Ione Woollacott

3.5k total citations · 2 hit papers
26 papers, 1.4k citations indexed

About

Ione Woollacott is a scholar working on Neurology, Physiology and Neurology. According to data from OpenAlex, Ione Woollacott has authored 26 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 10 papers in Physiology and 7 papers in Neurology. Recurrent topics in Ione Woollacott's work include Amyotrophic Lateral Sclerosis Research (11 papers), Alzheimer's disease research and treatments (10 papers) and Dementia and Cognitive Impairment Research (5 papers). Ione Woollacott is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (11 papers), Alzheimer's disease research and treatments (10 papers) and Dementia and Cognitive Impairment Research (5 papers). Ione Woollacott collaborates with scholars based in United Kingdom, Sweden and Germany. Ione Woollacott's co-authors include Jonathan D. Rohrer, Simon Mead, Jason D. Warren, Jonathan M. Schott, Nick C. Fox, Henrik Zetterberg, Andrew J. Nicoll, Karen Cleverley, Sebastian Grönke and J. Pietrzyk and has published in prestigious journals such as Science, Neurology and Journal of Neurochemistry.

In The Last Decade

Ione Woollacott

24 papers receiving 1.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins

2014 510 citations Sarah Mizielinska, Sebastian Grönke et al. Science profile →
Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia

2016 319 citations Jonathan D. Rohrer, Ione Woollacott et al. Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ione Woollacott United Kingdom	16	816	465	462	314	278	26	1.4k
Tim Van Langenhove Belgium	11	718 0.9×	339 0.7×	316 0.7×	263 0.8×	367 1.3×	23	1.1k
Jon Beck United Kingdom	17	1.0k 1.3×	699 1.5×	743 1.6×	249 0.8×	561 2.0×	25	1.8k
Anne Sieben Belgium	17	472 0.6×	335 0.7×	305 0.7×	174 0.6×	159 0.6×	50	1.1k
Harro Seelaar Netherlands	21	1.2k 1.5×	873 1.9×	417 0.9×	195 0.6×	425 1.5×	72	1.9k
Alice Vajda Ireland	26	1.6k 2.0×	372 0.8×	284 0.6×	655 2.1×	316 1.1×	54	1.9k
Linda Gibbons United Kingdom	13	555 0.7×	470 1.0×	191 0.4×	137 0.4×	209 0.8×	20	1.1k
Bi Zhao China	26	1.5k 1.8×	274 0.6×	410 0.9×	215 0.7×	383 1.4×	146	2.0k
Anna M. Karydas United States	18	733 0.9×	849 1.8×	514 1.1×	138 0.4×	380 1.4×	24	1.9k
Marsel Mesulam United States	8	512 0.6×	266 0.6×	338 0.7×	207 0.7×	138 0.5×	14	981
Edoardo Gioele Spinelli Italy	22	792 1.0×	396 0.9×	229 0.5×	257 0.8×	210 0.8×	58	1.5k

Countries citing papers authored by Ione Woollacott

Since Specialization

Citations

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

Fields of papers citing papers by Ione Woollacott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ione Woollacott

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

All Works

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20 of 20 papers shown

Cope, Heidi, Emma Heslop, Alexandra Johnson, et al.. (2024). Clinician Perspectives of Gene Therapy as a Treatment Option for Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases. 11(5). 1085–1093.

Sim, Peng Yong, et al.. (2021). Idiopathic intracranial hypertension presenting as iron deficiency anemia: a case report. Journal of Medical Case Reports. 15(1). 45–45. 4 indexed citations

Sogorb‐Esteve, Aitana, Imogen J. Swift, Ione Woollacott, et al.. (2021). Differential chemokine alteration in the variants of primary progressive aphasia—a role for neuroinflammation. Journal of Neuroinflammation. 18(1). 224–224. 15 indexed citations

Woollacott, Ione, Jennifer M. Nicholas, Carolin Heller, et al.. (2020). Cerebrospinal Fluid YKL-40 and Chitotriosidase Levels in Frontotemporal Dementia Vary by Clinical, Genetic and Pathological Subtype. Dementia and Geriatric Cognitive Disorders. 49(1). 56–76. 29 indexed citations

