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

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

Sensitivity and specificity of a seed amplification assay for diagnosis of multiple system atrophy: a multicentre cohort study

种子扩增检测法诊断多系统萎缩的敏感性和特异性:一项多中心队列研究

Ma, Yihua; Farris, Carly M; Weber, Sandrina; Schade, Sebastian; Nguyen, Hieu; Pérez-Soriano, Alexandra; Giraldo, Darly M; Fernández, Manel; Soto, Marta; Cámara, Ana; Painous, Celia; Muñoz, Esteban; Valldeoriola, Francesc; Martí, Maria J; Clarimon, Jordi; Kallunki, Pekka; Ma, Thong Chi; Alcalay, Roy N; Gomes, Bárbara Fernandez; Blennow, Kaj; Zetterberg, Henrik; Constantinescu, Julius; Mengel, David; Kadam, Vaibhavi; Parchi, Piero; Brockmann, Kathrin; Tropea, Thomas F; Siderowf, Andrew; Synofzik, Matthis; Kang, Un Jung; Compta, Yaroslau; Svenningsson, Per; Mollenhauer, Brit; Concha-Marambio, Luis

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

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

全基因组分析揭示了MAPT、MOBP和APOE基因位点在散发性额颞叶痴呆症中的潜在作用

Manzoni, Claudia; Kia, Demis A; Ferrari, Raffaele; Leonenko, Ganna; Costa, Beatrice; Saba, Valentina; Jabbari, Edwin; Tan, Manuela Mx; Albani, Diego; Alvarez, Victoria; Alvarez, Ignacio; Andreassen, Ole A; Angiolillo, Antonella; Arighi, Andrea; Baker, Matt; Benussi, Luisa; Bessi, Valentina; Binetti, Giuliano; Blackburn, Daniel J; Boada, Merce; Boeve, Bradley F; Borrego-Ecija, Sergi; Borroni, Barbara; Bråthen, Geir; Brooks, William S; Bruni, Amalia C; Caroppo, Paola; Bandres-Ciga, Sara; Clarimon, Jordi; Colao, Rosanna; Cruchaga, Carlos; Danek, Adrian; de Boer, Sterre Cm; de Rojas, Itziar; di Costanzo, Alfonso; Dickson, Dennis W; Diehl-Schmid, Janine; Dobson-Stone, Carol; Dols-Icardo, Oriol; Donizetti, Aldo; Dopper, Elise; Durante, Elisabetta; Ferrari, Camilla; Forloni, Gianluigi; Frangipane, Francesca; Fratiglioni, Laura; Kramberger, Milica G; Galimberti, Daniela; Gallucci, Maurizio; García-González, Pablo; Ghidoni, Roberta; Giaccone, Giorgio; Graff, Caroline; Graff-Radford, Neill R; Grafman, Jordan; Halliday, Glenda M; Hernandez, Dena G; Hjermind, Lena E; Hodges, John R; Holloway, Guy; Huey, Edward D; Illán-Gala, Ignacio; Josephs, Keith A; Knopman, David S; Kristiansen, Mark; Kwok, John B; Leber, Isabelle; Leonard, Hampton L; Libri, Ilenia; Lleo, Alberto; Mackenzie, Ian R; Madhan, Gaganjit K; Maletta, Raffaele; Marquié, Marta; Maver, Ales; Menendez-Gonzalez, Manuel; Milan, Graziella; Miller, Bruce L; Morris, Christopher M; Morris, Huw R; Nacmias, Benedetta; Newton, Judith; Nielsen, Jørgen E; Nilsson, Christer; Novelli, Valeria; Padovani, Alessandro; Pal, Suvankar; Pasquier, Florence; Pastor, Pau; Perneczky, Robert; Peterlin, Borut; Petersen, Ronald C; Piguet, Olivier; Pijnenburg, Yolande Al; Puca, Annibale A; Rademakers, Rosa; Rainero, Innocenzo; Reus, Lianne M; Richardson, Anna Mt; Riemenschneider, Matthias; Rogaeva, Ekaterina; Rogelj, Boris; Rollinson, Sara; Rosen, Howard; Rossi, Giacomina; Rowe, James B; Rubino, Elisa; Ruiz, Agustin; Salvi, Erika; Sanchez-Valle, Raquel; Sando, Sigrid Botne; Santillo, Alexander F; Saxon, Jennifer A; Schlachetzki, Johannes Cm; Scholz, Sonja W; Seelaar, Harro; Seeley, William W; Serpente, Maria; Sorbi, Sandro; Sordon, Sabrina; St George-Hyslop, Peter; Thompson, Jennifer C; Van Broeckhoven, Christine; Van Deerlin, Vivianna M; Van der Lee, Sven J; Van Swieten, John; Tagliavini, Fabrizio; van der Zee, Julie; Veronesi, Arianna; Vitale, Emilia; Waldo, Maria Landqvist; Yokoyama, Jennifer S; Nalls, Mike A; Momeni, Parastoo; Singleton, Andrew B; Hardy, John; Escott-Price, Valentina

A systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors

对超过7000人生物体液中前粒蛋白浓度进行系统性回顾——评估GRN基因突变的致病性及其他影响因素

Swift, Imogen J; Rademakers, Rosa; Finch, NiCole; Baker, Matt; Ghidoni, Roberta; Benussi, Luisa; Binetti, Giuliano; Rossi, Giacomina; Synofzik, Matthis; Wilke, Carlo; Mengel, David; Graff, Caroline; Takada, Leonel T; Sánchez-Valle, Raquel; Antonell, Anna; Galimberti, Daniela; Fenoglio, Chiara; Serpente, Maria; Arcaro, Marina; Schreiber, Stefanie; Vielhaber, Stefan; Arndt, Philipp; Santana, Isabel; Almeida, Maria Rosario; Moreno, Fermín; Barandiaran, Myriam; Gabilondo, Alazne; Stubert, Johannes; Gómez-Tortosa, Estrella; Agüero, Pablo; Sainz, M José; Gohda, Tomohito; Murakoshi, Maki; Kamei, Nozomu; Kittel-Schneider, Sarah; Reif, Andreas; Weigl, Johannes; Jian, Jinlong; Liu, Chuanju; Serrero, Ginette; Greither, Thomas; Theil, Gerit; Lohmann, Ebba; Gazzina, Stefano; Bagnoli, Silvia; Coppola, Giovanni; Bruni, Amalia; Quante, Mirja; Kiess, Wieland; Hiemisch, Andreas; Jurkutat, Anne; Block, Matthew S; Carlson, Aaron M; Bråthen, Geir; Sando, Sigrid Botne; Grøntvedt, Gøril Rolfseng; Lauridsen, Camilla; Heslegrave, Amanda; Heller, Carolin; Abel, Emily; Gómez-Núñez, Alba; Puey, Roger; Arighi, Andrea; Rotondo, Enmanuela; Jiskoot, Lize C; Meeter, Lieke H H; Durães, João; Lima, Marisa; Tábuas-Pereira, Miguel; Lemos, João; Boeve, Bradley; Petersen, Ronald C; Dickson, Dennis W; Graff-Radford, Neill R; LeBer, Isabelle; Sellami, Leila; Lamari, Foudil; Clot, Fabienne; Borroni, Barbara; Cantoni, Valentina; Rivolta, Jasmine; Lleó, Alberto; Fortea, Juan; Alcolea, Daniel; Illán-Gala, Ignacio; Andres-Cerezo, Lucie; Van Damme, Philip; Clarimon, Jordi; Steinacker, Petra; Feneberg, Emily; Otto, Markus; van der Ende, Emma L; van Swieten, John C; Seelaar, Harro; Zetterberg, Henrik; Sogorb-Esteve, Aitana; Rohrer, Jonathan D

Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease

可改变风险因素与阿尔茨海默病之间的遗传关联

Luo, Jiao; Thomassen, Jesper Qvist; Bellenguez, Céline; Grenier-Boley, Benjamin; de Rojas, Itziar; Castillo, Atahualpa; Parveen, Kayenat; Küçükali, Fahri; Nicolas, Aude; Peters, Oliver; Schneider, Anja; Dichgans, Martin; Rujescu, Dan; Scherbaum, Norbert; Jürgen, Deckert; Riedel-Heller, Steffi; Hausner, Lucrezia; Porcel, Laura Molina; Düzel, Emrah; Grimmer, Timo; Wiltfang, Jens; Heilmann-Heimbach, Stefanie; Moebus, Susanne; Tegos, Thomas; Scarmeas, Nikolaos; Clarimon, Jordi; Moreno, Fermin; Pérez-Tur, Jordi; Bullido, María J; Pastor, Pau; Sánchez-Valle, Raquel; Álvarez, Victoria; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Mir, Pablo; Real, Luis M; Piñol-Ripoll, Gerard; García-Alberca, Jose María; Royo, Jose Luís; Rodriguez-Rodriguez, Eloy; Soininen, Hilkka; Kuulasmaa, Teemu; de Mendonça, Alexandre; Mehrabian, Shima; Hort, Jakub; Vyhnalek, Martin; van der Lee, Sven; Graff, Caroline; Papenberg, Goran; Giedraitis, Vilmantas; Boland, Anne; Bacq-Daian, Delphine; Deleuze, Jean-François; Nicolas, Gael; Dufouil, Carole; Pasquier, Florence; Hanon, Olivier; Debette, Stéphanie; Grünblatt, Edna; Popp, Julius; Benussi, Luisa; Galimberti, Daniela; Arosio, Beatrice; Mecocci, Patrizia; Solfrizzi, Vincenzo; Parnetti, Lucilla; Squassina, Alessio; Tremolizzo, Lucio; Borroni, Barbara; Nacmias, Benedetta; Sorbi, Sandro; Caffarra, Paolo; Seripa, Davide; Rainero, Innocenzo; Daniele, Antonio; Masullo, Carlo; Spalletta, Gianfranco; Williams, Julie; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick; Tsolaki, Magda; Rossi, Giacomina; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Andreassen, Ole A; Hiltunen, Mikko; Van Duijn, Cornelia; Sims, Rebecca; van der Flier, Wiesje; Ruiz, Agustín; Ramirez, Alfredo; Lambert, Jean-Charles; Frikke-Schmidt, Ruth

Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes

对阿尔茨海默病和帕金森病中HLA基因座的多祖先分析揭示了一种由HLA-DRB1*04亚型介导的共同适应性免疫反应

Le Guen, Yann; Luo, Guo; Ambati, Aditya; Damotte, Vincent; Jansen, Iris; Yu, Eric; Nicolas, Aude; de Rojas, Itziar; Peixoto Leal, Thiago; Miyashita, Akinori; Bellenguez, Céline; Lian, Michelle Mulan; Parveen, Kayenat; Morizono, Takashi; Park, Hyeonseul; Grenier-Boley, Benjamin; Naito, Tatsuhiko; Küçükali, Fahri; Talyansky, Seth D; Yogeshwar, Selina Maria; Sempere, Vicente; Satake, Wataru; Alvarez, Victoria; Arosio, Beatrice; Belloy, Michael E; Benussi, Luisa; Boland, Anne; Borroni, Barbara; Bullido, María J; Caffarra, Paolo; Clarimon, Jordi; Daniele, Antonio; Darling, Daniel; Debette, Stéphanie; Deleuze, Jean-François; Dichgans, Martin; Dufouil, Carole; During, Emmanuel; Düzel, Emrah; Galimberti, Daniela; Garcia-Ribas, Guillermo; García-Alberca, José María; García-González, Pablo; Giedraitis, Vilmantas; Goldhardt, Oliver; Graff, Caroline; Grünblatt, Edna; Hanon, Olivier; Hausner, Lucrezia; Heilmann-Heimbach, Stefanie; Holstege, Henne; Hort, Jakub; Jung, Yoo Jin; Jürgen, Deckert; Kern, Silke; Kuulasmaa, Teemu; Lee, Kun Ho; Lin, Ling; Masullo, Carlo; Mecocci, Patrizia; Mehrabian, Shima; de Mendonça, Alexandre; Boada, Mercè; Mir, Pablo; Moebus, Susanne; Moreno, Fermin; Nacmias, Benedetta; Nicolas, Gael; Niida, Shumpei; Nordestgaard, Børge G; Papenberg, Goran; Papma, Janne; Parnetti, Lucilla; Pasquier, Florence; Pastor, Pau; Peters, Oliver; Pijnenburg, Yolande A L; Piñol-Ripoll, Gerard; Popp, Julius; Porcel, Laura Molina; Puerta, Raquel; Pérez-Tur, Jordi; Rainero, Innocenzo; Ramakers, Inez; Real, Luis M; Riedel-Heller, Steffi; Rodriguez-Rodriguez, Eloy; Ross, Owen A; Royo, Luis Jose; Rujescu, Dan; Scarmeas, Nikolaos; Scheltens, Philip; Scherbaum, Norbert; Schneider, Anja; Seripa, Davide; Skoog, Ingmar; Solfrizzi, Vincenzo; Spalletta, Gianfranco; Squassina, Alessio; van Swieten, John; Sánchez-Valle, Raquel; Tan, Eng-King; Tegos, Thomas; Teunissen, Charlotte; Thomassen, Jesper Qvist; Tremolizzo, Lucio; Vyhnalek, Martin; Verhey, Frans; Waern, Margda; Wiltfang, Jens; Zhang, Jing; Zetterberg, Henrik; Blennow, Kaj; He, Zihuai; Williams, Julie; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick G; Andreassen, Ole A; Van Duin, Cornelia; Tsolaki, Magda; Sánchez-Juan, Pascual; Frikke-Schmidt, Ruth; Sleegers, Kristel; Toda, Tatsushi; Zettergren, Anna; Ingelsson, Martin; Okada, Yukinori; Rossi, Giacomina; Hiltunen, Mikko; Gim, Jungsoo; Ozaki, Kouichi; Sims, Rebecca; Foo, Jia Nee; van der Flier, Wiesje; Ikeuchi, Takeshi; Ramirez, Alfredo; Mata, Ignacio; Ruiz, Agustín; Gan-Or, Ziv; Lambert, Jean-Charles; Greicius, Michael D; Mignot, Emmanuel

Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project

建立在线资源以促进全球合作和弱势群体参与:MJFF全球遗传帕金森病项目的经验

Vollstedt, Eva-Juliane; Madoev, Harutyun; Aasly, Anna; Ahmad-Annuar, Azlina; Al-Mubarak, Bashayer; Alcalay, Roy N; Alvarez, Victoria; Amorin, Ignacio; Annesi, Grazia; Arkadir, David; Bardien, Soraya; Barker, Roger A; Barkhuizen, Melinda; Basak, A Nazli; Bonifati, Vincenzo; Boon, Agnita; Brighina, Laura; Brockmann, Kathrin; Carmine Belin, Andrea; Carr, Jonathan; Clarimon, Jordi; Cornejo-Olivas, Mario; Correia Guedes, Leonor; Corvol, Jean-Christophe; Crosiers, David; Damásio, Joana; Das, Parimal; de Carvalho Aguiar, Patricia; De Rosa, Anna; Dorszewska, Jolanta; Ertan, Sibel; Ferese, Rosangela; Ferreira, Joaquim; Gatto, Emilia; Genç, Gençer; Giladi, Nir; Gómez-Garre, Pilar; Hanagasi, Hasmet; Hattori, Nobutaka; Hentati, Faycal; Hoffman-Zacharska, Dorota; Illarioshkin, Sergey N; Jankovic, Joseph; Jesús, Silvia; Kaasinen, Valtteri; Kievit, Anneke; Klivenyi, Peter; Kostic, Vladimir; Koziorowski, Dariusz; Kühn, Andrea A; Lang, Anthony E; Lim, Shen-Yang; Lin, Chin-Hsien; Lohmann, Katja; Markovic, Vladana; Martikainen, Mika Henrik; Mellick, George; Merello, Marcelo; Milanowski, Lukasz; Mir, Pablo; Öztop-Çakmak, Özgür; Pimentel, Márcia Mattos Gonçalves; Pulkes, Teeratorn; Puschmann, Andreas; Rogaeva, Ekaterina; Sammler, Esther M; Skaalum Petersen, Maria; Skorvanek, Matej; Spitz, Mariana; Suchowersky, Oksana; Tan, Ai Huey; Termsarasab, Pichet; Thaler, Avner; Tumas, Vitor; Valente, Enza Maria; van de Warrenburg, Bart; Williams-Gray, Caroline H; Wu, Ruey-Mei; Zhang, Baorong; Zimprich, Alexander; Solle, Justin; Padmanabhan, Shalini; Klein, Christine

