Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adultsSystematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachGlobal genetic architecture of an erythroid quantitative trait locus, HMIP-2Experimental generation of SNP haplotype signatures in patients with sickle cell anaemiaGenetic determinants of haemolysis in sickle cell anaemia.Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.Selection of housekeeping genes for gene expression studies in human reticulocytes using real-time PCR.The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease.Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin.Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.Tailoring iron chelation by iron intake and serum ferritin: the prospective EPIC study of deferasirox in 1744 patients with transfusion-dependent anemias.Multiple loci are associated with white blood cell phenotypes.Sickle cell/β0-thalassemia associated with the 1393 bp deletion can be associated with a severe phenotype.Extracranial internal carotid arterial disease in children with sickle cell anemia.Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency.Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years.Neurokinin-B transcription in erythroid cells: direct activation by the hematopoietic transcription factor GATA-1.The molecular basis of β-thalassemia.Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.Beta-thalassaemia prototype of a single gene disorder with multiple phenotypes.A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.Spectral domain optical coherence tomography in patients with sickle cell disease.The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC diseaseGenetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancerResponse of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias.Genetic insights into the clinical diversity of beta thalassaemia.Association between hemolysis and albuminuria in adults with sickle cell anemiaPulmonary Haemodynamics in Sickle Cell Disease Are Driven Predominantly by a High-Output State Rather Than Elevated Pulmonary Vascular Resistance: A Prospective 3-Dimensional Echocardiography/Doppler Study.New gene functions in megakaryopoiesis and platelet formationIntergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.Genetic modifiers of beta-thalassemia.Adult patients with Eisenmenger syndrome report flying safely on commercial airlines.Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in TanzaniaMolecular therapies in beta-thalassaemia.Genetic regulation of fetal haemoglobin in inherited bone marrow failure syndromes.Genetic modifiers of the beta-haemoglobinopathies.A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function
P50
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P50
description
US NIH researcher, ORCID id # 0000-0002-9835-6501
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onderzoekster uit Maleisië
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name
Swee Lay Thein
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Swee Lay Thein
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Swee Lay Thein
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Swee Lay Thein
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type
label
Swee Lay Thein
@ast
Swee Lay Thein
@en
Swee Lay Thein
@es
Swee Lay Thein
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prefLabel
Swee Lay Thein
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Swee Lay Thein
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Swee Lay Thein
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Swee Lay Thein
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P106
P19
P21
P31
P373
Swee Lay Thein
P496
0000-0002-9835-6501
P569
1952-01-01T00:00:00Z
P7578
swee-lay-thein