Marlene J. Huggins

1.6k citations
20 papers · 1.1k indexed · h-index 15
Topics
Genetic Neurodegenerative Diseases (9 papers)Biomedical Ethics and Regulation (2 papers)DNA Repair Mechanisms (2 papers)
Partner nations
CanadaUnited StatesItaly

In The Last Decade

Marlene J. Huggins

20 papers receiving 1.0k citations

Peers

Marlene J. Huggins
Comparison fields: 5 of 87
  • Genetics 553
  • Cellular and Molecular Neuroscience 422
  • Molecular Biology 313
  • Neurology 164
  • Pediatrics, Perinatology and Child Health 147
Replace Sandi Wiggins with:
Sandi Wiggins Canada
Maurice Bloch Canada
Claire O. Leonard United States
Petra G. Frets Netherlands
Andrea Boogaerts Belgium
Ann‐Marie Codori United States
Sheila A Simpson United Kingdom
L Kerzin-Storrar United Kingdom
Christie Barker‐Cummings United States
Julie S. Cohen United States
Marlene J. Huggins relative to Sandi Wiggins Canada Sandi Wiggins's profile →
Citations per field
00.5×2.8×
Sandi Wiggins · 1×
Citations per year

Countries citing papers authored by Marlene J. Huggins

Since Specialization
Citations

This map shows the geographic impact of Marlene J. Huggins'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 Marlene J. Huggins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marlene J. Huggins more than expected).

Fields of papers citing papers by Marlene J. Huggins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marlene J. Huggins. 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 Marlene J. Huggins. The network helps show where Marlene J. Huggins may publish in the future.

Co-authorship network of co-authors of Marlene J. Huggins

This figure shows the co-authorship network connecting the top 25 collaborators of Marlene J. Huggins. A scholar is included among the top collaborators of Marlene J. Huggins 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 Marlene J. Huggins. Marlene J. Huggins is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
#WorkIndexed citations
1 12
2 12
3 20
4 19
5 40
6 11
7 15
8 1
9 15
10 39
11 28
12
Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.
55
13 24
14 3
15 126
16 180
17 338
18
Linkage disequilibrium and modification of risk for Huntington disease.
16
19
Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington disease.
52
20 69

About Marlene J. Huggins

Marlene J. Huggins is a scholar working on Cellular and Molecular Neuroscience, Developmental Biology and Genetics, having authored 20 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (9 papers), Biomedical Ethics and Regulation (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (422 citations), Genetics (553 citations) and Neurology (164 citations). Marlene J. Huggins has collaborated with scholars based in Canada, United States and Italy. Frequent co-authors include Michael R. Hayden, Maurice Bloch, Shelin Adam, Jane Theilmann, Sandi Wiggins, Samuel B. Sheps, Martin T. Schechter, Patti Whyte, A Hedrick and Teresa Costa. Their work appears in journals such as New England Journal of Medicine, The American Journal of Human Genetics and Journal of Medical Genetics.

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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