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

A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions

GOLGA8A基因的重复扩增是伴有泛素阳性包涵体的非典型额颞叶变性的主要风险因素。

De Coster, Wouter; Van den Broeck, Marleen; Baker, Matt; Ghayal, Nikhil B; Wynants, Sarah; Batzler, Anthony; Pottier, Cyril; Alidadiani, Sara; Küçükali, Fahri; Jenkins, Gregory D; Policarpo, Rafaela; van Blitterswijk, Marka; DeJesus-Hernandez, Mariely; Soto-Beasley, Alexandra I; Faura, Júlia; Coopman, Elise; Hutten, Saskia; Mol, Merel O; Wallon, David; Sieben, Anne; Finger, Elizabeth C; Murray, Melissa E; Forrest, Shelley L; Tartaglia, Maria C; Troakes, Claire; van Rooij, Jeroen G J; Nguyen, Aivi T; Reichard, R Ross; Woodman, Natalie L; Nana, Alissa L; Weintraub, Sandra; Gefen, Tamar; De Vil, Bart; Bodi, Istvan; Lopez, Oscar L; Boluda, Susana; Belliard, Serge; Lebert, Florence; Marguet, Florent; Mao, Qinwen; Mesulam, Marsel M; Boxer, Adam L; Vandenbulcke, Mathieu; Suh, EunRan; Schaeverbeke, Jolien; Lambert, Jean-Charles; Scholz, Sonja W; Dalgard, Clifton L; Traynor, Bryan J; Gibbs, Raphael J; Schellenberg, Gerard D; Dormann, Dorothee; Joris, Geert; De Pooter, Tim; De Rijk, Peter; D'Hert, Svenn; Van Dongen, Jasper; van der Zee, Julie; Strazisar, Mojca; Gearing, Marla; Kukar, Thomas; Flanagan, Margaret; Engelborghs, Sebastiaan; Ghetti, Bernardino; Newell, Kathy L; King, Andrew; Roeber, Sigrun; Rosen, Howard J; Spina, Salvatore; Cras, Patrick; Ertekin-Taner, Nilüfer; Wszolek, Zbigniew K; Uitti, Ryan J; Cheshire, William P; Singer, Wolfgang; Herms, Jochen; Josephs, Keith A; Whitwell, Jennifer L; Petersen, Ronald C; Pasquier, Florence; Nicolas, Gaël; Castellani, Rudolph; Glass, Jonathan; Miller, Bruce L; Kovacs, Gabor G; Rissman, Robert A; Hiniker, Annie; Deramecourt, Vincent; Ang, Lee-Cyn; Lee-Way, Jin; Van Deerlin, Vivianna M; Dugger, Brittany N; Thal, Dietmar R; Grinberg, Lea T; Cruchaga, Carlos; Arzberger, Thomas; Munoz, David G; Keith, Julia; Zinman, Lorne; Rogaeva, Ekaterina; Lee, Edward B; Haggarty, Stephen J; Ansorge, Olaf; Husain, Masud; Halliday, Glenda M; Al-Sarraj, Safa; Ross, Owen A; Sleegers, Kristel; Vandenberghe, Rik; Boeve, Bradley F; Graff-Radford, Neill R; Kofler, Julia; White, Charles L 3rd; Lashley, Tammaryn; Neumann, Manuela; Biernacka, Joanna M; Seeley, William W; Seelaar, Harro; van Swieten, John C; Rohrer, Jonathan D; Dickson, Dennis W; Mackenzie, Ian R A; Rademakers, Rosa

Association between Human Leukocyte Antigen Alleles and Neuropathological Outcomes in Lewy Body Disease

人类白细胞抗原等位基因与路易体病神经病理学结果的关联

Gavrielatos, Marios; Heckman, Michael G; Soto-Beasley, Alexandra I; Blumenfeld, Sophia G; Hou, Xu; Koga, Shunsuke; Murray, Melissa E; Kasanuki, Koji; Ono, Daisuke; Fiesel, Fabienne C; Uitti, Ryan J; Fields, Julie A; Botha, Hugo; Ramanan, Vijay K; Kantarci, Kejal; Lowe, Val J; Jack, Clifford R; Ertekin-Taner, Nilufer; Gibbs, J Raphael; Traynor, Bryan J; Dalgard, Clifton L; Savica, Rodolfo; Graff-Radford, Jonathan; Petersen, Ronald C; Reichard, R Ross; Graff-Radford, Neill R; Ferman, Tanis J; Boeve, Bradley F; Wszolek, Zbigniew K; Springer, Wolfdieter; Gan-Or, Ziv; Mignot, Emmanuel; Scholz, Sonja W; Dickson, Dennis W; Ross, Owen A

Characterizing the expression profile of 3R tau pathology in Pick's disease

表征皮克氏病中3R tau病理的表达谱

Tamvaka, Nicole; Soto-Beasley, Alexandra I; Gavrielatos, Marios; Heckman, Michael G; Ren, Yingxue; Udine, Evan; Quicksall, Zachary S; Liskey, Delaney; Castanedes-Casey, Monica; Wszolek, Zbigniew K; Boeve, Bradley F; Josephs, Keith A; Graff-Radford, Neill; van Blitterswijk, Marka; Murray, Melissa E; Roemer, Shanu F; Dickson, Dennis W; Ross, Owen A

