Next‐generation sequencing based molecular testing is an equalizer for diagnostic service of rare genetic disorders in China

por Shen, Yiping
Publicado 2018

Editorial: Horizons of autism spectrum disorder and attention deficit hyperactivity disorder in clinical practice

por Li, Fei, Shen, Yiping, Li, Tingyu
Publicado 2023

Severe Systemic Rash in the Treatment of Hairy Cell Leukemia with Cladribine: Case Report and Literature Review

por Dong, Huijie, Shen, Yingying, Shen, Yiping, Wu, Dijiong
Publicado 2020

Trio-R: a script for assessing maternity and paternity in trio studies performed on Agilent chromosomal microarrays

por Xia, Daniel, Zhang, Chen, Lip, Va, Harris, Marian, Shen, Yiping
Publicado 2018

Evaluation of copy number variant detection from panel‐based next‐generation sequencing data

por Yao, Ruen, Yu, Tingting, Qing, Yanrong, Wang, Jian, Shen, Yiping
Publicado 2018

The rise of the genetic counseling profession in China

por Sun, Liya, Liang, Bo, Zhu, Liping, Shen, Yiping, He, Lin
Publicado 2019

Influence of the PZT Sensor Array Configuration on Lamb Wave Tomography Imaging with the RAPID Algorithm for Hole and Crack Detection

por Wang, Songlai, Wu, Wanrong, Shen, Yiping, Liu, Yi, Jiang, Shuai
Publicado 2020

The portrayal of people with dwarfism in Chinese art

por Wu, Liuyin, Zhou, Ying, Zhang, Dan, Shen, Yiping, Liu, Aixia
Publicado 2021

Case Report: A Case of Epileptic Disorder Associated With a Novel CNTN2 Frameshift Variant in Homozygosity due to Maternal Uniparental Disomy

por Chen, Wenjie, Chen, Fei, Shen, Yiping, Yang, Zhixian, Qin, Jiong
Publicado 2021

CTCF variant begets to short stature by down-regulation of IGF1

por Chen, Hong, Li, Weiyu, Zhang, Suping, Sun, Yunteng, Shen, Yiping, Chen, Ruimin
Publicado 2023

The Partial Reconstruction Symplectic Geometry Mode Decomposition and Its Application in Rolling Bearing Fault Diagnosis

por Liu, Yanfei, Cheng, Junsheng, Yang, Yu, Bin, Guangfu, Shen, Yiping, Peng, Yanfeng
Publicado 2023

The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability

por Ha, Kyungsoo, Shen, Yiping, Graves, Tyler, Kim, Cheol-Hee, Kim, Hyung-Goo
Publicado 2016

Novel Compound Heterozygous Variants in the LHCGR Gene in a Genetically Male Patient with Female External Genitalia

por Yan, Mei, Dilihuma, Julaiti, Luo, Yanfei, Reyilanmu, Baoerhan, Shen, Yiping, Mireguli, Maimaiti
Publicado 2019

Whole‐exome sequencing identified novel compound heterozygous variants in a Chinese neonate with liver failure and review of literature

por Qin, Zailong, Yang, Qi, Yi, Shang, Huang, Limei, Shen, Yiping, Luo, Jingsi
Publicado 2020

Preparation of high drug-loading celastrol nanosuspensions and their anti-breast cancer activities in vitro and in vivo

por Huang, Tiantian, Wang, Yian, Shen, Yiping, Ao, Hui, Guo, Yifei, Han, Meihua, Wang, Xiangtao
Publicado 2020

An Initial Survey of the Performances of Exome Variant Analysis and Clinical Reporting Among Diagnostic Laboratories in China

por Zhang, Kuo, Lin, Guigao, Han, Dongsheng, Han, Yanxi, Wang, Jian, Shen, Yiping, Li, Jinming
Publicado 2020

Antley-Bixler syndrome arising from compound heterozygotes in the P450 oxidoreductase gene: a case report

por Li, Haibo, Zhao, Aman, Xie, Min, Chen, Linqi, Wu, Haiying, Shen, Yiping, Wang, Hongying
Publicado 2021

The past, present, and future for constitutional ring chromosomes: A report of the international consortium for human ring chromosomes

por Li, Peining, Dupont, Barbara, Hu, Qiping, Crimi, Marco, Shen, Yiping, Lebedev, Igor, Liehr, Thomas
Publicado 2022

Autistic Children Exhibit Decreased Levels of Essential Fatty Acids in Red Blood Cells

por Brigandi, Sarah A., Shao, Hong, Qian, Steven Y., Shen, Yiping, Wu, Bai-Lin, Kang, Jing X.
Publicado 2015

Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data

por Yao, Ruen, Zhang, Cheng, Yu, Tingting, Li, Niu, Hu, Xuyun, Wang, Xiumin, Wang, Jian, Shen, Yiping
Publicado 2017