Marcy E. MacDonald
- Cellular and Molecular Neuroscience top 0.01%
- Genetic Neurodegenerative Diseases 132
- Neurology top 0.05%
- Neurological disorders and treatments 42
- Molecular Biology top 0.1%
- Mitochondrial Function and Pathology 85
- Muscle Physiology and Disorders 29
- Fungal and yeast genetics research 17
- DNA Repair Mechanisms 11
- CRISPR and Genetic Engineering 9
- Aging top 0.5%
- Cell Biology top 0.5%
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- Lysosomal Storage Disorders Research 10
- Co-authors
- James F. GusellaRichard H. MyersJean‐Paul VonsattelMabel P. DuyaoPeter W. FaberFrancesca PersichettiElena CattaneoMichael R. Hayden
- Journals
- Human Molecular Genetics (24 papers)Neurobiology of Disease (13 papers)Journal of Huntington s Disease (7 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Marcy E. MacDonald
182 papers receiving 21.8k citations
Hit Papers
Peers
Comparison fields: 5 of 150
- Cellular and Molecular Neuroscience 16.1k
- Neurology 7.1k
- Molecular Biology 16.0k
- Aging 393
- Cell Biology 1.9k
Countries citing papers authored by Marcy E. MacDonald
This map shows the geographic impact of Marcy E. MacDonald's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marcy E. MacDonald with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcy E. MacDonald more than expected).
Fields of papers citing papers by Marcy E. MacDonald
This network shows the impact of papers produced by Marcy E. MacDonald. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marcy E. MacDonald. The network helps show where Marcy E. MacDonald may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Marcy E. MacDonald, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 54 | |
| 2 | 2018 | 13 | |
| 3 | 2018 | 25 | |
| 4 | 2015 | 17 | |
| 5 | 2015 | 16 | |
| 6 | 2012 | 84 | |
| 7 | 2011 | 57 | |
| 8 | 2011 | 49 | |
| 9 | 2009 | 88 | |
| 10 | Psychiatric Symptoms in Huntington's Disease before Diagnosis : The Predict-HD Study. Commentary | 2007 | 3 |
| 11 | 2006 | 90 | |
| 12 | 2006 | 78 | |
| 13 | 2006 | 8 | |
| 14 | The mild neurodegenerative phenotype of CLN3(Delta ex7/8) knock-in mice is accompanied by prominent astrocytosis at the advanced stages of murine JNCL | 2005 | 1 |
| 15 | 2005 | 235 | |
| 16 | 2002 | 167 | |
| 17 | 1999 | 98 | |
| 18 | 1998 | 140 | |
| 19 | 1997 | 398 | |
| 20 | A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesbreakdown → | 1993 | 6516 |
About Marcy E. MacDonald
Marcy E. MacDonald is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Virology and Aging, having authored 183 papers that have together received 22.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (132 papers), Mitochondrial Function and Pathology (85 papers), Neurological disorders and treatments (42 papers), Muscle Physiology and Disorders (29 papers), Fungal and yeast genetics research (17 papers), DNA Repair Mechanisms (11 papers), Lysosomal Storage Disorders Research (10 papers) and CRISPR and Genetic Engineering (9 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (16.1k citations), Neurology (7.1k citations), Molecular Biology (16.0k citations), Aging (393 citations) and Cell Biology (1.9k citations). Marcy E. MacDonald has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include James F. Gusella, Richard H. Myers, Jean‐Paul Vonsattel, Mabel P. Duyao, Peter W. Faber, Francesca Persichetti, Elena Cattaneo, Michael R. Hayden, Chiara Zuccato and John B. Penney. Their work appears in journals such as Human Molecular Genetics, Neurobiology of Disease, Journal of Huntington s Disease, The American Journal of Human Genetics and Journal of Biological Chemistry.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.