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Rosa Rademakers

Active 2003–2025

270
Papers
55,541
Citations
116
h-index
259
i10-index

Citations

Citations per year for Rosa Rademakers1967: 1 citations1984: 1 citations1990: 1 citations1999: 2 citations2001: 3 citations2002: 4 citations2004: 5 citations2005: 16 citations2006: 109 citations2007: 251 citations2008: 273 citations2009: 295 citations2010: 357 citations2011: 460 citations2012: 726 citations2013: 850 citations2014: 802 citations2015: 827 citations2016: 1,035 citations2017: 1,170 citations2018: 968 citations2019: 2,625 citations2020: 2,728 citations2021: 2,826 citations2022: 2,127 citations2023: 1,816 citations2024: 2,466 citations2025: 1,445 citations2026: 45 citations1968–1983: no citations, so these years are not shown1985–1989: no citations, so these years are not shown1991–1998: no citations, so these years are not shown2000: no citations, so this year is not shown2003: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 5,924 citing papers, 27.6% of this breakdownUnited Kingdom: 2,165 citing papers, 10.1% of this breakdownChina: 1,335 citing papers, 6.2% of this breakdownGermany: 1,320 citing papers, 6.1% of this breakdownItaly: 1,056 citing papers, 4.9% of this breakdownCanada: 1,025 citing papers, 4.8% of this breakdownNetherlands: 777 citing papers, 3.6% of this breakdownAustralia: 748 citing papers, 3.5% of this breakdownFrance: 719 citing papers, 3.3% of this breakdownSpain: 627 citing papers, 2.9% of this breakdownJapan: 593 citing papers, 2.8% of this breakdownSweden: 586 citing papers, 2.7% of this breakdown
0%27.6%Other 21.5%

Institutions

Fields

  • Medicine56.7%
  • Biochemistry, Genetics and Molecular Biology21.3%
  • Neuroscience18.3%
  • Immunology and Microbiology1.7%
  • Computer Science0.4%
  • Agricultural and Biological Sciences0.4%
  • Other1.2%

Topics

  • Amyotrophic Lateral Sclerosis Research11.3%
  • Alzheimer's disease research and treatments10.3%
  • Neuroinflammation and Neurodegeneration Mechanisms6%
  • Neurogenetic and Muscular Disorders Research5%
  • Parkinson's Disease Mechanisms and Treatments4.7%
  • Dementia and Cognitive Impairment Research3.8%
  • Other58.9%

Coauthors

All papers

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  1. 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

  2. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS

    Authors: Mariely DeJesus‐Hernandez, Ian R. Mackenzie, Bradley F. Boeve, Adam L. Boxer, Matt Baker, Nicola J. Rutherford, Alexandra M. Nicholson, NiCole A. Finch, Heather C. Flynn, Jennifer Adamson, Naomi Kouri, Aleksandra Wojtas, Pheth Sengdy, Ging‐Yuek Robin Hsiung, Anna Karydas, William W. Seeley, Keith A. Josephs, Giovanni Coppola, Daniel H. Geschwind, Zbigniew K. Wszołek, Howard Feldman, David S. Knopman, Ronald C. Petersen, Bruce L. Miller, Dennis W. Dickson, Khrista Boylan, Neill R. Graff‐Radford, Rosa Rademakers - Neuron 2011 cited by 4,971

  3. Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report

    Authors: Peter T. Nelson, Dennis W. Dickson, John Q. Trojanowski, Clifford R. Jack, Patricia A. Boyle, Konstantinos Arfanakis, Rosa Rademakers, Irina Alafuzoff, Johannes Attems, Carol Brayne, Ian Coyle‐Gilchrist, Helena C. Chui, David W. Fardo, Margaret E. Flanagan, Glenda M. Halliday, Suvi R. K. Hokkanen, Sally Hunter, Gregory A. Jicha, Yuriko Katsumata, Claudia H. Kawas, C. Dirk Keene, Gábor G. Kovács, Walter A. Kukull, Allan I. Levey, Nazanin Makkinejad, Thomas J. Montine, Shigeo Murayama, Melissa E. Murray, Sukriti Nag, Robert A. Rissman, William W. Seeley, Reisa A. Sperling, Charles L. White, Lei Yu, Julie A. Schneider - Brain 2019 cited by 1,546

