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1 Long version search in PubMed, turkey genomics Master Author = Yigit, Serbulent Abstracts Association of MEFV gene mutations with rheumatoid factor levels in patients with rheumatoid arthritis. The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population. High Association of IL-4 Gene Intron 3 VNTR Polymorphism with Diabetic Peripheral Neuropathy. Association between interleukin 4 gene intron 3 VNTR polymorphism and recurrent aphthous stomatitis in a cohort of Turkish patients. Association of interleukin (IL)-4 gene intron 3 VNTR polymorphism with multiple sclerosis in Turkish population. IL-4 and MTHFR gene polymorphism in rheumatoid arthritis and their effects. Association of MTHFR gene C677T mutation with recurrent aphthous stomatitis and number of oral ulcers. Association between MEFV gene mutations and recurrent aphthous stomatitis in a cohort of Turkish patients. Association of MTHFR gene C677T mutation with diabetic peripheral neuropathy and diabetic retinopathy. Association of IL-4 gene VNTR variant with deep venous thrombosis in Behcet's disease and its effect on ocular involvement. Association of missense mutations of Mediterranean fever (MEFV) gene with multiple sclerosis in Turkish population. MTHFR gene C677T mutation and ACE gene I/D polymorphism in Turkish patients with osteoarthritis. DD genotype of ACE gene I/D polymorphism is associated with Behcet disease in a Turkish population. Association between fibromyalgia syndrome and polymorphism of the IL-4 gene in a Turkish population. Significance of MEFV gene R202Q polymorphism in Turkish familial Mediterranean fever patients. Association between sequence variations of the Mediterranean fever gene and fibromyalgia syndrome in a cohort of Turkish patients. Page of 44

2 Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and rheumatoid arthritis. Common Mediterranean fever (MEFV) gene mutations associated with ankylosing spondylitis in Turkish population. Significant association between insertion/deletion polymorphism of the angiotensin-convertig enzyme gene and ankylosing spondylitis. Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet's disease. 2 Gaziosmanpasa University, Faculty of Medicine, Department of Physical Medicine and Rehabilitation, Tokat, Turkey. ainanir@gmail.com Gaziosmanpasa University, Faculty of Medicine, Department of Dermatovenerology, Tokat, Turkey. Electronic address: goknurkalkan@yahoo.com. Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, 6000 Tokat, Turkey. yigit.serbulent@gmail.com Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. Department of Medical Biology, Faculty of Medicine, Gaziosmapasa University, Tokat, Turkey. serbulent.yigit@gmail.com Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. ainanir@gmail.com Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, 6000, Turkey. Electronic address: inanira@gmail.com. Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. inanira@gmail.com Faculty of Medicine, Department of Dermatology, Gaziosmanpasa University, 6000, Tokat, Turkey. Department of Dermatovenerology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. Faculty of Medicine, Department of Medical Biology, Ondokuz Mayis University, Samsun, Turkey. Page 2 of 44

3 Ondokuz Mayis University, Faculty of Medicine, Department of Medical Biology, Samsun, Turkey. Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Electronic address: Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Electronic address: Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Gaziosmanpasa University, Faculy of Medicine, Department of Medical Biology, Tokat, Turkey. Gaziosmanpasa University, School of Medicine, Department of Dermatology, Tokat, Turkey. Electronic address: Faculty of Medicine, Department of Emergency Medicine, Gaziosmanpasa University, 6000, Tokat, Turkey, 4 Karakus, Nevin 3 Inanir, Ahmet 8 Ates, Omer 7 Tural, Sengul 7 Kalkan, Goknur 3 Akkanet, Songul 3 Bas, Yalcin 3 Rustemoglu, Aydin 2 Pancar, Gunseli Sefika 2 Tekcan, Akin 2 Bozkurt, Nihan 2 Kaya, Suheyla Uzun 2 Inanir, Sema 2 Gul, Ulker Habiboglu, Abdulkadir Demir, Osman Page 3 of 44

