Alexis Brice

1987–2025 年に発表

392
論文数
80,046
被引用数
144
h 指数
382
i10 指数

被引用数

Alexis Brice の年別被引用数1967 年: 被引用 13 件1988 年: 被引用 1 件1989 年: 被引用 2 件1990 年: 被引用 8 件1991 年: 被引用 8 件1992 年: 被引用 13 件1993 年: 被引用 16 件1994 年: 被引用 20 件1995 年: 被引用 31 件1996 年: 被引用 86 件1997 年: 被引用 201 件1998 年: 被引用 217 件1999 年: 被引用 220 件2000 年: 被引用 350 件2001 年: 被引用 339 件2002 年: 被引用 349 件2003 年: 被引用 480 件2004 年: 被引用 457 件2005 年: 被引用 376 件2006 年: 被引用 538 件2007 年: 被引用 498 件2008 年: 被引用 573 件2009 年: 被引用 600 件2010 年: 被引用 628 件2011 年: 被引用 731 件2012 年: 被引用 768 件2013 年: 被引用 870 件2014 年: 被引用 808 件2015 年: 被引用 924 件2016 年: 被引用 890 件2017 年: 被引用 949 件2018 年: 被引用 968 件2019 年: 被引用 2,496 件2020 年: 被引用 2,861 件2021 年: 被引用 2,895 件2022 年: 被引用 2,281 件2023 年: 被引用 1,759 件2024 年: 被引用 2,607 件2025 年: 被引用 1,099 件2026 年: 被引用 30 件1968〜1987 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 8,027 件、この内訳の 24.2%イギリス: 引用元論文 3,084 件、この内訳の 9.3%ドイツ: 引用元論文 2,253 件、この内訳の 6.8%中国: 引用元論文 1,934 件、この内訳の 5.8%イタリア: 引用元論文 1,785 件、この内訳の 5.4%フランス: 引用元論文 1,692 件、この内訳の 5.1%カナダ: 引用元論文 1,462 件、この内訳の 4.4%オーストラリア: 引用元論文 1,043 件、この内訳の 3.2%オランダ: 引用元論文 996 件、この内訳の 3%スペイン: 引用元論文 924 件、この内訳の 2.8%日本: 引用元論文 901 件、この内訳の 2.7%ベルギー: 引用元論文 670 件、この内訳の 2%
0%24.2%その他 25.3%

分野

  • Medicine49.5%
  • Biochemistry, Genetics and Molecular Biology25.8%
  • Neuroscience22%
  • Immunology and Microbiology0.5%
  • Nursing0.4%
  • Agricultural and Biological Sciences0.3%
  • その他1.5%

トピック

  • Parkinson's Disease Mechanisms and Treatments10.6%
  • Genetic Neurodegenerative Diseases5.8%
  • Alzheimer's disease research and treatments4.8%
  • Mitochondrial Function and Pathology4.4%
  • Amyotrophic Lateral Sclerosis Research3.9%
  • Neurological disorders and treatments3.2%
  • その他67.3%

共著者

全論文

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  1. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lisa M. Shulman, Margaret Sutherland, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Ole A. Andreassen, Tushar Bangale, Alexis Brice, Jian Yang, Ziv Gan‐Or, Thomas Gasser, Peter Heutink, Joshua Shulman, Nicholas Wood, David A. Hinds, John Hardy, Huw R Morris, Jacob Gratten, Peter M. Visscher, Robert Graham, Andrew B Singleton, Astrid Adarmes‐Gómez, Miquel Aguilar, Akbota Aitkulova, Vadim Akhmetzhanov, Roy N. Alcalay, Ignacio Álvarez, Victoria Álvarez, Sara Bandrés‐Ciga, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Kimberley J. Billingsley, Cornelis Blauwendraat, Marta Blazquez, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, José Brás, Alexis Brice, Kathrin Brockmann, Vivien J. Bubb, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Viorica Chelban, Jordi Clarimón, Carl E Clarke, Yaroslau Compta, Mark Cookson, Jean‐Christophe Corvol, David W. Craig, Fabrice Danjou, Mónica Díez-Fairén, Oriol Dols‐Icardo, J. Duarte, Raquel Durán, Francisco Escamilla‐Sevilla, Valentina Escott‐Price, Mario Ezquerra, Faraz Faghri, Cici Feliz, Manel Fernández, Rubén Fernández‐Santiago, Steven Finkbeiner, Thomas Foltynie, Ziv Gan‐Or, Ciara García ほか 170 名 - The Lancet Neurology 2019 被引用: 2,541

