Prof.

SEVİLHAN ARTAN


Tıp Fakültesi

Dahili Tıp Bil. Bölüm

Tıbbi Genetik Anabilim Dalı

Education Information

1989 - 1992

1989 - 1992

Doctorate

Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Dr), Turkey

1985 - 1988

1985 - 1988

Postgraduate

Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Yl) (Tezli), Turkey

1978 - 1983

1978 - 1983

Undergraduate

Middle East Technical University, Faculty Of Arts And Sciences, Department Of Biology, Turkey

Dissertations

1992

1992

Doctorate

İlk trimester spontan abortus materyallerinde sitogenetik ve elektron mikroskobik analizler

Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Dr)

1989

1989

Postgraduate

Düşük doğum ağırlıklı yenidoğanlarda genetik ve dermatoglifik analizler

Eskisehir Osmangazi University, Sağlık Bilimleri Enstitüsü, Tıbbi Genetik (Yl) (Tezli)

Research Areas

Health Sciences, Natural Sciences

Academic Titles / Tasks

2004 - Continues

2004 - Continues

Professor

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm

1997 - 2002

1997 - 2002

Associate Professor

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm

1994 - 1998

1994 - 1998

Assistant Professor

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm

1985 - 1994

1985 - 1994

Research Assistant

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm

Managerial Experience

2014 - Continues

2014 - Continues

Director of the Center

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bil. Bölüm

2012 - Continues

2012 - Continues

Head of Department

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2002 - 2011

2002 - 2011

Head of Department

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

2007 - 2009

2007 - 2009

Deputy Head of Department

Eskisehir Osmangazi University, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü

Advising Theses

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

2021

2021

A pediatric BAL case with double Ph chromosomes and trisomy 5

Gunden G., Işık S. , Özdemir C. , Çilingir O. , Bör Ö. , Gokalp E. E. , et al.

Cancer Genetics, vol.258, pp.7-9, 2021 (Journal Indexed in SCI) identifier identifier identifier

2020

2020

A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency

BAŞ H. , ÇİLİNGİR O. , TEKİN N. , ŞAYLISOY S. , DURAK ARAS B. , Uzay E., et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol.182, no.4, pp.740-745, 2020 (Journal Indexed in SCI) identifier identifier identifier

2019

2019

The 15q11.2 BP1-BP2 Microdeletion Syndrome with Variable Expressivity.

Erzurumluoğlu Gökalp E. , Çilingir O., Durak Aras B. , Kocagil S., Susam E. , Artan S.

Balkan Journal Of Medical Genetics, vol.22, no.1, pp.92, 2019 (Journal Indexed in SCI Expanded)

2019

2019

Importance of Cytocenetic Analysis in Hematological Malignancies: with Two Rare Cases Reports

Işık S. , Günden G., Çilingir O., Eker İ., Üsküdar Teke H. , Gündüz E. , et al.

Balkan Journal Of Medical Genetics, vol.22, no.1, pp.76, 2019 (Journal Indexed in SCI Expanded)

2018

2018

Apolipoprotein E allelic variants and cerebral palsy

Gumus E., DURAK ARAS B. , ÇİLİNGİR O. , YARAR C. , ÇARMAN K. B. , Laciner-Gurlevik S., et al.

TURKISH JOURNAL OF PEDIATRICS, vol.60, no.4, pp.361-371, 2018 (Journal Indexed in SCI) Creative Commons License identifier identifier identifier

2017

2017

Association of functional RAGE gene polymorphisms with Parkinson’s disease in a Turkish cohort

ÇİLİNGİR O. , ÖZKAN S. , DURAK ARAS B. , ERZURUMLUOĞLU E. , KUTLAY Ö., EMİR B. , et al.

Biomedical Research-India, vol.28, no.19, pp.8454-8460, 2017 (Journal Indexed in SCI Expanded) identifier

2015

2015

Association of Alzheimer's Disease With APOE and IL-1 alpha Gene Polymorphisms

YILDIZ S. H. , Erdogan M. O. , ARTAN S. , SOLAK M., YAMAN M., Ozbabalik B. D. , et al.

AMERICAN JOURNAL OF ALZHEIMERS DISEASE AND OTHER DEMENTIAS, vol.30, no.8, pp.756-761, 2015 (Journal Indexed in SCI) identifier identifier identifier

2015

2015

Study of fluorescence in situ hybridization in malignant melanoma

DURAK ARAS B. , Isik S. , Tore T., CANAZ F. , Yilmaz H., Ozdemir M., et al.

CHROMOSOME RESEARCH, vol.23, 2015 (Journal Indexed in SCI) identifier

2014

2014

Investigation of key miRNAs and target genes in bladder cancer using miRNA profiling and bioinformatic tools

Canturk K. M. , Ozdemir M., Can C. , Oner S. , Emre R., Aslan H., et al.

MOLECULAR BIOLOGY REPORTS, vol.41, no.12, pp.8127-8135, 2014 (Journal Indexed in SCI) Sustainable Development identifier identifier identifier

2014

2014

Detection of kinase amplifications in gastric adenocarcinomas

Ozdemir M., Oznur M., Ciftci E., DURAK ARAS B. , Aslan H., Saygili H., et al.

TURKISH JOURNAL OF MEDICAL SCIENCES, vol.44, no.3, pp.461-470, 2014 (Journal Indexed in SCI) identifier identifier identifier

2014

2014

IDH2 Mutations in Primary Glioblastoma

Atli E. I. , Kalkan R., Ciftci E., Ozkara E., ÇİLİNGİR O. , Ozdemir M., et al.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, vol.31, no.4, pp.693-698, 2014 (Journal Indexed in SCI) identifier identifier

2012

2012

Conventional and Molecular Cytogenetic Analyses in Turkish Patients with Multiple Myeloma

DURAK ARAS B. , Akay O. M. , Sungar G., Bademci G., Aslan V., Caferler J., et al.

TURKISH JOURNAL OF HEMATOLOGY, vol.29, no.2, pp.135-142, 2012 (Journal Indexed in SCI) identifier identifier identifier

2011

2011

Association of estrogen receptor alpha and collagen type I alpha 1 gene polymorphisms with bone mineral density in postmenopausal women.

Erdogan M. O. , Yildiz H., Artan S. , Solak M., Tascioglu F. , Dundar U., et al.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, vol.22, no.4, pp.1219-25, 2011 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2010

2010

Is Recurrent Abortion an Indication for Subtelomeric Region Analysis?

DURAK ARAS B. , Yesil M., Ozdemir M., ÇİLİNGİR O. , Sener T., Bademci G., et al.

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI, vol.30, no.5, pp.1465-1468, 2010 (Journal Indexed in SCI) identifier identifier

2007

2007

An unusual case of cervical clear-cell meningioma in pediatric age

Vural M., Arslantas A. , Ciftci E., Artan S. , Atasoy M. A.

