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

Neuropathology, Localized Proteomics, and Imaging of the Choroid Plexus across the Alzheimer's Disease Continuum

阿尔茨海默病连续谱中脉络丛的神经病理学、局部蛋白质组学和成像

Strickland, Samantha L; Morel, Hélène; Prusinski, Christian; Allen, Mariet; Patel, Tulsi A; Carrasquillo, Minerva M; Conway, Olivia J; Lincoln, Sarah J; Reddy, Joseph S; Nguyen, Thuy; Malphrus, Kimberly G; Soto, Alexandra I; Walton, Ronald L; Crook, Julia E; Murray, Melissa E; Boeve, Bradley F; Petersen, Ronald C; Lucas, John A; Ferman, Tanis J; Uitti, Ryan J; Wszolek, Zbigniew K; Ross, Owen A; Graff-Radford, Neill R; Dickson, Dennis W; Ertekin-Taner, Nilüfer; Leitner, Dominique; Li, Chenyang; Pang, Huize; Bruno, Mary; Faustin, Arline; Devinsky, Orrin; Kanshin, Evgeny; Ueberheide, Beatrix; Zaim‐Wadghiri, Youssef; Zhang, Jiangyang; Ge, Yulin; Wisniewski, Thomas

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

Genome sequence analyses identify novel risk loci for multiple system atrophy

基因组序列分析发现了多系统萎缩的新风险位点

Chia, Ruth; Ray, Anindita; Shah, Zalak; Ding, Jinhui; Ruffo, Paola; Fujita, Masashi; Menon, Vilas; Saez-Atienzar, Sara; Reho, Paolo; Kaivola, Karri; Walton, Ronald L; Reynolds, Regina H; Karra, Ramita; Sait, Shaimaa; Akcimen, Fulya; Diez-Fairen, Monica; Alvarez, Ignacio; Fanciulli, Alessandra; Stefanova, Nadia; Seppi, Klaus; Duerr, Susanne; Leys, Fabian; Krismer, Florian; Sidoroff, Victoria; Zimprich, Alexander; Pirker, Walter; Rascol, Olivier; Foubert-Samier, Alexandra; Meissner, Wassilios G; Tison, François; Pavy-Le Traon, Anne; Pellecchia, Maria Teresa; Barone, Paolo; Russillo, Maria Claudia; Marín-Lahoz, Juan; Kulisevsky, Jaime; Torres, Soraya; Mir, Pablo; Periñán, Maria Teresa; Proukakis, Christos; Chelban, Viorica; Wu, Lesley; Goh, Yee Y; Parkkinen, Laura; Hu, Michele T; Kobylecki, Christopher; Saxon, Jennifer A; Rollinson, Sara; Garland, Emily; Biaggioni, Italo; Litvan, Irene; Rubio, Ileana; Alcalay, Roy N; Kwei, Kimberly T; Lubbe, Steven J; Mao, Qinwen; Flanagan, Margaret E; Castellani, Rudolph J; Khurana, Vikram; Ndayisaba, Alain; Calvo, Andrea; Mora, Gabriele; Canosa, Antonio; Floris, Gianluca; Bohannan, Ryan C; Moore, Anni; Norcliffe-Kaufmann, Lucy; Palma, Jose-Alberto; Kaufmann, Horacio; Kim, Changyoun; Iba, Michiyo; Masliah, Eliezer; Dawson, Ted M; Rosenthal, Liana S; Pantelyat, Alexander; Albert, Marilyn S; Pletnikova, Olga; Troncoso, Juan C; Infante, Jon; Lage, Carmen; Sánchez-Juan, Pascual; Serrano, Geidy E; Beach, Thomas G; Pastor, Pau; Morris, Huw R; Albani, Diego; Clarimon, Jordi; Wenning, Gregor K; Hardy, John A; Ryten, Mina; Topol, Eric; Torkamani, Ali; Chiò, Adriano; Bennett, David A; De Jager, Philip L; Low, Philip A; Singer, Wolfgang; Cheshire, William P; Wszolek, Zbigniew K; Dickson, Dennis W; Traynor, Bryan J; Gibbs, J Raphael; Dalgard, Clifton L; Ross, Owen A; Houlden, Henry; Scholz, Sonja W

