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Nancy Y. Ip
H-index:88
Citation Count:4.0万
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Genome-wide analysis of common structural variants in Alzheimer’s disease identifies a risk-associated regulatory CCG repeat in FAM193B
阿尔茨海默病中常见结构变异的全基因组分析鉴定了一个与风险相关的FAM193B基因中的CCG重复序列
APOE-stratified genome-wide association analyses provide insights into the genetic etiology of Alzheimers’s disease
APOE分层的全基因组关联分析为阿尔茨海默病的遗传病因提供了见解
Nature Genetics
IF29
Ethnic-specific effects of the LILRB2–LILRB5 locus and newly identified risk loci for Alzheimer's disease in the East Asian population
东亚人群中LILRB2–LILRB5基因座及新识别的阿尔茨海默症风险基因座的种族特异性效应
The TREM2 H157Y variant is associated with more severe neurodegeneration in Alzheimer's disease and altered immune-related processes
TREM2 H157Y变异体与阿尔茨海默病中更严重的神经退行性变以及改变的免疫相关过程相关。
Alzheimer's & Dementia
IF11.1
Transferability of European-derived Alzheimer’s disease polygenic risk scores across multiancestry populations
欧洲来源的阿尔茨海默病多基因风险评分在多祖先人群中的可转移性
Multi-ancestry genome-wide association meta-analysis of Parkinson's disease
帕金森病多血统全基因组关联meta分析
NATURE GENETICS
IF31.8
An IL1RL1 genetic variant lowers soluble ST2 levels and the risk effects of APOE-ε4 in female patients with Alzheimer's disease
IL1RL1遗传变异可降低女性阿尔茨海默病患者的可溶性ST2水平和APOE-ε4的风险影响
NATURE AGING
IF19.4

