Tom Cullup

671 total citations
7 papers, 174 citations indexed

About

Tom Cullup is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Tom Cullup has authored 7 papers receiving a total of 174 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cell Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Tom Cullup's work include Cellular transport and secretion (2 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Tom Cullup is often cited by papers focused on Cellular transport and secretion (2 papers), Cardiomyopathy and Myosin Studies (2 papers) and Genetic Neurodegenerative Diseases (2 papers). Tom Cullup collaborates with scholars based in United Kingdom, France and Australia. Tom Cullup's co-authors include Caroline A. Sewry, Heinz Jungbluth, Stephen Abbs, Francesco Muntoni, S. Robb, David Beeson, Matthew Pitt, Jocelyn Laporte, Lucy Feng and Suzanne Lillis and has published in prestigious journals such as British Journal of Dermatology, European Journal of Human Genetics and Neuromuscular Disorders.

In The Last Decade

Tom Cullup

6 papers receiving 174 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tom Cullup United Kingdom	6	112	78	57	48	41	7	174
S. Lillis United Kingdom	6	173 1.5×	56 0.7×	102 1.8×	74 1.5×	38 0.9×	6	237
Cristiane Araújo Martins Moreno Brazil	9	73 0.7×	43 0.6×	38 0.7×	19 0.4×	48 1.2×	28	143
Michaela Yuen Australia	8	169 1.5×	55 0.7×	93 1.6×	45 0.9×	26 0.6×	13	255
Estelle Healy United Kingdom	7	97 0.9×	23 0.3×	48 0.8×	22 0.5×	20 0.5×	20	171
M. Leach United States	8	92 0.8×	29 0.4×	23 0.4×	54 1.1×	12 0.3×	21	187
Daniel Lashley United Kingdom	8	122 1.1×	93 1.2×	35 0.6×	44 0.9×	238 5.8×	13	324
Mark Screen Finland	6	199 1.8×	29 0.4×	83 1.5×	49 1.0×	38 0.9×	7	252
Mridul Johari Finland	9	133 1.2×	18 0.2×	63 1.1×	39 0.8×	16 0.4×	28	194
Agnieszka Madej‐Pilarczyk Poland	11	270 2.4×	28 0.4×	69 1.2×	37 0.8×	8 0.2×	34	311

Countries citing papers authored by Tom Cullup

Since Specialization

Citations

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

Fields of papers citing papers by Tom Cullup

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tom Cullup

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

All Works

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7 of 7 papers shown

1.

D’Arco, Felice, Matías Morin, Tom Cullup, et al.. (2019). Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases. Genes. 10(7). 529–529. 8 indexed citations

2.

Menzies, Lara, Tom Cullup, Alistair Calder, Louise C. Wilson, & Francesca Faravelli. (2019). A novel homozygous variant in CANT1 in a patient with Kim-type Desbuquois dysplasia. Clinical Dysmorphology. 28(4). 219–223. 5 indexed citations

3.

Scoto, Mariacristina, Tom Cullup, Sebahattin Çırak, et al.. (2013). Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing. European Journal of Human Genetics. 21(11). 1249–1252.

4.

Robb, S., Caroline A. Sewry, James J. Dowling, et al.. (2011). Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies. Neuromuscular Disorders. 21(6). 379–386. 80 indexed citations

5.

Munot, Pinki, Daniel Lashley, Heinz Jungbluth, et al.. (2010). Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia. Neuromuscular Disorders. 20(12). 796–800. 41 indexed citations

6.

Jungbluth, Heinz, Tom Cullup, Suzanne Lillis, et al.. (2009). Centronuclear myopathy with cataracts due to a novel dynamin 2 (DNM2) mutation. Neuromuscular Disorders. 20(1). 49–52. 28 indexed citations

7.

Cullup, Tom, et al.. (2006). A novel ABCA12 mutation underlying a case of Harlequin ichthyosis. British Journal of Dermatology. 155(1). 204–206. 12 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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