litlas
Log inCreate account

Marcy E. MacDonald

Active 1986–2025

128
Papers
42,416
Citations
95
h-index
126
i10-index

Citations

Citations per year for Marcy E. MacDonald1967: 1 citations1971: 1 citations1976: 1 citations1983: 4 citations1986: 1 citations1987: 8 citations1988: 13 citations1989: 20 citations1990: 12 citations1991: 21 citations1992: 19 citations1993: 79 citations1994: 141 citations1995: 206 citations1996: 152 citations1997: 306 citations1998: 300 citations1999: 329 citations2000: 326 citations2001: 273 citations2002: 293 citations2003: 345 citations2004: 344 citations2005: 394 citations2006: 458 citations2007: 448 citations2008: 439 citations2009: 462 citations2010: 554 citations2011: 542 citations2012: 449 citations2013: 466 citations2014: 452 citations2015: 407 citations2016: 376 citations2017: 346 citations2018: 392 citations2019: 1,059 citations2020: 1,069 citations2021: 1,111 citations2022: 778 citations2023: 472 citations2024: 887 citations2025: 417 citations2026: 15 citations1968–1970: no citations, so these years are not shown1972–1975: no citations, so these years are not shown1977–1982: no citations, so these years are not shown1984–1985: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,896 citing papers, 33.9% of this breakdownUnited Kingdom: 1,363 citing papers, 9.4% of this breakdownGermany: 806 citing papers, 5.6% of this breakdownCanada: 699 citing papers, 4.8% of this breakdownChina: 630 citing papers, 4.4% of this breakdownItaly: 591 citing papers, 4.1% of this breakdownFrance: 558 citing papers, 3.9% of this breakdownAustralia: 431 citing papers, 3% of this breakdownSpain: 359 citing papers, 2.5% of this breakdownJapan: 343 citing papers, 2.4% of this breakdownNetherlands: 337 citing papers, 2.3% of this breakdownSwitzerland: 273 citing papers, 1.9% of this breakdown
0%33.9%Other 21.8%

Institutions

Fields

  • Neuroscience44.4%
  • Biochemistry, Genetics and Molecular Biology28.3%
  • Medicine18%
  • Immunology and Microbiology6.4%
  • Computer Science0.9%
  • Agricultural and Biological Sciences0.5%
  • Other1.5%

Topics

  • Genetic Neurodegenerative Diseases13.2%
  • Mitochondrial Function and Pathology7.9%
  • Neurological disorders and treatments3.9%
  • Alzheimer's disease research and treatments2.8%
  • Parkinson's Disease Mechanisms and Treatments2.3%
  • HIV Research and Treatment2.1%
  • Other67.8%

Coauthors

All papers

Open in search
  1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

    Authors: Marcy E. MacDonald - Cell 1993 cited by 8,458

  2. Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease

    Authors: Bin Zhang, Chris Gaiteri, Liviu‐Gabriel Bodea, Zhi Wang, Joshua McElwee, Alexei A. Podtelezhnikov, Chunsheng Zhang, Tao Xie, Linh M. Tran, Radu Dobrin, Eugene M. Fluder, Bruce E. Clurman, Stacey Melquist, Manikandan Narayanan, Christine Suver, Hardik Shah, Milind Mahajan, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Marcy E. MacDonald, John R. Lamb, David A. Bennett, Cliona Molony, David J. Stone, Vilmundur Guðnason, Amanda Myers, Eric E. Schadt, Harald Neumann, Jun Zhu, Valur Emilsson - Cell 2013 cited by 1,788

  3. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset

    Authors: Jong‐Min Lee, Kevin Correia, Jacob M. Loupe, Kyung‐Hee Kim, Douglas Barker, Eun Pyo Hong, Michael J. Chao, Jeffrey D. Long, Diane Lucente, Jean Paul Vonsattel, Ricardo Mouro Pinto, Kawther Abu Elneel, Eliana Marisa Ramos, Jayalakshmi Srinidhi Mysore, Tammy Gillis, Vanessa C. Wheeler, Marcy E. MacDonald, James F. Gusella, Branduff McAllister, Thomas H. Massey, Christopher Medway, Timothy Stone, Lynsey S. Hall, Lesley Jones, Peter Holmans, Seung Kwak, Anka G Ehrhardt, Cristina Sampaio, Marc Ciosi, Alastair Maxwell, Afroditi Chatzi, Darren G. Monckton, Michael Orth, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Ira Shoulson, Richard H. Myers - Cell 2019 cited by 576

