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

Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing

通过全基因组测序解析FTLD-TDP病理亚型的不同遗传风险因素

Pottier, Cyril; Küçükali, Fahri; Baker, Matt; Batzler, Anthony; Jenkins, Gregory D; van Blitterswijk, Marka; Vicente, Cristina T; De Coster, Wouter; Wynants, Sarah; Van de Walle, Pieter; Ross, Owen A; Murray, Melissa E; Faura, Júlia; Haggarty, Stephen J; van Rooij, Jeroen Gj; Mol, Merel O; Hsiung, Ging-Yuek R; Graff, Caroline; Öijerstedt, Linn; Neumann, Manuela; Asmann, Yan; McDonnell, Shannon K; Baheti, Saurabh; Josephs, Keith A; Whitwell, Jennifer L; Bieniek, Kevin F; Forsberg, Leah; Heuer, Hilary; Lago, Argentina Lario; Geier, Ethan G; Yokoyama, Jennifer S; Oddi, Alexis P; Flanagan, Margaret; Mao, Qinwen; Hodges, John R; Kwok, John B; Domoto-Reilly, Kimiko; Synofzik, Matthis; Wilke, Carlo; Onyike, Chiadi; Dickerson, Bradford C; Evers, Bret M; Dugger, Brittany N; Munoz, David G; Keith, Julia; Zinman, Lorne; Rogaeva, Ekaterina; Suh, EunRan; Gefen, Tamar; Geula, Changiz; Weintraub, Sandra; Diehl-Schmid, Janine; Farlow, Martin R; Edbauer, Dieter; Woodruff, Bryan K; Caselli, Richard J; Donker Kaat, Laura L; Huey, Edward D; Reiman, Eric M; Mead, Simon; King, Andrew; Roeber, Sigrun; Nana, Alissa L; Ertekin-Taner, Nilufer; Knopman, David S; Petersen, Ronald C; Petrucelli, Leonard; Uitti, Ryan J; Wszolek, Zbigniew K; Ramos, Eliana Marisa; Grinberg, Lea T; Tempini, Maria Luisa Gorno; Rosen, Howard J; Spina, Salvatore; Piguet, Olivier; Grossman, Murray; Trojanowski, John Q; Keene, C Dirk; Jin, Lee-Way; Prudlo, Johannes; Geschwind, Daniel H; Rissman, Robert A; Cruchaga, Carlos; Ghetti, Bernardino; Halliday, Glenda M; Beach, Thomas G; Serrano, Geidy E; Arzberger, Thomas; Herms, Jochen; Boxer, Adam L; Honig, Lawrence S; Vonsattel, Jean P; Lopez, Oscar L; Kofler, Julia; White, Charles L 3rd; Gearing, Marla; Glass, Jonathan; Rohrer, Jonathan D; Irwin, David J; Lee, Edward B; Van Deerlin, Vivianna; Castellani, Rudolph; Mesulam, Marsel M; Tartaglia, Maria C; Finger, Elizabeth C; Troakes, Claire; Al-Sarraj, Safa; Dalgard, Clifton L; Miller, Bruce L; Seelaar, Harro; Graff-Radford, Neill R; Boeve, Bradley F; Mackenzie, Ian Ra; van Swieten, John C; Seeley, William W; Sleegers, Kristel; Dickson, Dennis W; Biernacka, Joanna M; Rademakers, Rosa

Opposing role of phagocytic receptors MERTK and AXL in Progranulin deficient FTD.

吞噬受体 MERTK 和 AXL 在前粒蛋白缺乏型 FTD 中的相反作用

Clelland Claire Dudley, Fan Li, Saloner Rowan, Etchegaray Jon Iker, Altobelli Chad Richard, Salomonsson Sally, Maltos Alisha M, Sachdev Aradhana, Zhu Jingjie, Lee Se-In, Li Yaqiao, Zhou Yungui, Le David, Wang Chao, Carling Gillian, Kodama Lay, Sayed Faten, Perez-Bermejo Jaun A, Geier Ethan G, Yokoyama Jennifer S, Rosen Howie, Nana Alissa L, Spina Salvatore, Grinberg Lea T, Seeley William W, Elahi Fanny, Boxer Adam L, Arkin Michelle R, Gan Li

Early-onset Alzheimer's disease explained by polygenic risk of late-onset disease?

早发性阿尔茨海默病是否可以用晚发性疾病的多基因风险来解释?

