Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Screening, genetic analysis, and clinical transfusion implications of thalassaemia and glucose-6-phosphate dehydrogenase deficiency in blood donors.

Transfusion medicine (Oxford, England) - 1 Feb 2026

Chen Zhi-Xiao, Chen Bao-Ying, Liu Rong-Huo, Huang Jian-Cheng, Mo Jia-Min, Mai Zhen-Yuan, Zeng Yan-Qing, Huang Yu-Chan, Cao Yan-Bin, Lai Bai-Ru, Xu Wei-Feng, Yang Li-Ye

Abstract excerpt

BACKGROUND: This study aims to explore the prevalence, genotypes, and clinical applications of thalassaemia and glucose-6-phosphate dehydrogenase (G6PD) deficiency among blood donors, offering scientific support for the safety of clinical blood transfusions. MATERIALS AND METHODS: Haematological and G6PD enzyme activity tests were conducted on 1028 blood donors from one coastal city in southern China. A detailed...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to alpha-Thalassemia
Share to beta-Thalassemia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Blood Donors

Share to Blood Transfusion

Share to Glucosephosphate Dehydrogenase

Share to Glucosephosphate Dehydrogenase Deficiency

Share to Prevalence

Share to Thalassemia

Source

Identifiers

PMID: 41229149
DOI: 10.1111/tme.70018

Genes

G6PD
SEA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Screening, genetic analysis, and clinical transfusion implications of thalassaemia and glucose-6-phosphate dehydrogenase deficiency in blood donors.PMID 41229149Read ↗

Screening, genotyping and haematological analysis of glucose-6-phosphate dehydrogenase deficiency in the blood donors of Wuxi City, China.Semantic proximity Read ↗

High prevalence of G6PD mutations in blood donors from the Brazilian Amazon region.Semantic proximity Read ↗

Glucose-6-phosphate dehydrogenase deficiency in Italian blood donors: prevalence and molecular defect characterization.Semantic proximity Read ↗

Mutation spectrum and erythrocyte indices characterisation of α-thalassaemia and β-thalassaemia in Sichuan women in China: a thalassaemia screening survey of 42 155 women.Semantic proximity Read ↗

Analysis of genetic test results in 378 patients suspected of thalassaemia.Semantic proximity Read ↗

Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemiaSemantic proximity Read ↗

Evaluation of the phenotypic test and genetic analysis in the detection of glucose-6-phosphate dehydrogenase deficiencySemantic proximity Read ↗

Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand.Semantic proximity Read ↗

Clinical experience using peripheral blood parameters to analyse the mutation type of thalassemia carriers in pregnant women.Semantic proximity Read ↗

The prevalence and spectrum of alpha and beta thalassaemia in Guangdong Province: implications for the future health burden and population screening.Semantic proximity Read ↗

Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia.Semantic proximity Read ↗

Gene Mutation Spectrum among Alpha-Thalassaemia Patients in Northeast Peninsular MalaysiaSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.