Steve D. M. Brown

Active 1990–2025

Also published as
Steve D.M. Brown · Steve D M Brown
97
Papers
18,652
Citations
75
h-index
95
i10-index

Citations

Citations per year for Steve D. M. Brown1991: 2 citations1992: 3 citations1993: 2 citations1994: 4 citations1995: 11 citations1996: 19 citations1997: 47 citations1998: 71 citations1999: 93 citations2000: 87 citations2001: 138 citations2002: 133 citations2003: 129 citations2004: 151 citations2005: 141 citations2006: 133 citations2007: 147 citations2008: 157 citations2009: 164 citations2010: 175 citations2011: 164 citations2012: 172 citations2013: 183 citations2014: 145 citations2015: 178 citations2016: 164 citations2017: 216 citations2018: 177 citations2019: 573 citations2020: 596 citations2021: 585 citations2022: 377 citations2023: 243 citations2024: 392 citations2025: 152 citations2026: 5 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,399 citing papers, 26.9% of this breakdownUnited Kingdom: 1,054 citing papers, 11.8% of this breakdownGermany: 630 citing papers, 7% of this breakdownFrance: 459 citing papers, 5.1% of this breakdownChina: 454 citing papers, 5.1% of this breakdownCanada: 363 citing papers, 4.1% of this breakdownJapan: 281 citing papers, 3.1% of this breakdownItaly: 276 citing papers, 3.1% of this breakdownNetherlands: 258 citing papers, 2.9% of this breakdownAustralia: 256 citing papers, 2.9% of this breakdownSpain: 181 citing papers, 2% of this breakdownSwitzerland: 166 citing papers, 1.9% of this breakdown
0%26.9%Other 24.1%

Fields

  • Biochemistry, Genetics and Molecular Biology45.3%
  • Medicine27.4%
  • Neuroscience18.5%
  • Immunology and Microbiology1.6%
  • Psychology1.4%
  • Agricultural and Biological Sciences1.4%
  • Other4.4%

Topics

  • Hearing, Cochlea, Tinnitus, Genetics4.5%
  • Autophagy in Disease and Therapy3.4%
  • Parkinson's Disease Mechanisms and Treatments2.4%
  • CRISPR and Genetic Engineering2%
  • Genetics and Neurodevelopmental Disorders1.4%
  • Cellular transport and secretion1.3%
  • Other85%

Coauthors

All papers

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  1. High-throughput discovery of novel developmental phenotypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sara Johnson, Sowmya Kalaga, Lance C. Keith, Louise Lanoue, Thomas N. Lawson, Monkol Lek, Manuel Mark, Susan Marschall, Jeremy Mason, Melissa L. McElwee, Susan Newbigging, Lauryl M. J. Nutter, Kevin A. Peterson, Ramiro Ramírez‐Solis, Douglas J. Rowland, Edward J. Ryder, Kaitlin E. Samocha, John R. Seavitt, Mohammed Selloum, Zsombor Szoke-Kovacs, Masaru Tamura, Amanda Trainor, Ilinca Tudose, Shigeharu Wakana, Jonathan Warren, Olivia Wendling, David B. West, Leeyean Wong, Atsushi Yoshiki, Wolfgang Wurst, Daniel G. MacArthur, Glauco P. Tocchini‐Valentini, Xiang Gao, Paul Flicek, Allan Bradley, William C. Skarnes, Monica J. Justice, Helen Parkinson, Mark W. Moore, Sara Wells, Robert E. Braun, Karen L. Svenson, Martin Hrabě de Angelis, Yann Hérault, Tim Mohun, Ann‐Marie Mallon, R. Mark Henkelman, Steve D. M. Brown, David J. Adams, K. C. Kent Lloyd, Colin McKerlie, Arthur L. Beaudet, Maja Bućan, Stephen A. Murray - Nature 2016 cited by 1,307

  2. α-Synuclein impairs macroautophagy: implications for Parkinson’s disease

    Authors: , , , , , , , , , , , , - The Journal of Cell Biology 2010 cited by 827

  3. A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marie‐France Champy, Roy Combe, Petr Danecek, Armida Di Fenza, Hilary Gates, Anna-Karin Gerdin, Elisabetta Golini, John M. Hancock, Wolfgang Hans, Sabine M. Hölter, Tertius Hough, Pierre Jurdic, Thomas Keane, Hugh W. Morgan, Werner Müller, Frauke Neff, George Nicholson, Bastian Pasche, Laura-Anne Roberson, Jan Rozman, Mark Sanderson, Luís Santos, Mohammed Selloum, Carl Shannon, Anne Southwell, Glauco P. Tocchini‐Valentini, Valerie E. Vancollie, Henrik Westerberg, Wolfgang Wurst, Min Zi, Binnaz Yalcin, Ramiro Ramírez‐Solis, Karen P. Steel, Ann‐Marie Mallon, Martin Hrabě de Angelis, Yann Hérault, Steve D. M. Brown - Genome biology 2013 cited by 524