  4. Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease

    Authors: Jong‐Min Lee, Vanessa C. Wheeler, Michael J. Chao, Jean Paul Vonsattel, Ricardo Mouro Pinto, Diane Lucente, Kawther Abu-Elneel, Eliana Marisa Ramos, Jayalakshmi Srinidhi Mysore, Tammy Gillis, Marcy E. MacDonald, James F. Gusella, Denise Harold, Timothy Stone, Valentina Escott‐Price, Jun Han, Alexey Vedernikov, Peter Holmans, Lesley Jones, Seung Kwak, Mithra Mahmoudi, Michael Orth, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Ira Shoulson, Richard H. Myers - Cell 2015 cited by 684

  5. Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease

    Authors: Chiara Zuccato, Andrea Ciammola, Dorotea Rigamonti, Blair R. Leavitt, Donato Goffredo, Luciano Conti, Marcy E. MacDonald, Robert M. Friedlander, Vincenzo Silani, Michael R. Hayden, Tõnis Timmusk, Simonetta Sipione, Elena Cattaneo - Science 2001 cited by 1,329

  6. Huntington’s Disease Pathogenesis: Two Sequential Components

    Authors: Eun Pyo Hong, Marcy E. MacDonald, Vanessa C. Wheeler, Lesley Jones, Peter Holmans, Michael Orth, Darren G. Monckton, Jeffrey D. Long, Seung Kwak, James F. Gusella, Jong‐Min Lee - Journal of Huntington s Disease 2021 cited by 111

  7. Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

    Authors: Ella Dragileva, Audrey E. Hendricks, Allison Teed, Tammy Gillis, Edith Lopez, Errol C. Friedberg, Raju Kucherlapati, Winfried Edelmann, Kathryn L. Lunetta, Marcy E. MacDonald, Vanessa C. Wheeler - Neurobiology of Disease 2008 cited by 253

  8. Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

    Authors: Jong‐Min Lee, Yuan Huang, Michael Orth, Tammy Gillis, Jacqueline Siciliano, Eunpyo Hong, Jayalakshmi Srinidhi Mysore, Diane Lucente, Vanessa C. Wheeler, Ihn Sik Seong, Zachariah L. McLean, James A. Mills, Branduff McAllister, S. V. Lobanov, Thomas H. Massey, Marc Ciosi, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Ira Shoulson, Cristina Sampaio, Darren G. Monckton, Seung Kwak, Peter Holmans, Lesley Jones, Marcy E. MacDonald, Jeffrey D. Long, James F. Gusella - The American Journal of Human Genetics 2022 cited by 116

  9. Huntingtin Controls Neurotrophic Support and Survival of Neurons by Enhancing BDNF Vesicular Transport along Microtubules

    Authors: Laurent Gauthier, Bénédicte C. Charrin, María Borrell-Pagés, Jim Dompierre, Hélène Rangone, Fabrice P. Cordelières, Jan De Mey, Marcy E. MacDonald, Volkmar Leßmann, Sandrine Humbert, Frédéric Saudou - Cell 2004 cited by 1,158

  10. Trinucleotide repeat length instability and age of onset in Huntington's disease

    Authors: Mabel P. Duyao, C M Ambrose, Richard H. Myers, Andrea Novelletto, Francesca Persichetti, Marina Frontali, Susan E. Folstein, Christopher A. Ross, Mary L. Franz, M Abbott, J. Gray, P.M. Conneally, A. B. Young, John B. Penney, Zane Hollingsworth, Ira Shoulson, Alice Lazzarini, Arthur Falek, Walter J. Koroshetz, Daniel S. Sax, Edward J. Bird, Jean Paul Vonsattel, E. Bonilla, José Alvir, Jaime Conde, Jeong‐Heon Cha, Leon Dure, F. Gomez, María Ramos, Juan Sanchez‐Ramos, S. Robert Snodgrass, Margot de Young, Nancy S. Wexler, Chaya Moscowitz, Graciela K. Penchaszadeh, H MacFarlane, Mark J. Anderson, Bruce G. Jenkins, Jayalakshmi Srinidhi, Glenn Barnes, James F. Gusella, Marcy E. MacDonald - Nature Genetics 1993 cited by 1,099

