SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
EVALUATION of SMOOTH MUSCLE MYOSIN HEAVY CHAIN ISOFORM EXPRESSIONS in a BURIED PENIS
JOURNAL OF PEDIATRIC SURGERY
, sa.3, ss.1-13, 2024 (SCI-Expanded)
New results for monogenic diabetes with analysis of causative genes using next-generation sequencing: a tertiary centre experience from Turkey
International Journal of Diabetes in Developing Countries
, cilt.42, sa.4, ss.703-712, 2022 (SCI-Expanded)
The comparison of telomere length in cancer patients: Plasma, whole blood and tumor tissue
Medicine Science And The Law
, cilt.2021104111721, sa.2021;10(4):1117-21, ss.1117-1121, 2021 (SCI-Expanded)
Prevalence and mutations of ß-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey.
BALKAN JOURNAL OF MEDICAL GENETICS
, cilt.19, sa.1, ss.29-34, 2016 (SCI-Expanded)
The CYP4502D6*4 and*6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patients
EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS
, cilt.41, sa.3, ss.281-286, 2016 (SCI-Expanded)
Vitamin D Receptor Gene BSMI, FOKI, APAI, and TAQI Polymorphisms and the Risk of Atopic Dermatitis
JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY
, cilt.26, sa.2, ss.106-110, 2016 (SCI-Expanded)
Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population.
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
, cilt.4, sa.2, ss.120-7, 2015 (SCI-Expanded)
Contribution of the STAT4 rs7574865 gene polymorphism to the susceptibility to otoimmune thyroiditis in healthy population and psoriatic subgroups
CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY
, cilt.40, sa.4, ss.437-441, 2015 (SCI-Expanded)
Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris?
TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY
, cilt.48, sa.3, ss.131-134, 2014 (SCI-Expanded)
Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension.
ANNALS OF SAUDI MEDICINE
, cilt.34, sa.4, ss.340-345, 2014 (SCI-Expanded)
Association of Vitamin D Receptor Gene Polymorphisms in Children With Atopic Diseases
GENE THERAPY AND MOLECULAR BIOLOGY
, cilt.16, ss.55-60, 2014 (SCI-Expanded)
Double Translocation: An Interesting Family History.
BALKAN JOURNAL OF MEDICAL GENETICS
, cilt.1, ss.77-80, 2013 (SCI-Expanded)
Increased T allele frequency of 677 C>T polymorphism in the MTHFR gene in differentiated thyroid carcinoma.
GENETIC TESTING AND MOLECULAR BIOMARKERS
, sa.16, ss.780-784, 2012 (SCI-Expanded)
Branchio-oculo-facial syndrome with the atresia of external ear
International Journal of Pediatric Otorhinolaryngology
, cilt.69, sa.11, ss.1575-1578, 2005 (SCI-Expanded)
Non-Hodgkin's lymphoma and auricular hypoplasia: Associated with juvenile colloid milium or ligneous conjunctivitis?
Journal of the European Academy of Dermatology and Venereology
, cilt.19, sa.3, ss.348-351, 2005 (SCI-Expanded)
Syndromic etiology in children at schools for the deaf in Turkey
International Journal of Pediatric Otorhinolaryngology
, cilt.68, sa.11, ss.1399-1406, 2004 (SCI-Expanded)
Etiology of deafness at the Yeditepe School for the deaf in Istanbul
International Journal of Pediatric Otorhinolaryngology
, cilt.67, sa.5, ss.467-471, 2003 (SCI-Expanded)
Diğer Dergilerde Yayınlanan Makaleler
Investigation of TAp63 gene expression and follicle count using melatonin in cisplatin-induced ovarian toxicity
International Journal of Research in Medical Sciences
, cilt.9, sa.3, ss.658-664, 2021 (Hakemli Dergi)
Çanakkale İlimizdeki Jinekolojik Kanserlerde Yeni Nesil DNA Dizi Analizi ile Saptanan Mutasyon Profilleri
Uludağ Üniversitesi Tıp Fakültesi Dergisi
, cilt.46, sa.3, ss.349-356, 2020 (Hakemli Dergi)
Tedaviyi Etkileyen Tarama Testleri
Türkiye Klinikleri Sağlık Bilimleri Dergisi
, 2020 (Hakemli Dergi)
Prenatal diagnosis of aneuploidies and microdelation/duplication in amniotic fluid and fetal aborted material by QF-PCR and MLPA analysis.
