Alexis Brice
Active 1987–2025
- 392
- Papers
- 80,046
- Citations
- 144
- h-index
- 382
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Medicine49.5%
- Biochemistry, Genetics and Molecular Biology25.8%
- Neuroscience22%
- Immunology and Microbiology0.5%
- Nursing0.4%
- Agricultural and Biological Sciences0.3%
- Other1.5%
Topics
- 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%
- Other67.3%
Coauthors
- Alexandra Dürr133
- Giovanni Stévanin78
- Suzanne Lesage67
- Jean‐Christophe Corvol51
- Isabelle Le Ber43
- Yves Agid40
- Didier Hannequin39
- Éric Leguern31
- Agnès Camuzat29
- Marie Vidailhet29
- Nicholas Wood29
- Perrine Charles29
- Sylvie Forlani27
- Christel Depienne25
- Thomas Gasser25
- Cornelis Blauwendraat24
- Mathieu Anheim23
- Merle Ruberg23
- Bruno Dubois22
- Christelle Tesson22
- Andrew Singleton21
- Cyril Goizet21
- J. Raphael Gibbs21
- John Hardy21
All papers
- Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Authors: Mike A. Nalls, Cornelis Blauwendraat, Costanza L. Vallerga, Karl Heilbron, Sara Bandrés‐Ciga, Diana Chang, Manuela Tan, Demis A. Kia, Alastair J. Noyce, Angli Xue, José Brás, Emily Young, Rainer von Coelln, Javier Simón-Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Lasse Pihlstrøm, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Faraz Faghri, J Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Juan A. Botía, María Martínez, Jean‐Christophe Corvol, Suzanne Lesage, Joseph Jankovic, 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 and 170 more - The Lancet Neurology 2019 cited by 2,541
- Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Authors: E. Sidransky, Mike A. Nalls, Jan Aasly, J. Aharon‐Peretz, Grazia Annesi, Egberto Reis Barbosa, Anat Bar‐Shira, Daniela Berg, José Brás, Alexis Brice, Chien‐Ming Chen, Lorraine N. Clark, Christel Condroyer, Elvira Valeria De Marco, Alexandra Dürr, Michael J. Eblan, S Fahn, Matthew J. Farrer, Hon‐Chung Fung, Ziv Gan‐Or, Thomas Gasser, Ruth Gershoni‐Baruch, Nir Giladi, Alida Griffith, Tanya Gurevich, Cristina Januário, Peter Kropp, Anthony E. Lang, Guey‐Jen Lee‐Chen, Suzanne Lesage, 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 cited by 2,126
- Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Authors: Wouter van Rheenen, Rick A. A. van der Spek, Mark K. Bakker, Joke J.F.A. van Vugt, Paul J. Hop, Ramona A.J. Zwamborn, Niek de Klein, Harm-Jan Westra, Olivier B. Bakker, Patrick Deelen, Gemma Shireby, Eilís Hannon, Matthieu Moisse, Denis Baird, Restuadi Restuadi, Egor Dolzhenko, Annelot M. Dekker, Klara Gawor, Henk‐Jan Westeneng, Gijs H.P. Tazelaar, Kristel R. van Eijk, Maarten Kooyman, Ross P. Byrne, Mark A. Doherty, Mark Heverin, Ahmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, Nicola Ticozzi, Johnathan Cooper‐Knock, 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 and 182 more - Nature Genetics 2021 cited by 552
- Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Authors: Mike A. Nalls, 23andMe, GenePD, The Ashkenazi Jewish Dataset Investigator, Alzheimer Genetic Analysis Group, Nathan Pankratz, Christina M. Lill, Chuong B Do, Dena G. Hernandez, Mohamad Saad, Anita L. DeStefano, Eleanna Kara, José Brás, Manu Sharma, Claudia Schulte, Margaux F. Keller, Sampath Arepalli, Christopher T. Letson, Connor Edsall, Hreinn Stefánsson, Xinmin Liu, Hannah A. Pliner, Joseph H. Lee, Rong Cheng, M. Arfan Ikram, John P. A. Ioannidis, Georgios M. Hadjigeorgiou, Joshua C Bis, María Martínez, Joel S. Perlmutter, 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 cited by 1,964
- Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Authors: Vincenzo Bonifati, Patrizia Rizzu, Marijke J. van Baren, Onno Schaap, Guido J. Breedveld, Elmar Krieger, Marieke Dekker, Ferdinando Squitieri, Pablo Ibáñez, Marijke Joosse, Jeroen W. van Dongen, Nicola Vanacore, John C. van Swieten, Alexis Brice, G. Meco, Cornelia M. van Duijn, Ben A. Oostra, Peter Heutink - Science 2003 cited by 2,797
