Janice L. Holton

29.7k total citations · 6 hit papers
242 papers, 17.7k citations indexed

About

Janice L. Holton is a scholar working on Neurology, Molecular Biology and Physiology. According to data from OpenAlex, Janice L. Holton has authored 242 papers receiving a total of 17.7k indexed citations (citations by other indexed papers that have themselves been cited), including 166 papers in Neurology, 80 papers in Molecular Biology and 70 papers in Physiology. Recurrent topics in Janice L. Holton's work include Parkinson's Disease Mechanisms and Treatments (129 papers), Alzheimer's disease research and treatments (64 papers) and Neurological disorders and treatments (54 papers). Janice L. Holton is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (129 papers), Alzheimer's disease research and treatments (64 papers) and Neurological disorders and treatments (54 papers). Janice L. Holton collaborates with scholars based in United Kingdom, United States and Australia. Janice L. Holton's co-authors include Tamás Révész, Andrew J. Lees, Tammaryn Lashley, Henry Houlden, Niall Quinn, Helen Ling, David R. Williams, John Hardy, Rohan de Silva and Peter Kempster and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Janice L. Holton

238 papers receiving 17.3k citations

Hit Papers

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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.

Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation

2008 1.3k citations Jiayi Li, Elisabet Englund et al. Nature Medicine profile →
A common LRRK2 mutation in idiopathic Parkinson's disease

2005 575 citations Andrew Singleton, Andrew J. Lees et al. profile →
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism

2005 517 citations David R. Williams, Rohan de Silva et al. Brain profile →
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

2009 509 citations José Brás, Emma Deas et al. Brain profile →
Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?

2011 441 citations Laura Parkkinen, Sean S. O’Sullivan et al. Brain profile →
Prognosis and Neuropathologic Correlation of Clinical Subtypes of Parkinson Disease

2019 200 citations Eduardo De Pablo‐Fernández, Andrew J. Lees et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Janice L. Holton United Kingdom	71	11.6k	6.0k	4.7k	4.6k	3.9k	242	17.7k
Zbigniew K. Wszołek United States	73	12.5k 1.1×	5.6k 0.9×	4.6k 1.0×	5.3k 1.1×	5.0k 1.3×	461	18.9k
Tamás Révész United Kingdom	69	14.3k 1.2×	7.5k 1.2×	5.5k 1.2×	5.9k 1.3×	4.8k 1.2×	247	21.6k
Henry Houlden United Kingdom	70	7.0k 0.6×	6.7k 1.1×	8.9k 1.9×	7.0k 1.5×	5.1k 1.3×	512	20.7k
Christine Klein Germany	70	14.9k 1.3×	2.8k 0.5×	6.1k 1.3×	8.3k 1.8×	3.3k 0.8×	500	22.4k
Thomas Klockgether Germany	80	10.7k 0.9×	3.8k 0.6×	8.8k 1.9×	10.2k 2.2×	4.1k 1.1×	386	23.9k
Rob A. I. de Vos Netherlands	46	10.2k 0.9×	3.5k 0.6×	3.5k 0.8×	4.8k 1.0×	2.9k 0.7×	79	15.7k
Gen Sobue Japan	82	11.6k 1.0×	4.2k 0.7×	12.4k 2.7×	9.6k 2.1×	2.9k 0.7×	754	28.1k
Shigeo Murayama Japan	61	6.0k 0.5×	5.8k 1.0×	5.4k 1.2×	2.9k 0.6×	2.8k 0.7×	409	14.2k
Shoji Tsuji Japan	65	6.7k 0.6×	3.3k 0.5×	8.8k 1.9×	6.7k 1.5×	2.3k 0.6×	507	17.1k
Lawrence I. Golbe United States	41	12.5k 1.1×	4.1k 0.7×	3.2k 0.7×	5.4k 1.2×	3.0k 0.8×	99	15.9k

Countries citing papers authored by Janice L. Holton

Since Specialization

Citations

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

Fields of papers citing papers by Janice L. Holton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janice L. Holton. 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 Janice L. Holton. The network helps show where Janice L. Holton may publish in the future.