  2. Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , K. Marder, Ignácio F. Mata, Anat Mirelman, Jun Mitsui, Ikuko Mizuta, Giuseppe Nicoletti, Catarina R. Oliveira, Ruth Ottman, Avi Orr‐Urtreger, Lygia V. Pereira, Aldo Quattrone, Ekaterina Rogaeva, A. Rolfs, Hanna Rosenbaum, Roberto Rozenberg, Ali Samii, T. Samaddar, Claudia Schulte, Manu Sharma, Andrew Singleton, Mariana Spitz, Eng‐King Tan, N. Tayebi, Tatsushi Toda, A. R. Troiano, Shoji Tsuji, Matthias Wittstock, Tyra G. Wolfsberg, Yih‐Ru Wu, Cyrus P. Zabetian, Yirui Zhao, Shira G. Ziegler - New England Journal of Medicine 2009 被引用: 2,126

  3. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bradley Smith, Marta Gromicho, Siddharthan Chandran, Suvankar Pal, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Michael Sendtner, Thomas Meyer, Nazlı Başak, Anneke J. van der Kooi, Antonia Ratti, Isabella Fogh, Cinzia Gellera, Giuseppe Lauria, Stefania Corti, Cristina Cereda, Daisy Sproviero, Sandra D’Alfonso, Gianni Sorarú, Gabriele Siciliano, Massimiliano Filosto, Alessandro Padovani, Adriano Chiò, Andrea Calvo, Cristina Moglia, Maura Brunetti, Antonio Canosa, Maurizio Grassano, Ettore Beghi, Elisabetta Pupillo, Giancarlo Logroscino, Beatrice Nefussy, Alma Osmanovic, Angelica Nordin, Yossef Lerner, Michal Zabari, Marc Gotkine, Robert H. Baloh, Shaughn Bell, Patrick Vourc’h, Philippe Corcia, Philippe Couratier, Stéphanie Millecamps, Vincent Meininger, François Salachas, Jesús S. Mora Pardina, Abdelilah Assialioui, Ricardo Rojas-García, Patrick A. Dion, Jay P. Ross, Albert C. Ludolph, Jochen H. Weishaupt, Dávid Brenner, Axel Freischmidt, Gilbert Bensimon, Alexis Brice, Alexandra Durr, C. Payán, Safa Saker-Delye, Nicholas Wood, Simon Topp, Rosa Rademakers, Lukas Tittmann, Wolfgang Lieb, André Franke, Stephan Ripke, Alice Braun, Julia Kraft ほか 182 名 - Nature Genetics 2021 被引用: 552

  4. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alison Goate, Karen Marder, Brian Fiske, Margaret Sutherland, Georgia Xiromerisiou, Richard H. Myers, Lorraine N. Clark, Kāri Stefánsson, John Hardy, Peter Heutink, Honglei Chen, Nicholas Wood, Henry Houlden, Haydeh Payami, Alexis Brice, William K. Scott, Thomas Gasser, Lars Bertram, Nicholas Eriksson, Tatiana Foroud, Andrew Singleton - Nature Genetics 2014 被引用: 1,964