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Authors: Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman, Alexis Brice, Jan Aasly, Cyrus P. Zabetian, Stefano Goldwurm, Joaquim J. Ferreira, Eduardo Tolosa, Denise M. Kay, Christine Klein, David R. Williams, Connie Marras, Anthony E. Lang, Zbigniew K. Wszołek, José Berciano, Anthony H.V. Schapira, Timothy Lynch, Kailash P. Bhatia, Thomas Gasser, Andrew J. Lees, Nicholas Wood - The Lancet Neurology 2008 cited by 1,563
- Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
Authors: Victoria Campuzano, Laura Montermini, María Dolores Moltó, Luigi Pianese, Mireille Cossée, Francesca Cavalcanti, Eugènia Monrós, François Rodius, Franck Duclos, Antonella Monticelli, Federico Zara, Joaquı́n Cañizares, Hana Koutníková, Sanjay I. Bidichandani, Cinzia Gellera, Alexis Brice, P Trouillas, Giuseppe De Michele, Alessandro Filla, R. de Frutos, Francesc Palau, Pragna I. Patel, Stefano Di Donato, Jean‐Louis Mandel, Sergio Cocozza, Michel Koenig, Massimo Pandolfo - Science 1996 cited by 2,801
- Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
Authors: Elisa Majounie, Alan E. Renton, Kin Y. Mok, Elise G.P. Dopper, Adrian J. Waite, Sara Rollinson, Adriano Chiò, Gabriella Restagno, Nayia Nicolaou, Javier Simón‐Sánchez, John C. van Swieten, Yevgeniya Abramzon, Janel O. Johnson, Michael Sendtner, Roger Pamphlett, Richard W. Orrell, Simon Mead, Katie Sidle, Henry Houlden, Jonathan D. Rohrer, Karen Morrison, Hardev Pall, Kevin Talbot, Olaf Ansorge, Dena G. Hernandez, Sampath Arepalli, Mario Sabatelli, Gabriele Mora, Massimo Corbo, Fabio Giannini, 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 cited by 1,226
- Clinical Correlations With Lewy Body Pathology inLRRK2-Related Parkinson Disease
Authors: Lorraine V. Kalia, Anthony E. Lang, Lili‐Naz Hazrati, Shinsuke Fujioka, Zbigniew K. Wszołek, Dennis W. Dickson, Owen A. Ross, Vivianna M. Van Deerlin, John Q. Trojanowski, Howard I. Hurtig, Roy N. Alcalay, Karen Marder, Lorraine N. Clark, Carles Gaig, Eduardo Tolosa, Javier Ruiz‐Martínez, J.F. Martí-Massó, Isidró Ferrer, Adolfo López de Munaín, Samuel M. Goldman, Birgitt Schüle, J. William Langston, Jan Aasly, Maria Teresa Giordana, Vincenzo Bonifati, Andreas Puschmann, Margherita Canesi, Gianni Pezzoli, A. Maues de Paula, Kazuko Hasegawa, Charles Duyckaerts, Alexis Brice, A. Jon Stoessl, Connie Marras - JAMA Neurology 2014 cited by 407
- Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome
Authors: Catherine S. Storm, Demis A. Kia, Mona Mohammad Almramhi, Sara Bandrés‐Ciga, Chris Finan, Alastair J. Noyce, Rauan Kaiyrzhanov, Ben Middlehurst, Manuela Tan, Henry Houlden, Huw R. Morris, Hélène Plun‐Favreau, Peter Holmans, John Hardy, Daniah Trabzuni, John P. Quinn, Vivien J. Bubb, Kin Y. Mok, Kerri J. Kinghorn, Patrick A. Lewis, Sebastian R. Schreglmann, Ruth C. Lovering, Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, 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 and 75 more - Nature Communications 2021 cited by 214
- Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Authors: PARALS Registry, Wouter van Rheenen, SLALOM Group, SLAP Registry, NNIPPS Study Group, Aleksey Shatunov, Annelot M. Dekker, Russell L. McLaughlin, Frank P. Diekstra, Sara L. Pulit, Rick A. A. van der Spek, Urmo Võsa, Simone de Jong, Matthew R. Robinson, Jian Yang, Isabella Fogh, Perry Tc van Doormaal, Gijs Tazelaar, Max Koppers, Anna M. Blokhuis, William Sproviero, Ashley R Jones, Kevin P. Kenna, Kristel R. van Eijk, Oliver Harschnitz, Raymond D. Schellevis, William J. Brands, Jelena Medic, Androniki Menelaou, Alice Vajda, 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 and 81 more - Nature Genetics 2016 cited by 628
- Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases
Authors: Aree Witoelar, Iris E. Jansen, Yunpeng Wang, Rahul S. Desikan, J. Raphael Gibbs, Cornelis Blauwendraat, Wesley K. Thompson, Dena G. Hernandez, Srdjan Djurovic, Andrew J. Schork, Francesco Bettella, David Ellinghaus, Andre Franke, Benedicte A. Lie, Linda K. McEvoy, Tom H. Karlsen, Suzanne Lesage, Huw R. Morris, Alexis Brice, Nicholas Wood, Peter Heutink, John Hardy, Andrew B. Singleton, Anders M. Dale, Thomas Gasser, Ole A. Andreassen, Manu Sharma - JAMA Neurology 2017 cited by 378