4 Demir, Helin Deniz Cecen, Osman Basol, Nursah Balta, Ilknur Cevik, Betul Kisacik, Bunyamin Yildirim, Eren Kismali, Gorkem Kurt, Gulsum Semiha Kurt, Semiha Gulsum Okan, Sevil Ozturk, Sibel Demir Ozuguz, Pinar Pancar, Gunseli S Seckin, Havva Yildiz Takci, Zennure Tasliyurt, Turker Tekin, Saban Toprak, Huriye Kesici, Esra Page 4 of 44

5 Master Author 2 = Ustek, Duran Abstracts A novel TNFRSF gene mutation in a Turkish family: a report of three cases. Characterization of H3K9me3- and H4K20me3-associated circulating nucleosomal DNA by high-throughput sequencing in colorectal cancer. The relationship between coronary artery ectasia and enos intron 4a/b gene polymorphisms. Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: A case of mesial temporal lobe epilepsy with hippocampal sclerosis. Investigation of Arg399Gln and Arg94Trp polymorphisms of the XRCC (x-ray cross-complementing group ) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia. A novel partial sequence alignment tool for finding large deletions. A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology. Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993t>c mutation in the MT-ATP6 gene. Draft genome sequence of Halomonas smyrnensis AAD6T. Scientific and Technological Research Council of Turkey (TUBITAK), 4470 Kocaeli, Turkey. Medical Faculty, Deparment of Pediatrics, Division of Child Neurology, Kocaeli University, Kocaeli, Turkey. bulentkara@excite.com Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Kocaeli University, Umuttepe, Kocaeli, Turkey. fulcosan@gmail.com Department of Internal Medicine, Division of Medical Genetics, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey. Department of Genetics, Istanbul University, Institute for Experimental Medicine, Istanbul 34093, Turkey. dustek@istanbul.edu.tr Page 5 of 44

6 Department of Genetics, Institute for Experimental Medicine, Istanbul University, Istanbul, Turkey. Department of Cardiology, Siyami Ersek Cardiovascular and Thoracic Surgery Centre, Istanbul, Turkey. Department of Bioengineering, Marmara University, Istanbul, Turkey. Department of Basic Oncology, Istanbul University Oncology Institute, Capa, 34390, Istanbul, Turkey. 5 Cakiris, Aris 5 Abaci, Neslihan 3 Arikan, Muzaffer 2 Kursun, Olcay 2 Emrence, Zeliha 2 Azakli, Hulya 2 Cosan, Fulya Gul, Ahmet Gokyigit, Aysen Gezer, Ugur Eren, Mehmet Ekmekci, Ahmet Duman, Nilgun Dalay, Nejat Cefle, Ayse Gungor, Baris Cakar, Atilla Bilgic, Bilge Aydoseli, Aydin Aruk, Taner Arikan, Muzzaffer Arga, Kazim Yalcin Aras, Yavuz Aktan, Melih Cefle, Kivanc Oz, Dilaver Page 6 of 44

7 Yilmazer, Baris Yazici, Ayten Tosu, Rodi Toprak, Ercan Sogutcu, Elif Sirma, Sema Sencer, Altay Parlak, Mahmut Palanduz, Sukru Ozturk, Sukru Gulec, Cagri Ozbek, Ugur Gumus, Ergun Osmonov, Damirbek Oner, Ebru Toksoy Nalcaci, Meliha Mathew, Jaicy Maras, Hulya Leszinski, Gloria Kara, Bulent Holdenrieder, Stefan Gurses, Candan Yoruker, Ebru E Ozcan, Kazim Serhan Page 7 of 44

8 Master Author 3 = Ozdemir, Ozturk Abstracts Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers. Association Between ABCB (MDR) Gene Polymorphism and Unresponsiveness Combined Therapy in Chronic Hepatitis C virus. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations. Alterations in promoter methylation status of tumor suppressor HIC, SFRP2, and DAPK genes in prostate carcinomas. Increased T-allele frequency of 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene in differentiated thyroid carcinoma. The prevalence of VKORC 639 G>A and CYP2C9*2*3 genotypes in patients that requiring anticoagulant therapy in Turkish population. Department of Urology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey. Department of Pharmacology, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, 700, Turkey. csilan@yahoo.com Department of Nuclear Medicine, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey semozdemir@yahoo.com. Department of Nuclear Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey. semozdemir@yahoo.com Department of Medical Genetics, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey. ozdemir65@yahoo.com Department of Gastroenterology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey. 5 Ozdemir, Semra 4 Silan, Fatma Page 8 of 44

