Çukurova Üniversitesi
Akademik Veri Yönetim Sistemi
Yayınlar & Eserler
SCI,SSCI,AHCI İNDEKSLERİNE GİREN DERGİLERDE YAYINLANAN MAKALELER
Tunc E., Demirhan O., Sağlıker Y., Yıldız İ., Paylar N., Guzel A.I., "Chromosomal findings and sequence analysis of target exons of calcium-sensing receptor (CaSR) gene in patients with Sagliker syndrome", TURKİSH JOURNAL OF MEDİCAL SCİENCES, vol.47, pp.13-21, 2017
Demirhan O., Yilmaz M.B., Tanriverdi N., Kocaturk-Sel S., Erkoc M.A., Öksüz H., "Identification of the Short Arm of the Y Chromosome by Cytogenetic and Molecular Analyses", CYTOLOGY AND GENETİCS, vol.51, pp.60-64, 2017
Tunç E., Tanriverdi N., Demirhan O., Süleymanova D., Çetinel N., "Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions.", REPRODUCTIVE BIOMEDICINE ONLINE, vol.32, pp.414-419, 2016
Boğa Pekmezekmek A., Emre M., Sertdemir Y., Uncu İ., Binokay U.S., Demirhan O., "Effects of GSM-like radiofrequency irradiation during the oogenesis and spermiogenesis of Xenopus laevis", ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, vol.129, pp.137-144, 2016
Demirhan O., Tanriverdi N., Yilmaz M.B., Kocatürk Sel S. , Inandiklioglu N., Lüleyap H.Ü., et al., "Report of a new case with pentasomy X and novel clinical findings.", BALKAN JOURNAL OF MEDICAL GENETICS, vol.18, pp.85-92, 2015
Korkmaz D.T., Demirhan O., Abat D., Demirberk B., Tunc E., Kuleci S., "Microchimeric Cells, Sex Chromosome Aneuploidies and Cancer", PATHOLOGY & ONCOLOGY RESEARCH, vol.21, pp.1157-1165, 2015
Boğa Pekmezekmek A., Emre M., Sertdemir Y., Akillioğlu K., Binokay U.S., Demirhan O., "The effect of 900 and 1800 MHz GSM-like radiofrequency irradiation and nicotine sulfate administration on the embryonic development of Xenopus laevis", ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, vol.113, pp.378-390, 2015
Demirhan O., Sagliker Y., Akbal E., Paylar N., Sagliker H.S., Ozkaynak P.S., et al., "WHOLE 13 EXONS OF GNAS1 GENE IN SAGLIKER SYNDROME(SS). COMBINATION-COMPULSION OF BONE DYSPLASIAS-HEREDITARY OSTEODISTROPHIES(BD), CHRONIC KIDNEY DISEASES (CKD) AND SECONDARY HYPERPARATHYROIDISM(SH)", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.30, 2015
Demirhan O., "Gene mutations in chronic kidney disease patients with secondary hyperparathyroidism and Sagliker syndrome.", JOURNAL OF RENAL NUTRITION, vol.25, pp.176-186, 2015 (Link)
Demirhan O., Arslan A., Sagliker Y., Akbal E., Ergun S., Bayraktar R., et al., "NOVEL STRIKING MISMUTATIONS ON GNAS1, FGF23 AND FGFR3 GENES IN CKD WITH SECONDARY HYPERPARATHYROIDISM (SH) AND SAGLIKER SYNDROME (SS). SS IS ACOMBINATION-COMPULSION OF BONE DISPLASIAS-HEREDITARY OSTEODYSTROPHIES AND CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.30, 2015
Demirhan O., Tanriverdi N., Tunc E., Inandikioglu N., Suleymanova D., "Frequency and Types of Chromosomal Abnormalities in Turkish Women with Amenorrhea", JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY, vol.27, pp.274-277, 2014 (Link)
Abat D., Demirhan O., Inandiklioglu N., Tunc E., Erdoğan Ş., Tastemir D., et al., "Genetic alterations of chromosomes, p53 and p16 genes in low- and high-grade bladder cancer", ONCOLOGY LETTERS, vol.8, pp.25-32, 2014
