buccal tissue...  2008
    93  Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2)...  2008
    94  Clinical and radiographic delineation of odontochondrodysplasia...  2008
    95  ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features...  2008
    96  Scoliosis, blindness and arachnodactyly in a large Turkish family: is it a new syndrome?...  2008
    97  Can the classical euchromatic variants of 9q12/qh+ cause recurrent abortions?...  2008
    98  How the I1307K adenomatous polyposis coli gene variant contributes in the assessment of risk of colo...  2007
    99  Parental Karyotype and Genetic Markers for Thrombophilia in Recurrent Miscarriage...  2007
    100  Molybdenum cofactor deficiency:: Clinical features in a Turkish patient...  2007
    101  Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3?qter) and ...  2007
    102  Frequency Of The Common G985A Mutation In The Medium-chain Acyl-CoA Dehydrogenase Gene In Turkish Po...  2007
    103  Prenatal diagnosis of a fetus with partial trisomy 7p...  2007
  • NO NAME DATE
    1  Klinik Araştırma Merkezleri: Dokuz Eylül Üniversitesi Örneği... 28/11/2024 - 29/11/2024
    2  Endüstri Destekli Klinik Araştırmalarda Bütçeleme: Bir Üniversite Hastanesi Modeli Önerisi... 28/11/2024 - 29/11/2024
    3  Evaluation of Etiology, Diagnosis, Treatment and Follow-up Results of Patients With Epilepsy Under t... 20/06/2023 - 24/06/2023
    4  Çocukluk çağı miyastenia gravisin genetik, serolojik ve klinik değerlendirmesi- Alt grup analiz... 17/05/2023 - 21/05/2023
    5  Meme Kanseri Gelişiminde Etkili Olabilecek Bir Aday Genin Yeni Nesil Dizileme Yöntemiyle Tespiti... 04/05/2023 - 07/05/2023
    6  Klinik Önemi Bilinmeyen CHEK2 Geni Varyantlarının In Silico Değerlendirilmesi... 04/05/2023 - 07/05/2023
    7  Likit Biyopsi Uygulanmış Küçük Hücreli Dişi Akciğer Karsinomu Tanılı Olgularda Test Edilen... 04/05/2023 - 07/05/2023
    8  Demans ön tanılı hastaların yeni nesil dizileme panel yöntemi ile araştırılması... 09/11/2022 - 13/11/2022
    9  Pah Geni Varyantlarının Retrospektif Olarak Değerlendirilmesi: Tek Merkez Deneyimi... 09/11/2022 - 13/11/2022
    10  Primer İmmun Yetmezlik Ön Tanılı Olguların Genetik Altyapısının Yeni Nesil Dizileme Analizi ... 09/11/2022 - 13/11/2022
    11  Entelektüel Yetersizlik Ön Tanılı Hastaların Yeni Nesil Dizileme Yöntemi Ile Araştırılması... 09/11/2022 - 13/11/2022
    12  Renal Tubuler Hastalıkların Yeni Nesil Dizileme Analizi Yöntemi İle Araştırılması... 09/11/2022 - 13/11/2022
    13  A RARE CAUSE OF COMBINED HEPATIC AND RENAL FAILURE: NPHP19 DUE TO A NOVEL DCDC2 VARIANT IN TWO SIBLI... 22/06/2022 -
    14  Evaluation of supervision systems by PhD students in Dokuz Eylul University Graduate School of Healt... 12/05/2022 - 14/05/2022
    15  Dokuz Eylül University Graduate School of Health Sciences... 12/05/2022 - 14/05/2022
    16  Targeted next generation sequencing analysis of 30 Turkish patients with inherited cardiomyopathies... 20/11/2020 - 22/11/2020
    17  TUSC3 Mutasyonu Pozitif Mental Retarde Kardeşler, Vaka Takdimi... 05/03/2020 - 07/03/2020
    18  Pathogenic variations of MUTYH gene in hereditary cancer cases... 20/02/2020 - 22/02/2020
    19  Genetic analyses in understanding of renal tubulopathies... 20/02/2020 - 22/02/2020
    20  Identifying Common Pathogenesis of Diseases Using Literature Mined Gene Interactions... 17/10/2019 - 19/10/2019
    21  MACROD2 gene expression profile in autism spectrum disorder: a case-control study... 18/04/2019 - 21/04/2019