  5. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

    著者: , , , , , , , , , , , , , , , , , - Science 2003 被引用: 2,797

  6. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Neurology 2008 被引用: 1,563

  7. Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Science 1996 被引用: 2,801

  8. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea Calvo, Elisabet Englund, Giuseppe Borghero, Gianluca Floris, Anne M. Remes, Hannu Laaksovirta, Leo McCluskey, John Q. Trojanowski, Vivianna M. Van Deerlin, Gerard D. Schellenberg, Michael A. Nalls, Vivian E. Drory, Chin‐Song Lu, Tu‐Hsueh Yeh, Hiroyuki Ishiura, Yuji Takahashi, Shoji Tsuji, Isabelle Le Ber, Alexis Brice, Carsten Drepper, Nigel Williams, Janine Kirby, Pamela J. Shaw, John Hardy, Pentti J. Tienari, Peter Heutink, Huw R. Morris, Stuart Pickering‐Brown, Bryan J. Traynor - The Lancet Neurology 2012 被引用: 1,226

  9. Clinical Correlations With Lewy Body Pathology inLRRK2-Related Parkinson Disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Charles Duyckaerts, Alexis Brice, A. Jon Stoessl, Connie Marras - JAMA Neurology 2014 被引用: 407

  10. Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nigel Williams, Karen Morrison, Carl E Clarke, Kirsten Harvey, Benjamin M. Jacobs, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Susanne A. Schneider, Mark Cookson, Cornelis Blauwendraat, David W. Craig, Kimberley J. Billingsley, Mary B. Makarious, Derek P. Narendra, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hirotaka Iwaki, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, José Brás, Rita Guerreiro, Steven Lubbe, Timothy Troycoco, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Ryan J. Uitti, Owen A. Ross, Francis P. Grenn, Anni Moore, Roy N. Alcalay, Zbigniew K. Wszołek, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Kheireddin Mufti, Jacobus J. van Hilten, Johan Marinus, Astrid D. Adarmes-Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blázquez Estrada, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Ana Cámara, Fátima Carrillo, Mario Carrión‐Claro ほか 75 名 - Nature Communications 2021 被引用: 214

  11. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicola Ticozzi, Kuang Lin, Boris Rogelj, Katarina Vrabec, Metka Ravnik‐Glavač, Blaž Koritnik, Janez Zidar, Lea Leonardis, Leja Dolenc Grošelj, Stéphanie Millecamps, François Salachas, Vincent Meininger, Mamede de Carvalho, Susana Pinto, Jesús S. Mora, Ricardo Rojas-García, Meraida Polak, Siddharthan Chandran, Shuna Colville, Robert Swingler, Karen Morrison, Pamela J. Shaw, John Hardy, Richard W. Orrell, Alan Pittman, Katie Sidle, Pietro Fratta, Andrea Malaspina, Simon Topp, Susanne Petri, Susanne Abdulla, Carsten Drepper, Michael Sendtner, Thomas Meyer, Roel A. Ophoff, Kim A. Staats, Martina Wiedau‐Pazos, Catherine Lomen‐Hoerth, Vivianna M. Van Deerlin, John Q. Trojanowski, Lauren Elman, Leo McCluskey, A. Nazlı Başak, Ceren Tunca, Hamid Hamzeiy, Yeşim Parman, Thomas Meitinger, Peter Lichtner, Milena Radivojkov‐Blagojevic, Christian Andrés, Cindy Maurel, Gilbert Bensimon, G. Bernhard Landwehrmeyer, Alexis Brice, Christine Payan, Safaa Saker-Delye, Alexandra Dürr, Nicholas Wood, Lukas Tittmann, Wolfgang Lieb, André Franke, Marcella Rietschel, Sven Cichon, Markus M. Nöthen, Philippe Amouyel, Christophe Tzourio, Jean‐François Dartigues, André G. Uitterlinden, Fernando Rivadeneira, Karol Estrada ほか 81 名 - Nature Genetics 2016 被引用: 628

  12. Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - JAMA Neurology 2017 被引用: 378

