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

Charles Weissmann (1931–2025), an outstanding and captivating molecular biologist

查尔斯·魏斯曼(1931–2025),一位杰出而富有魅力的分子生物学家

van Rheenen, Wouter; van der Spek, Rick A A; Bakker, Mark K; van Vugt, Joke J F A; Hop, Paul J; Zwamborn, Ramona A J; de Klein, Niek; Westra, Harm-Jan; Bakker, Olivier B; Deelen, Patrick; Shireby, Gemma; Hannon, Eilis; Moisse, Matthieu; Baird, Denis; Restuadi, Restuadi; Dolzhenko, Egor; Dekker, Annelot M; Gawor, Klara; Westeneng, Henk-Jan; Tazelaar, Gijs H P; van Eijk, Kristel R; Kooyman, Maarten; Byrne, Ross P; Doherty, Mark; Heverin, Mark; Al Khleifat, Ahmad; Iacoangeli, Alfredo; Shatunov, Aleksey; Ticozzi, Nicola; Cooper-Knock, Johnathan; Smith, Bradley N; Gromicho, Marta; Chandran, Siddharthan; Pal, Suvankar; Morrison, Karen E; Shaw, Pamela J; Hardy, John; Orrell, Richard W; Sendtner, Michael; Meyer, Thomas; Başak, Nazli; van der Kooi, Anneke J; Ratti, Antonia; Fogh, Isabella; Gellera, Cinzia; Lauria, Giuseppe; Corti, Stefania; Cereda, Cristina; Sproviero, Daisy; D'Alfonso, Sandra; Sorarù, Gianni; Siciliano, Gabriele; Filosto, Massimiliano; Padovani, Alessandro; Chiò, Adriano; Calvo, Andrea; Moglia, Cristina; Brunetti, Maura; Canosa, Antonio; Grassano, Maurizio; Beghi, Ettore; Pupillo, Elisabetta; Logroscino, Giancarlo; Nefussy, Beatrice; Osmanovic, Alma; Nordin, Angelica; Lerner, Yossef; Zabari, Michal; Gotkine, Marc; Baloh, Robert H; Bell, Shaughn; Vourc'h, Patrick; Corcia, Philippe; Couratier, Philippe; Millecamps, Stéphanie; Meininger, Vincent; Salachas, François; Mora Pardina, Jesus S; Assialioui, Abdelilah; Rojas-García, Ricardo; Dion, Patrick A; Ross, Jay P; Ludolph, Albert C; Weishaupt, Jochen H; Brenner, David; Freischmidt, Axel; Bensimon, Gilbert; Brice, Alexis; Durr, Alexandra; Payan, Christine A M; Saker-Delye, Safa; Wood, Nicholas W; Topp, Simon; Rademakers, Rosa; Tittmann, Lukas; Lieb, Wolfgang; Franke, Andre; Ripke, Stephan; Braun, Alice; Kraft, Julia; Whiteman, David C; Olsen, Catherine M; Uitterlinden, Andre G; Hofman, Albert; Rietschel, Marcella; Cichon, Sven; Nöthen, Markus M; Amouyel, Philippe; Traynor, Bryan J; Singleton, Andrew B; Mitne Neto, Miguel; Cauchi, Ruben J; Ophoff, Roel A; Wiedau-Pazos, Martina; Lomen-Hoerth, Catherine; van Deerlin, Vivianna M; Grosskreutz, Julian; Roediger, Annekathrin; Gaur, Nayana; Jörk, Alexander; Barthel, Tabea; Theele, Erik; Ilse, Benjamin; Stubendorff, Beatrice; Witte, Otto W; Steinbach, Robert; Hübner, Christian A; Graff, Caroline; Brylev, Lev; Fominykh, Vera; Demeshonok, Vera; Ataulina, Anastasia; Rogelj, Boris; Koritnik, Blaž; Zidar, Janez; Ravnik-Glavač, Metka; Glavač, Damjan; Stević, Zorica; Drory, Vivian; Povedano, Monica; Blair, Ian P; Kiernan, Matthew C; Benyamin, Beben; Henderson, Robert D; Furlong, Sarah; Mathers, Susan; McCombe, Pamela A; Needham, Merrilee; Ngo, Shyuan T; Nicholson, Garth A; Pamphlett, Roger; Rowe, Dominic B; Steyn, Frederik J; Williams, Kelly L; Mather, Karen A; Sachdev, Perminder S; Henders, Anjali K; Wallace, Leanne; de Carvalho, Mamede; Pinto, Susana; Petri, Susanne; Weber, Markus; Rouleau, Guy A; Silani, Vincenzo; Curtis, Charles J; Breen, Gerome; Glass, Jonathan D; Brown, Robert H Jr; Landers, John E; Shaw, Christopher E; Andersen, Peter M; Groen, Ewout J N; van Es, Michael A; Pasterkamp, R Jeroen; Fan, Dongsheng; Garton, Fleur C; McRae, Allan F; Davey Smith, George; Gaunt, Tom R; Eberle, Michael A; Mill, Jonathan; McLaughlin, Russell L; Hardiman, Orla; Kenna, Kevin P; Wray, Naomi R; Tsai, Ellen; Runz, Heiko; Franke, Lude; Al-Chalabi, Ammar; Van Damme, Philip; van den Berg, Leonard H; Veldink, Jan H; Borst, Piet; Flavell, Richard A