    22  Çocukluk Çağı Kanserlerinde Herediter Kanser Predispozisyonu Sendromu... 02/05/2018 - 06/05/2018
    23  NIPBL Geninde Yeni Bir Missense Mutasyon Saptanan Ağır Fenotipli Cornelia De Lange Sendromlu Bir O... 11/10/2017 - 13/10/2017
    24  A Rare Genodermatosis: H Syndrome... 09/10/2017 - 10/10/2017
    25  When ataxia is not just ataxia ? why genetic testing matters. Physiotherapy management of the ataxia... 27/09/2017 - 27/09/2017
    26  FBOX07 mutation with juvenile Parkinsonism and behavioral disorders... 19/06/2016 - 23/06/2016
    27  Constitutional Mismatch Repair Defect Syndrome: New Insights from Whole Exome Sequencing Data and Fu... 05/05/2016 - 07/05/2016
    28  Ekzom Dizileme İle IFT80 Geninde Homozigot Delesyon Saptanan Yeni Bir Polidaktili... 22/10/2015 - 24/10/2015
    29  Otozomal Resesif Primer Mikrosefali Tip 1... 22/10/2015 - 24/10/2015
    30  The classical phenotype of glucose transporter-1 deficiency syndrome (GLUT-1 DS): Different clinical... 05/09/2015 - 09/09/2015
    31  Üç Kardeş Olguda Merozin Negatif Konjenital Muskuler Distrofi.... 06/05/2015 - 09/05/2015
    32  Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winkin... 22/06/2014 - 25/06/2014
    33  An Atypical Clinical Presentation of Tangier Disease, A Rare Cause of Neuropathy... 22/06/2014 - 25/06/2014
    34  Thiamine Metabolism Dysfunction Syndrome-4 (Bilateral Striatal Degeneration and Progressive Polyneur... 22/06/2014 - 25/06/2014
    35  New Mutations Detected in Primer Microcephaly genes by Whole-Exome Sequencing... 25/09/2013 - 29/09/2013
    36  A New Variant Detected in GRIN2A by Whole-Exome Sequencing in a Patient with Intellectual Disability... 25/09/2013 - 29/09/2013
    37  Whole Exome Sequencing Detected CEP135 Mutation... 05/06/2013 - 08/06/2013
    38  A new Turkish case with Ataxia-Oculomotor Apraxia syndrome type 1 diagnosed by whole-exome sequencin... 16/05/2012 - 19/05/2012
    39  A new case: Congenital myasthenic syndrome with epsilon subunit mutations... 16/05/2012 - 19/05/2012
    40  A first report of TMCO1 defect syndrome in a non-amish patient.... 16/05/2012 - 19/05/2012
    41  Molibden Kofaktör Eksikliği Ve Uniparental Dizomi... 26/05/2010 - 29/05/2010
    42  Rubinstein-Taybi syndrome with a novel mutation... 28/06/2009 - 01/07/2009
    43  First Turkish patient with Epidermolytic palmoplantar keratoderma due to keratin 9 gene mutation (Ar... 28/06/2009 - 01/07/2009
    44  Coffin-Lowry Syndrome in Two Siblings with A New Findings... 28/06/2009 - 01/07/2009
    45  MEFV Gene Compound Heterozygous Mutations in Familial Mediterranean Fever Phenotype... 28/06/2009 - 01/07/2009
    46  A new case with bilateral frontoparietal polymicrogyria due to GPR56 gene mutation... 28/06/2009 - 01/07/2009
    47  Can Heterochromatin Polymorphisms Affect Fertility?... 28/06/2009 - 01/07/2009
    48  Cytogenetic Results of 153 Patients with Mental Retardation in Middle Anatolia in Turkey... 28/06/2009 - 01/07/2009
    49  The angiotensin converting enzyme gene polymorphism is related with the acute aortic dissection.... 28/06/2009 - 01/07/2009
    50  Cytogenetic Results of 336 Patients with Recurrent Spontaneous Abortions in Middle Anatolia in Turke... 28/06/2009 - 01/07/2009
    51  Effect of Bedtime Levetiracetam or Carbamazepine Monotheraphy in Newly Diagnosed Benign Epilepsy of ... 10/06/2009 - 13/06/2009
    52  Epidemiological Findings of the Cerebral Palsy... 10/06/2009 - 13/06/2009
    53  Three Patient with Molybdenum Cofactor Deficiency without Disease-Causing Mutations: Is it a n New G... 10/06/2009 - 13/06/2009