9 3 Uludag, Ahmet 3 Atik, Sinem 2 Koksal, Binnur Kilinc, Devran Aksulu, Hakki Engin Alagozlu, Hakan Asgun, Halil Fatih Atik, Sinem Yalcintepe Cetin, Ali Dogan, Omer Tamer Erselcan, Taner Gol, Mert Gultekin, Yener E Akdur, Secil Hasbek, Zekiye Yenicesu, Gonca Imir Korgali, Esat Kukulguven, Fatma Mutlu Ozen, Filiz Silan, Coskun Timucin, Meryem Turgut, Bulent Uslu, Atilla Gungor, Buket Page 9 of 44

10 Master Author 4 = Budak, Hikmet Abstracts Physical mapping integrated with syntenic analysis to characterize the gene space of the long arm of wheat chromosome A. Genomics Approaches for Crop Improvement against Abiotic Stress. Unique and Conserved MicroRNAs in Wheat Chromosome 5D Revealed by Next-Generation Sequencing. Functional features of a single chromosome arm in wheat (AL) determined from its structure. Subgenomic analysis of micrornas in polyploid wheat. Sorting the wheat from the chaff: identifying mirnas in genomic survey sequences of Triticum aestivum chromosome AL. Sabanci University, Biological Sciences and Bioengineering Program, Tuzla, Istanbul, Turkey. Faculty of Engineering and Natural Sciences, Sabanci University, Tuzla, Istanbul, Turkey. Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Tuzla, Istanbul, Turkey. Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Tuzla, Istanbul, Turkey. Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Istanbul, Turkey. Biological Sciences and Bioengineering Program, Sabanci University, Tuzla, Istanbul, Turkey. 6 Lucas, Stuart J 3 Kantar, Melda 3 Dolezel, Jaroslav 3 Akpinar, Bala Ani 2 Vautrin, Sonia 2 Simkova, Hana 2 Safar, Jan Page 0 of 44

11 2 Bellec, Arnaud 2 Berges, Helene 2 Cattonaro, Federica Aydinoglu, Fatma Frenkel, Zeev Hernandez, Pilar Korol, Abraham Weinstein, Zohar Kurtoglu, Kuaybe Yucebilgili Magni, Federica Valarik, Miroslav Jurman, Irena search in PubMed, turkey genomics Page of 44

12 Master Author 5 = Unver, Turgay Abstracts Genome-wide identification of alternate bearing-associated micrornas (mirnas) in olive (Olea europaea L.). Transcriptome-wide identification of R2R3-MYB transcription factors in barley with their boron responsive expression analysis. Isolation and expression analysis of cdnas that are associated with alternate bearing in Olea europaea L. cv. Ayvalik. Nutrition metabolism plays an important role in the alternate bearing of the olive tree (Olea europaea L.). Genome-wide identification of mirnas responsive to drought in peach (Prunus persica) by high-throughput deep sequencing. Fen Edebiyat Fakultesi, Biyoloji Bolumu, Balikesir Universitesi, Balikesir, Turkey. dundar@balikesir.edu.tr Faculty of Science, Department of Biology, Cankiri Karatekin University, Cankiri, Turkey. Faculty of Science, Department of Biology, Cankiri Karatekin University, 800, Cankiri, Turkey. Department of Biology, Faculty of Arts and Science, Fatih University, Buyukcekmece, Istanbul, Turkey. htombuloglu@fatih.edu.tr Cankiri Karatekin University, Faculty of Science, Department of Biology, Cankiri, Turkey ; Istanbul University, Faculty of Science, Department of Biology, Istanbul, Turkey. 3 Dundar, Ekrem 2 Hernandez, Pilar 2 Turktas, Mine 2 Dorado, Gabriel Celikkol Akcay, Ufuk Dagdelen, Ayhan Eldem, Vahap Erkilic, Emine Gulden Page 2 of 44

