Ekaterina Rogaeva

Active 1992–2026

184
Papers
46,844
Citations
87
h-index
170
i10-index

Citations

Citations per year for Ekaterina Rogaeva1990: 2 citations1991: 2 citations1993: 14 citations1994: 15 citations1995: 41 citations1996: 115 citations1997: 160 citations1998: 125 citations1999: 152 citations2000: 199 citations2001: 157 citations2002: 199 citations2003: 174 citations2004: 188 citations2005: 159 citations2006: 190 citations2007: 211 citations2008: 257 citations2009: 178 citations2010: 231 citations2011: 291 citations2012: 451 citations2013: 506 citations2014: 572 citations2015: 678 citations2016: 806 citations2017: 739 citations2018: 788 citations2019: 2,095 citations2020: 2,107 citations2021: 2,021 citations2022: 1,551 citations2023: 1,208 citations2024: 1,625 citations2025: 860 citations2026: 24 citations1992: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,789 citing papers, 26.1% of this breakdownUnited Kingdom: 2,540 citing papers, 9.8% of this breakdownChina: 1,561 citing papers, 6% of this breakdownGermany: 1,552 citing papers, 6% of this breakdownCanada: 1,284 citing papers, 4.9% of this breakdownItaly: 1,114 citing papers, 4.3% of this breakdownNetherlands: 920 citing papers, 3.5% of this breakdownFrance: 886 citing papers, 3.4% of this breakdownAustralia: 874 citing papers, 3.4% of this breakdownSpain: 762 citing papers, 2.9% of this breakdownSweden: 746 citing papers, 2.9% of this breakdownJapan: 674 citing papers, 2.6% of this breakdown
0%26.1%Other 24.2%

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

All papers

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  1. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  2. TREM2 Variants in Alzheimer's Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2012 cited by 3,083

  3. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  5. Analysis of shared heritability in common disorders of the brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  6. Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  8. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , P. E. Fraser, Johanna M. Rommens, Peter St George‐Hyslop - Nature 1995 cited by 4,061

  9. TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  10. Late-onset vs nonmendelian early-onset Alzheimer disease

    Authors: , , - Neurology Genetics 2020 cited by 170

  11. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  13. Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  15. 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: , , , , , , , , , , , , , , , , , , , , - Nature 1995 cited by 2,067

  16. Serum neurofilament light chain in genetic frontotemporal dementia: a longitudinal, multicentre cohort study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  17. Early-Onset Alzheimer’s Disease: What Is Missing in Research?

    Authors: , , , , - Current Neurology and Neuroscience Reports 2021 cited by 194

  18. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  19. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  20. A complex of C9ORF72 and p62 uses arginine methylation to eliminate stress granules by autophagy

    Authors: , , , , , , , , , , , , , , , , - Nature Communications 2018 cited by 177

  21. Network structure and transcriptomic vulnerability shape atrophy in frontotemporal dementia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jonathan D. Rohrer, Bratislav Mišić, Simon Ducharme, Frontotemporal Lobar Degeneration Neuroimaging Initiative (FTLDNI), Howard Rosen, Bradford C. Dickerson, Kimoko Domoto-Reilly, David S. Knopman, Bradley F. Boeve, Adam L. Boxer, John Kornak, Bruce L. Miller, William W. Seeley, Maria‐Luisa Gorno‐Tempini, Scott McGinnis, Maria Luisa Mandelli, GENetic Frontotemporal dementia Initiative (GENFI), Aitana Sogorb‐Esteve, Annabel Nelson, Arabella Bouzigues, Carolin Heller, Caroline Greaves, David M. Cash, David L. Thomas, Emily Todd, Hanya Benotmane, Henrik Zetterberg, Imogen J. Swift, Jennifer Nicholas, Kiran Samra, Lucy L. Russell, Martina Bocchetta, Rachelle Shafei, Rhian S. Convery, Carolyn Timberlake, Thomas Cope, Timothy Rittman, Alberto Benussi, Enrico Premi, Roberto Gasparotti, Silvana Archetti, Stefano Gazzina, Valentina Cantoni, Andrea Arighi, Chiara Fenoglio, Elio Scarpini, Giorgio Fumagalli, Vittoria Borracci, Giacomina Rossi, Giorgio Giaccone, Giuseppe Di Fede, Paola Caroppo, Pietro Tiraboschi, Sara Prioni, Veronica Redaelli, David F. Tang‐Wai, Ekaterina Rogaeva, Miguel Castelo‐Branco, Morris Freedman, Ron Keren, Sandra E. Black, Sara Mitchell, Christen Shoesmith, Robart Bartha, Rosa Rademakers, Emma van der Ende, Jackie M. Poos, Janne M. Papma, Lucia Giannini, Rick van Minkelen and 70 more - Brain 2022 cited by 90

  22. Collagenosis of the Deep Medullary Veins: An Underrecognized Pathologic Correlate of White Matter Hyperintensities and Periventricular Infarction?

    Authors: , , , , , , , , - Journal of Neuropathology & Experimental Neurology 2017 cited by 172

  23. Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marie‐Christine Chartier‐Harlin, Eugénie Mutez, Kathrin Brockmann, Angela Deutschländer, G. Hadjigeorgiou, Efthimos Dardiotis, Leonidas Stefanis, Athina Maria Simitsi, Enza Maria Valente, Simona Petrucci, Letizia Straniero, Anna Zecchinelli, Gianni Pezzoli, Laura Brighina, Carlo Ferrarese, Grazia Annesi, Andrea Quattrone, Monica Gagliardi, Lena F. Burbulla, Hirotaka Matsuo, Yusuke Kawamura, Nobutaka Hattori, Kenya Nishioka, Sun Ju Chung, Yun Joong Kim, Lukas Pavelka, Bart P.C. van de Warrenburg, Bastiaan R. Bloem, Andrew Singleton, Jan Aasly, Mathias Toft, Leonor Correia Guedes, Joaquim J. Ferreira, Soraya Bardien, Jonathan Carr, Eduardo Tolosa, Mario Ezquerra, Pau Pástor, Mónica Díez-Fairén, Karin Wirdefeldt, Nancy L. Pedersen, Caroline Ran, Andrea Carmine Belin, Andreas Puschmann, Clara Hellberg, Carl E Clarke, Karen Morrison, Dimitri Krainc, Matthew J. Farrer, Rejko Krüger, Alexis Elbaz, Thomas Gasser, Manu Sharma - Neurology 2022 cited by 71

  24. Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Safa Al‐Sarraj, Tammaryn Lashley, Yaroslau Compta, Tamás Révész, Andrew J. Lees, Nigel J. Cairns, Glenda M. Halliday, David Mann, Stuart Pickering‐Brown, Dennis W. Dickson, Andrew Singleton, John Hardy - Human Molecular Genetics 2014 cited by 240