Year |
Citation |
Score |
2022 |
Min S, Xu Q, Qin L, Li Y, Li Z, Chen C, Wu H, Han J, Zhu X, Jin P, Tang B. Altered Hydroxymethylome in the substantia Nigra of Parkinson's disease. Human Molecular Genetics. PMID 35661211 DOI: 10.1093/hmg/ddac122 |
0.401 |
|
2021 |
Zhao F, Xu Y, Gao S, Qin L, Austria Q, Siedlak SL, Pajdzik K, Dai Q, He C, Wang W, O'Donnell JM, Tang B, Zhu X. METTL3-dependent RNA mA dysregulation contributes to neurodegeneration in Alzheimer's disease through aberrant cell cycle events. Molecular Neurodegeneration. 16: 70. PMID 34593014 DOI: 10.1186/s13024-021-00484-x |
0.404 |
|
2021 |
Min S, Li Z, Shieh A, Giase G, Bao R, Zhang C, Kuney L, Kopp R, Asif H, Alliey-Rodriguez N, Qin L, Craig DW, Faulkner GJ, Gershon ES, Tang B, et al. Absence of coding somatic single nucleotide variants within well-known candidate genes in late-onset sporadic Alzheimer's Disease based on the analysis of multi-omics data. Neurobiology of Aging. PMID 34392980 DOI: 10.1016/j.neurobiolaging.2021.07.010 |
0.327 |
|
2020 |
Qin L, Zhu X, Friedland RP. ApoE and mitochondrial dysfunction. Neurology. PMID 32457209 DOI: 10.1212/Wnl.0000000000009569 |
0.431 |
|
2019 |
Qin L, Xu Q, Li Z, Chen L, Li Y, Yang N, Liu Z, Guo J, Shen L, Allen EG, Chen C, Ma C, Wu H, Zhu X, Jin P, et al. Ethnicity-specific and overlapping alterations of brain hydroxymethylome in Alzheimer's disease. Human Molecular Genetics. PMID 31814020 DOI: 10.1093/Hmg/Ddz273 |
0.468 |
|
2019 |
Wang M, Qin L, Tang B. MicroRNAs in Alzheimer's Disease. Frontiers in Genetics. 10: 153. PMID 30881384 DOI: 10.3389/fgene.2019.00153 |
0.388 |
|
Show low-probability matches. |