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

Alzheimer's disease polygenic risk in early- and late-onset Alzheimer's disease

早发型和晚发型阿尔茨海默病的多基因风险

Pentchev, Julian V; Jackson, Trever; Khan, Naazneen; Rosewood, Thea J; Huang, Yen-Ning; Nho, Kwangsik; Saykin, Andrew J; Eloyan, Ani; Taurone, Alexander; Thangarajah, Maryanne; Riddle, Meghan; Salloway, Steven; Atri, Alireza; Honig, Lawrence S; Johnson, Erik C B; Turner, Raymond Scott; Masdeu, Joseph C; Foroud, Tatiana M; Clark, David; Hammers, Dustin B; Dage, Jeffrey L; Kirby, Kala; Ghetti, Bernardino; Newell, Kathy; Onyike, Chiadi U; Day, Gregory S; Graff-Radford, Neill R; Murray, Melissa E; Jones, David T; Jack, Clifford R Jr; Vemuri, Prashanthi; Touroutoglou, Alexandra; Duara, Ranjan; Grant, Ian; Sha, Sharon; Wingo, Thomas S; Beckett, Laurel A; Rogalski, Emily; Mendez, Mario F; Kramer, Joel; La Joie, Renaud; Blazhenets, Ganna; Grinberg, Lea T; Koeppe, Robert; Wolk, David A; Aisen, Paul; Raman, Rema; Toga, Arthur; Kukull, Walter A; Musiek, Erik; Womack, Kyle B; Carrillo, Maria C; Rabinovici, Gil D; Dickerson, Bradford C; Apostolova, Liana G; Nudelman, Kelly N H

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

Pathological TDP-43 filaments accumulate at synapses and cause synaptic dysfunction.

病理性 TDP-43 丝状物在突触处积聚,导致突触功能障碍。

Chen Renren, Stockwell Imogen, Pierce Jessica C, Peak-Chew Sew-Yeu, Huang Melissa, Newell Kathy, Ghetti Bernardino, Cousin Michael A, Greger Ingo H, Ryskeldi-Falcon Benjamin

Dissociable spatial topography of cortical atrophy in early-onset and late-onset Alzheimer's disease: A head-to-head comparison of the LEADS and ADNI cohorts

早发型和晚发型阿尔茨海默病皮质萎缩的空间地形可分离性:LEADS 和 ADNI 队列的直接比较

Katsumi, Yuta; Touroutoglou, Alexandra; Brickhouse, Michael; Eloyan, Ani; Eckbo, Ryan; Zaitsev, Alexander; La Joie, Renaud; Lagarde, Julien; Schonhaut, Daniel; Thangarajah, Maryanne; Taurone, Alexander; Vemuri, Prashanthi; Jack, Clifford R Jr; Dage, Jeffrey L; Nudelman, Kelly N H; Foroud, Tatiana; Hammers, Dustin B; Ghetti, Bernardino; Murray, Melissa E; Newell, Kathy L; Polsinelli, Angelina J; Aisen, Paul; Reman, Rema; Beckett, Laurel; Kramer, Joel H; Atri, Alireza; Day, Gregory S; Duara, Ranjan; Graff-Radford, Neill R; Grant, Ian M; Honig, Lawrence S; Johnson, Erik C B; Jones, David T; Masdeu, Joseph C; Mendez, Mario F; Musiek, Erik; Onyike, Chiadi U; Riddle, Meghan; Rogalski, Emily; Salloway, Stephen; Sha, Sharon; Turner, R Scott; Wingo, Thomas S; Wolk, David A; Womack, Kyle; Carrillo, Maria C; Rabinovici, Gil D; Apostolova, Liana G; Dickerson, Bradford C

Celebrating neuropathology's contributions to Alzheimer's Disease Research Centers

庆祝神经病理学对阿尔茨海默病研究中心的贡献

Fischer, D Luke; Grinberg, Lea T; Ahrendsen, Jared T; Beach, Thomas G; Bieniek, Kevin F; Castellani, Rudolph J; Chkheidze, Rati; Cobos, Inma; Cohen, Mark; Crary, John F; Dickson, Dennis W; Dugger, Brittany N; Dunlop, Sara R; Farrell, Kurt; Ghetti, Bernardino; Haeri, Mohammad; Harrison, William; Head, Elizabeth; Hiniker, Annie; Huang, Eric J; Huttner, Anita; Jamshidi, Pouya; Kapasi, Alifiya; Keene, C Dirk; Kofler, Julia; Latimer, Caitlin S; McKee, Ann C; Mente, Karin; Miller, Michael B; Montine, Thomas J; Morris, Meaghan; Murray, Melissa E; Nelson, Peter T; Newell, Kathy L; Perrin, Richard J; Ramani, Biswarathan; Reichard, R Ross; Roy, Subhojit; Schlachetzki, Johannes C M; Seeley, William W; Serrano, Geidy E; Spina, Salvatore; Teich, Andrew F; Wang, Shih-Hsiu J; Wisniewski, Thomas; Lee, Edward B

Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells

17q21.31拷贝数变异和单倍型分析揭示了进行性核上性麻痹风险增加以及神经元细胞基因表达变化。

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Si, Ya-Qin; Tucci, Albert; Patil, Vishakha; Valiente-Banuet, Leopoldo; Li, Chong; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Donker Kaat, Laura; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivianna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw R; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Compta, Yaroslau; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Tzeng, Jung-Ying; Geschwind, Daniel H; Schellenberg, Gerard D; Lee, Wan-Ping

Single‐nuclei transcriptomic identifies neuronal populations vulnerable to AD by leveraging AD variants

单核转录组学利用AD变异体识别易受AD影响的神经元群体

Deng, Guowei; Xia, Hui; Shang, De-Wei; Wen, Yuguan; Hu, Jinqing; Tan, Yaqian; Sannemann, Lena; Buerger, Katharina; Hellmann‐Regen, Julian; Kleineidam, Luca; Laske, Christoph; Perneczky, Robert; Peters, Oliver; Priller, Josef; Ramirez, Alfredo; Schneider, Anja; Spottke, Annika; Synofzik, Matthis; Teipel, Stefan J; Wagner, Michael; Wiltfang, Jens; Yakupov, Renat; Düzel, Emrah; Jessen, Frank; Ramirez, Aura M; Nasciben, Luciana Bertholim; Moura, Sofia; Coombs, Lauren E; Robayo, Maria C; Rajabli, Farid; DeRosa, Brooke A; Whitehead, Patrice G; Adams, Larry D; Starks, Takiyah D; Mena, Pedro R; Illanes‐Manrique, Maryenela Z; Tejada, Sergio J; Byrd, Goldie S; Cornejo‐Olivas, Mario; Feliciano‐Astacio, Briseida E; Wang, Liyong; Xu, Wanying; Jin, Fulai; Pericak‐Vance, Margaret; Dykxhoorn, Derek M; Griswold, Anthony J; Young, Juan I; Vance, Jeffery M; Pereira, Felipe Luiz; Lew, Caroline; Li, Song Hua; Rizzi, Liara; Araujo, Igor Prufer Q C; Soloviev, Alexander V; Spina, Salvatore; Rexach, Jessica E; Seeley, William W; Suemoto, Claudia Kimie; Leite, Renata Elaine Paraizo; Newell, Kathy L; Ghetti, Bernardino; Murray, Melissa E; Grinberg, Lea T

Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

全基因组测序分析揭示了与进行性核上性麻痹相关的新的易感基因位点和结构变异

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivanna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Schellenberg, Gerard D; Geschwind, Daniel H; Lee, Wan-Ping

Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy

更正:全基因组测序分析揭示了与进行性核上性麻痹相关的新的易感基因位点和结构变异

Wang, Hui; Chang, Timothy S; Dombroski, Beth A; Cheng, Po-Liang; Patil, Vishakha; Valiente-Banuet, Leopoldo; Farrell, Kurt; Mclean, Catriona; Molina-Porcel, Laura; Rajput, Alex; De Deyn, Peter Paul; Le Bastard, Nathalie; Gearing, Marla; Kaat, Laura Donker; Van Swieten, John C; Dopper, Elise; Ghetti, Bernardino F; Newell, Kathy L; Troakes, Claire; de Yébenes, Justo G; Rábano-Gutierrez, Alberto; Meller, Tina; Oertel, Wolfgang H; Respondek, Gesine; Stamelou, Maria; Arzberger, Thomas; Roeber, Sigrun; Müller, Ulrich; Hopfner, Franziska; Pastor, Pau; Brice, Alexis; Durr, Alexandra; Le Ber, Isabelle; Beach, Thomas G; Serrano, Geidy E; Hazrati, Lili-Naz; Litvan, Irene; Rademakers, Rosa; Ross, Owen A; Galasko, Douglas; Boxer, Adam L; Miller, Bruce L; Seeley, Willian W; Van Deerlin, Vivanna M; Lee, Edward B; White, Charles L 3rd; Morris, Huw; de Silva, Rohan; Crary, John F; Goate, Alison M; Friedman, Jeffrey S; Leung, Yuk Yee; Coppola, Giovanni; Naj, Adam C; Wang, Li-San; Dalgard, Clifton; Dickson, Dennis W; Höglinger, Günter U; Schellenberg, Gerard D; Geschwind, Daniel H; Lee, Wan-Ping