    54  Cerebral Palsy and Concomitant Abnormality... 10/06/2009 - 13/06/2009
    55  Cystic Leukoencephalopathy without Megalencephaly... 10/06/2009 - 13/06/2009
    56  Magnetic Resonance Imaging Findings in Cerebral Palsy... 10/06/2009 - 13/06/2009
    57  Autism with del15p.11.1: Case Report with New Cytogenetic Finding... 10/06/2009 - 13/06/2009
    58  No relationship among with aromatase and 5-alpha reductase genes polymorphisms and the idiopathic hi... 14/05/2009 - 17/05/2009
    59  DHCR7 mutations in Turkish SLOS patients and clinical description of four patients homozygous for th... 01/04/2009 - 03/04/2009
    60  Tekrarlayan gebelik kaybı olan bir ailede t(1;2) ve literatür taraması... 06/05/2008 - 09/05/2008
    61  Megarbane Sendromu: Literatüre katkı... 06/05/2008 - 09/05/2008
    62  Quantitative Determination of Aromatase and 5-Alpha Reductase mRNA In Women With Idiopathic Hirsutis... 02/05/2008 - 07/05/2008
    63  Tekrarlayan gebelik kaybı olan bayanlarda genetik risk faktörleri... 25/10/2007 - 29/10/2007
    64  Normalization of serum testosterone level alters local GnRH-II and IL-2R mRNA expression in peripher... 28/04/2007 - 02/05/2007
    65  Local Il-2R expression in peripheral lymphocytes in severe GH deficient patients with Sheehan's synd... 21/10/2006 - 24/10/2006
    66  Circulating testosterone regulates the local GnRH-II expression in peripheral lymphocytes: An in viv... 19/06/2006 - 22/06/2006
    67  A Novel Denovo Translocatıon t(4;7)(p15.2;p22)... 17/05/2006 - 20/05/2006
    68  Two case with klinefelter Syndrome presenting 48,XXYY karyotype... 17/05/2006 - 20/05/2006
    69  46,t(Y;Y) Karyotipi olan İnfertil bir erkek... 17/05/2006 - 20/05/2006
    70  Fetusta prenatal olarak tesbit edişmiş t(7;15) (q11.23;q26.3) In a Fetus... 17/05/2006 - 20/05/2006
    71  Down Syndrome Like Appearance With A Novel Denovo Translocation t(6;21)(p21;p13)... 17/05/2006 - 20/05/2006
    72  46,XY,t(12;13)(q24.33;q32) in a case... 17/05/2006 - 20/05/2006
    73  A Patient with Alstrom Syndrome... 17/05/2006 - 20/05/2006
    74  A Case With Turner Syndrome Presenting t(14;16)(q10;p10)... 17/05/2006 - 20/05/2006
    75  A Family with Pendred Syndrome... 17/05/2006 - 20/05/2006
    76  Segawa Hastalığı: Dört kardeş hastada exon 6 R 216 mutasyonu... 03/05/2006 - 06/05/2006
    77  Prenatal tanı alan Roberts sendromlu bir vaka... 21/04/2004 - 24/04/2004
    78  Holt-Oram Sendromlu bir vaka... 21/04/2004 - 24/04/2004
  • NO CHAPTER TITLE YEAR
    1  Yeni Nesil Dizileme Verilerinin Yorumlanması Yeni Nesil Dizileme ve Klinikteki Uygulamaları...  2024
    2  Nadir Hastalıklara Multi-omik Yaklaşım Yeni Nesil Dizileme ve Klinikteki Uygulamaları...  2024
    3  Spinoserebellar ataksilere genetik yaklaşım Nükleotid Tekrar Artışı Hastalıkları...  2023
    4  Otizm Spektrum Bozukluklarına Multiomik Yaklaşım Otizm Spektrum Bozukluklarinda Genetik Değerlendirme ve En Son Genetik Çalişmalar...  2022
    5  Gelecekteki Genom Tabanlı Tarama Yaklaşımları: Realite ve Potansiyel Güncel Genetik Tabanlı Tarama Testleri...  2020
    6  Meningiomlara Genetik Yaklaşım Meningiomlara Genel Bakış...  2020
    7  Anne Sütü ve Epigenetik Aile Hekimliğinde Anne Sütünün Anne ve Bebek Sağlığı Açısından Önemi - 2019...  2019
    8  Çoklu Konjenital Anomalisi Bulunan Hastalarda Güncel Tanı Yöntemleri: Laboratuvardan Kliniğe Sitogenetik...  2018
    9  Boy Kısalığına Yol açan Genetik Bozukluklar Çocuklarda ve Ergenlerde Büyüme...  2018
    10  Kraniyofasiyal anomaliler Tıbbi Genetik ve Klinik Uygulamaları...  2016
