Didier Hannequin
1982–2023 年に発表
- 104
- 論文数
- 21,733
- 被引用数
- 78
- h 指数
- 104
- i10 指数
被引用数
引用元
国・地域
機関
分野
- Medicine53.4%
- Biochemistry, Genetics and Molecular Biology22.1%
- Neuroscience18.4%
- Psychology2.1%
- Immunology and Microbiology0.9%
- Computer Science0.7%
- その他2.4%
トピック
- Alzheimer's disease research and treatments14.3%
- Neuroinflammation and Neurodegeneration Mechanisms4.4%
- Dementia and Cognitive Impairment Research4.2%
- Amyotrophic Lateral Sclerosis Research4.1%
- Genetic Associations and Epidemiology3.3%
- Parkinson's Disease Mechanisms and Treatments2.3%
- その他67.4%
共著者
- Alexis Brice36
- Isabelle Le Ber35
- Dominique Campion34
- Florence Pasquier30
- David Wallon24
- Bruno Dubois21
- Thierry Frébourg21
- Agnès Camuzat20
- Anne Rovelet‐Lecrux17
- Olivier Martinaud17
- Gaël Nicolas15
- Jérémie Pariente14
- Michèle Puel14
- Stéphane Rousseau13
- Lucette Lacomblez12
- Camille Charbonnier11
- Catherine Thomas-Antérion11
- Claire Boutoleau‐Bretonnière11
- Martine Vercelletto11
- Mira Didic11
- François Sellal10
- Philippe Couratier10
- Véronique Golfier10
- Adeline Rollin‐Sillaire9
全論文
- Analysis of shared heritability in common disorders of the brain
著者: Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Raymond K. Walters, José Brás, Laramie E. Duncan, Valentina Escott‐Price, Guido J. Falcone, Padhraig Gormley, Rainer Malik, Nikolaos A. Patsopoulos, Stephan Ripke, Zhi Wei, Dongmei Yu, Phil H. Lee, Patrick Turley, Benjamin Grenier‐Boley, Vincent Chouraki, Yoichiro Kamatani, Claudine Berr, Luc Letenneur, Didier Hannequin, Philippe Amouyel, Anne Boland, Jean‐François Deleuze, Emmanuelle Duron, Badri N. Vardarajan, Christiane Reitz, Alison Goate, Matthew J. Huentelman, M. Ilyas Kamboh, Eric B. Larson, Ekaterina Rogaeva, Peter St George‐Hyslop, Håkon Håkonarson, Walter A. Kukull, Lindsay A. Farrer, Lisa L. Barnes, Thomas G. Beach, F. Yesim Demirci, Elizabeth Head, Christine M. Hulette, Gregory A. Jicha, John S.K. Kauwe, Jeffrey A. Kaye, James B. Leverenz, Allan I. Levey, Andrew P. Lieberman, V. Shane Pankratz, Wayne W. Poon, Joseph F. Quinn, Andrew J. Saykin, Lon S. Schneider, Amanda Smith, Joshua A. Sonnen, Robert A. Stern, Vivianna M. Van Deerlin, Linda J. Van Eldik, Denise Harold, Giancarlo Russo, David C. Rubinsztein, Anthony Bayer, Magda Tsolaki, Petra Proitsi, Nick C. Fox, Harald Hampel, Michael J. Owen, Simon Mead, Peter Passmore, Kevin Morgan, Markus M. Nöthen, Jonathan M. Schott, Martin N. Rossor, Michelle K. Lupton, Per Hoffmann, Johannes Kornhuber, Brian Lawlor, Andrew McQuillin, Ammar Al‐Chalabi, Joshua C Bis, Agustı́n Ruiz, Merçé Boada, Sudha Seshadri, Alexa Beiser, Kenneth Rice, Sven J. van der Lee, Philip L. De Jager, Daniel H. Geschwind, Matthias Riemenschneider, Steffi G. Riedel‐Heller, Jerome I. Rotter, Gerhard Ransmayr, Bradley T. Hyman, Carlos Cruchaga, Montserrat Alegret, Bendik S. Winsvold, Priit Palta, Kai-How Farh, Ester Cuenca-León, Nicholas A. Furlotte ほか 477 名 - Science 2018 被引用: 2,050
- APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases
