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 |