  11. A novel approach to investigate tissue-specific trinucleotide repeat instability

    Authors: Jong-Min Lee, Jie Zhang, Andrew I. Su, John R. Walker, Tim Wiltshire, Kihwa Kang, Ella Dragileva, Tammy Gillis, Edith T. Lopez, Marie-Josee Boily, Michel Cyr, Isaac S. Kohane, James F. Gusella, Marcy E. MacDonald, Vanessa C. Wheeler - BMC Systems Biology, BMC Syst. Biol. 2010 cited by 152

  12. Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9

    Authors: Jun Wan Shin, Kyung‐Hee Kim, Michael J. Chao, Ranjit Singh Atwal, Tammy Gillis, Marcy E. MacDonald, James F. Gusella, Jong‐Min Lee - Human Molecular Genetics 2016 cited by 273

  13. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

    Authors: Branduff McAllister, Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards, Joseph Stone, S. V. Lobanov, Linda Elliston, Laura-Nadine Schuhmacher, Elliott Rees, Georgina Menzies, Marc Ciosi, Alastair Maxwell, Michael J. Chao, Eun Pyo Hong, Diane Lucente, Vanessa C. Wheeler, Jong‐Min Lee, Marcy E. MacDonald, Jeffrey D. Long, Elizabeth Aylward, G. Bernhard Landwehrmeyer, Anne Rosser, REGISTRY Investigators of the European Huntington’s disease network, Jane S. Paulsen, PREDICT-HD Investigators of the Huntington Study Group, Nigel Williams, James F. Gusella, Darren G. Monckton, Nicholas D. Allen, Peter Holmans, Lesley Jones, Thomas H. Massey - Nature Neuroscience 2022 cited by 89

  14. Homozygous Defect in HIV-1 Coreceptor Accounts for Resistance of Some Multiply-Exposed Individuals to HIV-1 Infection

    Authors: Rong Liu, William A. Paxton, Sunny Choe, Daniel J. Ceradini, Scott R. Martin, Richard Horuk, Marcy E. MacDonald, Heidi Stuhlmann, Richard A. Koup, Nathaniel R. Landau - Cell 1996 cited by 3,127

  15. Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out

    Authors: Jacob M. Loupe, Ricardo Mouro Pinto, Kyung‐Hee Kim, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Marissa A Andrew, Marina Kovalenko, Ryan Murtha, Ihnsik Seong, James F. Gusella, Seung Kwak, David Howland, Ramee Lee, Jong‐Min Lee, Vanessa C. Wheeler, Marcy E. MacDonald - Human Molecular Genetics 2020 cited by 90

  16. Detection of Huntington's disease decades before diagnosis: the Predict-HD study

    Authors: Jane S. Paulsen, Douglas R. Langbehn, Julie C. Stout, Elizabeth Aylward, C A Ross, Martha Nance, Mark Guttman, S Johnson, Marcy E. MacDonald, Leigh J. Beglinger, Karen Duff, Elise Kayson, Kevin Biglan, Ira Shoulson, David Oakes, Michael R. Hayden, The Predict-HD Investigators and Coordinators of the Huntington Study Group - Journal of Neurology Neurosurgery & Psychiatry 2007 cited by 812