Demirhan O., "Ckd Bone Disease", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.3, pp.394-405, 2014 (Link)
Inandiklioglu N., Demirhan O., Bayram I., Kasap M., Yilmaz S., Tanyeli A., "THE INVESTIGATION OF VEGF-A, MMP-2, MMP-9, TIMP-1, TIMP-2 GENES EXPRESSION ALTERATIONS AND METHYLATION LEVELS IN CHILDREN WITH ACUTE LYMPHOBLASTIC LEUKEMIA", LEUKEMIA RESEARCH, vol.38, pp.S42-S42, 2014
Dur O., Anarat A., Demirhan O., Inandiklioglu N., Bayazit A.K., "The Role Of Glucorticoid Receptor Gene (nr3c1 Gene) Polymorphism On Relapsing Of Idiopathic Nephrotic Syndrome In Children.", PEDIATRIC NEPHROLOGY, vol.29, pp.1730-1731, 2014
Sagliker Y., Demirhan O., Yildiz İ., Paylar N., Inandiklioglu N., Akbal E., et al., "THE WHOLE 13 EXONS OF GNAS1 GENE AND THE GENES FOR HEREDITARY OSTEODISTROPHIAS(HO) IN SAGLIKER SYNDROME(SS). COMBINATION-COMPULSION OF HEREDITARY OSTEODISTROPHIAS AND CHRONIC KIDNEY DISEASES (CKD) ?", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.29, pp.381-381, 2014
Tastemir-Korkmaz D., Demirhan O., Kuleci S., Hasturk S., "There is no Significant Association Between Death Receptor 4 (DR4) Gene Polymorphisms and Lung Cancer in Turkish Population", PATHOLOGY & ONCOLOGY RESEARCH, vol.19, pp.779-784, 2013
Dağlioğlu N., Akcan R., Efeoğlu P., Inandiklioglu N., Gülmen M.K., Demirhan O., "Polychlorinated biphenyls and organochlorine pesticides in amniotic fluids of pregnant women in south-central Turkey", TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY, vol.95, pp.954-961, 2013
Hakverdi S., Demirhan O., Tunc E., Inandiklioglu N., Uslu İ.N., Gungoren A., et al., "Chromosome Imbalances and Alterations in the p53 Gene in Uterine Myomas from the Same Family Members: Familial Leiomyomatosis in Turkey", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.14, pp.651-658, 2013
Tarkan Ö., Sari P., Demirhan O., Kiroğlu M.M., Tuncer Ü., Sürmelioğlu Ö., et al.,"Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey", JOURNAL OF LARYNGOLOGY AND OTOLOGY, vol.127, pp.33-37, 2013
Demirhan O., Çekin N., Tastemir D., Tunc E., Guzel A.I., Meral D., et al., "Are there fetal stem cells in the maternal brain?", NEURAL REGENERATION RESEARCH, vol.8, pp.593-598, 2013
Pazarbasi A., Demirhan O., Alptekin D., Ozgunen F.T., Ozpak L., Yilmaz M.B., et al., "INHERITANCE OF A CHROMOSOME 3 AND 21 TRANSLOCATION IN THE FETUSES, WITH ONE ALSO HAVING TRISOMY 21, IN THREE PREGNANCIES IN ONE FAMILY", BALKAN JOURNAL OF MEDICAL GENETICS, vol.16, pp.91-96, 2013
Guzel A., Yilmaz M.B., Demirhan O., Pazarbasi A., Kocaturk-Sel S., Erkoc M.A., et al., "RAPID DETECTION OF FETAL ANEUPLOIDIES BY QUANTITATIVE FLUORESCENT-POLYMERASE CHAIN REACTION FOR PRENATAL DIAGNOSIS IN THE TURKISH POPULATION", BALKAN JOURNAL OF MEDICAL GENETICS, vol.15, pp.11-17, 2012
Yildiz I., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Tasdemir D., et al.,"STRIKING AND PROMISING MIS-SENSE MUTATIONS ON THE GNAS1 GENE EXONS' 1,4,10 AND 4 IN SAGLIKER SYNDROME (SS). A UNIQUE CATASTROPHIC ENTITY. CYTOGENETIC STUDIES FOR CHROMOSOMAL ABNORMALITIES, CASR GENES AND GNAS 1 MUTATIONS. INTERNATIONAL EVALUATION OF UNRECOGNIZABLY UGLYFYING HUMAN FACES IN LATE AND SEVERE SH IN CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.27, pp.157-158, 2012
