Çanakkale Onsekiz Mart Üniversitesi
Akademik Veri Yönetim Sistemi
Yayınlar & Eserler
SCI,SSCI,AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
Velickovic J. , Silan F., Dinçsoy Bir F., Silan C., Albuz B., Özdemir Ö., "Blau syndrome with a rare mutation in exon 9 of NOD2 gene", AUTOIMMUNITY, vol.52, pp.1-8, 2019
Öztopuz R.Ö., Silan F., Akbal A., Çoşkun Ö., Özdemir Ö., "Assessment of BMP-6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients", JOURNAL OF BIOTECHNOLOGY, pp.23-23, 2016 (Link) (Abstract)
Hiz M.M., Oğuz S., Işik S., Öğretmen Z., Silan F., "Contribution of the STAT4 rs7574865 gene polymorphism to the susceptibility to autoimmune thyroiditis in healthy Turk population and psoriatic subgroups", CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY, vol.40, pp.437-441, 2016
Yalçintepe S., Özdemir Ö., Silan C., Özen F., Uludağ A., Candan F., et al.,"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, vol.41, pp.281-286, 2016 (Link)
Uyrum E., Balbay O., Annakkaya A.N., Balbay E.G., Silan F., Arbak P., "The Relationship Between Obstructive Sleep Apnea Syndrome And Apolipoprotein E Genetic Variants", RESPIRATION, vol.89, pp.195-200, 2015
Akbal A., Gökmen F., Reşorlu H., Gökmen F., Silan F., Özdemir Ö., "The relationship between C-reactive protein rs3091244 polymorphism and ankylosing spondylitis.", INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, pp.1-1, 2015
Yalçintepe S., Özdemir Ö., Hacivelioğlu S.Ö., Akurut Ç., Uludağ A., Coşar E., et al., "Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population.", INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, vol.4, pp.120-7, 2015
Akbal A., Reşorlu H., Gökmen F., Savaş Y., Zateri C., Sargin B., et al., "The relationship between C-reactive protein rs3091244 polymorphism and ankylosing spondylitis", INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, pp.1-1, 2015
Özdemir S., Aşik M., Silan F., Özdemir Ö., Tan Y.Z., Ari E., et al.,"The RFLP profiles at BRAF V600E mutations in thyroid FNAB nodules", JOURNAL OF BIOTECHNOLOGY, vol.208, pp.S85-S85, 2015
Özkan A., Silan F., Uludağ A., Degirmenci Y., Özişik Karaman H.I., "Tumour necrosis factor alpha, ınterleukin 10 and ınterleukin 6 gene polymorphisms of ıschemic stroke patients ın south Marmara region of Turkey", INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY, vol.8, pp.13500-13500, 2015
Özdemir Ö., Kayatas M., Cetinkaya S., Yildirim M.E., Silan F., Kurtulgan H.K., et al.,"Bcii-RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis", RENAL FAILURE, vol.37, pp.292-296, 2015
Yalçintepe S., Özdemir Ö., Silan C., Özen F., Uludağ A., Candan F., et al., "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, pp.1-1, 2015
Djurovic J., Stojkovic O., Özdemir Ö., Silan F., Akurut Ç., Todorovic J., et al., "Association Between Foki, Apai And Taqi Rflp Polymorphisms In Vdr Gene And Hashimoto'S Thyroiditis: Preliminary Data From Female Patients In Serbia.", INTERNATIONAL JOURNAL OF IMMUNOGENETICS, no.29, pp.1-1, 2015
Akbal A., Oğuz S., Gökmen F., Reşorlu H., Silan F., Uludağ A., "C-Reactive Protein Gene And Toll-Like Receptor 4 Gene Polymorphisms Can Relate To The Development Of Psoriatic Arthritis.", CLINICAL RHEUMATOLOGY, no.3, pp.3-4, 2014
Uludağ A., Silan C., Yalçintepe S., Akurut Ç., Silan F., Özdemir Ö., "Relationship Between Response To Colchicine Treatment And Mdr1 Polymorphism In Familial Mediterranean Fever Patients ", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.18, pp.73-76, 2014 (Abstract)
Şen H.M., Silan F., Silan C., Degirmenci Y., Özişik Karaman H.I., "EFFECTS OF CYP2C19 AND P2Y12 GENE POLYMORPHISMS ON CLINICAL RESULTS OF PATIENTS USING CLOPIDOGREL AFTER ACUTE ISCHEMIC CEREBROVASCULAR DISEASE", BALKAN JOURNAL OF MEDICAL GENETICS, vol.17, pp.37-41, 2014 (Link)
Asgun H.F., Kirilmaz B., Saygi S., Ozturk O., Silan F., Karatag O., et al., "Association Between Inherited Thrombophilia And Impaired Right Ventricular Function In Deep Vein Thrombosis Without Symptomatic Pulmonary Embolism", CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS, vol.20, pp.270-277, 2014
Öğretmen Z., Hiz M.M., Silan F., Koşar Ş., Özdemir Ö., "Is The Hla B27 Genotype A Risc Faktor For Psoriatic Arthritis And Psoriasis Vulgaris?", TURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY, vol.48, pp.131-134, 2014