Co-authorship network of co-authors of Janice L. Holton

This figure shows the co-authorship network connecting the top 25 collaborators of Janice L. Holton. A scholar is included among the top collaborators of Janice L. Holton 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 Janice L. Holton. Janice L. Holton 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

Vichayanrat, Ekawat, Fernanda Valério, Eduardo De Pablo‐Fernández, et al.. (2022). Diagnosing Premotor Multiple System Atrophy. Neurology. 99(11). e1168–e1177. 6 indexed citations

Holton, Janice L., et al.. (2021). Neurodegenerative movement disorders: An epigenetics perspective and promise for the future. Neuropathology and Applied Neurobiology. 47(7). 897–909. 18 indexed citations

Pablo‐Fernández, Eduardo De, et al.. (2021). Faster disease progression in Parkinson’s disease with type 2 diabetes is not associated with increased α‐synuclein, tau, amyloid‐β or vascular pathology. Neuropathology and Applied Neurobiology. 47(7). 1080–1091. 22 indexed citations

Bugiardini, Enrico, Emanuela Bottani, Silvia Marchet, et al.. (2020). Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations. Neurology Genetics. 6(1). e381–e381. 25 indexed citations

Heras‐Garvin, Antonio, et al.. (2020). Signs of Chronic Hypoxia Suggest a Novel Pathophysiological Event in α‐Synucleinopathies. Movement Disorders. 35(12). 2333–2338. 12 indexed citations

Lamb, Ruth, Jonathan D. Rohrer, Raquel Real, et al.. (2019). A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders. Molecular Case Studies. 5(3). a003913–a003913. 22 indexed citations

Olivier, P.A.S., Boél De Paepe, Eleonora Aronica, et al.. (2019). Idiopathic inflammatory myopathy. Neurology. 93(9). e889–e894. 15 indexed citations

Jabbari, Edwin, John Woodside, Manuela Tan, et al.. (2019). The genetic and clinico‐pathological profile of early‐onset progressive supranuclear palsy. Movement Disorders. 34(9). 1307–1314. 16 indexed citations

Batla, Amit, Eduardo De Pablo‐Fernández, Roberto Erro, et al.. (2018). Young‐onset multiple system atrophy: Clinical and pathological features. Movement Disorders. 33(7). 1099–1107. 24 indexed citations

10.

Ling, Helen, Gábor G. Kovács, Jean Paul Vonsattel, et al.. (2016). Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology. Brain. 139(12). 3237–3252. 101 indexed citations

11.

Pelayo‐Negro, Ana L., Zane Jaunmuktane, R. Scalco, et al.. (2015). Transthyretin V122I amyloidosis with clinical and histological evidence of amyloid neuropathy and myopathy. Neuromuscular Disorders. 25(6). 511–515. 19 indexed citations

12.

Massey, Luke A., Hans Rolf Jäger, Dominic Paviour, et al.. (2013). The midbrain to pons ratio. Neurology. 80(20). 1856–1861. 120 indexed citations

13.

Sallum, Adriana Maluf Elias, Hemlata Varsani, Janice L. Holton, Suely Kazue Nagahashi Marie, & Lucy R. Wedderburn. (2013). Morphometric analyses of normal pediatric brachial biceps and quadriceps muscle tissue.. PubMed. 28(4). 525–30. 15 indexed citations

14.

Ozawa, Tetsutaro, Tamás Révész, Dominic Paviour, et al.. (2012). Difference in MSA Phenotype Distribution between Populations: Genetics or Environment?. Journal of Parkinson s Disease. 2(1). 7–18. 29 indexed citations

15.

Massey, Luke A., Ludvic Zrinzo, Harold G. Parkes, et al.. (2011). High resolution MR anatomy of the subthalamic nucleus: Imaging at 9.4T with histological validation. NeuroImage. 59(3). 2035–2044. 74 indexed citations

16.

Brás, José, Emma Deas, Sean S. O’Sullivan, et al.. (2009). Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain. 132(7). 1783–1794. 509 indexed citations breakdown →

17.

Li, Jiayi, Elisabet Englund, Janice L. Holton, et al.. (2008). Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation. Nature Medicine. 14(5). 501–503. 1325 indexed citations breakdown →

18.

Williams, David R., Janice L. Holton, Catherine Strand, et al.. (2007). Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome. Brain. 130(6). 1566–1576. 303 indexed citations

19.

Williams, David R., Rohan de Silva, Dominic Paviour, et al.. (2005). Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism. Brain. 128(6). 1247–1258. 517 indexed citations breakdown →

20.

Frangione, B, T Révész, Rubén Vidal, et al.. (2001). Familial cerebral amyloid angiopathy related to stroke and dementia.. PubMed. 8 Suppl 1. 36–42. 23 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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