- A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Authors: Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, Emmanuelle C. Genin, Sandra Lacas‐Gervais, Konstantina Fragaki, Laetitia Berg-Alonso, Yusuke Kageyama, Valérie Serre, David Moore, Annie Verschueren, Cécile Rouzier, Isabelle Le Ber, Gaëlle Augé, Charlotte Cochaud, Françoise Lespinasse, Karine Nguyen, Anne de Septenville, Alexis Brice, Patrick Yu‐Wai‐Man, Hiromi Sesaki, Jean Pouget, Véronique Paquis‐Flucklinger - Brain 2014 cited by 497
- Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Authors: Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy, Aude Nicolas, Florence Cormier‐Dequaire, Sidi Mohamed Hassoun, Claire Pujol, Sorana Ciura, Zoi Erpapazoglou, Tatiana Usenko, Claude‐Alain Maurage, Mourad Sahbatou, Stefan Liebau, Jinhui Ding, Başar Bılgıç, Murat Emre, Nihan Erginel‐Ünaltuna, Gamze Güven, François Tison, Christine Tranchant, Marie Vidailhet, Jean‐Christophe Corvol, Paul Krack, Anne‐Louise Leutenegger, Michael A. Nalls, Dena G. Hernandez, Peter Heutink, J. Raphael Gibbs, 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 and 123 more - The American Journal of Human Genetics 2016 cited by 447
- Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
Authors: Cornelis Blauwendraat, Karl Heilbron, Costanza L. Vallerga, Sara Bandrés‐Ciga, Rainer von Coelln, Lasse Pihlstrøm, Javier Simón‐Sánchez, Claudia Schulte, Manu Sharma, Lynne Krohn, Ari Siitonen, Hirotaka Iwaki, Hampton L. Leonard, Alastair J. Noyce, Manuela Tan, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Joseph Jankovic, Lisa M. Shulman, Suzanne Lesage, Jean‐Christophe Corvol, Alexis Brice, Jacobus J. van Hilten, Johan Marinus, Johanna Eerola‐Rautio, Pentti J. Tienari, Kari Majamaa, Mathias Toft, Donald G. Grosset, 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 cited by 374
- A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
Authors: Michael A. Nalls, Raquel Durán, Grisel Lopez, Marzena Kurzawa‐Akanbi, Ian G. McKeith, Patrick F. Chinnery, Christopher M. Morris, Jessie Theuns, David Crosiers, Patrick Cras, Sebastiaan Engelborghs, Peter Paul De Deyn, Christine Van Broeckhoven, David M. A. Mann, Julie S. Snowden, Stuart Pickering‐Brown, Nicola Halliwell, Yvonne S. Davidson, Linda Gibbons, Jenny Harris, Una‐Marie Sheerin, José Brás, John Hardy, Lorraine N. Clark, Karen Marder, Lawrence S. Honig, Daniela Berg, Walter Maetzler, Kathrin Brockmann, Thomas Gasser, 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 cited by 444
- Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
Authors: Cornelis Blauwendraat, Xylena Reed, Lynne Krohn, Karl Heilbron, Sara Bandrés‐Ciga, Manuela Tan, J. Raphael Gibbs, Dena Hernández, Ravindran Kumaran, Rebekah G. Langston, Luis Bonet‐Ponce, Roy N. Alcalay, Sharon Hassin‐Baer, Lior Greenbaum, Hirotaka Iwaki, Hampton L. Leonard, Francis P. Grenn, Jennifer A. Ruskey, Marya S. Sabir, Sarah Ahmed, Mary B. Makarious, Lasse Pihlstrøm, Mathias Toft, Jacobus J. van Hilten, Johan Marinus, Claudia Schulte, Kathrin Brockmann, Manu Sharma, Ari Siitonen, Kari Majamaa, 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 cited by 245
- Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
Authors: Demis A. Kia, David Zhang, Sebastian Guelfi, Claudia Manzoni, Leon Hubbard, Regina H. Reynolds, Juan A. Botía, Mina Ryten, Raffaele Ferrari, Patrick A. Lewis, Nigel Williams, Daniah Trabzuni, John Hardy, Nicholas Wood, Alastair J. Noyce, Rauan Kaiyrzhanov, Ben Middlehurst, Demis A. Kia, Manuela Tan, Henry Houlden, Huw R. Morris, Hélène Plun‐Favreau, Peter Holmans, John Hardy, Daniah Trabzuni, José Brás, John P. Quinn, Kin Y. Mok, Kerri J. Kinghorn, Kimberley J. Billingsley, 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 and 63 more - JAMA Neurology 2021 cited by 203
- APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
Authors: 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 cited by 1,253
- Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
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