Topaloğlu N., Oğuz S., Silan F., Uludağ A., Işik S., Akurut Ç., "Association of Vitamin D Receptor Gene Polymorphisms in Children With Atopic Diseases", GENE THERAPY AND MOLECULAR BIOLOGY, vol.16, pp.55-60, 2014
Özdemir Ö., Silan F., Urfali M., Uludağ A., Arı E., Kayataş M., "Variable R.Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677T gene polymorphism: from genetics to epigenetics", GENE THERAPY AND MOLECULAR BIOLOGY, vol.16, pp.77-87, 2014
Öğretmen Z., Hiz M.M., Silan F., Uludag A., Özdemir Ö., "Association Of Endothelial Nitric Oxide Synthase Glu298asp Gene Polymorphism In Psoriasis Cases With Hypertension.", ANNALS OF SAUDI MEDICINE, vol.34, pp.340-5, 2014
Yalçintepe S., Silan F., Hacivelioğlu S.Ö., Uludağ A., Coşar E., Özdemir Ö., "Fetal Vegf Genotype Is More Important For Abortion Risk Than Mother Genotype.", Int J Mol Cell Med., no.2, pp.88-94, 2014 (Abstract)
Silan F., "Two Siblings With Currarino Syndrome With 7q34 Deletion Due To Maternal T(7;14)(Q34;P13)", HONG KONG JOURNAL OF PAEDIATRICS, vol.19, pp.181-184, 2014
Gazi E., Temiz A., Barutçu A., Silan F., Özdemir Ö., "Endothelial Function And Germ-Line Ace-Id, Enos And Pai-1 Gene Profiles In Patients With Coronary Slow Flow In The Canakkale Population: Multiple Thrombophilic Gene Profiles In Coronary Slow Flow", CARDIOVASCULAR JOURNAL OF AFRICA, vol.25, pp.9-14, 2014 (Abstract)
Gazi E., Barutçu A., Altun B., Temiz A., Bekler A., Urfali M., et al., "Intercellular Adhesion Molecule-1 K469e And Angiotensinogen T207m Polymorphisms In Coronary Slow Flow", MEDICAL PRINCIPLES AND PRACTICE, vol.23, pp.346-350, 2014 (Abstract)
Özdemir S., Uludağ A., Silan F., Yalçintepe S., Turgut B., Özdemir Ö., "Possible Roles Of The Xenobiotic Transporter P-Glycoproteins Encoded By The Mdr1 3435 C>T Gene Polymorphism In Differentiated Thyroid Cancers. ", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.3213-3217, 2013 (Abstract)
Silan F., Özdemir Ö., "The Proto-Oncogene Kras And Braf Profiles And Some Clinical Characteristics In Colorectal Cancer In The Turkish Population.", Genet Test Mol Biomarkers, vol.17, pp.135-139, 2013 (Abstract)
Şık E., Silan F., Uludağ A., Özdemir Ö., "Germ-Line Mthfr C677t, Fv H1299r And Pai-1 5g/4g Variations In Breast Carcinoma.", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.2903-2908, 2013 (Abstract)
Silan F., Özdemir Ö., Uysal A., Uludağ A., Erçelen N., "Double Translocation: An Interesting Family History.", BALKAN JOURNAL OF MEDICAL GENETICS, vol.1, pp.77-80, 2013
Silan F., Çakir Güngör A.N., Oguz S., Uludag A., Gencer M., Öğretmen Z., et al., "Stria Gravidarum Is Genetic But Not Related With Collagen Gene Polymorphism", GENE THERAPY AND MOLECULAR BIOLOGY, vol.15, pp.131-137, 2013
Silan C., Silan F., Kukul Güven F.M., Özdemir S., Uludağ A., Yalçintepe S., et al., "The Prevalence Of Vkorc1 1639 G>A And Cyp2c9*2*3 Genotypes In Patients That Requiring Anticoagulant Therapy In Turkish Population.", Mol Biol Rep, vol.39, pp.11017-11022, 2012 (Abstract)
Silan C., Dogan O., Silan F., Kukulguven F., Aşgün H.F., Özdemir S., et al.,"The prevalence of VKORC1 1639 G>A and CYP2C9*2*3 genotypes in patients that requiring anticoagulant therapy in Turkish population.", MOLECULAR BIOLOGY REPORTS, vol.39, pp.11017-22, 2012 (Link)
Özdemir S., Silan F., Özkan Hasbek Z., Uludağ A., Yalçintepe S., Erselcan T., et al., "Increased T-Allele Frequency Of 677 C>T Polymorphism In The Methylenetetrahydrofolate Reductase Gene In Differentiated Thyroid Carcinoma.", Genet Test Mol Biomarkers, vol.16, pp.780-784, 2012 (Abstract)
Özdemir Ö., Silan F., Yalçintepe S., "Recurrent Pregnancy Loss And Its Relation To Combined Parental Thrombophilic Gene Mutations.", Genet Test Mol Biomarkers, vol.16, pp.279-286, 2012 (Abstract)
Uludağ A., Silan F., "Does The Maxillary Sinus Have A Triggering Role In Nasal Nitric Oxide Synthesis? ", RHINOLOGY, vol.50, pp.402-407, 2012 (Abstract)
Silan F., Uludağ A., Özdemir Ö., Yalçintepe S., Özdemir S., Erselcan T., et al., "Increased T Allele Frequency Of 677 C>T Polymorphism In The Mthfr Gene In Differentiated Thyroid Carcinoma. ", Genetic Testing and Molecular Biomarkers, pp.780-784, 2012
Silan F., Yalçintepe S., Uludağ A., Özdemir Ö., "Combined Point Mutations In Codon 12 And 13 Of Kras Oncogene In Prostate Carcinomas.", Mol Biol Rep, vol.39, pp.1595-1590, 2012 (Abstract)