    11  Dysmorphology and Databases Atlas of Dysmorphology and Diagnosis...  2015
    12  Gen Tedavisi Modern Biyoteknoloji ve Uygulamaları...  2010
    13  Lomber dejeneratif disk hastalığında genetik etiopatogenez ve güncel genetik tedavi yöntemleri Lomber Dejeneratif Disk Hastalığı,...  2010
  • NO NAME DATE
    1  Enhancing Genetic Knowledge and Decision-making for Neurodegenerative Disorders through gamification...  10/2024 - 9/2027
    2  Nörodejeneratif Hastalıklara Agnostik Yaklaşım: Gba1 Varyantlarına Sahip Hastalarda Yığın Ve Tek Hücreli Multi-Omikler Yoluyla Yeni İlaç Ve Biyobelirteç Adaylarının Keşfi...  4/2024 - 4/2026
    3  Sirkadiyen ritm ilişkili CRY1'e spesifik olan M47 molekülünün, prostat kanserinde normal ve uzatılmış aydınlatma koşullarında potansiyel anti-tümoral etkisininincelenmesi...  5/2023 - 5/2025
    4  Saglık Bilimlerinde Arastırma Projeleri Hazırlama Egitimi...  4/2023 - 4/2023
    5  Spinal Musküler Atrofi (SMA) Hastalığına Yönelik Hızlı Genetik Tarama ve Tanı Kiti Geliştirilmesi...  6/2022 - 1/2024
    6  Kalıtsal Karaciğer Hastalıklarına Sebep Olan Gen Mutasyonlarının Tüm Ekzom Sekanslama Yöntemi ile Araştırılması...  9/2022 - 8/2023
    7  Koroner Yoğun Bakım'a yatan hastalarda ilaçla-indüklenen QT uzaması prevalansı ve risk faktörleri...  1/2021 - 10/2022
    8  Kawasaki hastalığının epidemiyolojik karakteristiği, sorumlu genlerin tüm ekzom ve genom dizileme yöntemleriyle tesbit edilmesi...  4/2019 - /
    9  Obezite ve Metabolik Sendromun Kardiyovasküler Sistem Üzerine Etkisi ve FTO rs9939609 gen Polimorfizm İlişkisi...  10/2019 - /
    10  Nörogenetik hastalıklarda yeni nesil dizileme teknolojisi ile genetik etyolojinin araştırılması ve bilinmeyen genlerin tanılanması...  7/2019 - /
    11  Otizm Spektrum Bozukluğu Hastalarında Adenosin Reseptörü 2A (ADORA 2A) geni ekspresyonunun İncelenmesi...  9/2018 - 9/2019
    12  Otizm Spektrum Bozukluğu Hastalarında Hedef Gen TMLHE Ekspresyon Profilinin İncelenmesi...  9/2017 - 9/2019
  • NO NAME DATE
    1  TÜBİTAK MSCA Above-Threshold-Award...  2020
    2  Birincilik...  2007
    3  Eskişehir Osmangazi Üniversitesi tıp Fakültesi Mezuniyet Üçüncülüğü...  2001
  • NO Responsibility
    1 Graduate School of Health Sciences Moleküler Tip Anabilim Dali , Director of Science Branch, June 2024-Continues
    2 Graduate School of Health Sciences , Member of The Institute Council, June 2024-Continues
    3 Teaching Hospital , Vice Head Doctor, February 2024-Continues
    4 Teaching Hospital , Vice Head Doctor, January 2024- February 2024
    5 DEÜ Rectorate Bilimsel Araştırmalar ve Yayın Etiği Kurulu (Sağlık Bilimleri) Member, January 2024- May 2024
    6 Teaching Hospital , Vice Head Doctor, November 2023- January 2024
    7 Teaching Hospital , Vice Head Doctor, November 2023- November 2023
    8 DEÜ Rectorate Girişimsel Olmayan Araştırmalar Etik Kurulu Member, May 2023- January 2024
    9 Graduate School of Health Sciences , Member of The Institute Council, June 2022- November 2023
    10 Graduate School of Health Sciences , Member of The Institute Council, June 2022- November 2023
    11 Graduate School of Health Sciences , Vice Director of The Institute, June 2022- November 2023
    12 Graduate School of Health Sciences , Member of The Institute Council, January 2022- June 2022
    13 Graduate School of Health Sciences , Member of The Institute Council, January 2022- June 2022
    14 Graduate School of Health Sciences , Vice Director of The Institute, January 2022- June 2022
    15 DEÜ Rectorate Girişimsel Olmayan Araştırmalar Etik Kurulu Member, May 2021- May 2023