Genome-wide association study of neuropathological features in Lewy body disease

路易体病神经病理特征的全基因组关联研究

Valentino, Rebecca R; Koga, Shunsuke; Soto-Beasley, Alexandra I; Ono, Daisuke; Wieczorek, Mikolaj A; Johnson, Patrick W; White, Launia J; Watkins, Molly M; Murray, Melissa E; Kasanuki, Koji; McLean, Pamela J; Springer, Wolfdieter; Uitti, Ryan J; Fields, Julie A; Botha, Hugo; Ramanan, Vijay K; Kantarci, Kejal; Lowe, Val J; Jack, Clifford R Jr; Bras, Jose; Guerreiro, Rita; Ertekin-Taner, Nilufer; Savica, Rodolfo; Graff-Radford, Jonathan; Petersen, Ronald C; Parisi, Joseph E; Reichard, R Ross; Graff-Radford, Neill R; Ferman, Tanis J; Boeve, Bradley F; Wszolek, Zbigniew K; Dickson, Dennis W; Heckman, Michael G; Ross, Owen A

Genome-wide association analysis identifies APOE as a mitophagy modifier in Lewy body disease.

全基因组关联分析发现 APOE 是路易体病中的线粒体自噬调节因子

Hou Xu, Heckman Michael G, Fiesel Fabienne C, Koga Shunsuke, Soto-Beasley Alexandra I, Watzlawik Jens O, Zhao Jing, Valentino Rebecca R, Johnson Patrick W, White Launia J, Quicksall Zachary S, Reddy Joseph S, Bras Jose, Guerreiro Rita, Zhao Na, Bu Guojun, Dickson Dennis W, Ross Owen A, Springer Wolfdieter

Describing the diversity of MAPT transcripts in the parietal cortex of Pick's disease patients

描述皮克氏病患者顶叶皮层中MAPT转录本的多样性

Tamvaka, Nicole; Stuber, Maximilian G; Gavrielatos, Marios; Soto-Beasley, Alexandra I; Heckman, Michael G; Murray, Melissa E; Boeve, Bradley F; Josephs, Keith A; Roemer, Shanu F; Graff-Radford, Neill R; Dickson, Dennis W; Ross, Owen A

MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

在Pick病国际联盟中,MAPT H2单倍型与Pick病风险的关系:一项遗传关联研究

Valentino, Rebecca R; Scotton, William J; Roemer, Shanu F; Lashley, Tammaryn; Heckman, Michael G; Shoai, Maryam; Martinez-Carrasco, Alejandro; Tamvaka, Nicole; Walton, Ronald L; Baker, Matthew C; Macpherson, Hannah L; Real, Raquel; Soto-Beasley, Alexandra I; Mok, Kin; Revesz, Tamas; Christopher, Elizabeth A; DeTure, Michael; Seeley, William W; Lee, Edward B; Frosch, Matthew P; Molina-Porcel, Laura; Gefen, Tamar; Redding-Ochoa, Javier; Ghetti, Bernardino; Robinson, Andrew C; Kobylecki, Christopher; Rowe, James B; Beach, Thomas G; Teich, Andrew F; Keith, Julia L; Bodi, Istvan; Halliday, Glenda M; Gearing, Marla; Arzberger, Thomas; Morris, Christopher M; White, Charles L 3rd; Mechawar, Naguib; Boluda, Susana; MacKenzie, Ian R; McLean, Catriona; Cykowski, Matthew D; Wang, Shih-Hsiu J; Graff, Caroline; Nagra, Rashed M; Kovacs, Gabor G; Giaccone, Giorgio; Neumann, Manuela; Ang, Lee-Cyn; Carvalho, Agostinho; Morris, Huw R; Rademakers, Rosa; Hardy, John A; Dickson, Dennis W; Rohrer, Jonathan D; Ross, Owen A

Role of GBA variants in Lewy body disease neuropathology.

GBA变异在路易体病神经病理学中的作用

Walton Ronald L, Koga Shunsuke, Beasley Alexandra I, White Launia J, Griesacker Teresa, Murray Melissa E, Kasanuki Koji, Hou Xu, Fiesel Fabienne C, Springer Wolfdieter, Uitti Ryan J, Fields Julie A, Botha Hugo, Ramanan Vijay K, Kantarci Kejal, Lowe Val J, Jack Clifford R, Ertekin-Taner Nilufer, Savica Rodolfo, Graff-Radford Jonathan, Petersen Ronald C, Parisi Joseph E, Reichard R Ross, Graff-Radford Neill R, Ferman Tanis J, Boeve Bradley F, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen A, Heckman Michael G

Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

出版商更正:弥漫性嗜银颗粒病伴TDP-43蛋白病和神经元中间丝包涵体病:伴混合tau蛋白、TDP-43蛋白和FUS蛋白病理的FTLD

Koga, Shunsuke; Murakami, Aya; Soto-Beasley, Alexandra I; Walton, Ronald L; Baker, Matthew C; Castanedes-Casey, Monica; Josephs, Keith A; Ross, Owen A; Dickson, Dennis W

CWH43 Variants Are Associated With Disease Risk and Clinical Phenotypic Measures in Patients With Normal Pressure Hydrocephalus

CWH43 变异与正常压力脑积水患者的疾病风险和临床表型指标相关

Tipton, Philip W; Atik, Merve; Soto-Beasley, Alexandra I; Day, Gregory S; Grewal, Sanjeet S; Chaichana, Kaisorn; Fermo, Olga P; Ball, Colleen T; Heckman, Michael G; White, Launia J; Quicksall, Zachary S; Reddy, Joseph S; Ramanan, Vijay K; Vemuri, Prashanthi; Elder, Benjamin D; Ertekin-Taner, Nilufer; Ross, Owen; Graff-Radford, Neill