  13. A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

    著者: , , , , , , , , , , , , , , , , , , , , , , - Brain 2014 被引用: 497

  14. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , John Hardy, Nicholas Wood, Thomas Gasser, Alexandra Dürr, Jean‐François Deleuze, Mériem Tazir, A. Destée, Ebba Lohmann, Edor Kabashi, Andrew Singleton, Olga Corti, Alexis Brice, Suzanne Lesage, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Yves Agid, Mathieu Anheim, Anne-Marie Bonnet, Michel Borg, Emmanuel Broussolle, Philippe Damier, A. Destée, Alexandra Dürr, Franck Durif, Paul Krack, Stephan Klebe, Ebba Lohmann, María Martínez, Pierre Pollak, Olivier Rascol, Christine Tranchant, Marc Vérin, François Viallet, Alexis Brice, Suzanne Lesage, Elisa Majounie, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Michael A. Nalls, Dena G. Hernandez, J. Raphael Gibbs, Alexandra Dürr, Sampath Arepalli, Roger A. Barker, Yoav Ben‐Shlomo, Daniela Berg, Francesco Bettella, Kailash P. Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bastiaan R. Bloem, Zoltán Bochdanovits, Michael von Bonin, Suzanne Lesage, François Tison, Marie Vidailhet, Jean‐Christophe Corvol, Yves Agid, Mathieu Anheim, Anne-Marie Bonnet, Michel Borg, Emmanuel Broussolle, Philippe Damier, A. Destée, Alexandra Dürr, Franck Durif, Paul Krack, Stephan Klebe ほか 123 名 - The American Journal of Human Genetics 2016 被引用: 447

  15. Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas Gasser, Peter Heutink, Joshua Shulman, Nicolas Wood, John Hardy, Huw R. Morris, David A. Hinds, Jacob Gratten, Peter M. Visscher, Ziv Gan‐Or, Mike A. Nalls, Andrew Singleton - Movement Disorders 2019 被引用: 374

  16. A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fabiana Novellino, Aldo Quattrone, Grazia Annesi, Elvira Valeria De Marco, Ekaterina Rogaeva, Mario Masellis, Sandra E. Black, Juan M. Bilbao, Tatiana Foroud, Bernardino Ghetti, William C. Nichols, Nathan Pankratz, Glenda M. Halliday, Suzanne Lesage, Stephan Klebe, Alexandra Dürr, Charles Duyckaerts, Alexis Brice, Benoit I. Giasson, John Q. Trojanowski, Howard I. Hurtig, Nahid Tayebi, Claudia Landazabal, Melanie A. Knight, Margaux F. Keller, Andrew Singleton, Tyra G. Wolfsberg, Ellen Sidransky - JAMA Neurology 2013 被引用: 444

  17. Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Johanna Eerola‐Rautio, Pentti J. Tienari, Alexander Pantelyat, Argye E. Hillis, Ted M. Dawson, Liana S. Rosenthal, Marilyn S. Albert, Susan M. Resnick, Luigi Ferrucci, Christopher M. Morris, Olga Pletnikova, Juan C. Troncoso, Donald G. Grosset, Suzanne Lesage, Jean‐Christophe Corvol, Alexis Brice, Alastair J. Noyce, Eliezer Masliah, Nick Wood, John Hardy, Lisa M. Shulman, Joseph Jankovic, Joshua Shulman, Peter Heutink, Thomas Gasser, Paul Cannon, Sonja W. Scholz, Huw R. Morris, Mark Cookson, Mike A. Nalls, Ziv Gan‐Or, Andrew Singleton - Brain 2019 被引用: 245

