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Robert W. Taylor

Active 1899–2025

255
Papers
35,398
Citations
108
h-index
235
i10-index

Citations

Citations per year for Robert W. Taylor1966: 1 citations1967: 1 citations1968: 1 citations1969: 2 citations1971: 2 citations1972: 3 citations1973: 6 citations1974: 15 citations1975: 26 citations1976: 36 citations1977: 24 citations1978: 28 citations1979: 32 citations1980: 12 citations1981: 19 citations1982: 17 citations1983: 14 citations1984: 8 citations1985: 16 citations1986: 14 citations1987: 14 citations1988: 9 citations1989: 12 citations1990: 7 citations1991: 8 citations1992: 7 citations1993: 9 citations1994: 6 citations1995: 6 citations1996: 17 citations1997: 10 citations1998: 7 citations1999: 26 citations2000: 39 citations2001: 36 citations2002: 37 citations2003: 80 citations2004: 91 citations2005: 139 citations2006: 170 citations2007: 210 citations2008: 260 citations2009: 285 citations2010: 307 citations2011: 284 citations2012: 233 citations2013: 311 citations2014: 323 citations2015: 366 citations2016: 397 citations2017: 344 citations2018: 345 citations2019: 1,016 citations2020: 1,266 citations2021: 1,272 citations2022: 1,035 citations2023: 725 citations2024: 1,205 citations2025: 618 citations2026: 15 citations1970: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,178 citing papers, 25.1% of this breakdownUnited Kingdom: 1,294 citing papers, 10.2% of this breakdownChina: 1,014 citing papers, 8% of this breakdownGermany: 805 citing papers, 6.3% of this breakdownItaly: 668 citing papers, 5.3% of this breakdownCanada: 465 citing papers, 3.7% of this breakdownFrance: 459 citing papers, 3.6% of this breakdownAustralia: 407 citing papers, 3.2% of this breakdownSpain: 365 citing papers, 2.9% of this breakdownNetherlands: 342 citing papers, 2.7% of this breakdownJapan: 303 citing papers, 2.4% of this breakdownSweden: 252 citing papers, 2% of this breakdown
0%25.1%Other 24.6%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology59.5%
  • Medicine26.1%
  • Computer Science5.2%
  • Neuroscience3.5%
  • Agricultural and Biological Sciences1.2%
  • Immunology and Microbiology1%
  • Other3.5%

Topics

  • Mitochondrial Function and Pathology16%
  • Metabolism and Genetic Disorders6.6%
  • ATP Synthase and ATPases Research5.6%
  • RNA modifications and cancer2.4%
  • Genetic Neurodegenerative Diseases2%
  • Autophagy in Disease and Therapy1.9%
  • Other65.5%

Coauthors

All papers

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  1. Mitochondrial DNA mutations in human disease

    Authors: Robert W. Taylor, Douglass M. Turnbull - Nature Reviews Genetics 2005 cited by 1,842

  2. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

    Authors: Gráinne S. Gorman, Andrew M. Schaefer, Yi Shiau Ng, Nicholas C. Gomez, Emma L. Blakely, Charlotte L. Alston, Catherine Feeney, Rita Horváth, Patrick Yu‐Wai‐Man, Patrick F. Chinnery, Robert W. Taylor, Douglass M. Turnbull, Robert McFarland - Annals of Neurology 2015 cited by 943

  3. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

    Authors: Andreas Bender, Kim J. Krishnan, Christopher M. Morris, Geoffrey A. Taylor, Amy K. Reeve, Robert H. Perry, Evelyn Jaros, Joshua Hersheson, Joanne Betts, Thomas Klopstock, Robert W. Taylor, Douglass M. Turnbull - Nature Genetics 2006 cited by 1,580

  4. Emerging roles of ATG7 in human health and disease

    Authors: Jack J. Collier, Fumi Suomi, Monika Oláhová, Thomas G. McWilliams, Robert W. Taylor - EMBO Molecular Medicine 2021 cited by 189

