Citations (15)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (6)
Sedat Yılmaz. (2019) The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Hemoglobin 43:3, pages 174-181.
Read now
Read now
Rakesh Kumar, Chandan Sagar, Dharmesh Sharma & Purnima Kishor. (2015) β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt. Hemoglobin 39:1, pages 1-8.
Read now
Read now
Emily Giannopoulou, Marina Bartsakoulia, Christina Tafrali, Alexandra Kourakli, Konstantinos Poulas, Eleana F. Stavrou, Adamantia Papachatzopoulou, Marianthi Georgitsi & George P. Patrinos. (2012) A Single Nucleotide Polymorphism in the HBBP1 Gene in the Human β-Globin Locus is Associated with a Mild β-Thalassemia Disease Phenotype. Hemoglobin 36:5, pages 433-445.
Read now
Read now
Ahmet Genc, Deniz Tastemir Korkmaz, Mehmet Buyukleyla & Murat Celiker. (2012) Prevalence and Molecular Analysis of β-Thalassemia in Adiyaman, Turkey. Hemoglobin 36:2, pages 131-138.
Read now
Read now
Christoforos Kalleas, Kostas Anagnostopoulos, Klio Sinopoulou, Evangelia Delaki, Dimitrios Margaritis, Georgios Bourikas, Constantinos Tsatalas, Alexandros Kortsaris & Ioannis Tentes. (2012) Phenotype and Genotype Frequency of β-Thalassemia and Sickle Cell Disease Carriers in Halkidiki, Northern Greece. Hemoglobin 36:1, pages 64-72.
Read now
Read now
Marianthi Georgitsi, Adamantia Papachatzopoulou, Emmanouella Linardaki, Vassilis Maroulis, Manoussos N. Papadakis & George P. Patrinos. (2011) First Report of Hb A2-NYU (HBD:c.39T>A) in the Hellenic Population. Hemoglobin 35:1, pages 91-95.
Read now
Read now
Articles from other publishers (9)
Seung Jun ChoiHanwool ChoKi-Seong EomJong Wook LeeYonggoo KimJihyang Lim. (2018) Effective sickle hemoglobin reduction by automated red cell exchange using Spectra Optia in three Emirati patients with sickle cell disease before allogeneic hematopoietic stem cell transplantation. Blood Research 53:4, pages 325.
Crossref
Crossref
Theodora Katsila & George P. Patrinos. 2018. Human Genome Informatics. Human Genome Informatics
91
107
.
Nikolaos Sousos, Despoina Adamidou, Philippos Klonizakis, Alexandra Agapidou, Stamatia Theodoridou, Georgios Spanos, Kyriakos Psarras, Evaggelia Vetsiou, Timoleon-Achilleas Vyzantiadis & Efthymia Vlachaki. (2017) Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence. Acta Haematologica 137:3, pages 175-182.
Crossref
Crossref
Christina Tafrali, Arsinoi Paizi, Joseph Borg, Milena Radmilovic, Marina Bartsakoulia, Emily Giannopoulou, Olga Giannakopoulou, Maja Stojiljkovic-Petrovic, Branka Zukic, Konstantinos Poulas, Eleana F Stavrou, Polyxeni Lambropoulou, Alexandra Kourakli, Alexander E Felice, Adamantia Papachatzopoulou, Sjaak Philipsen, Sonja Pavlovic, Marianthi Georgitsi & George P Patrinos. (2013)
Genomic variation in the
MAP3K5
gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy
. Pharmacogenomics 14:5, pages 469-483.
Crossref
Crossref
Vasilis Goulas, Alexandra Kourakli-Symeonidis & Charalambos Camoutsis. (2012) Comparative Effects of Three Iron Chelation Therapies on the Quality of Life of Greek Patients with Homozygous Transfusion-Dependent Beta-Thalassemia. ISRN Hematology 2012, pages 1-8.
Crossref
Crossref
George P. Patrinos, Timothy D. Smith, Heather Howard, Fahd Al-Mulla, Lotfi Chouchane, Andreas Hadjisavvas, Sherifa A. Hamed, Xi-Tao Li, Makia Marafie, Rajkumar S. Ramesar, Feliciano J. Ramos, Thomy de Ravel, Mona O. El-Ruby, Tilak Ram Shrestha, María-Jesús Sobrido, Ghazi Tadmouri, Martina Witsch-Baumgartner, Bin Alwi Zilfalil, Arleen D. Auerbach, Kevin Carpenter, Garry R. Cutting, Vu Chi Dung, Wayne Grody, Julia Hasler, Lynn Jorde, Jim Kaput, Milan Macek, Yoichi Matsubara, Carmancita Padilla, Helen Robinson, Augusto Rojas-Martinez, Graham R. Taylor, Mauno Vihinen, Tom Weber, John Burn, Ming Qi, Richard G. H. Cotton & David Rimoin. (2012) Human variome project country nodes: Documenting genetic information within a country. Human Mutation 33:11, pages 1513-1519.
Crossref
Crossref
Joseph Borg, Marios Phylactides, Marina Bartsakoulia, Christina Tafrali, Carsten Lederer, Alexander E Felice, Adamantia Papachatzopoulou, Alexandra Kourakli, Eleana F Stavrou, Soteroula Christou, Jun Hou, Sophia Karkabouna, Christina Lappa-Manakou, Zeliha Özgur, Wilfred van IJcken, Marieke von Lindern, Frank G Grosveld, Marianthi Georgitsi, Marina Kleanthous, Sjaak Philipsen & George P Patrinos. (2012)
KLF10
gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients
. Pharmacogenomics 13:13, pages 1487-1500.
Crossref
Crossref
Konstantinos Mitropoulos, Federico Innocenti, Ron H van Schaik, Alexander Lezhava, Giannis Tzimas, Panagoula Kollia, Milan Macek, Paolo Fortina & George P Patrinos. (2012) Institutional Profile: Golden Helix Institute of Biomedical Research: interdisciplinary research and educational activities in pharmacogenomics and personalized medicine. Pharmacogenomics 13:4, pages 387-392.
Crossref
Crossref
George P. Patrinos, Jumana Al Aama, Aida Al Aqeel, Fahd Al-Mulla, Joseph Borg, Andrew Devereux, Alex E. Felice, Finlay Macrae, Makia J. Marafie, Michael B. Petersen, Ming Qi, Rajkumar S. Ramesar, Joel Zlotogora & Richard G.H. Cotton. (2011) Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection. Human Mutation 32:1, pages 2-9.
Crossref
Crossref