Shiping Chen

Shenzhen, China

Last Updated: 09/26/2026

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Found 20 publications

An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletion.

An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletion.

Journal: Annals of hematology

Published: November 05, 2024

High efficiency of thalassemia prevention by next-generation sequencing: a real-world cohort study in two centers of China.

High efficiency of thalassemia prevention by next-generation sequencing: a real-world cohort study in two centers of China.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: June 18, 2024

A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient.

A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient.

Journal: Hemoglobin

Published: May 01, 2024

Prevalence and genetic analysis of triplicated α-globin gene in Ganzhou region using high-throughput sequencing.

Prevalence and genetic analysis of triplicated α-globin gene in Ganzhou region using high-throughput sequencing.

Journal: Frontiers in genetics

Published: July 27, 2023

Carrier rate of thalassemia among 25,910 high school students in Shaoguan area, China.

Carrier rate of thalassemia among 25,910 high school students in Shaoguan area, China.

Journal: Journal of medical screening

Published: July 13, 2023

Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China.

Novel Promoter Mutation (HBB:C.-139_-138del) Associated with β-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China.

Journal: Hemoglobin

Published: March 03, 2023

Characterization of a novel HBB:c.194dup variant of the β-globin gene combined with six alpha genes.

Characterization of a novel HBB:c.194dup variant of the β-globin gene combined with six alpha genes.

Journal: The Journal of international medical research

Published: May 13, 2022

A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family.

A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family.

Journal: Hemoglobin

Published: June 04, 2021

Report of Two Novel Thalassemia Variants, HBB: c.181delG and HBA1: c.121_126delAAGACC, in Chinese Individuals.

Report of Two Novel Thalassemia Variants, HBB: c.181delG and HBA1: c.121_126delAAGACC, in Chinese Individuals.

Journal: Hemoglobin

Published: April 01, 2021

Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals.

Identification of Two Novel Thalassemia Variants, HBA1: c.263delA and HBA2: c.376dupC, in Chinese Individuals.

Journal: Hemoglobin

Published: April 01, 2021

A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene

A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: January 10, 2021

Effect of high-throughput sequencing for the prevention and control of thalassemia

Effect of high-throughput sequencing for the prevention and control of thalassemia

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 31, 2020

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Last Updated: 09/26/2026