Yao Wang
Fudan University
9 Papers
3 Citations
Yao Wang is an academic researcher from Fudan University. The author has contributed to research in topics: Medicine & Exome sequencing. The author has an hindex of 1, co-authored 4 publications.
Chat about Author
Papers
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project.
Bingbing Wu,Wenqing Kang,Yingyuan Wang,Deyi Zhuang,Liping Chen,Long Li,Yajie Su,Xinnian Pan,Qiufen Wei,Zezhong Tang,Yangfang Li,Jin Gao,Rui Cheng,Wei Zhou,Zhangxing Wang,Gang Qiu,Jian Wang,Lin Yang,Ping Zhang,Xuemei Zhao,Yao Wang,Mingyu Gan,Gang Li,Renchao Liu,Qi Ni,Feifan Xiao,Kai Yan,Yun Cao,Guoping Lu,Yulan Lu,Huijun Wang,Wenhao Zhou +31 more
TL;DR: In this paper, the diagnostic and clinical utility of the trio-rapid genome sequencing in critically ill infants was evaluated in 13 member hospitals of the China Neonatal Genomes Project spanning 10 provinces.
54
Diagnostic and clinical utility of next‐generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project
Huijun Wang,Feifan Xiao,Xinran Dong,Yulan Lu,Guoqiang Cheng,Lai-Shuan Wang,Wei Lu,Lin Yang,Liping Chen,Wenqing Kang,Long Li,Xinnian Pan,Qiufen Wei,Deyi Zhuang,Dongmei Chen,Zhaoqing Yin,Ling Yang,Qi Ni,Renchao Liu,Gang Li,Ping Zhang,Yanyan Qian,Xu Li,Xiaomin Peng,Yao Wang,Fang Liu,Dahui Wang,Hao Li,Chun Shen,Liling Qian,Yun Cao,Bingbing Wu,Wenhao Zhou,Wenhao Zhou +33 more
TL;DR: In this article, the authors investigated the genetic causes and characteristics of clinical outcomes in a large cohort of neonates with multiple congenital anomalies (MCAs) at birth, and showed that both CNVs and SNVs contribute to the genetic cause of MCAs, and earlier genetic assertion may lead to better clinical management for patients.
26
Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes?
Haiyan Ma,Ze-zhong Tang,Feifan Xiao,Long Li,Yangfang Li,Wenyan Tang,Liping Chen,Wenqing Kang,Yulan Lu,Xinran Dong,Guoqiang Cheng,Laishuan Wang,Wei Lu,Lin Yang,Qi Ni,Xiaomin Peng,Yao Wang,Yun Cao,Bingbing Wu,Wenhao Zhou,Wenhao Zhou,Deyi Zhuang,Guang Lin,Huijun Wang +23 more
TL;DR: In this paper, the authors performed next-generation sequencing (NGS) on neonates with metabolic acidosis (NMA) from January 2016 to December 2019 to provide an overview of the genetic causes of NMA in patients from NICUs.
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome Project
Zhe-Lan Huang,Qian Shen,Bingbing Wu,Huijun Wang,Xinran Dong,Yulan Lu,Guoqiang Cheng,Laishuan Wang,Wei Lu,Liping Chen,W. Y. Kang,Long Li,Xinnian Pan,Qiu-Fen Wei,Deyi Zhuang,Dong-shen Chen,Zhaoqing Yin,Lin Yang,Qi Ni,Renchao Liu,Gang Liu,Ping Zhang,Yanyan Qian,Xiaomin Peng,Yao Wang,Yun-tao Cao,Hong Xu,Liyuan Hu,Lin Yang,Wenhao Zhou +29 more
TL;DR: This study shows the heterogeneous genetic etiologies in a Chinese CAKUT neonatal cohort by using WES and suggests patients with CAK UT who have extrarenal manifestations are more likely to harbor genetic diagnoses.
4
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes Project.
Feifan Xiao,Bingbing Wu,Chenbin Dong,Guoqiang Cheng,Yun Cao,Laishuan Wang,Xinran Dong,Yulan Lu,Lin Yang,Liping Chen,Long Li,Xinnian Pan,Qiufen Wei,Deyi Zhuang,Dong-shen Chen,Zhaoqing Yin,Qi Ni,Ren-chao Liu,Suzhen Xu,Gang Liu,Ping Zhang,Yanyan Qian,Xu Li,Xiaomin Peng,Yao Wang,Huijun Wang,Wenhao Zhou +26 more
TL;DR: A high incidence of genetic causes in critically ill neonates with CADs is identified, with a combination of single-nucleotide variations and CNVs among the genetic causes of CAD.
2