Inandiklioglu N., Yilmaz S., Demirhan O., Erdoğan Ş., Tanyeli A., "Chromosome Imbalances and Alterations of AURKA and MYCN Genes in Children with Neuroblastoma", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.13, pp.5391-5397, 2012
Hanta , Tastemir-Korkmaz D., Demirhan O., Hanta D., Kuleci S., Seydaoglu G., "Association of the Nramp1 gene polymorphisms and clinical forms in patients with tuberculosis", BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY, vol.113, pp.657-660, 2012
Yildiz I., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Tasdemir D., et al., "STRIKING AND PROMISING MIS-SENSE MUTATIONS ON THE GNAS1 GENE EXONS' 1,4,10 AND 4 IN SAGLIKER SYNDROME (SS). A UNIQUE CATASTROPHIC ENTITY. CYTOGENETIC STUDIES FOR CHROMOSOMAL ABNORMALITIES, CASR GENES AND GNAS 1 MUTATIONS. INTERNATIONAL EVALUATION OF UNRECOGNIZABLY UGLYFYING HUMAN FACES IN LATE AND SEVERE SH IN CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.27, pp.157-158, 2012
Yildiz I., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Tasdemir D., et al.,"STRIKING AND PROMISING MIS-SENSE MUTATIONS ON THE GNAS1 GENE EXONS' 1,4,10 AND 4 IN SAGLIKER SYNDROME (SS). A UNIQUE CATASTROPHIC ENTITY. CYTOGENETIC STUDIES FOR CHROMOSOMAL ABNORMALITIES, CASR GENES AND GNAS 1 MUTATIONS. INTERNATIONAL EVALUATION OF UNRECOGNIZABLY UGLYFYING HUMAN FACES IN LATE AND SEVERE SH IN CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.27, pp.157-158, 2012
Yildiz I., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Tasdemir D., et al.,"STRIKING AND PROMISING MIS-SENSE MUTATIONS ON THE GNAS1 GENE EXONS' 1,4,10 AND 4 IN SAGLIKER SYNDROME (SS). A UNIQUE CATASTROPHIC ENTITY. CYTOGENETIC STUDIES FOR CHROMOSOMAL ABNORMALITIES, CASR GENES AND GNAS 1 MUTATIONS. INTERNATIONAL EVALUATION OF UNRECOGNIZABLY UGLYFYING HUMAN FACES IN LATE AND SEVERE SH IN CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.27, pp.157-158, 2012
Yildiz İ., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Taşdemir D., et al.,"International Evaluation of Unrecognizably Uglifying Human Faces in Late and Severe Secondary Hyperparathyroidism in Chronic Kidney Disease. Sagliker Syndrome. A Unique Catastrophic Entity, Cytogenetic Studies for Chromosomal Abnormalities, Calcium-Sensing Receptor Gene and GNAS1 Mutations. Striking and Promising Missense Mutations on the GNAS1 Gene Exons 1, 4, 10, 4", JOURNAL OF RENAL NUTRITION, vol.22, pp.157-161, 2012
Yildiz İ., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Taşdemir D., et al., "International Evaluation of Unrecognizably Uglifying Human Faces in Late and Severe Secondary Hyperparathyroidism in Chronic Kidney Disease. Sagliker Syndrome. A Unique Catastrophic Entity, Cytogenetic Studies for Chromosomal Abnormalities, Calcium-Sensing Receptor Gene and GNAS1 Mutations. Striking and Promising Missense Mutations on the GNAS1 Gene Exons 1, 4, 10, 4", JOURNAL OF RENAL NUTRITION, vol.22, pp.157-161, 2012
