Comprehensive evaluation of deep and graph learning on drug–drug interactions prediction

X Lin, L Dai, Y Zhou, ZG Yu, W Zhang… - Briefings in …, 2023 - academic.oup.com
Recent advances and achievements of artificial intelligence (AI) as well as deep and graph
learning models have established their usefulness in biomedical applications, especially in …

[HTML][HTML] Novel epigenetic techniques provided by the CRISPR/Cas9 system

N Xie, Y Zhou, Q Sun, B Tang - Stem cells international, 2018 - hindawi.com
Epigenetics classically refers to the inheritable changes of hereditary information without
perturbing DNA sequences. Understanding mechanisms of how epigenetic factors …

[HTML][HTML] Genetics of progressive supranuclear palsy: a review

Y Wen, Y Zhou, B Jiao, L Shen - Journal of Parkinson's …, 2021 - content.iospress.com
Progressive supranuclear palsy (PSP) is an atypical parkinsonism with prominent 4R-tau
neuropathology, and the classical clinical phenotype is characterized by vertical …

[HTML][HTML] Neural biomarker diagnosis and prediction to mild cognitive impairment and Alzheimer's disease using EEG technology

B Jiao, R Li, H Zhou, K Qing, H Liu, H Pan, Y Lei… - Alzheimer's Research & …, 2023 - Springer
Background Electroencephalogram (EEG) has emerged as a non-invasive tool to detect the
aberrant neuronal activity related to different stages of Alzheimer's disease (AD). However …

[HTML][HTML] Identification of CHIP as a Novel Causative Gene for Autosomal Recessive Cerebellar Ataxia

Y Shi, J Wang, JD Li, H Ren, W Guan, M He, W Yan… - PloS one, 2013 - journals.plos.org
Autosomal recessive cerebellar ataxias are a group of neurodegenerative disorders that are
characterized by complex clinical and genetic heterogeneity. Although more than 20 …

Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

Y Tian, L Zhou, J Gao, B Jiao, S Zhang… - Journal of Neurology …, 2022 - jnnp.bmj.com
Background Abnormal expanded GGC repeats within the NOTCH2HLC gene has been
confirmed as the genetic mechanism for most Asian patients with neuronal intranuclear …

[HTML][HTML] Polygenic analysis of late-onset Alzheimer's disease from mainland China

B Jiao, X Liu, L Zhou, MH Wang, Y Zhou, T Xiao… - PloS one, 2015 - journals.plos.org
Recently, a number of single nucleotide polymorphisms (SNPs) were identified to be
associated with late-onset Alzheimer disease (LOAD) through genome-wide association …

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias

B Jiao, L Zhou, Y Zhou, L Weng, X Liao, Y Tian… - Neurobiology of …, 2020 - Elsevier
Recently, the (GGC) n repeat expansion in the NOTCH2NLC gene has been identified to be
associated with neuronal intranuclear inclusion disease (NIID). Given the clinical overlap of …

Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China

B Jiao, X Liu, B Tang, L Hou, L Zhou, F Zhang… - Neurobiology of …, 2014 - Elsevier
Recently, 3 rare coding variants significantly associated with Alzheimer's disease (AD) risk
have been identified in western populations using whole exome sequencing method …

[HTML][HTML] A DEA-based approach for fair reduction and reallocation of emission permits

H Wu, S Du, L Liang, Y Zhou - Mathematical and computer modelling, 2013 - Elsevier
How to allocate initial emission permits is vital for the cap-and-trade system in controlling the
total emission level and improving the operation efficiency of the trade mechanism. And data …