  4. 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

  5. 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

  6. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

    Authors: Hong Joo Kim, Nam Chul Kim, Yong‐Dong Wang, Emily A. Scarborough, Jennifer C. Moore, Zamia Diaz, Kyle S. MacLea, Brian D. Freibaum, Songqing Li, Amandine Molliex, Anderson Kanagaraj, Robert Carter, Khrista Boylan, Aleksandra Wojtas, Rosa Rademakers, Jack L. Pinkus, Steven A. Greenberg, John Q. Trojanowski, Bryan J. Traynor, Bradley Smith, Simon Topp, Athina-Soragia Gkazi, Jack W. Miller, Christopher E. Shaw, Michael Kottlors, Janbernd Kirschner, Alan Pestronk, Leslie A. Lange, Alice F. Ford, Aaron D. Gitler, Michael Benatar, Oliver D. King, Virginia Kimonis, Eric D. Ross, Conrad C. Weihl, James Shorter, J. Paul Taylor - Nature 2013 cited by 1,518

  7. Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

    Authors: Hansen Lui, Jiasheng Zhang, Stefanie Ritter Makinson, Michelle K. Cahill, Kevin W. Kelley, Hsin‐Yi Huang, Yulei Shang, Michael C. Oldham, Lauren Herl Martens, Fuying Gao, Giovanni Coppola, Steven A. Sloan, Christine L. Hsieh, Charles C. Kim, Eileen H. Bigio, Sandra Weıntraub, Marek-Marsel Mesulam, Rosa Rademakers, Ian R. Mackenzie, William W. Seeley, Anna Karydas, Bruce L. Miller, Barbara Borroni, Roberta Ghidoni, Robert V. Farese, Jeanne T. Paz, Ben A. Barres, Eric J. Huang - Cell 2016 cited by 757

  8. TDP-43 pathology disrupts nuclear pore complexes and nucleocytoplasmic transport in ALS/FTD

    Authors: Ching‐Chieh Chou, Yi Zhang, Mfon Umoh, Spencer Vaughan, Ileana Lorenzini, Feilin Liu, Melissa Sayegh, Paul Donlin-Asp, Yu Han Chen, Duc M. Duong, Nicholas T. Seyfried, Maureen A. Powers, Thomas Kukar, Chadwick M. Hales, Marla Gearing, Nigel J. Cairns, Khrista Boylan, Dennis W. Dickson, Rosa Rademakers, Yong‐Jie Zhang, Leonard Petrucelli, Rita Sattler, Daniela C. Zarnescu, Jonathan D. Glass, Wilfried Rossoll - Nature Neuroscience 2018 cited by 604

  9. Apolipoprotein E Is a Ligand for Triggering Receptor Expressed on Myeloid Cells 2 (TREM2)

    Authors: Yuka Atagi, Chia‐Chen Liu, Meghan M. Painter, Xiao‐Fen Chen, Christophe Verbeeck, Honghua Zheng, Xia Li, Rosa Rademakers, Silvia S. Kang, Huaxi Xu, Steven G. Younkin, Pritam Das, John Denis Fryer, Guojun Bu - Journal of Biological Chemistry 2015 cited by 628

  10. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

    Authors: Matt Baker, Ian R. Mackenzie, Stuart Pickering‐Brown, Jennifer Gass, Rosa Rademakers, Caroline Lindholm, Julie S. Snowden, Jennifer Adamson, A. Dessa Sadovnick, Sara Rollinson, Ashley Cannon, Emily Dwosh, David Neary, Stacey Melquist, Anna Richardson, Dennis W. Dickson, Zdenek Berger, Jason L. Eriksen, Todd Robinson, Cynthia Zehr, Chad A. Dickey, Richard Crook, Eileen McGowan, David Mann, Bradley F. Boeve, Howard Feldman, Mike Hutton - Nature 2006 cited by 2,121

  11. Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS

    Authors: Peter E.A. Ash, Kevin F. Bieniek, Tania F. Gendron, Thomas R. Caulfield, Wen-Lang Lin, Mariely DeJesus‐Hernandez, Marka van Blitterswijk, Karen Jansen‐West, Joseph W. Paul, Rosa Rademakers, Khrista Boylan, Dennis W. Dickson, Leonard Petrucelli - Neuron 2013 cited by 1,110