Yildiz I., Sagliker Y., Demirhan O., Tunc E., Inandiklioglu N., Tasdemir D., et al.,"STRIKING AND PROMISING MIS-SENSE MUTATIONS ON THE GNAS1 GENE EXONS' 1,4,10 AND 4 IN SAGLIKER SYNDROME (SS). A UNIQUE CATASTROPHIC ENTITY. CYTOGENETIC STUDIES FOR CHROMOSOMAL ABNORMALITIES, CASR GENES AND GNAS 1 MUTATIONS. INTERNATIONAL EVALUATION OF UNRECOGNIZABLY UGLYFYING HUMAN FACES IN LATE AND SEVERE SH IN CKD", NEPHROLOGY DIALYSIS TRANSPLANTATION, vol.27, pp.157-158, 2012
Demirhan O., Pazarbaşi A., Guzel A.I., Tastemir D., Yilmaz B., Kasap M., et al.,"The Reliability of Maternal Serum Triple Test in Prenatal Diagnosis of Fetal Chromosomal Abnormalities of Pregnant Turkish Women", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.15, pp.701-707, 2011 (Link)
Yilmaz M.B., Pazarbasi A., Guzel A.I., Kocaturk-Sel S., Kasap H., Kasap M., et al., "Association of serum sex steroid levels and bone mineral density with CYP17 and CYP19 gene polymorphisms in postmenopausal women in Turkey", GENETICS AND MOLECULAR RESEARCH, vol.10, pp.1999-2008, 2011
Izmirli M., Inandiklioglu N., Abat D., Alptekin D., Demirhan O., Tansug Z., et al., "MTHFR Gene Polymorphisms in Bladder Cancer in the Turkish Population", ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, vol.12, pp.1833-1835, 2011
Demirhan O., Demir C., Tunc E., Inandiklioglu N., Sutcu E., Sadikoglu N., et al., "The genotoxic effect of nicotine on chromosomes of human fetal cells: The first report described as an important study", INHALATION TOXICOLOGY, vol.23, pp.829-834, 2011
Demirhan O., Ozgunen F.T., Tastemir D., "CLINICAL MANIFESTATIONS OF PARTIAL TRISOMY 4p", BALKAN JOURNAL OF MEDICAL GENETICS, vol.13, pp.61-63, 2010
Cetiner S., Demirhan O., Inal T.C., Tastemir D., Sertdemir Y., "Analysis of peripheral blood T-cell subsets, natural killer cells and serum levels of cytokines in children with Down syndrome", INTERNATIONAL JOURNAL OF IMMUNOGENETICS, vol.37, pp.233-237, 2010
Demirhan O., Tastemir D., Hastuerk S., Kuleci S., Hanta İ., "Alterations in p16 and p53 genes and chromosomal findings in patients with lung cancer: Fluorescence in situ hybridization and cytogenetic studies", CANCER EPIDEMIOLOGY, vol.34, pp.472-477, 2010
Demirhan O., Pazarbasi A., Tanriverdi N., Aridogan A., Karahan D., "THE CLINICAL EFFECTS OF ISOCHROMOSOME Xq IN KLINEFELTER SYNDROME: REPORT OF A CASE AND REVIEW OF LITERATURE", GENETIC COUNSELING, vol.20, pp.235-242, 2009
Demirhan O., Tastemir D., Sertdemir Y., "The Expression of Folate Sensitive Fragile Sites in Patients with Bipolar Disorder", YONSEI MEDICAL JOURNAL, vol.50, pp.137-141, 2009
Guzel A.I., Demirhan O., Pazarbaşi A., Ozgunen F.T., Kocaturk-Sel S., Tastemir D., "Detection of Parental Origin and Cell Stage Errors of a Double Nondisjunction in a Fetus by QF-PCR", GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.13, pp.73-77, 2009 (Link)
Demirhan O., Pazarbasi A., Tunc E., Karahan D., Tanriverdi N., Avci A., et al., "THE EFFECT OF A DE NOVO PERICENTRIC INVERSION (10)(p11.1;q22.1) ON AGGRESSIVE BEHAVIOR AND HYPERACTIVITY", GENETIC COUNSELING, vol.20, pp.69-71, 2009
Guzel A., Demirhan O., Pazarbasi A., Yuksel B., "PARENTAL ORIGIN AND CELL STAGE ERRORS IN X-CHROMOSOME POLYSOMY 49,XXXXY", BALKAN JOURNAL OF MEDICAL GENETICS, vol.12, pp.45-50, 2009