CHILDS NERVOUS SYSTEM, vol.23, no.2, pp.225-229, 2007 (Journal Indexed in SCI) identifier identifier identifier

2007

2007

Genomic alterations in low-grade, anaplastic astrocytomas and glioblastomas

Arslantas A. , Artan S. , Oner U., Muslumanoglu M. H. , Ozdemir M., Durmaz R., et al.

PATHOLOGY & ONCOLOGY RESEARCH, vol.13, no.1, pp.39-46, 2007 (Journal Indexed in SCI) identifier identifier identifier

2006

2006

Germ cell tumor showing partial trisomy 1 in a gonadectomized intersex child with monosomy X and double Y mosaicism

Ogur G., Pinarli F. G. , Dagdemir A., Artan S. , Ariturk E., Elli M., et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, vol.28, no.11, pp.750-754, 2006 (Journal Indexed in SCI) identifier identifier identifier

2006

2006

A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda.

Muslumanoglu M. H. , Saracoglu N., Cilingir O. , Basmaci T., Urer S., Sabuncu I., et al.

The British journal of dermatology, vol.155, no.2, pp.467-9, 2006 (Journal Indexed in SCI Expanded) identifier identifier identifier

2006

2006

Fish detected p53 deletion and N-MYC amplification in colorectal cancer.

Ozakyol A. , Ozdemir M., Artan S.

Hepato-gastroenterology, vol.53, no.68, pp.192-5, 2006 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2005

2005

Trisomy 7 in synovial fluid cells of patients with rheumatoid arthritis

Tascioglu F. , Durak B. , Oner C., Artan S.

RHEUMATOLOGY INTERNATIONAL, vol.25, no.8, pp.571-575, 2005 (Journal Indexed in SCI) identifier identifier identifier

2005

2005

Role of the AZFd locus in spermatogenesis.

Muslumanoglu M., Turgut M., Cilingir O. , Can C. , Ozyurek Y., Artan S.

Fertility and sterility, vol.84, no.2, pp.519-22, 2005 (Journal Indexed in SCI Expanded) identifier identifier identifier

2005

2005

Genetic imbalances in endometrial hyperplasia and endometrioid carcinoma detected by comparative genomic hybridization.

Muslumanoglu H., Oner U., Ozalp S., Acikalin M. F. , YALÇIN Ö. T. , Ozdemir M., et al.

European journal of obstetrics, gynecology, and reproductive biology, vol.120, no.1, pp.107-14, 2005 (Journal Indexed in SCI Expanded) identifier identifier identifier

2004

2004

Chromosomal abnormalities, p53 and Bcl-2 expression and clinical outcome in choroidal melanoma.

EROL N. , Oner U., Artan S. , Isiksoy S., Yurdakul S.

Melanoma research, vol.14, no.6, pp.473-8, 2004 (Journal Indexed in SCI Expanded) identifier identifier identifier

2004

2004

The importance of genomic copy number changes in the prognosis of glioblastoma multiforme.

Arslantas A. , Artan S. , Oner U., Muslumanoglu H., Durmaz R., Cosan E., et al.

Neurosurgical review, vol.27, no.1, pp.58-64, 2004 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

2000

2000

Penoscrotal hypospadias and coarctation of the aorta with mixed gonadal dysgenesis

Konrad D., Sossai R., Winklehner H., Binkert F., Artan S. , Scharli A.

PEDIATRIC SURGERY INTERNATIONAL, vol.16, no.3, pp.226-228, 2000 (Journal Indexed in SCI) identifier identifier identifier

2000

2000

Prognostic significance of deletion and over-expression of the p53 gene in epithelial ovarian cancer.

Ozalp S., YALÇIN Ö. T. , Basaran N., Artan S. , Kabukcuoglu S., Minsin T.

European journal of gynaecological oncology, vol.21, no.3, pp.282-6, 2000 (Journal Indexed in SCI Expanded) Sustainable Development identifier identifier identifier

1999

1999

FISH analysis with locus-specific probes in sperm from two translocation carrier men

Durak B. , Ozon Y., Ozdemir M., Artan S. , Basaran N., Basaran S., et al.

CLINICAL GENETICS, vol.56, no.2, pp.129-135, 1999 (Journal Indexed in SCI) identifier identifier identifier

1998

1998

The deletion of 22q13 region in both intracranial and spinal meningiomas in a patient (case report).

Durmaz R., Arslantas A. , Artan S. , Ozon Y., Isiksoy S., Basaran N., et al.

Clinical neurology and neurosurgery, vol.100, no.3, pp.219-23, 1998 (Journal Indexed in SCI Expanded) identifier identifier identifier

1998

1998

Experimental tractional retinal detachment: an immunohistochemical study.

Basmak H., Isiksoy S., Topbas S., Artan S. , Yurdakul S.

European journal of ophthalmology, vol.8, no.2, pp.112-7, 1998 (Journal Indexed in SCI Expanded) identifier identifier identifier

1995

1995

Confined placental mosaicism in term placentae: analysis of 125 cases.

Artan S. , Basaran N., Hassa H., Ozalp S., Sener T., Sayli B., et al.

Prenatal diagnosis, vol.15, no.12, pp.1135-42, 1995 (Journal Indexed in SCI Expanded) identifier identifier identifier

1995

1995

Sister chromatid exchange analysis in acute leukemia patients.

Tuna M., Artan S. , Gezer S., Sayli B. S. , Başaran N.

Cancer genetics and cytogenetics, vol.79, pp.86-8, 1995 (Journal Indexed in SCI) identifier identifier identifier

1994

1994

Effects of consanguinity on anthropometric measurements of newborn infants.

BASARAN N., ARTAN S. , YAZICIOGLU S., SAYLI B.

Clinical genetics, vol.45, no.4, pp.208-11, 1994 (Journal Indexed in SCI Expanded) identifier identifier identifier

1994

1994

Chromosome analysis in pleural effusions. Efficiency of this method in the differential diagnosis of pleural effusions.

METINTAS M. , OZDEMIR N., SOLAK M., ARTAN S. , OZDEMIR M., BASARAN N., et al.

Respiration; international review of thoracic diseases, vol.61, no.6, pp.330-5, 1994 (Journal Indexed in SCI Expanded) identifier identifier identifier

1993

1993

Dacryocystitis associated with osteopoikilosis.

GUNAL I., SEBER S., BASARAN N., ARTAN S. , GUNAL K., GOKTURK E.

Clinical genetics, vol.44, no.4, pp.211-3, 1993 (Journal Indexed in SCI Expanded) identifier identifier identifier

1992

1992

Consanguineous marriages among parents of Down patients.