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis

大规模外显子组分析揭示了肌萎缩侧索硬化症中新的罕见变异贡献

Hop, Paul J; Kooyman, Maarten; Kenna, Brendan J; Zwamborn, Ramona A J; van Eijk, Kristel R; Wang, Yan; van Dijk, Charlotte H; Bekema, Erwin; van Rheenen, Wouter; Beele, Paul; van Vugt, Joke J F A; Khleifat, Ahmad Al; Iacoangeli, Alfredo; Cooper-Knock, Johnathan; Smith, Bradley N; Topp, Simon; van der Kooi, Anneke J; Fominykh, Vera; Drory, Vivian; Lerner, Yossef; Shovman, Yehuda; Rowe, Dominic B; Williams, Kelly L; McLaughlin, Russell L; Hurt, Jessica; Huang, Yunfeng; Chen, Chia-Yen; Tsai, Ellen; Runz, Heiko; Aronica, Eleonora; Groen, Ewout J N; van Es, Michael A; Pasterkamp, R Jeroen; Farhan, Sali M K; Garton, Fleur C; McRae, Allan F; McCombe, Pamela A; Henderson, Robert D; Fan, Dongsheng; Šlachtová, Lenka; Høyer, Helle; Nishimura, Agnes L; Cauchi, Ruben J; Brylev, Lev; Rogelj, Boris; Koritnik, Blaž; Zidar, Janez; Salas, Teresa; Mora Pardina, Jesus S; Gotkine, Marc; Povedano, Monica; Corcia, Philippe; Vourc'h, Patrick; Couratier, Philippe; Weber, Markus; Kiernan, Matthew C; Pamphlett, Roger; Blair, Ian P; de Carvalho, Mamede; Başak, Nazli A; Ingre, Caroline; Andersen, Peter M; Zinman, Lorne; Rogaeva, Ekaterina; MacKenzie, Ian R; Dupre, Nicolas; Rouleau, Guy A; Traynor, Bryan J; Ticozzi, Nicola; Chiò, Adriano; Silani, Vincenzo; Hardiman, Orla; Phatnani, Hemali; Harms, Matthew B; Dalgard, Clifton L; Glass, Jonathan D; Landers, John E; Van Damme, Philip; Morrison, Karen E; Shaw, Pamela J; Shaw, Chris E; Al-Chalabi, Ammar; van den Berg, Leonard H; Kenna, Kevin P; Veldink, Jan H

Bi-allelic intermediate ATXN2 repeat expansions are associated with slow progressing, leg-onset familial ALS

双等位基因中间型 ATXN2 重复序列扩增与进展缓慢、腿部起病的家族性 ALS 相关。

Demaegd, Koen Cedric; Koole, Wouter; van Vugt, Joke Jfa; Dankbaar, Jan Willem; Hendrikse, Jeroen; Nazlı Başak, A; de Carvalho, Mamede; Corcia, Philippe; Codron, Philippe; Bernard, Emilien; Guissart, Claire; Couratier, Philippe; Povedano Panades, Mónica; van Doorn, Pieter A; Warrenburg, Bart P; Cooper-Knock, Johnathan; Pasterkamp, R Jeroen; van Rheenen, Wouter; van Damme, Philip; van den Berg, Leonard H; Veldink, Jan Herman; van Es, Michael A

Reldesemtiv in Amyotrophic Lateral Sclerosis: Results From the COURAGE-ALS Randomized Clinical Trial

Reldesemtiv治疗肌萎缩侧索硬化症:COURAGE-ALS随机临床试验结果

Shefner, Jeremy M; Cudkowicz, Merit E; Genge, Angela; Hardiman, Orla; Al-Chalabi, Ammar; Andrews, Jinsy A; Chio, Adriano; Corcia, Philippe; Couratier, Philippe; de Carvalho, Mamede; Heiman-Patterson, Terry; Henderson, Robert D; Ingre, Caroline; Johnston, Wendy; Ludolph, Albert; Maragakis, Nicholas J; Miller, Timothy M; Mora, Jesus S; Petri, Susanne; Simmons, Zachary; van den Berg, Leonard H; Zinman, Lorne; Kupfer, Stuart; Malik, Fady I; Meng, Lisa; Simkins, Tyrell J; Wei, Jenny; Wolff, Andrew A; Rudnicki, Stacy A

