Yajun Chen

Shaoguan, China

Last Updated: 09/26/2026

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Found 12 publications

A multiplex allele specific PCR capillary electrophoresis (mASPCR-CE) assay for simultaneously analysis of SMN1/SMN2/NAIP copy number and SMN1 loss-of-function variants.

A multiplex allele specific PCR capillary electrophoresis (mASPCR-CE) assay for simultaneously analysis of SMN1/SMN2/NAIP copy number and SMN1 loss-of-function variants.

Journal: Clinical chemistry and laboratory medicine

Published: February 14, 2025

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

Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--SEA) carriers.

Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--SEA) carriers.

Journal: Journal of clinical pathology

Published: January 12, 2022

Application of an optimized interpretation model in capillary hemoglobin electrophoresis for newborn thalassemia screening.

Application of an optimized interpretation model in capillary hemoglobin electrophoresis for newborn thalassemia screening.

Journal: International journal of laboratory hematology

Published: April 23, 2021

NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study.

NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study.

Journal: European journal of human genetics : EJHG

Published: June 07, 2019

Long non‑coding RNA LINC00312 regulates breast cancer progression through the miR‑9/CDH1 axis.

Long non‑coding RNA LINC00312 regulates breast cancer progression through the miR‑9/CDH1 axis.

Journal: Molecular medicine reports

Published: March 12, 2019

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.

Journal: Human mutation

Published: March 03, 2019

Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR

Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR

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

Published: December 05, 2018

LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies.

LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathies.

Journal: Human mutation

Published: March 09, 2018

Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples.

Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples.

Journal: European journal of human genetics : EJHG

Published: February 15, 2018

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

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

Journal: EBioMedicine

Published: June 29, 2017

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression.

A Genetic Variant Ameliorates β-Thalassemia Severity by Epigenetic-Mediated Elevation of Human Fetal Hemoglobin Expression.

Journal: American journal of human genetics

Published: December 28, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026