  4. Human and mouse essentiality screens as a resource for disease gene discovery

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Radislav Sedláček, David J. Adams, John R. Seavitt, Glauco P. Tocchini‐Valentini, Fabio Mammano, Robert E. Braun, Colin McKerlie, Yann Hérault, Martin Hrabě de Angelis, Ann‐Marie Mallon, K. C. Kent Lloyd, Steve D. M. Brown, Helen Parkinson, Terrence F. Meehan, Damian Smedley, J. C. Ambrose, Paramasivam Arumugam, E. L. Baple, Marta Bleda, F. Boardman-Pretty, J. M. Boissiere, C. R. Boustred, H. Brittain, Mark J. Caulfield, Gcf Chan, C. E. H. Craig, Louise C. Daugherty, A. de Burca, A. Devereau, Greg Elgar, Rebecca E. Foulger, Tom Fowler, P. Furió-Tarí, J.M. Hackett, Dina Halai, Angela Hamblin, Seton Henderson, J. E. Holman, Tim Hubbard, Kristina Ibáñez, Richard V. Jackson, Lesley Jones, Dalia Kasperavičiūtė, M. Kayikci, L. Lahnstein, Kim Lawson, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Joanne Mason, Ellen M. McDonagh, L. Moutsianas, Michael Mueller, Nirupa Murugaesu, A. C. Need, Christopher A. Odhams, C. Patch, D. Perez-Gil, Dimitris Polychronopoulos, J. Pullinger, T. Rahim, Álvaro Rendón, Pablo Riesgo-Ferreiro, Tim Rogers, Mina Ryten, K Savage, K. Sawant, Richard H. Scott, A. Siddiq and 96 more - Nature Communications 2020 cited by 127

  5. CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells

    Authors: , , , , , , , , , , , , - Nature Communications 2017 cited by 194

  6. Prevalence of sexual dimorphism in mammalian phenotypic traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Luís Santos, John R. Seavitt, Damian Smedley, Tania Sorg, Anneliese O. Speak, Karen P. Steel, Karen L. Svenson, Yuichi Obata, Tomohiro Suzuki, Masaru Tamura, Hideki Kaneda, Tamio Furuse, Kimio Kobayashi, Ikuo Miura, Ikuko Yamada, Nobuhiko Tanaka, Atsushi Yoshiki, Shinya Ayabe, David Clary, Heather Tolentino, Michael Schuchbauer, Todd Tolentino, J Aprile, Sheryl Pedroia, Lois Kelsey, Igor Vukobradovic, Zorana Berberovic, Celeste Owen, Dawei Qu, Ruolin Guo, Susan Newbigging, Lily Morikawa, Napoleon Law, Xueyuan Shang, Patricia Feugas, Yanchun Wang, Mohammad Eskandarian, Yingchun Zhu, Lauryl M. J. Nutter, Patricia Penton, Valerie Laurin, Shannon Clarke, Qing Lan, Khondoker Sohel, D. Craig Miller, Greg Clark, Jane Hunter, Jorge Cabezas, Mohammed Bubshait, Tracy Carroll, Sandra Tondat, S. MacMaster, Monica Pereira, Marina Gertsenstein, Ozge Danisment, Elsa Jacob, Amie Creighton, Gillian Sleep, James D. Clark, Lydia Teboul, Martin Fray, Adam Caulder, Jorik Loeffler, Gemma Codner, James Cleak, Sara Johnson, Zsombor Szoke-Kovacs, Adam Radage, Marina Maritati, Joffrey Mianné and 102 more - Nature Communications 2017 cited by 272

  7. Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lynette R Bower, Mark W. Moore, Iva Morse, Xiang Gao, Glauco P. Tocchini‐Valentini, Yuichi Obata, Soo Young Cho, Je Kyung Seong, John Seavitt, Arthur L. Beaudet, Mary E. Dickinson, Yann Hérault, Wolfgang Wurst, Martin Hrabě de Angelis, K. C. Kent Lloyd, Ann M. Flenniken, Lauryl M. J. Nutter, Susan Newbigging, Colin McKerlie, Monica J. Justice, Stephen A. Murray, Karen L. Svenson, Robert E. Braun, Jacqueline K. White, Allan Bradley, Paul Flicek, Sara Wells, William C. Skarnes, David J. Adams, Helen Parkinson, Ann‐Marie Mallon, Steve D M Brown, Damian Smedley - Nature Genetics 2017 cited by 268

