Yayın Ağı
SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients
Modifications of the locomotor system in habitually quadrupedal humans
”Chromosomal alterations in patients with breast cancer”,
European Journal Of Human Genetics
, cilt.26, ss.536, 2018 (SCI-Expanded)
Chromosomal findings and sequence analysis of target exons of calcium-sensing receptor (CaSR) gene in patients with Sagliker syndrome
Effects of GSM-like radiofrequency irradiation during the oogenesis and spermiogenesis of Xenopus laevis
Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions
Microchimeric Cells, Sex Chromosome Aneuploidies and Cancer
Gene Mutations in Chronic Kidney Disease Patients With Secondary Hyperparathyroidism and Sagliker Syndrome
REPORT OF A NEW CASE WITH PENTASOMY X AND NOVEL CLINICAL FINDINGS
Frequency and Types of Chromosomal Abnormalities in Turkish Women with Amenorrhea
JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGY
, cilt.27, sa.5, ss.274-277, 2014 (SCI-Expanded)
The Role Of Glucorticoid Receptor Gene (nr3c1 Gene) Polymorphism On Relapsing Of Idiopathic Nephrotic Syndrome In Children.
PEDIATRIC NEPHROLOGY
, cilt.29, sa.9, ss.1730-1731, 2014 (SCI-Expanded)
Genetic alterations of chromosomes, p53 and p16 genes in low- and high-grade bladder cancer
There is no Significant Association Between Death Receptor 4 (DR4) Gene Polymorphisms and Lung Cancer in Turkish Population
Polychlorinated biphenyls and organochlorine pesticides in amniotic fluids of pregnant women in south-central Turkey
TOXICOLOGICAL AND ENVIRONMENTAL CHEMISTRY
, cilt.95, sa.6, ss.954-961, 2013 (SCI-Expanded)
Are there fetal stem cells in the maternal brain?
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
, cilt.14, sa.2, ss.651-658, 2013 (SCI-Expanded)
INHERITANCE OF A CHROMOSOME 3 AND 21 TRANSLOCATION IN THE FETUSES, WITH ONE ALSO HAVING TRISOMY 21, IN THREE PREGNANCIES IN ONE FAMILY
RAPID DETECTION OF FETAL ANEUPLOIDIES BY QUANTITATIVE FLUORESCENT-POLYMERASE CHAIN REACTION FOR PRENATAL DIAGNOSIS IN THE TURKISH POPULATION
Chromosome Imbalances and Alterations of AURKA and MYCN Genes in Children with Neuroblastoma
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION
, cilt.13, sa.11, ss.5391-5397, 2012 (SCI-Expanded)
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
Association of the Nramp1 gene polymorphisms and clinical forms in patients with tuberculosis
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY
, cilt.113, sa.11, ss.657-660, 2012 (SCI-Expanded)
The genotoxic effect of nicotine on chromosomes of human fetal cells: The first report described as an important study
The Reliability of Maternal Serum Triple Test in Prenatal Diagnosis of Fetal Chromosomal Abnormalities of Pregnant Turkish Women
GENETIC TESTING AND MOLECULAR BIOMARKERS
, cilt.15, sa.10, ss.701-707, 2011 (SCI-Expanded)
Polymorphisms in NRAMP1 and MBL2 genes and their relations with tuberculosis in Turkish children.
