Ekaterina Rogaeva
Active 1992–2026
- 184
- Papers
- 46,844
- Citations
- 87
- h-index
- 170
- i10-index
Citations
Citation sources
Countries
Institutions
- University College London1.3%
- Harvard University1.1%
- Inserm0.7%
- Mayo Clinic in Florida0.7%
- Massachusetts General Hospital0.6%
- University of Toronto0.6%
- Other95%
Fields
- Medicine56.6%
- Biochemistry, Genetics and Molecular Biology22.4%
- Neuroscience15.1%
- Computer Science1.2%
- Immunology and Microbiology1.2%
- Psychology1.1%
- Other2.4%
Topics
- Alzheimer's disease research and treatments12%
- Amyotrophic Lateral Sclerosis Research5.6%
- Parkinson's Disease Mechanisms and Treatments5%
- Neuroinflammation and Neurodegeneration Mechanisms4.6%
- Dementia and Cognitive Impairment Research3.2%
- Genetic Associations and Epidemiology2.7%
- Other66.9%
Coauthors
- Peter St George‐Hyslop58
- Anthony E. Lang38
- Christine Sato34
- Daniela Galimberti34
- Maria Carmela Tartaglia34
- Mario Masellis34
- Elizabeth Finger33
- Caroline Graff32
- Robert Laforce27
- John C. van Swieten25
- Sandra E. Black25
- Sandro Sorbi25
- Barbara Borroni24
- James B. Rowe23
- Lorne Zinman23
- Alexandre de Mendonça22
- Martina Bocchetta21
- David M. Cash20
- Raquel Sánchez‐Valle20
- Toshitaka Kawarai20
- Rik Vandenberghe18
- Fermín Moreno17
- Julia Keith17
- Lize C. Jiskoot17
All papers
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Authors: European Alzheimer's Disease Initiative (EADI), Jean‐Charles Lambert, Genetic and Environmental Risk in Alzheimer's Disease (GERAD), Carla A. Ibrahim‐Verbaas, Denise Harold, Adam C. Naj, Rebecca Sims, Céline Bellenguez, Gyungah Jun, Anita L. DeStefano, Joshua C Bis, Gary W. Beecham, Benjamin Grenier‐Boley, Giancarlo Russo, Tricia A. Thornton‐Wells, Nicola Jones, Albert V. Smith, Vincent Chouraki, Charlene Thomas, M. Arfan Ikram, Diana Zélénika, Badri N. Vardarajan, Yoichiro Kamatani, Chiao‐Feng Lin, Amy Gerrish, Helena Schmidt, Brian W. Kunkle, Melanie Dunstan, Agustı́n Ruiz, Marie‐Thérèse Bihoreau, Seung‐Hoan Choi, Christiane Reitz, Florence Pasquier, Paul Hollingworth, Alfredo Ramı́rez, Olivier Hanon, Annette L. Fitzpatrick, Joseph D. Buxbaum, Dominique Campion, Paul K. Crane, Clinton T. Baldwin, Tim Becker, Vilmundur Guðnason, Carlos Cruchaga, David Craig, Najaf Amin, Claudine Berr, Oscar L Lopez, Philip L. De Jager, Vincent Deramecourt, Janet Johnston, Denis A. Evans, Simon Lovestone, Luc Letenneur, Francisco Jesús Morón, David C. Rubinsztein, Gudny Eiriksdottir, Kristel Sleegers, Alison Goate, Nathalie Fiévet, Matthew J. Huentelman, Michael Gill, Kristelle Brown, M. Ilyas Kamboh, Lina Keller, Pascale Barberger‐Gateau, Bernadette McGuinness, Eric B. Larson, Robert C. Green, Amanda Myers, Carole Dufouil, Stephen Todd, David Wallon, Seth Love, Ekaterina Rogaeva, John Gallacher, Peter St George‐Hyslop, Jordi Clarimón, Alberto Lleó, Anthony Bayer, Debby W. Tsuang, Lei Yu, Magda Tsolaki, Paola Bossù, Gianfranco Spalletta, Petroula Proitsi, John Collinge, Sandro Sorbi, Florentino Sánchez-García, Nick C. Fox, John Hardy, María Cándida Déniz Naranjo, Paolo Bosco, Robert Clarke, Carol Brayne, Daniela Galimberti, Michelangelo Mancuso, Fiona E. Matthews, Susanne Moebus, Patrizia Mecocci and 84 more - Nature Genetics 2013 cited by 4,659