Demirel Y., Doğan S., Uludağ A., Silan C., Atik S., Silan F., et al., "Combined Effect Of Factor V Leiden, Mthfr, And Angiotensin-Converting Enzyme (Insertion/Deletion) Gene Mutations In Hypertensive Adult Individuals: A Population-Based Study From Sivas And Canakkale, Turkey", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.15, no.11, pp.785-791, 2011 (Link) (Abstract)
Silan C., Uludağ A., Silan F., Özdemir S., Atik S., Özdemir Ö., "Association Between Abcb1 (Mdr1) Gene 3435 C>T Polymorphism And Colchicine Unresponsiveness Of Fmf Patients. ", Ren Fail, vol.33, pp.899-903, 2011 (Abstract)
Silan F., Güçlü O., Kadioglu L.E., Silan C., Atik S., Uludağ A., et al., "Gjb2 35delg And Mitochondrial A1555g Mutations And Etiology Of Deafness At The Gelibolu School For The Deaf In Turkey", JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY, vol.7, pp.361-371, 2011
Silan F., "Anophthalmia, Cleft Lip/Palate, Absent Vomer Bone, Nystagmus, And Mental-Motor Retardation: A New Syndrome Or Fryns "Anophthalmia-Plus" Syndrome?", Cleft Palate Craniofac J, vol.45, pp.256-260, 2008 (Abstract)
Silan F., "A New Subtype Of Brachydactyly Type B Caused By Point Mutations In The Bone Morphogenetic Protein Antagonist Noggin.", Am J Hum Genet, vol.81, pp.388-396, 2007 (Abstract)
Silan F., "Partial Trisomy 1(Q25qter) Due To A De Novo Unbalanced 1;19 Translocation In A Neonate.", Genet Couns, vol.18, pp.409-416, 2007 (Abstract)
Silan F., "Partial Trisomy 4(Q31qter) Due To Maternal 4;5 Balanced Translocation In A Neonate.", Genet Couns, vol.18, pp.163-170, 2007 (Abstract)
Silan F., "Waardenburg Syndrome In The Turkish Deaf Population.", Genet Couns, vol.17, pp.41-48, 2006 (Abstract)
Silan F., "Congenital Sialoblastoma (Embryoma) Associated With Premature Centromere Division And High Level Of Alpha-Fetoprotein.", Prenat Diagn, vol.25, pp.687-689, 2005 (Abstract)
Silan F., "Branchio-Oculo-Facial Syndrome With The Atresia Of External Ear.", Int J Pediatr Otorhinolaryngol, vol.69, pp.1575-1578, 2005 (Abstract)
Silan F., "Non-Hodgkin'S Lymphoma And Auricular Hypoplasia: Associated With Juvenile Colloid Milium Or Ligneous Conjunctivitis?", J Eur Acad Dermatol Venereol, vol.19, pp.348-351, 2005 (Abstract)
Silan F., "Evaluation Of Deaf Children In A Large Series In Turkey.", Int J Pediatr Otorhinolaryngol, vol.69, pp.367-373, 2005 (Abstract)
Silan F., "A Novel L1cam Mutation With L1 Spectrum Disorders.", Prenat Diagn, vol.25, pp.57-59, 2005 (Abstract)
Silan F., "Syndromic Etiology In Children At Schools For The Deaf In Turkey.", Int J Pediatr Otorhinolaryngol, vol.68, pp.1399-1406, 2004 (Abstract)
Silan F., "Sall4 Deletions Are A Common Cause Of Okihiro And Acro-Renal-Ocular Syndromes And Confirm Haploinsufficiency As The Pathogenic Mechanism.", J Med Genet, vol.41, pp.1-1, 2004
Silan F., "Incontinentia Pigmenti With Nemo Mutation In A Turkish Family.", Int J Dermatol, vol.43, pp.527-529, 2004
Silan F., "A New Mutation Of The Fukutin Gene In A Non-Japanese Patient.", Ann Neurol, vol.53, pp.392-396, 2003 (Abstract)
Silan F., "Etiology Of Deafness At The Yeditepe School For The Deaf In Istanbul.", Int J Pediatr Otorhinolaryngol, vol.67, pp.467-471, 2003 (Abstract)
Silan F., "Protective Effect Of Melatonin On Beta-Cell Damage In Streptozotocin-Induced Diabetes In Rats.", Acta Histochem, vol.105, pp.261-266, 2003 (Abstract)
DİĞER DERGİLERDE YAYINLANAN MAKALELER
Gönlügür U., Gönlügür T., Özdemir Ö., Silan F., "Warfarin Resistance: A Case Report", EURASIAN JOURNAL OF EMERGENCY MEDICINE, vol.18, pp.61-63, 2019 (Link)
Öztopuz R.Ö., Silan F., Çoşkun Ö., Akbal A., "“Ankilozan Spondilitli Hastalarda BMP-6 (rs267196 ve rs267192) Genetik Polimorfizmi” b", Türk Hijyen ve Deneysel Biyoloji Dergisi, cilt.1, no.1, ss.1-6, 2019
Silan F., Silan F., "Kanser Etyolojisinde Tetikleyici Moleküler Mekanizmalar", Turkiye Klinikleri Journal of Medical Genetics-Special Topics, cilt.2, ss.74-87, 2017
Silan F., Silan F., Türünz V., Özdemir Ö., "The GJB2 gene mutation profiles in hearing impaired patients from Western Turkey, Canakkale", Biomedical Genetics and Genomics, vol.2, pp.1-5, 2017 (Link)
Silan F., Akbal A., Reşorlu H., Savaş Y., Zateri C., Silan F., et al., "THE FREQUENCY OF TOLL-LİKE RECEPTOR 4 GENE POLYMORPHİSM İN ANKYLOSİNG SPONDYLİTİS AND İTS RELATİONSHİP BETWEEN DİSEASE ACTİVİTY", THE EUROPEAN RESEARCH JOURNAL, 2017 (Link)
