Marcy E. MacDonald

8.2k total citations · 1 hit paper
53 papers, 4.7k citations indexed

About

Marcy E. MacDonald is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Marcy E. MacDonald has authored 53 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 45 papers in Cellular and Molecular Neuroscience and 10 papers in Neurology. Recurrent topics in Marcy E. MacDonald's work include Genetic Neurodegenerative Diseases (45 papers), Mitochondrial Function and Pathology (26 papers) and Neurological disorders and treatments (10 papers). Marcy E. MacDonald is often cited by papers focused on Genetic Neurodegenerative Diseases (45 papers), Mitochondrial Function and Pathology (26 papers) and Neurological disorders and treatments (10 papers). Marcy E. MacDonald collaborates with scholars based in United States, United Kingdom and Germany. Marcy E. MacDonald's co-authors include James F. Gusella, William A. Paxton, Richard Horuk, Nathaniel R. Landau, Rong Liu, Richard A. Koup, Heidi Stuhlmann, Sunny Choe, Daniel J. Ceradini and Jong‐Min Lee and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Marcy E. MacDonald

52 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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

1996 2.4k citations Rong Liu, William A. Paxton et al. Cell profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marcy E. MacDonald United States	29	2.4k	1.7k	1.5k	1.3k	747	53	4.7k
Pamela J. Skinner United States	27	2.1k 0.9×	991 0.6×	1.6k 1.1×	1.3k 1.0×	332 0.4×	57	3.9k
Naoko Tanese United States	34	4.2k 1.8×	500 0.3×	1.4k 1.0×	405 0.3×	431 0.6×	55	5.3k
John Colicelli United States	37	3.2k 1.4×	618 0.4×	442 0.3×	345 0.3×	401 0.5×	60	4.7k
François Rougeon France	36	4.0k 1.7×	384 0.2×	401 0.3×	1.2k 0.9×	363 0.5×	109	6.4k
Orna Elroy‐Stein Israel	37	3.5k 1.5×	355 0.2×	241 0.2×	556 0.4×	417 0.6×	75	5.2k
Frédérick Libert Belgium	37	2.2k 0.9×	497 0.3×	629 0.4×	969 0.7×	197 0.3×	88	4.7k
Marek Fischer Switzerland	38	3.7k 1.6×	2.6k 1.5×	309 0.2×	927 0.7×	1.9k 2.5×	63	6.7k
Laurel Thomas United States	29	2.4k 1.0×	592 0.3×	362 0.2×	570 0.4×	349 0.5×	41	4.2k
Georgina Miller United States	29	2.1k 0.9×	197 0.1×	507 0.3×	514 0.4×	570 0.8×	43	4.1k
George Kassiotis United Kingdom	38	2.1k 0.9×	221 0.1×	404 0.3×	2.9k 2.2×	329 0.4×	100	6.3k

Countries citing papers authored by Marcy E. MacDonald

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Marcy E. MacDonald

This figure shows the co-authorship network connecting the top 25 collaborators of Marcy E. MacDonald. A scholar is included among the top collaborators of Marcy E. MacDonald based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marcy E. MacDonald. Marcy E. MacDonald is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Handley, Renée R., Suzanne J. Reid, Skye R. Rudiger, et al.. (2021). A Multi-Omic Huntington’s Disease Transgenic Sheep-Model Database for Investigating Disease Pathogenesis. Journal of Huntington s Disease. 10(4). 423–434. 8 indexed citations

Loupe, Jacob M., Ricardo Mouro Pinto, Kyung‐Hee Kim, et al.. (2020). Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out. Human Molecular Genetics. 29(18). 3044–3053. 50 indexed citations

Tebaldi, Toma, Toshimi Yoshida, Serkan Erdin, et al.. (2019). Hypomorphic mutation of the mouse Huntington’s disease gene orthologue. PLoS Genetics. 15(3). e1007765–e1007765. 13 indexed citations

Handley, Renée R., Stefano Patassini, Skye R. Rudiger, et al.. (2011). Characterisation of a transgenic ovine model of Huntington’s disease. Clinical Genetics. 1 indexed citations