13 Bakir, Yakup Kekec, Guzin Yanik, Huriye Okay, Sezer Ozhuner, Esma Sakcali, Mehmet Serdal Suakar, Oznur Tombuloglu, Huseyin Uranbey, Serkan Inal, Behcet Page 3 of 44

14 Master Author 6 = Akar, Nejat Abstracts Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis. Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis. Prohemostatic and antithrombin activities of Ankaferd hemostat are linked to fibrinogen gamma chain and prothrombin by functional proteomic analyses. Intron F G79A polymorphism of the protein Z gene in Turkish Behcet patients. Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis. Proteomics Department, Central Laboratory of Ankara University Biotechnology Institute, Ankara, Turkey. ozel@medicine.ankara.edu.tr Department of Ophthalmology, Gaziosmanpasa University, Tokat, Turkey. helindeniz@hotmail.com BilGen Genetics and Biotechnology Center, Department of Molecular Biology and Genetics, Bilkent University, Ankara, Turkey. Ankara University Biotechnology Institute, Ankara, Turkey. ozel@medicine.ankara.edu.tr Ankara University Biotechnology Institute, Ankara, Turkey. 2 Peker, Selen 2 Demiralp, Duygu Ozel Karademir, Sedat Ayhan, Beycan Bagislar, Sevgi Bilen, Biter Bozkaya, Hakan Page 4 of 44

15 Cetin-Atalay, Rengul Demir, Helin Deniz Egin, Yonca Erdal, Esra Gursoy-Yuzugullu, Ozge Haznedaroglu, Ibrahim C Igci, Nasit Arslan-Ergul, Ayca Ilk, Ozlem Yuzugullu, Haluk Konu, Ozlen Mizrak, Dilsa Ozdag, Hilal Ozel-Demiralp, Duygu Ozen, Cigdem Ozturk, Aysenur Ozturk, Mehmet Ozturk, Nuri Sagol, Ozgul Turgut, Burhan Yalcindag, F Nilufer Yildiz, Gokhan Ilk, Hakki Gokhan Page 5 of 44

16 Master Author 7 = Berdeli, Afig Abstracts Determination of the effects of alcohol dehydrogenase (ADH) B and ADHC polymorphisms on alcohol dependence in Turkey. Gene polymorphism of complement factor H in a Turkish patient with membranoproliferative glomerulonephritis type II. Novel mutations and diverse clinical phenotypes in recombinaseactivating gene deficiency. SPP gene polymorphisms associated with nephrolithiasis in Turkish pediatric patients. [Familial Mediterranean fever with pulmonary manifestations alone; early diagnosis with genetic analysis]. Ege University School of Medicine, Department of Forensic Medicine, Izmir, Turkey. ekin.aktas@ege.edu.tr Department of Pediatrics, Faculty of Medicine, Ege University, 3500 Bornova, Izmir, Turkey. Department of Pediatric Nephrology, Ege University Faculty of Medicine, Bornova, Izmir, Turkey. betulsozeri@yahoo.com Department of Pediatric Nephrology, Celal Bayar University, Manisa, Turkey. Department of Chest Diseases, Faculty of Medicine, Sifa University, Izmir, Turkey. fidanyildiz@yahoo.com Kutukculer, Necil Aktas, Ekin Ozgur Aydin, Hikmet Hakan Celik, Handan Ak Coskunol, Hakan Dincel, Nida Ertan, Pelin Gulez, Nesrin Horasan, Gonul Page 6 of 44

17 Aksu, Guzide Kocak, Aytac Yalcin, Murat Mir, Sevgi Sanal, Salahattin Sarsik, Banu Senol, Ender Sever, Fidan Sever, Mustafa Sozeri, Betul Tekin, Gokhan Karaca, Neslihan Edeer Page 7 of 44

