A. Dalton

741 citations

17 papers · 448 indexed · h-index 13

Neurology top 10%
- Neurological diseases and metabolism 2
- Botulinum Toxin and Related Neurological Disorders 2
Cellular and Molecular Neuroscience top 10%
- Hereditary Neurological Disorders 4
Genetics
- Connective tissue disorders research 3
- Genomics and Rare Diseases 2
Clinical Biochemistry top 10%
Neurology
- Neurological diseases and metabolism 2
- Botulinum Toxin and Related Neurological Disorders 2
Pulmonary and Respiratory Medicine
- Neonatal Respiratory Health Research 3
- Tracheal and airway disorders 2
Molecular Biology
- Mitochondrial Function and Pathology 2

Co-authors: Alan Sprigg Patrick F. Chinnery Christopher McDermott Janine Kirby Channa Hewamadduma Pamela J. Shaw Jayne Leggo Patrick J. Morrison
Cited by: Neurology Cellular and Molecular Neuroscience Genetics
Journals: Neurology (4 papers)Journal of Inherited Metabolic Disease (2 papers)Journal of Medical Genetics (2 papers)
Partner nations: United Kingdom Australia Denmark

In The Last Decade

A. Dalton

17 papers receiving 434 citations

Peers

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

The 25 scholars most cited alongside A. Dalton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with A. Dalton Line = papers co-authored together A. Dalton links everyone, so they are left out of the graph.

All Works

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17 of 17 papers shown

#	Work
1	Specialist integrated haematological malignancy diagnostic services: an Activity Based Cost (ABC) analysis of a networked laboratory service model Journal of Clinical Pathology ·Taiyu Chen,Hasan Basarir,Camila Pineda Sepulvéda,Malee Fernando,D Pearson,Sue Ward,A Valverde Conde,Manuel Ángel Romero-García,Glenn V. Wilson,A. Dalton,P. Talley,David Barnett,云七,Nancy Porter,John T. Reilly,John A. Snowden	2015	3
2	The documentation of consent and disclosure of neurogenetic testing outside clinical genetics Neurogenetics ·Christine Lo,Joanne Martindale,Marios Hadjivassiliou,Paul Martin,A. Dalton,Oliver Bandmann	2014	2
3	Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth Bone ·A.P.H. Trivelli,Paul Arundel,Jackson Stermer,A. Dalton,Xingyu Gao,Jeanne Freeman,Nick Bishop	2010	14
4	HSP60 IS A RARE CAUSE OF HEREDITARY SPASTIC PARAPARESIS, BUT MAY ACT AS A GENETIC MODIFIER Neurology ·Channa Hewamadduma,Janine Kirby,Christopher J. Kershaw,Joanne Martindale,A. Dalton,Christopher McDermott,Pamela J. Shaw	2008	16
5	Unexplained fractures in infancy: looking for fragile bones Archives of Disease in Childhood ·Nivedita Shahane,Alan Sprigg,A. Dalton	2007	71
6	High frequency of missense mutations in glycogen storage disease type VI Journal of Inherited Metabolic Disease ·Nicholas Beauchamp,Joanna Taybert,M. P. Champion,Valérie Layet,Peter Heinz‐Erian,A. Dalton,M S Tanner,Ewa Pronicka,Mark Sharrard	2007	31
7	Children with recurrent fractures and low bone mass or idiopathic juvenile osteoporosis may have abnormalities in the canonical Wnt-signalling pathway through LRP5 Bone ·F.B.F. Alvarenga,R. J. Pollitt,A. Dalton,Anne Saarinen,Nick Bishop	2007	2
8	Pulmonary infection in mild variant cystic fibrosis: Implications for care Journal of Cystic Fibrosis ·Ethem Aplaydin,J McGaw,A. Dalton,P. Wb,Mark L. Everard,Chris Taylor	2006	15
9	Clinical features of hereditary spastic paraplegia due to spastin mutation Neurology ·Christopher McDermott,Christine Burness,Janine Kirby,Laura Cox,Dasappaiah Ganesh Rao,Channa Hewamadduma,Basil Sharrack,Marios Hadjivassiliou,Patrick F. Chinnery,A. Dalton,Pamela J. Shaw	2006	84
10	Strokelike presentation of Wilson disease with homozygosity for a novel T766R mutation Neurology ·Sarah T. Pendlebury,P M Rothwell,A. Dalton,Edward A. Burton	2004	13
11	Infantile hereditary spastic paraparesis due to codominant mutations in the spastin gene Neurology ·Patrick F. Chinnery,Sharon Keers,Max Märtens,Ramesh S. Ve,A. Dalton	2004	28
12	Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency Journal of Inherited Metabolic Disease ·S. E. Olpin,Y. Vargas-Luna,Geo. N. Carter,N. J. Manning,James R. Bonham,A. Dalton,J. V. Leonard,John M. Land,Brage Storstein Andresen,A. A. M. Morris,F. Muntoni,Douglass M. Turnbull,Morteza Pourfarzam,中村春樹,R. J. Pollitt	2003	43
13	Time-Course of Hypericin Phototoxicity and Effect on Mitochondrial Energies in EMT6 Mouse Mammary Carcinoma Cells Free Radical Biology and Medicine ·N. G. Han,A. Dalton,Ronald S. Pardini	1998	20
14	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 ·Jayne Leggo,A. Dalton,Patrick J. Morrison,A Dodge,Farnoush Farshidi,Maritha J. Kotze,David C. Rubinsztein	1997	64
15	Neonatal Screening for Cystic Fibrosis in the Trent Region (UK): Two-Stage Immunoreactive Trypsin Screening Compared with a Three-Stage Protocol with DNA Analysis as an Intermediate Step Journal of Medical Screening ·R. J. Pollitt,A. Dalton,G. Jellinek,H. Hughes,H. Namatsu	1997	20
16	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 ·Daniela T. Pilz,A. Dalton,Aidan A. Long,T. Jaspan,Edna L. Maltby,Oliver Quarrell	1995	8
17	Synergistic effects of azathioprine and ultraviolet light detected by sister chromatid exchange analysis Cancer Genetics and Cytogenetics ·A. Dalton,David Curtis,C.I. Harrington	1990	14

About A. Dalton

A. Dalton is a scholar working on Neurology, Orthopedics and Sports Medicine, Cellular and Molecular Neuroscience, Genetics and Clinical Biochemistry, having authored 17 papers that have together received 448 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (4 papers), Neonatal Respiratory Health Research (3 papers), Connective tissue disorders research (3 papers), Genomics and Rare Diseases (2 papers), Neurological diseases and metabolism (2 papers), Mitochondrial Function and Pathology (2 papers), Botulinum Toxin and Related Neurological Disorders (2 papers) and Tracheal and airway disorders (2 papers). The work is most often cited by research in Neurology (92 citations), Cellular and Molecular Neuroscience (179 citations), Genetics (73 citations), Clinical Biochemistry (46 citations) and Neurology (64 citations). A. Dalton has collaborated with scholars based in United Kingdom, Australia and Denmark. Frequent co-authors include Alan Sprigg, Patrick F. Chinnery, Christopher McDermott, Janine Kirby, Channa Hewamadduma, Pamela J. Shaw, Jayne Leggo, Patrick J. Morrison, David C. Rubinsztein and A Dodge. Their work appears in journals such as Neurology, Journal of Inherited Metabolic Disease, Journal of Medical Genetics, Bone and Journal of Clinical Pathology.

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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