Robin E. Williamson

4.6k citations
33 papers · 2.1k indexed · 1 hit paper · h-index 12

Impact in

  • Neurology top 1%
    • Parkinson's Disease Mechanisms and Treatments
    • Neurological disorders and treatments
    • Neurological diseases and metabolism
  • Physiology top 5%
    • Alzheimer's disease research and treatments

Papers in

    • Hearing, Cochlea, Tinnitus, Genetics 3
    • Genomic variations and chromosomal abnormalities 3

Robin E. Williamson

32 papers receiving 2.0k citations

Hit Papers

Acceleration of oligomerization, not fibrillization, is a shared property of both α-synuclein mutations linked to early-onset Parkinson's disease: Implications for pathogenesis and therapy 2000 · 1.3k citations
1.3k20002026200820174008001.2k

Peers

Robin E. Williamson
Comparison fields: 5 of 122
  • Neurology 1.1k
  • Neurology 289
  • Physiology 711
  • Cellular and Molecular Neuroscience 467
  • Sensory Systems 91
Replace Chunni Zhu with:
Chunni Zhu United States
Marcie A. Glicksman United States
Seungkyu Lee United States
Sonja W. Scholz United States
Nanping Wu United States
Karine Madiona France
Sandra Pritzkow United States
Marçal Vilar Spain
Majid Hafezparast United Kingdom
Edward A. Burton United States
Robin E. Williamson relative to Chunni Zhu United States Chunni Zhu's profile →
Citations per field
00.5×3.0×
Chunni Zhu · 1×
Citations per year

Countries citing papers authored by Robin E. Williamson

Since Specialization
Citations

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

Fields of papers citing papers by Robin E. Williamson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robin E. Williamson. 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 Robin E. Williamson. The network helps show where Robin E. Williamson may publish in the future.

Co-authors

The 25 scholars most cited alongside Robin E. Williamson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Robin E. Williamson Line = papers co-authored together Robin E. Williamson links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Acceleration of oligomerization, not fibrillization, is a shared property of both α-synuclein mutations linked to early-onset Parkinson's disease: Implications for pathogenesis and therapy
Hit paper breakdown →
20001269
2 2000179
3 1990145
4
Gene delivery and expression mediated by an integrin-binding peptide.
1995114
5 201193
6 200172
7 198657
8
On genetic and environmental factors in Menière's disease.
199440
9
The MEL gene: a new member of the RAB/YPT class of RAS-related genes.
199119
10 200818
11 198315
12
Wireless Temperature Monitoring in Remote Systems Analog
200213
13
Local area network design
198611
14 200710
15
Gene therapy for familial adenomatous polyposis. Prolonged expression of the adenomatous polyposis coli gene after lipofection into mouse colon in vivo.
19986
16 20085
17 20025
18
MOLECULAR STUDIES OF MONOSOMY-22Q11 AND ITS CLINICAL CONSEQUENCES
19914
19 20093
20 20093

About Robin E. Williamson

Robin E. Williamson is a scholar working on Sensory Systems, Genetics, Neurology, Otorhinolaryngology and Gastroenterology, having authored 33 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), Neurological disorders and treatments (2 papers), RNA regulation and disease (2 papers), RNA Interference and Gene Delivery (2 papers), Congenital heart defects research (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Neurology (1.1k citations), Neurology (289 citations), Physiology (711 citations), Cellular and Molecular Neuroscience (467 citations) and Sensory Systems (91 citations). Robin E. Williamson has collaborated with scholars based in United States, United Kingdom and Switzerland. Frequent co-authors include Peter T. Lansbury, Jean‐Christophe Rochet, Kelly A. Conway, Tomas T. Ding, Seung‐Jae Lee, Cynthia C. Morton, James D. Harper, Douglas D. Dykeman, W. Doeringer and Bernd Meister. Their work appears in journals such as The American Journal of Human Genetics, Proceedings of the National Academy of Sciences, IEEE Journal on Selected Areas in Communications, Journal of Clinical Pathology and Reproductive BioMedicine Online.

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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