Biomed Genet Genomics
, cilt.3, sa.1, ss.1-6, 2018 (Hakemli Dergi)
Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar
Turkiye Klinikleri Journal of Medical Genetics-Special Topics
, cilt.2, sa.2, ss.74-87, 2017 (Hakemli Dergi)
Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler
Turkiye Klinikleri Journal of Medical Genetics-Special Topics
, cilt.2, sa.2, ss.113-122, 2017 (Hakemli Dergi)
Kanser Etiyolojisinde Tetikleyici Moleküler Mekanizmalar
Turkiye Klinikleri J Med Genet-Special Topics
, cilt.2, sa.2, ss.74-87, 2017 (Hakemli Dergi)
A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus
Biomedical Genetics and Genomics
, cilt.2, sa.1, ss.1-3, 2017 (Hakemli Dergi)
Hypermethylated promoter profiles for tumour suppressor APC p53 MSH6 and MGMT genes in CRC tumours
journal of biomedical research
, cilt.2, sa.6, ss.41-47, 2016 (Scopus)
9qh liği Molar Gebelik İçin Bir Risk Faktörü mü
Jinekoloji - Obstetrik ve Neonatoloji Tıp Dergisi
, 2016 (Hakemli Dergi)
Epileptik nöbet bulgusu ile gelen temporal kemik osteomu: Nadir bir olgu sunumu
ODU Journal of Medicine
, cilt.2015, sa.2, ss.83-86, 2015 (Hakemli Dergi)
PATAU SENDROMU, KOMPLET VEYA İNKOMPLET YAŞAM SÜRESİNDE ÖNEMLİ Mİ?
Anatol J Clin Investig
, cilt.8, sa.4, ss.187-188, 2014 (Hakemli Dergi)
Increased Sister Chromatid Exchanges in Patients with Gastrointestinal Cancers and in their First-Degree Relatives
European Journal of Health Science
, cilt.11, sa.2, ss.94, 2014 (Hakemli Dergi)
Larenks Kanserli Hastalarımızda K-Ras Mutasyonları
International Journal of Clinical Research
, cilt.2, sa.1, ss.6-11, 2014 (Hakemli Dergi)
Characteristic findings of alstrom syndrome with a case report
Journal of Clinical Diagnostics
, sa.3, ss.75-77, 2013 (Hakemli Dergi)
Onsekiz Haftalık Spontan Olarak Sonlanan ve QF-PCR ile Saptanan Triploidik Fetus; Olgu Sunumu
International Journal of Clinical Research
, cilt.1, ss.31-34, 2013 (Hakemli Dergi)
Fetal Anöploidi Açısından Yüksek Riskli Gebeliklerin QF-PCR İle Analizi
International Journal of Clinical Research
, cilt.1, sa.1, ss.17-21, 2013 (Hakemli Dergi)
Tc-99m DMSA Scintigraphy in the Diagnosis of Renal Anomalies: A Turner Syndrome Case
Turkiye Klinikleri Journal of Pediatrics
, cilt.22, sa.1, ss.37-40, 2013 (Hakemli Dergi)
Tc 99 m DMSA scintigraphy in the diagnosis of renal anomalies A Turner case
Türkiye Klinikleri Pediatri Dergisi
, cilt.22, sa.1, ss.37-40, 2013 (Hakemli Dergi)
Nöral tüp defekti gebeliği olan olguda terminasyon kararı
Smyrna Tıp Dergisi
, ss.27-30, 2012 (Hakemli Dergi)
Çok Sayıda Konjenital Anomalinin Eşlik Ettiği Trizomi 8 Mozaisizm Olgusu
Turkiye Klinikleri Journal of Pediatrics
, cilt.18, sa.4, ss.324-327, 2009 (Hakemli Dergi)
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar
Mowat-Wilson Syndrome: A Case Report With Novel Splice Site Mutation In Zeb2 Gene
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022
Importance of genetic diagnosis in demyelinating diseases; adult-onset Alexander Disease case with novel GFAP mutation
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022
Ailesel Kanser Sendromu Tanısında Göz Ardı Edilmemesi Gereken Bir Gen ‘’Pms1’’: Çanakkale’Den Vaka Serisi
15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022
A rare Malpuech, Mignarelli, Michels, Carnevale Syndrome (3MC Syndrome); Novel variant in the MASP1 gene
EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022
A novel homozygous mutation in CC2D1A gene: two case from a Turkish family in Canakkale
EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022
A patient with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome due to 16p11.2 deletion: a case report from Çanakkale
EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022
A novel BRPF1 variant in a family with intellectual disability and dysmorphic face, from Çanakkale
EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022
The significance of the BRCA2 c.9934A>G variant is really unknown?A series of patients with BRCA2 c.9934A>G variant among Çanakkale patients
EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022