- TREM2 Variants in Alzheimer's Disease
Authors: Rita Guerreiro, Aleksandra Wojtas, José Brás, Minerva M. Carrasquillo, Ekaterina Rogaeva, Elisa Majounie, Carlos Cruchaga, Celeste Sassi, John Kauwe, Steven G. Younkin, Lili‐Naz Hazrati, John Collinge, Jennifer M. Pocock, Tammaryn Lashley, Julie Williams, Jean‐Charles Lambert, Philippe Amouyel, Alison Goate, Rosa Rademakers, Kevin Morgan, John Powell, Peter St George‐Hyslop, Andrew Singleton, John Hardy - New England Journal of Medicine 2012 cited by 3,083
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Authors: Alan E. Renton, Elisa Majounie, Adrian J. Waite, Javier Simón‐Sánchez, Sara Rollinson, J. Raphael Gibbs, Jennifer C. Schymick, Hannu Laaksovirta, John C. van Swieten, Liisa Myllykangas, Hannu Kalimo, Anders Paetau, Yevgeniya Abramzon, Anne M. Remes, Alice Kaganovich, Sonja W. Scholz, Jamie Duckworth, Jinhui Ding, Daniel W. Harmer, Dena G. Hernandez, Janel O. Johnson, Kin Y. Mok, Mina Ryten, Daniah Trabzuni, Rita Guerreiro, Richard W. Orrell, James Neal, Alex Murray, Justin Pearson, Iris E. Jansen, David Sondervan, Harro Seelaar, Derek J. Blake, Kate Young, Nicola Halliwell, Janis Bennion Callister, Greg Toulson, Anna Richardson, Alexander Gerhard, Julie S. Snowden, David Mann, David Neary, Michael A. Nalls, Terhi Peuralinna, Lilja Jansson, Veli‐Matti Isoviita, Anna-Lotta Kaivorinne, Maarit Hölttä‐Vuori, Elina Ikonen, Raimo Sulkava, Michael Benatar, Joanne Wuu, Adriano Chiò, Gabriella Restagno, Giuseppe Borghero, Mario Sabatelli, David Heckerman, Ekaterina Rogaeva, Lorne Zinman, Jeffrey D. Rothstein, Michael Sendtner, Carsten Drepper, Evan E. Eichler, Can Alkan, Ziedulla Abdullaev, Svetlana Pack, Amalia Dutra, Evgenia Pak, John Hardy, Andrew Singleton, Nigel Williams, Peter Heutink, Stuart Pickering‐Brown, Huw R. Morris, Pentti J. Tienari, Bryan J. Traynor - Neuron 2011 cited by 4,469
- 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
- Analysis of shared heritability in common disorders of the brain
Authors: 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 and 477 more - Science 2018 cited by 2,050
- Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference
Authors: Alexandra L. Young, Razvan Marinescu, Neil P. Oxtoby, Martina Bocchetta, Keir Yong, Nicholas C. Firth, David M. Cash, David L. Thomas, Katrina M. Dick, M. Jorge Cardoso, John C. van Swieten, Barbara Borroni, Daniela Galimberti, Mario Masellis, Maria Carmela Tartaglia, James B. Rowe, Caroline Graff, Fabrizio Tagliavini, Giovanni B. Frisoni, Robert Laforce, Elizabeth Finger, Alexandre de Mendonça, Sandro Sorbi, Jason D. Warren, Sebastian J. Crutch, Nick C. Fox, Sébastien Ourselin, Jonathan M. Schott, Jonathan D. Rohrer, Daniel C. Alexander, The Genetic FTD Initiative (GENFI), Christin Andersson, Silvana Archetti, Andrea