PubRank

Pranee Winichagoon

Author PubWeight™ 24.55‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. Hum Genet 2010 1.75
2 Haemoglobinopathies in southeast Asia. Indian J Med Res 2011 1.34
3 A scoring system for the classification of beta-thalassemia/Hb E disease severity. Am J Hematol 2008 1.04
4 Thalassemia and abnormal hemoglobin. Int J Hematol 2002 1.04
5 Simple method for screening of alpha-thalassaemia 1 carriers. Int J Hematol 2009 0.97
6 Hydroxyurea responses and fetal hemoglobin induction in beta-thalassemia/HbE patients' peripheral blood erythroid cell culture. Ann Hematol 2006 0.90
7 Molecular analysis of beta-thalassemia in South Vietnam. Am J Hematol 2002 0.90
8 Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study. BMC Med Genet 2010 0.84
9 Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations. Hemoglobin 2007 0.84
10 Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease. Ann Hematol 2007 0.83
11 In vivo and in vitro studies of fetal hemoglobin induction by hydroxyurea in beta-thalassemia/hemoglobin E patients. Exp Hematol 2005 0.83
12 Association of SNP in exon 1 of HBS1L with hemoglobin F level in beta0-thalassemia/hemoglobin E. Int J Hematol 2008 0.83
13 Heart rate variability in beta-thalassemic mice. Int J Cardiol 2006 0.82
14 Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice. Haematologica 2009 0.81
15 Expression of microRNA-451 in normal and thalassemic erythropoiesis. Ann Hematol 2010 0.81
16 Genetic analysis of candidate modifier polymorphisms in Hb E-beta 0-thalassemia patients. Ann N Y Acad Sci 2005 0.80
17 Detection and haplotype differentiation of Southeast Asian alpha-thalassemia using polymerase chain reaction and a piezoelectric biosensor immobilized with a single oligonucleotide probe. Transl Res 2008 0.80
18 Rapid diagnosis of alpha-thalassemia by melting curve analysis. J Mol Diagn 2010 0.79
19 Molecular analysis of globin gene expression in different thalassaemia disorders: individual variation of β(E) pre-mRNA splicing determine disease severity. Br J Haematol 2011 0.79
20 Quantitative analysis of Hb Bart's in cord blood by capillary electrophoresis system. Ann Hematol 2010 0.78
21 Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, α2) and Paksé (codon 142, TAA>TAT, α2) mutations in Thailand. Hemoglobin 2010 0.78
22 Rescued mice with Hb E transgene-developed red cell changes similar to human beta-thalassemia/HbE disease. Ann N Y Acad Sci 2005 0.78
23 Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in Thailand. Hemoglobin 2004 0.77
24 The signaling pathways of erythropoietin and interferon-gamma differ in preventing the apoptosis of mature erythroid progenitor cells. Int J Hematol 2003 0.77
25 Cardiomyocyte ultrastructural damage in β-thalassaemic mice. Int J Exp Pathol 2013 0.76
26 Role of interleukin-3 and signaling pathways on beta-thalassemia/HbE erythroid progenitor cell in culture. Southeast Asian J Trop Med Public Health 2007 0.76
27 Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect. Hemoglobin 2002 0.76
28 A reduced curcuminoid analog as a novel inducer of fetal hemoglobin. Ann Hematol 2012 0.75
29 Hb Kodaira II [beta146(HC3)His --> Gln] detected in Thailand. Hemoglobin 2003 0.75
30 Chicken egg yolk antibodies specific for the gamma chain of human hemoglobin for diagnosis of thalassemia. Int J Hematol 2006 0.75
31 Double heterozygosity for Hb Pyrgos [beta83(EF7)Gly-->Asp] and Hb E [beta26(B8)Glu-->Lys] found in association with alpha-thalassemia. Hemoglobin 2002 0.75
32 Molecular mechanism of high hemoglobin F production in Southeast Asian-type hereditary persistence of fetal hemoglobin. Int J Hematol 2006 0.75
33 Hb Kurosaki [alpha7(A5)Lys -->Glu (AAG --> GAG)]: an alpha2-globin gene mutation found in Thailand. Hemoglobin 2005 0.75
34 Molecular mechanism of beta-thalassaemia caused by 22-bp duplication. Ann Hematol 2008 0.75
35 Expression of betaE and gamma-globin genes in infants heterozygous for hemoglobin E and double heterozygous for hemoglobin E and alpha-thalassemia. Haematologica 2007 0.75
36 Characterization of a novel deletion causing (deltabeta)0-thalassemia in a Thai family. Am J Hematol 2007 0.75
37 Effect of human beta-globin bacterial artificial chromosome transgenesis on embryo cryopreservation in mouse models. Reprod Fertil Dev 2010 0.75