Genetic Screening, Diagnosis and Treatment for Newborns

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ORIGINAL RESEARCH

Published on 11 Jun 2024

Single-cell transcriptomic analysis reveals heterogeneous features of myeloid-derived suppressor cells in newborns

Meng Yao
Yingjiao Cao
Juan He
Rui Dong
Gaoyu Liu
Yingying Chen
Jun Wang
Jie Zhou

Single-cell transcriptomic analysis reveals heterogeneous features of myeloid-derived suppressor cells in newborns

doi 10.3389/fimmu.2024.1367230

1,841 views

ORIGINAL RESEARCH

Published on 11 Jan 2024

Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case–control study based on the China Neonatal Genomes Project

Xiao Wang
Tiantian Xiao
Jin Wang
Bingbing Wu
Huijun Wang
Yulan Lu
Yaqiong Wang
Bin Chen
Liyuan Hu
7 more
Wenhao Zhou

Clinical and genetic risk factors associated with neonatal severe hyperbilirubinemia: a case–control study based on the China Neonatal Genomes Project

doi 10.3389/fgene.2023.1292921

1,205 views

ORIGINAL RESEARCH

Published on 06 Dec 2023

Primary carnitine deficiency: Estimation of prevalence in Chinese population and insights into newborn screening

Xiaoshan Ji
Yanzhuang Ge
Qi Ni
Suhua Xu
Zhongmeng Xiong
Lin Yang
Liyuan Hu
Yun Cao
Yulan Lu
4 more
Xinran Dong

Primary carnitine deficiency: Estimation of prevalence in Chinese population and insights into newborn screening

doi 10.3389/fgene.2023.1304458

2,192 views
3 citations

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Frontiers in Genetics

Human and Medical Genomics

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