Rhona MacLeod

1.8k citations
43 papers · 1.3k indexed · h-index 20
Topics
BRCA gene mutations in cancer (15 papers)Genetic Neurodegenerative Diseases (12 papers)Family Support in Illness (5 papers)

In The Last Decade

Rhona MacLeod

41 papers receiving 1.2k citations

Peers

Rhona MacLeod
Comparison fields: 5 of 111
  • Genetics 486
  • Pediatrics, Perinatology and Child Health 260
  • Neurology 257
  • Molecular Biology 183
  • Cellular and Molecular Neuroscience 182
Replace Alessandro Orsini with:
Alessandro Orsini Italy
Christie Barker‐Cummings United States
Kai Eriksson Finland
George R. Beauchamp United States
Emily Harris United States
Wojciech Kułąk Poland
Amy Goldstein United States
Arthur R. Van Gool Netherlands
Martina Baethmann Germany
Michael Harbord Australia
Rhona MacLeod relative to Alessandro Orsini Italy Alessandro Orsini's profile →
Citations per field
00.5×3.4×
Alessandro Orsini · 1×
Citations per year

Countries citing papers authored by Rhona MacLeod

Since Specialization
Citations

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

Fields of papers citing papers by Rhona MacLeod

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rhona MacLeod. 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 Rhona MacLeod. The network helps show where Rhona MacLeod may publish in the future.

Co-authorship network of co-authors of Rhona MacLeod

This figure shows the co-authorship network connecting the top 25 collaborators of Rhona MacLeod. A scholar is included among the top collaborators of Rhona MacLeod 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 Rhona MacLeod. Rhona MacLeod 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 0
2 2
3 14
4 11
5 1
6 6
7 4
8 27
9 16
10 36
11 158
12 22
13 37
14 42
15 82
16 66
17 40
18 55
19
Vitamin deficiency in the elderly.
5
20 53

About Rhona MacLeod

Rhona MacLeod is a scholar working on Cellular and Molecular Neuroscience, Genetics and Neurology, having authored 43 papers that have together received 1.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (15 papers), Genetic Neurodegenerative Diseases (12 papers) and Family Support in Illness (5 papers). The work is most often cited by research in Genetics (486 citations), Neurology (257 citations) and Pediatrics, Perinatology and Child Health (260 citations). Rhona MacLeod has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Dian Donnai, Marion McAllister, Linda Davies, Katherine Payne, Stuart G. Nicholls, David Craufurd, Marina Frontali, D. Gareth Evans, Aad Tibben and Alison L Jones. Their work appears in journals such as Gastroenterology, Neurology and The Journal of Physiology.

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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