18 Master Author 8 = Sogut, Erkan Abstracts Protective effect of paraoxonase gene variant L55M in retinal vein occlusion. Association of MMP2-306C/T and TIMP2G-48C polymorphisms in retinal vein occlusion. Predictive value of the vitamin K epoxide reductase complex subunit G-639A and C73T single nucleotide polymorphisms in retinal vein occlusion. Manganese-superoxide dismutase and glutathione peroxidase polymorphisms in recurrent tonsillitis and tonsillar hypertrophy. Gaziosmanpasa University Faculty of Medicine, Department of Ophthalmology, Tokat, Turkey. huseyin.ortak@hotmail.com Gaziosmanpasa University Faculty of Medicine, Department of Ophthalmology, Tokat, Turkey. Electronic address: huseyin.ortak@hotmail.com. Department of Otorhinolaryngology, Gaziosmanpasa University, School of Medicine, Tokat, Turkey. gurbuzler@yahoo.com Department of Ophthalmology, Gaziosmanpasa University, Faculty of Medicine, Tokat, Turkey. huseyin.ortak@hotmail.com 3 Ortak, Huseyin 3 Benli, Ismail 2 Demir, Selim 2 Ates, Omer Aksakal, Ceyhun Alim, Sait Ardagil, Aylin Demir, Helin Akbas, Ali Eyibilen, Ahmet Yelken, Kursat Page 8 of 44

19 Gurbuzler, Levent Koc, Sema Ozyurt, Huseyin Sahin, Semsettin Senkal, Hilmi A Erkorkmaz, Unal Page 9 of 44

20 Master Author 9 = Agar, Guleray Abstracts Determination of protective role of selenium against aflatoxin B- induced DNA damage. Determination of the genotoxic effects of Convolvulus arvensis extracts on corn (Zea mays L.) seeds. Molecular determination of genotoxic effects of cobalt and nickel on maize (Zea mays L.) by RAPD and protein analyses. Determination of genetic diversity of Vitis vinifera cv. Kabarcik populations from the Coruh Valley using SSR markers. 2 Department of Biology, Ataturk University, Erzurum, Turkey. Faculty of Science, Department of Biology, Ataturk University, Erzurum, Turkey. Department of Biology, Ataturk University, Turkey. 3 Yildirim, Nalan 2 Erturk, Filiz Aygun Yuksel, Canan Sunar, Serap Nardemir, Gokce Ergul, Ali Ercisli, Sezai Bozari, Sedat Ay, Hilal Alpsoy, Lokman Aksakal, Ozkan Page 20 of 44

21 Master Author 0 = Oztuzcu, Serdar Abstracts Role of rho-kinase gene polymorphisms and protein expressions in colorectal cancer development. Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory Distress syndrome. Association between Rho-kinase (ROCK2) gene polymorphisms and Behcet's disease. Mutational screening of the SOCS3 gene promoter in metastatic colorectal cancer patients. Faculty of Medicine, Division of Neonatology, Department of Pediatrics, University of Gaziantep, Gaziantep, Turkey. Department of Pathology, Faculty of Medicine, University of Gaziantep, Gaziantep, Turkey. isari@gantep.edu.tr Department of Medical Pharmacology, University of Gaziantep, Gaziantep, Turkey. Department of Medical Biology, Gaziantep University, Gaziantep, Turkey. mehriigci@gantep.edu.tr 3 Ozkara, Esma 3 Camci, Celaletdin 2 Demiryurek, Abdullah T 2 Arslan, Ahmet Bayram, Ali Berberoglu, Betul Cakmak, Ecir Ali Cengiz, Beyhan Coskun, M Yavuz Demircubuk, Ayse G Demiryurek, A Tuncay Alasehirli, Belgin Dokuyucu, Recep Page 2 of 44

22 Taviloglu, Z Safak Gogebakan, Bulent Igci, Mehri Igci, Yusuf Ziya Kisacik, Bunyamin Oguz, Elif Onat, Ahmet Mesut Pehlivan, Yavuz Sari, Ibrahim Sivasli, Ercan Demiryurek, Seniz Page 22 of 44