Türkiye NRXN1 intragenik delesyonlarının fenotipik spektrumu: Çanakkale’den bir vaka serisi
7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022
A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region
7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022
Primary Coenzyme Q10 Deficiency; Determination of Patient and Carrier Frequency in the Çanakkale Cohort
7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022
22q11.2 duplication syndrome showing clinical variability and overlapping with the features of Digeorge/Velocardiofacial Syndrome: case series from Çanakkale
7.Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 Mayıs 2022, ss.161-162
Geniş Kapsamlı Panel Analizlerinin Klinik Faydası: Ailesinde Yaygın Kanser Öyküsü Olan Pankreas Kanseri Ve Memede Kitle Sebebiyle Takipli Genç Yaş Kadın Hastada Saptanan Chek2 Ve Nbn Patojenik/muhtemel Patojenik Varyantları
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1
Ailevi Kanser Sendromu Ön Tanılı Vakalarda Tp53 Ve Chek2 Genlerinin Analizi: Bir Vaka Serisi
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1
Palb2 Genotip Fenotip Korelasyonu: Vaka Serisi
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1
İzole Pankreas Kanserli Bir Olgunun Ailesinde Saptanan M.patojenik Novel Vhl Mutasyonu Bildirimi
1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1
Pericentric invertion and duplication deletion of chromosome 8p Syndrome
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
NBN gene mutations with clinical spectrum in our patients who applied to our outpatient clinic
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
From tissue to diagnosis; a case report of Proteus Syndrome Report
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
A rare 22q11.2 microduplication in a boy with poor head control
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
The evaluation of FMF course and colchicine treatment in the patients with or without COVID-19 symptoms during the pandemic
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
De novo GABRB3 c.103G>A mutation detected in a patient with epilepsy and speech retardation
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 Eylül 2021
The role of balanced chromosomal translocation in the etiology of habitual abortion and the importance of traditional karyotype analysis in definitive diagnosis
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
Uniparental disomic effects by CNVs and structural point mutations in ELN gene
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
Submicroscopic evaluation with chromosomal microarray to elucidate the genetic etiology of patients with cerebral palsy
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
The acquitition of mosaic trisomy 8 associated with corpus callosum agenesis in Warkany Syndrome 2;A case report
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1
Characterization of a rare mosaicism of an autosomal translocation of t(6;9) underlying mental retardation by using conventional cytogenetics and MicroArray CGH methods: a case report
13th European Cytogenomics Conferece, Bari, İtalya, 3 - 05 Temmuz 2021, ss.0-1
Cytogenetic and molecular analyses of balanced reciprocal translocation in an infertile female patient with 46,XX,t(11;17)pat karyotype
13th European Cytogenomics Conferece, Bari, İtalya, 3 - 05 Temmuz 2021, ss.0-1
De novo pericentric inversion of chromosome 1(p13q21) and male infertility A case report
13th European Cytogenomics Conferece, Bari, İtalya, 3 - 05 Temmuz 2021, ss.0-1
A 15 mb interstitial duplication in band Xq27.1 q28 in a female infant with hypotonia, microcephaly, prominent forehead and retrognathia a case report
13th European Cytogenomics Conferece, Bari, İtalya, 3 - 05 Temmuz 2021, ss.0-1
A rare Koolen de Vries syndrome caused by 17q21.31 deletion that encompassing KANSL1 gene
13th European Cytogenomics Conferece, Bari, İtalya, 3 - 05 Temmuz 2021, ss.0-1
Preliminary results to propose the prognostic algorithm for PET/CT SUVmax values and BRCA1/2 mutations in breast cancers.
