Peter S. Harper
Impact in
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases
- Neurology top 0.2%
- Neurofibromatosis and Schwannoma Cases
- Neurological disorders and treatments
Papers in
-
- Mitochondrial Function and Pathology 35
- Muscle Physiology and Disorders 34
- RNA Research and Splicing 12
-
- Genetic Neurodegenerative Diseases 90
- Co-authors
- D. A. S. Compston (7 shared papers)Susan Huson (13 shared papers)Duncan J. Shaw (21 shared papers)Meena Upadhyaya (26 shared papers)M. Sarfarazi (31 shared papers)Nick Thomas (12 shared papers)Peter Lunt (8 shared papers)H G Harley (16 shared papers)
- Journals
- Journal of Medical Genetics (49 papers)Human Genetics (31 papers)Clinical Genetics (14 papers)Archives of Disease in Childhood (10 papers)The Lancet (9 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Peter S. Harper
247 papers receiving 8.4k citations
Peter S. Harper's Hit Papers
Peers
Comparison fields: 5 of 174
- Cellular and Molecular Neuroscience 3.1k
- Neurology 2.5k
- Genetics 1.9k
- Molecular Biology 4.6k
- Genetics 641
Countries citing papers authored by Peter S. Harper
This map shows the geographic impact of Peter S. Harper'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 Peter S. Harper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter S. Harper more than expected).
Fields of papers citing papers by Peter S. Harper
This network shows the impact of papers produced by Peter S. Harper. 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 Peter S. Harper. The network helps show where Peter S. Harper may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter S. Harper, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 251 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease Hit paper breakdown → | 1993 | 558 |
| 2 | VON RECKLINGHAUSEN NEUROFIBROMATOSIS Hit paper breakdown → | 1988 | 483 |
| 3 | 1989 | 385 | |
| 4 | 1983 | 309 | |
| 5 | 1996 | 268 | |
| 6 | 1988 | 240 | |
| 7 | Anticipation in myotonic dystrophy: new light on an old problem. | 1992 | 199 |
| 8 | 1987 | 199 | |
| 9 | Promoting safe and effective genetic testing in the United States: Final Report of the Task Force on Genetic Testing. | 1998 | 166 |
| 10 | 1992 | 143 | |
| 11 | George Otto Gey. (1899-1970). The HeLa cell and a reappraisal of its origin. | 1971 | 129 |
| 12 | 1989 | 122 | |
| 13 | 1998 | 112 | |
| 14 | 2000 | 108 | |
| 15 | 1991 | 105 | |
| 16 | 1990 | 104 | |
| 17 | 1984 | 95 | |
| 18 | 1991 | 95 | |
| 19 | 1993 | 93 | |
| 20 | 1999 | 92 |
About Peter S. Harper
Peter S. Harper is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Genetics, having authored 251 papers that have together received 8.8k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (90 papers), Mitochondrial Function and Pathology (35 papers), Muscle Physiology and Disorders (34 papers), BRCA gene mutations in cancer (24 papers), Neurological disorders and treatments (18 papers), Neurogenetic and Muscular Disorders Research (18 papers), Neurofibromatosis and Schwannoma Cases (16 papers) and RNA Research and Splicing (12 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.1k citations), Neurology (2.5k citations), Genetics (1.9k citations), Molecular Biology (4.6k citations) and Genetics (641 citations). Peter S. Harper has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include D. A. S. Compston, Susan Huson, Duncan J. Shaw, Meena Upadhyaya, M. Sarfarazi, Nick Thomas, Peter Lunt, H G Harley, Peggy Clark and William Reardon. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, Clinical Genetics, Archives of Disease in Childhood and The Lancet.
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.