Arighi, Luisa Benussi, Giuliano Binetti, Sandra E. Black, Maura Cosseddu, Marie Fallström, Carlos Ferreira, Chiara Fenoglio, Morris Freedman, Giorgio Fumagalli, Stefano Gazzina, Roberta Ghidoni, Marina Grisoli, Vesna Jelić, Lize C. Jiskoot, Ron Keren, Gemma Lombardi, Carolina Maruta, Lieke Meeter, Simon Mead, Rick van Minkelen, Benedetta Nacmias, Linn Öijerstedt, Alessandro Padovani, Jessica Panman, Michela Pievani, Cristina Polito, Enrico Premi, Sara Prioni, Rosa Rademakers, Veronica Redaelli, Ekaterina Rogaeva, Giacomina Rossi, Martin N. Rossor, Elio Scarpini, David F. Tang‐Wai, Håkan Thonberg, Pietro Tiraboschi, Ana Verdelho, The Alzheimer’s Disease Neuroimaging Initiative (ADNI), Michael W. Weiner, Paul Aisen, Ronald Petersen, Clifford R. Jack, William J. Jagust, John Q. Trojanowki, Arthur W. Toga, Laurel Beckett, Robert C. Green, Andrew J. Saykin, John C. Morris, Leslie M. Shaw, Zaven S. Khachaturian, Greg Sorensen, Lew Kuller, Marc Raichle, Steven M. Paul, Peter Davies, Howard Fillit, Franz Hefti, Davie Holtzman, M. Marcel Mesulam, William C. Potter, Peter J. Snyder, Adam Schwartz, Tom Montine, Ronald G. Thomas and 280 more - Nature Communications 2018 cited by 586
- Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Authors: Adam C. Naj, Gyungah Jun, Gary W. Beecham, Li‐San Wang, Badri N. Vardarajan, Jacqueline L. Buros, Paul J. Gallins, Joseph D. Buxbaum, Gail P. Jarvik, Paul K. Crane, Eric B. Larson, Thomas D. Bird, Bradley F. Boeve, Neill R. Graff‐Radford, Philip L. De Jager, Denis A. Evans, Julie A. Schneider, Minerva M. Carrasquillo, Nilüfer Ertekin‐Taner, Steven G. Younkin, Carlos Cruchaga, John Kauwe, Petra Nowotny, Patricia Kramer, John Hardy, Matthew J. Huentelman, Amanda Myers, M. Michael Barmada, F. Yesim Demirci, Clinton T. Baldwin, Robert C. Green, Ekaterina Rogaeva, Peter St George‐Hyslop, Steven E. Arnold, Robert C. Barber, Thomas G. Beach, Eileen H. Bigio, James D. Bowen, Adam Boxer, James R. Burke, Nigel J. Cairns, Chris Carlson, Regina M. Carney, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason J. Corneveaux, Carl W. Cotman, Jeffrey L. Cummings, Charles DeCarli, Steven T. DeKosky, Ramon Diaz‐Arrastia, Malcolm Dick, Dennis W. Dickson, William G. Ellis, Kelley M. Faber, Kenneth B. Fallon, Martin R. Farlow, Steven H. Ferris, Matthew P. Frosch, Douglas Galasko, Mary Ganguli, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Sid Gilman, Bruno Giordani, Jonathan D. Glass, John H. Growdon, Ronald L. Hamilton, Lindy E. Harrell, Elizabeth Head, Lawrence S. Honig, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin, Nancy Johnson, Jason Karlawish, Anna Karydas, Jeffrey Kaye, Ronald Kim, Edward H. Koo, Neil W. Kowall, James J. Lah, Allan I. Levey, Andrew P. Lieberman, Oscar L. López, Wendy J. Mack, Daniel Marson, Frank Martiniuk, Deborah C. Mash, Eliezer Masliah, Wayne C. McCormick, Susan M. McCurry, Andrew McDavid, Ann C. McKee, Marsel Mesulam, Bruce L. Miller and 55 more - Nature Genetics 2011 cited by 2,014
- Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