Demirhan O., Pazarbaşi A., Suleymanova-Karahan D., Tanriverdi N., Kilinç Y., "Correlation of clinical phenotype with a pericentric inversion of chromosome 9 and genetic counseling", SAUDI MEDICAL JOURNAL, vol.29, pp.946-951, 2008 (Link)
Pazarbasi A., Demirhan O., Sleymanova-Karahan D., Tastemir D., Tunc E., Guemuerduelue D., "PRENATAL DIAGNOSIS OF TRANSLOCATION 13;13 PATAU SYNDROME: CLINICAL FEATURES OF TWO CASES", BALKAN JOURNAL OF MEDICAL GENETICS, vol.11, pp.69-73, 2008
Tuerkmen S., Hoffmann K., Demirhan O., Aruoba D., Humphrey N., Mundlos S., "Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene", EUROPEAN JOURNAL OF HUMAN GENETICS, vol.16, pp.1070-1074, 2008
Demirhan O., Tunali N., Erdoğan Ş., Tastemir D., Tunc E., "Different segregation of chromosomes 5 and 7 in two generations and related phenotypic findings", TURKISH JOURNAL OF MEDICAL SCIENCES, vol.38, pp.287-292, 2008
Demirhan O., Tastemir D., "Cytogenetic effects of ethanol on chronic alcohol users", ALCOHOL AND ALCOHOLISM, vol.43, pp.127-136, 2008
Pazarbasi A., Demirhan O., Turgut M., Guzel I., Tastemir D., "INHERITANCE OF A TRANSLOCATION BETWEEN CHROMOSOMES 12 AND 16 IN A FAMILY WITH RECURRENT MISCARRIAGES AND A NEWBORN WITH DOWN SYNDROME CARRYING THE SAME TRANSLOCATION", GENETIC COUNSELING, vol.19, pp.301-308, 2008
Yilmaz M., Demirhan O., Kucukosmanoglu E., Pehlivan M., Okan V., Balat O., et al., "Pregnancy in patients with chronic myeloid leukemia treated with imatinib", LEUKEMIA, vol.48, pp.2454-2456, 2007
Pazarbasi A., Kasap M., Demirhan O., Vardar M.A., Suleymanova-Karahan D., Doran F., "Chromosomal abnormalities in endometrial and ovarian carcinomas", BALKAN JOURNAL OF MEDICAL GENETICS, vol.10, pp.61-69, 2007
Tunc E., Demirhan O., Demir C., Tastemir D., "Cytogenetic study of recurrent miscarriages and their parents", RUSSIAN JOURNAL OF GENETICS, vol.43, pp.437-443, 2007
Demirhan O., Tastemir D., Narli N., Soyupak S., Ozcan K., "Chromosome and p63 gene analysis of an infant with ectrodactyly-split hand and foot malformation", TURKISH JOURNAL OF MEDICAL SCIENCES, vol.37, pp.167-171, 2007
Demirhan O., Tastemir D., Özpoyraz N., "Chromosomal variations in patients with bipolar affective disorder", KOREAN JOURNAL OF GENETICS, vol.29, pp.43-49, 2007
Tastemir D., Demirhan O., Sertdemir Y., "Chromosomal fragile site expression in Turkish psychiatric patients", PSYCHIATRY RESEARCH, vol.144, pp.197-203, 2006
Demirhan O., Taşdemir D., Sertdemir Y., "Chromosomal fragile sites in schizophrenic patients", RUSSIAN JOURNAL OF GENETICS, vol.42, pp.810-817, 2006
Demirhan O., Tastemir D., Sertdemir Y., "Chromosomal fragile sites in schizophrenic patients", RUSSIAN JOURNAL OF GENETICS, vol.42, pp.810-817, 2006
Gülderen Özlü F., Yapicioğlu Yildizdaş H., Satar M., Narli N., Ozcan K., Buyukcelik M., et al.,"Barttin mutations in antenatal Bartter syndrome with sensorineural deafness", PEDIATRIC NEPHROLOGY, vol.21, pp.1056-1057, 2006
Turkmen S., Demirhan O., Hoffmann K., Diers A., Zimmer C., Sperling K., et al., "Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p", JOURNAL OF MEDICAL GENETICS, vol.43, pp.461-464, 2006
