日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Single-cell RNA-seq reveals alterations in peripheral CX3CR1 and nonclassical monocytes in familial tauopathy

单细胞 RNA 测序揭示家族性 tau 蛋白病中外周 CX3CR1 和非经典单核细胞的改变

Daniel W Sirkis #, Caroline Warly Solsberg #, Taylor P Johnson, Luke W Bonham, Virginia E Sturm, Suzee E Lee, Katherine P Rankin, Howard J Rosen, Adam L Boxer, William W Seeley, Bruce L Miller, Ethan G Geier, Jennifer S Yokoyama2

Radiogenomics of C9orf72 Expansion Carriers Reveals Global Transposable Element Derepression and Enables Prediction of Thalamic Atrophy and Clinical Impairment

C9orf72 扩增携带者的放射基因组学揭示了整体转座因子去抑制,并能够预测丘脑萎缩和临床损伤

Luke W Bonham, Ethan G Geier, Daniel W Sirkis, Josiah K Leong, Eliana Marisa Ramos, Qing Wang, Anna Karydas, Suzee E Lee, Virginia E Sturm, Russell P Sawyer, Adit Friedberg, Justin K Ichida, Aaron D Gitler, Leo Sugrue, Michael Cordingley, Walter Bee, Eckard Weber, Joel H Kramer, Katherine P Rankin, 

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

神经元蜡样脂褐素沉积症基因 MFSD8 中的罕见变异是额颞叶痴呆的候选风险因素

Ethan G Geier, Mathieu Bourdenx, Nadia J Storm, J Nicholas Cochran, Daniel W Sirkis, Ji-Hye Hwang, Luke W Bonham, Eliana Marisa Ramos, Antonio Diaz, Victoria Van Berlo, Deepika Dokuru, Alissa L Nana, Anna Karydas, Maureen E Balestra, Yadong Huang, Silvia P Russo, Salvatore Spina, Lea T Grinberg, Wil

Identification of a rare coding variant in TREM2 in a Chinese individual with Alzheimer's disease

在患有阿尔茨海默病的中国患者中鉴定出 TREM2 的罕见编码变异

Luke W Bonham, Daniel W Sirkis, Jia Fan, Renan E Aparicio, Marian Tse, Eliana Marisa Ramos, Qing Wang, Giovanni Coppola, Howard J Rosen, Bruce L Miller, Jennifer S Yokoyama