  17. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion

    Authors: J.-M. Lee, E.M. Ramos, J.-H. Lee, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Michael R. Hayden, Simon C. Warby, PJ Morrison, Martha Nance, Christopher A. Ross, Russell L. Margolis, Ferdinando Squitieri, S. Orobello, Stefano Di Donato, Estrella Gómez‐Tortosa, Carmen Ayuso, Oksana Suchowersky, R J Trent, Elizabeth McCusker, Andrea Novelletto, Marina Frontali, Randi Jones, Tetsuo Ashizawa, Samuel Frank, Marie Saint‐Hilaire, Steven M. Hersch, H. Diana Rosas, Diane Lucente, Madeline Harrison, Andrea Zanko, Ruth K. Abramson, Karen Marder, Jorge Sequeiros, Jane S. Paulsen, G. Bernhard Landwehrmeyer, Richard H. Myers, Marcy E. MacDonald, James F. Gusella, Alexandra Dürr, Adam Rosenblatt, Luigi Frati, Susan B. Perlman, P. M. Conneally, Mary Lou Klimek, Melissa Diggin, Tiffany C. Hadzi, Ayana Duckett, Anwar Ahmed, Paul Allen, David Ames, Christine Anderson, Karla J. Anderson, Karen Anderson, Thomasin Andrews, John Ashburner, Eric Axelson, Elizabeth Aylward, Roger A. Barker, Katrin Barth, Stacey K. Barton, Kathleen Baynes, Alexandra Bea, Erik B. Beall, Mirza Faisal Beg, Leigh J. Beglinger, Kevin Biglan, K. Björk, Steve Blanchard, Jeremy Bockholt, Sudharshan Reddy Bommu, Bradley G. Brossman, Maggie Burrows, Vince D. Calhoun, Noelle E. Carlozzi, Amy M. Chesire, Edmond Chiu, Phyllis Chua, R.J. Connell, Carmela Connor, Jody Corey‐Bloom, David Craufurd, Stephen Cross, Lucette A. Cysique, Rachelle Dar Santos, Jennifer Davis, Joji Decolongon, A. Dipietro, Nicholas Doucette, Nancy R. Downing, Ann Dudler, Steve Dunn, Daniel Ecker, Eric A. Epping, Diane Erickson, Cheryl Erwin, Kenneth Evans, Stewart A. Factor, Sarah Tomaszewski Farias, Marta Fatas, Jess G. Fiedorowicz and 611 more - Neurology 2012 cited by 391

  18. Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects

    Authors: Kyung‐Hee Kim, Eun Pyo Hong, Jun Wan Shin, Michael J. Chao, Jacob M. Loupe, Tammy Gillis, Jayalakshmi Srinidhi Mysore, Peter Holmans, Lesley Jones, Michael Orth, Darren G. Monckton, Jeffrey D. Long, Seung Kwak, Ramee Lee, James F. Gusella, Marcy E. MacDonald, Jong‐Min Lee - The American Journal of Human Genetics 2020 cited by 74

  19. Splice modulators target PMS1 to reduce somatic expansion of the Huntington’s disease-associated CAG repeat

    Authors: Zachariah L. McLean, Dadi Gao, Kevin Correia, Jennie C. L. Roy, Shota Shibata, Iris N. Farnum, Zoe Valdepenas-Mellor, Marina Kovalenko, Manasa Rapuru, Elisabetta Morini, Jayla Ruliera, Tammy Gillis, Diane Lucente, Benjamin P. Kleinstiver, Jong‐Min Lee, Marcy E. MacDonald, Vanessa C. Wheeler, Ricardo Mouro Pinto, James F. Gusella - Nature Communications 2024 cited by 41

  20. Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease

    Authors: Branduff McAllister, James F. Gusella, G. Bernhard Landwehrmeyer, Jong‐Min Lee, Marcy E. MacDonald, Michael Orth, Anne Rosser, Nigel Williams, Peter Holmans, Lesley Jones, Thomas H. Massey, on behalf of the REGISTRY Investigators of the European Huntington's Disease Network - Neurology 2021 cited by 117

  21. Brain urea increase is an early Huntington’s disease pathogenic event observed in a prodromal transgenic sheep model and HD cases

    Authors: Renée R. Handley, Suzanne J. Reid, Rüdiger Bräuning, Paul Maclean, Emily Mears, Imche Fourie, Stefano Patassini, Garth J. S. Cooper, Skye R. Rudiger, Clive J. McLaughlan, Paul J. Verma, James F. Gusella, Marcy E. MacDonald, Henry J. Waldvogel, C. Simon Bawden, Richard L. M. Faull, Russell G. Snell - National Academy of Sciences, Proceedings of the National Academy of Sciences 2017 cited by 108

  22. Huntington’s disease: nearly four decades of human molecular genetics

    Authors: James F. Gusella, Jong‐Min Lee, Marcy E. MacDonald - Human Molecular Genetics 2021 cited by 50

  23. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

    Authors: Russell G. Snell, John MacMillan, Jeremy P. Cheadle, Iain Fenton, L. Lazarou, Peter J. Davies, Marcy E. MacDonald, James F. Gusella, Peter S. Harper, Duncan J. Shaw - Nature Genetics 1993 cited by 719

  24. CAG repeat number governs the development rate of pathology in Huntington's disease

    Authors: John B. Penney, Jean‐Paul Vonsattel, Marcy E. MacDonald, James F. Gusella, Richard H. Myers - Annals of Neurology 1997 cited by 676