  12. 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

  13. Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia

    Authors: Mercedes Prudencio, Jack Humphrey, Sarah Pickles, Anna‐Leigh Brown, Sarah E. Hill, Jennifer M. Kachergus, Jianhua Shi, Michael G. Heckman, Matthew R. Spiegel, Casey Cook, Yuping Song, Mei Yue, Lillian M. Daughrity, Yari Carlomagno, Karen Jansen‐West, Cristhoper Fernandez De Castro, Michael DeTure, Shunsuke Koga, Ying‐Chih Wang, Prasanth Sivakumar, Cristian Bodo, Ana Candalija, Kevin Talbot, Bhuvaneish T. Selvaraj, Karen Burr, Siddharthan Chandran, Jia Newcombe, Tammaryn Lashley, Isabel Hubbard, Demetra Catalano, Duyang Kim, Nadia Propp, Samantha Fennessey, Delphine Fagegaltier, Hemali Phatnani, Maria Secrier, Elizabeth Fisher, Björn Oskarsson, Marka van Blitterswijk, Rosa Rademakers, N. R. Graff-Radford, Bradley F. Boeve, David S. Knopman, Ronald C. Petersen, Keith A. Josephs, E. Aubrey Thompson, Towfique Raj, Michael E. Ward, Dennis W. Dickson, Tania F. Gendron, Pietro Fratta, Leonard Petrucelli - Journal of Clinical Investigation 2020 cited by 257

  14. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

    Authors: Vivianna M. Van Deerlin, Patrick Sleiman, Maria Martinez‐Lage, Alice Chen‐Plotkin, Li-San Wang, Neill R. Graff‐Radford, Dennis W. Dickson, Rosa Rademakers, Bradley F. Boeve, Murray Grossman, Steven E. Arnold, David Mann, Stuart Pickering‐Brown, Harro Seelaar, Peter Heutink, John C. van Swieten, Jill R. Murrell, Bernardino Ghetti, Salvatore Spina, Jordan Grafman, John R. Hodges, Maria Grazia Spillantini, Sid Gilman, Andrew P. Lieberman, Jeffrey Kaye, Randall L. Woltjer, Eileen H. Bigio, Marsel Mesulam, Safa Al‐Sarraj, Claire Troakes, Roger N. Rosenberg, Charles L. White, Isidró Ferrer, Albert Lladó, Manuela Neumann, Hans A. Kretzschmar, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, Bruce L. Miller, Ainhoa Alzualde, Adolfo López de Munain, Ann C. McKee, Marla Gearing, Allan I. Levey, James J. Lah, John Hardy, Jonathan D. Rohrer, Tammaryn Lashley, Ian R. Mackenzie, Howard Feldman, Ronald L. Hamilton, Steven T. DeKosky, Julie van der Zee, Samir Kumar‐Singh, Christine Van Broeckhoven, Richard Mayeux, Jean Paul Vonsattel, Juan C. Troncoso, Jillian J. Kril, John B. Kwok, Glenda M. Halliday, Thomas D. Bird, Paul G. Ince, Pamela J. Shaw, Nigel J. Cairns, John C. Morris, Catriona McLean, Charles DeCarli, William G. Ellis, Stefanie H. Freeman, Matthew P. Frosch, John H. Growdon, Daniel P. Perl, Mary Sano, David A. Bennett, Julie A. Schneider, Thomas G. Beach, Eric M. Reiman, Bryan K. Woodruff, Jeffrey L. Cummings, Harry V. Vinters, Carol A. Miller, Helena C. Chui, Irina Alafuzoff, Päivi Hartikainen, Danielle Seilhean, Douglas Galasko, Eliezer Masliah, Carl W. Cotman, MJ Tuñón, Mònica Martínez, David G. Muñoz, Steven L. Carroll, Daniel Marson, Peter Riederer, Nenad Bogdanović, Gerard D Schellenberg, Håkon Håkonarson, John Q. Trojanowski, Virginia M.‐Y. Lee - Nature Genetics 2010 cited by 609

  15. TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

    Authors: Ian R. Mackenzie, Rosa Rademakers, Manuela Neumann - The Lancet Neurology 2010 cited by 973

