Jon Warner

2.9k total citations
37 papers, 1.8k citations indexed

About

Jon Warner is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Jon Warner has authored 37 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in Jon Warner's work include Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (5 papers) and Colorectal Cancer Screening and Detection (4 papers). Jon Warner is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (5 papers) and Colorectal Cancer Screening and Detection (4 papers). Jon Warner collaborates with scholars based in United Kingdom, United States and Switzerland. Jon Warner's co-authors include Robert J. Krushell, Alain‐Charles Masquelet, Christian Gerber, D. J. H. Brock, David T. Bonthron, D. J. H. Brock, Mary Porteous, David Fitzpatrick, David J. Dow and David Goudie and has published in prestigious journals such as Nature Genetics, Journal of Bone and Joint Surgery and Biochemical Journal.

In The Last Decade

Jon Warner

37 papers receiving 1.7k citations

Peers

Countries citing papers authored by Jon Warner

Since Specialization

Citations

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

Fields of papers citing papers by Jon Warner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jon Warner

This figure shows the co-authorship network connecting the top 25 collaborators of Jon Warner. A scholar is included among the top collaborators of Jon Warner 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 Jon Warner. Jon Warner 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

#	Work	Indexed citations
1	Survey of Pathologic Microorganisms in the Streams Along the Tahoe Rim Trail 2025 ·Wilderness and Environmental Medicine ·Heather J. Miller, (unknown), Jon Warner, (unknown), (unknown), Adrian G. Cummins, (unknown), David C. Fiore	1
2	Relationship between neuropsychiatric disorders and cognitive and behavioural change in MND 2019 ·Journal of Neurology Neurosurgery & Psychiatry ·Caroline McHutchison, Danielle Leighton, Andrew M. McIntosh, Elaine Cleary, Jon Warner, Mary Porteous, Siddharthan Chandran, Suvankar Pal, Sharon Abrahams	17
3	De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1 2018 ·European Journal of Human Genetics ·Sarah A. Cumming, Mark Hamilton, (unknown), Helen Gregory, Catherine McWilliam, Anneli Cooper, Berit Adam, (unknown), Graham Hamilton, Pawel Herzyk, Michael Tschannen, Elizabeth A. Worthey, Richard Petty, (unknown), Jon Warner, Maria Elena Farrugia, Cheryl Longman, Darren G. Monckton	69
4	PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption 2018 ·Frontiers in Cellular Neuroscience ·Suran Nethisinghe, (unknown), Sally Pemble, Mary G. Sweeney, Robyn Labrum, Katarina Manso, David Moore, Jon Warner, Mary B. Davis, Paola Giunti	16
5	Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis 2017 ·Acta Neuropathologica ·Christopher M. Henstridge, (unknown), Emily Carroll, (unknown), (unknown), Makis Tzioras, Chris-Anne McKenzie, Colin Smith, Christine A. F. Von Arnim, Albert C. Ludolph, Dorothée Lulé, Danielle Leighton, Jon Warner, Elaine Cleary, Judith Newton, Robert Swingler, Siddharthan Chandran, Thomas H. Gillingwater, Sharon Abrahams, Tara L. Spires‐Jones	85
6	Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions 2016 ·Molecular and Cellular Probes ·Elaine Cleary, Suvankar Pal, (unknown), David Moore, Robert Swingler, George Gorrie, Laura Stephenson, Shuna Colville, Siddharthan Chandran, Mary Porteous, Jon Warner	33
7	Genetic epidemiology of motor neuron disease-associated variants in the Scottish population 2016 ·Neurobiology of Aging ·(unknown), Danielle Leighton, Elaine Cleary, (unknown), Laura Stephenson, Shuna Colville, David Ross, Jon Warner, Mary Porteous, George Gorrie, Robert Swingler, David B. Goldstein, Matthew Harms, Peter Connick, Suvankar Pal, Timothy J. Aitman, Siddharthan Chandran	33
8	Semi-dominant X-chromosome linked learning disability with progressive ataxia, spasticity and dystonia associated with the novel MECP2 variant p.V122A: Akin to the new MECP2 duplication syndrome? 2009 ·European Journal of Paediatric Neurology ·Catherine McWilliam, Andrew Cooke, Daniela Lobo, Jon Warner, Matthew R.G. Taylor, John Tolmie	1
9	Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings 2007 ·Acta Neurologica Scandinavica ·Lorna Torrens, Edith Burns, Jon Stone, Cynthia A. Graham, (unknown), David Summers, Robin Sellar, Mary Porteous, Jon Warner, Adam Zeman	19
10	Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer 2007 ·Human Mutation ·Rebecca A. Barnetson, (unknown), (unknown), (unknown), (unknown), Susan M. Farrington, Nicola Williams, Jon Warner, Harry Campbell, Mary Porteous, Malcolm G. Dunlop	59
11	Spinocerebellar ataxia type 8 in Scotland 2004 ·Journal of Neurology Neurosurgery & Psychiatry ·Adam Zeman, Jon Stone, Mary Porteous, Edith Burns, L Barron, Jon Warner	1
12	Organization of the Human Glucokinase Regulator GeneGCKR 1998 ·Genomics ·Bruce E. Hayward, (unknown), (unknown), J.P. Leek, Alex Markham, Jon Warner, David T. Bonthron	19
13	BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland 1997 ·British Journal of Cancer ·Peter Mullen, WR Miller, James Mackay, David Fitzpatrick, SP Langdon, Jon Warner	8
14	Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23 1996 ·Mammalian Genome ·Bruce E. Hayward, Judy Fantes, Jon Warner, (unknown), J.P. Leek, Alex Markham, David T. Bonthron	21
15	A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12. 1995 ·Genome Research ·David W. Johnson, Jonathan Berg, Carol J. Gallione, Kimberly A. McAllister, Jon Warner, E.A. Helmbold, Dorene S. Markel, Charles E. Jackson, Mary Porteous, Douglas A. Marchuk	124
16	Chromosomal organisation of a repeated gene cluster expressed in mammalian stages of Leishmania 1995 ·Gene ·Ben L. Kelly, Sabrina D. Dyall, Jon Warner, Jun Tang, Deborah F. Smith	6
17	The ASP1 gene of Saccharomyces cerevisiae, encoding the intracellular isozyme of l-asparaginase 1994 ·Gene ·Kathryn Sinclair, Jon Warner, David T. Bonthron	21
18	A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population 1994 ·Human Molecular Genetics ·(unknown), (unknown), S Holloway, D. J. H. Brock, Jon Warner	23
19	A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes 1993 ·Molecular and Cellular Probes ·Jon Warner, (unknown), D. J. H. Brock	188
20	Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig 1992 ·Prenatal Diagnosis ·Yun‐Ling Zheng, M.A. Ferguson‐Smith, Jon Warner, (unknown), Carole A. Sargent, N. P. Carter	38

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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