Authors: Robin Sherrington, Е. И. Рогаев, Yuh‐Jin Liang, Ekaterina Rogaeva, Georges Lévesque, Masaki Ikeda, Hongbo Chi, Chiao‐Feng Lin, Li Guo, K. Holman, T. Tsuda, Lynn Mar, J F Foncin, Amalia C. Bruni, M. P. Montesi, Sandro Sorbi, Innocenzo Rainero, Lorenzo Pinessi, Linda E. Nee, Ilya Chumakov, D. A. Pollen, Anthony J. Brookes, Philippe Sanséau, Ronald J. Polinsky, Wilma Wasco, H. A. R. Da Silva, Jonathan L. Haines, Margaret A. Pericak‐Vance, Rudolph E. Tanzi, Allen D. Roses, P. E. Fraser, Johanna M. Rommens, Peter St George‐Hyslop - Nature 1995 cited by 4,061
- TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
Authors: Ian R. Mackenzie, Alexandra M. Nicholson, Mohona Sarkar, James Messing, Maria D. Purice, Cyril Pottier, Kavya Annu, Matt Baker, Ralph B. Perkerson, Aishe Kurti, Billie J. Matchett, Tanja Mittag, Jamshid Temirov, Ging‐Yuek Robin Hsiung, Charles Krieger, Melissa E. Murray, Masato Kato, John Denis Fryer, Leonard Petrucelli, Lorne Zinman, Sandra Weıntraub, Marsel Mesulam, Julia Keith, Sasha Živković, Veronica Hirsch‐Reinshagen, Raymond P. Roos, Stephan Züchner, Neill R. Graff‐Radford, Ronald C. Petersen, Richard J. Caselli, Zbigniew K. Wszołek, Elizabeth Finger, Carol F. Lippa, David Lacomis, Heather Stewart, Dennis W. Dickson, Hong Joo Kim, Ekaterina Rogaeva, Eileen H. Bigio, Khrista Boylan, J. Paul Taylor, Rosa Rademakers - Neuron 2017 cited by 651
- Late-onset vs nonmendelian early-onset Alzheimer disease
Authors: Christiane Reitz, Ekaterina Rogaeva, Gary W. Beecham - Neurology Genetics 2020 cited by 170
- The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease
Authors: Ekaterina Rogaeva, Yan Meng, Joseph H. Lee, Yongjun Gu, Toshitaka Kawarai, Fanggeng Zou, Taiichi Katayama, Clinton T. Baldwin, Rong Cheng, Hiroshi Hasegawa, Fusheng Chen, Nobuto Shibata, Kathryn L. Lunetta, Raphaëlle Pardossi‐Piquard, Christopher Böhm, Yosuke Wakutani, L. Adrienne Cupples, Karen T. Cuenco, Robert C. Green, Lorenzo Pinessi, Innocenzo Rainero, Sandro Sorbi, Amalia C. Bruni, Ranjan Duara, Robert P. Friedland, Rivka Inzelberg, Wolfgang Hampe, Hideaki Bujo, You‐Qiang Song, Olav M. Andersen, Thomas E. Willnow, Neill R. Graff‐Radford, Ronald Petersen, Dennis W. Dickson, Sandy D. Der, Paul E. Fraser, Gerold Schmitt‐Ulms, Steven G. Younkin, Richard Mayeux, Lindsay A. Farrer, Peter St George‐Hyslop - Nature Genetics 2007 cited by 1,169
- 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
- Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
Authors: Jonathan D. Rohrer, Jennifer Nicholas, David M. Cash, John C. van Swieten, Elise G.P. Dopper, Lize C. Jiskoot, Rick van Minkelen, Serge A.R.B. Rombouts, M. Jorge Cardoso, Shona Clegg, Miklos Espak, Simon Mead, David L. Thomas, Enrico De Vita, Mario Masellis, Sandra E. Black, Morris Freedman, Ron Keren, Bradley J. MacIntosh, Ekaterina Rogaeva, David F. Tang‐Wai, Maria Carmela Tartaglia, Robert Laforce, Fabrizio Tagliavini, Pietro Tiraboschi, Veronica Redaelli, Sara Prioni, Marina Grisoli, Barbara Borroni, Alessandro