Carmel Toomes

6.2k total citations
65 papers, 2.4k citations indexed

About

Carmel Toomes is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Carmel Toomes has authored 65 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Ophthalmology. Recurrent topics in Carmel Toomes's work include Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Ubiquitin and proteasome pathways (7 papers). Carmel Toomes is often cited by papers focused on Retinal Development and Disorders (11 papers), Retinal Diseases and Treatments (7 papers) and Ubiquitin and proteasome pathways (7 papers). Carmel Toomes collaborates with scholars based in United Kingdom, United States and Egypt. Carmel Toomes's co-authors include Chris F. Inglehearn, Sandra Bell, David A. Mackey, Jamie E. Craig, Louise Downey, Alan J. Mighell, C. Geoffrey Woods, Ian Carr, Colin A. Johnson and Gulshan Karbani and has published in prestigious journals such as PLoS ONE, Scientific Reports and Brain Research.

In The Last Decade

Carmel Toomes

63 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carmel Toomes United Kingdom 24 1.8k 741 349 278 178 65 2.4k
Waixing Tang United States 20 1.6k 0.9× 573 0.8× 291 0.8× 342 1.2× 195 1.1× 26 2.5k
Ordan J. Lehmann Canada 29 1.5k 0.8× 685 0.9× 276 0.8× 810 2.9× 422 2.4× 56 2.6k
Karen Grønskov Denmark 27 1.6k 0.9× 925 1.2× 624 1.8× 252 0.9× 107 0.6× 90 2.3k
Sheikh Riazuddin United States 26 2.0k 1.1× 504 0.7× 224 0.6× 700 2.5× 318 1.8× 98 2.5k
Philip J. Gage United States 31 2.4k 1.3× 1.0k 1.4× 227 0.7× 290 1.0× 529 3.0× 52 3.7k
Vasiliki Kalatzis France 27 1.3k 0.7× 390 0.5× 163 0.5× 197 0.7× 129 0.7× 69 2.6k
Erwin van Wijk Netherlands 27 1.8k 1.0× 692 0.9× 433 1.2× 249 0.9× 101 0.6× 75 2.7k
Orly Goldstein United States 21 1.1k 0.6× 446 0.6× 148 0.4× 120 0.4× 62 0.3× 60 1.6k
Carolina Mailhos United Kingdom 15 1.3k 0.7× 189 0.3× 199 0.6× 214 0.8× 216 1.2× 20 1.9k
Ling Hou China 26 1.2k 0.7× 261 0.4× 967 2.8× 176 0.6× 65 0.4× 64 2.1k

Countries citing papers authored by Carmel Toomes

Since Specialization
Citations

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

Fields of papers citing papers by Carmel Toomes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmel Toomes

This figure shows the co-authorship network connecting the top 25 collaborators of Carmel Toomes. A scholar is included among the top collaborators of Carmel Toomes 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 Carmel Toomes. Carmel Toomes 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.
Watson, Christopher M., Ian Carr, Martin McKibbin, et al.. (2023). Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. Molecular Diagnosis & Therapy. 27(4). 525–535. 4 indexed citations
2.
McKibbin, Martin, Susanne Roosing, Manir Ali, et al.. (2023). Effective smMIPs-Based Sequencing of Maculopathy-Associated Genes in Stargardt Disease Cases and Allied Maculopathies from the UK. Genes. 14(1). 191–191. 2 indexed citations
3.
Taylor, Rachel L., Simon G. Williams, Jane Ashworth, et al.. (2022). Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia. Orphanet Journal of Rare Diseases. 17(1). 110–110. 5 indexed citations
4.
El‐Asrag, Mohammed E., Marta Cortón, Martin McKibbin, et al.. (2022). Novel homozygous mutations in the transcription factor NRL cause non-syndromic retinitis pigmentosa. PubMed Central. 8 indexed citations
5.
Toomes, Carmel, et al.. (2021). The Role of Csmd1 during Mammary Gland Development. Genes. 12(2). 162–162. 5 indexed citations
6.
Lord, Emma, James A. Poulter, Andrew R. Webster, et al.. (2017). Mutations in SLC38A8 and FOXD1 in patients with nystagmus and foveal hypoplasia.. Investigative Ophthalmology & Visual Science. 58(8). 2786–2786. 1 indexed citations
7.
Khan, Kamron N., Mohammed E. El‐Asrag, Cristy A. Ku, et al.. (2017). Specific Alleles of CLN7 / MFSD8 , a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy. Investigative Ophthalmology & Visual Science. 58(7). 2906–2906. 38 indexed citations
8.
Kamal, Mohamed, Deborah L. Holliday, Ewan E. Morrison, et al.. (2017). Loss of CSMD1 expression disrupts mammary duct formation while enhancing proliferation, migration and invasion. Oncology Reports. 38(1). 283–292. 18 indexed citations
9.
Taylor, Rachel L., Gavin Arno, James A. Poulter, et al.. (2017). Association of Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation With Early-Onset Retinal Dystrophy. JAMA Ophthalmology. 135(4). 339–339. 32 indexed citations
10.
Sergouniotis, Panagiotis I., Martin McKibbin, Anthony G. Robson, et al.. (2015). Disease Expression in Autosomal Recessive Retinal Dystrophy Associated With Mutations in theDRAM2Gene. Investigative Ophthalmology & Visual Science. 56(13). 8083–8083. 12 indexed citations
11.
Edwards, Thomas L., Benjamin Burt, Graeme C. Black, et al.. (2012). Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations. Clinical and Experimental Ophthalmology. 40(5). 476–483. 7 indexed citations
12.
Carr, Ian, Colin A. Johnson, Alex Markham, et al.. (2011). DominantMapper: Rule-based analysis of SNP data for rapid mapping of dominant diseases in related nuclear families. Human Mutation. 32(12). 1359–1366. 4 indexed citations
13.
Booth, Adam, et al.. (2008). Confirmation of a Locus for Primary Congenital Glaucoma (PCG) on Chromosome 14q24 in a Pakistani Pedigree. Investigative Ophthalmology & Visual Science. 49(13). 5123–5123. 1 indexed citations
14.
Craig, Jamie E., Alex W. Hewitt, David P. Dimasi, et al.. (2006). The role of the Met98Lys optineurin variant in inherited optic nerve diseases. British Journal of Ophthalmology. 90(11). 1420–1424. 13 indexed citations
15.
Williams, G. A., Eamonn Sheridan, Carmel Toomes, et al.. (2005). Investigation of Candidate Loci for Familial Nonsyndromic Human Strabismus. Investigative Ophthalmology & Visual Science. 46(13). 3825–3825.
16.
17.
Downey, Louise, et al.. (2004). Autosomal Recessive Inheritance of Familial Exudative Vitreoretinopathy. Investigative Ophthalmology & Visual Science. 45(13). 4760–4760.
18.
Toomes, Carmel, H.M. Bottomley, Richard M. Jackson, et al.. (2004). Mutations in LRP5 or FZD4 underlie the common FEVR locus on chromosome 11q13. Investigative Ophthalmology & Visual Science. 45(13). 1021–1021. 3 indexed citations
19.
Craig, Jamie E., et al.. (2002). Deletion of the OPA1 gene in a family with dominant optic atrophy: evidence that haploinsufficiency is the cause of disease. Journal of Medical Genetics. 39. 47–48. 4 indexed citations
20.
Ishwad, Chandramohan S., Michèle Shuster, Nalin Thakker, et al.. (1999). Frequent allelic loss and homozygous deletion in chromosome band 8p23 in oral cancer. International Journal of Cancer. 80(1). 25–31. 48 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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