23 Master Author = Ozkinay, Ferda Abstracts Genotyping of beta-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders. A novel KIF mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family. Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish children. Analysis of the beta-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele. Division of Pediatric Infectious Diseases, Dr. Behcet Uz Child Diseases and Pediatric Surgery Training and Research Hospital, Izmir, Turkey. Department of Medical Genetics, Ege University, Faculty of Medicine, Bornova, Izmir, Turkey. burak.durmaz@ege.edu.tr Department of Medical Genetics, Ege University Faculty of Medicine, Bornova-Izmir, Turkey. karacaemin@gmail.com Department of Medical Genetics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey. filizhazan@hotmail.com 3 Onay, Huseyin 2 Karaca, Emin Aydinok, Yesim Aykut, Ayca Bayram, Nuri Coker, Mahmut Durmaz, Burak Hazan, Filiz Jeffery, Steve Kalkan, Sema Page 23 of 44

24 Atlihan, Fusun Kantekin, Esin Yilmaz-Ciftdogan, Dilek Ostergaard, Pia Ozturk, Taylan Tavmergen, Erol Traeger-Synodinos, Jan Tufan, Senem Vardar, Fadil Vrettou, Christina Kanavakis, Emmanuel Page 24 of 44

25 Master Author 2 = Cetin, Zafer Abstracts Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 4q3.q3.3 regions in a patient with azoospermia. A 5q2.-5q2.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement. Mixed gonadal dysgenesis in a patient with de novo tas(y;9)(p.3;q3.4) and 45,X mosaicism. A patient with Down syndrome with a de novo derivative chromosome 2. 3 Department of Medical Biology and Genetics, Faculty of Medicine, Akdeniz University, Antalya, Turkey. Department of Medical Biology, Faculty of Medicine, Akdeniz University, Antalya, Turkey. 4 Luleci, Guven 3 Yakut, Sezin 3 Berker, Sibel 2 Mihci, Ercan 2 Clark, Ozden Altiok Usta, Mustafa Faruk Parlak, Mesut Manguoglu, Ayse Esra Keser, Ibrahim Karaguzel, Gungor Bircan, Iffet Berker-Karauzum, Sibel Altiok Clark, Ozden Page 25 of 44

26 Master Author 3 = Tukun, Ajlan Abstracts A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type. Disruption of HDX gene in premature ovarian failure. Relationship between antimetabolite toxicity and pharmacogenetics in Turkish cancer patients. Hypochondroplasia in a child with 620C>G (Asn540Lys) mutation in FGFR3. Ondokuz Mayis University, Faculty of Medicine, Department of Medical Biology, Samsun, Turkey. Dr. Behcet Uz Children Disease and Surgery Training and Research Hospital, Department of Pediatric Endocrinology, Izmir, Turkey. drkorkmazanil@hotmail.com Dept of Medical Oncology, School of Medicine, Ankara University, Ankara, Turkey. mutludogan@yahoo.com Department of Medical Genetics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey. filizhazan@hotmail.com 2 Hazan, Filiz Kocak, Idris Akbulut, Hakan Demirkazik, Ahmet Dincol, Dilek Dizdarer, Ceyhun Dogan, Mutlu Gunes, Sezgin Adibelli, Hamit Karabulut, Halil G Yalcin, Bulent Korkmaz, Huseyin Anil Page 26 of 44

27 Okten, Gulsen Onat, Onur Emre Ozcelik, Tayfun Ozturk, A Taylan Unal, Nurettin Utkan, Gungor Icli, Fikri Page 27 of 44

28 Master Author 4 = Kayserili, Hulya Abstracts Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome. A large duplication involving the IHH locus mimics acrocallosal syndrome. A novel c.255g>t (p.d49y) mutation in SH3BP2 gene causes cherubism in a Turkish family. 2 Department of Medical Genetics, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey. Department of Medical Biology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey. ersankalay@hotmail.com Li, Yun Akarsu, Nurten A Aktoren, Oya Apak, Selcuk Aslan, Yakup Bogershausen, Nina Cansu, Aysegul Chellappa, Vasant Dinckan, Nuriye Grzeschik, Karl-Heinz Gulgoren, Ayan Guven, Yeliz Kalay, Ersan Abdalla, Ebtesam Mohammed Kreiger, Elmar Yuksel-Apak, Memnune Milz, Esther Page 28 of 44

