Robert H. Brown

Active 1951–2025

Also published as
ROBERT H. BROWN
267
Papers
63,500
Citations
132
h-index
255
i10-index

Citations

Citations per year for Robert H. Brown1967: 2 citations1968: 5 citations1969: 5 citations1970: 2 citations1971: 3 citations1972: 4 citations1973: 2 citations1974: 3 citations1975: 4 citations1976: 2 citations1977: 3 citations1978: 3 citations1979: 1 citations1980: 5 citations1981: 5 citations1982: 1 citations1983: 3 citations1984: 3 citations1985: 1 citations1986: 1 citations1987: 7 citations1988: 43 citations1989: 51 citations1990: 49 citations1991: 72 citations1992: 77 citations1993: 108 citations1994: 93 citations1995: 126 citations1996: 146 citations1997: 157 citations1998: 158 citations1999: 241 citations2000: 258 citations2001: 280 citations2002: 326 citations2003: 348 citations2004: 352 citations2005: 389 citations2006: 532 citations2007: 415 citations2008: 481 citations2009: 553 citations2010: 610 citations2011: 652 citations2012: 661 citations2013: 719 citations2014: 565 citations2015: 630 citations2016: 676 citations2017: 718 citations2018: 640 citations2019: 1,874 citations2020: 2,224 citations2021: 2,158 citations2022: 1,631 citations2023: 1,200 citations2024: 1,711 citations2025: 805 citations2026: 24 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 7,011 citing papers, 30.9% of this breakdownUnited Kingdom: 1,902 citing papers, 8.4% of this breakdownChina: 1,373 citing papers, 6% of this breakdownItaly: 1,263 citing papers, 5.6% of this breakdownGermany: 1,151 citing papers, 5.1% of this breakdownCanada: 1,054 citing papers, 4.6% of this breakdownFrance: 858 citing papers, 3.8% of this breakdownJapan: 851 citing papers, 3.7% of this breakdownAustralia: 763 citing papers, 3.4% of this breakdownNetherlands: 586 citing papers, 2.6% of this breakdownSpain: 490 citing papers, 2.1% of this breakdownSwitzerland: 408 citing papers, 1.8% of this breakdown
0%30.9%Other 22%

Fields

  • Medicine50.8%
  • Biochemistry, Genetics and Molecular Biology35.8%
  • Neuroscience8%
  • Immunology and Microbiology1.1%
  • Energy0.9%
  • Engineering0.8%
  • Other2.6%

Topics

  • Amyotrophic Lateral Sclerosis Research11%
  • Neurogenetic and Muscular Disorders Research6.2%
  • Muscle Physiology and Disorders3.6%
  • Parkinson's Disease Mechanisms and Treatments2.8%
  • Alzheimer's disease research and treatments2.7%
  • Genetic Neurodegenerative Diseases2.6%
  • Other71.1%

Coauthors

All papers

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  1. Decoding ALS: from genes to mechanism

    Authors: , , - Nature 2016 cited by 2,131

  2. Amyotrophic Lateral Sclerosis

    Authors: , - New England Journal of Medicine 2017 cited by 2,121

  3. Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2009 cited by 2,573

  4. Efficacy and safety of minimally invasive surgery with thrombolysis in intracerebral haemorrhage evacuation (MISTIE III): a randomised, controlled, open-label, blinded endpoint phase 3 trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael R. Chicoine, Hiren C. Patel, Robert Dodd, Paul J. Camarata, Stacey Q Wolfe, Agnieszka Stadnik, Patricia Lynn Money, Patrick Mitchell, Rosario Sarabia, Sagi Harnof, Pál Barzó, Andreas Unterberg, Jeanne Teitelbaum, Weimin Wang, Craig S Anderson, A. D. Mendelow, Barbara Gregson, Scott Janis, Paul Vespa, Wendy Ziai, Mario Zuccarello, Issam A. Awad, Azmil H. Abdul‐Rahim, Amal Abou‐Hamden, Michael Abraham, Azam Ahmed, Carlos Alarcon Alba, E. François Aldrich, David Altschul, Sepideh Amin‐Hanjani, Doug Anderson, Safdar Ansari, David Antezana, Agnieszka Ardelt, Fuat Arikán, M. Báguena, Alexandra Baker, Steven J. Barrer, Kyra J. Becker, Thomas Bergman, Azize Boström, Jamie Braun, Peter G. Brindley, William C. Broaddus, Robert H. Brown, András Büki, Bing Cao, Ying Cao, Julián Carrión‐Penagos, Julio A. Chalela, Tiffany Chang, Indalecio Moran Chorro, Shakeel Chowdhry, Luisa Corral, László Csiba, Jason M. Davies, Alberto Torres Díaz, Colin P. Derdeyn, Michael N. Diringer, Rachel Dlugash, Robert D. Ecker, Tracey Economas, Pedro Enríquez, Erzsébet Ezer, Yuhua Fan, Hua Feng, Douglas Franz, William D. Freeman, Matthew R. Fusco, Walter Galicich and 129 more - The Lancet 2019 cited by 899

