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

In memoriam: Professor Dan J. Stein (1962-2025) — a global pioneer with an African heart

缅怀:丹·J·斯坦教授(1962-2025)——一位拥有非洲情怀的全球先驱

Nalls, Mike A; Pankratz, Nathan; Lill, Christina M; Do, Chuong B; Hernandez, Dena G; Saad, Mohamad; DeStefano, Anita L; Kara, Eleanna; Bras, Jose; Sharma, Manu; Schulte, Claudia; Keller, Margaux F; Arepalli, Sampath; Letson, Christopher; Edsall, Connor; Stefansson, Hreinn; Liu, Xinmin; Pliner, Hannah; Lee, Joseph H; Cheng, Rong; Ikram, M Arfan; Ioannidis, John P A; Hadjigeorgiou, Georgios M; Bis, Joshua C; Martinez, Maria; Perlmutter, Joel S; Goate, Alison; Marder, Karen; Fiske, Brian; Sutherland, Margaret; Xiromerisiou, Georgia; Myers, Richard H; Clark, Lorraine N; Stefansson, Kari; Hardy, John A; Heutink, Peter; Chen, Honglei; Wood, Nicholas W; Houlden, Henry; Payami, Haydeh; Brice, Alexis; Scott, William K; Gasser, Thomas; Bertram, Lars; Eriksson, Nicholas; Foroud, Tatiana; Singleton, Andrew B; Wegener, Gregers; Lerer, Bernard; Frazer, Alan; Grace, Anthony; Ikeda, Kazutaka; Gobbi, Gabriella; Young, Allan; Zohar, Joseph; Blier, Pierre; Kasper, Siegfried; Krystal, John; Yamawaki, Shigeto; Philips, Anthony; Möller, Hans-Jürgen; Belmaker, Robert H; Atwoli, Lukoye; Nutt, David; Harvey, Brian H; Seedat, Soraya; Berk, Michael; Emsley, Robin

Domain mapping of disease mutations reveals pathogenic SORL1 variants in Alzheimer's disease

疾病突变的结构域定位揭示了阿尔茨海默病中的致病性SORL1变异

Andersen, Olav M; de Waal, Matthijs W J; Monti, Giulia; Tesi, Niccolo; Jensen, Anne Mette G; de Geus, Christa; van Spaendonk, Rosalina; Vogel, Maartje; Ahmad, Shahzad; Amin, Najaf; Amouyel, Philippe; Beecham, Gary W; Bellenguez, Céline; Berr, Claudine; Bis, Joshua C; Boland, Anne; Bossù, Paola; Bouwman, Femke; Bras, Jose; Charbonnier, Camille; Clarimon, Jordi; Cruchaga, Carlos; Daniele, Antonio; Dartigues, Jean-François; Debette, Stéphanie; Deleuze, Jean-François; Denning, Nicola; DeStefano, Anita L; Dols-Icardo, Oriol; van Duijn, Cornelia M; Farrer, Lindsay A; Fernández, Maria Victoria; van der Flier, Wiesje M; Fox, Nick C; Galimberti, Daniela; Genin, Emmanuelle; Gille, Johan J P; Grenier-Boley, Benjamin; Grozeva, Detelina; Guen, Yann Le; Guerreiro, Rita; Haines, Jonathan L; Holmes, Clive; Hummerich, Holger; Arfan Ikram, M; Kamran Ikram, M; Kawalia, Amit; Kraaij, Robert; Lambert, Jean-Charles; Lathrop, Marc; Lemstra, Afina W; Lleó, Alberto; Myers, Richard M; Mannens, Marcel M A M; Marshall, Rachel; Martin, Eden R; Masullo, Carlo; Mayeux, Richard; Mead, Simon; Mecocci, Patrizia; Meggy, Alun; Mol, Merel O; Nacmias, Benedetta; Naj, Adam C; Napolioni, Valerio; Nicholas Cochran, J; Nicolas, Gaël; Pasquier, Florence; Pastor, Pau; Pericak-Vance, Margaret A; Pijnenburg, Yolande A L; Piras, Fabrizio; Quenez, Olivier; Ramirez, Alfredo; Raybould, Rachel; Redon, Richard; Reinders, Marcel J T; Richard, Anne-Claire; Riedel-Heller, Steffi G; Rivadeneira, Fernando; van Rooij, Jeroen G J; Rousseau, Stéphane; Ryan, Natalie S; Sanchez-Juan, Pascual; Schellenberg, Gerard D; Scheltens, Philip; Schott, Jonathan M; Seshadri, Sudha; Sie, Daoud; Sims, Rebecca; Sistermans, Erik A; Sorbi, Sandro; van Swieten, John C; Tijms, Betty; Uitterlinden, André G; Visser, Pieter Jelle; Wagner, Michael; Wallon, David; Wang, Li-San; Williams, Julie; Yokoyama, Jennifer S; Zarea, Aline; van der Lee, Sven J; Olsen, Johan G; Hulsman, Marc; Holstege, Henne

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

Ide Copy Number Variant Does Not Influence Stroke Severity in 2 C57BL/6J Mouse Models nor in Humans: An Exploratory Study.

