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Molecular Psychiatry|June 8, 2018
A comparative study of the genetic components of three subcategories of autism spectrum disorderJinchen Li, Shanshan Hu, Kun Zhang, et al.
Science China. Life Sciences|April 28, 2023
Genome-wide DNA methylation landscape of four Chinese populations and epigenetic variation linked to Tibetan high-altitude adaptationZeshan Lin, Yan Lu, Guoliang Yu, et al.
Scientific Reports|November 18, 2015
Investigation of Pathogenic Genes in Chinese sporadic Hypertrophic Cardiomyopathy Patients by Whole Exome SequencingJing Xu, Zhongshan Li, Xianguo Ren, et al.
Molecular Oncology|April 12, 2019
A 17 gene panel for non-small-cell lung cancer prognosis identified through integrative epigenomic-transcriptomic analyses of hypoxia-induced epithelial-mesenchymal transitionYue-Lei Chen, Yihe Zhang, Junwen Wang, et al.
Computational and Structural Biotechnology Journal|June 6, 2022
Transcriptomic signatures associated with autoimmune thyroiditis in papillary thyroid carcinoma and cancer immunotherapy-induced thyroid dysfunctionYi Li, Yue Zang, Tianda Fan, et al.
Translational Psychiatry|February 19, 2020
Genetic evidence of gender difference in autism spectrum disorder supports the female-protective effectYi Zhang, Na Li, Chao Li, et al.
Scientific Reports|August 15, 2015
Wide mutation spectrum and frequent variant Ala27Thr of FBN1 identified in a large cohort of Chinese patients with sporadic TAADJun Guo, Lun Cai, Lixin Jia, et al.
Carcinogenesis|December 27, 2011
MicroRNA-34a inhibits migration and invasion of colon cancer cells via targeting to Fra-1Jianmin Wu, Gang Wu, Lu Lv, et al.
Nucleic Acids Research|October 24, 2017
CirGRDB: a database for the genome-wide deciphering circadian genes and regulatorsXianfeng Li, Leisheng Shi, Kun Zhang, et al.
Neurobiology of Aging|October 8, 2013
Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigreeZhanjun Wang, Wanshi Cai, Fang Cui, et al.
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