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

Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease

罕见APOE错义变异V236E和R251G与阿尔茨海默病风险的关联

Le Guen, Yann; Belloy, Michael E; Grenier-Boley, Benjamin; de Rojas, Itziar; Castillo-Morales, Atahualpa; Jansen, Iris; Nicolas, Aude; Bellenguez, Céline; Dalmasso, Carolina; Küçükali, Fahri; Eger, Sarah J; Rasmussen, Katrine Laura; Thomassen, Jesper Qvist; Deleuze, Jean-François; He, Zihuai; Napolioni, Valerio; Amouyel, Philippe; Jessen, Frank; Kehoe, Patrick G; van Duijn, Cornelia; Tsolaki, Magda; Sánchez-Juan, Pascual; Sleegers, Kristel; Ingelsson, Martin; Rossi, Giacomina; Hiltunen, Mikko; Sims, Rebecca; van der Flier, Wiesje M; Ramirez, Alfredo; Andreassen, Ole A; Frikke-Schmidt, Ruth; Williams, Julie; Ruiz, Agustín; Lambert, Jean-Charles; Greicius, Michael D; Arosio, Beatrice; Benussi, Luisa; Boland, Anne; Borroni, Barbara; Caffarra, Paolo; Daian, Delphine; Daniele, Antonio; Debette, Stéphanie; Dufouil, Carole; Düzel, Emrah; Galimberti, Daniela; Giedraitis, Vilmantas; Grimmer, Timo; Graff, Caroline; Grünblatt, Edna; Hanon, Olivier; Hausner, Lucrezia; Heilmann-Heimbach, Stefanie; Holstege, Henne; Hort, Jakub; Jürgen, Deckert; Kuulasmaa, Teemu; van der Lugt, Aad; Masullo, Carlo; Mecocci, Patrizia; Mehrabian, Shima; de Mendonça, Alexandre; Moebus, Susanne; Nacmias, Benedetta; Nicolas, Gael; Olaso, Robert; Papenberg, Goran; Parnetti, Lucilla; Pasquier, Florence; Peters, Oliver; Pijnenburg, Yolande A L; Popp, Julius; Rainero, Innocenzo; Ramakers, Inez; Riedel-Heller, Steffi; Scarmeas, Nikolaos; Scheltens, Philip; Scherbaum, Norbert; Schneider, Anja; Seripa, Davide; Soininen, Hilkka; Solfrizzi, Vincenzo; Spalletta, Gianfranco; Squassina, Alessio; van Swieten, John; Tegos, Thomas J; Tremolizzo, Lucio; Verhey, Frans; Vyhnalek, Martin; Wiltfang, Jens; Boada, Mercè; García-González, Pablo; Puerta, Raquel; Real, Luis M; Álvarez, Victoria; Bullido, María J; Clarimon, Jordi; García-Alberca, José María; Mir, Pablo; Moreno, Fermin; Pastor, Pau; Piñol-Ripoll, Gerard; Molina-Porcel, Laura; Pérez-Tur, Jordi; Rodríguez-Rodríguez, Eloy; Royo, Jose Luís; Sánchez-Valle, Raquel; Dichgans, Martin; Rujescu, Dan