European Biotechnology Congress 24-26 September 2020 Prague, VIENNA, Viyana, Avusturya, 24 - 26 Eylül 2020, cilt.1, ss.7-9
ÇOMÜ Tıbbi Genetik Tanı Merkezi’nde Spinal Musküler Atrofi Taşıyıcılığı Açısından Genotiplendirilen Olguların SMN1/SMN2 Genlerinin Kopya Sayılarının Analizi
Ulusal tıbbi genetik kongresi 2020, Online, Türkiye, 20 Kasım 2020
Tekrarlayan Gebelik Kaybı olan olguların kopya sayısı değişikliklerinin profillemesi
Ulusal tıbbi genetik kongresi 2020, Online, Türkiye, 20 Kasım 2020
Multiple pterygia, joint contractures, hypoplastic lungs and hydrops: A rare case of lethal multiple pterygium syndrome
Ulusal tıbbi genetik kongresi 2020, Online, Türkiye, 20 Kasım 2020
Oculocutaneous albinism caused by a compound heterozygous mutations in TYR gene: a case report
Ulusal tıbbi genetik kongresi 2020, Online, Türkiye, 20 Kasım 2020
HbF veya HbA2 seviyelerinde farklılığı bulunan bireylerde Kruppel-like factor 1 (KLF1) ve Hemoglobin subunit delta (HBD) genlerinde saptanan mutasyonların genotip-fenotip ilişkisinin incelenmesi
Ulusal tıbbi genetik kongresi 2020, Online, Türkiye, 20 Kasım 2020
Additional point mutations in ACAN and GATA4 genes in an atypical achondroplasia patient with platyspondyly and congenital heart defect.
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
A novel variant for SQSTM1 gene in a patient with frontotemporal dementia.
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
A Case Of Coffin-Siris Syndrome With Atypical Phenotype Caused By A Novel De Novo Mutation In ARID1B Gene.
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
A Homozygous Nonsense Mutation In MTHFR Gene Causes A Severe Phenotype: Hypotonia And Hydrocephalus. Poster presentation
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
Investigation of autoinflammatory genes in patients with conventional treatment-resistant dermatological diseases Poster presentation,
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
Chromatin remodelling dysfunction and CHD2 related epilepsy:Reports of two unrelated child.
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
A rare lethal multiple pterygium syndrome caused by a homozygous point mutation In CHRNG gene:a case report.
European Biotechnology Congress 2020, Çek Cumhuriyeti, 24 Eylül 2020
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
European Biotechnology Congress 2020, Prag, Çek Cumhuriyeti, 24 Eylül 2020
Balanced Reciprocal Translocation Detected in an Infertile Couple
6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.1
A Rare Chromosomal Aneuploidy That Diagnosed With Array CGH And MLPA Validation : Trisomy 4 in a fetus
V.International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Türkiye, 20 Şubat 2020
HOMOZYGOUS FRAMESHİFT MUTATİON İN DDB2 GENE İNDUCED SQUAMOUS CELL AND BASAL CELL CARCİNOMAS İN A CHİLD WİTH XERODERMA PİGMENTOSUM
V.International Participated Erciyes Medical Genetics Days Congress, Nevşehir, Türkiye, 20 Şubat 2020
Novel Missense Mutation in Phosoholipase C-Gamme-2 Gene (PLCG2) Causes Cold-Induced Psorıasıs : A Case raport
1st Bursa International Genetics Days: Dermatogenetics Symposium, Bursa, Türkiye, 09 Ocak 2020
A Novel Combined C.1630T>C AND C.1579G>A Point Mutations in ALOX12B Gene in A Rare Autosomal Recessive Congenital Ichthyosis : A Case Report
1st Bursa International Genetics Days: Dermatogenetics Symposium, Bursa, Türkiye, 09 Ocak 2020
BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q
13th Balkan Congress of Human Genetics, Edirne, Türkiye, 17 - 20 Nisan 2019, cilt.22, ss.156-1156
ÇOCUKLARDA MENTAL RETARDASYON ETİYOLOJİSİNİN BELİRLENMESİNDE ARRAY CGH TEKNİĞİNİN YERİ
