Catherine Winchester

968 total citations
21 papers, 712 citations indexed

About

Catherine Winchester is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Catherine Winchester has authored 21 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Catherine Winchester's work include Genetic Neurodegenerative Diseases (4 papers), Phosphodiesterase function and regulation (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Catherine Winchester is often cited by papers focused on Genetic Neurodegenerative Diseases (4 papers), Phosphodiesterase function and regulation (4 papers) and Neuroscience and Neuropharmacology Research (3 papers). Catherine Winchester collaborates with scholars based in United Kingdom, United States and Australia. Catherine Winchester's co-authors include Judith A. Pratt, Brian Morris, Mark J. Salji, Neil Dawson, Keith Johnson, Alice Egerton, Billah Morris, Catherine Boucher, Mark E.S. Bailey and Nessa Carey and has published in prestigious journals such as Nature, Nucleic Acids Research and Nature Reviews Drug Discovery.

In The Last Decade

Catherine Winchester

21 papers receiving 695 citations

Peers

Catherine Winchester

CMN

GENET

Hiroaki Kawasaki Japan

Jean‐François Théroux Canada

Jocelyn Widagdo Australia

Heather McKellar United States

Steven Chao United States

Chiara Cerri Italy

Mari Kondo Japan

Maria Vittoria Simonini United States

K. Haddley United Kingdom

Rolando Meloni France

Hiroaki Kawasaki Japan

Catherine Winchester

398 ×1.0

246 ×0.7

CMN

93 ×0.9

GENET

71 ×0.8

20 ×0.3

Citations per year, relative to Catherine Winchester Catherine Winchester (= 1×) peers Hiroaki Kawasaki

Countries citing papers authored by Catherine Winchester

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Winchester

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Winchester

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

Winchester, Catherine. (2018). Give every paper a read for reproducibility. Nature. 557(7705). 281–281. 12 indexed citations

Udovicich, Cristian, Veeru Kasivisvanathan, & Catherine Winchester. (2017). Communicating your research (part 2): to the wider community. Journal of Clinical Urology. 11(3). 208–214. 1 indexed citations

Salji, Mark J., Imran Ahmad, & Catherine Winchester. (2016). Non-clinical research – laboratory based. Journal of Clinical Urology. 9(6). 362–364. 1 indexed citations

Udovicich, Cristian, Veeru Kasivisvanathan, & Catherine Winchester. (2016). Communicating your research (part 1) – to the scientific community. Journal of Clinical Urology. 10(4). 396–399. 2 indexed citations

Winchester, Catherine & Mark J. Salji. (2016). Writing a literature review. Journal of Clinical Urology. 9(5). 308–312. 62 indexed citations

Dawson, Neil, Masaki Kurihara, David M. Thomson, et al.. (2015). Altered functional brain network connectivity and glutamate system function in transgenic mice expressing truncated Disrupted-in-Schizophrenia 1. Translational Psychiatry. 5(5). e569–e569. 35 indexed citations

Rajan, Prabhakar, et al.. (2015). Framing a research question: The first and most vital step in planning research. Journal of Clinical Urology. 8(6). 409–411. 2 indexed citations

Dawson, Neil, Catherine Winchester, Zoë A. Hughes, et al.. (2014). Poster #M9 DISC1 MUTATION INDUCED ALTERATIONS IN CEREBRAL METABOLISM AND IN THE RESPONSE TO ACUTE SUBANAESTHETIC KETAMINE: A COMPARISON OF THREE DIFFERENT DISC1 MUTATIONS. Schizophrenia Research. 153. S192–S192. 2 indexed citations

Winchester, Catherine, Judith A. Pratt, & Brian Morris. (2014). Risk genes for schizophrenia: Translational opportunities for drug discovery. Pharmacology & Therapeutics. 143(1). 34–50. 21 indexed citations

10.

Pratt, Judith A., Catherine Winchester, Neil Dawson, & Brian Morris. (2012). Advancing schizophrenia drug discovery: optimizing rodent models to bridge the translational gap. Nature Reviews Drug Discovery. 11(7). 560–579. 113 indexed citations

11.

Winchester, Catherine, Demetrius A. Vouyiouklis, Rachel Thompson, et al.. (2012). Converging evidence that sequence variations in the novel candidate gene MAP2K7 (MKK7) are functionally associated with schizophrenia. Human Molecular Genetics. 21(22). 4910–4921. 42 indexed citations

12.

Winchester, Catherine, et al.. (2011). Using next generation sequencing to investigate DPYSL2 gene variants in schizophrenia. Journal of Psychopharmacology. 25. 1 indexed citations

13.

Pratt, Judith A., Neil Dawson, Catherine Winchester, David M. Thomson, & Brian Morris. (2010). DISTINCT ASPECTS OF PREFRONTAL CORTEX DYSFUNCTION IN SCHIZOPHRENIA MODELLED BY ACUTE AND REPEATED PCP TREATMENT: IMPACT OF MODAFINIL. Schizophrenia Research. 117(2-3). 509–509. 1 indexed citations

14.

Pratt, Judith A., et al.. (2008). Modelling prefrontal cortex deficits in schizophrenia: implications for treatment. British Journal of Pharmacology. 153(S1). S465–70. 130 indexed citations

15.

Harris, Sarah E., Catherine Winchester, & Keith Johnson. (2000). Functional analysis of the homeodomain protein SIX5. Nucleic Acids Research. 28(9). 1871–1878. 22 indexed citations

16.

Boucher, Catherine, Catherine Winchester, Graham Hamilton, et al.. (2000). Structure, mapping and expression of the human gene encoding the homeodomain protein, SIX2. Gene. 247(1-2). 145–151. 31 indexed citations

17.

Winchester, Catherine, et al.. (2000). Expression of a homeobox gene (SIX5) in borderline ovarian tumours. Journal of Clinical Pathology. 53(3). 212–217. 16 indexed citations

18.

Winchester, Catherine. (1999). Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy. Human Molecular Genetics. 8(3). 481–492. 63 indexed citations

19.

Johnson, Keith, Catherine Boucher, Catherine Winchester, et al.. (1996). Is myotonic dystrophy a single-gene disorder?. Biochemical Society Transactions. 24(2). 510–513. 6 indexed citations

20.

Boucher, Catherine, Nessa Carey, Ralf Krahe, et al.. (1995). A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)_n repeat. Human Molecular Genetics. 4(10). 1919–1925. 147 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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