Associated Papers
Full-length haplotype reconstruction of CD36 by long-read sequencing: uncovers a novel structural variant.
Liang S et al.
Bmc Genomics, 2026
Genetic spectrum analysis of high-carrier-frequency monogenic disorders based on whole-exome sequencing in the Chinese general population.
Hao N et al.
Human Genomics, 2026
Comparative genetic analysis of blood and semen samples in sperm donors from Hunan, China.
Huang C et al.
Annals of Medicine, 2025
Two novel mutations (c.878T>C and c.1316delA) in CD36 alleles lead to CD36 antigen deficiency.
He H et al.
Transfusion, 2025
Development and clinical application of a low-cost high-resolution melting curve assay for CD36 gene variant screening in a chinese population.
Liu Z et al.
Molecular Biology Reports, 2025
Haplotypes analysis reveals the genetic basis of type I CD36 deficiency.
Xia W et al.
Scientific Reports, 2024
Genetic disease risks of under-represented founder populations in New York City.
Isshiki M et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
The polymorphism analysis for CD36 among platelet donors.
Lyu Q et al.
Scientific Reports, 2024
High-Throughput CD36 Phenotyping on Human Platelets Based on Sandwich ELISA and Mutant Gene Analysis.
He H et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie, 2024
Frequency and molecular basis of CD36 deficiency among platelet donors in Kunming, China.
Lyu Q et al.
Platelets, 2023
Primary lymphoma of bone in children: Three case reports and literature review.
Zhang M et al.
Pediatric Discovery, 2023
Application of circulating tumour DNA in terms of prognosis prediction in Chinese follicular lymphoma patients.
Zhao M et al.
Frontiers in Genetics, 2023
Analysis of clinically relevant variants from ancestrally diverse Asian genomes.
Chan SH et al.
Nature Communications, 2022
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.
Cong PK et al.
Nature Communications, 2022
Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.
Maegawa T et al.
Plos One, 2022
Platelet CD36 deficiency is present in 2.6% of Arabian individuals and can cause NAIT and platelet refractoriness.
Flesch BK et al.
Transfusion, 2021
New molecular basis associated with CD36-negative phenotype in the sub-Saharan African population.
Le Toriellec E et al.
Transfusion, 2020
Reinterpretation of common pathogenic variants in ClinVar revealed a high proportion of downgrades.
Xiang J et al.
Scientific Reports, 2020
Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.
Sha Y et al.
Bmc Medical Genetics, 2019
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Chen X et al.
Bmc Medical Genetics, 2019
Fetal/neonatal alloimmune thrombocytopenia due to anti-CD36 antibodies: antibody evaluations by CD36-transfected cell lines.
Lin M et al.
Transfusion, 2018