P.S. Harper
Impact in
-
- Genetic Neurodegenerative Diseases
- Physiology top 5%
- Lysosomal Storage Disorders Research
Papers in
-
- Genetic Neurodegenerative Diseases 34
- Genetics 28
- Genomics and Rare Diseases 11
- Genomic variations and chromosomal abnormalities 7
- Genetic Associations and Epidemiology 5
- Co-authors
- Ian D. Young (8 shared papers)Paul Richard Dyken (1 shared paper)Angus John Clarke (4 shared papers)Meena Upadhyaya (10 shared papers)Manuela C. Koch (2 shared papers)Robert Gordon Newcombe (4 shared papers)Mansoor Sarfarazi (7 shared papers)T O'Brien (6 shared papers)
- Journals
- Journal of Medical Genetics (20 papers)The Lancet (17 papers)Archives of Disease in Childhood (6 papers)Clinical Genetics (5 papers)Developmental Medicine & Child Neurology (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
P.S. Harper
96 papers receiving 2.9k citations
Peers
Comparison fields: 5 of 103
- Cellular and Molecular Neuroscience 1k
- Physiology 558
- Genetics 511
- Pediatrics, Perinatology and Child Health 179
- Genetics 113
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 99 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 244 | |
| 2 | 1995 | 176 | |
| 3 | 1975 | 141 | |
| 4 | 1983 | 135 | |
| 5 | Genetic risks for children of women with myotonic dystrophy. | 1991 | 126 |
| 6 | 1982 | 119 | |
| 7 | 1972 | 118 | |
| 8 | 1982 | 103 | |
| 9 | 1990 | 93 | |
| 10 | 2000 | 83 | |
| 11 | Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. | 1991 | 81 |
| 12 | 1983 | 73 | |
| 13 | 1999 | 73 | |
| 14 | Carcinoma of the oesophagus with tylosis. | 1970 | 71 |
| 15 | 1992 | 70 | |
| 16 | Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions. | 1999 | 69 |
| 17 | 1989 | 66 | |
| 18 | 1990 | 60 | |
| 19 | 1982 | 53 | |
| 20 | 1981 | 50 |
About P.S. Harper
P.S. Harper is a scholar working on Cellular and Molecular Neuroscience, Genetics, Physiology, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 99 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (34 papers), Muscle Physiology and Disorders (17 papers), Lysosomal Storage Disorders Research (12 papers), Genomics and Rare Diseases (11 papers), Medical and Health Sciences Research (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Associations and Epidemiology (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1k citations), Physiology (558 citations), Genetics (511 citations), Pediatrics, Perinatology and Child Health (179 citations) and Genetics (113 citations). P.S. Harper has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Ian D. Young, Paul Richard Dyken, Angus John Clarke, Meena Upadhyaya, Manuela C. Koch, Robert Gordon Newcombe, Mansoor Sarfarazi, T O'Brien, Audrey Tyler and Peter Lunt. Their work appears in journals such as Journal of Medical Genetics, The Lancet, Archives of Disease in Childhood, Clinical Genetics and Developmental Medicine & Child Neurology.
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.