Ide 拷贝数变异不影响 2 个 C57BL/6J 小鼠模型和人类的中风严重程度:一项探索性研究

Foddis Marco, Blumenau Sonja, Mueller Susanne, Messerschmidt Clemens, Rocca Clarissa, Pagnamenta Alistair T, Winek Katarzyna, Endres Matthias, Meisel Andreas, Tucci Arianna, Bras Jose, Guerreiro Rita, Beule Dieter, Dirnagl Ulrich, Sassi Celeste

Treatment of traumatic disruption of the suspensory apparatus in Thoroughbred racehorses at risk of proximal interphalangeal joint subluxation using a locking compression-distal femur plate for double arthrodesis

采用锁定加压远端股骨钢板进行双关节融合术,治疗纯种赛马近端指间关节半脱位风险的悬韧带损伤。

Orozco Lopez, David; Garcia-Lopez, Jose M; Carpenter, Ryan; Bras, Jose J; Richardson, Dean W; Ortved, Kyla F

Genome-wide association study identifies APOE and ZMIZ1 variants as mitophagy modifiers in Lewy body disease

全基因组关联研究发现 APOE 和 ZMIZ1 变异体是路易体病中线粒体自噬的调节因子。

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

Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease

溶酶体多基因风险与路易体病神经病理学的严重程度相关

Tunold, Jon-Anders; Tan, Manuela M X; Koga, Shunsuke; Geut, Hanneke; Rozemuller, Annemieke J M; Valentino, Rebecca; Sekiya, Hiroaki; Martin, Nicholas B; Heckman, Michael G; Bras, Jose; Guerreiro, Rita; Dickson, Dennis W; Toft, Mathias; van de Berg, Wilma D J; Ross, Owen A; Pihlstrøm, Lasse

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease

外显子组测序发现ATP8B4和ABCA1基因中的罕见有害变异是阿尔茨海默病风险因素。

Holstege, Henne; Hulsman, Marc; Charbonnier, Camille; Grenier-Boley, Benjamin; Quenez, Olivier; Grozeva, Detelina; van Rooij, Jeroen G J; Sims, Rebecca; Ahmad, Shahzad; Amin, Najaf; Norsworthy, Penny J; Dols-Icardo, Oriol; Hummerich, Holger; Kawalia, Amit; Amouyel, Philippe; Beecham, Gary W; Berr, Claudine; Bis, Joshua C; Boland, Anne; Bossù, Paola; Bouwman, Femke; Bras, Jose; Campion, Dominique; Cochran, J Nicholas; Daniele, Antonio; Dartigues, Jean-François; Debette, Stéphanie; Deleuze, Jean-François; Denning, Nicola; DeStefano, Anita L; Farrer, Lindsay A; Fernández, Maria Victoria; Fox, Nick C; Galimberti, Daniela; Genin, Emmanuelle; Gille, Johan J P; Le Guen, Yann; Guerreiro, Rita; Haines, Jonathan L; Holmes, Clive; Ikram, M Arfan; Ikram, M Kamran; Jansen, Iris E; Kraaij, Robert; Lathrop, Marc; Lemstra, Afina W; Lleó, Alberto; Luckcuck, Lauren; Mannens, Marcel M A M; Marshall, Rachel; Martin, Eden R; Masullo, Carlo; Mayeux, Richard; Mecocci, Patrizia; Meggy, Alun; Mol, Merel O; Morgan, Kevin; Myers, Richard M; Nacmias, Benedetta; Naj, Adam C; Napolioni, Valerio; Pasquier, Florence; Pastor, Pau; Pericak-Vance, Margaret A; Raybould, Rachel; Redon, Richard; Reinders, Marcel J T; Richard, Anne-Claire; Riedel-Heller, Steffi G; Rivadeneira, Fernando; Rousseau, Stéphane; Ryan, Natalie S; Saad, Salha; Sanchez-Juan, Pascual; Schellenberg, Gerard D; Scheltens, Philip; Schott, Jonathan M; Seripa, Davide; Seshadri, Sudha; Sie, Daoud; Sistermans, Erik A; Sorbi, Sandro; van Spaendonk, Resie; Spalletta, Gianfranco; Tesi, Niccolo'; Tijms, Betty; Uitterlinden, André G; van der Lee, Sven J; Visser, Pieter Jelle; Wagner, Michael; Wallon, David; Wang, Li-San; Zarea, Aline; Clarimon, Jordi; van Swieten, John C; Greicius, Michael D; Yokoyama, Jennifer S; Cruchaga, Carlos; Hardy, John; Ramirez, Alfredo; Mead, Simon; van der Flier, Wiesje M; van Duijn, Cornelia M; Williams, Julie; Nicolas, Gaël; Bellenguez, Céline; Lambert, Jean-Charles

Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer's disease

更正:挑战已接受:揭示罕见基因变异在阿尔茨海默病中的作用

Khani, Marzieh; Gibbons, Elizabeth; Bras, Jose; Guerreiro, Rita