29 Morsy, Heba Mutlu, Mehmet Nurnberg, Gudrun Nurnberg, Peter Pawlik, Barbara Pillai, Shiv Sezgin, Orhan Toraman, Bayram Uyguner, Oya Uyguner, Oya Zehra Wollnik, Bernd Karaman, Birsen Page 29 of 44

30 Master Author 5 = Cakmakoglu, Bedia Abstracts G-->C and -95 A-->G promoter variants of the cyclooxygenase- 2 gene decrease the risk for preeclampsia. Association of the CC chemokine receptor 5 (CCR5) polymorphisms with preeclampsia in Turkish women. Association of polymorphisms in MCP-, CCR2, and CCR5 genes with the risk and clinicopathological characteristics of prostate cancer. Department of Biochemistry, Istanbul University, Istanbul, Turkey. figur@istanbul.edu.tr Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey. figur@istanbul.edu.tr Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey. 2 Isbilen, Elif 2 Gurdol, Figen Yurdum, Leman M Seckin, Sule Sanli, Oner Ozturk, Ummuhan Kucukgergin, Canan Isman, Ferruh K Isbir, Turgay Dasdemir, Selcuk Bekpinar, Seldag Page 30 of 44

31 Master Author 6 = Tekin, Mustafa Abstracts A novel COL4A3 mutation causes autosomal-recessive Alport syndrome in a large Turkish family. ATP6VB mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families. Autosomal recessive nonsyndromic deafness genes: a review. Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, Dikimevi, Ankara, Turkey. Department of Medical Genetics, Erciyes University School of Medicine, Kayseri, Turkey. Department of Medical Genetics, Erciyes University School of Medicine, Kayseri, Turkey. Yalcinkaya, Fatos Uzak, Asli Subasioglu Tokgoz, Bulent Subasioglu Uzak, Asli Dundar, Munis Duman, Duygu Comak, Elif Cakar, Nilgun Page 3 of 44

32 Master Author 7 = Ozturk, Ozlem Abstracts Goruroglu HLA class-ii allele frequencies in Turkish breast cancer patients. Diversity of killer cell immunoglobulin-like receptor genes in Southern Turkey. Evaluation of KIR genes in recurrent miscarriage. Faculty of Medicine, Department of Clinical Biochemistry, Cukurova University, Adana, Turkey. ozlem_goruroglu@yahoo.com Department of Clinical Biochemistry, Faculty of Medicine, Cukurova Universitesi, Tip Fakultesi, Tibbi Biyokimya AD, 0330 Adana, Turkey. ozlem_goruroglu@yahoo.com Birecik State Hospital, Sanliurfa, Turkey. 2 Polat, Gurbuz Sahin, Gulhan Polat, Ayse Kucukgoz, Umran Karacor, Esin Damla Ziyanoglu Gun, Faik Deniz Atik, Ugur Page 32 of 44

33 Master Author 8 = Bozdayi, A Mithat Abstracts Clonal analysis of the quasispecies of antiviral-resistant HBV genomes in patients with entecavir resistance during rescue treatment and successful treatment of entecavir resistance with tenofovir. Potential proteomic biomarkers in assessing liver fibrosis using SELDI- TOF MS. Molecular characterization of hepatitis A virus isolated from acute infections in Turkey. Ankara University, School of Medicine Institute of Hepatology, Ankara, Turkey. mithat.bozdayi@medicine.ankara.edu.tr Ankara University, Institute of Hepatology, Ankara, Turkey. Ankara University, Institute of Hepatology, Ankara University, Cebeci Hospital, Dikimevi Ankara, Turkey Phone: * Fax: bozdayi@medicine.ankara.edu.tr. 2 Karatayli, Ersin 2 Karatayli, Senem Ceren 2 Yurdaydin, Cihan 2 Idilman, Ramazan Alagoz, S Gokce Berk, Elife Berktas, Mustafa Bozdayi, Gulendam Celik, Inci Cevik, Emrah Cinar, Kubilay Dinc, Bedia Erden, Esra Akguc, Miray Page 33 of 44

