Gemma Codner

2.5k total citations
19 papers, 460 citations indexed

About

Gemma Codner is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Gemma Codner has authored 19 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Immunology. Recurrent topics in Gemma Codner's work include CRISPR and Genetic Engineering (8 papers), T-cell and B-cell Immunology (4 papers) and Pluripotent Stem Cells Research (3 papers). Gemma Codner is often cited by papers focused on CRISPR and Genetic Engineering (8 papers), T-cell and B-cell Immunology (4 papers) and Pluripotent Stem Cells Research (3 papers). Gemma Codner collaborates with scholars based in United Kingdom, France and Netherlands. Gemma Codner's co-authors include Lydia Teboul, Sara Wells, Shirley A. Ellis, Adam Caulder, Joffrey Mianné, Marie Hutchison, J.R. Birch, Lauren Chessum, Carlos Aguilar and Andrew Parker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Scientific Reports.

In The Last Decade

Gemma Codner

19 papers receiving 457 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Gemma Codner United Kingdom	11	275	116	70	53	49	19	460
U. Philipp Germany	15	275 1.0×	310 2.7×	28 0.4×	20 0.4×	28 0.6×	39	735
James Cleak United Kingdom	7	488 1.8×	422 3.6×	40 0.6×	12 0.2×	20 0.4×	9	869
Toh Hean Ch’ng United States	16	363 1.3×	154 1.3×	143 2.0×	7 0.1×	25 0.5×	24	937
Yu Qi China	17	537 2.0×	150 1.3×	37 0.5×	70 1.3×	7 0.1×	62	856
Nathan Anderson United States	6	273 1.0×	407 3.5×	33 0.5×	25 0.5×	7 0.1×	10	606
Ying-Tao Zhao United States	16	674 2.5×	213 1.8×	77 1.1×	17 0.3×	9 0.2×	25	1.2k
Stephanie S. Anguiano-Zarate United States	7	211 0.8×	102 0.9×	43 0.6×	7 0.1×	9 0.2×	7	372
Elvis Huarcaya Najarro United States	8	265 1.0×	18 0.2×	22 0.3×	158 3.0×	26 0.5×	8	484
Eillen Tecle United States	10	245 0.9×	57 0.5×	70 1.0×	4 0.1×	61 1.2×	13	477
Elizabeth E. Marr United States	8	241 0.9×	138 1.2×	79 1.1×	23 0.4×	20 0.4×	10	561

Countries citing papers authored by Gemma Codner

Since Specialization

Citations

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

Fields of papers citing papers by Gemma Codner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gemma Codner

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

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

Codner, Gemma, Adam Caulder, Skevoulla Christou, et al.. (2024). Long-read sequencing for fast and robust identification of correct genome-edited alleles: PCR-based and Cas9 capture methods. PLoS Genetics. 20(3). e1011187–e1011187. 3 indexed citations

Jones, Emma, Elizabeth Hill, Jacqueline M. Linehan, et al.. (2023). Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6. Neurobiology of Disease. 190. 106363–106363. 3 indexed citations

Mackenzie, Matthew, et al.. (2023). Genotyping Genome-Edited Founders and Subsequent Generation. Methods in molecular biology. 2631. 103–134. 1 indexed citations

Stewart, Michelle, Gemma Codner, Steffen Mayerl, et al.. (2022). An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1 Y446C/Y446C mutation. Human Molecular Genetics. 31(17). 2951–2963. 8 indexed citations

Aguilar, Carlos, Andrew Parker, Gemma Codner, et al.. (2022). Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing. PLoS Genetics. 18(1). e1009937–e1009937. 7 indexed citations

Hannan, Fadil, Mark Stevenson, Victoria Stokes, et al.. (2021). Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2. Human Molecular Genetics. 30(10). 880–892. 12 indexed citations

Bunton-Stasyshyn, Rosie, Gemma Codner, & Lydia Teboul. (2021). Screening and validation of genome-edited animals. Laboratory Animals. 56(1). 69–82. 9 indexed citations

Codner, Gemma, Lauren Chessum, Adam Caulder, et al.. (2020). Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination. Methods. 191. 59–67. 16 indexed citations

Codner, Gemma, et al.. (2019). The guanine nucleotide exchange factor, Spata13, influences social behaviour and nocturnal activity. Mammalian Genome. 30(3-4). 54–62. 6 indexed citations

10.

Warr, Nick, Pam Siggers, Joffrey Mianné, et al.. (2019). Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight. Scientific Reports. 9(1). 17195–17195. 10 indexed citations

11.

Owens, Dominic D. G., Adam Caulder, Vincent Frontera, et al.. (2019). Microhomologies are prevalent at Cas9-induced larger deletions. Nucleic Acids Research. 47(14). 7402–7417. 85 indexed citations

12.

Mianné, Joffrey, Gemma Codner, Adam Caulder, et al.. (2017). Analysing the outcome of CRISPR-aided genome editing in embryos: Screening, genotyping and quality control. Methods. 121-122. 68–76. 48 indexed citations

13.

Codner, Gemma, Adam Caulder, Marie Wattenhofer‐Donzé, et al.. (2016). Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction. BMC Cell Biology. 17(1). 30–30. 20 indexed citations

14.

Mianné, Joffrey, Lauren Chessum, Saumya Kumar, et al.. (2016). Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. Genome Medicine. 8(1). 16–16. 97 indexed citations

15.

Maywood, Elizabeth S., Lesley Drynan, Johanna E. Chesham, et al.. (2013). Analysis of core circadian feedback loop in suprachiasmatic nucleus of mCry1-luc transgenic reporter mouse. Proceedings of the National Academy of Sciences. 110(23). 9547–9552. 50 indexed citations

16.

Codner, Gemma, J.R. Birch, John A. Hammond, & Shirley A. Ellis. (2012). Constraints on haplotype structure and variable gene frequencies suggest a functional hierarchy within cattle MHC class I. Immunogenetics. 64(6). 435–445. 19 indexed citations

17.

Ellis, Shirley A. & Gemma Codner. (2011). The impact of MHC diversity on cattle T cell responses. Veterinary Immunology and Immunopathology. 148(1-2). 74–77. 12 indexed citations

18.

Codner, Gemma, M.J. Stear, Richard Reeve, Louise Matthews, & S. A. Ellis. (2011). Selective forces shaping diversity in the class I region of the major histocompatibility complex in dairy cattle. Animal Genetics. 43(3). 239–249. 24 indexed citations

19.

Birch, J.R., Gemma Codner, Efrain Guzman, & Shirley A. Ellis. (2008). Genomic location and characterisation of nonclassical MHC class I genes in cattle. Immunogenetics. 60(5). 267–273. 30 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