Padovani, Daniela Galimberti, Elio Scarpini, Andrea Arighi, Giorgio Fumagalli, James B. Rowe, Ian Coyle‐Gilchrist, Caroline Graff, Marie Fallström, Vesna Jelić, Anne Kinhult Ståhlbom, Christin Andersson, Håkan Thonberg, Lena Lilius, Giovanni B. Frisoni, Giuliano Binetti, Michela Pievani, Martina Bocchetta, Luisa Benussi, Roberta Ghidoni, Elizabeth Finger, Sandro Sorbi, Benedetta Nacmias, Gemma Lombardi, Cristina Polito, Jason D. Warren, Sébastien Ourselin, Nick C. Fox, Martin N. Rossor - The Lancet Neurology 2015 cited by 544
- Frontotemporal dementia and its subtypes: a genome-wide association study
Authors: 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 and 58 more - The Lancet Neurology 2014 cited by 402
- Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
Authors: Е. И. Рогаев, Robin Sherrington, Ekaterina Rogaeva, Georges Lévesque, Masaki Ikeda, Yuh‐Jin Liang, Hongbo Chi, Chen-Xi Lin, K. Holman, T. Tsuda, Lynn Mar, Sandro Sorbi, Benedetta Nacmias, Silvia Piacentini, L. Amaducci, Ilya Chumakov, Daniel Cohen, Lars Lannfelt, Paul E. Fraser, Johanna M. Rommens, Peter St George‐Hyslop - Nature 1995 cited by 2,067
- Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study
Authors: Emma L. van der Ende, Lieke Meeter, Jackie M. Poos, Jessica Panman, Lize C. Jiskoot, Elise G.P. Dopper, Janne M. Papma, Frank Jan de Jong, Inge M.W. Verberk, Charlotte E. Teunissen, Dimitris Rizopoulos, Carolin Heller, Rhian S. Convery, Katrina Moore, Martina Bocchetta, Mollie Neason, David M. Cash, Barbara Borroni, Daniela Galimberti, Raquel Sánchez‐Valle, Robert Laforce, Fermín Moreno, Matthis Synofzik, Caroline Graff, Mario Masellis, Maria Carmela Tartaglia, James B. Rowe, Rik Vandenberghe, Elizabeth Finger, Fabrizio Tagliavini, Alexandre de Mendonça, Isabel Santana, Christopher Butler, Simon Ducharme, Alexander Gerhard, Adrian Danek, Johannes Levin, Markus Otto, Giovanni B. Frisoni, Stefano F. Cappa, Yolande A.L. Pijnenburg, Jonathan D. Rohrer, John C. van Swieten, Martin N. Rossor, Jason D. Warren, Nick C. Fox, Ione Woollacott, Rachelle Shafei, Caroline Greaves, Rita Guerreiro, José Brás, David L. Thomas, Jennifer Nicholas, Simon Mead, Rick van Minkelen, Myriam Barandiarán, Begoña Indakoetxea, Alazne Gabilondo, Mikel Tainta, María de Arriba, Ana Gorostidi, Miren Zulaica, Jorge Villanúa, Zigor Díaz, Sergi Borrego‐Écija, Jaume Olives, Albert Lladó, Mircea Balasa, Anna Antonell, Núria Bargalló, Enrico Premi, Maura Cosseddu, Stefano Gazzina, Alessandro Padovani, Roberto Gasparotti, Silvana Archetti, Sandra E. Black, Sara Mitchell, Ekaterina Rogaeva, Morris Freedman, Ron Keren, David F. Tang‐Wai, Linn Öijerstedt, Christin Andersson, Vesna Jelić, Håkan Thonberg, Andrea Arighi, Chiara Fenoglio, Elio Scarpini, Giorgio Fumagalli, Thomas Cope, Carolyn Timberlake, Timothy Rittman, Christen Shoesmith, Robart Bartha, Rosa Rademakers, Carlo Wilke, Hans‐Otto Karnath, Benjamin Bender, Rose Bruffaerts and 33 more - The Lancet Neurology 2019 cited by 186
- Early-Onset Alzheimer’s Disease: What Is Missing in Research?