Swift, Imogen J., Martina Bocchetta, Hanya Benotmane, et al.. (2020). Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature. Neurobiology of Aging. 99. 100.e9–100.e15. 14 indexed citations

Foiani, Martha, Claudia Cicognola, Natalia Ermann, et al.. (2019). Searching for novel cerebrospinal fluid biomarkers of tau pathology in frontotemporal dementia: an elusive quest. Journal of Neurology Neurosurgery & Psychiatry. 90(7). 740–746. 24 indexed citations

Brinkmalm, Ann, Martha Foiani, Ione Woollacott, et al.. (2019). CSF synaptic protein concentrations are raised in those with atypical Alzheimer’s disease but not frontotemporal dementia. Alzheimer s Research & Therapy. 11(1). 105–105. 42 indexed citations

Bond, Rebecca L., Charles R. Marshall, Chris JD Hardy, et al.. (2019). Sleep symptoms in syndromes of frontotemporal dementia and Alzheimer’s disease: A proof-of-principle behavioural study. eNeurologicalSci. 17. 100212–100212. 22 indexed citations

Shafei, Rachelle, Ione Woollacott, Catherine J. Mummery, et al.. (2019). Two pathologically confirmed cases of novel mutations in the MAPT gene causing frontotemporal dementia. Neurobiology of Aging. 87. 141.e15–141.e20. 7 indexed citations

10.

Woollacott, Ione, Martina Bocchetta, Carole H. Sudre, et al.. (2018). Pathological correlates of white matter hyperintensities in a case of progranulin mutation associated frontotemporal dementia. Neurocase. 24(3). 166–174. 35 indexed citations

11.

Foiani, Martha, Ione Woollacott, Carolin Heller, et al.. (2018). Plasma tau is increased in frontotemporal dementia. Journal of Neurology Neurosurgery & Psychiatry. 89(8). 804–807. 44 indexed citations

12.

Woollacott, Ione, Jennifer M. Nicholas, Amanda Heslegrave, et al.. (2018). Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup. Alzheimer s Research & Therapy. 10(1). 79–79. 47 indexed citations

13.

Bocchetta, Martina, Emilie Brotherhood, Ione Woollacott, et al.. (2016). The clinical, neuroanatomical, and neuropathologic phenotype of TBK1‐associated frontotemporal dementia: A longitudinal case report. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 6(1). 75–81. 26 indexed citations

14.

Rohrer, Jonathan D., Ione Woollacott, Katrina M. Dick, et al.. (2016). Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia. Neurology. 87(13). 1329–1336. 319 indexed citations breakdown →

15.

Clark, Camilla N., Jennifer M. Nicholas, Susie M.D. Henley, et al.. (2015). Humour processing in frontotemporal lobar degeneration: A behavioural and neuroanatomical analysis. Cortex. 69. 47–59. 37 indexed citations

16.

Mizielinska, Sarah, Sebastian Grönke, Teresa Niccoli, et al.. (2014). C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins. Science. 345(6201). 1192–1194. 510 indexed citations breakdown →

17.

Woollacott, Ione, Phillip D. Fletcher, Luke A. Massey, et al.. (2014). Compulsive versifying after treatment of transient epileptic amnesia. Neurocase. 21(5). 548–553. 5 indexed citations

18.

Woollacott, Ione & Simon Mead. (2014). The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues. Acta Neuropathologica. 127(3). 319–332. 44 indexed citations

19.

Jones, Ashley, Ione Woollacott, Aleksey Shatunov, et al.. (2013). Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeat. Neurobiology of Aging. 34(9). 2234.e1–2234.e7. 16 indexed citations

20.

Woollacott, Ione, Catherine Scott, David R. Fish, Shelagh M. Smith, & Matthew C. Walker. (2010). When do psychogenic nonepileptic seizures occur on a video/EEG telemetry unit?. Epilepsy & Behavior. 17(2). 228–235. 16 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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