Demirhan O., Turkmen S., Schwabe G., Soyupak S., Akgul E., Tastemir D., et al., "A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies", JOURNAL OF MEDICAL GENETICS, vol.42, pp.314-317, 2005
Demirhan O., "Clinical findings and phenotype in a toddler with 48,XXYY syndrome", AMERICAN JOURNAL OF MEDICAL GENETICS, vol.119A, pp.393-394, 2003
Demirhan O., Tastemir D., Diler R., Firat S., Avei A., "A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome", YONSEI MEDICAL JOURNAL, vol.44, pp.583-592, 2003
Demirhan O., Tastemir D., "Chromosome aberrations in a schizophrenia population", SCHIZOPHRENIA RESEARCH, vol.65, pp.1-7, 2003
Coucke P., Van Hauwe P., Everett L., Demirhan O., Kabakkaya Y., Dietrich N., et al.,"Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome", JOURNAL OF MEDICAL GENETICS, vol.36, pp.475-477, 1999
Coucke P., Vancamp G., Demirhan O., Kabakkaya Y., Balemans W., Vanhauwe P., et al.,"The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q", GENOMICS, vol.40, pp.48-54, 1997
Satar M., Temocin A., Atici A., Demirhan O., "A case of spondylocostal dysostosis with a fra(5)(q32)", TURKISH JOURNAL OF PEDIATRICS, vol.39, pp.547-549, 1997
Kasap H., Kasap M., Demirhan O., Alptekin D., "DEVELOPMENT OF PLASMODIUM-VIVAX IN ANOPHELES-SUPERPICTUS UNDER EXPERIMENTAL CONDITIONS", AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, vol.37, pp.241-245, 1987
DİĞER DERGİLERDE YAYIMLANAN MAKALELER
Demirhan O., Tanriverdi N., Süleymanova D., "Chromosomal Analysis of Couples with Bad Obstetric History", Journal of Clinical Developmental Biology, vol.1, pp.16-16, 2016
Tunç E., Demirhan O., Sağlıker Y., Güzel A.İ., "Chromosomal Findings and Calcium Sensing Receptor (CaSR) Gene Analysis in Patients with Sağlıker Syndrome", Turk Journal Med Sci., vol.46, pp.1-9, 2016
Demirhan O., Tanriverdi N., Süleymanova D., "Chromosomal aberrations in Turkish infertile couples with reproductive problems", Global Journal of Fertility and Research, vol.1, pp.6-10, 2016
Demirhan O., Tanriverdi N., Süleymanova D., Çetinel N., Yaşar Y., "The frequency and types of chromosomal aberrations in the patients with hypogonodism", Human Genetics and Embryology, vol.5, pp.124-129, 2015
Tunç E., Demirhan O., Pazarbaşi A., Tastemir D., Guzel A.I., Kasap M., et al.,"The effect of conception time and maternal age upon fetal sex ratio in Çukurova population, Adana-Turkey", Cukurova Medical Journal, cilt.39, ss.248-255, 2014 (Link)
Tanriverdi N., Pazarbaşi A., Suleymanova-Karahan D., Avcı A., Tahiroglu A.Y., Tunc E., et al.,"10. Kromozomdaki Perisentrik İnversiyonun Agresif Davranış ve Hiperaktivite Üzerine Etkisi", Cukurova Medical Journal, cilt.38, ss.108-113, 2013 (Link)
HAKEMLİ KONGRE / SEMPOZYUMLARIN BİLDİRİ KİTAPLARINDA YER ALAN YAYINLAR
Alptekin D., Pazarbaşi A., Lüleyap H.Ü., Erkoc M.A., Yilmaz M.B., Cömertpay G., et al.,"The Presence Of One Trisomic Diallelic Marker Of A Fetus For D21s1411 With Normal Karyotype", European Human Genetics Conference 2013, PARİS, FRANSA, 8-11 Haziran 2013, vol.21, pp.57-57