Özdemir Ö., Silan F., Silan F., "A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus", Biomedical Genetics and Genomics, vol.2, pp.1-3, 2017 (Link)
Silan F., Topaloğlu N., Tekin M., Silan F., "A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion.", Acta Medica Iranica, 2017
Yalçintepe S., Silan F., Silan F., "Günümüzde Kanser Tanısında Kullanılan Geçerli ve Güvenilir Moleküler Tetkikler", Turkiye Klinikleri Journal of Medical Genetics-Special Topics, cilt.2, ss.113-122, 2017
Yildirim Ş., Topaloğlu N., Tekin M., Silan F., "A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion.", Acta Medica Iranica, vol.55, pp.661-663, 2017
Altinbaş K., Yeşilbaş D., İnce B., Cansiz A., Silan F., Silan F., et al., "Evaluation of The Association Between Lithium Treatment and GSK3ß Polymorphism in Bipolar Disorder Patients. January 2017 Turk psikiyatri dergisi = DOI:", Turkish journal of psychiatry, 2017
Akbal A., Reşorlu H., Savaş Y., Zateri C., Silan F., Silan F., "The frequency of toll-like receptor 4 gene polymorphism in ankylosing spondylitis and its relationship between disease activity.", The European Research Journal, 2017
Silan F., Silan F., "A mosaic infertile case of isodicentric Y-chromosome with duplicated SRY, SHOX and deleted AZF locus", Biomedical Genetics and Genomics, vol.2, pp.1-3, 2017
Çakir Güngör A.N., Silan F., Kilinç N., Gencer M., Uludağ A., Coşar E., et al., "9qh liği Molar Gebelik İçin Bir Risk Faktörü mü", Jinekoloji - Obstetrik ve Neonatoloji Tıp Dergisi, 2016
Özdemir Ö., Gürgen A., Urfali M., Yildiz O., Uludağ A., Silan F., "An infertile case of 47 XYY syndromewithout autistic spectrum Cost effectivewell define of extra Y chromosome byGTG C bandings QF PCR and FISHanalyses", Cumhuriyet Tıp Dergisi, 2016
Özdemir Ö., Küçük Kurtulgan H., Urfali M., Silan F., "Hypermethylated promoter profiles for tumoursupressor APC p53 MSH6 and MGMT genes in CRCtumours", Pyrex Journal of Biomedical Research, 2016
Silan F., Yildiz O., Urfali M., Özdemir Ö., "A mental and motor retarded dysmorphic case withheterozygous 1p36 deletion Comparable results fromcytogenetic MicroArray CGH FISH and MLPAtechniques", merit research journal of medicine and medical sciences, 2016
Semerci C.N., Alatas E., Silan F., Tufan N.L., Dodurga Y., Satiroglu H., "Mutation analysis of HSFY gene by DNA sequencing in Turkish men with idiopathic infertility", Pamukkale Tip Dergisi, cilt.9, ss.1-4, 2016
Yildiz O., Silan F., Özdemir Ö., Mosse I., Kilchevsky A., Gonchar A., et al., "Comparison of the thrombophilic gene polymorphismsand recurrent pregnancy loss Results on combined geneeffect of FV Leiden FVR2 FXIII MTHFR A1298Cand C677T PAI 1 4G 5G and ACE I D genes in RPLWomen from Misk Belarus and Canakkale Sivas Turkey", Biomedical Genetics and Genomics, 2016
Şen H., Silan F., Binnetoğlu E., Güneş F., Akurut Ç., Uludağ A., "Hyperimmunoglobulin D syndrome: case report", Turkish Journal of Rheumatology., vol.30, pp.244-244, 2015
Silan F., Çakir Güngör A.N., Urfali M., Uludağ A., Çavuş E., Koç E., et al., "Triploidy/Diploidy Mosaisizm, Diandry and Uniparental Isodisomy: Fetus with Omphalocele and Contracted Finger", Family Medicine & Medical Science Research , vol.4, pp.1000180-1000180, 2015 (Link)
Silan F., Çakir Güngör A.N., Urfali M., Uludağ A., Özdemir Ö., "Triploidy Diploidy Mosaisizm Diandry and Uniparental Isodisomy Fetus withOmphalocele and Contracted Finger", Family Medicine & Medical ScienceResearch, 2015
Güven M., Akman T., Aras A.B., Topaloğlu N., Şen H.M., Silan F., et al., "Epileptik Nöbet Bulgusu Ile Gelen Temporal Kemik Osteomu: Nadir Bir Olgu Sunumu ", Odü Tıp Dergisi, no.2, ss.83-86, 2015
Turgut T., Yaşar M. , Yaykaşlı K.O. , Ertaş E. , Silan F., "Increased Sister Chromatid Exchanges In Patients With Gastrointestinal Cancers And In Their First-Degree Relatives", European Journal of Health Science, vol.11, pp.94-94, 2014 (Özet)
Kara M., Dereköy F.S., Güçlü O., Özdemir Ö., Silan F., Barutçu O., et al., "Larenks Kanserli Hastalarımızda K-Ras Mutasyonları", International Journal of Clinical Research, cilt.2, ss.6-11, 2014
Yildirim Ş., Topaloğlu N., Tekin M., Silan F., "Patau Sendromu, Komplet Veya İnkomplet Yaşam Süresinde Önemli Mi?", Anatol J Clin Investig, cilt.8, ss.187-188, 2014
