Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler
Diğer Dergilerde Yayınlanan Makaleler
Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

Ethical, Legal, and Social ImplicaKons (ELSI) of Biobanking in Turkey

ETHICAL, LEGAL AND SOCIETAL INSIGHTS & OUTLOOK FOR BIOBANKS AND MEDICAL RESEARCH, Lyon, Fransa, 4 - 07 Haziran 2024

Hereditary hemolytic anemia cases in Turkey by whole exome sequencing

EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects, Budapest, Macaristan, 3 - 04 Kasım 2023

Characterization of Hereditary Hemolytic Anemia cases in Turkey by Whole Exome Sequencing

EHA-SWG Scientific Meeting on Red Cell and Iron Metabolism Defects: From Basic Science to Clinical Case Application, Budapest, Macaristan, 12 - 14 Ekim 2023

Lenfoma ve İmmünyetmezliğe Sahip İndeks Olguda Somatik ve Germline Varyasyonların Ekzom Dizi Analizi ile Analizi

XIII. AZİZ SANCAR DENEYSEL TIP ARAŞTIRMA ENSTİTÜSÜ GÜNLERİ Yaşam Bilimlerinde Omik Teknolojileri: Genomdan Tedaviye, İstanbul, Türkiye, 21 - 22 Aralık 2021, cilt.12

CD70 mutations in a family with affected CID indivuduals

Highlights of Bertinoro, Predisposition to hereditary Leukemia and Lymphoma Training School, 11 - 12 Ekim 2019

A translational perspective on diffuse large B-cell lymphoma

9th International Eurasian Hematology Oncology Congress (EHOC), İstanbul, Türkiye, 17 - 20 Ekim 2018, cilt.73 identifier

Comprehensive analysis of transcriptomic portrait of T-cell acute lymphoblastic leukemia by RNA sequencing

9th International Eurasian Hematology Oncology Congress (EHOC), İstanbul, Türkiye, 17 - 20 Ekim 2018, cilt.73 identifier

Nörogenetik verinin analizi: İnteraktif eğitim ve uygulama- ACMG Klavuzu

Nadir Görülen Hastalıklar Sempozyumu ve Nörogenetik Kursu, Türkiye, 31 Mayıs 2018

AccessDistribution of Biospecimens: Practical Issues

International Workshop on Biobanking for Rare Diseases, 2 - 03 Mayıs 2018

IKZF1 Deletions at Diagnose and Relapse of Childhood B-ALL

59th Annual Meeting of the American-Society-of-Hematology (ASH), Georgia, Amerika Birleşik Devletleri, 9 - 12 Aralık 2017, cilt.130 identifier

PTEN AND AKT1 GENE VARIATIONS IN CHILDHOODT-ALL PATIENTS

6th International Congress onLeukemia – Lymphoma – Myeloma, 11 - 13 Mayıs 2017

Biyobankalarda Pre Analitik Süreçler ve Standartlar

Biyobankada Laboratuvar Süreçleri Kursu, Türkiye, 27 Mayıs - 28 Haziran 2016

Pathway Analizi Enrichment Analizi

Biyobankalamada Veri Analizi Yöntemleri Kursu, Türkiye, 30 - 31 Mayıs 2016

Geleceğe Yatırım BİYOBANKA Projesi kapsamında Biyobankalama Protokolleri

Biyobankada Protokol ve Kalite Çalıştayı, Türkiye, 06 Nisan 2016

Hematolojik malignitelerde genetik belirteçler

Ulusal Çocuk Genetik Sempozyumu, Türkiye, 22 - 24 Ekim 2015

Downregulation of SnoN SKIL gene in T ALL

European Society of Human Genetics Meeting, Glasgow, İngiltere, 6 - 09 Haziran 2015

Pathways associated with relapse and high risk in childhood acute lymphoblastic leukemia

European Society of Human Genetics, Glasgow, Birleşik Krallık, 6 - 09 Haziran 2015, ss.445

Pathways associated with relapse and high risk in childhood ALL

European Society of Human Genetics Meeting, Glasgow, İngiltere, 6 - 09 Haziran 2015

Downregulation of Sno SKIL gene in T ALL

5th International Leukemia Lymphoma Myeloma Meeting, İstanbul, Türkiye, 21 - 23 Mayıs 2015