  5. Dystrophin: The protein product of the duchenne muscular dystrophy locus

    Authors: , , - Cell 1987 cited by 4,711

  6. SOD1 Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS

    Authors: , , , , , , , , , , , , , , , - New England Journal of Medicine 2020 cited by 252

  7. Suppression of mutant C9orf72 expression by a potent mixed backbone antisense oligonucleotide

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2021 cited by 174

  8. Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jack W. Miller, Soragia Athina Gkazi, Ammar Al‐Chalabi, Leonard H. van den Berg, Jan H. Veldink, Vincenzo Silani, Nicola Ticozzi, Christopher E. Shaw, Robert H. Baloh, Stanley H. Appel, Ericka Simpson, Clotilde Lagier‐Tourenne, Stefan M. Pulst, Summer Gibson, John Q. Trojanowski, Lauren Elman, Leo McCluskey, Murray Grossman, Neil A. Shneider, Wendy K. Chung, John Ravits, Jonathan D. Glass, Katherine B. Sims, Vivianna M. Van Deerlin, Tom Maniatis, Sebastian Hayes, Alban Ordureau, Sharan Swarup, John E. Landers, Frank Baas, Andrew S. Allen, Richard Bedlack, J. Wade Harper, Aaron D. Gitler, Guy A. Rouleau, Robert H. Brown, Matthew B. Harms, Gregory M. Cooper, Tim Harris, R Myers, David B. Goldstein - Science 2015 cited by 992

  9. dSarm/Sarm1 Is Required for Activation of an Injury-Induced Axon Death Pathway

    Authors: , , , , , , , , , , , , , , , , , , , , , - Science 2012 cited by 724

  10. Deferoxamine mesylate in patients with intracerebral haemorrhage (i-DEF): a multicentre, randomised, placebo-controlled, double-blind phase 2 trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Chad Tremont, Chitra Venkatasubramanian, Rosita Thiessen, Supriya Save, Steven Verrault, Karin Collard, Michael DeGeorgia, Valerie Cwiklinski, Bradford Thompson, Lesley Wasilewski, Charles Andrews, Robert Burfeind, Michel Torbey, Mohammad Hamed, Kenneth Butcher, Leka Sivakumar, Nicolaou Varelas, Kathleen Mays-Wilson, Enrique C. Leira, Heena Olalde, Scott Silliman, Rhonda Calhoun, Neha Dangayach, Ricardo Renvill, Rishi Malhotra, Kristina Kordesch, Aaron Lord, Thomas Calahan, Romergryko G. Geocadin, Michelle Burke Parish, James L. Frey, Mary Harrigan, Dana Leifer, Ryna Mathias, Michael Schneck, Tara Bernier, Sergio Gonzales-Arias, Josette Elysée, George Α. Lopez, Josephine Volgi, Robert H. Brown, Sara Jasak, Stephen Phillips, J Jarrett, João Gomes, Moneen McBride, François Aldrich, Charlene Aldrich, Joshua Kornbluth, Michelle Bettle, Joshua N. Goldstein, Gregory Philip Tirrell, Qaisar Shaw, Karin Jonczak - The Lancet Neurology 2019 cited by 249