  8. A resource of targeted mutant mouse lines for 5,061 genes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ruairidh King, Ralf Kühn, Ho Lee, Young Jae Lee, Zhiwei Liu, K. C. Kent Lloyd, Isabel Lorenzo, Ann‐Marie Mallon, Colin McKerlie, Terrence F. Meehan, Violeta Muñoz‐Fuentes, Stuart Newman, Lauryl M. J. Nutter, Goo Taeg Oh, Guillaume Pavlovic, Ramiro Ramírez‐Solis, Barry P. Rosen, Edward J. Ryder, Luís Santos, Joel Schick, John R. Seavitt, Radislav Sedláček, Claudia Seisenberger, Je Kyung Seong, William C. Skarnes, Tania Sorg, Karen P. Steel, Masaru Tamura, Glauco P. Tocchini‐Valentini, Chi‐Kuang Leo Wang, Hannah Wardle‐Jones, Marie Wattenhofer‐Donzé, Sara Wells, Michael V. Wiles, Brandon Willis, Joshua A. Wood, Wolfgang Wurst, Ying Xu, Juan Gallegos, Jennie R. Green, Ritu Bohat, Katie Zimmel, Monica Pereira, S. MacMaster, Sandra Tondat, Linda Wei, Tracy Carroll, Jorge Cabezas, Qing Fan-Lan, Elsa Jacob, Amie Creighton, Patricia Castellanos-Penton, Ozge Danisment, Shannon Clarke, Joanna Joeng, Deborah F. Kelly, Christine To, Rebekah van Bruggen, Valerie Gailus-Durner, Helmut Fuchs, Susan Marschall, Stefanie Dunst, Markus Romberger, Bernhard Rey, Sabine Fessele, Philipp Gormanns, Roland H. Friedel, Cornelia Kaloff, Andreas Hörlein, Sandy Teichmann and 125 more - Nature Genetics 2021 cited by 114

  9. The mammalian gene function resource: the international knockout mouse consortium

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pieter J. de Jong, James A. Kadin, Cornelia Kaloff, Karen L. Kennedy, Manousos Koutsourakis, K. C. Kent Lloyd, Susan Marschall, Jeremy Mason, Colin McKerlie, Michael P. McLeod, Harald von Melchner, Mark W. Moore, Alejandro O. Mujica, András Nagy, Mikhail Nefedov, Lauryl M. J. Nutter, Guillaume Pavlovic, Jane L. Peterson, Jonathan D. Pollock, Ramiro Ramírez‐Solis, Derrick E. Rancourt, Marcello Raspa, Jacques Remacle, Martin Ringwald, Barry P. Rosen, Nadia Rosenthal, Janet Rossant, Patricia Ruíz, Edward J. Ryder, Joel Schick, Frank Schnütgen, Paul N. Schofield, Claudia Seisenberger, Mohammed Selloum, Elizabeth M. Simpson, William C. Skarnes, Damian Smedley, William L. Stanford, A. Francis Stewart, Kevin Stone, Kate Swan, Hamsa D. Tadepally, Lydia Teboul, Glauco P. Tocchini‐Valentini, David M. Valenzuela, Anthony P. West, Ken‐ichi Yamamura, Yuko Yoshinaga, Wolfgang Wurst - Mammalian Genome 2012 cited by 328

  10. Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair

    Authors: , , , , , , , , , , , , - Genome Medicine 2016 cited by 144

  11. Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

    Authors: , , , , , , , , , , , , , , - Current Biology 2003 cited by 622

  12. The International Mouse Phenotyping Consortium (IMPC): a functional catalogue of the mammalian genome that informs conservation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Conservation Genetics 2018 cited by 133

  13. Helios is a key transcriptional regulator of outer hair cell maturation

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature 2018 cited by 126

  14. Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

    Authors: , , , , , - Mammalian Genome 1997 cited by 803

  15. Dynein mutations impair autophagic clearance of aggregate-prone proteins

    Authors: , , , , , , , - Nature Genetics 2005 cited by 451

  16. The mouse ascending: perspectives for human-disease models

    Authors: , - Nature Cell Biology 2007 cited by 444

  17. IGF-1 receptor antagonism inhibits autophagy

    Authors: , , , , , , , , , , , , , - Human Molecular Genetics 2013 cited by 91

  18. Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Physiological Genomics 2008 cited by 284

  19. Hyaluronic Acid Production in Bacillus subtilis

    Authors: , , , , , , , , , - Applied and Environmental Microbiology 2005 cited by 281

  20. Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David A. Blizard, Connie R. Bezzina, David J. Adams, Paul Franken, Tom Weaver, Sara Wells, Steve D. M. Brown, Paul Potter, Paul Klenerman, Arimantas Lionikas, Richard Mott, Jonathan Flint - Nature Genetics 2016 cited by 160

  21. Defective myosin VIIA gene responsible for Usher syndrome type IB

    Authors: , , , , , , , , , , , , , , , , , , - Nature 1995 cited by 1,074

  22. Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochlea

    Authors: , , , , , , , - The Journal of Physiology 2020 cited by 47

  23. The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William C. Skarnes, Ann-Marie Mallon, Helen E. Parkinson - Nucleic Acids Research, Nucleic Acids Res. 2013 cited by 290

  24. Genome-Wide Association Study Using Extreme Truncate Selection Identifies Novel Genes Affecting Bone Mineral Density and Fracture Risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Albert Hofman, Mark A. Kotowicz, Joanna Makovey, Sing C. Nguyen, Tuan V. Nguyen, Julie A. Pasco, Karena Pryce, David M. Reid, Fernando Rivadeneira, Christian Roux, Kāri Stefánsson, Unnur Styrkársdóttir, Guðmar Þorleifsson, Rumbidzai Tichawangana, David M. Evans, Matthew A. Brown - PLoS Genetics 2011 cited by 281