Nüks Akut Lenfoblastik Lösemi Hastalarında Tüm Genom Analizleri

DETAE Genç Araştırıcılar Toplantısı, Türkiye, 19 - 20 Ocak 2015

Epigenetic profile of early relapsed Childhood ALL

40 Ulusal Hematoloji Kongresi, Antalya, Türkiye, 22 - 25 Ekim 2014, ss.20

Next Generation Sequencing Of The BCR ABL1 Domain May Be Beneficial In Decision Makin

55th Annual Meeting of the American-Society-of-Hematology, New Orleans, Amerika Birleşik Devletleri, 7 - 10 Aralık 2013

Normalization methods and analysis packages for 450k data analysis

High-Throughput Methylome Analysis & Its Impact on Human Health and Disease Workshop, İstanbul, Türkiye, 31 Mayıs 2013

Elevated Trib2 with Notch1 activation in pediatric adult T ALL

BRITISH JOURNAL OF HAEMATOLOGY, Glasgow, İngiltere, 2 - 04 Aralık 2012, cilt.157, ss.6

Mutations in AXIN1, APC and B-catenin Genes in T-cell Acute Leukemia Patients

T-cell Acute Lymphoblastic Leukemia (T-ALL) Meets Normal T-cell Development, Mandelieu, Fransa, 7 - 09 Mayıs 2010, ss.28

WNT pathway mutations in acute leukemia patients

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.55 identifier

WNT5A gene expression and promoter methylation in acute leukemia patients

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.55 identifier

Increased level of B-catenin mRNA and mutational alterations in APC gene are present in acute leukemia

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.62 identifier

Methylation status of the wnt antagonist DICKKOPF-1 gene in acute leukemias

12th Congress of the European-Hematology-Association, Vienna, Avusturya, 7 - 10 Haziran 2007, cilt.92, ss.403 identifier

Different activation of WNT signaling pathway in B-cell and T-cell acute leukemias.

48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108 identifier

Upregulation of FZ5 results in abberant expression of beta-catenin and LEF/TCF complex in acute myeloid leukemia.

48th Annual Meeting of the American-Society-of-Hematology, Florida, Amerika Birleşik Devletleri, 9 - 12 Aralık 2006, cilt.108 identifier
Kitap & Kitap Bölümleri

The Human Genome and Inheritance: Key Concepts

Pathological Basis of Oral and Maxillofacial Diseases, Khurram Syed Ali, Kujan Omar, Prabhu Soorebettu, SOLUK TEKKEŞİN MERVA, Editör, Willey, ss.227-244, 2024

Germline Predisposition to Childhood Cancers

Cancer: From Genomics to Pharmaceutics, KARAKAŞ ZEYNEP, ERDAL MERYEM SEDEF, SAYİTOĞLU MÜGE, SOLUK TEKKEŞİN MERVA, Editör, Istanbul University Press, ss.147-175, 2024

EPİGENETİK HAFIZA VE EPİGENETİK KALITIM

Epigenetik, Hikmet AKGÜL, Editör, Türkiye Klinikleri Tıbbi Genetik, ss.69-74, 2023

Biyobankalar

Tıp Bilişimi, Nilgün Bozbuğa,Sevinç Gülseçen, Editör, Istanbul University, İstanbul, ss.159-169, 2021

Genetikte Temel Kavramlar

”Cerebral Palsy” ve Genetik, Hande Akçakaya, Uğur Özbek, Editör, Boyut, ss.1-8, 2019

GENETİKTE TEMEL KAVRAMLAR

Genetik, Güner Hayri Özsan, Müge Sayitoğlu, Editör, Galenos, ss.1-8, 2019

AKUT LENFOBLASTİK LÖSEMİ GENETİĞİ

Genetik, Güner Hayri Özsan, Müge Sayitoğlu, Editör, Galenos, ss.78-90, 2019

Biyobankalamada Protokol ve Kalite Kılavuzu

İstanbul Medikal Sağlık ve Yayıncılık Hiz. Tic. Ltd. Şti., İstanbul, 2017

Epigenetics, Inflammation and Inflammation Associated Diseases

Epigenetics, Yıldız Dinçer, Editör, NOVA Publications , New York, ss.175-211, 2016
Metrikler

Yayın

149

Atıf (WoS)

279

H-İndeks (WoS)

8

Atıf (Scopus)

290

H-İndeks (Scopus)

9

Proje

19

Tez Danışmanlığı

1

Açık Erişim

10
BM Sürdürülebilir Kalkınma Amaçları