P.S. Harper
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 2%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
Papers in
-
- Muscle Physiology and Disorders 13
- Mitochondrial Function and Pathology 10
-
- Genetic Neurodegenerative Diseases 29
- Co-authors
- I D Young (8 shared papers)Meena Upadhyaya (9 shared papers)Angus Clarke (2 shared papers)Manuela C. Koch (2 shared papers)T O'Brien (6 shared papers)Audrey Tyler (3 shared papers)M. Sarfarazi (7 shared papers)Peter Lunt (6 shared papers)
- Journals
- Journal of Medical Genetics (17 papers)The Lancet (11 papers)Archives of Disease in Childhood (6 papers)Clinical Genetics (5 papers)Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
P.S. Harper
82 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 104
- Cellular and Molecular Neuroscience 1.2k
- Neurology 500
- Genetics 243
- Physiology 522
- Molecular Biology 1.2k
Countries citing papers authored by P.S. Harper
This map shows the geographic impact of P.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 P.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 P.S. Harper more than expected).
Fields of papers citing papers by P.S. Harper
This network shows the impact of papers produced by P.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 P.S. Harper. The network helps show where P.S. Harper may publish in the future.
Co-authors
The 25 scholars most cited alongside P.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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 240 | |
| 2 | 1995 | 161 | |
| 3 | 1975 | 141 | |
| 4 | 1983 | 134 | |
| 5 | Genetic risks for children of women with myotonic dystrophy. | 1991 | 121 |
| 6 | 1982 | 117 | |
| 7 | 1972 | 117 | |
| 8 | 1982 | 99 | |
| 9 | 1990 | 91 | |
| 10 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 82 |
| 11 | 1983 | 71 | |
| 12 | Carcinoma of the oesophagus with tylosis. | 1970 | 70 |
| 13 | 1992 | 66 | |
| 14 | 1999 | 65 | |
| 15 | 1990 | 59 | |
| 16 | Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions. | 1999 | 57 |
| 17 | 1982 | 53 | |
| 18 | 1984 | 51 | |
| 19 | 1981 | 48 | |
| 20 | 1993 | 45 |
About P.S. Harper
P.S. Harper is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Genetics and Neurology, having authored 85 papers that have together received 2.9k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (29 papers), Muscle Physiology and Disorders (13 papers), Neurogenetic and Muscular Disorders Research (10 papers), Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.2k citations), Neurology (500 citations), Genetics (243 citations), Physiology (522 citations) and Molecular Biology (1.2k citations). P.S. Harper has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include I D Young, Meena Upadhyaya, Angus Clarke, Manuela C. Koch, T O'Brien, Audrey Tyler, M. Sarfarazi, Peter Lunt, Robert G. Newcombe and R G Newcombe. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Archives of Disease in Childhood, Clinical Genetics and Human 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.