著者: Hélène-Marie Lanoiselée, Gaël Nicolas, David Wallon, Anne Rovelet‐Lecrux, Morgane Lacour, Stéphane Rousseau, Anne‐Claire Richard, Florence Pasquier, Adeline Rollin‐Sillaire, Olivier Martinaud, Muriel Quillard‐Muraine, Vincent de La Sayette, Claire Boutoleau‐Bretonnière, Frédérique Etcharry‐Bouyx, Valérie Chauviré, Marie Sarazin, Isabelle Le Ber, Stéphane Epelbaum, Thérèse Jonveaux, Olivier Rouaud, Mathieu Ceccaldi, Olivier Félician, Olivier Godefroy, Maïté Formaglio, Bernard Croisile, Sophie Auriacombe, Ludivine Chamard, Jean‐Louis Vincent, Mathilde Sauvée, Cécilia Marelli, Audrey Gabelle, Canan Özsancak, Jérémie Pariente, Claire Paquet, Didier Hannequin, Dominique Campion, collaborators of the CNR-MAJ project - PLoS Medicine 2017 被引用: 609
- Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
著者: the European Alzheimer's Disease Initiative Investigators, Jean‐Charles Lambert, Simon Heath, Gaël Even, Dominique Campion, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, Diana Zélénika, María J. Bullido, Béatrice Tavernier, Luc Letenneur, Karolien Bettens, Claudine Berr, Florence Pasquier, Nathalie Fiévet, Pascale Barberger‐Gateau, Sebastiaan Engelborghs, Peter Paul De Deyn, Ignacio Mateo, A. Franck, Seppo Helisalmi, Elisa Porcellini, Olivier Hanon, Marian M. de Pancorbo, Corinne Lendon, Carole Dufouil, Céline Jaillard, Thierry Léveillard, Victoria Álvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Paola Piccardi, Giorgio Annoni, Davide Seripa, Daniela Galimberti, Didier Hannequin, Federico Licastro, Hilkka Soininen, Karen Ritchie, Hélène Blanché, Jean‐François Dartigues, Christophe Tzourio, Marta Gut, Christine Van Broeckhoven, Annick Alpérovitch, Mark Lathrop, Philippe Amouyel - Nature Genetics 2009 被引用: 2,271
- A trial of gantenerumab or solanezumab in dominantly inherited Alzheimer’s disease
著者: Stephen Salloway, Martin R. Farlow, Eric McDade, David B. Clifford, Guoqiao Wang, Jorge J. Llibre‐Guerra, Janice M. Hitchcock, Susan L. Mills, Anna Santacruz, Andrew J. Aschenbrenner, Jason Hassenstab, Tammie L.S. Benzinger, Brian A. Gordon, Anne M. Fagan, Kelley A. Coalier, Carlos Cruchaga, Alison Goate, Richard J. Perrin, Chengjie Xiong, Yan Li, John C. Morris, B. Joy Snider, Catherine J. Mummery, Ghulam M. Surti, Didier Hannequin, David Wallon, Sarah Berman, James J. Lah, Ivonne Z. Jiménez‐Velázquez, Erik D. Roberson, Christopher H. van Dyck, Lawrence S. Honig, Raquel Sánchez‐Valle, William S. Brooks, Serge Gauthier, Douglas Galasko, Colin L. Masters, Jared R. Brosch, Ging‐Yuek Robin Hsiung, Suman Jayadev, Maïté Formaglio, Mario Masellis, Roger Clarnette, Jérémie Pariente, Bruno Dubois, Florence Pasquier, Clifford R. Jack, Robert A. Koeppe, Peter J. Snyder, Paul Aisen, Ronald G. Thomas, Scott Berry, Barbara Wendelberger, Scott W. Andersen, Karen C. Holdridge, Mark A. Mintun, R. Yaari, John R. Sims, Monika Baudler, Paul Delmar, Rachelle S. Doody, Paulo Fontoura, Caroline Giacobino, Geoffrey A. Kerchner, Randall J. Bateman, the Dominantly Inherited Alzheimer Network–Trials Unit, Maïté Formaglio, Susan L. Mills, Jérémie Pariente, Christopher H. van Dyck - Nature Medicine 2021 被引用: 365
- Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
著者: Rebecca Sims, GERAD/PERADES, CHARGE, ADGC, EADI, Sven J. van der Lee, Adam C. Naj, Céline Bellenguez, Nandini Badarinarayan, Jóhanna Jakobsdóttir, Brian W. Kunkle, Anne Boland, Rachel Raybould, Joshua C Bis, Eden R. Martin, Benjamin Grenier‐Boley, Stefanie Heilmann‐Heimbach, Vincent Chouraki, Amanda Kuzma, Kristel Sleegers, Maria Vronskaya, Agustı́n Ruiz, Robert Graham, Robert Olaso, Per Hoffmann, Megan L. Grove, Badri N. Vardarajan, Mikko Hiltunen, Markus M. Nöthen, Charles C. White, Kara L. Hamilton‐Nelson, Jacques Epelbaum, Wolfgang