Association of serum sex steroid levels and bone mineral density with CYP17 and CYP19 gene polymorphisms in postmenopausal women in Turkey
Analysis of peripheral blood T-cell subsets, natural killer cells and serum levels of cytokines in children with Down syndrome
INTERNATIONAL JOURNAL OF IMMUNOGENETICS
, cilt.37, sa.4, ss.233-237, 2010 (SCI-Expanded)
Alterations in p16 and p53 genes and chromosomal findings in patients with lung cancer: Fluorescence in situ hybridization and cytogenetic studies
CLINICAL MANIFESTATIONS OF PARTIAL TRISOMY 4p
The Expression of Folate Sensitive Fragile Sites in Patients with Bipolar Disorder
Detection of Parental Origin and Cell Stage Errors of a Double Nondisjunction in a Fetus by QF-PCR
GENETIC TESTING AND MOLECULAR BIOMARKERS
, cilt.13, sa.1, ss.73-77, 2009 (SCI-Expanded)
PARENTAL ORIGIN AND CELL STAGE ERRORS IN X-CHROMOSOME POLYSOMY 49,XXXXY
Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene
Cytogenetic effects of ethanol on chronic alcohol users
PRENATAL DIAGNOSIS OF TRANSLOCATION 13;13 PATAU SYNDROME: CLINICAL FEATURES OF TWO CASES
Cytogenetic study of recurrent miscarriages and their parents
Pregnancy in patients with chronic myeloid leukemia treated with imatinib
Chromosomal abnormalities in endometrial and ovarian carcinomas
Chromosomal fragile site expression in Turkish psychiatric patients
Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages
Barttin mutations in antenatal Bartter syndrome with sensorineural deafness
Chromosomal fragile sites in schizophrenic patients
Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p
A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
Chromosome aberrations in a schizophrenia population
A cytogenetic study in 120 Turkish children with intellectual disability and characteristics of fragile X syndrome
Clinical findings and phenotype in a toddler with 48,XXYY syndrome
Results of cytogenetic investigation in adolescent patients with primary or secondary amenorrhea.
Journal of pediatric and adolescent gynecology
, cilt.10, ss.86-8, 1997 (SCI-Expanded)
A case spondylocostal dysostosis with fra (5Q32).
CYTOGENETICS AND CELL GENETICS
, cilt.77, 1997 (SCI-Expanded)
DEVELOPMENT OF PLASMODIUM-VIVAX IN ANOPHELES-SUPERPICTUS UNDER EXPERIMENTAL CONDITIONS
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE
, cilt.37, sa.2, ss.241-245, 1987 (SCI-Expanded)
Diğer Dergilerde Yayınlanan Makaleler
A Cytogenetic Study of Turkish Children with Global Developmental Delay
Cytogenetic differences in blood and cancer tissue samples of the same patient group
Journal of Cancer Research and Cellular Therapeutics
, cilt.4, sa.1, ss.1-3, 2020 (Hakemli Dergi)
The Genotoxic Effect of Interventional Cardiac Radiologic Procedures on Human Chromosomes
Chromosomal Aberrations in agricultural farmers exposed to pesticides.
Frequency and types of chromosomal abnormalities in acute lymphoblastic leukemia patients in Turkey
Microchimerism may be the cause of psychiatric disorders.
<i>In vitro</i> cytogenotoxic evaluation of sertraline.
Alteration of Peripheral Blood T-cell Subsets in Patients with Cardiovascular Disease Exposure to Ionizing Radiation (X-rays) and Contrast Medium
International Journal of Cardiology and Research
, cilt.5, sa.2, ss.104-108, 2018 (Hakemli Dergi)
Cancerous cell lines alter their genomic organization and karyotype with increased passage number: a cytogenetic study
Constitutional chromosome 16q mosaicism: inheritance and phenotypic effects
The chromosomal effects of GSM-like electromagneticradiation exposure on human fetal cells
Statin and MTHFR C677T Polymorphism in Patients with Cardiovascular Diseases
Sıgaradaki Kanserojen Maddelerle Gen Bölgeleri Arasındaki İlişki
Tubitak, Bilim Ve Teknik Dergisi
, cilt.86, ss.65, 2006 (Hakemli Dergi)
Sıgaradaki Kanserojen Maddelerle Gen Bölgeleri Arasındaki İlişki. , Ocak 200665.
Tubitak, Bilim Ve Teknik Dergisi
, cilt.65, ss.144-150, 2006 (Hakemli Dergi)
Alkol Bağımlılığı Ve Genetik Yönü. 200217(1):53-60.
