Associated Papers
Association between G6PD gene variants and adverse pregnancy outcomes.
Guo D et al.
Bmc Pregnancy and Childbirth, 2026
Ethnic Variation in G6PD Deficiency: Epidemiology and Mutation Spectrum in Southern China's Multiethnic Hub, Nanning.
Yang J et al.
Clinical Genetics, 2026
Rapid detection of G6PD deficiency SNPs using a novel amplicon-based minion sequencing assay.
Tacoli C et al.
Scientific Reports, 2025
Screening, genetic analysis, and clinical transfusion implications of thalassaemia and glucose-6-phosphate dehydrogenase deficiency in blood donors.
Chen ZX et al.
Transfusion Medicine (oxford, England), 2025
Establishment of reference interval (RI) for G6PD/6PGD ratio in adults from Yangjiang, China.
Wang Z et al.
Annals of Hematology, 2025
Rapid detection of G6PD deficiency SNPs using a novel amplicon-based MinION Sequencing Assay.
Tacoli C et al.
Biorxiv : the Preprint Server for Biology, 2025
Screening results and mutation frequency analysis of G6PD deficiency in 1,291,274 newborns in Huizhou, China: a twenty-year experience.
Zhang Z et al.
Annals of Hematology, 2024
Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China.
Xu JX et al.
World Journal of Clinical Cases, 2023
Etiology analysis and G6PD deficiency for term infants with jaundice in Yangjiang of western Guangdong.
Yang YK et al.
Frontiers in Pediatrics, 2023
Molecular epidemiological investigation of G6PD deficiency in Yangjiang region, western Guangdong province.
Liang HF et al.
Frontiers in Genetics, 2023
Glucose-6-phosphate dehydrogenase deficiency screening and gene analysis in blood donors of Guangdong province.
Liang HF et al.
Hematology (amsterdam, Netherlands), 2022
Identification of a Novel Hb H Disease with Glucose-6-Phosphate Dehydrogenase Deficiency Using Whole Genome Sequencing.
Ren ZM et al.
Hemoglobin, 2022
Clinical pharmacogenetic analysis in 5,001 individuals with diagnostic Exome Sequencing data.
Lanillos J et al.
Npj Genomic Medicine, 2022
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in neonates in Wuhan: Description of four novel variants.
Shen S et al.
Frontiers in Genetics, 2022
Simultaneous detection of G6PD mutations using SNPscan in a multiethnic minority area of Southwestern China.
Wei H et al.
Frontiers in Genetics, 2022
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
Xu JX et al.
Bmc Pediatrics, 2021
Epidemiology, evolutionary origin, and malaria-induced positive selection effects of G6PD-deficient alleles in Chinese populations.
Zheng Y et al.
Molecular Genetics & Genomic Medicine, 2020
High resolution melting curve analysis enables rapid and reliable detection of G6PD variants in heterozygous females.
Islam MT et al.
Bmc Genetics, 2018
Molecular newborn screening of four genetic diseases in Guizhou Province of South China.
Huang S et al.
Gene, 2016
Large cohort screening of G6PD deficiency and the mutational spectrum in the Dongguan District in Southern China.
Peng Q et al.
Plos One, 2015
Glucose-6-phosphate dehydrogenase--beyond the realm of red cell biology.
Ho HY et al.
Free Radical Research, 2014
Spatial distribution of G6PD deficiency variants across malaria-endemic regions.
Howes RE et al.
Malaria Journal, 2013
A reverse dot blot assay for the expanded screening of eleven Chinese G6PD mutations.
Lu X et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2013
G6PD deficiency prevalence and estimates of affected populations in malaria endemic countries: a geostatistical model-based map.
Howes RE et al.
Plos Medicine, 2012
Rapid and reliable detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations in Han Chinese using high-resolution melting analysis.
Yan JB et al.
The Journal of Molecular Diagnostics : Jmd, 2010
The first case of a class I glucose-6-phosphate dehydrogenase deficiency, G6PD Santiago de Cuba (1339 G > A), in a Chinese population as found in a survey for G6PD deficiency in northeastern and central China.
Wang J et al.
Acta Medica Okayama, 2010
Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population.
Jiang W et al.
Human Genetics, 2006
[Identification of G6PD gene variants from Hakka population in Guangdong province].
Yu GL et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2004
A novel mis-sense mutation (G1381A) in the G6PD gene identified in a Chinese man.
Ren X et al.
Chinese Medical Journal, 2001
[The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province].
Yang Z et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2000
[Detection of R277Q mutation of SRD5alpha2 gene by amplification refractory mutation system].
Guang W et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 1999
Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system.
Du CS et al.
Human Heredity, 1999
[Detection of three common G6PD gene point mutations in Guangdong province by using ARMS].
Du C et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 1999