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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 8, 2018
Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patientsHang Zhang, Wanshi Cai, Siyu Chen, et al.
Plos Computational Biology|September 26, 2014
A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing dataQing Xie, Qi Liu, Fengbiao Mao, et al.
Epigenetics|July 28, 2015
Q-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analysesKangli Wang, Xianfeng Li, Shanshan Dong, et al.
Nucleic Acids Research|May 9, 2019
MFEprimer-3.0: quality control for PCR primersKun Wang, Haiwei Li, Yue Xu, et al.
Human Mutation|August 7, 2012
Mutations of ANK3 identified by exome sequencing are associated with autism susceptibilityCheng Bi, Jinyu Wu, Tao Jiang, et al.
International Journal of Biological Sciences|August 16, 2017
Acetylation of hMOF Modulates H4K16ac to Regulate DNA Repair Genes in Response to Oxidative StressJianing Zhong, Liying Ji, Huiqian Chen, et al.
Biochemical and Biophysical Research Communications|April 17, 2007
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathyYi Tong, Yijian Mao, Xiangtian Zhou, et al.
The Journal of Pathology|November 17, 2017
Genetic landscape of papillary thyroid carcinoma in the Chinese populationJialong Liang, Wanshi Cai, Dongdong Feng, 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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