P E Campbell

661 total citations · 1 hit paper
8 papers, 451 citations indexed

About

P E Campbell is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, P E Campbell has authored 8 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in P E Campbell's work include Connective tissue disorders research (3 papers), Dermatological and Skeletal Disorders (2 papers) and Bone health and treatments (1 paper). P E Campbell is often cited by papers focused on Connective tissue disorders research (3 papers), Dermatological and Skeletal Disorders (2 papers) and Bone health and treatments (1 paper). P E Campbell collaborates with scholars based in Australia. P E Campbell's co-authors include D. M. Danks, B. Stevens, B Turner, J A Walker‐Smith, J. M. Gillespie, Jeanette Blomfield, Howard Williams, Barry W. Oakes, David M. Danks and William G. Cole and has published in prestigious journals such as The Lancet, Archives of Disease in Childhood and Journal of Medical Genetics.

In The Last Decade

P E Campbell

8 papers receiving 393 citations

Hit Papers

MENKES' KINKY-HAIR SYNDROME 1972 2026 1990 2008 1972 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P E Campbell Australia 7 219 133 83 79 67 8 451
Olivier LaRochelle Canada 10 154 0.7× 138 1.0× 114 1.4× 71 0.9× 56 0.8× 12 440
David Kimball United States 9 73 0.3× 56 0.4× 22 0.3× 32 0.4× 44 0.7× 14 300
Masato Itoh Japan 12 87 0.4× 115 0.9× 51 0.6× 11 0.1× 112 1.7× 31 418
H Høyer Denmark 9 76 0.3× 62 0.5× 17 0.2× 77 1.0× 6 0.1× 15 336
Shigehiro Fujimoto Japan 9 37 0.2× 95 0.7× 10 0.1× 107 1.4× 12 0.2× 19 337
R. Öner Türkiye 14 79 0.4× 132 1.0× 8 0.1× 101 1.3× 42 0.6× 36 693
Nicole Wilkinson Canada 8 204 0.9× 164 1.2× 19 0.2× 21 0.3× 63 0.9× 9 615
Antoinette Sakaris United States 5 161 0.7× 241 1.8× 13 0.2× 48 0.6× 38 0.6× 8 806
P. Mocetti Italy 10 36 0.2× 129 1.0× 22 0.3× 34 0.4× 22 0.3× 16 314
Pauline L. Lee United States 15 559 2.6× 168 1.3× 88 1.1× 26 0.3× 13 0.2× 29 959

Countries citing papers authored by P E Campbell

Since Specialization
Citations

This map shows the geographic impact of P E Campbell'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 E Campbell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P E Campbell more than expected).

Fields of papers citing papers by P E Campbell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P E Campbell. 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 E Campbell. The network helps show where P E Campbell may publish in the future.

Co-authorship network of co-authors of P E Campbell

This figure shows the co-authorship network connecting the top 25 collaborators of P E Campbell. A scholar is included among the top collaborators of P E Campbell 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 E Campbell. P E Campbell is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
2.
Sillence, David, et al.. (1991). Ehlers-Danlos syndrome type IV: phenotypic consequences of a splicing mutation in one COL3A1 allele.. Journal of Medical Genetics. 28(12). 840–845. 10 indexed citations
3.
Cole, William G., P E Campbell, John Rogers, & John F. Bateman. (1990). The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissues.. Journal of Medical Genetics. 27(9). 545–551. 15 indexed citations
4.
Oakes, Barry W., David M. Danks, & P E Campbell. (1976). Human copper deficiency: Ultrastructural studies of the aorta and skin in a child with Menkes' syndrome. Experimental and Molecular Pathology. 25(1). 82–98. 28 indexed citations
5.
Campbell, P E, et al.. (1974). Proceedings: Primary hepatic cancer in childhood.. Archives of Disease in Childhood. 49(6). 496–496. 5 indexed citations
6.
Danks, D. M., P E Campbell, J A Walker‐Smith, et al.. (1972). MENKES' KINKY-HAIR SYNDROME. The Lancet. 299(7760). 1100–1103. 301 indexed citations breakdown →
7.
Danks, D. M., et al.. (1971). IS MENKES' SYNDROME A HERITABLE DISORDER OF CONNECTIVE TISSUE ?. The Lancet. 298(7733). 1089–1089. 17 indexed citations
8.
Williams, Howard & P E Campbell. (1960). Generalized Bronchiectasis associated with Deficiency of Cartilage in the Bronchial Tree. Archives of Disease in Childhood. 35(180). 182–191. 60 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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