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

Type I interferon drives T cell responses to amyloid beta in the central nervous system

I型干扰素驱动中枢神经系统中T细胞对β-淀粉样蛋白的反应

Michel, Julius J; Sanghvi, Khwab; Rosenbauer, Jakob; Humbs, Lea; Dierssen, Clara Tejido; Grudzenski-Theis, Saskia; Sachs, Viktoria; Jähne, Kristine; Degenhardt, Karoline; Frölich, Lutz; Herms, Jochen; Fatar, Marc; Platten, Michael; Bunse, Lukas

Longitudinal monitoring of tau aggregation in progressive supranuclear palsy with [(18)F]PI-2620 PET

利用[(18)F]PI-2620 PET对进行性核上性麻痹患者的tau蛋白聚集进行纵向监测

Gnörich, Johannes; Kusche-Palenga, Julia; Palleis, Carla; Neubauer, Antonia; Frontzkowski, Lukas; Jäck, Alexander; Kling, Agnes; Bauer, Theresa; Eyob, Hannah; Probst, Katharina; Roemer-Cassiano, Sebastian N; Bernhardt, Alexander M; Katzdobler, Sabrina; Marth, Lena; Zaganjori, Mirlind; Hopfner, Franziska; Zwergal, Andreas; Häckert, Jan; Rullmann, Michael; Sabri, Osama; Barthel, Henryk; Stöcklein, Sophia; Werner, Rudolf A; Simons, Mikael; Levin, Johannes; Herms, Jochen; Franzmeier, Nicolai; Höglinger, Günter U; Brendel, Matthias

The Phenotypic Spectrum of Sporadic Creutzfeldt-Jakob Disease Cortical Subtype

散发型克雅氏病皮质亚型的表型谱

Baiardi, Simone; Vargiu, Claudia Marina; Appleby, Brian S; Barria, Marcelo; Bentivenga, Giuseppe Mario; Calì, Ignazio; Carlà, Benedetta; Cohen, Mark; Giese, Armin; Herms, Jochen; Kortelainen, Aino-Minerva; Ladogana, Anna; Mammana, Angela; Ritchie, Diane; Windl, Otto; Capellari, Sabina; Parchi, Piero

Accuracy of clinical diagnosis in neurodegenerative diseases - a study of 455 autopsy cases

神经退行性疾病临床诊断的准确性——一项基于455例尸检病例的研究

Vöglein, Jonathan; Arzberger, Thomas; Ebner, Irena; Herms, Jochen; Roeber, Sigrun; Ruf, Viktoria; Danek, Adrian; Giese, Armin; Höglinger, Günter U; Levin, Johannes

Distinct TAF15 amyloid filament folds define multiple subtypes of FTLD-TAF15

不同的TAF15淀粉样蛋白丝折叠定义了FTLD-TAF15的多种亚型

Tetter, Stephan; Varghese, Nikhil R; Murzin, Alexey G; De Coster, Wouter; Van den Broeck, Marleen; Roeber, Sigrun; Joseph, Jeffrey T; Newell, Kathy; Castellani, Rudolf; Das, Sumit; Ang, Lee-Cyn; Synofzik, Matthis; Herms, Jochen; Rademakers, Rosa; Ghetti, Bernardino; Lashley, Tammaryn; Mackenzie, Ian R A; Neumann, Manuela; Ryskeldi-Falcon, Benjamin

Clinical Predictors of Intracranial Pathology in Emergency Department Patients with Non-traumatic Headache and No Neurological Deficits: Prospective Study

急诊科非创伤性头痛且无神经功能缺损患者颅内病变的临床预测因素:前瞻性研究

Zhang, Lei; Jiang, Yankai; Zhu, Jie; Liang, Huazheng; He, Xiangyang; Qian, Jiahong; Lin, Hai; Tao, Yubo; Zhu, Keqing; Song, Xiaoxuan; Vecchi, Teodoro De; Widmann, Jeannine; Fierli, Federico; Ruf, Viktoria; Tang, Qilin; Arzberger, Thomas; Roeber, Sigrun; Köglsperger, Thomas; Windl, Otto; Haass, Christian; Winkelmann, Juliane; Herms, Jochen; Strübing, Felix; Serinken, Mustafa; Eken, Cenker; Güngör, Faruk; Akdağ, Ömer; Citisli, Veli

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

Early Locus Coeruleus noradrenergic axon loss drives olfactory dysfunction in Alzheimer's disease.

蓝斑核早期去甲肾上腺素能轴突丢失是阿尔茨海默病嗅觉功能障碍的驱动因素

Meyer Carolin, Niedermeier Theresa, Feyen Paul L C, Strübing Felix L, Rauchmann Boris-Stephan, Karali Katerina, Gentz Johanna, Tillmann Yannik E, Landgraf Nicolas F, Rumpf Svenja-Lotta, Ochs Katharina, Wind-Mark Karin, Biechele Gloria, Wagner Jessica, Guersel Selim, Kurz Carolin I, Schweiger Meike, Prtvar Danilo, Shi Yuan, Banati Richard B, Liu Guo-Jun, Middleton Ryan J, Mitteregger-Kretzschmar Gerda, Perneczky Robert, Koeglsperger Thomas, Neher Jonas J, Tahirovic Sabina, Brendel Matthias, Herms Jochen, Paeger Lars

Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-U

脑转录组学研究揭示了aFTLD-U患者非神经元细胞中大量基因表达和剪接改变。

Alidadiani, Sara; Faura, Júlia; Wynants, Sarah; Peeters, Nele; Van den Broeck, Marleen; De Witte, Linus; Policarpo, Rafaela; Cheung, Simon; Pottier, Cyril; Ghayal, Nikhil B; Mol, Merel O; van Blitterswijk, Marka; Udine, Evan; DeJesus-Hernandez, Mariely; Baker, Matthew; Finch, NiCole A; Asmann, Yan W; van Rooij, Jeroen G J; Nguyen, Aivi T; Ross Reichard, R; Nana, Alissa L; Lopez, Oscar L; Boxer, Adam L; Rosen, Howard J; Spina, Salvatore; Herms, Jochen; Josephs, Keith A; Petersen, Ronald C; Rissman, Robert A; Hiniker, Annie; Ang, Lee-Cyn; Grinberg, Lea T; Halliday, Glenda M; Boeve, Bradley F; Graff-Radford, Neill R; Seelaar, Harro; Neumann, Manuela; Kofler, Julia; White, Charles L 3rd; Seeley, William W; van Swieten, John C; Dickson, Dennis W; Mackenzie, Ian R A; De Coster, Wouter; Rademakers, Rosa