Mantyh, William G; Cochran, J Nicholas; Taylor, Jared W; Broce, Iris J; Geier, Ethan G; Bonham, Luke W; Anderson, Ashlyn G; Sirkis, Daniel W; Joie, Renaud La; Iaccarino, Leonardo; Chaudhary, Kiran; Edwards, Lauren; Strom, Amelia; Grant, Harli; Allen, Isabel E; Miller, Zachary A; Gorno-Tempini, Marilu L; Kramer, Joel H; Miller, Bruce L; Desikan, Rahul S; Rabinovici, Gil D; Yokoyama, Jennifer S

Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

TET2基因中的非编码变异和功能丧失型编码变异与多种神经退行性疾病相关

Cochran, J Nicholas; Geier, Ethan G; Bonham, Luke W; Newberry, J Scott; Amaral, Michelle D; Thompson, Michelle L; Lasseigne, Brittany N; Karydas, Anna M; Roberson, Erik D; Cooper, Gregory M; Rabinovici, Gil D; Miller, Bruce L; Myers, Richard M; Yokoyama, Jennifer S

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

基因组测序在早发性或非典型痴呆症中的应用:诊断率高,且经常观察到多个致病等位基因

Cochran, J Nicholas; McKinley, Emily C; Cochran, Meagan; Amaral, Michelle D; Moyers, Bryan A; Lasseigne, Brittany N; Gray, David E; Lawlor, James M J; Prokop, Jeremy W; Geier, Ethan G; Holt, James M; Thompson, Michelle L; Newberry, J Scott; Yokoyama, Jennifer S; Worthey, Elizabeth A; Geldmacher, David S; Love, Marissa Natelson; Cooper, Gregory M; Myers, Richard M; Roberson, Erik D

Recent advances in the genetics of frontotemporal dementia

额颞叶痴呆遗传学的最新进展

Sirkis, Daniel W; Geier, Ethan G; Bonham, Luke W; Karch, Celeste M; Yokoyama, Jennifer S

CXCR4 involvement in neurodegenerative diseases

CXCR4参与神经退行性疾病

Bonham, Luke W; Karch, Celeste M; Fan, Chun C; Tan, Chin; Geier, Ethan G; Wang, Yunpeng; Wen, Natalie; Broce, Iris J; Li, Yi; Barkovich, Matthew J; Ferrari, Raffaele; Hardy, John; Momeni, Parastoo; Höglinger, Günter; Müller, Ulrich; Hess, Christopher P; Sugrue, Leo P; Dillon, William P; Schellenberg, Gerard D; Miller, Bruce L; Andreassen, Ole A; Dale, Anders M; Barkovich, A James; Yokoyama, Jennifer S; Desikan, Rahul S

Protein network analysis reveals selectively vulnerable regions and biological processes in FTD

蛋白质网络分析揭示了额颞叶痴呆症中选择性易损区域和生物学过程。

Bonham, Luke W; Steele, Natasha Z R; Karch, Celeste M; Manzoni, Claudia; Geier, Ethan G; Wen, Natalie; Ofori-Kuragu, Aaron; Momeni, Parastoo; Hardy, John; Miller, Zachary A; Hess, Christopher P; Lewis, Patrick; Miller, Bruce L; Seeley, William W; Baranzini, Sergio E; Desikan, Rahul S; Ferrari, Raffaele; Yokoyama, Jennifer S

Genetic Variation in the Androgen Receptor and Measures of Plasma Testosterone Levels Suggest Androgen Dysfunction in Alzheimer's Disease

雄激素受体基因变异和血浆睾酮水平测量结果提示阿尔茨海默病存在雄激素功能障碍

Carr, Jessie S; Bonham, Luke W; Morgans, Alicia K; Ryan, Charles J; Yokoyama, Jennifer S; Geier, Ethan G

Insulin-Like Growth Factor Binding Protein 2 Is Associated With Biomarkers of Alzheimer's Disease Pathology and Shows Differential Expression in Transgenic Mice

胰岛素样生长因子结合蛋白2与阿尔茨海默病病理生物标志物相关,并在转基因小鼠中表现出差异表达

Bonham, Luke W; Geier, Ethan G; Steele, Natasha Z R; Holland, Dominic; Miller, Bruce L; Dale, Anders M; Desikan, Rahul S; Yokoyama, Jennifer S