Jiangfen Wu

Guiyang, China

Last Updated: 09/26/2026

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Found 8 publications

Large-Scale Analysis of the Thalassemia Mutation Spectrum in Guizhou Province, Southern China, Using Third-Generation Sequencing.

Large-Scale Analysis of the Thalassemia Mutation Spectrum in Guizhou Province, Southern China, Using Third-Generation Sequencing.

Journal: Clinical genetics

Published: November 24, 2024

Epidemiological study of thalassemia in the Buyi population of Qiannan Prefecture, Guizhou Province, China based on third-generation sequencing.

Epidemiological study of thalassemia in the Buyi population of Qiannan Prefecture, Guizhou Province, China based on third-generation sequencing.

Journal: Annals of hematology

Published: November 07, 2024

Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation.

Long Non-Coding RNA H19 Leads to Upregulation of γ-Globin Gene Expression during Erythroid Differentiation.

Journal: Hemoglobin

Published: February 29, 2024

A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non-syndromic deafness 2A in a Chinese family.

A novel variant c.902C>A (p. A301D) in KCNQ4 associated with non-syndromic deafness 2A in a Chinese family.

Journal: Molecular genetics & genomic medicine

Published: October 12, 2023

Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy.

Identification of Two Novel Variants of the DMD Gene in Chinese Families with Duchenne Muscular Dystrophy.

Journal: Pharmacogenomics and personalized medicine

Published: April 08, 2023

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.

Journal: Medicine

Published: February 17, 2023

Application of third-generation sequencing for genetic testing of thalassemia in Guizhou Province, Southwest China.

Application of third-generation sequencing for genetic testing of thalassemia in Guizhou Province, Southwest China.

Journal: Hematology (Amsterdam, Netherlands)

Published: December 15, 2022

Whole-exome sequencing identified five novel de novo variants in patients with unexplained intellectual disability.

Whole-exome sequencing identified five novel de novo variants in patients with unexplained intellectual disability.

Journal: Journal of clinical laboratory analysis

Published: March 10, 2022

Showing 1-8 of 8

Last Updated: 09/26/2026