Emma J. Stringer

420 total citations
9 papers, 267 citations indexed

About

Emma J. Stringer is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Emma J. Stringer has authored 9 papers receiving a total of 267 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Surgery. Recurrent topics in Emma J. Stringer's work include Congenital gastrointestinal and neural anomalies (3 papers), Digestive system and related health (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Emma J. Stringer is often cited by papers focused on Congenital gastrointestinal and neural anomalies (3 papers), Digestive system and related health (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Emma J. Stringer collaborates with scholars based in United Kingdom, Netherlands and Poland. Emma J. Stringer's co-authors include Felix Beck, Catrin Pritchard, Jean‐Noël Freund, Jacqueline Deschamps, Monika Bialecka, Nick Barker, Hans Clevers, Isabelle Duluc, Doug J. Winton and Nicholas A. Wright and has published in prestigious journals such as Circulation, Development and FEBS Letters.

In The Last Decade

Emma J. Stringer

9 papers receiving 266 citations

Peers

Emma J. Stringer

MB

GENET

SURGE

ONCOL

IMMUN

Martina Owens United Kingdom

Angeline Lai Singapore

Signe Perlman Denmark

Tzu-Ping Lin Taiwan

Xiangjie Xu China

Anja Schrade United States

Colleen Macmurdo United States

Clémentine Mahaut France

Jeannette Connerney United States

Mamiko Yamada Japan

Martina Owens United Kingdom

Emma J. Stringer

163 ×1.0

MB

128 ×1.1

GENET

116 ×1.8

SURGE

35 ×0.9

ONCOL

13 ×0.9

IMMUN

Citations per year, relative to Emma J. Stringer Emma J. Stringer (= 1×) peers Martina Owens

Countries citing papers authored by Emma J. Stringer

Since Specialization

Citations

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

Fields of papers citing papers by Emma J. Stringer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emma J. Stringer. 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 Emma J. Stringer. The network helps show where Emma J. Stringer may publish in the future.

Co-authorship network of co-authors of Emma J. Stringer

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

All Works

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9 of 9 papers shown

1.

Karp, Natasha A., et al.. (2022). A qualitative study of the barriers to using blinding in in vivo experiments and suggestions for improvement. PLoS Biology. 20(11). e3001873–e3001873. 15 indexed citations

2.

McVey, David G., Sander W. van der Laan, Kenneth Chan, et al.. (2020). The FES gene, located at the chromosome 15Q21.6 coronary-artery-disease locus, modulates atherosclerotic plaque vulnerability. Atherosclerosis. 315. e19–e19. 1 indexed citations

3.

Morris, G E, Peter D. Jones, Michael Kaiser, et al.. (2019). HHIPL1 , a Gene at the 14q32 Coronary Artery Disease Locus, Positively Regulates Hedgehog Signaling and Promotes Atherosclerosis. Circulation. 140(6). 500–513. 28 indexed citations

4.

Kanber, Baris, Kumar V. Ramnarine, David G. Lambert, et al.. (2018). A preclinical ultrasound method for the assessment of vascular disease progression in murine models. Ultrasound. 27(2). 85–93. 3 indexed citations

5.

Ven, Cesca van de, Monika Bialecka, Roel Neijts, et al.. (2011). Concerted involvement of Cdx/Hox genes and Wnt signaling in morphogenesis of the caudal neural tube and cloacal derivatives from the posterior growth zone. Development. 138(16). 3451–3462. 63 indexed citations

6.

Ven, Cesca van de, Monika Białecka, Roel Neijts, et al.. (2011). Concerted involvement of Cdx/Hox genes and Wnt signaling in morphogenesis of the caudal neural tube and cloacal derivatives from the posterior growth zone. Development. 138(17). 3859–3859. 7 indexed citations

7.

Stringer, Emma J., Isabelle Duluc, Irwin Davidson, et al.. (2011). Cdx2 determines the fate of postnatal intestinal endoderm. Development. 139(3). 465–474. 78 indexed citations

8.

Beck, Felix & Emma J. Stringer. (2010). The role of Cdx genes in the gut and in axial development. Biochemical Society Transactions. 38(2). 353–357. 52 indexed citations

9.

Stringer, Emma J., Catrin Pritchard, & Felix Beck. (2008). Cdx2 initiates histodifferentiation of the midgut endoderm. FEBS Letters. 582(17). 2555–2560. 20 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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