Maier, Seung-Hoan Choi, Gary W. Beecham, Cécile Dulary, Stefan Herms, Albert V. Smith, Cory C. Funk, Céline Derbois, Andreas J. Forstner, Shahzad Ahmad, Hong‐Dong Li, Delphine Bacq, Denise Harold, Claudia L. Satizábal, Otto Valladares, Alessio Squassina, Rhodri Thomas, Jennifer A. Brody, Liming Qu, Pascual Sánchez‐Juan, Taniesha Morgan, Frank J. Wolters, Yi Zhao, Florentino Sánchez-García, Nicola Denning, Myriam Fornage, John Malamon, María Cándida Déniz Naranjo, Elisa Majounie, Thomas H. Mosley, Beth A. Dombroski, David Wallon, Michelle K. Lupton, Josée Dupuis, Patrice L. Whitehead, Laura Fratiglioni, Christopher Medway, Xueqiu Jian, Shubhabrata Mukherjee, Lina Keller, Kristelle Brown, Honghuang Lin, Laura B. Cantwell, Francesco Panza, Bernadette McGuinness, Sonia Moreno–Grau, Jeremy D. Burgess, Vincenzo Solfrizzi, Petra Proitsi, Hieab H.H. Adams, Mariet Allen, Davide Seripa, Pau Pástor, L. Adrienne Cupples, Nathan D. Price, Didier Hannequin, Ana Frank, Daniel Levy, Paramita Chakrabarty, Paolo Caffarra, Ina Giegling, Alexa Beiser, Vilmantas Giedraitis, Harald Hampel, Melissa E. Garcia, Xue Wang, Lars Lannfelt, Patrizia Mecocci, Gudny Eiriksdottir, Paul K. Crane, Florence Pasquier ほか 350 名 - Nature Genetics 2017 被引用: 1,104
- APOE and Alzheimer disease: a major gene with semi-dominant inheritance
著者: Emmanuelle Génin, Didier Hannequin, David Wallon, Kristel Sleegers, Mikko Hiltunen, Onofre Combarros, María J. Bullido, Sebastiaan Engelborghs, Peter Paul De Deyn, Claudine Berr, Florence Pasquier, Bruno Dubois, Gloria Tognoni, Nathalie Fiévet, Nathalie Brouwers, Karolien Bettens, Beatrice Arosio, Eliécer Coto, Maria Del Zompo, Ignacio Mateo, Jacques Epelbaum, Ana Frank, Seppo Helisalmi, Elisa Porcellini, Alberto Pilotto, Paola Forti, Raffaele Ferri, Elio Scarpini, Gabriele Siciliano, Vincenzo Solfrizzi, Sandro Sorbi, Gianfranco Spalletta, Fernando Valdivieso, Saila Vepsäläinen, Victoria Álvarez, Paolo Bosco, Michelangelo Mancuso, Francesco Panza, Benedetta Nacmias, Paola Bossù, Olivier Hanon, Paola Piccardi, G Annoni, Davide Seripa, Daniela Galimberti, Federico Licastro, Hilkka Soininen, Dartigues Jf, M. Ilyas Kamboh, Christine Van Broeckhoven, Jean‐Charles Lambert, Philippe Amouyel, Dominique Campion - Molecular Psychiatry 2011 被引用: 703
- APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
著者: Anne Rovelet‐Lecrux, Didier Hannequin, Grégory Raux, Nathalie Le Meur, Annie Laquerrière, Anne Vital, Cécile Dumanchin, Sébastien Feuillette, Alexis Brice, Martine Vercelletto, Frédéric Dubas, Thierry Frébourg, Dominique Campion - Nature Genetics 2005 被引用: 1,253
- Frontotemporal dementia and its subtypes: a genome-wide association study
著者: Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, William S. Brooks, Peter R. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George‐Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim Van Langenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri, Jørgen E. Nielsen, Lena E. Hjermind, Matthias Riemenschneider, Manuel Mayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N. Rossor ほか 58 名 - The Lancet Neurology 2014 被引用: 402
- Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export