Yalçintepe S., Gencer M., Uludağ A., Çakir Güngör A.N., Kumcular T., Coşar E., et al., "Onsekiz Haftalık Spontan Olarak Sonlanan Ve Qf-Pcr Ile Saptanan Triploi'Dik Fetus: Olgu Sunumu", International Journal of Clinical Research, cilt.1, ss.31-34, 2013
Silan F., Gür S., Kadioglu L.E., Yalçintepe S., Ükinç K., Uludağ A., et al., "Characteristic Findings Of Alstrom Syndrome With A Case Report", Journal of Clinical Diagnostics, pp.75-77, 2013
Özdemir S., Tan Y.Z., Topaloğlu N., Silan F., Tekin M., "Tc-99m Dmsa Scintigraphy In The Diagnosis Of Renal Anomalies: A Turner Syndrome Case", Turkiye Klinikleri Journal of Pediatrics, cilt.22, ss.37-40, 2013
Çakir Güngör A.N., Hacivelioğlu S.Ö., Uludağ A., Gencer M., Uysal A., Atik S., et al., "Fetal Anöploidi Açısından Yüksek Riskli Gebeliklerin Qf-Pcr İle Analizi", International Journal of Clinical Research, cilt.1, ss.17-21, 2013
Çakir Güngör A.N., Gencer M., Yücesoy K., Hacivelioğlu S.Ö., Kizildağ B., Silan F., "Nöral Tüp Defekti Gebeliği Olan Olguda Terminasyon Kararı ", Smyrna Tıp Dergisi, ss.27-30, 2012
Silan F., "Çok Sayıda Konjenital Anomalinin Eşlik Ettiği Trizomi 8 Mozaisizm Olgusu", Turkiye Klinikleri Journal of Pediatrics, cilt.18, ss.324-327, 2009
HAKEMLİ KONGRE / SEMPOZYUMLARIN BİLDİRİ KİTAPLARINDA YER ALAN YAYINLAR
Silan F., Silan F., Özdemir Ö., "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,
Silan F., Silan F., Yildiz O., Urfali M., Özdemir Ö., "Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?", World BioDiscovery Congress 2017, Sofia, Bulgaria, Sofya, BULGARISTAN, , vol.20, pp.20113-20113
Silan F., Silan F., Yildiz O., Urfali M., Özdemir Ö., "A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype–phenotype correlation in a case report", European Biotechnology Congress 2017, Dubrovnik,Croatia, Dubrovnik, HIRVATISTAN, , vol.256, pp.78-79
Özdemir Ö., Urfali M., Silan F., Yildiz O., Silan F., "A balanced non-reciprocal translocated case with recurrent abortions: The importance and validity of conventional cytogenetics analysis in balanced translocations detection when comparing to the MicroArray-CGH technique", European Biotechnology Congress 2017, Dubrovnik, Croatia, Dubrovnik, HIRVATISTAN, , vol.256, pp.79-79
Silan F., Urfali M., Silan F., Özdemir Ö., "Clinical and molecular characterization of SLC7A gene that located in 14q11.2 locus in a seconder infertile rare case with lysinuric protein intolerance", European Biotechnology Congress 2017, Dubrovnik,Croatia, Dubrovnik, HIRVATISTAN, , vol.256, pp.78-78
Özdemir Ö., Yildiz O., Silan F., Urfali M., Silan F., "The microdeletion of 15q11.2 locus encompassing TUBGCP5, NIPA1, NIPA2, and CYFIP1 genes in an epileptic case with macrocephaly, attention-deficit/hyperactivity disorder (ADHD), speech and motor delay", European Biotechnology Congress 2017, Dubrovnik, Croatia, Dubrovnik, HIRVATISTAN, , vol.256, pp.78-78
Urfali M., Silan F., Silan F., "The comparison of telomeric DNA length in different biological materials in various cancers by real-time PCR amplification of circulating tumour DNA.", European Biotechnology Congress, Dubrovnik, , , pp.79-79
Kankaya D., Silan F., Yildiz O., Urfali M., Güler Z., Özdemir Ö., "THE MOLECULAR ETHIOLOGICAL PARAMETERS IN PRELINGUAL SENSORINEURAL HEARING LOSS", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP21, pp.S16-S16
Öztopuz R.Ö., Silan F., Akbal A., Çoşkun Ö., Özdemir Ö., "Assessment of BMP 6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients", EUROPEAN BİOTECHNOLOGY CONFERENCE, RIGA, ,
Bakirdöğen S., Silan F., Özkul F., Arik M., Silan C., Özdemir Ö., "UGT1A1 GENE MUTATIONS MAY CAUSE MYCOPHENOLATE MOFETIL INDUCED LEUCOPENIA AFTER RENALTRANSPLANTATION: A CASE REPORT", Medical Genetics andClinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP53, pp.S28-S28
Özdemir Ö., Paksoy B., Gürgen A., Urfali M., Yildiz O., Uysal D., et al., "AN İNFERTILE CASE OF 47, XYY SYNDROME WITHOUT AUTISTIC SPECTRUM: COST EFFECTIVE WELL-DEFINE OF EXTRA Y CHROMOSOME BY GTG, C BANDINGS, QF-PCR AND FISH ANALYSE", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP06, pp.s9-s9
Silan F., Urfali M., Özdemir Ö., Paksoy B., Uysal D. , "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, KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP05, pp.s9-s9
