A. Dalton

741 total citations
17 papers, 448 citations indexed

About

A. Dalton is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, A. Dalton has authored 17 papers receiving a total of 448 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in A. Dalton's work include Hereditary Neurological Disorders (4 papers), Neonatal Respiratory Health Research (3 papers) and Connective tissue disorders research (3 papers). A. Dalton is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Neonatal Respiratory Health Research (3 papers) and Connective tissue disorders research (3 papers). A. Dalton collaborates with scholars based in United Kingdom, France and Austria. A. Dalton's co-authors include Alan Sprigg, Patrick F. Chinnery, Channa Hewamadduma, Pamela J. Shaw, Janine Kirby, Christopher McDermott, Maritha J. Kotze, David C. Rubinsztein, Jayne Leggo and A Dodge and has published in prestigious journals such as Neurology, Free Radical Biology and Medicine and Bone.

In The Last Decade

A. Dalton

17 papers receiving 434 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Dalton United Kingdom 13 179 137 92 73 71 17 448
Mariona Guitart‐Mampel Spain 17 37 0.2× 252 1.8× 17 0.2× 62 0.8× 53 0.7× 40 578
T. M. Vanier United Kingdom 9 94 0.5× 106 0.8× 9 0.1× 55 0.8× 28 0.4× 15 343
Athina Xaidara Greece 10 16 0.1× 121 0.9× 18 0.2× 19 0.3× 55 0.8× 21 355
Megumi Shibata Japan 11 40 0.2× 98 0.7× 14 0.2× 24 0.3× 21 0.3× 34 351
Muhammad Talal Alrifai Saudi Arabia 12 47 0.3× 157 1.1× 9 0.1× 11 0.2× 82 1.2× 28 444
Stephen O’Riordan United Kingdom 12 56 0.3× 113 0.8× 9 0.1× 14 0.2× 185 2.6× 17 709
Jackie Imrie United Kingdom 15 16 0.1× 110 0.8× 16 0.2× 16 0.2× 37 0.5× 22 773
Akiyo Hineno Japan 13 31 0.2× 101 0.7× 69 0.8× 48 0.7× 4 0.1× 34 432
Norberto Guelbert Argentina 16 25 0.1× 148 1.1× 8 0.1× 30 0.4× 58 0.8× 39 651

Countries citing papers authored by A. Dalton

Since Specialization
Citations

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

Fields of papers citing papers by A. Dalton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Dalton

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

All Works

17 of 17 papers shown
1.
Basarir, Hasan, Malee Fernando, D Pearson, et al.. (2015). Specialist integrated haematological malignancy diagnostic services: an Activity Based Cost (ABC) analysis of a networked laboratory service model. Journal of Clinical Pathology. 68(4). 292–300. 3 indexed citations
2.
Lo, Christine, Joanne Martindale, Marios Hadjivassiliou, et al.. (2014). The documentation of consent and disclosure of neurogenetic testing outside clinical genetics. Neurogenetics. 15(1). 19–21. 2 indexed citations
3.
Arundel, Paul, et al.. (2010). Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth. Bone. 47(5). 989–994. 14 indexed citations
4.
Hewamadduma, Channa, Janine Kirby, Christopher J. Kershaw, et al.. (2008). HSP60 IS A RARE CAUSE OF HEREDITARY SPASTIC PARAPARESIS, BUT MAY ACT AS A GENETIC MODIFIER. Neurology. 70(19). 1717–1718. 16 indexed citations
5.
Sprigg, Alan, et al.. (2007). Unexplained fractures in infancy: looking for fragile bones. Archives of Disease in Childhood. 92(3). 251–256. 71 indexed citations
6.
Beauchamp, Nicholas, Joanna Taybert, M. P. Champion, et al.. (2007). High frequency of missense mutations in glycogen storage disease type VI. Journal of Inherited Metabolic Disease. 30(5). 722–734. 31 indexed citations
7.
8.
McGaw, J, et al.. (2006). Pulmonary infection in mild variant cystic fibrosis: Implications for care. Journal of Cystic Fibrosis. 5(2). 101–104. 15 indexed citations
9.
McDermott, Christopher, Christine Burness, Janine Kirby, et al.. (2006). Clinical features of hereditary spastic paraplegia due to spastin mutation. Neurology. 67(1). 45–51. 84 indexed citations
10.
Chinnery, Patrick F., et al.. (2004). Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene. Neurology. 63(4). 710–712. 28 indexed citations
11.
Pendlebury, Sarah T., P M Rothwell, A. Dalton, & Edward A. Burton. (2004). Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation. Neurology. 63(10). 1982–1983. 13 indexed citations
12.
Olpin, S. E., N. J. Manning, James R. Bonham, et al.. (2003). Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency. Journal of Inherited Metabolic Disease. 26(6). 543–557. 43 indexed citations
13.
Dalton, A., et al.. (1998). Time-Course of Hypericin Phototoxicity and Effect on Mitochondrial Energies in EMT6 Mouse Mammary Carcinoma Cells. Free Radical Biology and Medicine. 25(2). 144–152. 20 indexed citations
14.
Leggo, Jayne, A. Dalton, Patrick J. Morrison, et al.. (1997). Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.. Journal of Medical Genetics. 34(12). 982–985. 64 indexed citations
15.
16.
Pilz, Daniela T., A. Dalton, Aidan A. Long, et al.. (1995). Detecting deletions in the critical region for lissencephaly on 17p13.3 using fluorescent in situ hybridisation and a PCR assay identifying a dinucleotide repeat polymorphism.. Journal of Medical Genetics. 32(4). 275–278. 8 indexed citations
17.
Dalton, A., David Curtis, & C.I. Harrington. (1990). Synergistic effects of azathioprine and ultraviolet light detected by sister chromatid exchange analysis. Cancer Genetics and Cytogenetics. 45(1). 93–99. 14 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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