著者: Andrea Legati, Donatella Giovannini, Gaël Nicolas, Uriel López-Sánchez, Beatriz Quintáns, João Ricardo Mendes de Oliveira, Renee Sears, Eliana Marisa Ramos, Elizabeth Spiteri, María-Jesús Sobrido, Ãngel Carracedo, Cristina Castro-Fernández, Stéphanie Cubizolle, Brent L. Fogel, Cyril Goizet, Joanna C. Jen, Suppachok Kirdlarp, Anthony E. Lang, Zosia Miedzybrodzka, Witoon Mitarnun, Martin Paucar, Henry L. Paulson, Jérémie Pariente, Anne-Claire Richard, Naomi Salins, Sheila A Simpson, Pasquale Striano, Per Svenningsson, François Tison, Vivek K. Unni, Olivier Vanakker, Marja W. Wessels, Suppachok Wetchaphanphesat, Michele Yang, François Boller, Dominique Campion, Didier Hannequin, Marc Sitbon, Daniel H. Geschwind, Jean‐Luc Battini, Giovanni Coppola - Nature Genetics 2015 被引用: 316
- Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum
著者: Dominique Campion, Cécile Dumanchin, Didier Hannequin, Bruno Dubois, Serge Belliard, Michèle Puel, Catherine Thomas-Antérion, Agnès Michon, Cosette Martin, Françoise Charbonnier, Grégory Raux, Agnès Camuzat, Christiane Penet, Valérie Mesnage, María Martínez, Françoise Clerget‐Darpoux, Alexis Brice, Thierry Frébourg - The American Journal of Human Genetics 1999 被引用: 788
- Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
著者: Annika Keller, Ana Westenberger, María Jesús Sobrido, María García-Murias, Aloysius Domingo, Renee Sears, Roberta R. Lemos, Andrés Ordóñez‐Ugalde, Gaël Nicolas, José Eriton Gomes da Cunha, Elisabeth J. Rushing, Michael Hugelshofer, Moritz C. Wurnig, Andres Kaech, Regina Reimann, Katja Lohmann, Valerija Dobričić, Ãngel Carracedo, Igor Petrović, Janis M. Miyasaki, Irina Abakumova, Maarja Andaloussi Mäe, Elisabeth Raschperger, Mayana Zatz, Katja Zschiedrich, Jörg Klepper, Elizabeth Spiteri, José M. Prieto, Inmaculada Navas, Michael Preuß, Carmen Dering, Milena Janković, Martin Paucar, Per Svenningsson, Kioomars Saliminejad, Hamid Reza Khorram Khorshid, Ivana Novaković, Adriano Aguzzi, Andreas Boss, Isabelle Le Ber, Gilles Defer, Didier Hannequin, Vladimir S Kostić, Dominique Campion, Daniel H. Geschwind, Giovanni Coppola, Christer Betsholtz, Christine Klein, João Ricardo Mendes de Oliveira - Nature Genetics 2013 被引用: 328
- Comparison of Pittsburgh compound B and florbetapir in cross‐sectional and longitudinal studies
著者: Yi Su, Shaney Flores, Guoqiao Wang, Russ C. Hornbeck, Benjamin Speidel, Nelly Joseph‐Mathurin, Andrei G. Vlassenko, Brian A. Gordon, Robert A. Koeppe, William E. Klunk, Clifford R. Jack, Martin R. Farlow, Stephen Salloway, Barbara J. Snider, Sarah Berman, Erik D. Roberson, Jared R. Brosch, Ivonne Jimenez-Velazques, Christopher H. van Dyck, Douglas Galasko, Shauna H. Yuan, Suman Jayadev, Lawrence S. Honig, Serge Gauthier, Ging‐Yuek Robin Hsiung, Mario Masellis, William S. Brooks, Michael Fulham, Roger Clarnette, Colin L. Masters, David Wallon, Didier Hannequin, Bruno Dubois, Jérémie Pariente, Raquel Sánchez‐Valle, Catherine J. Mummery, John M. Ringman, Michel Bottlaender, Gregory Klein, Smiljana Milosavljevic‐Ristic, Eric McDade, Chengjie Xiong, John C. Morris, Randall J. Bateman, Tammie L.S. Benzinger - Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring 2019 被引用: 138
- A novel Alzheimer disease locus located near the gene encoding tau protein