Ç.Ü. Sağlık Bilimleri Dergisi
, cilt.17, sa.1, ss.53-60, 2002 (Hakemli Dergi)
Alkol Bağımlılığı Ve Genetik Yönü
Ç.Ü. Sağlık Bilimleri Dergisi
, cilt.17, sa.1, ss.53-60, 2002 (Hakemli Dergi)
Sıtma Vektörü Anopheles sacharovi'nin Lipid Düzeyinin Mevsimsel Değişimi. 1994, 18: 161-165.
Tr. J. Of Zoology,
, cilt.18, ss.161-165, 1994 (Hakemli Dergi)
Sıtma Vektörü Anopheles sacharovi’xxnin Lipid Düzeyinin Mevsimsel Değişimi
Tr. J. Of Zoology,
, cilt.18, ss.161-165, 1994 (Scopus)
Kafes büyüklüğünün sıtma vektörü Anopheles sacharovi'nin döllenme, ömür uzunluğuna ve yumurta verimine etkisi. .1991,6(1,2,3):21-16.
Ç.Ü.Sağ.Bil.Der
, cilt.6, ss.16-21, 1991 (Hakemli Dergi)
. Sıtma Vektörü Anopheles sacharovi'nin Kan Emme Aktivitesi. 1991, Sayı 3-4:131-136.
Türk. Parazitol. Dergisi,
, cilt.3-4, ss.131-136, 1991 (Hakemli Dergi)
Sıtma Vektörü Anopheles sacharovi’xxnin Kan Emme Aktivitesi.
Türk. Parazitol. Dergisi,
, ss.131-136, 1991 (Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
Results of karyotype analysis of 7975 pregnancies prenataly identified with amniocentesis in Turkey
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.883-884, (Özet Bildiri)
Detection of chromosomal anomalies from South of Turkey: QF PCR versus cytogenetic
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, İtalya, 16 - 19 Haziran 2018, cilt.27, ss.885, (Özet Bildiri)
STRIKING NOVEL MULTI- MISMUTATIONS ON GNAS1, FGF23 AND FGFR3 GENES IN CKD WITH SECONDARY HYPERPARATHYROIDISM(SH) . SAGLIKER SYNDROME(SS) . SS IS A COMBINATION -COMPULSION OF BONE DISPLASIAS-HEREDITARY OSTEODYSTROPHIES AND SH AND CKD
56th Congress of the European-Renal-Association (ERA)-European-Dialysis-and-Transplant-Association (EDTA) - Burden, Access and Disparities in Kidney Disease, Budapest, Macaristan, 13 - 16 Haziran 2019, cilt.34, ss.199-201, (Özet Bildiri)
Analysis of maternal polymorphism of CBS gene and risk of Down syndrome offspring
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.827, (Özet Bildiri)
Kisspeptin Induce Aromatase Expression via Kisspeptin Receptor (GPR54) in MCF 7 Breast Cancer Cell Line
50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.968, (Özet Bildiri)
MULTIPLE GNAS1, FGF23, FGFR3 GENES’xx STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS)
55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA, Birleşik Krallık, 24 - 27 Mayıs 2018, cilt.33, ss.168-169, (Özet Bildiri)
MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRIKING MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDITARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS)
55th Congress of the European-Renal-Association (ERA) and European-Dialysis-and-Transplantation-Association (EDTA), Copenhagen, Danimarka, 24 - 27 Mayıs 2018, cilt.33, (Özet Bildiri)
EXPRESSION AND METHYLATION LEVELS OF VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF-C) AND BASIC FIBROBLAST GROWTH FACTORS (BFGF) IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA
8th International Eurasian Hematology Oncology Congress (EHOC), İstanbul, Türkiye, 18 - 21 Ekim 2017, cilt.61, (Özet Bildiri)
Kisspeptin induce aromatase expression via kisspeptin receptor (GPR54) in MCF 7 breast cancer cell line
Eurpean Human Genetics Conference 2017, Kopenhag, Danımarka, 27 - 30 Mayıs 2017, (Tam Metin Bildiri)
Chromosomal alteraĕons in paĕents with breast cancer
