Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Diğer Dergilerde Yayınlanan Makaleler

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

BRCA MUTASYONLU HASTALARIN KLİNİKOPATOLOJİK ÖZELLİKLERİ

8. TÜRK TIBBİ ONKOLOJİ KONGRESİ, Antalya, Türkiye, 3 - 07 Kasım 2021, sa.187, ss.112 Sürdürülebilir Kalkınma

Importance of detection of ALK gene rearrengement with FISH method in non-small cell lung carcinoma patients

50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Danimarka, 27 - 30 Mayıs 2017, cilt.26, ss.962 identifier

NGS based ctDNA-liquide biopsy analysis in Turkish Cancer patients

5th Central-Eastern European Congresson Cell-Free Nucleic Acids, 21 - 22 Haziran 2018 Sürdürülebilir Kalkınma

Importance of structural abnormalities detected by array comparative genomic hybridızation in recurrent miscarriage: a retrospective study

25th European Congress of Obstetrics and Gynaecology 15th Congress of Turkish Society of Obstetrics and Gynaecology, Antalya, Türkiye, 17 - 21 Mayıs 2017

Importance Of Structural Abnormalities Detected By Array Comparative Genomic Hybridization In Recurrent Miscarriage: A Retrospective Study

25th European Congress of Obstetrics and Gynaecology15th Congress of Turkish Society of Obstetrics and Gynaecology, 17 - 21 Mayıs 2017

Mosaic Trisomy 9: A case study

11. Ulusal Tıbbi Genetik Kongresi, Türkiye, 24 Ağustos - 27 Eylül 2014

Olgu sunumu: 9p tetrazomisi

13. Ulusal Tıbbi biyoloji ve Genetik Kongresi, Türkiye, 27 - 30 Ekim 2013

Konuşma bozuklukları ve genetik

7. Ulusal dil ve konuşma bozuklukları kongresi, Türkiye, 5 - 07 Mayıs 2013

Comparative genomic hybridization array study in non-syndromic (primary) autism patients

24th Congress Meeting of European-College-of-Neuropsychopharmacology, Paris, Fransa, 3 - 07 Eylül 2011, cilt.21 identifier

Split hand food malformation associated with sensorineural hearig loss: a case study

Tıbbi Genetik Deneği 9. Ulusal Tıbbi Genetik Kongresi, Türkiye, 1 - 05 Aralık 2010

Detectıon of genetıc abnormalities by array comperative genomic hybridization for prenatal diagnosis

9th National Medical Genetics Congress of Turkish Medical Genetics, Türkiye, 1 - 05 Aralık 2010, cilt.78, ss.14

Detection of genetic abnormalities by array comparative genomic hybridization for prenatal diagnosis

9 th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 1 - 05 Aralık 2010, cilt.78, ss.14

Split Hand/Foot Malformation Associated with Sensorineural Hearing Loss: A case study.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 01 Ekim 2010

Complex Hemihyperplasia with Associated Cutis Marmorata: A case study.

9th National Medical Genetics Congress of Turkish Medical Genetics Society with International Participation, 01 Ekim 2010

Epilepsy DNA Bank Project in Istanbul University

Idiopathic Generalized Epilepsies (IGE): Developmental Aspects Bridging Basic Science and Clinical Research, Türkiye, 3 - 06 Ekim 2007

Determinationof E352K mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsy

Idiopathic Generalized Epilepsies (IGE): Developmental Aspects Bridging Basic Science and Clinical Research, Türkiye, 3 - 06 Ekim 2007

Predictive C3435T polymorphism in the MDR1 for carbamazepine plasma levels

6th European Congress on Epileptology, Vienna, Avusturya, 30 Mayıs - 03 Haziran 2004, cilt.45, ss.121 identifier

Evaluation of gabra1 gene in idiopathic epilepsies

6th European Congress on Epileptology, Vienna, Avusturya, 30 Mayıs - 03 Haziran 2004, cilt.45, ss.118-119 identifier

Autosomal recessive idiopathic epilepsy: linkage to chromosome 9q32-33

6th European Congress on Epileptology, Vienna, Avusturya, 30 Mayıs - 03 Haziran 2004, cilt.45, ss.123 identifier

Effect of methylenetetrahydrofolate reductase gene polymorphism on methotrexate toxicity after bone marrow transplantation

29th Annual Meeting of the European-Group-for-Blood-and-Marrow-Transplantation/19th Meeting of the EBMT-Nurses-Group/2nd Meeting of the EBMT-Data-Management-Group, İstanbul, Türkiye, 23 - 26 Mart 2003 identifier

The association of endothelial constitutive nitric oxide synthase gene polymorphism (ecNOS) in the Turkish population

19th Meeting of the International-Society-for-Hypertension/12th European-Society-of-Hypertension Meeting, PRAGUE, Çek Cumhuriyeti, 23 - 27 Haziran 2002, cilt.20 identifier

The association of endothelial dysfunction with endothelial constitutive nitric oxide synthase gene polymorphism in different patient populations

19th Meeting of the International-Society-for-Hypertension/12th European-Society-of-Hypertension Meeting, PRAGUE, Çek Cumhuriyeti, 23 - 27 Haziran 2002 identifier

Kitap & Kitap Bölümleri

Epigenetiği İnceleme Yöntemleri, Konsorsiyumlar/Veri Tabanları

Epigenetik, Yelda Tarkan Ergügen, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.1-137, 2023

Epilepsilerin genetik yönü

Epilepsi, İbrahim Bora, Naz Yeni, Candan Gürses, Editör, Nobel, İstanbul, ss.111-128, 2018

Çevresel Etkiler ve Genetik

Nörogenetik Özel Sayısı, Prof.Dr. Yeşim Parman, Editör, Türkiye Klinikleri Yayınevi, İstanbul, ss.16-25, 2011

Metrikler

Yayın

175

Atıf (WoS)

927

H-İndeks (WoS)

17

Atıf (Scopus)

1140

H-İndeks (Scopus)

19

Proje

9

Tez Danışmanlığı

1

Açık Erişim

6
BM Sürdürülebilir Kalkınma Amaçları