著者: Gyungah Jun, Carla A. Ibrahim‐Verbaas, Maria Vronskaya, J-C Lambert, Jaeyoon Chung, Adam C. Naj, Brian W. Kunkle, Li‐Shun Wang, Joshua C. Bis, Céline Bellenguez, Denise Harold, Kathryn L. Lunetta, Anita L. DeStefano, Benjamin Grenier‐Boley, Rebecca Sims, Gary W. Beecham, Albert V. Smith, Vincent Chouraki, Kara L. Hamilton‐Nelson, M. Arfan Ikram, Nathalie Fiévet, Nicola Denning, Eden R. Martin, Helena Schmidt, Y Kamatani, Melanie Dunstan, Otto Valladares, Agustín Ruiz Laza, Diana Zélénika, Alfredo Ramı́rez, Tatiana Foroud, S-H Choi, Anne Boland, Tim Becker, Walter A. Kukull, Sven J. van der Lee, Florence Pasquier, Carlos Cruchaga, Duane Beekly, Annette L. Fitzpatrick, Olivier Hanon, Michael Gill, Robert C. Barber, Vilmundur Guðnason, Dominique Campion, Seth Love, David A. Bennett, Najaf Amin, Claudine Berr, Magda Tsolaki, Joseph D. Buxbaum, Oscar L. López, Vincent Deramecourt, Nick C. Fox, Laura B. Cantwell, Lluís Tárraga, Carole Dufouil, John Hardy, Paul K. Crane, Gudny Eiriksdottir, Didier Hannequin, Robert Clarke, Denis A. Evans, Thomas H. Mosley, Luc Letenneur, Carol Brayne, Wolfgang Maier, Philip L. De Jager, Valur Emilsson, Dartigues Jf, Harald Hampel, M. Ilyas Kamboh, Renée F.A.G. de Bruijn, Christophe Tzourio, Pau Pástor, Eric B. Larson, Jerome I. Rotter, Michael O‘Donovan, Thomas J. Montine, Michael A. Nalls, Simon Mead, Eric M. Reiman, Pálmi V. Jónsson, Clive Holmes, Peter St George‐Hyslop, Merçé Boada, Peter Passmore, Jens R. Wendland, R. Schmidt, Kevin Morgan, Ashley R. Winslow, John Powell, M Carasquillo, Steven G. Younkin, Jóhanna Jakobsdóttir, John Kauwe, K C Wilhelmsen, Dan Rujescu, Markus M. Nöthen, Albert Hofman ほか 329 名 - Molecular Psychiatry 2015 被引用: 309
- High frequency of potentially pathogenic SORL1 mutations in autosomal dominant early-onset Alzheimer disease
著者: Cyril Pottier, Didier Hannequin, Sophie Coutant, Anne Rovelet‐Lecrux, David Wallon, Simon Rousseau, Solenn Legallic, Claire Paquet, Stéphanie Bombois, Jérémie Pariente, C. Thomas-Antérion, Agnès Michon, Bernard Croisile, Frédérique Etcharry‐Bouyx, Claudine Berr, Dartigues Jf, Philippe Amouyel, Hélène Dauchel, Claire Boutoleau‐Bretonnière, Christel Thauvin, Thierry Frébourg, J-C Lambert, Dominique Campion, PHRC GMAJ Collaborators - Molecular Psychiatry 2012 被引用: 318
- Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification
著者: Gaël Nicolas, Cyril Pottier, David Maltête, Sophie Coutant, Anne Rovelet‐Lecrux, Solenn Legallic, Stéphane Rousseau, Yvan Vaschalde, Lucie Guyant‐Maréchal, Jérôme Augustin, Olivier Martinaud, Luc Defebvre, Pierre Krystkowiak, Jérémie Pariente, Michel Clanet, Pierre Labauge, Xavier Ayrignac, Romain Lefaucheur, Isabelle Le Ber, Thierry Frébourg, Didier Hannequin, Dominique Campion - Neurology 2012 被引用: 277
- Plasma NfL levels and longitudinal change rates in C9orf72 and GRN-associated diseases: from tailored references to clinical applications
著者: Dario Saracino, Karim Dorgham, Agnès Camuzat, Daisy Rinaldi, Armelle Rametti‐Lacroux, Marion Houot, Fabienne Clot, Philippe Martin-Hardy, Ludmila Jornéa, Carole Azuar, Raffaella Migliaccio, Florence Pasquier, Philippe Couratier, Sophie Auriacombe, Mathilde Sauvée, Claire Boutoleau‐Bretonnière, Jérémie Pariente, Mira Didic, Didier Hannequin, David Wallon, the PREV-DEMALS and Predict-PGRN study groups, Olivier Colliot, Bruno Dubois, Alexis Brice, Richard Lévy, Sylvie Forlani, Isabelle Le Ber - Journal of Neurology Neurosurgery & Psychiatry 2021 被引用: 54
- Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
