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 India. Jon Warner's co-authors include Robert J. Krushell, Christian Gerber, Alain‐Charles Masquelet, D. J. H. Brock, David T. Bonthron, D. J. H. Brock, Mary Porteous, David Fitzpatrick, David Goudie and Lisa Strain 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

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Jon Warner 770 533 387 378 292 37 1.8k
Ann Curtis 674 0.9× 361 0.7× 117 0.3× 410 1.1× 88 0.3× 53 1.6k
M. Sarfarazi 1.7k 2.2× 435 0.8× 247 0.6× 192 0.5× 85 0.3× 67 3.0k
Rein P. Stulp 767 1.0× 98 0.2× 544 1.4× 235 0.6× 284 1.0× 20 1.8k
L. J. Rubinstein 550 0.7× 267 0.5× 161 0.4× 480 1.3× 214 0.7× 32 1.6k
Joy Kahn 694 0.9× 279 0.5× 290 0.7× 198 0.5× 74 0.3× 29 1.8k
Daniëlle Majoor‐Krakauer 1.0k 1.4× 101 0.2× 360 0.9× 333 0.9× 136 0.5× 55 2.2k
Yuichi Kawagashira 665 0.9× 480 0.9× 74 0.2× 887 2.3× 118 0.4× 62 1.7k
Haipeng Xue 1.3k 1.6× 386 0.7× 211 0.5× 131 0.3× 44 0.2× 69 2.2k
Steven Sparagana 669 0.9× 286 0.5× 138 0.4× 231 0.6× 88 0.3× 60 2.8k
Marc Valentine 932 1.2× 156 0.3× 122 0.3× 526 1.4× 67 0.2× 31 1.7k

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

20 of 20 papers shown
1.
Miller, Heather J., et al.. (2025). Survey of Pathologic Microorganisms in the Streams Along the Tahoe Rim Trail. Wilderness and Environmental Medicine. 36(2). 194–200. 1 indexed citations
2.
McHutchison, Caroline, Danielle Leighton, Andrew M. McIntosh, et al.. (2019). Relationship between neuropsychiatric disorders and cognitive and behavioural change in MND. Journal of Neurology Neurosurgery & Psychiatry. 91(3). 245–253. 17 indexed citations
3.
Cumming, Sarah A., Mark Hamilton, Helen Gregory, et al.. (2018). De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1. European Journal of Human Genetics. 26(11). 1635–1647. 69 indexed citations
4.
Nethisinghe, Suran, Sally Pemble, Mary G. Sweeney, et al.. (2018). PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption. Frontiers in Cellular Neuroscience. 12. 200–200. 16 indexed citations
5.
Henstridge, Christopher M., Emily Carroll, Makis Tzioras, et al.. (2017). Synapse loss in the prefrontal cortex is associated with cognitive decline in amyotrophic lateral sclerosis. Acta Neuropathologica. 135(2). 213–226. 85 indexed citations
6.
Cleary, Elaine, Suvankar Pal, David Moore, et al.. (2016). Improved PCR based methods for detecting C9orf72 hexanucleotide repeat expansions. Molecular and Cellular Probes. 30(4). 218–224. 33 indexed citations
7.
Leighton, Danielle, Elaine Cleary, Laura Stephenson, et al.. (2016). Genetic epidemiology of motor neuron disease-associated variants in the Scottish population. Neurobiology of Aging. 51. 178.e11–178.e20. 33 indexed citations
8.
Soares, Dinesh C., Sachin Wani, Antonia Sophocleous, et al.. (2015). Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone. Human Molecular Genetics. 24(11). 3286–3295. 25 indexed citations
9.
McWilliam, Catherine, Andrew Cooke, Daniela Lobo, et al.. (2009). 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?. European Journal of Paediatric Neurology. 14(3). 267–269. 1 indexed citations
10.
Torrens, Lorna, Edith Burns, Jon Stone, et al.. (2007). Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings. Acta Neurologica Scandinavica. 0(0). 4026748930–???. 19 indexed citations
11.
Zeman, Adam, Jon Stone, Mary Porteous, et al.. (2004). Spinocerebellar ataxia type 8 in Scotland. Journal of Neurology Neurosurgery & Psychiatry. 75(3). 1 indexed citations
12.
13.
Mullen, Peter, WR Miller, James Mackay, et al.. (1997). BRCA1 5382insC mutation in sporadic and familial breast and ovarian carcinoma in Scotland. British Journal of Cancer. 75(9). 1377–1380. 8 indexed citations
14.
Hayward, Bruce E., Judy Fantes, Jon Warner, et al.. (1996). Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23. Mammalian Genome. 7(6). 454–458. 21 indexed citations
15.
Johnson, David W., Jonathan Berg, Carol J. Gallione, et al.. (1995). A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.. Genome Research. 5(1). 21–28. 124 indexed citations
16.
Kelly, Ben L., Sabrina D. Dyall, Jon Warner, Jun Tang, & Deborah F. Smith. (1995). Chromosomal organisation of a repeated gene cluster expressed in mammalian stages of Leishmania. Gene. 163(1). 145–149. 6 indexed citations
17.
Strain, Lisa, et al.. (1995). A human parthenogenetic chimaera. Nature Genetics. 11(2). 164–169. 120 indexed citations
18.
19.
Zheng, Yun‐Ling, et al.. (1992). Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig. Prenatal Diagnosis. 12(11). 931–943. 38 indexed citations
20.
Cole, Charlotte G., Stephen Abbs, Victor Dubowitz, et al.. (1992). Linkage of emery-dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIII. Neuromuscular Disorders. 2(1). 51–57. 6 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

Breakdown of academic impact, for papers by Ann Curtis Breakdown of academic impact, for papers by M. Sarfarazi Breakdown of academic impact, for papers by Rein P. Stulp Breakdown of academic impact, for papers by L. J. Rubinstein Breakdown of academic impact, for papers by Joy Kahn Breakdown of academic impact, for papers by Daniëlle Majoor‐Krakauer Breakdown of academic impact, for papers by Yuichi Kawagashira Breakdown of academic impact, for papers by Haipeng Xue Breakdown of academic impact, for papers by Steven Sparagana Breakdown of academic impact, for papers by Marc Valentine
Rankless by CCL
2026