1ST INTERNATIONAL AHI EVRAN MEDICINE CONGRESS, Kırşehir, Türkiye, 11 - 14 Nisan 2019
Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
13th Balcan Human Genetic Congress, Edirne, Türkiye, 17 - 20 Nisan 2019
Cytogenetics and molecular genecs diagnostic testing and the future of clinical genomics: Experience from Medical Genec Diagnostic Center in Canakkale, Turkey
VII Baltıc Genetıcs Congress, 24 - 27 Ekim 2018
AİLEVİ AKDENİZ ATEŞİ TANISI ALAN ÇOCUKLARDA ATRİYAL İLETİ PARAMETRELERİNİN DEĞERLENDİRİLMESİ
14. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Türkiye, 11 - 14 Mart 2018
Kliniğimizde Takip Edilen Kadın Hastalarda Servikal Neoplaziyi Değerlendirmek İçin Kullanılan Pap Smear ve HPV DNA Test Sonuçlarının Retrospektif Analizi
İstanbul Üniversitesi 7. Kadın Doğum Günleri, İstanbul, Türkiye, 7 - 10 Aralık 2017
A unique keratosis pattern in a case of epidermolytic hyperkeratosis: Report of a case in 46,XX,9qh karyotype”
2nd International Dermatology and Cosmetology Congress (INDERCOS 2017), İstanbul, Türkiye, 15 - 18 Mart 2017
Fenotipik olarak normal fakat habitüel abortus öyküsü olan bayanda nadir rastlanılan dengeli non resiprokal 5p 14p translokasyonu Dengeli transloke olguların doğru tanısında kromozom analiznin önemi ve MicroArray CGH yöntemine üstünlüğü
XII. Ulusal Tıbbi Genetik Kongrresi., İzmir, Türkiye, 5 - 09 Ekim 2016
The crucial role of Factor V Leiden mutation in cardiovascular complications in psoriasis
25TH EADV, 28 Eylül - 02 Ekim 2016
A Case report of an infertile man with Isodicentric Y Chromosome mosaicism with duplicated SRY SHOX and deleted AZF regions
Eurobiotech2016, 5 - 07 Mayıs 2016
Assessment of BMP 6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients 05 07 May 2016 Riga LATVIA Journal of Biotechnology 231 S23
European Biotchnology Congress, Riga, Letonya, 5 - 07 Mayıs 2016
UGT1A1 GENE MUTATIONS MAY CAUSE MYCOPHENOLATE MOFETIL INDUCED LEUCOPENIA AFTER RENAL TRANSPLANTATION A CASE REPORT
Gevher Nesibe Tıp Günleri 2016 ve Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Kayseri, Türkiye, 11 - 13 Şubat 2016
Kardiyovasküler Hastalıkların Genetiği
Medical Genetics and Clinical Applications (with International Participation), Türkiye, 11 - 13 Şubat 2016
RECURRENT PREGNANCY LOSS AND PARENTAL CARRIER OF A STRUCTURAL CHROMOSOME TRANSLOCATION: A CASE REPORT OF A MOTHER WITH T(9;13)
Medical Genetics and Clinical Applications, Kayseri, Türkiye, 11 - 13 Şubat 2016
Medical genetics in Canakkale and Turkey
II INTERNATIONAL SCIENTIFIC CONFERENCE ON “GENETICS AND BIOTECHNOLOGY OF THE 21ST CENTURY: POBLEMS, ACHIEVEMENTS AND PERSPECTIVES, Minsk, Belarus, 13 - 15 Ekim 2015
Familial X chromosome translocation Xqtriplication and SHOX gene deletion with short stature
International Biotechnology Congress, BÜKREŞ, Romanya, 7 - 09 Mayıs 2015
The relationship between germ line MTHFR C677T and A1298C polymorphisms and psoriasis
International Biotechnology Congress, BÜKREŞ, Romanya, 7 - 09 Mayıs 2015
A case of 47 XYY syndrome without behavioraland emotional difficulties Cost effective well define of extra Y chromosome by GTG Cbandings and FISH analysis
International Biotechnology Congress, BÜKREŞ, Romanya, 7 - 09 Mayıs 2015
Epileptik Nöbet Bulgusu İle Gelen Temporal Kemik Osteomu Nadir Bir Olgu Sunumu
2015 yılı Türk Nöroşirürji Derneği 29.Bilimsel Kongresi, 17 - 21 Nisan 2015
TNF Alpha G308A polymorphism is a risk factor for diabet among psoriatic patients P 1650
23rd EADV Congress Building Bridges, Amsterdam, Hollanda, 8 - 12 Ekim 2014
Association of eNOS Glu298Asp gene polymorphism with family history of psoriasis.