Silan F., Özdil Kahveci D., Urfali M., Paksoy B., Özdemir Ö., "THE PREVALENCE AND HIGH-RISK GENOTYPE DISTRUBUTIONS OF HUMAN PAPILLOMA VIRUS (HPV) FROM CERVICAL PAPSEMEAR IN WOMEN FROM ÇANAKKALE COHORT.", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP4, pp.s9-s9
Urfali M., Silan F., Kuru B., Özdemir Ö., "GENETIC SCREENING FOR CFTR AND AZF REGION OF Y CHROMOSOME MICRODELETIONS IN IDIOPATHIC CASES OF AZOOSPERMIA AND OLIGOZOOSPERMIA:A MOLECULAR AND CYTOGENETIC APPROACHE", Medical Genetics andClinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP33, pp.S20-S20
Silan F., Yildiz O., Güler Z., Küçük Kurtulgan H. , Özdemir Ö., "THE COMBINED MUTATION EFFECT OF PROTROMBIN G20210A AND ACE I/D GENES IN ESSENTIAL HYPERTENSION", Medical Genetics andClinical Applications, KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP22, pp.S16-S16
Kuru B., Silan F., Uludağ A., Urfali M., Yildiz O., Özdemir Ö., "“FISHED” OUT THE CORRECT DIAGNOSIS: A CASE OF DIGEORGE SYNDROME WITH MENTAL RETARDATION, SHORT STATURE AND DYSMORPHIC FACIAL FINDINGS", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP20, pp.S15-S15
Silan F., Karaağaçli D., Kuru B., Uludağ A., Paksoy B., Urfali M., et al., "THE 22Q11.21 DUPLICATION IN A NORMAL INTELLIGENCE CASE WITH PREMATURE OVARIAN FAILURE AND HIGH MYOPIA", Medical Genetics andClinical Applications, KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.0P019, pp.S15-S15
Silan F., Yildiz O., Urfali M., Özdemir Ö., "INCREASED POINT MUTATION FREQUENCY IN K-RAS ONCOGENE IN CRC TUMOURS IN CANAKKALE POPULATION", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP23, pp.S16-S16
Özdemir Ö., Yildiz O., Kuru B. , Paksoy B., Uysal D., Silan F., "The possible role of chromosome 9q11.1-1.2 duplication resulting with infertility and recurrent pregnancy loss", European Human Genetics Conference 2016, BARCELONA, ISPANYA, 21-24 Mayıs 2016, pp.E-P01.38-E-P01.38
Urfali M., Silan F., Tan Y.Z., Türker Çelik F., Güler Z., Özdemir Ö., "Alterations in the telomere length distribution of cell-free DNA in human cancer", EUROPEAN BIOTECHNOLOGY CONGRESS 2016, RİGA, LITVANYA, 5-7 Mayıs 2016, cilt.231, ss.S109-S109 (Link)
Silan F., Paksoy B., Özdemir Ö., "Clinical characteristics and cytogenetic abnormalities of chromosome 22q11. 2 syndrome: Results from thirteen patients with variable phenotypes", EUROPEAN BIOTECHNOLOGY CONGRESS 2016, RİGA, LITVANYA, 5-7 Mayıs 2016, vol.231, pp.S82-S82 (Link)
Silan F., Işin B., Urfali M., Yildiz O., Uludağ A., Özdemir Ö., "A CASE DIRECTLY REQUESTED GENETIC COUNSELLING FROM MEDICAL GENETIC OUTPATIENT CLINIC AND DIAGNOSED MOSAIC KLEINFELTER SYNDROME AFTER KARYOTYPE AND FISH ANALYSES", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP07, pp.S10-S10
Yildiz O., Uludağ A., Silan F., Güler Z., Özdemir Ö., "MICROGNATIA, FACIAL DYSMORPHISM, AORTIC VALVE PATHOLOGY, LOW WEIGHT, CHEST DEFORMITIES AND MENTAL RETARDATION: A CASE WITH WILLIAMS SYNDROME", Medical Genetics andClinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP58, pp.S30-S30
Silan C., Yildiz O., Özdemir Ö., Silan F., "Pharmacogenetic analysis of CYP genes, VKORC1, UGT1A1 and MDR1 at West Anatolia Region", European Human Genetics Conference 2016, BARCELONA, ISPANYA, 21-24 Mayıs 2016, pp.E-P15.11 -E-P15.11
Silan F., Urfali M., Yildiz O., Paksoy B., Uludağ A., Özdemir Ö., ". Familial X chromosome translocation, Xq triplication and SHOX gene deletion with short stature;Conflicting results of QF-PCR analysis for Xq segmental triplication. ", European Human Genetics Conference 2016, BARCELONA, ISPANYA, 21-24 Mayıs 2016, pp.E-P13.17 -E-P13.17
Silan F., Has H., Işin B., Uludağ A., Urfali M., Yildiz O., et al., "A MOSAIC TURNER PHENOTYPE WITH SECONDARY AMENORREA, INFERTILITY AND NORMAL HORMONAL STATUS THAT DETERMINED BY FISH ANALYSIS", Medical Genetics and Clinical Applications , KAYSERİ, TÜRKIYE, 11-13 Şubat 2016, no.OP08, pp.S10-S10
Kuru B., Silan F., Uludağ A., Urfali M., Yildiz O., Özdemir Ö., "Mental Retardasyon, Kısa Boy ve Dismorfik Yüz Bulguları ile Karakterize DiGeorge Sendromlu Olgu FISH Yöntemi ile Doğru Tanı: Çanakkale Deneyimi.", 1. Trakya Üniversiteler Birliği Yüksek Lisans Öğrenci Kongresi , ÇANAKKALE, TÜRKIYE, 29-30 Nisan 2016, ss.1-1
Silan F., Mosse I. , Gonchar A., Sedlyar N. , Kilchevsky A.V., Kuru B., et al., "The thrombophilic gene polymorphisms and recurrent pregnancy loss dilemma: From Minsk/Belarus and Canakkale–Sivas/Turkish populations", EUROPEAN BIOTECHNOLOGY CONGRESS 2016, RIGA, LITVANYA, 5-7 Mayıs 2016, vol.231, pp.S20-S20 (Link)
