P.S. Harper

4.1k total citations
83 papers, 2.7k citations indexed

About

P.S. Harper is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, P.S. Harper has authored 83 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 30 papers in Cellular and Molecular Neuroscience and 18 papers in Genetics. Recurrent topics in P.S. Harper's work include Genetic Neurodegenerative Diseases (29 papers), Muscle Physiology and Disorders (13 papers) and Mitochondrial Function and Pathology (11 papers). P.S. Harper is often cited by papers focused on Genetic Neurodegenerative Diseases (29 papers), Muscle Physiology and Disorders (13 papers) and Mitochondrial Function and Pathology (11 papers). P.S. Harper collaborates with scholars based in United Kingdom, United States and Germany. P.S. Harper's co-authors include I D Young, Meena Upadhyaya, Manuela C. Koch, Angus Clarke, Audrey Tyler, M. Sarfarazi, T O'Brien, Peter Lunt, R G Newcombe and Robert G. Newcombe and has published in prestigious journals such as The Lancet, Philosophical Transactions of the Royal Society B Biological Sciences and Human Molecular Genetics.

In The Last Decade

P.S. Harper

82 papers receiving 2.5k 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	31	1.3k	1.2k	548	508	459	83	2.7k
Patrick MacLeod Canada	29	1.3k 1.1×	644 0.6×	266 0.5×	250 0.5×	910 2.0×	74	3.1k
Eiichiro Uyama Japan	24	757 0.6×	366 0.3×	499 0.9×	364 0.7×	172 0.4×	85	1.8k
Raji P. Grewal United States	19	1.3k 1.0×	729 0.6×	388 0.7×	1.1k 2.2×	258 0.6×	77	2.6k
M. Priscilla Short United States	34	1.5k 1.2×	591 0.5×	877 1.6×	1.1k 2.2×	1.2k 2.6×	55	4.2k
David W. Stockton United States	32	3.3k 2.6×	1.3k 1.1×	483 0.9×	429 0.8×	1.3k 2.9×	70	4.9k
Fernando Kok Brazil	31	2.1k 1.6×	544 0.5×	802 1.5×	559 1.1×	1.1k 2.3×	177	3.9k
Jacek Zaremba Poland	22	881 0.7×	451 0.4×	361 0.7×	200 0.4×	328 0.7×	97	1.9k
Jaakko Leisti Finland	27	1.1k 0.9×	338 0.3×	178 0.3×	156 0.3×	873 1.9×	82	2.1k
Nicole I. Wolf Netherlands	41	3.1k 2.4×	594 0.5×	411 0.8×	664 1.3×	692 1.5×	169	4.8k
Gaëtan Lesca France	33	1.2k 1.0×	610 0.5×	382 0.7×	329 0.6×	1.0k 2.3×	160	3.4k

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Phillips, Margaret, et al.. (1999). Daytime somnolence in myotonic dystrophy. Journal of Neurology. 246(4). 275–282. 59 indexed citations

Upadhyaya, Meena, et al.. (1995). Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: Construction of a laser microdissection library. American Journal of Medical Genetics. 60(3). 244–251. 7 indexed citations

Harper, P.S.. (1995). Genetic testing, common diseases, and health service provision. The Lancet. 346(8991-8992). 1645–1646. 21 indexed citations

Lunt, Peter, Philip Jardine, Manuela C. Koch, et al.. (1995). Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD). Human Molecular Genetics. 4(5). 951–958. 150 indexed citations

Harper, P.S.. (1993). Insurance and genetic testing. The Lancet. 341(8839). 224–227. 43 indexed citations

Harper, P.S.. (1992). The epidemiology of Huntington's disease. Human Genetics. 89(4). 365–76. 211 indexed citations

Harper, P.S., et al.. (1992). Myotonic Dystrophy: Advances in Molecular Genetics. Neuromuscular Disorders. 2(4). 241–243. 6 indexed citations

Upadhyaya, Meena, Robert A. Smith, N S Thomas, Andrew Norman, & P.S. Harper. (1990). Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA. Clinical Genetics. 37(6). 456–462. 15 indexed citations

Harper, P.S. & Angus Clarke. (1990). Should we test children for "adult" genetic diseases?. The Lancet. 335(8699). 1205–1206. 85 indexed citations

10.

Al-Jader, Layla N., M C Goodchild, H C Ryley, & P.S. Harper. (1990). Attitudes of parents of cystic fibrosis children towards neonatal screening and antenatal diagnosis. Clinical Genetics. 38(6). 460–465. 55 indexed citations

11.

Smith, Robert A., J R Sibert, & P.S. Harper. (1990). EARLY DEVELOPMENT OF BOYS WITH DUCHENNE MUSCULAR DYSTROPHY. Developmental Medicine & Child Neurology. 32(6). 519–527. 35 indexed citations

12.

Harper, P.S., et al.. (1989). A regional register for inherited cancers.. BMJ. 298(6689). 1689–1691. 4 indexed citations

13.

Harper, P.S. & M. Sarfarazi. (1985). Genetic prediction and family structure in Huntington's chorea.. BMJ. 290(6486). 1929–1931. 34 indexed citations

14.

O'Brien, T & P.S. Harper. (1984). COURSE, PROGNOSIS AND COMPLICATIONS OF CHILDHOOD‐ONSET MYOTONIC DYSTROPHY. Developmental Medicine & Child Neurology. 26(1). 62–67. 42 indexed citations

15.

O'Brien, T, J R Sibert, & P.S. Harper. (1983). Implications of diagnostic delay in Duchenne muscular dystrophy.. BMJ. 287(6399). 1106–1107. 13 indexed citations

16.

O'Brien, T, R. G. Newcombe, & P.S. Harper. (1983). Outlook for a clinically normal child in a sibship with congenital myotonic dystrophy. The Journal of Pediatrics. 103(5). 762–763. 5 indexed citations

17.

Young, I D & P.S. Harper. (1982). Incidence of Hunter's syndrome. Human Genetics. 60(4). 391–392. 41 indexed citations

18.

Harper, P.S., et al.. (1982). An autosomal dominant syndrome of uveal colobomata, cleft lip and palate, and mental retardation.. Journal of Medical Genetics. 19(6). 444–446. 12 indexed citations

19.

Harper, P.S., et al.. (1980). Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibship.. Journal of Medical Genetics. 17(3). 212–215. 6 indexed citations

20.

Harper, P.S., et al.. (1970). Severe hypercalcaemia from hyperthyroidism with unusual features.. BMJ. 1(5690). 213–214. 9 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.

Explore authors with similar magnitude of impact