BASARAN N., CENANI A., SAYLI B., OZKINAY C., ARTAN S. , SEVEN H., et al.

Clinical genetics, vol.42, no.1, pp.13-5, 1992 (Journal Indexed in SCI Expanded) identifier identifier identifier

1989

1989

The effect of consanguinity on the reproductive wastage in the Turkish population.

BASARAN N., HASSA H., BASARAN A., ARTAN S. , STEVENSON J., SAYLI B.

Clinical genetics, vol.36, no.3, pp.168-73, 1989 (Journal Indexed in SCI Expanded) identifier identifier identifier

1988

1988

Consanguineous marriages in the Turkish population.

Başaran N., Sayli B. S. , Başaran A., Solak M., Artan S. , Stevenson J. D.

Clinical genetics, vol.34, pp.339-41, 1988 (Journal Indexed in SCI Expanded) identifier identifier

Articles Published in Other Journals

2021

2021

Extra Chromosome, Extra Love

Aras B. D. , Işık S. , Baş H. , Ocal E. E. , Gokalp E. , Çilingir O. , et al.

GAZI MEDICAL JOURNAL, vol.32, no.1, pp.83-87, 2021 (Journal Indexed in ESCI) identifier identifier

2020

2020

Bağımlılıkta Genetiğin Katkısına Genel Bir Bakış

ERZURUMLUOĞLU GÖKALP E. , ARTAN S.

Türkiye Klinikleri Farmakoloji - Özel Konular, 2020 (National Non-Refereed Journal)

2020

2020

Correlation of HER2/TOP2A Gene Aberrations with RASSF1A/APC Gene Methylation Status in High-Risk Breast Cancer

Nursal A. F. , Çilingir O. , Eroğlu O., Durak Aras B. , Ciftci E., Baydemir C., et al.

TURK ONKOLOJI DERGISI-TURKISH JOURNAL OF ONCOLOGY, vol.35, pp.8-14, 2020 (Journal Indexed in ESCI) Sustainable Development identifier identifier

2019

2019

İnterlökin-6 Geni Promotor Bölge Polimorfizmi ve Serebral Palsi İlişkisinin İncelenmesi

GÜMÜŞ E., ÇİLİNGİR O. , YARAR C. , ÇARMAN K. B. , KOÇAK O., LAÇİNEL GÜRLEVİK S., et al.

Ege Klinikleri Tıp Dergisi, vol.57, no.1, pp.18-22, 2019 (Other Refereed National Journals)

2019

2019

Investigation of DNAmethylation of TWIST Gene in Breast Cancer and Its Relationship to Histopathological Features

EROĞLU O., ÇİLİNGİR O. , ARTAN S. , DURAK ARAS B.

Advances in Breast Cancer Research, vol.8, no.1, pp.45-59, 2019 (Refereed Journals of Other Institutions) Creative Commons License Sustainable Development

2018

2018

Glutathıone S-Transferases M1/T1 and P1 Polymorphisms in Patıents with Alopecia Areata

Çilingir O. , Saraçoğlu Z. N. , Durak Aras B. , Haziyeva K., Kutlay Ö., Erzurumluoğlu E. , et al.

International Journal of Research Studies in Medical and Health Sciences V, vol.3, no.2, pp.1-8, 2018 (Refereed Journals of Other Institutions) Creative Commons License

2018

2018

The Relationship between Glutathione-S-Transferases Polymorphisms and Lichen Planus Susceptibility

ÇİLİNGİR O., bulur I., DURAK ARAS B. , kutlay ö., ERZURUMLUOĞLU E., haziyeva k., et al.

International Journal of Research Studies in Medical and Health Sciences (IJRSMHS), 2018 (Refereed Journals of Other Institutions)

2018

2018

The Relationship between Glutathione-S-Transferases Polymorphisms and Lichen Planus Susceptibility

ÇİLİNGİR O. , BULUR I., DURAK ARAS B. , KUTLAY Ö., ERZURUMLUOĞLU E. , HAZİYEVA K., et al.

International Journal of Research Studies in Medical and Health Sciences, vol.3, no.1, pp.15-22, 2018 (Refereed Journals of Other Institutions)

2018

2018

Prenatal Sitogenetik Anomalilerde İleri Tanı Yöntemi Olarak Array CGH

ERZURUMLUOĞLU E. , ARTAN S.

Türkiye Klinikleri Tıbbi Genetik Özel Dergisi, vol.3, no.1, pp.63-69, 2018 (National Non-Refereed Journal)

2015

2015

The effects of a heterochromatin polymorphism in chromosome 6 on premature ovarian failure

KÜÇÜK H., AYDIN Y. , ERZURUMLUOĞLU E. , ÖZDEMİR M. , HASSA H. , ARTAN S.

Asian Pacific Journal of Reproduction, vol.4, no.1, pp.41-43, 2015 (Refereed Journals of Other Institutions)

2013

2013

Ailevi Akdeniz Ateşli hastalarda gen mutasyonu ile Klinik bulgular arasındaki ilişkilerin değerlendirilmesi

ÇETİN N. , YILDIZ B., KURAL N., ARTAN S.

Turkish Journal of Pediatric Disease, vol.7, no.4, pp.173-177, 2013 (Other Refereed National Journals)

2013

2013

ICSI Sonraıs Fertilizasyon Sonuçlarına Azoospermik ve Oligospermik Hastalardaki Genetik Anomalilerinin Etkisi

ALDEMİR Ö., MÜSLÜMANOĞLU M. H. , CAN C., BAL C. , CANTÜRK M., EMRE R., et al.

Tıp Araştırmaları Dergisi, vol.11, no.3, pp.111-115, 2013 (Other Refereed National Journals)

2013

2013

ICSI sonrası fertilizasyon sonuçlarına Azospermik ve oligospermik hastalardaki genetik anomalilerin etkisi

ALDEMİR Ö., MÜSLÜMANOĞLU M. H. , CAN Y. S. C. , BAL C. , CANTURK K. M. , EMRE R., et al.

Tıp Araştırmaları Dergisi, vol.11, no.3, pp.111-115, 2013 (Other Refereed National Journals)

2011

2011

The First Report of a Patient with Probable Variant Creutzfeldt-Jakob Disease in Turkey

Adapinar D. O. , ŞAYLISOY S. , YENİLMEZ Ç. , Aslan H., Ertan B., ARTAN S. , et al.

DEMENTIA AND GERIATRIC COGNITIVE DISORDERS EXTRA, vol.1, no.1, pp.429-432, 2011 (Journal Indexed in ESCI) Creative Commons License identifier identifier

2010

2010

Performance of MLPA as a screening method for aneuploidy in uncultured ammniocytes

Yurdakul H., DURAK ARAS B. , Muslumanoglu M. H. , Ozdemir M., ÇİLİNGİR O. , Sener T., et al.

JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION, vol.11, no.4, pp.199-203, 2010 (Journal Indexed in ESCI) identifier identifier identifier

2010

2010

Evaluation of the Results of Cordocentesis: 9 Years of Experience

ŞENER T., TANIR H. M. , ÖZALP E., UYSAL E., DURAK ARAS B. , ÇİLİNGİR O. , et al.

Perinatal Journal, vol.18, no.2, pp.35-42, 2010 (Other Refereed National Journals)

2007

2007

Tip 2 Diyabetes Mellitus ile β3 Adrenerjik Reseptör Gen Polimorfizmi Arasındaki İlişki

ÇAKIR B., ÖZDEMİR M., MÜSLÜMANOĞLU M. H. , ÇİLİNGİR O. , GÜLER S., KURTULUŞ A., et al.

Turkish Journal Of Medical Sciences, vol.1, no.2, pp.55-60, 2007 (Other Refereed National Journals) Sustainable Development

2007

2007

Kliniğimizde 7 Yıllık Amniyosentez Sonuçları

ŞENER T., DURAK ARAS B. , TANIR H. M. , TEPELİ E., KAYA M., ARTAN S.

Perinatoloji Dergisi, vol.4, no.2, pp.127-133, 2007 (Other Refereed National Journals)

2002

2002

Kapak tümörleri ve flep dokularında p53 gen mutasyonu ve erbB2 protoonkogen amplifikasyonu

YILDIRIM N. , EROL N. , ARTAN S.

MN Oftalmoloji, vol.9, no.1, pp.62-65, 2002 (Other Refereed National Journals)

Refereed Congress / Symposium Publications in Proceedings

2021

2021

A NOVEL FRAMESHIFT VARIANT IN A PATIENT WITH CHD8-RELATED OVERGROWTH SYNDROME

KOCAGİL S. , KEKLİKCİ A. R. , KILIÇ YILDIRIM G. , ÇİLİNGİR O. , ERZURUMLUOĞLU GÖKALP E. , DURAK ARAS B. , et al.

31TH EUROPEAN MEETING ON DYSMORPHOLOGY ONLINE, Germany, 23 - 25 September 2021, vol.1, pp.34-35

2020

2020

İzole Del13q Kronik Lenfositik Lösemi Olgularında NOTCH1 ve SF3B1 Genlerinin Mutasyonel Durumu

günden g., IŞIK S. , ÜSKÜDAR TEKE H. , ERZURUMLUOĞLU GÖKALP E. , ÇİLİNGİR O. , ARTAN S. , et al.

14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.28

2020

2020

A complex chromosomal rearrangement in a patient with developmental delay and dysmorphic features

AYNACI S., TOSUMOĞLU E., KEKLİKÇİ A. R. , KOCAGİL S. , ERZURUMLUOĞLU GÖKALP E. , ÇİLİNGİR O. , et al.

14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.94

2020

2020

Genetic analysis of a large Osteogenesis Imperfecta Family

günden g., IŞIK S., ÜSKÜDAR TEKE H. , ERZURUMLUOĞLU GÖKALP E., ÇİLİNGİR O., ARTAN S. , et al.

14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.48

2020

2020

Genetic variants associated with atrial fibrillation n Turkish patients

ULUS T., DURAL M. , meşe p., YETMİŞ F. , MERT K. U. , GÖRENEK B. , et al.

36. Uluslararası Katılımlı Türk Kardiyoloji Kongresi, Turkey, 3 - 06 December 2020

2020

2020

Atipik bulguları olan Smith-Magenis sendromlu bir olgu sunumu

SARAÇ E. , ÖZBAKIR D. H. , KOCAGİL S. , ERZURUMLUOĞLU GÖKALP E. , ÇİLİNGİR O. , DURAK ARAS B. , et al.

14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Turkey, 20 - 22 November 2020, vol.31, pp.92

2020

2020

A Rare Form Of Constitutional Chromoanasynthesis: Ring Chromosome 18

Susam E. , Erzurumluoğlu Gökalp E. , Tosumoğlu E., Kocagil S. , Çilingir O. , Durak Aras B. , et al.

14. ULUSAL TIBBİ GENETİK KONGRESİ’xx’xxULUSLARAARSI KATILIMLI’xx’xx, Ankara, Turkey, 20 - 22 November 2020, vol.31, pp.15

2020

2020

A rare homozygous variant in CUL7 gene in two syblings with variable features of 3M syndrome

KOCAGİL S. , KILIÇ YILDIRIM G. , ARTAN S.

14. ULUSAL TIBBİ GENETİK KONGRESİ“Uluslararası Katılımlı”, Turkey, 20 - 22 November 2020

2019

2019

Akne vulgaris’de IL-17A ve RORγt Gen Polimorfiziminin Araştırılması

BULUR I., KAYA ERDOĞAN H. , ÇİLİNGİR O. , ağaoğlu e., temena a., ARTAN S. , et al.

XXIV. Prof. Dr. A. Lütfü Tat Sempozyumu, Ankara, Turkey, 20 - 24 November 2019

2019

2019

KLL’de 13q delesyon büyüklüğünün önemi

IŞIK S. , GÜNDEN G., AKAY O. M. , ÇİLİNGİR O. , ERZURUMLUOĞLU GÖKALP E. , GÜNDÜZ E. , et al.

45.Ulusal Hematoloji Kongresi, Turkey, 30 October - 02 November 2019

2019

2019

The 15q11.2 BP1–BP2 Microdeletion Syndrome with Variable Expressivity

ERZURUMLUOĞLU GÖKALP E. , ÇİLİNGİR O. , DURAK ARAS B. , KOCAGİL S. , SUSAM E. , ARTAN S.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.95

2019

2019

A rare case of severe microcephaly caused by pathogenic variant of NDE1

BAŞ H. , ÇİLİNGİR O. , DURAK ARAS B. , KOCAGİL S. , ARTAN S.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.67

2019

2019

IMPORTANCE OF CYTOGENETIC ANALYSIS IN HEMATOLOGICAL MALIGNANCIES: WITH TWO RARE CASES REPORTS

IŞIK S., GÜNDEN G., ÇİLİNGİR O. , EKER İ., ÜSKÜDAR TEKE H. , GÜNDÜZ E. , et al.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.76

2019

2019

THE RARE ABNORMALITIES OF CHROMOSOME 1 IN MYELOIDMALIGNANCIES

Gunden G., Isik S. , Cilingir O., Davutoglu N. O. , Yavasoglu F., EKER İ., et al.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.184

2019

2019

THE RARE ABNORMALITIES OF CHROMOSOME 1 IN MYELOIDMALIGNANCIES

günden g., ışık s., ÇİLİNGİR O. , OĞUZ DAVUTOĞLU N. , YAVAŞOĞLU F., EKER İ., et al.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.184

2019

2019

IMPORTANCE OF CYTOGENETIC ANALYSIS IN HEMATOLOGICALMALIGNANCIES: WITH TWO RARE CASES REPORTS

IŞIK S. , Gunden G., Cilingir O., EKER İ., USKUDAR TEKE H. , Gunduz E. , et al.

