C. Pollitt

1.4k total citations
11 papers, 460 citations indexed

About

C. Pollitt is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, C. Pollitt has authored 11 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Cell Biology. Recurrent topics in C. Pollitt's work include Muscle Physiology and Disorders (5 papers), Calpain Protease Function and Regulation (3 papers) and Genetic Neurodegenerative Diseases (3 papers). C. Pollitt is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Calpain Protease Function and Regulation (3 papers) and Genetic Neurodegenerative Diseases (3 papers). C. Pollitt collaborates with scholars based in United Kingdom, Germany and Finland. C. Pollitt's co-authors include Robert Pogue, Kate Bushby, Angela Pyle, Ana María Fortuna, George D. Yancopoulos, Michael Oldridge, Robert B. Kimble, Andrew O.M. Wilkie, Monika Maringa and David M. Valenzuela and has published in prestigious journals such as Nature Genetics, Developmental Medicine & Child Neurology and European Journal of Clinical Microbiology & Infectious Diseases.

In The Last Decade

C. Pollitt

10 papers receiving 443 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Pollitt United Kingdom	7	379	136	103	68	65	11	460
Stephanie K. Mewborn United States	7	473 1.2×	44 0.3×	102 1.0×	123 1.8×	82 1.3×	7	596
Ravi Knight United Kingdom	6	211 0.6×	55 0.4×	60 0.6×	76 1.1×	24 0.4×	6	295
Janet E. Sowden United States	12	298 0.8×	213 1.6×	91 0.9×	35 0.5×	61 0.9×	23	577
H. Jacobus Gilhuis Netherlands	12	165 0.4×	29 0.2×	40 0.4×	42 0.6×	67 1.0×	23	379
Jeffrey Murray United Kingdom	7	605 1.6×	100 0.7×	30 0.3×	90 1.3×	284 4.4×	8	766
Amandine Boyer France	11	587 1.5×	136 1.0×	143 1.4×	12 0.2×	57 0.9×	15	797
Giovanni Marrosu Italy	12	227 0.6×	57 0.4×	48 0.5×	50 0.7×	13 0.2×	19	349
E. Hammouda France	4	1.1k 2.8×	62 0.5×	148 1.4×	260 3.8×	48 0.7×	4	1.1k
A. J. van Essen Netherlands	11	188 0.5×	60 0.4×	26 0.3×	43 0.6×	66 1.0×	11	287
Patrick Frosk Canada	10	495 1.3×	119 0.9×	74 0.7×	140 2.1×	81 1.2×	18	618

Countries citing papers authored by C. Pollitt

Since Specialization

Citations

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

Fields of papers citing papers by C. Pollitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C. Pollitt. 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 C. Pollitt. The network helps show where C. Pollitt may publish in the future.

Co-authorship network of co-authors of C. Pollitt

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

All Works

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11 of 11 papers shown

1.

Gray, J. A. Muir, Sharon Keers, Elizabeth Vafiadaki, et al.. (2001). Secondary changes in dysferlin expression. Neuromuscular Disorders. 1 indexed citations

2.

Pogue, Robert, Louise V.B. Anderson, Angela Pyle, et al.. (2001). Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies. Neuromuscular Disorders. 11(1). 80–87. 32 indexed citations

3.

Pollitt, C., et al.. (2001). The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach. Neuromuscular Disorders. 11(3). 287–296. 67 indexed citations

4.

Oldridge, Michael, Ana María Fortuna, Monika Maringa, et al.. (2000). Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nature Genetics. 24(3). 275–278. 163 indexed citations

5.

Anderson, Louise V.B., Robert Pogue, Elizabeth Vafiadaki, et al.. (2000). Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscular Disorders. 10(8). 553–559. 113 indexed citations

6.

Eagle, Michelle, et al.. (2000). Multicore myopathy: respiratory failure and paraspinal muscle contractures are important complications. Developmental Medicine & Child Neurology. 42(5). 340–343. 1 indexed citations

7.

Eagle, Michelle, et al.. (2000). Multicore myopathy: respiratory failure and paraspinal muscle contractures are important complications. Developmental Medicine & Child Neurology. 42(5). 340–343. 13 indexed citations

8.

Bushby, Kate, C. Pollitt, Mary Ann Johnson, Mark T. Rogers, & Patrick F. Chinnery. (1998). Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports. Neuromuscular Disorders. 8(8). 574–579. 55 indexed citations

9.

Graham, Julie, Deborah A. Tweddle, David R. Jenkins, C. Pollitt, & S.J. Pedler. (1998). Non-tuberculous mycobacterial infection in children with cancer. European Journal of Clinical Microbiology & Infectious Diseases. 17(6). 394–397. 11 indexed citations

10.

Graham, Julie, Deborah A. Tweddle, David R. Jenkins, C. Pollitt, & S.J. Pedler. (1998). Non-Tuberculous Mycobacterial Infection in Children with Cancer. European Journal of Clinical Microbiology & Infectious Diseases. 17(6). 394–397. 1 indexed citations

11.

Bushby, K., Caroline A. Sewry, Robert Pogue, et al.. (1997). Dystrophinopathy or sarcoglycanopathy: the importance of a full diagnostic assessment in suspected manifesting carriers of Duchenne and Becker muscular dystrophy. Neuromuscular Disorders. 7(6-7). 438–438. 3 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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