Marcy E. MacDonald
Impact in
- Virology top 0.2%
- HIV Research and Treatment
-
- Genetic Neurodegenerative Diseases
Papers in
-
- Genetic Neurodegenerative Diseases 45
-
- Mitochondrial Function and Pathology 22
- CRISPR and Genetic Engineering 9
- DNA Repair Mechanisms 8
- Fungal and yeast genetics research 6
- Ubiquitin and proteasome pathways 5
- Muscle Physiology and Disorders 4
- Co-authors
- James F. Gusella (44 shared papers)Richard Horuk (1 shared paper)Richard A. Koup (1 shared paper)Daniel J. Ceradini (1 shared paper)Sunny Choe (1 shared paper)Heidi Stuhlmann (1 shared paper)Nathaniel R. Landau (1 shared paper)William A. Paxton (1 shared paper)
- Journals
- Genomics (8 papers)Nature Genetics (4 papers)Human Molecular Genetics (3 papers)Cell (2 papers)Nucleic Acids Research (2 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Marcy E. MacDonald
52 papers receiving 4.7k citations
Marcy E. MacDonald's Hit Papers
Peers
Comparison fields: 5 of 120
- Virology 1.6k
- Cellular and Molecular Neuroscience 1.5k
- Immunology 1.2k
- Infectious Diseases 651
- Neurology 493
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-authors
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
Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Homozygous Defect in HIV-1 Coreceptor Accounts for Resistance of Some Multiply-Exposed Individuals to HIV-1 Infection Hit paper breakdown → | 1996 | 2379 |
| 2 | 2016 | 208 | |
| 3 | 2005 | 151 | |
| 4 | 1992 | 118 | |
| 5 | 1997 | 117 | |
| 6 | 2014 | 105 | |
| 7 | 2006 | 104 | |
| 8 | 1987 | 100 | |
| 9 | 1997 | 99 | |
| 10 | 1987 | 86 | |
| 11 | 1995 | 82 | |
| 12 | 1989 | 79 | |
| 13 | 1993 | 74 | |
| 14 | 1995 | 70 | |
| 15 | Complex patterns of linkage disequilibrium in the Huntington disease region. | 1991 | 63 |
| 16 | Defined physical limits of the Huntington disease gene candidate region. | 1991 | 59 |
| 17 | A yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease gene. | 1990 | 56 |
| 18 | 1987 | 54 | |
| 19 | 2020 | 52 | |
| 20 | 1992 | 50 |
About Marcy E. MacDonald
Marcy E. MacDonald is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Genetics and Infectious Diseases, having authored 53 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (45 papers), Mitochondrial Function and Pathology (22 papers), Neurological disorders and treatments (9 papers), CRISPR and Genetic Engineering (9 papers), DNA Repair Mechanisms (8 papers), Fungal and yeast genetics research (6 papers), Ubiquitin and proteasome pathways (5 papers) and Muscle Physiology and Disorders (4 papers). The work is most often cited by research in Virology (1.6k citations), Cellular and Molecular Neuroscience (1.5k citations), Immunology (1.2k citations), Infectious Diseases (651 citations) and Neurology (493 citations). Marcy E. MacDonald has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include James F. Gusella, Richard Horuk, Richard A. Koup, Daniel J. Ceradini, Sunny Choe, Heidi Stuhlmann, Nathaniel R. Landau, William A. Paxton, Rong Liu and Jong‐Min Lee. Their work appears in journals such as Genomics, Nature Genetics, Human Molecular Genetics, Cell and Nucleic Acids Research.
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.