  5. Effect of Probiotics on Incident Ventilator-Associated Pneumonia in Critically Ill Patients

    Authors: Jennie Johnstone, Maureen O. Meade, François Lauzier, John C. Marshall, Erick Duan, Joanna C. Dionne, Yaseen M. Arabi, Diane Heels‐Ansdell, Lehana Thabane, Daphnée Lamarche, Michael G. Surette, Nicole Zytaruk, Sangeeta Mehta, Peter Dodek, Lauralyn McIntyre, Shane English, Bram Rochwerg, Tim Karachi, William R. Henderson, Gordon Wood, Daniel Ovakim, Margaret S. Herridge, John Granton, M. Elizabeth Wilcox, Alberto Goffi, Henry T. Stelfox, Daniel J. Niven, John Muscedere, François Lamontagne, Frédérick D’Aragon, Charles St.-Arnaud, Ian Ball, Dave Nagpal, Martin Girard, Pierre Aslanian, Emmanuel Charbonney, David Williamson, Wendy Sligl, Jan O. Friedrich, Neill K. J. Adhikari, François Marquis, Patrick Archambault, Kosar Khwaja, Arnold S. Kristof, James Kutsogiannis, Ryan Zarychanski, Bojan Paunovic, Brenda Reeve, François Lellouche, Paul Hosek, Jennifer Tsang, Alexandra Binnie, Sébastien Trop, Osama Loubani, Richard Hall, Robert Cirone, Steve Reynolds, Paul Lysecki, Eyal Golan, Rodrigo Cartin‐Ceba, Robert W. Taylor, Deborah Cook, Prevention of Severe Pneumonia and Endotracheal Colonization Trial (PROSPECT) Investigators and the Canadian Critical Care Trials Group, Christine Wallace, Gita Sobhi, Jennie Johnstone, François Lauzier, Deborah Cook, Erick Duan, Joanna C. Dionne, Bram Rochwerg, John Centoanti, Simon Oczkowski, Daphne Lamarche, Michael G. Surette, Dawn M. E. Bowdish, Andreas Laupacis, Robin Roberts, Christian Brun‐Buisson, Steve Reynolds, Sue Willems, Tina Sekhon, Peter Dodek, Najib Ayas, Maria Agda, Victoria Alcuaz, Betty-Jean Ashley, Kelsey Brewer, Janice L. Palmer, Glen Brown, Mara Pavan, William R. Henderson, Donald Greisdale, Mypinder S. Sekhon, Denise Foster, Suzie Logie, Judy Yip, Gordon Wood, Daniel Ovakim, F. C. Auld and 562 more - JAMA 2021 cited by 218

  6. Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans

    Authors: Jack J. Collier, Claire Guissart, Monika Oláhová, Souphatta Sasorith, Florence Piron‐Prunier, Fumi Suomi, David Zhang, Nuria Martinez-Lopez, Nicolas Leboucq, Angela Bahr, Silvia Azzarello‐Burri, Selina Reich, Lüdger Schöls, Tuomo Polvikoski, Pierre Meyer, Lise Larrieu, Andrew M. Schaefer, Hessa S. Alsaif, Suad Alyamani, Stephan Züchner, Inês A. Barbosa, Charu Deshpande, Angela Pyle, Anita Rauch, Matthis Synofzik, Fowzan S. Alkuraya, François Rivier, Mina Ryten, Robert McFarland, Agnés Delahodde, Thomas G. McWilliams, Michel Koenig, Robert W. Taylor - New England Journal of Medicine 2021 cited by 194

  7. LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding

    Authors: Chun-Shik Shin, Shuxia Meng, Spiros D. Garbis, Annie Moradian, Robert W. Taylor, Michael J. Sweredoski, Brett Lomenick, David C. Chan - Nature Communications 2021 cited by 131

  8. Mitochondrial signalling and homeostasis: from cell biology to neurological disease

    Authors: Jack J. Collier, Monika Oláhová, Thomas G. McWilliams, Robert W. Taylor - Trends in Neurosciences 2023 cited by 125

  9. Mitochondrial disease in adults: recent advances and future promise

    Authors: Yi Shiau Ng, Laurence A. Bindoff, Gráinne S. Gorman, Thomas Klopstock, Cornelia Kornblum, Michelangelo Mancuso, Robert McFarland, Carolyn M. Sue, Anu Suomalainen, Robert W. Taylor, David R. Thorburn, Douglass M. Turnbull - The Lancet Neurology 2021 cited by 217

  10. Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways

    Authors: Jia Xin Tang, Kyle Thompson, Robert W. Taylor, Monika Oláhová - International Journal of Molecular Sciences 2020 cited by 186

  11. mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease

    Authors: John P. Grady, Sarah J. Pickett, Yi Shiau Ng, Charlotte L. Alston, Emma L. Blakely, Steven Hardy, Catherine Feeney, Alexandra Bright, Andrew M. Schaefer, Gráinne S. Gorman, Richard McNally, Robert W. Taylor, Douglass M. Turnbull, Robert McFarland - EMBO Molecular Medicine 2018 cited by 288

  12. The genetics and pathology of mitochondrial disease

    Authors: Charlotte L. Alston, Mariana C. Rocha, Nichola Z. Lax, Douglass M. Turnbull, Robert W. Taylor - The Journal of Pathology 2016 cited by 446

  13. Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

    Authors: Amy E. Vincent, Kathryn White, Tracey Davey, Jonathan Philips, R. Todd Ogden, Conor Lawless, Charlotte Warren, Matt G. Hall, Yi Shiau Ng, Gavin Falkous, T. M. Holden, David J. Deehan, Robert W. Taylor, Douglass M. Turnbull, Martin Picard - Cell Reports 2019 cited by 202