Wang, Jin, Sílvia Ginés, Marcy E. MacDonald, & James F. Gusella. (2005). Reversal of a full-length mutant huntingtin neuronal cell phenotype by chemical inhibitors of polyglutamine-mediated aggregation. BMC Neuroscience. 6(1). 1–1. 152 indexed citations

Namura, Shobu, Lorenz Hirt, Vanessa C. Wheeler, et al.. (2002). The HD Mutation Does Not Alter Neuronal Death in the Striatum of HdhQ92 Knock-in Mice after Mild Focal Ischemia. Neurobiology of Disease. 11(1). 147–154. 7 indexed citations

Fenner, Martin, Julia Parrish, Yvonne Boyd, et al.. (1998). MSG1(Melanocyte-Specific Gene 1): Mapping to Chromosome Xq13.1, Genomic Organization, and Promoter Analysis. Genomics. 51(3). 401–407. 23 indexed citations

Ferrante, Robert J., Francesca Persichetti, Sandra McNeil, et al.. (1997). Heterogeneous Topographic and Cellular Distribution of Huntingtin Expression in the Normal Human Neostriatum. Journal of Neuroscience. 17(9). 3052–3063. 117 indexed citations

McNeil, Sandra, Andrea Novelletto, Jayalakshmi Srinidhi, et al.. (1997). Reduced Penetrance of the Huntington's Disease Mutation. Human Molecular Genetics. 6(5). 775–779. 99 indexed citations

10.

Liu, Rong, William A. Paxton, Sunny Choe, et al.. (1996). Homozygous Defect in HIV-1 Coreceptor Accounts for Resistance of Some Multiply-Exposed Individuals to HIV-1 Infection. Cell. 86(3). 367–377. 2375 indexed citations breakdown →

11.

MacDonald, Marcy E., et al.. (1994). Synteny conservation of the Huntington's disease gene and surrounding loci on mouse Chromosome 5. Mammalian Genome. 5(7). 424–428. 11 indexed citations

12.

Gusella, James F. & Marcy E. MacDonald. (1993). Hunting for Huntington's Disease. Elsevier eBooks. 3. 139–158. 16 indexed citations

13.

Youngman, S, Gillian P. Bates, Andrea I. McClatchey, et al.. (1992). The telomeric 60 kb of chromosome arm 4p is homologous to telomeric regions on 13p, 15p, 21p, and 22p. Genomics. 14(2). 350–356. 28 indexed citations

14.

Altherr, Michael R., Sarah J. Plummer, Gillian P. Bates, et al.. (1992). Radiation hybrid map spanning the huntington disease gene region of chromosome 4. Genomics. 13(4). 1040–1046. 11 indexed citations

15.

Gusella, James F., Michael R. Altherr, Andrea I. McClatchey, et al.. (1992). Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate region. Genomics. 13(1). 75–80. 12 indexed citations

16.

Allitto, Bernice A., Andrea I. McClatchey, Glenn Barnes, et al.. (1992). Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4. Molecular and Cellular Probes. 6(6). 513–520. 4 indexed citations

17.

Lin, Carol Sze Ki, Michael R. Altherr, Gillian P. Bates, et al.. (1991). New DNA markers in the Huntington's disease gene candidate region. Somatic Cell and Molecular Genetics. 17(5). 481–488. 23 indexed citations

18.

MacDonald, Marcy E., Hamish S. Scott, William L. Whaley, et al.. (1991). Huntington disease-linked locusD4S111 exposed as the ?-l-iduronidase gene. Somatic Cell and Molecular Genetics. 17(4). 421–425. 27 indexed citations

19.

Whaley, William L., Frank Michiels, Marcy E. MacDonald, et al.. (1988). Mapping ofD4S98/S114/S113confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4. Nucleic Acids Research. 16(24). 11769–11780. 39 indexed citations

20.

MacDonald, Marcy E., Mary Anne Anderson, Sheldon Milstien, et al.. (1987). Physical and genetic localization of quinonoid dihydropteridine reductase gene (QDPR) on short arm of chromosome 4. Somatic Cell and Molecular Genetics. 13(5). 569–574. 10 indexed citations

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.

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