Annabelle Lewis

3.2k total citations
38 papers, 1.9k citations indexed

About

Annabelle Lewis is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Annabelle Lewis has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Pathology and Forensic Medicine. Recurrent topics in Annabelle Lewis's work include Epigenetics and DNA Methylation (13 papers), Genetic Syndromes and Imprinting (11 papers) and Genetic factors in colorectal cancer (11 papers). Annabelle Lewis is often cited by papers focused on Epigenetics and DNA Methylation (13 papers), Genetic Syndromes and Imprinting (11 papers) and Genetic factors in colorectal cancer (11 papers). Annabelle Lewis collaborates with scholars based in United Kingdom, United States and France. Annabelle Lewis's co-authors include Wolf Reik, Hayley L. Belnoue-Davis, Ian Tomlinson, Kohzoh Mitsuya, Wendy Dean, Michael J. Higgins, David Umlauf, Robert Feil, Joern Walter and Paul D. Smith and has published in prestigious journals such as Nature Genetics, The Journal of Experimental Medicine and The Journal of Cell Biology.

In The Last Decade

Annabelle Lewis

37 papers receiving 1.9k citations

Peers

Annabelle Lewis
Elena M. Pugacheva United States
Karim Malik United Kingdom
S. A. Schonberg United States
Rahul Karnik United States
Heinz-Ulrich Weier United States
Elena M. Pugacheva United States
Annabelle Lewis
Citations per year, relative to Annabelle Lewis Annabelle Lewis (= 1×) peers Elena M. Pugacheva

Countries citing papers authored by Annabelle Lewis

Since Specialization
Citations

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

Fields of papers citing papers by Annabelle Lewis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annabelle Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Annabelle Lewis. A scholar is included among the top collaborators of Annabelle Lewis 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 Annabelle Lewis. Annabelle Lewis 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
2.
Harvey, Amanda, et al.. (2023). Therapeutic Potential of Protein Tyrosine Kinase 6 in Colorectal Cancer. Cancers. 15(14). 3703–3703. 5 indexed citations
3.
Brown, Matthew, Hayley L. Belnoue-Davis, John P. Lydon, et al.. (2023). Functional analysis reveals driver cooperativity and novel mechanisms in endometrial carcinogenesis. EMBO Molecular Medicine. 15(10). e17094–e17094. 2 indexed citations
4.
Bridger, Joanna M., et al.. (2022). Alterations to Genome Organisation in Stem Cells, Their Differentiation and Associated Diseases. Results and problems in cell differentiation. 70. 71–102. 2 indexed citations
5.
O’Cathail, Séan M., Chieh‐Hsi Wu, Annabelle Lewis, et al.. (2020). NRF2 metagene signature is a novel prognostic biomarker in colorectal cancer. Cancer Genetics. 248-249. 1–10. 13 indexed citations
6.
Buchanan, Daniel D., Rachael Thomas, Emma Tham, et al.. (2020). The MLH1 polymorphism rs1800734 and risk of endometrial cancer with microsatellite instability. Clinical Epigenetics. 12(1). 102–102. 8 indexed citations
7.
Rayner, Emily, Rachael Thomas, Daniela Moralli, et al.. (2019). CRISPR-Cas9 Causes Chromosomal Instability and Rearrangements in Cancer Cell Lines, Detectable by Cytogenetic Methods. The CRISPR Journal. 2(6). 406–416. 49 indexed citations
8.
Thomas, Rachael, Markéta Tomková, Ceres Fernández–Rozadilla, et al.. (2019). The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression. Scientific Reports. 9(1). 13463–13463. 6 indexed citations
9.
Lewis, Annabelle, Luke Freeman-Mills, Elisa de la Calle‐Mustienes, et al.. (2014). A Polymorphic Enhancer near GREM1 Influences Bowel Cancer Risk through Differential CDX2 and TCF7L2 Binding. Cell Reports. 8(4). 983–990. 34 indexed citations
10.
Belnoue-Davis, Hayley L., Annabelle Lewis, Axel Behrens, & Ian Tomlinson. (2013). Investigation of the atypical FBXW7 mutation spectrum in human tumours by conditional expression of a heterozygous propellor tip missense allele in the mouse intestines. Gut. 63(5). 792–799. 48 indexed citations
11.
Leedham, Simon J., Pedro Rodenas-Cuadrado, Kimberley Howarth, et al.. (2012). A basal gradient of Wnt and stem-cell number influences regional tumour distribution in human and mouse intestinal tracts. Gut. 62(1). 83–93. 69 indexed citations
12.
Lewis, Annabelle, Hayley L. Belnoue-Davis, Maesha Deheragoda, et al.. (2011). The C‐terminus of Apc does not influence intestinal adenoma development or progression. The Journal of Pathology. 226(1). 73–83. 14 indexed citations
13.
Belnoue-Davis, Hayley L., Annabelle Lewis, Bradley Spencer‐Dene, et al.. (2011). FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development. The Journal of Pathology. 224(2). 180–189. 19 indexed citations
14.
Green, Kelly, Annabelle Lewis, Claire Dawson, et al.. (2007). A developmental window of opportunity for imprinted gene silencing mediated by DNA methylation and the Kcnq1ot1 noncoding RNA. Mammalian Genome. 18(1). 32–42. 31 indexed citations
15.
Lewis, Annabelle & Wolf Reik. (2006). How imprinting centres work. Cytogenetic and Genome Research. 113(1-4). 81–89. 147 indexed citations
16.
Lewis, Annabelle, et al.. (2005). Genetic Imprinting: Conflict at the Callipyge Locus. Current Biology. 15(8). R291–R294. 22 indexed citations
17.
Lewis, Annabelle & Adele Murrell. (2004). Genomic Imprinting: CTCF Protects the Boundaries. Current Biology. 14(7). R284–R286. 69 indexed citations
18.
Reik, Wolf, Adele Murrell, Annabelle Lewis, et al.. (2004). Chromosome Loops, Insulators, and Histone Methylation: New Insights into Regulation of Imprinting in Clusters. Cold Spring Harbor Symposia on Quantitative Biology. 69(0). 29–38. 17 indexed citations
19.
Lewis, Annabelle, Kohzoh Mitsuya, David Umlauf, et al.. (2004). Imprinting on distal chromosome 7 in the placenta involves repressive histone methylation independent of DNA methylation. Nature Genetics. 36(12). 1291–1295. 347 indexed citations
20.
Reik, Wolf, Annabelle Lewis, Hugh D. Morgan, et al.. (2004). IMPRINTING AND EPIGENETIC REPROGRAMMING IN MAMMALIAN DEVELOPMENT. Cold Spring Harbor Symposia on Quantitative Biology. 69(1). 1–1. 1 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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