13 th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.76

2019

2019

Assesment of Genes Known to be Assosiated with MODY by Next Generation Sequencing.

ÇİLİNGİR O., DURAK ARAS B. , ŞİMŞEK E. , ÇINAR D., TEMENA M. A. , ARSLAN S., et al.

European Human Genetics Conference, Gothenburg, Sweden, 15 June 2019, vol.27, pp.1260

2019

2019

Macroorchidism as a Uniq Sign in 3q13.31 Deletion Syndrome.

SUSAM E. , ÇİLİNGİR O. , DURAK ARAS B. , ERZURUMLUOĞLU GÖKALP E., KOCAGİL S. , ARTAN S. , et al.

European Human Genetics Conference, Gothenburg, Sweden, 15 June 2019, vol.27, pp.1843

2018

2018

NPHP1 homozigot gen delesyonu saptanan Joubert Sendromu tip 4 tanılı iki olgu sunumu

KOCAGİL S. , EREN M. C. , ELMAS M., YARAR C. , ERZURUMLUOĞLU E., ÇİLİNGİR O., et al.

Uluslararası Katılımlı XIII. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018

2018

2018

PGRN RS5848 POLİMORFİZMİ TÜRK FTLD KOHORTU İÇİN BİR RİSK FAKTÖRÜ MÜDÜR?

ERZURUMLUOĞLU GÖKALP E. , ÖZBABALIK ADAPINAR B. D. , ÇİLİNGİR O. , EKENEL E. Q. , ARTAN S.

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Turkey, 7 - 11 November 2018, pp.149

2018

2018

NPHP1 HOMOZİGOT GEN DELESYONU SAPTANAN JOUBERT SENDROMU TİP 4 TANILI İKİ OLGU SUNUMU

KOCAGİL S., eren m. c. , ELMAS M., YARAR C. , ERZURUMLUOĞLU GÖKALP E. , ÇİLİNGİR O. , et al.

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018, pp.119

2018

2018

NPHP1 homozigot gen delesyonu saptanan Joubert sendromu tip 4 tanılı iki olgu sunumu

KOCAGİL S., EREN M. C. , ELMAS M., YARAR C. , ERZURUMLUOĞLU E., ÇİLİNGİR O., et al.

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018

2018

2018

Konjenital Adrenal Hiperplazi Olgularında Fenotip Genotip İlişkisi

ŞİMŞEK E. , Binay C., ÇİLİNGİR O. , DEMİRAL M., ARTAN S.

XXII. Ulusal Pediatrik Endokrinoloji ve Diyabet Kongresi, Turkey, 18 - 22 April 2018

2018

2018

Türkiye’de Çocukluk Çağı Adrenokortikal Karsinomlarda TP53 Mutasyonu Taraması

ŞİMŞEK E. , ÇİLİNGİR O. , BİNAY Ç., DEMİRAL M., HAZİYEVA K., ARTAN S. , et al.

22. ULUSAL PEDİATRİK ENDOKRİNOLOJİ VE DİYABET KONGRESİ, Antalya, Turkey, 18 - 22 April 2018

2018

2018

Parsiyel Trizomi 15 tanımlanan 2 kardeş olgu

KOCAGİL S. , TEKİN A. N. , ERZURUMLUOĞLU E. , ÇAKIL SAĞLIK A. , Tosumoğlu E., ARTAN S.

Ulusal Neonatoloji Kongresi (UNEKO-26), Girne, Cyprus (Kktc), 14 - 18 April 2018, pp.221

2017

2017

APO E GENOTYPE AND CEREBRAL PALSY

GÜMÜŞ E., DURAK ARAS B. , YARAR C. , LAÇİNEL GÜRLEVİK S., KOÇAK O., ARTAN S. , et al.

12TH EUROPEAN PEDIATRIC NEUROLOGY SOCIETY CONGRESS, 20 - 24 June 2017

2017

2017

Diagnosis rate of DNA fragment analysis for patients with SMA symptoms

ÖZDEMİR M., ARTAN S. , YARAR C. , DURAK ARAS B. , ÇARMAN K. B. , BAŞ H. , et al.

European Human Genetics Conference 2017, Copenhagen, Denmark, 27 - 30 May 2017

2017

2017

Yapısal kromozom anomalilerinin oluşum mekanizmaları

ARTAN S.

Erciyes Tıp Günleri, Turkey, 11 - 13 May 2017

2016

2016

Epigenetik

ARTAN S.

Gevher Nesibe Tıp Günleri 2016 & Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Turkey, 11 - 13 February 2016

2016

2016

Küçük Hücre Dışı Akciğer Kanserinde EGFR Gen Mutasyonları-Tek Merkez Deneyimi.

ÇİLİNGİR O. , ASLAN H., METİNTAŞ M. , DİNCER M. , DURAK ARAS B. , KUTLAY Ö., et al.

XII. Ulusal Tıbbi Genetik Kongresi, İzmir, Turkey, 05 November 2016, vol.2, pp.324 Sustainable Development

2016

2016

BECKWİTH WİEDEMANN SENDROMU. BİR OLGU

ASLAN H. , ÖZDEMİR M. , ÇİLİNGİR O., KOCAGİL S., KÜÇÜK H., DURAK ARAS B. , et al.

12. ULUSAL TIBBİ GENETİK KONGRESİ, Turkey, 5 - 09 October 2016

2016

2016

Beckwith Wiedemann Sendromu: Bir Olgu Sunumu.

ASLAN H., ÖZDEMİR M., ÇİLİNGİR O. , KOCAGİL S. , KÜÇÜK H., DURAK ARAS B. , et al.

XII. Ulusal Tıbbi Genetik Kongresi, İzmir, Turkey, 05 October 2016, vol.2, pp.330

2016

2016

Malign Melanom Olgularında Sitogenetik Çalışmalar.

DURAK ARAS B. , IŞIK S. , TÖRE T., CANAZ F. , YILMAZ H., ÖZDEMİR M., et al.

2. Ege Hematoloji Onkoloji Kongresi, İzmir, Turkey, 18 March 2016, pp.160

2016

2016

Malign Melanom Olgularında Moleküler Sitogenetik Çalışmalar

DURAK ARAS B. , IŞIK S. , töre t., CANAZ F. , yılmaz h., ÖZDEMİR M., et al.

2. Ege Hematoloji Onkoloji Kongresi, Turkey, 18 - 20 March 2016

2016

2016

KML ve ALL Tanılı Hastalarda BCR/ABL Füzyon Geni Mutasyonlarının Taranması.

