P.S. Harper
Impact in
-
- Genetic Neurodegenerative Diseases
- Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
Papers in ⓘ
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- Genetic Neurodegenerative Diseases 29
- Genetics 10
- Neurogenetic and Muscular Disorders Research 10
- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 5
- Co-authors
- I D Young (8 shared papers)Meena Upadhyaya (9 shared papers)Angus Clarke (2 shared papers)Manuela C. Koch (2 shared papers)Audrey Tyler (3 shared papers)T O'Brien (6 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 (5 papers)Clinical Genetics (5 papers)Human Molecular Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
P.S. Harper
82 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 111
- Cellular and Molecular Neuroscience 1.2k
- Neurology 548
- Genetics 245
- Physiology 508
- Molecular Biology 1.3k
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 83 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 211 | |
| 2 | 1995 | 150 | |
| 3 | 1975 | 129 | |
| 4 | 1983 | 125 | |
| 5 | Genetic risks for children of women with myotonic dystrophy. | 1991 | 114 |
| 6 | 1982 | 110 | |
| 7 | 1972 | 104 | |
| 8 | 1982 | 92 | |
| 9 | 1990 | 85 | |
| 10 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 80 |
| 11 | 1983 | 65 | |
| 12 | 1999 | 59 | |
| 13 | 1992 | 58 | |
| 14 | Carcinoma of the oesophagus with tylosis. | 1970 | 57 |
| 15 | 1990 | 55 | |
| 16 | Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions. | 1999 | 53 |
| 17 | 1981 | 48 | |
| 18 | 1982 | 48 | |
| 19 | 1993 | 43 | |
| 20 | 1984 | 42 |
About P.S. Harper
P.S. Harper is a scholar working on Cellular and Molecular Neuroscience, Genetics, Clinical Biochemistry, Neurology and Genetics, having authored 83 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (29 papers), Muscle Physiology and Disorders (13 papers), Mitochondrial Function and Pathology (11 papers), Neurogenetic and Muscular Disorders Research (10 papers), Metabolism and Genetic Disorders (6 papers), Genomics and Rare Diseases (6 papers), Cardiomyopathy and Myosin Studies (5 papers) and BRCA gene mutations in cancer (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.2k citations), Neurology (548 citations), Genetics (245 citations), Physiology (508 citations) and Molecular Biology (1.3k citations). P.S. Harper has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include I D Young, Meena Upadhyaya, Angus Clarke, Manuela C. Koch, Audrey Tyler, T O'Brien, M. Sarfarazi, Peter Lunt, R G Newcombe and Robert G. Newcombe. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Archives of Disease in Childhood, Clinical Genetics 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.