  11. Genetics of Amyotrophic Lateral Sclerosis

    Authors: , - Cold Spring Harbor Perspectives in Medicine 2017 cited by 262

  12. AAV gene therapy for Tay-Sachs disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Medicine 2022 cited by 137

  13. Lipid production in Nannochloropsis gaditana is doubled by decreasing expression of a single transcriptional regulator

    Authors: , , , , , , , , , , , , , , , , , , - Nature Biotechnology 2017 cited by 479

  14. TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2018 cited by 298

  15. Intrinsic Membrane Hyperexcitability of Amyotrophic Lateral Sclerosis Patient-Derived Motor Neurons

    Authors: , , , , , , , , , , , , , , , - Cell Reports 2014 cited by 686

  16. NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Frank Baas, Anneke J. van der Kooi, Marianne de Visser, Anneloor L.M.A. ten Asbroek, Peter C. Sapp, Diane McKenna‐Yasek, Meraida Polak, Seneshaw Asress, José Luís Muñoz-Blanco, Tim M. Strom, Thomas Meitinger, Karen Morrison, Giuseppe Lauria, Kelly L. Williams, P. Nigel Leigh, Garth A. Nicholson, Ian P. Blair, Claire S. Leblond, Patrick A. Dion, Guy A. Rouleau, Hardev Pall, Pamela J. Shaw, Martin R. Turner, Kevin Talbot, Franco Taroni, Khrista Boylan, Marka van Blitterswijk, Rosa Rademakers, Jesús Esteban‐Pérez, Alberto García‐Redondo, Phillip Van Damme, Wim Robberecht, Adriano Chiò, Cinzia Gellera, Carsten Drepper, Michael Sendtner, Antonia Ratti, Jonathan D. Glass, Jesús S. Mora, Nazlı Başak, Orla Hardiman, Albert C. Ludolph, Peter M. Andersen, Jochen H. Weishaupt, Robert H. Brown, Ammar Al‐Chalabi, Vincenzo Silani, Christopher E. Shaw, Leonard H. van den Berg, Jan H. Veldink, John E. Landers - Nature Genetics 2016 cited by 294

  17. Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Florian P. Thomas, Katherine R. Chao, Chamindra G. Konersman, Megan T. Cho, Tracy Brandt, Volker Straub, Anne M. Connolly, Ulrike Schara, Andreas Roos, Mark A. Tarnopolsky, Ahmet Höke, Robert H. Brown, Chia‐Hsueh Lee, Thorsten Hornemann, Teresa Dunn, Carsten G. Bönnemann - Nature Medicine 2021 cited by 152

  18. A randomized placebo‐controlled phase 3 study of mesenchymal stem cells induced to secrete high levels of neurotrophic factors in amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , - Muscle & Nerve 2021 cited by 114

  19. CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2022 cited by 70

  20. Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules

    Authors: , , , , , , , , , - Human Molecular Genetics 2010 cited by 517

  21. Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alberto García‐Redondo, Jesús Esteban‐Pérez, Cinzia Tiloca, Federico Verde, Stefano Duga, Nigel Leigh, Hardev Pall, Karen Morrison, Ammar Al‐Chalabi, Pamela J. Shaw, Janine Kirby, Martin R. Turner, Kevin Talbot, Orla Hardiman, Jonathan D. Glass, Jacqueline de Belleroche, Masatoshi Maki, Stephen E. Moss, Christopher C.J. Miller, Cinzia Gellera, Antonia Ratti, Safa Al‐Sarraj, Robert H. Brown, Vincenzo Silani, John E. Landers, Christopher E. Shaw - Science Translational Medicine 2017 cited by 247

  22. Molecular biology of amyotrophic lateral sclerosis: insights from genetics

    Authors: , - Nature reviews. Neuroscience 2006 cited by 1,101

  23. Immediate and long-term consequences of COVID-19 infections for the development of neurological disease

    Authors: , , , , - Alzheimer s Research & Therapy 2020 cited by 578

  24. Excessive release of inorganic polyphosphate by ALS/FTD astrocytes causes non-cell-autonomous toxicity to motoneurons

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Katharine Nicholson, Miguel Sena‐Esteves, Rodolfo Madrid, Diego Varela, Martı́n Montecino, Robert H. Brown, Brigitte van Zundert - Neuron 2022 cited by 87