M. Hutton

2.3k total citations
16 papers, 1.4k citations indexed

About

M. Hutton is a scholar working on Physiology, Neurology and Molecular Biology. According to data from OpenAlex, M. Hutton has authored 16 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Physiology, 5 papers in Neurology and 4 papers in Molecular Biology. Recurrent topics in M. Hutton's work include Alzheimer's disease research and treatments (8 papers), Cellular transport and secretion (3 papers) and Amyotrophic Lateral Sclerosis Research (2 papers). M. Hutton is often cited by papers focused on Alzheimer's disease research and treatments (8 papers), Cellular transport and secretion (3 papers) and Amyotrophic Lateral Sclerosis Research (2 papers). M. Hutton collaborates with scholars based in United States, United Kingdom and Canada. M. Hutton's co-authors include Michelle Wragg, Alison Goate, Chris J. Talbot, John Hardy, H. Backhovens, A. Hofman, Anita Wehnert, Marc Cruts, Peter St George‐Hyslop and Robin Sherrington and has published in prestigious journals such as The Lancet, Brain and Neurology.

In The Last Decade

M. Hutton

16 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Hutton United States 10 1.1k 546 426 314 238 16 1.4k
Marianne Hallupp Australia 17 727 0.7× 675 1.2× 460 1.1× 165 0.5× 303 1.3× 25 1.3k
Sally Serneels Belgium 11 753 0.7× 402 0.7× 270 0.6× 153 0.5× 113 0.5× 14 1.0k
H. Backhovens Belgium 15 678 0.6× 608 1.1× 189 0.4× 180 0.6× 177 0.7× 27 1.1k
Steven G. Younkin United States 12 680 0.6× 476 0.9× 246 0.6× 128 0.4× 147 0.6× 25 1.1k
Ellen Corsmit Belgium 14 558 0.5× 425 0.8× 312 0.7× 145 0.5× 203 0.9× 21 949
Michael W. DeLucia United States 11 882 0.8× 340 0.6× 456 1.1× 129 0.4× 207 0.9× 11 1.2k
Cécile Dumanchin France 12 1.4k 1.3× 988 1.8× 374 0.9× 322 1.0× 378 1.6× 17 2.2k
Janusz Frackowiak United States 21 888 0.8× 462 0.8× 254 0.6× 91 0.3× 164 0.7× 43 1.3k
Sumi Chakraverty United States 12 601 0.6× 448 0.8× 873 2.0× 118 0.4× 169 0.7× 16 1.3k
Steven G. Younkin United States 12 1.0k 1.0× 616 1.1× 85 0.2× 178 0.6× 260 1.1× 14 1.4k

Countries citing papers authored by M. Hutton

Since Specialization
Citations

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

Fields of papers citing papers by M. Hutton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Hutton

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

All Works

16 of 16 papers shown
1.
Fountain, Daniel M., et al.. (2022). Getting it right first time: national survey of surgical site infection 2019. Annals of The Royal College of Surgeons of England. 105(6). 513–522. 5 indexed citations
2.
Sewell, Mathew David, et al.. (2017). Assessing the amount of distraction needed for expandable anterior column cages in the cervical spine. Annals of The Royal College of Surgeons of England. 99(8). 659–660. 3 indexed citations
3.
Romanowski, C.A.J., M. Hutton, Jeremy Rowe, et al.. (2011). The Anatomy of the Medial Lemniscus within the Brainstem Demonstrated at 3 Tesla with High Resolution Fat Suppressed T1-Weighted Images and Diffusion Tensor Imaging. The Neuroradiology Journal. 24(2). 171–176. 8 indexed citations
4.
O’Farrell, Casey, Karen L. M. Martin, M. Hutton, et al.. (2009). Mutant torsinA interacts with tyrosine hydroxylase in cultured cells. Neuroscience. 164(3). 1127–1137. 15 indexed citations
5.
Baba, Yasuhiko, Isabelle Le Ber, Alexis Brice, et al.. (2007). Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation. Journal of Neural Transmission. 114(7). 947–950. 23 indexed citations
6.
Mackenzie, I. R. A., Matthew Baker, Stuart Pickering‐Brown, et al.. (2006). The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene. Brain. 129(11). 3081–3090. 226 indexed citations
7.
Boeve, Bradley F., Matthew B. Baker, Dennis W. Dickson, et al.. (2006). Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study. Brain. 129(11). 3103–3114. 84 indexed citations
8.
Utton, Michelle A., James W. Connell, Ayodeji A. Asuni, et al.. (2002). The mechanism of slow axonal transport of the microtubule-associated protein tau and the transport rates of different isoforms and mutants. UCL Discovery (University College London). 1 indexed citations
9.
Morris, Huw R., Matt Baker, Koji Yasojima, et al.. (2002). Analysis of tau haplotypes in Pick’s disease. Neurology. 59(3). 443–445. 34 indexed citations
10.
Cruts, Marc, Cornelia M. van Duijn, H. Backhovens, et al.. (1998). Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease. Human Molecular Genetics. 7(1). 43–51. 323 indexed citations
11.
Harvey, Richard, David W. Ellison, John Hardy, et al.. (1998). Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucineright-arrowserine (L250S) substitution at codon 250 of the presenilin 1 gene. Journal of Neurology Neurosurgery & Psychiatry. 64(1). 44–49. 46 indexed citations
12.
Hutton, M.. (1997). The presenilins and Alzheimer's disease. Human Molecular Genetics. 6(10). 1639–1646. 292 indexed citations
13.
Scheuner, Donalyn, Christopher B. Eckman, Martin Citron, et al.. (1996). 149 The Presenilin 1 and 2 mutations linked to familial Alzheimer's Disease increase the extracellular concentration of amyloid 0 protein (Aβ) ending at Aβ42(43). Neurobiology of Aging. 17(4). S38–S38. 2 indexed citations
14.
Wragg, Michelle, Chris J. Talbot, M. Hutton, & Alison Goate. (1996). Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. The Lancet. 347(9000). 509–512. 195 indexed citations
15.
Clark, Robert, M. Hutton, Chris J. Talbot, et al.. (1996). . Cold Spring Harbor Symposia on Quantitative Biology. 61(1). 551–558. 6 indexed citations
16.
Mann, D.M.A., Takeshi Iwatsubo, N. J. Cairns, et al.. (1996). Amyloid β protein (Aβ) deposition in chromosome 14–linked Alzheimer's disease: Predominance of Aβ42(43). Annals of Neurology. 40(2). 149–156. 155 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marianne Hallupp Breakdown of academic impact, for papers by Sally Serneels Breakdown of academic impact, for papers by H. Backhovens Breakdown of academic impact, for papers by Steven G. Younkin Breakdown of academic impact, for papers by Ellen Corsmit Breakdown of academic impact, for papers by Michael W. DeLucia Breakdown of academic impact, for papers by Cécile Dumanchin Breakdown of academic impact, for papers by Janusz Frackowiak Breakdown of academic impact, for papers by Sumi Chakraverty Breakdown of academic impact, for papers by Steven G. Younkin
Rankless by CCL
2026