Silan F., Yildiz O., Özdemir Ö., Taş Z.T., "Microtia micrognati facial dysmorphism short stature and mental retardation A rare case with Meirer Gorlin syndrome", European Biotechnology Congress, , , pp.86-86
Silan F., "Medical genetics in Canakkale and Turkey", II INTERNATIONAL SCIENTIFIC CONFERENCE ON “GENETICS AND BIOTECHNOLOGY OF THE 21ST CENTURY: POBLEMS, ACHIEVEMENTS AND PERSPECTIVES, Minsk, BEYAZ RUSYA,
Silan F., Uludağ A., Yildiz O., Urfali M., Özdemir Ö., "The microdeletion microduplication profiles in spontaneously aborted fetal materials Double blind results of QF PCR and MLPA techniques", European Biotechnology Congress, , , pp.85-85
Özdemir S., Aşik M., Silan F., Özdemir Ö., Tan Y.Z., Ükinç K., " The Rflp Profiles At Braf V600e Mutations In Thyroid Fnab Nodules. ", European Biotechnology Congress, Bükreş, ROMANYA, 7-9 Mayıs 2015, vol.208, pp.85-85
Özdemir Ö., Silan F., Urfali M., "Bcii – Rflp Profiles For Serum Amiloid A1 And Mutated Mefv Gene Prevelance In Chronic Renal Failure Patients Requiring Long-Term Haemodialysis.", 11. Ulusal Tıbbi Genetik kongresi, İSTANBUL, TÜRKIYE, 24-27 Eylül 2014, ss.160-160
Silan F., Urfali M., Özdemir Ö., "İzole Malign Periferal Sinir Kılıf Tümörlü Hastada Nf1 Ve Omgp Gen Delesyonu. ", 11. Ulusal Tıbbi Genetik kongresi,, İSTANBUL, TÜRKIYE, 24-27 Eylül 2014, ss.82-82
Özdemir Ö., Urfali M., Uludağ A., Uysal D., Silan F., "Erkekte Azospermi, Kadında Translokasyon Taşıyıcılığı Saptanan Infertilite Çifti. ", Ulusal Tıbbi Genetik kongresi, İSTANBUL, TÜRKIYE, 24-27 Eylül 2014, ss.120-120
Şık E., Özdemir Ö., Silan F., Uludağ A., Urfali M., "Aberrantly Methylated Promoter Regions Of Tumour Supressor Apc, P53, Mgmt, Dapk1 And Mlh3 Genes That Commonly Affected By Dna Hypermethylation In Colorectal Cancer. ", 11. Ulusal Tıbbi Genetik kongresi, , İSTANBUL, TÜRKIYE, 24 Eylül - 27 Ekim 2014, ss.41-41
Urfali M., Özdemir Ö., Uysal D., Çakir Güngör A.N., Silan F., "Aynı Ailede Boy Kısalığının Iki Farklı Genetik Etyolojisi.", 11. Ulusal Tıbbi Genetik kongresi,, İSTANBUL, TÜRKIYE, 24-27 Eylül 2014, ss.81-81
Gazi E., Barutçu A., Altun B., Temiz A., Bekler A., Urfali M., et al., "Intercellular Adhesion Molecule-1 K469e And Angiotensinogen T207m Polymorphisms In Coronary Slow Flow", INTERNATIONAL CONGRESS OF UPDATE IN CARDIOLOGY AND CARDIOVASCULAR SURGERY , ANTALYA, TÜRKIYE, 13-16 Mart 2014, ss.122-122
Akurut Ç. , Silan F., Çakir Güngör A.N., Özdemir Ö., "Maternal Kandan Fetal DNA İzolasyonu ve Fetal RhD Analizi. ", Ulusal Tıbbi Genetik kongresi, İSTANBUL, TÜRKIYE, 24-24 Eylül 2014, ss.141-141
Merve Meliha H., Aki C., Öğretmen Z., Silan F., "Lack of association of apolipoprotein E Apo E epsilon 2 epsilon 3 epsilon 4 polymorphisms with depression among Turkish psoriatic patients", FEBS EMBO 2014 Conference, ,
Silan F., Yalçintepe S., Özdemir Ö., Hacivelioğlu S.Ö., Akurut Ç., Kumcular T., "Maternal-Fetal Enos Genotipleri Ile Spontan Abortus İlişkisi", Erişkin Yaşta Görülen Genetik Hastalılar Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık
Silan F., Yalçintepe S., Hacivelioğlu S.Ö., Uludağ A., Coşar E., Özdemir Ö., "Abortus Riskinde Fetal Vegf Genotipinin Önemi. Erişkin Yaşta Görülen Genetik Hastalılar Sempozyumu", Erişkin Yaşta Görülen Genetik Hastalıklar Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık 2013
Silan F., Akurut Ç., Urfali M., Şık E., Özdemir Ö., "Kliniğimizde Herediter Trombofili Saptanan 5 Olgu", Erişkin Yaş Genetik Hastalıkları Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık 2013
Öğretmen Z., Silan F., Sinem Atik Y., Kirilmaz B., Özdemir Ö., "The relationship between psoriasis and tnf alpha g308a and g238a polymorphisms", JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY, ,
Silan F., Akurut Ç., Yalçintepe S., Coşar E., Gencer M., Özdemir Ö., "Sayısal Kromozom Anomalilerinin Ve Uniparental Disomi Olgularının Mikrosatellit Markerlarla Analizi", Erişkin Yaşta Görülen Genetik Hastalılar Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık
Uludağ A., Silan C., Atik S., Akurut Ç., Silan F., Özdemir Ö., "Relationship Between Response To Colchicine Treatment And Mdr1 Polymorphism In Fmf Patients", European Human Genetics Conference, PARİS, FRANSA, 8-11 Haziran 2013, pp.04-57