34 Karatayli, Senem C Koyuncu, Duygu Mizrak, Dilsa Ozkan, Muhip Parlak, Mehmet Savas, Berna Sayki, Muyesser Sertoz, Ruchan Seven, Gulseren Yakut, Mustafa Kabacam, Gokhan Page 34 of 44

35 Master Author 9 = Sunguroglu, Asuman Abstracts Effect of lomeguatrib-temozolomide combination on MGMT promoter methylation and expression in primary glioblastoma tumor cells. Variations in glutathione-s-transferase genes influence risk of chronic myeloid leukemia. The effect of CYPA, GSTT and GSTM polymorphisms on the risk of lung cancer: a case-control study. Department of Thoracic Surgery, Kirikkale University, Kirikkale, Turkey. Department of Medical Biology, School of Medicine, Ankara University, Ankara, Turkey. nurozten@uic.edu Department of Medical Biology, Ankara University School of Medicine, Ankara, Turkey. mtaspinartr@gmail.com 2 Taspinar, Mehmet 2 Oztuna, Derya Ozten, Nur Bosland, Maarten C Canpinar, Hande Castresana, Javier S Ilgaz, Seda Oz, Gurhan Atinkaya, Cansel Ozkan, Tulin Yazici, Ulku Rey, Juan A Sakiragaoglu, Onur Tastepe, Irfan Ugur, Hasan Caglar Ozdemir, Mevci Page 35 of 44

36 Master Author 20 = Eroz, R Abstracts Is there any relationship between decreased AgNOR protein synthesis and human hair loss? Does higher NORs expression affect the developmental stages of Down syndrome infants? EEC syndrome with a de novo mutation (c.953g > a) on exon 7 of P63 gene: a case report. Duzce University Medical Faculty, Department of Pediatrics, Duzce, Turkey. okurmesut@yahoo.com Duzce University Medical Faculty, Department of Medical Genetics, Duzce, Turkey. Department of Medical Genetics, Duzce University Medical School, Duzce, Turkey. receperoz@duzce.edu.tr 2 Okur, M Ulgen, E Tasdemir, S Senses, D A Ozkan, A Ozcelik, D Mundlos, S Ismailler, Z B Gunes, C Dogan, H Berik, O Page 36 of 44

37 Master Author 2 = Bilaloglu, Rahmi Abstracts Radioprotection by two phenolic compounds: chlorogenic and quinic acid, on X-ray induced DNA damage in human blood lymphocytes in vitro. Influence of naringin on cadmium-induced genomic damage in human lymphocytes in vitro. Genotoxic and anti-genotoxic effects of vanillic acid against mitomycin C-induced genomic damage in human lymphocytes in vitro. Uludag University, Faculty of Arts and Sciences, Department of Biology, Cell Culture and Genetic Toxicology Laboratory, Bursa, Turkey. aydemirn@uludag.edu.tr Department of Biology, Uludag University Faculty of Science and Arts, Gorukle, Bursa, Turkey. Department of Biology, Faculty of Science and Arts, Cell Culture and Genetic Toxicology Laboratory, Bursa, Turkey. 3 Yilmaz, Dilek 3 Vatan, Ozgur 2 Cinkilic, Nilufer Zorlu, Tolga Tuzun, Ece Tunc, Sema Ozkan, Lutfi Erdem, Merve Guler Cetintas, Sibel Kahraman Cavas, Tolga Bagdas, Deniz Aydemir, Nilufer Cinkilic Page 37 of 44