P S Harper

4.8k total citations
35 papers, 1.3k citations indexed

About

P S Harper is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, P S Harper has authored 35 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in P S Harper's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (4 papers) and Muscle Physiology and Disorders (4 papers). P S Harper is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (4 papers) and Muscle Physiology and Disorders (4 papers). P S Harper collaborates with scholars based in United Kingdom, Netherlands and Germany. P S Harper's co-authors include Jeffrey Murray, Linda Meredith, C R Mueller, Kay E. Davies, R. Williamson, J. MacMillan, Jonathan M. Boutell, Victoria Weston, P. Thomas and J. W. Neal and has published in prestigious journals such as Nature, Science and Human Molecular Genetics.

In The Last Decade

P S Harper

35 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
P S Harper United Kingdom	15	856	613	378	283	89	35	1.3k
Sibylle Jakubiczka Germany	21	814 1.0×	261 0.4×	606 1.6×	180 0.6×	72 0.8×	54	1.4k
Ann Curtis United Kingdom	22	674 0.8×	361 0.6×	170 0.4×	410 1.4×	232 2.6×	53	1.6k
Elizabeth Ives Canada	21	895 1.0×	417 0.7×	526 1.4×	172 0.6×	32 0.4×	28	1.5k
S. Igarashi Japan	12	1.3k 1.5×	1.3k 2.2×	323 0.9×	530 1.9×	109 1.2×	26	1.9k
Elisabeth Rosser United Kingdom	17	657 0.8×	301 0.5×	347 0.9×	173 0.6×	49 0.6×	35	1.1k
Emanuela Manfredini Italy	15	271 0.3×	330 0.5×	284 0.8×	572 2.0×	72 0.8×	27	1.1k
Sahar Al‐Mahdawi United Kingdom	25	1.5k 1.7×	1.1k 1.8×	242 0.6×	196 0.7×	67 0.8×	52	1.9k
Loreto Martorell Spain	22	1.0k 1.2×	735 1.2×	366 1.0×	333 1.2×	65 0.7×	73	1.4k
R. J. M. Gardner New Zealand	18	766 0.9×	126 0.2×	682 1.8×	134 0.5×	101 1.1×	27	1.6k
Friedmar R. Kreuz Germany	17	498 0.6×	441 0.7×	197 0.5×	129 0.5×	105 1.2×	30	923

Countries citing papers authored by P S Harper

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of P S Harper

This figure shows the co-authorship network connecting the top 25 collaborators of P S Harper. A scholar is included among the top collaborators of P S Harper based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with P S Harper. P S Harper is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Harper, P S, et al.. (2010). The Human Genetics Historical Library: an international resource for geneticists and historians. Clinical Genetics. 77(3). 214–220. 2 indexed citations

Newcombe, R., et al.. (2002). Developing a quality scoring system for epidemiological surveys of genetic disorders. Clinical Genetics. 62(3). 230–234. 16 indexed citations

Boutell, Jonathan M., P. Thomas, J. W. Neal, et al.. (1999). Aberrant Interactions of Transcriptional Repressor Proteins with the Huntington's Disease Gene Product, Huntingtin. Human Molecular Genetics. 8(9). 1647–1655. 248 indexed citations

Upadhyaya, Meena, Julie Maynard, Michael J. Osborn, & P S Harper. (1997). Six novel mutations in the neurofibromatosis type 1 (NF1) gene. Human Mutation. 10(3). 248–250. 12 indexed citations

Harper, P S, et al.. (1996). Clinical Genetics Services into the 21st Century. Journal of the Royal College of Physicians of London. 30(4). 296–301. 1 indexed citations

Harper, P S. (1996). New genes for old diseases: the molecular basis of myotonic dystrophy and Huntington's disease. The Lumleian Lecture 1995.. PubMed. 30(3). 221–31. 18 indexed citations

Upadhyaya, Meena, Julie Maynard, M. Osborn, et al.. (1995). Characterisation of germline mutations in the neurofibromatosis type 1 (NF1) gene.. Journal of Medical Genetics. 32(9). 706–710. 35 indexed citations

MacMillan, J. & P S Harper. (1994). Clinical genetics in neurological disease.. Journal of Neurology Neurosurgery & Psychiatry. 57(1). 7–15. 15 indexed citations

Roberts, Susan, Meena Upadhyaya, M. Sarfarazi, & P S Harper. (1989). Further evidence localising the gene for Hunter's syndrome to the distal region of the X chromosome long arm.. Journal of Medical Genetics. 26(5). 309–313. 27 indexed citations

10.

Suthers, G K, David F. Callen, V.J. Hyland, et al.. (1989). A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA ). Science. 246(4935). 1298–1300. 54 indexed citations

11.

Harper, P S. (1989). Gene mapping and the muscular dystrophies.. PubMed. 306. 29–49. 6 indexed citations

12.

Harper, P S, et al.. (1987). Report of the delegation of clinical geneticists to China, Spring 1986.. PubMed. 4(2). 61–77. 13 indexed citations

13.

Tsipouras, Petros, et al.. (1986). Marfan syndrome: exclusion of genetic linkage to the COL1A2 gene.. PubMed. 30(5). 428–32. 30 indexed citations

14.

Emery, Alan E H, et al.. (1978). A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party.. Journal of Medical Genetics. 15(6). 435–442. 21 indexed citations

15.

Harper, P S. (1976). Genetic variation in Wales.. PubMed. 10(4). 321–32. 6 indexed citations

16.

Harper, P S. (1973). The Prenatal Diagnosis of Metabolic Disorders. Journal of the Royal College of Physicians of London. 7(3). 251–258. 1 indexed citations

17.

Harper, P S, Peter O Jenkins, & K. M. Laurence. (1973). Spondyloepiphyseal dysplasia tarda: a report of four cases in two families. British Journal of Radiology. 46(549). 676–684. 14 indexed citations

18.

Harper, P S. (1971). Turban tumors (cylindromatosis).. PubMed. 7(8). 338–41. 3 indexed citations

19.

Harper, P S. (1971). Calcifying epithelioma of Malherbe and myotonic dystrophy in sisters.. PubMed. 7(8). 343–5. 11 indexed citations

20.

Harper, P S, et al.. (1971). Klippel-Trénaunay-Weber syndrome.. PubMed. 7(8). 315–8. 6 indexed citations

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.

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