ARSLAN S., ÇİLİNGİR O. , ASLAN H., AKAY O. M. , DURAK ARAS B. , ÖZDEMİR M., et al.

II. Hematolojik Genetik Sempozyumu, İzmir, Turkey, 24 February 2016, pp.35

2016

2016

MALİGN MELANOM OLGULARINDA SİTOGENETİK ÇALIŞMALAR

DURAK ARAS B. , IŞIK S. , TÖRE T., CANAZ F. , YILMAZ H. , ÖZDEMİR M. , et al.

2. EGE HEMATOLOJİ ONKOLOJİ KONGRESİ, Turkey, 18 - 20 March 2016

2016

2016

EGFR MUTATİONS İN TURKİSH NON-SMALL CELL LUNG CASES

ASLAN H. , ÇİLİNGİR O., DİNÇER M., DURAK ARAS B. , ASLAN S., HAZİYAVA K., et al.

2. EGE HEMATOLOJİ ONKOLOJİ KONGRESİ, Turkey, 18 - 20 March 2016

2016

2016

PATERNALLY INHERITED PROXIMAL 22Q11.2 DELETION IN TWOSIBLINGS

ÖZDEMİR M. , KÜÇÜK H., TEKİN A. N. , ERZURUMLUOĞLU E. , ASLAN H. , DURAK ARAS B. , et al.

Medical Genetics and Clinical Applications (with International Participation), Turkey, 11 - 13 February 2016

2016

2016

A CLİNİCAL REPORT OF AN İNFANT WİTH RUSSEL-SİLVER SENDROM

UZAY E., ASLAN H. , ÇİLİNGİR O., AYNACI S., ÖZDEMİR M. , DURAK ARAS B. , et al.

GEVHER NESİBE TIP GÜNLERİ, Turkey, 11 - 13 February 2016

2016

2016

A clinical report of an infant with Russel Silver Syndrome

Uzay E., ASLAN H. , ÇİLİNGİR O. , Aynacı S., ÖZDEMİR M. , DURAK ARAS B. , et al.

Gevher Nesibe Tıp Günleri 2016 & Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Turkey, 11 - 13 February 2016

2016

2016

A Clinical Report of an Infant with Russel Silver Sendrom

ÖZDEMİR M. , ÖNÜR H., TEKİN A. N. , ERZURUMLUOĞLU E. , ASLAN H. , DURAK ARAS B. , et al.

Gevher Nesibe Tıp Günleri 2016 Tıbbi Genetik ve Klinik Uygulamaları Kongresi, Turkey, 11 - 13 February 2016

2010

2010

Determination of MIRNAS’ Expressions in Bladder Cancer by Microarray Technology

Canturk K. M. , Artan S. , Can Y. S. C. , Öner K. S. , Özen M., Özdemir M., et al.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, İstanbul, Turkey, 1 - 05 November 2010 Sustainable Development

2015

2015

Study of In Situ Hybridization in Malignant Melanoma

DURAK ARAS B. , IŞIK S. , töre t., CANAZ F. , yılmaz h., ÖZDEMİR M., et al.

10th European Cytogenetics Conference, 4 - 07 July 2015

2014

2014

Miller-Dieker Sendromlu Bir Olgu Sunumu

GÜMÜŞ E., AYNACI S., ERZURUMLUOĞLU E. , ASLAN H., ÇİLİNGİR O. , ARTAN S.

11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014

2014

2014

Xq21.32-23 Duplikasyon Saptanan Olgu Sunumu

KÜÇÜK H., ASLAN H., ÇARMAN K. B. , ERZURUMLUOĞLU E., DÜZKALE N., ÖZDEMİR M., et al.

11.Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014

2014

2014

Xq21 32 23 Duplikasyonu Saptanan Olgu Sunumu

KÜÇÜK H., ASLAN H. , ÇARMAN K. B. , ERZURUMLUOĞLU E. , DÜZKALE N., ÖZDEMİR M. , et al.

11. Ulusal Tıbbi Genetik Kongresi, Turkey, 24 - 27 September 2014

2014

2014

De Novo 4p deletion and 4q duplication in a female dysmorphic child

ÖZDEMİR M., küçük h., ŞİMŞEK E. , ÇİLİNGİR O. , DÜZKALE N., DURAK ARAS B. , et al.

European Human Genetics Conference 2014, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.444

2014

2014

A rare case with De Novo Isochromosome 18p Syndrome

ARTAN S. , ERZURUMLUOĞLU E. , ÇARMAN K. B. , GÜMÜŞ E., ÖZDEMİR M., DURAK ARAS B. , et al.

European Human Genetics Conference 2014, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.448

2014

2014

Molecular cytogenetic diagnosis of melanocytic lesions

DURAK ARAS B. , IŞIK S. , CANAZ F. , ÖZDEMİR M., ÇİLİNGİR O. , ASLAN H., et al.

EUROPEAN JOURNAL OF HUMAN GENETİCS, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.470

2014

2014

Apoe Allele frequency in Alzheimer’s disease in turkish population

ÇİLİNGİR O. , özbabalık d., ASLAN H., ÖZDEMİR M., DURAK ARAS B. , özden k., et al.

European Human Genetics Conference 2014, 31 May - 03 June 2014, vol.22, pp.429

2014

2014

Sequence variants of PRNP gene in probable prion disease patiens

ASLAN H., özbabalık d., ÇİLİNGİR O. , DURAK ARAS B. , ÖZDEMİR M., KUTLAY Ö., et al.

European Human Genetics Conference 2014, 31 May - 03 June 2014, vol.22, pp.437

2014

2014

Investigation of the promoter hypermethylation in ILC and IDC of the breast

EROĞLU O., erci baysak m., DURAK ARAS B. , ARTAN S. , ÖZDEMİR M., ÇİLİNGİR O.

EUROPEAN JOURNAL OF HUMAN GENETICS 2014, Milan, Italy, 31 May - 03 June 2014, vol.22, pp.494

2014

2014

Molecular cytogenetics diagnosis of melanocytic lesions

DURAK ARAS B., IŞIK S. , CANAZ F. , ÖZDEMİR M., ÇİLİNGİR O., ASLAN H., et al.

European Human Genetics Conference, European Journal of Human Genetics, 31 May - 03 June 2014

2013

2013

Miyeloid Haalıklarda Nadir Görülen İzokromozom 5p Anomalisi

IŞIK S. , AKAY O. M. , ÖZDEMİR M., ANDIÇ N., ÇİLİNGİR O., GÜNDÜZ E. , et al.

