Robert Barber

4.6k total citations
31 papers, 2.4k citations indexed

About

Robert Barber is a scholar working on Psychiatry and Mental health, Physiology and Neurology. According to data from OpenAlex, Robert Barber has authored 31 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Psychiatry and Mental health, 8 papers in Physiology and 5 papers in Neurology. Recurrent topics in Robert Barber's work include Dementia and Cognitive Impairment Research (10 papers), Alzheimer's disease research and treatments (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (4 papers). Robert Barber is often cited by papers focused on Dementia and Cognitive Impairment Research (10 papers), Alzheimer's disease research and treatments (7 papers) and Neuroinflammation and Neurodegeneration Mechanisms (4 papers). Robert Barber collaborates with scholars based in United Kingdom, United States and Australia. Robert Barber's co-authors include John T. O’Brien, Raj N. Kalaria, Paul G. Ince, Fiona E. Matthews, Evelyn Jaros, Robert H. Perry, Stephen B. Wharton, Pamela J. Shaw, Carol Brayne and Malee Fernando and has published in prestigious journals such as Brain, Neurology and Stroke.

In The Last Decade

Robert Barber

30 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert Barber United Kingdom 21 858 707 694 593 413 31 2.4k
Robert Barber United Kingdom 26 1.4k 1.6× 658 0.9× 906 1.3× 687 1.2× 642 1.6× 38 2.7k
Young Noh South Korea 27 773 0.9× 396 0.6× 581 0.8× 508 0.9× 418 1.0× 114 1.9k
Ling Zheng United States 25 922 1.1× 409 0.6× 575 0.8× 346 0.6× 222 0.5× 54 2.4k
Byoung Seok Ye South Korea 30 1.0k 1.2× 515 0.7× 842 1.2× 871 1.5× 417 1.0× 149 2.6k
John Wade United Kingdom 18 804 0.9× 307 0.4× 674 1.0× 547 0.9× 207 0.5× 34 2.5k
Franco Giubilei Italy 29 484 0.6× 386 0.5× 440 0.6× 526 0.9× 265 0.6× 80 2.5k
Alessandra Canuto Switzerland 27 833 1.0× 384 0.5× 400 0.6× 529 0.9× 178 0.4× 63 2.0k
Joel H. Kramer United States 25 1.4k 1.6× 407 0.6× 1.2k 1.7× 719 1.2× 466 1.1× 51 3.5k
Raija Ylikoski Finland 28 1.2k 1.4× 789 1.1× 482 0.7× 511 0.9× 308 0.7× 36 2.9k
Ana Verdelho Portugal 29 1.0k 1.2× 718 1.0× 341 0.5× 560 0.9× 376 0.9× 65 2.6k

Countries citing papers authored by Robert Barber

Since Specialization
Citations

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

Fields of papers citing papers by Robert Barber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Barber

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Barber. A scholar is included among the top collaborators of Robert Barber 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 Robert Barber. Robert Barber 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.
Barber, Robert, et al.. (2025). miRNA mediated mitochondrial function and gene regulation associated with Alzheimer’s disease. Frontiers in Aging. 6. 1582812–1582812. 1 indexed citations
2.
Allan, Louise, Tara Homer, Shannon Robalino, et al.. (2019). An intervention to improve outcomes of falls in dementia: the DIFRID mixed-methods feasibility study. Health Technology Assessment. 23(59). 1–208. 7 indexed citations
3.
Bamford, Claire, Fiona Beyer, Chris Fox, et al.. (2019). Developing an Intervention for Fall-Related Injuries in Dementia (DIFRID): an integrated, mixed-methods approach. BMC Geriatrics. 19(1). 57–57. 5 indexed citations
4.
Allan, Louise, Chris Fox, Denise Howel, et al.. (2018). Is it feasible to deliver a complex intervention to improve the outcome of falls in people with dementia? A protocol for the DIFRID feasibility study. Pilot and Feasibility Studies. 4(1). 170–170. 5 indexed citations
6.
Edwards, Melissa, et al.. (2014). Regional specific groundwater arsenic levels and neuropsychological functioning: a cross-sectional study. International Journal of Environmental Health Research. 24(6). 546–557. 20 indexed citations
7.
Barber, Robert, et al.. (2013). Therapeutic lying in dementia care. Nursing Standard. 28(1). 35–39. 36 indexed citations
8.
Burton, Emma J., Elizabeta B. Mukaetova‐Ladinska, Robert H. Perry, et al.. (2011). Neuropathological correlates of volumetric MRI in autopsy-confirmed Lewy body dementia. Neurobiology of Aging. 33(7). 1228–1236. 36 indexed citations
9.
Firbank, Michael, Louise Allan, Emma J. Burton, et al.. (2011). Neuroimaging predictors of death and dementia in a cohort of older stroke survivors. Journal of Neurology Neurosurgery & Psychiatry. 83(3). 263–267. 20 indexed citations
10.
Köhler, Sebastian, Alan Thomas, Adrian J. Lloyd, et al.. (2010). White matter hyperintensities, cortisol levels, brain atrophy and continuing cognitive deficits in late-life depression. The British Journal of Psychiatry. 196(2). 143–149. 96 indexed citations
11.
12.
Simpson, Julie E., Paul G. Ince, Catherine Gelsthorpe, et al.. (2007). Microglial activation in white matter lesions and nonlesional white matter of ageing brains. Neuropathology and Applied Neurobiology. 33(6). 670–683. 113 indexed citations
13.
Fernando, M. Shanika, Luke Clark, Paul G. Ince, et al.. (2007). White matter lesions in an unselected cohort of the elderly: astrocytic, microglial and oligodendrocyte precursor cell responses. Neuropathology and Applied Neurobiology. 33(4). 410–419. 171 indexed citations
14.
Fernando, Malee, Julie E. Simpson, Fiona E. Matthews, et al.. (2006). White Matter Lesions in an Unselected Cohort of the Elderly. Stroke. 37(6). 1391–1398. 463 indexed citations
15.
Lloyd, Adrian J., I. Nicol Ferrier, Robert Barber, et al.. (2004). Hippocampal volume change in depression: Late- and early-onset illness compared. The British Journal of Psychiatry. 184(6). 488–495. 138 indexed citations
16.
Barber, Robert. (2002). Volumetric MRI study of the caudate nucleus in patients with dementia with Lewy bodies, Alzheimer's disease, and vascular dementia. Journal of Neurology Neurosurgery & Psychiatry. 72(3). 406–407. 73 indexed citations
17.
Ballard, Clive, Ian Powell, Ian James, et al.. (2002). Can psychiatric liaison reduce neuroleptic use and reduce health service utilization for dementia patients residing in care facilities. International Journal of Geriatric Psychiatry. 17(2). 140–145. 44 indexed citations
18.
Barber, Robert, et al.. (2001). Dementia with Lewy bodies: diagnosis and management. International Journal of Geriatric Psychiatry. 16(S1). S12–S18. 66 indexed citations
19.
McKeith, Ian G., Clive Ballard, Robert H. Perry, et al.. (2000). Prospective validation of Consensus criteria for the diagnosis of dementia with Lewy bodies. Neurology. 54(5). 1050–1058. 335 indexed citations
20.
Stewart, Alice, et al.. (1962). Adult Leukaemias and Diagnostic X Rays. BMJ. 2(5309). 882–890. 56 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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