Eurpean Human Genetics Conference, Kopenhag, DANIMARKA, 27 - 30 Mayıs 2017, (Tam Metin Bildiri)
Kisspeptin induce aromatose expression via kisspeptin receptor (GPR54) in MCF 7 breast cancer cell line
Eurpean Human Genetics Conference, Kpenhag, Danimarka, 27 Mayıs 2017 - 30 Mayıs 2015, ss.21, (Tam Metin Bildiri)
Chromosomal alteration in patients with breast cancer
Eurpean Human Genetics Conference, Kpenhag, Danimarka, 27 Mayıs 2017 - 30 Haziran 2015, cilt.P12, ss.454, (Tam Metin Bildiri)
Turner fenotipine sahip kadınlardaki cinsiyet kromozomu anomalilerinin sıklık ve dağılımları uzun süreli retrospektif çalışma
Innovation in Medicine Meetings 3, Türkiye, 11 - 13 Mayıs 2017, ss.70, (Özet Bildiri)
Turner fenotipine sahip kadınlardaki cinsiyet kromozomu anomalilerinin sıklık ve dağılımları; uzun süreli retrospektif çalışma. Innovation in Medicine Meetings 3, May 11-13, 2017. Innovation summit book 2017; pp: 70. The University of Sanko, GAZİANTEP/TURKEY.
Innovation in Medicine Meetings 3, Gaziantep, Türkiye, 11 - 13 Mayıs 2017, ss.70, (Tam Metin Bildiri)
Maternal Mıcrochımerıc Cells Turn Into Cancer.
6. Multidisipliner Kanser Araştırma Kongresi,, Konya, Türkiye, 27 - 30 Ekim 2016, ss.2, (Tam Metin Bildiri)
Maternal Mıcrochımerıc Cells Turn Into Cancer Stem Cells?
6. Multidisipliner Kanser Araştırma Kongresi,, Konya, Türkiye, 27 - 30 Ekim 2016, ss.2, (Tam Metin Bildiri)
Maternal Mıcrochımerıc Cells Turn Into Cancer Stem Cells?
6. Multidisipliner Kanser Araştırma Kongresi,, Konya, Türkiye, 27 - 30 Ekim 2016, ss.2, (Tam Metin Bildiri)
MULTIPLE GENE MUTATIONS IN GNAS1, FGF23 AND FGFR3 GENES IN CKD PATIENTS WITH SH SAGLIKER SYNDROME
53rd ERA-EDTA Congress, Vienna, Avusturya, 21 - 24 Mayıs 2016, cilt.31, ss.1468, (Özet Bildiri)
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)
52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri)
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
52nd Congress of the European-Renal-Association-European-Dialysis-and-Transplant-Assocation, London, Kanada, 28 - 31 Mayıs 2015, cilt.30, (Özet Bildiri)
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
5th International Eurasian Hematology Congress, Antalya, Türkiye, 15 - 19 Ekim 2014, cilt.38, (Özet Bildiri)
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) ?
51st Congress of the European-Renal-Association(ERA)/European-Dialysis-and-Transplant-Association (EDTA), Amsterdam, Hollanda, 31 Mayıs - 03 Haziran 2014, cilt.29, ss.381, (Özet Bildiri)
microchimeric cells, sex chromosome aneuploidies and cancer.
1. Uluslararası Katılımlı Kök Hücre ve Hücresel Tedaviler Kongresi, 20-23 Mart 2014, Kartepe Green Park Resort Hotel., Kocaeli, Türkiye, 20 - 23 Mart 2014, ss.1, (Tam Metin Bildiri)
. Pazarbasi, O Demirhan, M. Kasap, D. Alptekin, U. Luleyap, B. Yilmaz, A. I. Guzel, S. K. Sel, E. Tunc, L. Özpak, F. T. Özgunen, H. Kasap The reliability of maternal serum triple screening for the prenatal diagnosis of fetal chromosomal abnormalities in Turkish women
European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics, 23 - 26 Haziran 2012, ss.5-65, (Özet Bildiri)
The reliability of maternal serum triple screening for the prenatal diagnosis of fetal chromosomal abnormalities in Turkish women. European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics June 23 - 26, 2012, NCC Ost, Nürnberg, Germany, P05.65.