  18. Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas Wood, Patrick A. Lewis, Sebastian R. Schreglmann, Rita Guerreiro, Ruth C. Lovering, Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, Nigel Williams, Alexis Brice, Fabrice Danjou, Suzanne Lesage, Jean‐Christophe Corvol, María Martínez, Claudia Schulte, Kathrin Brockmann, Javier Simón‐Sánchez, Peter Heutink, Patrizia Rizzu, Manu Sharma, Thomas Gasser, Aude Nicolas, Mark Cookson, Sara Bandrés‐Ciga, Cornelis Blauwendraat, David W. Craig, Faraz Faghri, J. Raphael Gibbs, Dena Hernández, Kendall Van Keuren‐Jensen, Joshua Shulman, Hampton L. Leonard, Mike A. Nalls, Laurie Robak, Steven Lubbe, Steven Finkbeiner, Niccolò E. Mencacci, Codrin Lungu, Andrew Singleton, Sonja W. Scholz, Xylena Reed, Roy N. Alcalay, Ziv Gan‐Or, Guy A. Rouleau, Lynne Krohn, Jacobus J. van Hilten, Johan Marinus, Astrid Adarmes‐Gómez, Miquel Aguilar, Ignacio Álvarez, Victoria Álvarez, Francisco Javier Barrero, Jesús Alberto Bergareche Yarza, Inmaculada Bernal‐Bernal, Marta Blázquez Estrada, Marta Bonilla‐Toribio, Juan A. Botía, María Teresa Boungiorno, Dolores Buiza‐Rueda, Anna Maria Novella Càmara, Fátima Carrillo, Mario Carrión‐Claro, Debora Cerdan, Jordi Clarimón, Yaroslau Compta ほか 63 名 - JAMA Neurology 2021 被引用: 203

  19. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

    著者: , , , , , , , , , , , , - Nature Genetics 2005 被引用: 1,253

  20. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Paola Caroppo, Roberta Ghidoni, Michela Pievani, Luisa Benussi, Giuliano Binetti, Bradford C. Dickerson, Diane Lucente, Samantha Krivensky, Caroline Graff, Linn Öijerstedt, Marie Fallström, Håkan Thonberg, Nupur Ghoshal, John C. Morris, Barbara Borroni, Alberto Benussi, Alessandro Padovani, Daniela Galimberti, Elio Scarpini, Giorgio Fumagalli, Ian R. Mackenzie, Ging‐Yuek Robin Hsiung, Pheth Sengdy, Adam L. Boxer, Howie Rosen, Joanne Taylor, Matthis Synofzik, Carlo Wilke, Patricia Sulzer, John R. Hodges, Glenda M. Halliday, John B. Kwok, Raquel Sánchez‐Valle, Albert Lladó, Sergi Borrego‐Écija, Isabel Santana, Maria Rosário Almeida, Miguel Tábuas‐Pereira, Fermín Moreno, Myriam Barandiarán, Begoña Indakoetxea, Johannes Levin, Adrian Danek, James B. Rowe, Thomas Cope, Markus Otto, Sarah Anderl‐Straub, Alexandre de Mendonça, Carolina Maruta, Mario Masellis, Sandra E. Black, Philippe Couratier, Géraldine Lautrette, Edward D. Huey, Sandro Sorbi, Benedetta Nacmias, Robert Laforce, Marie-Pier L Tremblay, Rik Vandenberghe, Philip Van Damme, Emily Rogalskı, Sandra Weıntraub, Alexander Gerhard, Chiadi U. Onyike, Simon Ducharme, Sokratis G. Papageorgiou, Adeline Su Lyn Ng, Amy Brodtmann, Elizabeth Finger, Rita Guerreiro ほか 71 名 - The Lancet Neurology 2019 被引用: 311

  21. Frontotemporal dementia and its subtypes: a genome-wide association study

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  22. G51D α‐synuclein mutation causes a novel Parkinsonian–pyramidal syndrome

    著者: , , , , , , , , , , , , - Annals of Neurology 2013 被引用: 723

  23. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron - PLoS Genetics 2014 被引用: 664

  24. Association between Early-Onset Parkinson's Disease and Mutations in theParkinGene

    著者: , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2000 被引用: 1,426