  16. Temporal order of clinical and biomarker changes in familial frontotemporal dementia

    Authors: Adam M. Staffaroni, Melanie Quintana, Barbara Wendelberger, Hilary W. Heuer, Lucy L. Russell, Yann Cobigo, Amy Wolf, Sheng‐Yang M. Goh, Leonard Petrucelli, Tania F. Gendron, Carolin Heller, Annie L Clark, Jack C. Taylor, Amy B. Wise, Elise Ong, Leah K. Forsberg, Danielle Brushaber, Julio C. Rojas, Lawren VandeVrede, Peter A. Ljubenkov, Joel H. Kramer, Kaitlin B. Casaletto, Brian S. Appleby, Yvette Bordelon, Hugo Botha, Bradford C. Dickerson, Kimiko Domoto‐Reilly, Julie A. Fields, Tatiana Foroud, Ralitza H. Gavrilova, Daniel H. Geschwind, Nupur Ghoshal, Jill Goldman, Jonathon Graff-Radford, Neill R. Graff‐Radford, Murray Grossman, Matthew Hall, Ging‐Yuek Robin Hsiung, Edward D. Huey, David J. Irwin, David T. Jones, Kejal Kantarci, Daniel Kaufer, David S. Knopman, Walter K. Kremers, Argentina Lario Lago, Maria I. Lapid, Irene Litvan, Diane Lucente, Ian R. Mackenzie, Mario F. Mendez, Carly Mester, Bruce L. Miller, Chiadi U. Onyike, Rosa Rademakers, Vijay K. Ramanan, Eliana Marisa Ramos, Meghana Rao, Katya Rascovsky, Katherine P. Rankin, Erik D. Roberson, Rodolfo Savica, Maria Carmela Tartaglia, Sandra Weıntraub, Bonnie Wong, David M. Cash, Arabella Bouzigues, Imogen J. Swift, Georgia Peakman, Martina Bocchetta, Emily Todd, Rhian S. Convery, James B. Rowe, Barbara Borroni, Daniela Galimberti, Pietro Tiraboschi, Mario Masellis, Elizabeth Finger, John C. van Swieten, Harro Seelaar, Lize C. Jiskoot, Sandro Sorbi, Christopher Butler, Caroline Graff, Alexander Gerhard, Tobias Langheinrich, Robert Laforce, Raquel Sánchez‐Valle, Alexandre de Mendonça, Fermín Moreno, Matthis Synofzik, Rik Vandenberghe, Simon Ducharme, Isabelle Le Ber, Johannes Levin, Adrian Danek, Markus Otto, Florence Pasquier, Isabel Santana, John Kornak and 148 more - Nature Medicine 2022 cited by 138

  17. Frontotemporal lobar degeneration

    Authors: Murray Grossman, William W. Seeley, Adam L. Boxer, Argye E. Hillis, David S. Knopman, Peter A. Ljubenov, Bruce L. Miller, Olivier Piguet, Rosa Rademakers, Jennifer L. Whitwell, Henrik Zetterberg, John C. van Swieten - Nature Reviews Disease Primers 2023 cited by 156

  18. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

    Authors: Marc Cruts, Ilse Gijselinck, Julie van der Zee, Sebastiaan Engelborghs, Hans Wils, Daniel Pirici, Rosa Rademakers, Rik Vandenberghe, Bart Dermaut, Jean‐Jacques Martin, Cornelia M. van Duijn, Karin Peeters, Raf Sciot, Patrick Santens, Tim De Pooter, Maria Mattheijssens, Marleen Van den Broeck, Ivy Cuijt, Krist’l Vennekens, Peter Paul De Deyn, Samir Kumar‐Singh, Christine Van Broeckhoven - Nature 2006 cited by 1,542

  19. Validation of serum neurofilaments as prognostic and potential pharmacodynamic biomarkers for ALS

    Authors: Michael Benatar, Lanyu Zhang, Lily Wang, Volkan Granit, Jeffrey Statland, Richard J. Barohn, Andrea Swenson, John Ravits, Carlayne E. Jackson, Ted M. Burns, Jaya Trivedi, Erik P. Pioro, James B. Caress, Jonathan Katz, Jacob L. McCauley, Rosa Rademakers, Andrea Malaspina, Lyle W. Ostrow, Joanne Wuu, Sumaira Hussain, Anne Cooley, Yindi Li, Marielle Wallace, Julie Steele, Jessica Hernandez, Jéssica Medina, Maria Elena Paredes, Ashley Manso, Natalia Ravelo, Wendy Levy, Patrice L. Whitehead, Stephan Züchner, Mamatha Pasnoor, Omar Jawdat, Duaa Jabari, Constantine Farmakidis, Melanie Glenn, Mazen M. Dimachkie, Laura Herbelin, Hellen Tanui, Sherri Anderson, Michaela Walker, Tina Liu, Ayla McCally, Andrew Heim, Melissa Currence, Yolanda Harness, Jeri Sieren, Emilee Gibson, G. Garcia Gutierrez, Danielle Bussey, Rose Previte, Pamella Kittrell, Amruta Joshi, Amy Conger, Debbie Hastings, Irys Caristo, Mozhdeh Marandi, Simon Carty, J. Paul Taylor, Gang Wu, Evadnie Rampersaud, Rebecca Schüle, Marka van Blitterswijk - Neurology 2020 cited by 202