39. Ulusal Hematoloji Kongresi, Turkey, 23 - 26 October 2013

2012

2012

Prognostic Genetic Markers in Glial Tumors

KARAKURT C., ÖZDEMİR M., ARSLANTAŞ A. , ÇİFTÇİ E., DURAK ARAS B. , ÇİLİNGİR O. , et al.

European Journal of Human Genetics, 23 - 26 June 2012

2010

2010

A Clinical Report Of A Prenatally Diagnosed inv Dup (15) Syndrome

DURAK ARAS B. , ÖZDEMİR M., TANIR H. M. , dikoğlu e., YÜKSEL Z., ERZURUMLUOĞLU E. , et al.

9 th National Medical Genetics Congress of turkısh Medical Genetics Society with İnternational Participation, Turkey, 1 - 05 December 2010, vol.78, pp.104-110

2010

2010

Analysis Of Copy Number Alterations Of EGFR, HER2 and TOP2A Genes in Gastric Carsinomas

saygılı h., ÖZDEMİR M., DURAK ARAS B. , ÖZNUR M., MÜSLÜMANOĞLU M. H. , ÇİLİNGİR O. , et al.

9th National Medical Genetics Congress of Turkısh Medical Genetics Society with International Participation, Turkey, 1 - 05 December 2010

2008

2008

Nadir Görülen Trizomi 18 ve Ektrodaktili Birlikteliği

BADEMCİ G., ASLAN H., ÖZDEMİR M., ÇİLİNGİR O. , GÖKMEYDAN E., DURAK ARAS B. , et al.

Uluslararası Katılımlı 8.Ulusal Tıbbi Genetik Kongresi, Çanakkale, Turkey, 6 - 09 May 2008

2009

2009

Effects of Fluoxetine in Peripheral Blood by Using Cytokinesis Blocked Micronucleus CBMN Technique

ÜSTÜNER D., ÖZDEMİR M. , ÜSTÜNER M. C. , DURAK B., ARTAN S.

3th Internatıonal Congress Of Molecular Medıcıne, İstanbul, Turkey, 5 - 08 May 2009, vol.61, pp.0-357

2008

2008

Kordosentez: 8 Yıllık Değerlendirme.

ÖZALP E., TANIR H. M. , ŞENER T., ARTAN S. , BADEMCİ G.

6. Ulusal Jinekoloji ve Obstetrik Kongresi 14-19 Mayıs 2008, Susesi Deluxe Otel, Antalya., Turkey, 14 - 19 May 2008

2008

2008

Nadir Görülen Trizomi 18 ve Ektrodaktili Birlikteliği

Bademci G., ASLAN H., ÖZDEMİR M., ÇİLİNGİR O. , gökmeydan e., DURAK ARAS B. , et al.

VIII. Ulusal Tıbbi Genetik Kongresi-Uluslararası Katılımlı, Turkey, 6 - 09 May 2008

2008

2008

Subtelomerik FISH Yöntemiyle Saptanan kriptik 14q Delesyonu ve 19p Duplikasyonlu Olgu

CANTURK K. M. , ÇİLİNGİR O. , ÖZDEMİR M., EMRE R., ALDEMİR Ö., DURAK ARAS B. , et al.

VIII. Ulusal Tıbbi Genetik Kongresi-Uluslararası Katılımlı, Turkey, 6 - 09 May 2008

2008

2008

Multipl Konjenital Anomalide Sui4q Monozomisi ve 8q Trizomisi Olan Olgu

gökmeydan e., SATILMIŞ E., ÖZDEMİR M., CANTURK K. M. , YARAR C. , ÇİLİNGİR O. , et al.

VIII. Ulusal Tıbbi Genetik Kongresi-Uluslararası katılımlı, Çanakkale, Turkey, 6 - 09 May 2008

2008

2008

Apoptosis patterns in eutopic endometrium and normal-looking endometrium from women with or without endometriosis

TANIR H. M. , HASSA H., KIRILMAZ S., TEKİN A. B. , ARTAN S. , DÜNDAR E.

AGES XVIII Annual Scientific Meeting WCE 2008 ArtScience of Endometriosis, Melbourne, Australia, 11-14 March, 2008, 11 - 14 March 2008 Sustainable Development

2008

2008

Apoptosis in the adhesions and normal-looking peritoneum in women with different stages of endometriosis

TANIR H. M. , HASSA H., KIRILMAZ S., TEKİN A. B. , ARTAN S. , DÜNDAR E.

AGES XVIII Annual Scientific Meeting WCE 2008 ArtScience of Endometriosis, Melbourne, Australia, 11-14 March, 2008., 11 - 14 March 2008 Sustainable Development

2007

2007

Genomic alterations in low grade anaplastic astrocytomas and glioblastomas

ARSLANTAŞ A. , ARTAN S. , ÖNER Ü., ÖZKARA E. , MÜSLÜMANOĞLU M. H. , DURMAZ R. , et al.

5. Meeting of Asian society of neurooncology, Turkey, 2 - 04 November 2007

2007

2007

Chromosome constitutions of primary infertile men and women

ÖZDEMİR M., DURAK ARAS B. , ÇİLİNGİR O. , Bademci G., CANTÜRK M., ARTAN S.

6th European Cytogenetics Conference, 7 - 10 July 2007, vol.15, pp.95 Sustainable Development

2006

2006

Detection of chromosomal aberrations in CLL and correlation with clinical staging.

Durak B. , Akay M. O. , Kaytaz B., Burul I., Ozdemir M., Artan S. , et al.

48th Annual Meeting of the American-Society-of-Hematology, Florida, United States Of America, 9 - 12 December 2006, vol.108 identifier

2006

2006

METHYLATION PROFİLES P16, RASSF1C, AND HMLH1 PROMOTER CPG ISLANDS IN BRAIN TUMORS

DURMAZ R. , ULUDAĞ A., ARTAN S. , ARSLANTAŞ A. , KARAKAŞ Z., ÇİLİNGİR O.

The 7th European Association NeuroOncology Congress, 14 - 17 September 2006, pp.34

2006

2006

Metilation profile of p16 RASSF1cand pmlh1 promoter CPG islands in brain tumors

DURMAZ R. , ULUDAĞ A., ARTAN S. , TEPELİ E., ARSLANTAŞ A. , KARAKAŞ Z., et al.

The European Assosiation for Neurooncology, Austria, 7 - 11 September 2006

2006

2006

Cordocentesis of 198 cases in a university clinic of Turkey during a 7-year period

ŞENER T., TANIR H. M. , DURAK ARAS B. , KAYA M., ÖGE T. , TEPELİ E., et al.

XX European Congress of Perinatal and Neonatal Medicine,24-27 May 2006 Prague, Czech Republic., 24 - 27 May 2006

2006

2006

Chorionic vilus sampling (CVS) of 68 cases: a retrospective analysis.

ŞENER T., TANIR H. M. , DURAK ARAS B. , KAYA M., ÖGE T. , TEPELİ E., et al.