Quantifying multimodal longitudinal brain changes in presymptomatic C9orf72 disease

量化C9orf72疾病前驱期多模态纵向脑部变化

Saracino, Dario; Cipriano, Lorenzo; Houot, Marion; Querin, Giorgia; Rinaldi, Daisy; Rametti-Lacroux, Armelle; Wallon, David; Gerardin, Emmanuel; Couratier, Philippe; Boncoeur, Marie-Paule; Lebouvier, Thibaud; Colliot, Olivier; Pradat, Pierre-François; Migliaccio, Raffaella; Le Ber, Isabelle

Oligogenic structure of amyotrophic lateral sclerosis has genetic testing, counselling and therapeutic implications

肌萎缩侧索硬化症的寡基因结构具有基因检测、咨询和治疗意义。

Iacoangeli, Alfredo; Dilliott, Allison A; Al Khleifat, Ahmad; Andersen, Peter M; Başak, Nazlı A; Cooper-Knock, Johnathan; Corcia, Philippe; Couratier, Philippe; deCarvalho, Mamede; Drory, Vivian E; Glass, Jonathan D; Gotkine, Marc; Lerner, Yosef M; Hardiman, Orla; Landers, John E; McLaughlin, Russell L; Pardina, Jesus S Mora; Morrison, Karen; Pinto, Susana; Povedano, Monica; Shaw, Christopher E; Shaw, Pamela J; Silani, Vincenzo; Ticozzi, Nicola; van Damme, Philip; van den Berg, Leonard H; Vourc'h, Patrick; Weber, Markus; Veldink, Jan Herman; Dobson, Richard; Rouleau, Guy A; Al-Chalabi, Ammar; Farhan, Sali M K

Improving ALS Molecular Diagnosis Through Functional Assays: Reassessment of a SOD1 Variant of Uncertain Significance

通过功能性检测改进ALS分子诊断:重新评估意义未明的SOD1变异体

Bedja-Iacona, Léa; Forget, Arthur; Boisseau, Chloé; Marouillat, Sylviane; Chudinova, Aleksandra; Veyrat-Durebex, Charlotte; Guissart, Claire; Lumbroso, Serge; Raoul, Cédric; Andres, Christian R; Blasco, Hélène; Couratier, Philippe; Corcia, Philippe; Verschueren, Annie; Mouzat, Kevin; Vourc'h, Patrick

MAPT mutations in amyotrophic lateral sclerosis: clinical, neuropathological and functional insights

肌萎缩侧索硬化症中的MAPT基因突变:临床、神经病理学和功能方面的见解

De Bertier, Sibylle; Lautrette, Géraldine; Amador, Maria-Del-Mar; Miki, Tomoko; Boillée, Séverine; Lobsiger, Christian Stefan; Bohl, Delphine; Darios, Frederic; Machat, Selma; Duchesne, Mathilde; Vourc'h, Patrick; Fauret-Amsellem, Anne-Laure; Corcia, Philippe; Guy, Nathalie; Couratier, Philippe; Seilhean, Danielle; Millecamps, Stéphanie

Epidemiology, disease evolution and economic burden of amyotrophic lateral sclerosis in France using the French national health data system

利用法国国家健康数据系统研究法国肌萎缩侧索硬化症的流行病学、疾病演变和经济负担

Corcia, Philippe; Stenson, Katie; Doutriaux, Agathe; Hadjrabia, Hicham; Boer, François; Issa, Seham; Marguet, Sophie; Bernard, Frederic; Nasanbat, Enkhgerel; Nowacki, Gregoire; de Pouvourville, Gérard; Couratier, Philippe

Prevalence of SOD1 and C9orf72 Variants Among French ALS Population: The GENIALS Study

法国ALS人群中SOD1和C9orf72变异体的患病率:GENIALS研究

Corcia, P; Erazo, D; Amador, M D M; Beltran, S; Bernard, E; Blasco, H; Boutoleau-Bretonniere, C; Bruneteau, G; Camdessanche, J P; Camu, W; Cassereau, J; Choumert, A; Codron, P; Cintas, P; De La Cruz, E; Danel, V; Desnuelle, C; Eyraud, N; Esselin, F; Fauret, A L; Lefilliatre, M; Fleury, M C; Genestet, S; Grapperon, A M; Guy, N; Jacquin-Piques, A; Beauvais, K; Lautrette, G; Le Masson, G; Mathis, S; Piegay, A S; Pittion-Vouyovitch, S; Sauleau, P; Soriani, M H; Vershueren, A; Mouzat, K; Guissart, C; Couratier, P; Vourc'h, P