  14. FBXL4 suppresses mitophagy by restricting the accumulation of NIX and BNIP3 mitophagy receptors

    Authors: Giang Nguyen, Keri‐Lyn Kozul, Yi Cui, Brendan Townsend, Prajakta Gosavi, Soo Siang Ooi, Antonio Marzio, Nissa Carrodus, Steven Zuryn, Michele Pagano, Robert G. Parton, Michael Lazarou, S. Sean Millard, Robert W. Taylor, Brett M. Collins, Mathew V. Jones, Julia K. Pagan - The EMBO Journal 2023 cited by 75

  15. Mosaic dysfunction of mitophagy in mitochondrial muscle disease

    Authors: Takayuki Mito, Amy E. Vincent, Julie Faitg, Robert W. Taylor, Nahid Khan, Thomas G. McWilliams, Anu Suomalainen - Cell Metabolism 2022 cited by 90

  16. Defining mitochondrial protein functions through deep multiomic profiling

    Authors: Jarred W. Rensvold, Evgenia Shishkova, Yuriy Sverchkov, Ian Miller, Arda Çetinkaya, Angela Pyle, Mateusz Manicki, Dain R. Brademan, Yasemin Alanay, Julian Raiman, Adam Jochem, Paul D. Hutchins, Sean R. Peters, Vanessa Linke, Katherine A. Overmyer, Austin Z. Salome, Alexander S. Hebert, Catherine E. Vincent, Nicholas W. Kwiecien, Matthew J. P. Rush, Michael S. Westphall, Mark Craven, Nurten Akarsu, Robert W. Taylor, Joshua J. Coon, David J. Pagliarini - Nature 2022 cited by 118

  17. Mitochondrial DNA mutations and human disease

    Authors: Helen Tuppen, Emma L. Blakely, Douglass M. Turnbull, Robert W. Taylor - Biochimica et Biophysica Acta (BBA) - Bioenergetics 2009 cited by 683

  18. Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis

    Authors: Anna L. Smith, Julia C. Whitehall, Carla Bradshaw, David M. Gay, Fiona Robertson, Alasdair Blain, Gavin Hudson, Angela Pyle, David Houghton, Matthew Hunt, James N. Sampson, Craig Stamp, Grace Mallett, Shoba Amarnath, Jack Leslie, Fiona Oakley, Laura Wilson, Angela Baker, Oliver M. Russell, Riem Johnson, Claire Richardson, Bhavana Gupta, Iain McCallum, Stuart A.C. McDonald, Seamus B. Kelly, John C. Mathers, Rakesh Heer, Robert W. Taylor, Neil D. Perkins, Douglass M. Turnbull, Owen J. Sansom, Laura C. Greaves - Nature Cancer 2020 cited by 135

  19. Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing

    Authors: Laura C. Greaves, Marco Nooteboom, Joanna L. Elson, Helen Tuppen, Geoffrey A. Taylor, Daniel M. Commane, Ramesh Arasaradnam, Konstantin Khrapko, Robert W. Taylor, Thomas B. L. Kirkwood, John C. Mathers, Douglass M. Turnbull - PLoS Genetics 2014 cited by 175

  20. Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies

    Authors: Robert W. Taylor, Angela Pyle, Helen Griffin, Emma L. Blakely, Jennifer Duff, Langping He, Tania Smertenko, Charlotte L. Alston, Vivienne C. M. Neeve, Andrew Best, John W. Yarham, Janbernd Kirschner, Ulrike Schara, Beril Talim, Haluk Topaloğlu, Ivo Barić, Elke Holinski‐Feder, Angela Abicht, Birgit Czermin, Stephanie Kleinle, Andrew A. M. Morris, Grace Vassallo, Gráinne S. Gorman, Venkateswaran Ramesh, Douglass M. Turnbull, Mauro Santibanez‐Koref, Robert McFarland, Rita Horváth, Patrick F. Chinnery - JAMA 2014 cited by 365

  21. Mitochondrial DNA and disease

    Authors: Laura C. Greaves, Amy K. Reeve, Robert W. Taylor, Douglass M. Turnbull - The Journal of Pathology 2011 cited by 309

  22. The Spectrum of Mitochondrial Ultrastructural Defects in Mitochondrial Myopathy

    Authors: Amy E. Vincent, Yi Shiau Ng, Kathryn White, Tracey Davey, Carmen A. Mannella, Gavin Falkous, Catherine Feeney, Andrew M. Schaefer, Robert McFarland, Gráinne S. Gorman, Robert W. Taylor, Douglass M. Turnbull, Martin Picard - Scientific Reports 2016 cited by 240

  23. Mutations causing mitochondrial disease: What is new and what challenges remain?

    Authors: Robert N. Lightowlers, Robert W. Taylor, Douglass M. Turnbull - Science 2015 cited by 345

  24. Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines

    Authors: Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L. Alston, Cathy E. Woodward, Conrad Smith, Charlotte V. Y. Knowles, Yogen Patel, Philip Hodsdon, Jack P. Baines, Emma L. Blakely, James M. Polke, Robert W. Taylor, Carl Fratter - European Journal of Human Genetics 2022 cited by 82