Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder

Xiujuan Du, Xueren Gao, Xin Liu, +12

Frontiers in Genetics

Bioinformatics identification of crucial genes and pathways associated with hepatocellular carcinoma

Xueren Gao, Xixi Wang, Shulong Zhang

Bioscience Reports

Meta-Analysis of the Association between Vitamin D Receptor Polymorphisms and the Risk of Autoimmune Thyroid Disease

Xueren Gao, Yongguo Yu

International Journal of Endocrinology

Integrated Bioinformatics Analysis of Hub Genes and Pathways in Anaplastic Thyroid Carcinomas

Xueren Gao, Jianguo Wang, Shulong Zhang

International Journal of Endocrinology

High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study

Yu Sun, Xiantao Ye, Yanjie Fan, +14

Clinical Chemistry

The Association Between STAT4 rs7574865 Polymorphism and the Susceptibility of Autoimmune Thyroid Disease: A Meta-Analysis

Xueren Gao, Jianguo Wang, Yongguo Yu

Frontiers in Genetics

Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

Xiaomei Luo, Jiacheng Hu, Xueren Gao, +4

BMC Medical Genetics

A Functional Mutation in HDAC8 Gene as Novel Diagnostic Marker for Cornelia De Lange Syndrome

Xueren Gao, Zhuo Huang, Yanjie Fan, +5

Cellular Physiology and Biochemistry

Identification of RUNX2 variants associated with cleidocranial dysplasia

Xueren Gao, Kunxia Li, Yanjie Fan, +9

Hereditas