Wanjun Zhou

发表

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

Ping Fang, Liang Li, Jian Zeng, 2015, BMC Musculoskeletal Disorders.

Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography.

Wanjun Zhou, Xiangmin Xu, W. Luo, 2012, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia

Yuanping Du, Zhuo Song, Wanjun Zhou, 2019, Advanced science.

Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping

Wanjun Zhou, Tizhen Yan, Xiangmin Xu, 2018, Journal of Human Genetics.

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.

Liang Li, Wanjun Zhou, Xiangmin Xu, 2013, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations.

Wanjun Zhou, Haiping Liu, Qiang Zhang, 2020, The Journal of molecular diagnostics : JMD.

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

Wanjun Zhou, Tizhen Yan, Xiang-min Xu, 2011, PloS one.

Molecular spectrum of thalassemia in tropical Hainan Island of southern China：high allele frequency with low health burden.

Wanjun Zhou, Min-Nung Huang, Yun Zou, 2022, Journal of genetics and genomics = Yi chuan xue bao.

One-step genotyping of α-thalassaemia by multiplex symmetric PCR melting curve

Wanjun Zhou, Jun He, Yang Li, 2022, Journal of clinical pathology.

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing

Wanjun Zhou, Tizhen Yan, Yuhua Ye, 2020, Molecular Genetics and Genomics.

[Rapid preimplantation genetic diagnosis of α-thalassemia SEA deletion with blastocyst cell whole genome amplification and short fragment Gap-PCR method].

Wanjun Zhou, Ping Yan, Yanhui Liu, 2018, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases

Wanjun Zhou, Qiang Zhang, X. Fan, 2017, Hemoglobin.

Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα

Wanjun Zhou, Qiang Zhang, X. Fan, 2017, Hemoglobin.

[Rapid detection of alpha-globin gene αααanti-3.7 triplets with droplet digital PCR].

Wanjun Zhou, Xiaoqian Gong, X. Yang, 2017, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects.

Wanjun Zhou, Li Lin, Xiang-min Xu, 2015, Blood cells, molecules & diseases.

Rapid genotyping of known mutations and polymorphisms in beta-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes.

Liang Li, Wanjun Zhou, Xiang-min Xu, 2008, Clinical biochemistry.

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

Liang Li, Jian Zeng, Wanjun Zhou, 2017, Clinical chemistry and laboratory medicine.

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Asan, Huanming Yang, Jian Wang, 2017, EBioMedicine.

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

J. Li, B. Tang, Wanjun Zhou, 2019, Brain : a journal of neurology.

A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction.

Jian-hui Jiang, Wanjun Zhou, Ze-yan Zhong, 2012, Analytical biochemistry.

Human STEAP3 mutations with no phenotypic red cell changes.

Wanjun Zhou, Li Lin, N. Mohandas, 2016, Blood.

Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay.

Liang Li, Wanjun Zhou, Xiang-min Xu, 2011, Blood cells, molecules & diseases.

Target-allele-specific probe single-base extension (TASP-SBE): a novel MALDI–TOF–MS strategy for multi-variants analysis and its application in simultaneous detection of α-/β-thalassemia mutations

Wanjun Zhou, Yang Li, Ziyan Li, 2023, Human Genetics.

Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay

Liang Li, Wanjun Zhou, Xiang-min Xu, 2013, Clinical chemistry and laboratory medicine.

A multiplex qPCR gene dosage assay for rapid genotyping and large-scale population screening for deletional α-thalassemia.

Wanjun Zhou, Xiangmin Xu, F. Xiong, 2013, The Journal of molecular diagnostics : JMD.

A splicing mutation in VPS4B causes dentin dysplasia I

Wanjun Zhou, Jinzhong Liu, Yuhua Ye, 2016, Journal of Medical Genetics.

Nanopore Third-Generation Sequencing for Comprehensive Analysis of Hemoglobinopathy Variants.

Wanjun Zhou, Wanqing Han, Weilun Huang, 2023, Clinical chemistry.

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing

Wanjun Zhou, Tizhen Yan, Yuhua Ye, 2020, Molecular Genetics and Genomics.