European Meeting on Psychosocial Aspects of Genetics and the German Society of Human Genetics, Nünberg, Almanya, 23 - 26 Haziran 2012, ss.5-65, (Tam Metin Bildiri)
Effects of common Methylene Tetrahydrofolate Reductase MTHFR polymorfhisms on the risk of bladder cancer in Turkey European Society of Human Genetics
European Human Genetics Conference, Amsterdam, Hollanda, 28 - 31 Mayıs 2011, (Özet Bildiri)
Effects of common methylene tetrahydrofolate Reductase (mtHFR) Polymorfhisms on the Risk of Bladder cancer in turkey. P06.150. European Human Genetics Conference 2011, Amsterdam Rai Congress Centre Amsterdam, The Netherlands Saturday, May 28 ? Tuesday, May 31, 2011.
European Human Genetics Conference 2011, Amsterdam Rai Congress Centre Amsterdam,, Amsterdam, Hollanda, 28 - 31 Mayıs 2011, ss.6-150, (Tam Metin Bildiri)
Effects of common Methylene Tetrahydrofolate Reductase (MTHFR) polymorfhisms on the risk of bladder cancer in Turkey
European Society of Human Genetics. European Human Genetics Conference 2011, Amsterdam, Hollanda, 28 - 31 Mayıs 2011, cilt.06, sa.150, ss.223-224, (Tam Metin Bildiri)
?Akciğer Kanserli Hastaların Malign ve Normal Bronş Epitel Dokularında Gözlenen Kromozom Düzensizlikleri?
XI. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Hotel Diamond, Bodrum., Muğla, Türkiye, 28 - 31 Ekim 2009, ss.34, (Tam Metin Bildiri)
Alterations in p16 and p53 genes and chromosomal findings in patients with lung cancer: FISH and cytogenetic study.
European Human Genetics Conference, Viyana, Avusturya, 23 - 26 Mayıs 2009, ss.7, (Tam Metin Bildiri)
Naturel Resistance-associated Macrophage Protein 1 (NRAMP1) Gene Polymorphisms, Susceptibility and Clinical Forms of Tuberculosis in a Turkish Population.
XX. International Congress of Genetics,, Berlin, Almanya, 12 - 17 Haziran 2008, ss.29-444, (Tam Metin Bildiri)
Cytogenetic effects of chronic alcohol Users.
The American Society of Human Genetics, 55th Annual Meeting,, Salt Lake City,, Amerika Birleşik Devletleri, 25 Ekim - 29 Aralık 2005, ss.779, (Tam Metin Bildiri)
History Of The Use Of Adulticides İn Malaria Control İn Turkey With Reference To The Detection Of Resistance To Some İnsecticides And The Management Of Malaria İncidence To Acceptable Low Levels
Iranian Congress Of Malaria, Zahedan,, İran, 22 - 28 Şubat 1992, ss.45, (Tam Metin Bildiri)
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, İran, 22 - 26 Şubat 1992, cilt.24, ss.42-43, (Tam Metin Bildiri)
Sıtma Paraziti Plasmodium vivax'ın vektör Anopheles sacharovi'deki sporogonik gelişimi
5. Ulusal Parazitoloji Kongresi, Adana, Türkiye, 15 - 17 Eylül 1987, cilt.87, sa.1, ss.55, (Özet Bildiri)
Kitaplar
Tobacco Use and Its Genotoxic Effects in Pregnancy, Tobacco Addiction: Effect on Human Health,
Tobacco Use and Its Genotoxic Effects in Pregnancy, Tobacco Addiction: Effect on Human Health, Chapter 5., Demirha O, Editör, Open Access, Washington, ss.1-15, 2018
