Marion Hamshere
Impact in
-
- Genetic Neurodegenerative Diseases
-
- Mitochondrial Function and Pathology
- Muscle Physiology and Disorders
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- RNA modifications and cancer
Papers in
-
- Mitochondrial Function and Pathology 6
- RNA Research and Splicing 3
- Muscle Physiology and Disorders 3
- RNA and protein synthesis mechanisms 2
- Ubiquitin and proteasome pathways 1
-
- Genetic Neurodegenerative Diseases 7
- Co-authors
- J. David Brook (7 shared papers)Robert J. Osborne (1 shared paper)Ian C. Eperon (3 shared papers)B.S. Athwal (1 shared paper)Edward M. Newman (1 shared paper)Ian R. Graham (1 shared paper)John F. Y. Brookfield (2 shared papers)P.S. Harper (1 shared paper)
- Journals
- Molecular and Cellular Biology (2 papers)Genomics (2 papers)Proceedings of the National Academy of Sciences (1 paper)Parasitology (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomUnited StatesBrazil
In The Last Decade
Marion Hamshere
13 papers receiving 457 citations
Peers
Comparison fields: 5 of 46
- Cellular and Molecular Neuroscience 273
- Molecular Biology 398
- Neurology 77
- Aging 6
- Cardiology and Cardiovascular Medicine 68
Countries citing papers authored by Marion Hamshere
This map shows the geographic impact of Marion Hamshere'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 Marion Hamshere with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marion Hamshere more than expected).
Fields of papers citing papers by Marion Hamshere
This network shows the impact of papers produced by Marion Hamshere. 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 Marion Hamshere. The network helps show where Marion Hamshere may publish in the future.
Co-authors
The 24 scholars most cited alongside Marion Hamshere, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 110 | |
| 2 | A genome-wide map showing common regions of loss of heterozygosity/allelic imbalance in breast cancer. | 2000 | 68 |
| 3 | 1999 | 63 | |
| 4 | 1993 | 56 | |
| 5 | Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions. | 1999 | 53 |
| 6 | 1992 | 42 | |
| 7 | 1991 | 24 | |
| 8 | 1992 | 17 | |
| 9 | 1996 | 14 | |
| 10 | 1998 | 7 | |
| 11 | 2005 | 5 | |
| 12 | 2000 | 3 | |
| 13 | 1999 | 1 |
About Marion Hamshere
Marion Hamshere is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Neurology, Genetics and Pathology and Forensic Medicine, having authored 13 papers that have together received 463 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Mitochondrial Function and Pathology (6 papers), RNA Research and Splicing (3 papers), Muscle Physiology and Disorders (3 papers), RNA and protein synthesis mechanisms (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers), Neurological disorders and treatments (2 papers) and Ubiquitin and proteasome pathways (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (273 citations), Molecular Biology (398 citations), Neurology (77 citations), Aging (6 citations) and Cardiology and Cardiovascular Medicine (68 citations). Marion Hamshere has collaborated with scholars based in United Kingdom, United States and Brazil. Frequent co-authors include J. David Brook, Robert J. Osborne, Ian C. Eperon, B.S. Athwal, Edward M. Newman, Ian R. Graham, John F. Y. Brookfield, P.S. Harper, George Dickson and Jean‐Paul Thirion. Their work appears in journals such as Molecular and Cellular Biology, Genomics, Proceedings of the National Academy of Sciences, Parasitology and Human Molecular 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.