Pazarbaşi A., Tunç E., Alptekin D., Lüleyap H.Ü., Demirhan O., Tanriverdi N., et al.,"Chromosomal Abnormalities Identified At Prenatal Diagnosis", European Human Genetics Conference 2013, PARİS, FRANSA, 8-11 Haziran 2013, vol.21, pp.78-78
Pazarbaşi A., Alptekin D., Tunç E., Tanriverdi N., Demirhan O., Özgünen F.T., et al.,"Amniyosentez Ile Prenatal Tanı Konulan 5671 Olguda Sitogennetik Bulgular", 10. Ulusal Tıbbi Genetik Kongresi , BURSA, TÜRKIYE, 19-23 Eylül 2012, cilt.PB0177, ss.63-63
Pazarbaşi A., Demirhan O., Kasap M., Alptekin D., Lüleyap H.Ü., Guzel A.I., et al.,""The Reliability Of Maternal Serum Triple Screening For The Parental Diagnosis Of Fetal Chromosomal Abnormalities In Turkish Women"", European Human Genetics Conference, NÜRNBERG, ALMANYA, 23-26 Haziran 2012, vol.05, pp.65-65
Pazarbaşi A., Alptekin D., Lüleyap H.Ü., Tansug Z., Izmirli M., Yilmaz M.B., et al.," "Genetic Polymorphisms In The Estrogen Receptor Alpha Gene In Turkish Patients With Familial Prostate Carcinoma"", IV. International Congress of Molecular Medicine, İSTANBUL, TÜRKIYE, 27-30 Haziran 2011, cilt.231, ss.97-98
Pazarbaşi A., Demirhan O., Tanriverdi N., Avci A., Yolga Tahiroğlu A., "Perisentrik İnversiyon (10)(p11.1;q22.1)?un Agresif Davranış ve Hiperaktivite Üzerine Etkisi", 19. Ulusal Ulusal Çocuk ve Ergen Ruh Sağlığı ve Hastalıkları Kongresi , HATAY, TÜRKIYE, 14-16 Nisan 2009, ss.134-134
Kasap H., Kasap M., Alptekin D., Demirhan O., Lüleyap H.Ü., Pazarbaşi A., ""Population Density And Nocturnal Activity Of Anopheles Sacharovi And Anopheles Hyrcanus Collected By Different Sampling Methods"", 8th International Congress of Parasitology, İZMİR, TÜRKIYE, 10-14 Ekim 1994, vol.2, pp.414-414
Kasap H., Kasap M., Alptekin D., Demirhan O., Lüleyap H.Ü., Pazarbaşi A., ""Culicinae Erginlerinin Mayıs-Ekim Aylarında Tarsus Yöresinde Gece Aktiviteleri Ve Populasyon Yoğunluğu", ", XII. Ulusal Biyoloji Kongresi,, EDİRNE, TÜRKIYE, 6-8 Temmuz 1994, ss.26-26
Kasap H., Kasap M., Akbaba M., Alptekin D., Demirhan O., Lüleyap H.Ü., et al.,"The History Of Use Of Adulticides In Malaria Control In Turkey With Reference To The Detection Of Resistance To Carbamates And Some Organophosphorus Insecticides And The Management Of Malaria Incidence To Acceptable Low Levels"", Iranian Congress of Malaria, Zahedan, IRAN, 22-26 Şubat 1992, vol.24, pp.42-43
Özcel M., Kasap H., Alkan M., Kasap M., Ak M., Alptekin D., et al.,""Entomological Studies On Anopheles Sacharovi In Çukurova, Turkey"", XIIIth International Congress for Tropical Medicine and Malaria, PATTAYA, TAYLAND, 29-4 Kasım 1992, vol.2, pp.15-15
Kasap H., Kasap M., Akbaba M., Alptekin D., Demirhan O., Lüleyap H.Ü., et al.,""Residual Efficacy Of Primiphos Methyl (Actellic) On Anopheles Sacharovi In Çukurova, Turkey"", VII. International Congress of Parasitology,, PARİS, FRANSA, 8-12 Kasım 1990, vol.8, pp.1198-1198
KİTAP ve KİTAP BÖLÜMLERİ
Kasap H., Kasap M., Demirhan O., Alptekin D., Lüleyap H.Ü., Pazarbaşi A., et al.,"Tıbbi Biyoloji ve Genetik ", Nobel, ADANA, 2009
Kasap H., Kasap M., Alptekin D., Lüleyap H.Ü., Demirhan O., "Tıbbi Biyoloji ve Genetik-I", Ç.Ü Tıp Fakültesi Yayınları, ADANA, 2006