Xiaoge Li

发表

Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2021, Translational Psychiatry.

Identification of two novel pathogenic compound heterozygous MYO7A mutations in Usher syndrome by whole exome sequencing.

Yi Xu, Xin Li, Dong Yang, 2018, International journal of pediatric otorhinolaryngology.

Altered Urinary Amino Acids in Children With Autism Spectrum Disorders

Mingbang Wang, Wei Zhou, Wenhao Zhou, 2019, Front. Cell. Neurosci..

Whole Exome Sequencing Revealed Clinical Relevant Variants in A Family Affected with Autism Spectrum Disorder

Mingbang Wang, F. He, Xiaoge Li, 2016 .

Gene4HL: An Integrated Genetic Database for Hearing Loss

X. Wang, Kuokuo Li, Guihu Zhao, 2021, Frontiers in Genetics.

Elevated Expression of LYPD3 Is Associated with Lung Adenocarcinoma Carcinogenesis and Poor Prognosis.

Yan Wang, Ping Hu, Yuanyuan Gao, 2020, DNA and cell biology.

Association of novel rare coding variants with juvenile idiopathic arthritis

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2021, Annals of the Rheumatic Diseases.

HPV Testing Can Be Used As a Primary Screening Method for Cervical Lesions among Women in Western China

Xiaoge Li, Yutong Wu, Zhaoning Duan, 2022 .

Identification of a Mutation in the Novel Compound Heterozygous CFTR in a Chinese Family with Cystic Fibrosis

Ming Zhang, Qi Wu, Junping Wu, 2020, Canadian respiratory journal.