23rd EADV Congress Building Bridges, Amsterdam, Hollanda, 8 - 12 Ekim 2014, ss.1109
PS 035 C 14 Üre Nefes Testi ile Helikobakter Pilori Tedavi Direnci Saptanan Olgularda MDR1 Gen Polimorfizminin Etkisi
26.Ulusal Nükleer Tıp Kongresi. 16-20 Nisan 2014, Antalya, Türkiye, 16 - 20 Nisan 2014, ss.36
ÇANAKKALE DE AİLEVİ AKDENİZ ATEŞİ OLAN ÇOCUKLARDA Mefv GEN MUTASYONLARI VE FENOTİP GENOTİP İLİŞKİSİ
10. ULUDAĞ PEDİATRİ KIŞ KONGRESİ, Türkiye, 16 - 19 Mart 2014, ss.35-36
Maternal-Fetal eNOS Genotipleri ile Spontan Abortus İlişkisi
Erişkin Yaşta Görülen Genetik Hastalılar Sempozyumu, İstanbul, Türkiye, 1 - 04 Aralık 2013, ss.14
The prevelance of VKORC1 1639 G A and CYP2C9 2 3 genotypes in patients that requiring anticoagulant therapy in Turkish population
European Human Genetics Conference, Nuremberg, Almanya, 23 - 26 Haziran 2012, ss.356
P06 205 Evaluation of CYP2C9 and CYP2D6 gene polymorphisms in thyroid cancer
European Human Genetics Conference. Nürnberg-GERMANY 23-26 June 2012, 23 - 26 Haziran 2012, cilt.20, ss.198
P06 206 The possible role of the xenobiotic transporter P glycoprotein polymorphism that encoded by the MDR1 3435 C T gene in the susceptibility of differentiated thyroid cancer
European Human Genetics Conference.Nürnberg-GERMANY 23-26 June 2012., NÜRNBERG, Almanya, 23 - 26 Haziran 2012, cilt.20, ss.199
6 P76 Increased T allele frequency in MTHFR C677T gene in thyroid carcinoma
8th European Cytogenetic Conference, 02-05 July 2011, Porto, Portekiz, 2 - 05 Temmuz 2011, cilt.19, ss.175
Kitap & Kitap Bölümleri
Biyoteknoloji esasları ve tıbbi genetikte yeni uygulama alanları
Tıbbi Genetik ve Klinik Uygulamaları, Munis DÜNDAR, Editör, MG GRUP MATBAACILIK, KAYSERİ 2016;syf 935- 958, Kayseri, ss.539-556, 2016
Kardiyovasküler sistem hastalıklarına genetik yaklaşım
Tıbbi Genetik ve Klinik Uygulamaları, Munis DÜNDAR, Editör, MG GRUP MATBAACILIK, Kayseri, ss.935-958, 2016
Kardiyovasküler Hastalıkların Genetiği
Tıbbi Genetik ve Klinik Uygulamaları, Munis Dündar, Editör, Erciyes Üniversitesi, 2016