Trevor Cole

17.2k total citations
62 papers, 3.2k citations indexed

About

Trevor Cole is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Trevor Cole has authored 62 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Genetics, 30 papers in Molecular Biology and 12 papers in Surgery. Recurrent topics in Trevor Cole's work include Genetic Syndromes and Imprinting (21 papers), Prenatal Screening and Diagnostics (9 papers) and Genomics and Rare Diseases (6 papers). Trevor Cole is often cited by papers focused on Genetic Syndromes and Imprinting (21 papers), Prenatal Screening and Diagnostics (9 papers) and Genomics and Rare Diseases (6 papers). Trevor Cole collaborates with scholars based in United Kingdom, United States and Germany. Trevor Cole's co-authors include Helen E. Hughes, Eamonn R. Maher, D. Gareth Evans, Katrina Tatton‐Brown, Nazneen Rahman, Janusz Jankowski, Frances M. Richards, M. Helen Rajpar, C. McKeown and Shane McKee and has published in prestigious journals such as The Lancet, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Trevor Cole

61 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Trevor Cole United Kingdom 31 1.7k 1.7k 489 386 321 62 3.2k
Dvorah Abeliovich Israel 31 1.5k 0.8× 1.4k 0.8× 450 0.9× 340 0.9× 229 0.7× 98 3.0k
Howard M. Saal United States 33 1.3k 0.7× 2.4k 1.4× 765 1.6× 470 1.2× 256 0.8× 114 4.2k
Kenjiro Kosaki Japan 35 2.7k 1.6× 1.8k 1.1× 591 1.2× 623 1.6× 193 0.6× 363 5.2k
Margherita Silengo Italy 29 2.0k 1.2× 1.7k 1.0× 617 1.3× 489 1.3× 163 0.5× 114 3.3k
Sally Ann Lynch Ireland 34 1.6k 0.9× 1.4k 0.8× 379 0.8× 744 1.9× 184 0.6× 146 3.7k
Thomy de Ravel Belgium 38 2.0k 1.2× 1.9k 1.2× 720 1.5× 382 1.0× 165 0.5× 112 4.2k
Mariëlle Alders Netherlands 36 2.1k 1.2× 1.2k 0.7× 494 1.0× 364 0.9× 153 0.5× 114 4.0k
Giandomenico Palka Italy 31 1.5k 0.9× 1.5k 0.9× 515 1.1× 247 0.6× 252 0.8× 145 3.3k
Damien Sanlaville France 33 1.6k 0.9× 2.2k 1.3× 585 1.2× 356 0.9× 140 0.4× 189 3.7k
Hidenobu Soejima Japan 35 2.6k 1.5× 1.2k 0.7× 655 1.3× 225 0.6× 130 0.4× 117 3.4k

Countries citing papers authored by Trevor Cole

Since Specialization
Citations

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

Fields of papers citing papers by Trevor Cole

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Trevor Cole

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

All Works

20 of 20 papers shown
1.
Gerrish, Amy, E. C. Stone, Samuel Clokie, et al.. (2019). Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humour. British Journal of Ophthalmology. 103(5). 721–724. 48 indexed citations
2.
Maddux, Michele H., et al.. (2019). Initial Validation of IBD KNOW-IT: Measuring Patient and Caregiver Knowledge of a Child’s Disease and Treatment Regimen. Journal of Clinical Psychology in Medical Settings. 27(3). 480–489. 10 indexed citations
3.
Parks, Michael, Siobhán Cleary, Samuel Clokie, et al.. (2017). Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage. European Journal of Human Genetics. 25(4). 416–422. 74 indexed citations
4.
Tatton‐Brown, Katrina, Chey Loveday, Shawn Yost, et al.. (2017). Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. The American Journal of Human Genetics. 100(5). 725–736. 128 indexed citations
5.
Moss, Joanna, et al.. (2015). The behavioral characteristics of Sotos syndrome. American Journal of Medical Genetics Part A. 167(12). 2945–2956. 21 indexed citations
6.
Zweier, Christiane, Olaf Rittinger, Ingrid Bader, et al.. (2014). Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(3). 290–301. 20 indexed citations
7.
Zweier, Christiane, Cornelia Kraus, Louise Brueton, et al.. (2013). A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. Journal of Medical Genetics. 50(12). 838–847. 32 indexed citations
8.
Hopman, Saskia, Johannes H. M. Merks, Corianne A.J.M. de Borgie, et al.. (2013). The development of a clinical screening instrument for tumour predisposition syndromes in childhood cancer patients. European Journal of Cancer. 49(15). 3247–3254. 14 indexed citations
9.
Hanson, Dan, Philip Murray, James O’Sullivan, et al.. (2011). Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth. The American Journal of Human Genetics. 89(1). 148–153. 88 indexed citations
10.
Hoornaert, Kristien, K. Kozlowski, Trevor Cole, et al.. (2007). Czech dysplasia metatarsal type: another type II collagen disorder. European Journal of Human Genetics. 15(12). 1269–1275. 33 indexed citations
11.
Lonie, Lorne, Daniel Porter, Maria Fraser, et al.. (2006). Determination of the mutation spectrum of theEXT1/EXT2genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes inEXTnegative cases. Human Mutation. 27(11). 1160–1160. 45 indexed citations
12.
Vos, Michel De, Bruce E. Hayward, Ruth Charlton, et al.. (2006). PMS2 Mutations in Childhood Cancer. JNCI Journal of the National Cancer Institute. 98(5). 358–361. 63 indexed citations
13.
Trochet, Delphine, Louise M. O’Brien, David Gozal, et al.. (2005). PHOX2B Genotype Allows for Prediction of Tumor Risk in Congenital Central Hypoventilation Syndrome. The American Journal of Human Genetics. 76(3). 421–426. 183 indexed citations
14.
Tatton‐Brown, Katrina, Jenny Douglas, Kim Coleman, et al.. (2005). Genotype-Phenotype Associations in Sotos Syndrome: An Analysis of 266 Individuals with NSD1 Aberrations. The American Journal of Human Genetics. 77(2). 193–204. 221 indexed citations
15.
Douglas, Jenny, Kim Coleman, Katrina Tatton‐Brown, et al.. (2004). Evaluation of NSD2 and NSD3 in overgrowth syndromes. European Journal of Human Genetics. 13(2). 150–153. 30 indexed citations
16.
Møller, Lisbeth Birk, Zeynep Tümer, Connie Lund, et al.. (2000). Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome. The American Journal of Human Genetics. 66(4). 1211–1220. 84 indexed citations
17.
Richards, Frances M., Shane McKee, M. Helen Rajpar, et al.. (1999). Germline E-cadherin Gene (CDH1) Mutations Predispose to Familial Gastric Cancer and Colorectal Cancer. Human Molecular Genetics. 8(4). 607–610. 251 indexed citations
18.
Cole, Trevor, et al.. (1996). Sotos syndrome: Evolution of facial phenotype subjective and objective assessment. American Journal of Medical Genetics. 65(1). 13–20. 54 indexed citations
19.
Cole, Trevor, et al.. (1992). Weaver syndrome.. Journal of Medical Genetics. 29(5). 332–337. 24 indexed citations
20.
Rutter, S. & Trevor Cole. (1991). PSYCHOLOGICAL CHARACTERISTICS OF SOTOS SYNDROME. Developmental Medicine & Child Neurology. 33(10). 898–902. 38 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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