Sheng He

发表

The first two Chinese Myhre syndrome patients with the recurrent SMAD4 pathogenic variants: functional consequences and clinical diversity.

Yiping Shen, Ling Li, Hongyan Wang, 2019, Clinica chimica acta; international journal of clinical chemistry.

Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases

P. Agrawal, Shaoke Chen, S. Luo, 2019, Scientific Reports.

The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang β-thalassemia intermedia patients.

Ze Yang, Hongwei Wei, Shang Yi, 2017, Blood cells, molecules & diseases.

Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang β-Thalassemia Intermedia Patients

Guojian Li, Hongwei Wei, Sheng Yi, 2016, Hemoglobin.

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.

First Identification of the 3.5 kb Deletion (NC_000011.10: g.5224302-5227791del3490bp) on the β-Globin Gene Cluster in a Chinese Family

X. Qiu, Sheng He, Chenguang Zheng, 2018, Hemoglobin.

Performance of Cell-Free DNA Screening for Fetal Common Aneuploidies and Sex Chromosomal Abnormalities: A Prospective Study from a Less Developed Autonomous Region in Mainland China

T. Leung, Z. Dong, Hongwei Wei, 2021, Genes.

Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α0-Thalassemia in a Chinese Family

Shang Yi, Sheng He, Chenguang Zheng, 2017, Hemoglobin.

Geographical Clustering Analysis of Birth Defects in Guangxi

Hongwei Wei, X. Qiu, Sheng He, 2021 .

Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China.

Shaoke Chen, Shang Yi, Sheng He, 2017, Gene.

De Novo CSNK2B Mutations in Five Cases of Poirier–Bienvenu Neurodevelopmental Syndrome

Z. Qin, Shan Ou, Qinle Zhang, 2022, Frontiers in Neurology.

Molecular characterisation of Hb Akron [β52 (D3) Asp→Val] combined with thalassaemia in a Chinese family

Hongwei Wei, Shang Yi, Sheng He, 2022, Journal of Clinical Pathology.

Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in Guangxi

Xiangmin Xu, Jingsi Luo, Sheng He, 2022, International journal of laboratory hematology.

The Clinical Significance of the Spectrum of Interactions of the Rare IVS-II-5 G>C (HBB: c.315+5 G>C) Variation with Other β-Thalassemia Mutations in Southern China

Qiuying Huang, Sheng He, Xiaolin Yin, 2022, Mediterranean journal of hematology and infectious diseases.

Molecular characterization of α- and β-thalassemia in the Yulin region of Southern China.

X. Qiu, Shang Yi, Yi Liang, 2018, Gene.

Identification of a Novel 9.7 kb Deletion Causing α0-Thalassemia in Two Pregnant Women in Southern China

Xiangmin Xu, X. Qiu, Sheng He, 2018, Hemoglobin.

Characterization of Hb Bart’s Hydrops Fetalis Caused by – –SEA and a Large Novel α0-Thalassemia Deletion

Xiao-Xian Tian, X. Qiu, Sheng He, 2018, Hemoglobin.

The prevalence and molecular characterization of (δβ)0‐thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang population

Hongwei Wei, X. Qiu, Shang Yi, 2017, Journal of clinical laboratory analysis.

Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family

Guojian Li, Hongwei Wei, X. Qiu, 2016, Hemoglobin.

Hb H Hydrops Fetalis Syndrome Caused by Association of the − −SEA Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family

Xiao-Xian Tian, Shaoke Chen, Qiang Zhang, 2015, Hemoglobin.

Deletion and Hb Constant Spring (HBA2: c.427T4C) Mutation in a Chinese Family

Xiao-Xian Tian, Shaoke Chen, Qiang Zhang, 2015 .

Prevention and control of Hb Bart's disease in Guangxi Zhuang Autonomous Region, China.

Shaoke Chen, Qiang Zhang, Sheng He, 2014, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal diagnosis of β-thalassemia in Guangxi Zhuang Autonomous Region, China

Qiang Zhang, Sheng He, Chenguang Zheng, 2013, Archives of Gynecology and Obstetrics.

A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33.

Yiping Shen, Xuyun Hu, Shaoke Chen, 2016, Gene.

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

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

Safety and efficacy of thalidomide in patients with transfusion-dependent β-thalassemia: a randomized clinical trial

Guang-Biao Zhou, Saijuan Chen, Ken Huang, 2021, Signal Transduction and Targeted Therapy.

Molecular Characterization of α- and β-Thalassaemia Among Children From 1 to 10 Years of Age in Guangxi, A Multi-Ethnic Region in Southern China

Chaofan Zhou, Hongwei Wei, Shang Yi, 2021, Frontiers in Pediatrics.

First Detection of a Splice Acceptor Site β-Thalassemia Mutation: IVS-I-130 (HBB: c.93-1G > C) in a Chinese Patient

Shaoke Chen, Qiang Zhang, Sheng He, 2015, Hemoglobin.

Complex Interaction of Hb Q-Thailand with α0- and β0-Thalassemia in a Chinese Family

X. Qiu, Shang Yi, Sheng He, 2017, Hemoglobin.

A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA)

Guojian Li, Hongwei Wei, X. Qiu, 2017, Hemoglobin.

Genotypes of thalassemia in children: an analysis of 30 417 cases.

Dong-ming Li, Sheng He, 2021, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

de novo interstitial deletions at the 11q23.3-q24.2 region

Yiping Shen, Xuyun Hu, Shaoke Chen, 2016, Molecular Cytogenetics.

Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 cases

P. Agrawal, Shaoke Chen, S. Luo, 2019, Scientific Reports.

First Detection of a Splice Site β-Thalassemia Mutation, IVS-I-6 (T > C) (HBB: c.92 + 6T > C) in a Chinese Family

Qiang Zhang, Shang Yi, Sheng He, 2015, Hemoglobin.