XX European Congress of Perinatal and Neonatal Medicine,24-27 May 2006 Prague, Czech Republic, 24 - 27 May 2006

2006

2006

Evaluation of 894 amniocentesis in a 7- year period in an university hospital of mid-Anatolian region of Turkey.

ŞENER T., TANIR H. M. , DURAK ARAS B. , KAYA M., ÖGE T. , TEPELİ E., et al.

XX European Congress of Perinatal and Neonatal Medicine,24-27 May 2006 Prague, Czech Republic., 24 - 27 May 2006

2006

2006

Mal De Meladalı Olgularda ARS (COMPONENT B) Geninde Saptanan Yeni Mutasyonlar

MÜSLÜMANOĞLU M. H. , ÇİLİNGİR O. , SARAÇOĞLU Z. N. , DEMİR S., ürer s., Bademci G., et al.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006

2006

2006

Tekrarlayan Gebelik Kayıpları Olan Çiftlerde Subtelomerik FISH Analizi

DURAK ARAS B. , YEŞİL M., KAYTAZ B., ÇİLİNGİR O. , ÖZDEMİR M., MÜSLÜMANOĞLU M. H. , et al.

VII. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Kayseri, Turkey, 17 - 20 May 2006

2005

2005

A case of prenatal diagnosis of 3p deletion

ÇİLİNGİR O. , TEPELİ E., ÜSTÜNER D., ÖZDEMİR M., MÜSLÜMANOĞLU M. H. , DURAK ARAS B. , et al.

5th European Cytogenetics Conference, 4 - 07 June 2005, vol.13, pp.22

2005

2005

A case Prenatal Diagnosis of 3p Deletions

ÇİLİNGİR O., TEPELİ E., ÜSTÜNER D. , ÖZDEMİR M., MÜSLÜMANOĞLU M. H. , DURAK ARAS B. , et al.

5th European Cytogenetics Conference, Chromosome Research, 4 - 07 June 2005, vol.13, pp.22

2004

2004

Apoptotic markers from placentas of pregnancies associated with intrauterine growth retardation.

TANIR H. M. , ŞENER T., ARTAN S. , DEMİR S., MUTLU F. , TEKİN A. B. , et al.

The 5th World Congress On Controversies In Obstetrics and Gynecology Infertility, Las Vegas, USA, 3-6 June, 2004., 3 - 06 June 2004

2004

2004

Apoptotic markers from placentas of pregnancies associated with preeclampsia

TANIR H. M. , ŞENER T., ARTAN S. , KAYTAZ B., TEKİN A. N. , MUTLU F.

The 5th World Congress On Controversies In Obstetrics and Gynecology Infertility, Las Vegas, USA, 3-6 June, 2004., 3 - 06 June 2004

2004

2004

Programmed cell death (apoptosis) from placentas of pregnancies complicated by term and preterm premature rupture of membranes (tPPROM /pPROM)

TANIR H. M. , ŞENER T., ARTAN S. , KAYTAZ B., TEKİN A. B. , MUTLU F. , et al.

The 5th World Congress On Controversies In Obstetrics and Gynecology Infertility, Las Vegas, USA, 3-6 June, 2004., 3 - 06 June 2004

2004

2004

Fluoksetin in kromozomlar ve mitotik indeks üzerine in vitro ve in vivo etkilerinin incelenmesi

ÜSTÜNER D., ÖZDEMİR M. , EROL K. , DURAK ARAS B., TEPELİ E., ÜSTÜNER M. C. , et al.

6. Ulusal Prenatal Tanı ve Tıbbi Genetik Kongresi, Antalya, Turkey, 21 - 24 April 2004, pp.0-111

2001

2001

Copy Number Changes In Breast Tumors Preliminary Findings

ARTAN S. , ÖNER U., MÜSLÜMANOĞLU M. H. , IŞIKSOY S. , OZON H., YAŞAR B., et al.

10TH European Journal of Human Genetics, 15 - 19 May 2001, vol.9, pp.139

2000

2000

Results of cytogenetics and FISH studies in patients with chronicmyeloid leukemia

DURAK ARAS B. , Aslan V., GÜLBAŞ Z., ÜSTÜNER D., ÇİLİNGİR O. , ARTAN S. , et al.

10TH European Journal of Human Genetics, 27 - 30 May 2000, vol.8, pp.102

2000

2000

Results of Cytogenetics and FISH Studies in Patients with Chronic Myeloid Leukemia

Durak Aras B. , Aslan V., Gülbaş Z., Üstüner D. , Çilingir O. , Artan S. , et al.

European Journal of Human Genetics, Amsterdam, Netherlands, 27 - 30 May 2000, vol.8, pp.102

Books & Book Chapters

2021

2021

Genetics of frontotemporal dementia

ERZURUMLUOĞLU GÖKALP E. , ÖZBABALIK ADAPINAR B. D. , ARTAN S.

in: Factors Affecting Neurological Aging , Colin Martin, Victor Preedy, Rajkumar Rajendram, Editor, Academic Press , pp.3-16, 2021

2021

2021

Genetics of frontotemporal dementia

ERZURUMLUOĞLU GÖKALP E., ÖZBABALIK ADAPINAR B. D. , ARTAN S.

in: Factors Affecting Neurological Aging Genetics, Neurology, Behavior, and Diet, Colin Martin, Victor Preedy, Rajkumar Rajendram, Editor, Academic Press , pp.3-16, 2021

2020

2020

The Usage Of Genetıc Abnormalıtıes In Glıal Tumor Classıfıcatıon

KALKAN R., ARSLANTAŞ A. , ARTAN S.

in: Theory And Research ın Health Sciences, Prof. Dr. Cem EVEREKLİOĞLU, Editor, Gece Kitap, Ankara, pp.33-55, 2020

2020

2020

The Usage Of Genetıc Abnormalıtıes In Glıal Tumor Classıfıcatıon

KALKAN R., ARSLANTAŞ A. , ARTAN S.

in: Theory And Research ın Health Scıences, Prof. Dr. Cem EVEREKLİOĞLU, Editor, Gece Kitap, Ankara, pp.35-55, 2020

2016

2016

Tıbbi Genetik ve Klinik Uygulamaları

Artan S.

MGRUP MATBAACILIK KAYSERİ, Kayseri, 2016

2016

2016

Epigenetik

ARTAN S.

in: Tıbbi Genetik ve Klinik Uygulamaları, Dündar, Munis, Editor, MGRUP MATBAACILIK KAYSERİ, pp.177-224, 2016

Supported Projects

Memberships / Tasks in Scientific Organizations

2012 - Continues

2012 - Continues

European Cytogenetics Association

Executive Board Member



Citations

Total Citations (WOS): 595

h-index (WOS): 14