著者: Yi‐Jun Ge, Ya‐Nan Ou, Yue‐Ting Deng, Bang‐Sheng Wu, Yang Liu, Ya-Ru Zhang, Shi-Dong Chen, Yuyuan Huang, Qiang Dong, Lan Tan, Jin‐Tai Yu, Raffaele Ferrari, Dena Hernandez, Michael A. Nalls, Jonathan D. Rohrer, Adaikalavan Ramasamy, John B. Kwok, Carol Dobson‐Stone, William S. Brooks, Peter R. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, Lauren Bartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustı́n Ruiz, Merçé Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga, Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Gianluigi Forloni, Daniela Galimberti, Chiara Fenoglio, María Serpente, Elio Scarpini, Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, Karin Nilsson, Christer Nilsson, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, David Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems, Timothy D. Griffiths, Ian G. McKeith, Alan Thomas, Pietro Pietrini, Edward D. Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C. Tierney, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Elena Alonso, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Alexander Kurz, Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, Peter St George‐Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone, James B. Rowe, Johannes C. M. Schlachetzki, James Uphill, John Collinge, Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman, John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim Van Langenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa, Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto, Alexis Brice, Benedetta Nacmias, Sandro Sorbi ほか 69 名 - Biological Psychiatry 2022 被引用: 50
- Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study
著者: Cyril Pottier, Xiaolai Zhou, Ralph B. Perkerson, Matt Baker, Gregory D. Jenkins, Daniel Serie, Roberta Ghidoni, Luisa Benussi, Giuliano Binetti, Adolfo López de Munain, Miren Zulaica, Fermín Moreno, Isabelle Le Ber, Florence Pasquier, Didier Hannequin, Raquel Sánchez‐Valle, Anna Antonell, Albert Lladó, Tammee M. Parsons, NiCole A. Finch, Elizabeth Finger, Carol F. Lippa, Edward D. Huey, Manuela Neumann, Peter Heutink, Matthis Synofzik, Carlo Wilke, Robert A. Rissman, Jarosław Sławek, Emilia J. Sitek, Peter Johannsen, Jørgen E. Nielsen, Yingxue Ren, Marka van Blitterswijk, Mariely DeJesus‐Hernandez, Elizabeth Christopher, Melissa E. Murray, Kevin F. Bieniek, Bret M. Evers, Camilla Ferrari, Sara Rollinson, Anna Richardson, Elio Scarpini, Giorgio Fumagalli, Alessandro Padovani, John Hardy, Parastoo Momeni, Raffaele Ferrari, Francesca Frangipane, Raffaele Maletta, Maria Anfossi, Maura Gallo, Leonard Petrucelli, EunRan Suh, Oscar L Lopez, Tsz Hang Wong, Jeroen van Rooij, Harro Seelaar, Simon Mead, Richard J. Caselli, Eric M. Reiman, Marwan N. Sabbagh, Mads Kjølby, Anders Nykjær, Anna M. Karydas, Adam L. Boxer, Lea T. Grinberg, Jordan Grafman, Salvatore Spina, Adrian L. Oblak, M-Marsel Mesulam, Sandra Weıntraub, Changiz Geula, John R. Hodges, Olivier Piguet, William S. Brooks, David J. Irwin, John Q. Trojanowski, Edward B. Lee, Keith A. Josephs, Joseph E. Parisi, Nilüfer Ertekin‐Taner, David S. Knopman, Benedetta Nacmias, Irene Piaceri, Silvia Bagnoli, Sandro Sorbi, Marla Gearing, Jonathan D. Glass, Thomas G. Beach, Sandra E. Black, Mario Masellis, Ekaterina Rogaeva, Jean‐Paul Vonsattel, Lawrence S. Honig, Julia Kofler, Amalia C. Bruni, Julie S. Snowden, David Mann, Stuart Pickering‐Brown ほか 33 名 - The Lancet Neurology 2018 被引用: 129
- Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification
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