Ergül Berber

Istanbul Arel University — Turkey

Medicine · Health Sciences

10h-index344citations30works0.02yr avg
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Research Topics

Platelet Disorders and Treatments(13), Hemophilia Treatment and Research(8), Blood Coagulation and Thrombosis Mechanisms(6), Blood groups and transfusion(6), Coagulation, Bradykinin, Polyphosphates, and Angioedema(6)

Publications29 total

Gene therapy in haemophilia: literature review and regional perspectives for Turkey
Therapeutic Advances in Hematology·2022· 10 citedOpen Access
Whole exome sequencing reveals novel candidate gene variants for MODY
Clinica Chimica Acta·2020· 9 cited
Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation
Cumhuriyet Tıp Dergisi/Cumhuriyet Üniversitesi Tıp Fakültesi dergisi·2018
Exploring the role of miRNAs in the diagnosis of MODY3
TURKISH JOURNAL OF MEDICAL SCIENCES·2018· 5 citedOpen Access
A correlation between the genotype and clinical course in hemophilia B patients
2018
Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p.M771I, p.L881R and p.P1413L.
PubMed·2017· 4 citedOpen Access
Regional hemophilia project in Turkey
2016
Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p.Cys398Tyr mutation.
PubMed·2014· 2 citedOpen Access
HNF1A gene analysis in the MODY suspected Turkish patients
2013
GCK mutations are not common cause for MODY2 and gestational diabetes in Turkey
2013
Functional Characterization of the Type 1 VWD Candidate VWF Gene Variants: P.M771I, p.L881R, p.P1413L, and p.Q1475X
Blood·2012
A Common VWF Exon 28 Haplotype in the Turkish Population
Clinical and Applied Thrombosis/Hemostasis·2012· 7 citedOpen Access
Front & Back Matter
Acta Haematologica·2012
The Molecular Genetics of von Willebrand Disease
Turkish Journal of Hematology·2012· 13 citedOpen Access
The Molecular Genetics of von Willebrand Disease Von Willebrand Hastaliği'nin Moleküler Genetiği
2012
Higher Expression of the Novel Gene Upregulated Gene 4 in Two Acute Lymphoblastic Leukemia Patients with Poor Prednisolone Response
Acta Haematologica·2012· 1 cited
Türk mody hastalarında GCK ve HNF1A gen analizi
2012
Molecular Characterization of FXI Deficiency
Clinical and Applied Thrombosis/Hemostasis·2010· 16 cited
Characterization of the genetic basis of FXI deficiency in two Turkish patients
Haemophilia·2009· 6 citedOpen Access
Presence of a Common Haplotype in the Turkish VWD Patients.
Blood·2009
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Frequent Co-authors

David Lillicrap(8), Christine Hough(5), S. Hande Çağlayan(4), Colleen Notley(3), Christine Brown(3), Bülent Zülfikar(3), Özlem Yalçın Çapan(3), Lee A. O’Brien(2), Cherie Cameron(2), Carol Hegadorn(2), Paula James(2), C. Brown(2), Nejat Akar(2), Hande Çağlayan(2), Kaan Kavaklı(2), Neslihan Aydın(2), Temel Yılmaz(2), Funda Pehlevan(2), Mehmet Akın(2), Kaan Kavaklı(2)