Authors: Temitope Ayodele, Ekaterina Rogaeva, Jiji T. Kurup, Gary W. Beecham, Christiane Reitz - Current Neurology and Neuroscience Reports 2021 cited by 194
- Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Authors: ITALSGEN, Janel O. Johnson, Erik P. Pioro, Ashley Boehringer, Ruth Chia, Howard Feit, Alan E. Renton, Hannah A. Pliner, Yevgeniya Abramzon, Giuseppe Marangi, Brett J Winborn, J. Raphael Gibbs, Michael A. Nalls, Sarah Morgan, Maryam Shoai, John Hardy, Alan Pittman, Richard W. Orrell, Andrea Malaspina, Katie Sidle, Pietro Fratta, Matthew B. Harms, Robert H. Baloh, Alan Pestronk, Conrad C. Weihl, Ekaterina Rogaeva, Lorne Zinman, Vivian E. Drory, Giuseppe Borghero, Gabriele Mora, Andrea Calvo, Jeffrey D. Rothstein, Carsten Drepper, Michael Sendtner, Andrew Singleton, J. Paul Taylor, Mark Cookson, Gabriella Restagno, Mario Sabatelli, Robert Bowser, Adriano Chiò, Bryan J. Traynor - Nature Neuroscience 2014 cited by 443
- Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
Authors: Rita Guerreiro, Owen A. Ross, Célia Kun‐Rodrigues, Dena Hernández, Tatiana Orme, John D. Eicher, Claire E. Shepherd, Laura Parkkinen, Lee Darwent, Michael G. Heckman, Sonja W. Scholz, Juan C. Troncoso, Olga Pletnikova, Olaf Ansorge, Jordi Clarimón, Alberto Lleó, Estrella Morenas‐Rodríguez, Lorraine N. Clark, Lawrence S. Honig, Karen Marder, Afina W. Lemstra, Ekaterina Rogaeva, Peter St George‐Hyslop, Elisabet Londos, Henrik Zetterberg, Imelda Barber, Anne Braae, Kristelle Brown, Kevin Morgan, Claire Troakes, Safa Al‐Sarraj, Tammaryn Lashley, Janice L. Holton, Yaroslau Compta, Vivianna M. Van Deerlin, Geidy E. Serrano, Thomas G. Beach, Suzanne Lesage, Douglas Galasko, Eliezer Masliah, Isabel Santana, Pau Pástor, Mónica Díez-Fairén, Miquel Aguilar, Pentti J. Tienari, Liisa Myllykangas, Minna Oinas, Tamás Révész, Andrew J. Lees, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Valentina Escott‐Price, Caroline Graff, Nigel J. Cairns, John C. Morris, Stuart Pickering‐Brown, David Mann, Glenda M. Halliday, John Hardy, John Q. Trojanowski, Dennis W. Dickson, Andrew Singleton, David J. Stone, José Brás - The Lancet Neurology 2017 cited by 289
- A complex of C9ORF72 and p62 uses arginine methylation to eliminate stress granules by autophagy
Authors: Maneka Chitiprolu, Chantal Jagow, Véronique Tremblay, Emma Bondy‐Chorney, Geneviève Paris, Alexandre Savard, Gareth Palidwor, Francesca A. Barry, Lorne Zinman, Julia Keith, Ekaterina Rogaeva, Janice Robertson, Mathieu Lavallée‐Adam, John Woulfe, Jean‐François Couture, Jocelyn Côté, Derrick Gibbings - Nature Communications 2018 cited by 177
- Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia
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