  20. Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases

    Authors: Andrew Chang, Xinyu Xiang, Jing Wang, Carolyn Lee, Tamta Arakhamia, Marija Simjanoska, Chi Wang, Yari Carlomagno, Guoan Zhang, Shikhar Dhingra, Manon Thierry, Jolien Perneel, Bavo Heeman, Lauren M. Forgrave, Michael DeTure, Mari L. DeMarco, Casey Cook, Rosa Rademakers, Dennis W. Dickson, Leonard Petrucelli, Michael H. B. Stowell, Ian R. Mackenzie, Anthony W. P. Fitzpatrick - Cell 2022 cited by 166

  21. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

    Authors: Rosa Rademakers, Matt Baker, Alexandra M. Nicholson, Nicola J. Rutherford, NiCole A. Finch, Alexandra I. Soto‐Ortolaza, Jennifer Lash, Christian Wider, Aleksandra Wojtas, Mariely DeJesus‐Hernandez, Jennifer Adamson, Naomi Kouri, Christina Sundal, Elizabeth A. Shuster, Jan Aasly, J. M. MacKenzie, Sigrun Roeber, Hans A. Kretzschmar, Bradley F. Boeve, David S. Knopman, Ronald C. Petersen, Nigel J. Cairns, Bernardino Ghetti, Salvatore Spina, James Garbern, Alexandros Tselis, Ryan J. Uitti, Pritam Das, Jay A. van Gerpen, James F. Meschia, Shawn Levy, Daniel F. Broderick, Neill R. Graff‐Radford, Owen A. Ross, Bradley B. Miller, Russell H. Swerdlow, Dennis W. Dickson, Zbigniew K. Wszołek - Nature Genetics 2011 cited by 579

  22. Detection of long repeat expansions from PCR-free whole-genome sequence data

    Authors: Egor Dolzhenko, Joke J.F.A. van Vugt, Richard J. Shaw, Mitchell A. Bekritsky, Marka van Blitterswijk, Giuseppe Narzisi, Subramanian S. Ajay, Vani Rajan, Bryan R. Lajoie, Nathan Johnson, Zoya Kingsbury, Sean Humphray, Raymond D. Schellevis, William J. Brands, Matt Baker, Rosa Rademakers, Maarten Kooyman, Gijs H.P. Tazelaar, Michael A. van Es, Russell L. McLaughlin, William Sproviero, Aleksey Shatunov, Ashley Jones, Ahmad Al Khleifat, Alan Pittman, Sarah Morgan, Orla Hardiman, Ammar Al‐Chalabi, Christopher E. Shaw, Bradley Smith, Edmund Jin Rui Neo, Karen Morrison, Pamela J. Shaw, Catherine Reeves, Lara Winterkorn, Nancy S. Wexler, David E. Housman, Christopher Ng, Alina Li, Ryan J. Taft, Leonard H. van den Berg, David Bentley, Jan H. Veldink, Michael A. Eberle - Genome Research 2017 cited by 437

  23. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    Authors: PSP Genetics Study Group, Günter U. Höglinger, Nadine M Melhem, Dennis W. Dickson, Patrick Sleiman, Li-San Wang, Lambertus Klei, Rosa Rademakers, Rohan de Silva, Irene Litvan, David E. Riley, John C. van Swieten, Peter Heutink, Zbigniew K. Wszołek, Ryan J. Uitti, Jana Vandrovcová, Howard I. Hurtig, Owen A. Ross, Walter Maetzler, Stefano Goldwurm, Eduardo Tolosa, Barbara Borroni, Pau Pástor, Laura B. Cantwell, Mi Ryung Han, Allissa Dillman, Marcel P. van der Brug, J. Raphael Gibbs, Mark Cookson, Dena G. Hernandez, Andrew Singleton, Matthew J. Farrer, Chang-En Yu, Lawrence I. Golbe, Tamás Révész, John Hardy, Andrew J. Lees, Bernie Devlin, Håkon Håkonarson, Ulrich Müller, Gerard D Schellenberg - Nature Genetics 2011 cited by 632

  24. Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS

    Authors: Tania F. Gendron, Kevin F. Bieniek, Yong‐Jie Zhang, Karen Jansen‐West, Peter E.A. Ash, Thomas R. Caulfield, Lillian M. Daughrity, Judith Dunmore, Monica Castanedes‐Casey, Jeannie Chew, Danielle M. Cosio, Marka van Blitterswijk, Chris W. Lee, Rosa Rademakers, Khrista Boylan, Dennis W. Dickson, Leonard Petrucelli - Acta Neuropathologica 2013 cited by 589