Özdemir Ö., Silan F., Atik S., "The Mefv Mutation Profiles And Saa1 Gene Bcii Polymorphism In Chronic Renal Failure Patients That Requiring Long-Term Haemodialysis In Turkish Population.", European Human Genetics Conference, PARİS, FRANSA, 8-11 Haziran 2013, pp.04-49
Silan F., Urfali M., Özdemir Ö., Uysal D., Ari E., Göveç H., "Sitogenetik Sonuçları Olan Bir Tek Gen Defekti: Prematur Chromatide Separation", Erişkin Yaşta Görülen Genetik Hastalılar Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık
Silan F., Özdemir Ö., Uysal D., Urfali M., Yalçintepe S., Coşar E., et al., "Tekrarlayan Düşükleri Olan Çiftlerde D16z2 Lokus Polimorfizminin Fish Yöntemiyle Analizi", Erişkin Yaşta Görülen Genetik Hastalıklar Sempzyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık 2013
Silan F., Yalçintepe S., Hacivelioğlu S.Ö., Koç E., Coşar E., Uludağ A., et al., "Apo E Polimorfizmi: Fetal Genotipler Anne Genotiplerine Karşı? ", Erişkin Yaş Genetik Hastalıkları Sempozyumu, İSTANBUL, TÜRKİYE, 6-7 Aralık 2013
Özdemir S., Uludağ A., Silan F., Atik S., Turgut B., Özdemir Ö., ".The Possible Role Of The Xenobiotic Transporter P-Glycoproteinpolymorphism That Encoded By The Mdr1 3435 C>T Gene In The Susceptibility Of Differentiated Thyroid Cancer", European Human GeneticsConference , NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.198-198
Silan F., Atik S., Uludağ A., Özdemir Ö., "Combined Point Mutations In Codon 12 And 13 Of Kras Oncogene In Prostate Carcinomas With High Gleason Score", European Human Genetics Conference, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.171-171
Silan F., Atik S., Uludağ A., Özdemir Ö., "Combined Point Mutations In Codon 12 And 13 Of Kras Oncogene In Prostate Carcinomas With High Gleason Score", European Journal of Human Genetics, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.171-171
Atik S., Uludağ A., Silan C., Silan F., Özdemir Ö., "Polymorphism In Gene Encoding Drugs And Xenobiotic Metabolizing Enzyme Cyp2d6 As A Risk Factor For Drug Response In Colchicine Unresponsive Fmf Patients", European Human Genetics Conference, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.199-199
Silan C., Silan F., Uludağ A., Aşgün H.F., Atik S., Güngör B., et al., "The Prevalence Of Vkorc1 1639 G>A And Cyp2c9*2*3 Genotypes In Patients That Requiring Anticoagulant Therapy In Turkish Population", .European Human Genetics Conference , Nürnberg, ALMANYA, 23-26 Haziran 2012, vol.20, no.1, pp.1-1 (Link)
Uludağ A., Özdemir S., Silan C., Atik S., Silan F., Özdemir Ö., "Evaluation Of Cyp2c9, Cyp2c19 And Cyp2d6 Gene Polymorphisms In Thyroid Cancer", European Human Genetics Conference, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.187-187
Uludağ A., Silan F., Silan C., Atik S., Özdemir Ö., "What About The Relatives Who Have Mthfr C677t Polymorphism?", European Human Genetics Conference, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, pp.182-182
Atik S., Silan C., Uludağ A., Silan F., Özdemir S., Özdemir Ö., "Increased T Allele Frequency In Multidrug Transporter Abcb1 (Mdr1) Gene In Fmf Patients Of Colchicine Unresponsiveness", European Journal of Human Genetics, AMSTERDAM, HOLLANDA, 5-5 Mayıs 2011, pp.477-477
Silan F., Uludağ A., Silan C., Özdemir Ö., Atik S., "Combine Effect Of Factor V Leiden, Mthfr And Angiotensin Converting Enzyme (Insertion/Deletion) Gene Mutations In Hypertensive Adult Individuals: A Population-Based Study From Sivas And Canakkale, Turkey", European Journal of Human Genetics, AMSTERDAM, HOLLANDA, 12-12 Mayıs 2011, pp.295-295
Silan F., Silan C., Uludağ A., Atik S., Özdemir Ö., "Gjb2 35delg And Mitochondrial A1555g Mutations And Etiology Of Deafness At The Gelibolu School For The Deaf In Turkey", European Human Genetics , AMSTERDAM, HOLLANDA, 28-31 Mayıs 2011, pp.285-285
Özdemir S., Silan F., Erselcan T., Uludağ A., Atik S., "Increased T Allele Frequency In Mthfr C677t Gene In Thyroid Carcinom", European Cytogenetic Conference, PORTO, PORTEKIZ, 2-5 Temmuz 2011, pp.166-166
KİTAP ve KİTAP BÖLÜMLERİ
Silan F., Özdemir Ö., "Kardiyovasküler Hastalıkların Genetiği", Tıbbi Genetik ve Klinik Uygulamaları, Munis Dündar, Ed., Erciyes Üniversitesi, 2016
Özdemir Ö., Silan F., "Biyoteknoloji esasları ve tıbbi genetikte yeni uygulama alanları", Tıbbi Genetik ve Klinik Uygulamaları, Munis Dündar, Ed., Erciyes Üniversitesi, 2016
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