Katie Sidle

10.6k total citations · 3 hit papers
25 papers, 3.8k citations indexed

About

Katie Sidle is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Katie Sidle has authored 25 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 14 papers in Neurology and 11 papers in Neurology. Recurrent topics in Katie Sidle's work include Neurological diseases and metabolism (14 papers), Prion Diseases and Protein Misfolding (14 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Katie Sidle is often cited by papers focused on Neurological diseases and metabolism (14 papers), Prion Diseases and Protein Misfolding (14 papers) and Amyotrophic Lateral Sclerosis Research (9 papers). Katie Sidle collaborates with scholars based in United Kingdom, Austria and Germany. Katie Sidle's co-authors include John Collinge, Andrew F. Hill, James W. Ironside, Julie Meads, Mark S. Palmer, Miles A. Whittington, John G. R. Jefferys, Anthony R. Clarke, Corinne J. Smith and John Collinge and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Katie Sidle

23 papers receiving 3.7k 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.

Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD

1996 1.3k citations John Collinge, Katie Sidle et al. Nature profile →
Prion protein is necessary for normal synaptic function

1994 595 citations John Collinge, Miles A. Whittington et al. Nature profile →
Neurofilament light chain

2015 390 citations Ching‐Hua Lu, Corrie Macdonald‐Wallis 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
Katie Sidle United Kingdom	17	3.2k	1.9k	1.1k	783	375	25	3.8k
Regina Kascsak United States	27	2.5k 0.8×	1.1k 0.6×	1.0k 0.9×	247 0.3×	351 0.9×	40	2.8k
Richard J. Kascsak United States	29	2.4k 0.7×	1.1k 0.6×	911 0.8×	159 0.2×	601 1.6×	56	2.8k
Anna Ladogana Italy	31	2.6k 0.8×	1.3k 0.7×	512 0.5×	1.0k 1.3×	519 1.4×	67	3.2k
Emmanuel A. Asante United Kingdom	23	2.2k 0.7×	1.1k 0.6×	673 0.6×	160 0.2×	494 1.3×	40	2.4k
Wen‐Quan Zou United States	29	2.8k 0.9×	1.6k 0.8×	944 0.9×	693 0.9×	552 1.5×	99	3.4k
Samantha L. Eaton United Kingdom	19	1.3k 0.4×	328 0.2×	290 0.3×	111 0.1×	260 0.7×	42	1.7k
S. B. Prusiner United States	31	3.5k 1.1×	1.9k 1.0×	1.5k 1.4×	224 0.3×	413 1.1×	56	3.6k
Nicole Salès France	18	1.4k 0.4×	475 0.3×	316 0.3×	119 0.2×	219 0.6×	24	1.7k
Martin Jeffrey United Kingdom	30	2.5k 0.8×	1.3k 0.7×	1.1k 1.0×	117 0.1×	344 0.9×	80	2.8k
Hao Pang China	24	947 0.3×	414 0.2×	71 0.1×	282 0.4×	282 0.8×	112	2.0k

Countries citing papers authored by Katie Sidle

Since Specialization

Citations

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

Fields of papers citing papers by Katie Sidle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katie Sidle

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Zampedri, Luca, Oliver J. Ziff, Christopher D. J. Sinclair, et al.. (2025). Muscle MRI quantifies disease progression in amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 96(9). 908–911.

Latorre, Anna, Lorenzo Rocchi, María Stamelou, et al.. (2018). Tremor in motor neuron disease may be central rather than peripheral in origin. European Journal of Neurology. 26(3). 394–394. 5 indexed citations

Morgan, Sarah, Aleksey Shatunov, William Sproviero, et al.. (2017). A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UK. Brain. 140(6). 1611–1618. 68 indexed citations

Lu, Ching‐Hua, Corrie Macdonald‐Wallis, Elizabeth Gray, et al.. (2015). Neurofilament light chain. Neurology. 84(22). 2247–2257. 390 indexed citations breakdown →

Rohrer, Jonathan D., Adrian M. Isaacs, Sarah Mizielinska, et al.. (2015). C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. The Lancet Neurology. 14(3). 291–301. 169 indexed citations

Morgan, Sarah, Maryam Shoai, Pietro Fratta, et al.. (2014). Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis. Neurobiology of Aging. 36(3). 1600.e5–1600.e8. 30 indexed citations

Fratta, Pietro, Toby Collins, Anny Devoy, et al.. (2013). Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 85(5). 506–508. 17 indexed citations

Spillane, Jennifer, Gerry Christofi, Katie Sidle, Dimitri M. Kullmann, & Robin Howard. (2013). Myasthenia gravis and neuromyelitis opica: A causal link. Multiple Sclerosis and Related Disorders. 2(3). 233–237. 11 indexed citations

Hill, Andrew F., Susan Joiner, Jonathan D. F. Wadsworth, et al.. (2003). Molecular classification of sporadic Creutzfeldt–Jakob disease. Brain. 126(6). 1333–1346. 254 indexed citations

10.

Almer, Gabriele, Johannes A. Hainfellner, Thomas Brücke, et al.. (1999). Fatal familial insomnia: a new Austrian family. Brain. 122(1). 5–16. 66 indexed citations

11.

Hill, Andrew F., et al.. (1998). Molecular screening of sheep for bovine spongiform encephalopathy. Neuroscience Letters. 255(3). 159–162. 80 indexed citations

12.

Collinge, John, Andrew F. Hill, Katie Sidle, & James W. Ironside. (1997). Biochemical typing of scrapie strains. Nature. 386(6625). 564–564. 25 indexed citations

13.

Windl, Otto, Maureen Dempster, J. Peter Estibeiro, et al.. (1996). Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Human Genetics. 98(3). 259–264. 164 indexed citations

14.

Collinge, John, Katie Sidle, Julie Meads, James W. Ironside, & Andrew F. Hill. (1996). Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. Nature. 383(6602). 685–690. 1308 indexed citations breakdown →

15.

Whittington, Miles A., Katie Sidle, Ian Gowland, et al.. (1995). Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein. Nature Genetics. 9(2). 197–201. 102 indexed citations

16.

Collinge, John, Miles A. Whittington, Katie Sidle, et al.. (1994). Prion protein is necessary for normal synaptic function. Nature. 370(6487). 295–297. 595 indexed citations breakdown →

17.

Telling, Glenn C., Michael Scott, Karen Hsiao, et al.. (1994). Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.. Proceedings of the National Academy of Sciences. 91(21). 9936–9940. 233 indexed citations

18.

Palmer, Mark S., Sukhvir P. Mahal, Tracy Campbell, et al.. (1993). Deletions in the prion protein gene are not associated with CJD. Human Molecular Genetics. 2(5). 541–544. 71 indexed citations

19.

Collinge, John, et al.. (1993). Inherited prion disease (PrP lysine 200) in Britain: two case reports.. BMJ. 306(6873). 301–302. 24 indexed citations

20.

Palmer, Mark S., Katie Sidle, Tracy Campbell, et al.. (1992). Absence of PRP gene mutation in patient showing PRP immunostaining. Neurobiology of Aging. 13. S94–S94. 2 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