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

Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease

创建皮克氏病国际联盟:MAPT H2 单倍型与皮克氏病风险的关联研究

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; Warner, Thomas T; Jaunmuktane, Zane; Boeve, Bradley F; Christopher, Elizabeth A; DeTure, Michael; Duara, Ranjan; Graff-Radford, Neill R; Josephs, Keith A; Knopman, David S; Koga, Shunsuke; Murray, Melissa E; Lyons, Kelly E; Pahwa, Rajesh; Parisi, Joseph E; Petersen, Ronald C; Whitwell, Jennifer; Grinberg, Lea T; Miller, Bruce; Schlereth, Athena; Seeley, William W; Spina, Salvatore; Grossman, Murray; Irwin, David J; Lee, Edward B; Suh, EunRan; Trojanowski, John Q; Van Deerlin, Vivianna M; Wolk, David A; Connors, Theresa R; Dooley, Patrick M; Frosch, Matthew P; Oakley, Derek H; Aldecoa, Iban; Balasa, Mircea; Gelpi, Ellen; Borrego-Écija, Sergi; de Eugenio Huélamo, Rosa Maria; Gascon-Bayarri, Jordi; Sánchez-Valle, Raquel; Sanz-Cartagena, Pilar; Piñol-Ripoll, Gerard; Molina-Porcel, Laura; Bigio, Eileen H; Flanagan, Margaret E; Gefen, Tamar; Rogalski, Emily J; Weintraub, Sandra; Redding-Ochoa, Javier; Chang, Koping; Troncoso, Juan C; Prokop, Stefan; Newell, Kathy L; Ghetti, Bernardino; Jones, Matthew; Richardson, Anna; Robinson, Andrew C; Roncaroli, Federico; Snowden, Julie; Allinson, Kieren; Green, Oliver; Rowe, James B; Singh, Poonam; Beach, Thomas G; Serrano, Geidy E; Flowers, Xena E; Goldman, James E; Heaps, Allison C; Leskinen, Sandra P; Teich, Andrew F; Black, Sandra E; Keith, Julia L; Masellis, Mario; Bodi, Istvan; King, Andrew; Sarraj, Safa-Al; Troakes, Claire; Halliday, Glenda M; Hodges, John R; Kril, Jillian J; Kwok, John B; Piguet, Olivier; Gearing, Marla; Arzberger, Thomas; Roeber, Sigrun; Attems, Johannes; Morris, Christopher M; Thomas, Alan J; Evers, Bret M; White, Charles L; Mechawar, Naguib; Sieben, Anne A; Cras, Patrick P; De Vil, Bart B; De Deyn, Peter Paul P P; Duyckaerts, Charles; Le Ber, Isabelle; Seihean, Danielle; Turbant-Leclere, Sabrina; MacKenzie, Ian R; McLean, Catriona; Cykowski, Matthew D; Ervin, John F; Wang, Shih-Hsiu J; Graff, Caroline; Nennesmo, Inger; Nagra, Rashed M; Riehl, James; Kovacs, Gabor G; Giaccone, Giorgio; Nacmias, Benedetta; Neumann, Manuela; Ang, Lee-Cyn; Finger, Elizabeth C; Blauwendraat, Cornelis; Nalls, Mike A; Singleton, Andrew B; Vitale, Dan; Cunha, Cristina; Carvalho, Agostinho; Wszolek, Zbigniew K; Morris, Huw R; Rademakers, Rosa; Hardy, John A; Dickson, Dennis W; Rohrer, Jonathan D; Ross, Owen A

Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures

路易体痴呆症中线粒体基因组变异:与疾病风险和神经病理学指标的关联

Valentino, Rebecca R; Ramnarine, Chloe; Heckman, Michael G; Johnson, Patrick W; Soto-Beasley, Alexandra I; Walton, Ronald L; Koga, Shunsuke; Kasanuki, Koji; Murray, Melissa E; 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

Dancing Feet Dyskinesia in a Patient with GBA-PD

GBA-PD患者的舞蹈足运动障碍

Olszewska, Diana A; McCarthy, Allan; Soto-Beasley, Alexandra I; Walton, Ronald L; Ross, Owen A; Lynch, Tim

PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson's disease in Ireland

爱尔兰早发性帕金森病患者的PARKIN、PINK1和DJ1基因分析

Olszewska, Diana A; McCarthy, Allan; Soto-Beasley, Alexandra I; Walton, Ronald L; Ross, Owen A; Lynch, Tim

Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease

线粒体DNA基因组变异与皮克病风险的关联

Valentino, Rebecca R; Heckman, Michael G; Johnson, Patrick W; Baker, Matthew C; Soto-Beasley, Alexandra I; Walton, Ronald L; Koga, Shunsuke; Roemer, Shanu F; Suh, EunRan; Uitti, Ryan J; Trojanowski, John Q; Grossman, Murray; Van Deerlin, Vivianna M; Rademakers, Rosa; Wszolek, Zbigniew K; Dickson, Dennis W; Ross, Owen A