Gemma F. Codner
Impact in
- Sensory Systems top 2%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- Genomics and Rare Diseases
- Animal Genetics and Reproduction
- Genetic and phenotypic traits in livestock
- Genetic Associations and Epidemiology
Papers in
- Genetics 19
- Animal Genetics and Reproduction 5
- Genetic and phenotypic traits in livestock 5
- Genomics and Rare Diseases 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Hearing, Cochlea, Tinnitus, Genetics 4
- Co-authors
- Lydia Teboul (10 shared papers)Adam Caulder (6 shared papers)Shirley A. Ellis (3 shared papers)Sara E. Wells (6 shared papers)Joffrey Mianné (4 shared papers)Marella F. T. R. De Bruijn (1 shared paper)Joe R. Harman (1 shared paper)Efrain Guzman (1 shared paper)
- Journals
- Nature Communications (4 papers)Human Molecular Genetics (3 papers)Nature Genetics (3 papers)The EMBO Journal (2 papers)Methods (2 papers)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Gemma F. Codner
35 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 97
- Sensory Systems 205
- Genetics 447
- Endocrine and Autonomic Systems 63
- Molecular Biology 636
- Small Animals 82
Countries citing papers authored by Gemma F. Codner
This map shows the geographic impact of Gemma F. 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 F. 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 F. Codner more than expected).
Fields of papers citing papers by Gemma F. Codner
This network shows the impact of papers produced by Gemma F. 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 F. Codner. The network helps show where Gemma F. Codner may publish in the future.
Co-authors
The 25 scholars most cited alongside Gemma F. Codner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 196 | |
| 2 | 2017 | 181 | |
| 3 | 2018 | 125 | |
| 4 | 2017 | 122 | |
| 5 | 2015 | 118 | |
| 6 | 2019 | 93 | |
| 7 | 2018 | 88 | |
| 8 | 2020 | 81 | |
| 9 | 2021 | 80 | |
| 10 | 2018 | 70 | |
| 11 | 2017 | 63 | |
| 12 | 2013 | 54 | |
| 13 | 2018 | 53 | |
| 14 | 2022 | 38 | |
| 15 | 2008 | 31 | |
| 16 | 2011 | 26 | |
| 17 | 2016 | 23 | |
| 18 | 2012 | 21 | |
| 19 | 2019 | 21 | |
| 20 | 2020 | 18 |
About Gemma F. Codner
Gemma F. Codner is a scholar working on Genetics, Sensory Systems, Molecular Biology, Neurology and Cellular and Molecular Neuroscience, having authored 36 papers that have together received 1.6k indexed citations. Recurring topics across this work include CRISPR and Genetic Engineering (9 papers), Animal Genetics and Reproduction (5 papers), Genetic and phenotypic traits in livestock (5 papers), Genomics and Rare Diseases (5 papers), Hearing, Cochlea, Tinnitus, Genetics (4 papers), Bioinformatics and Genomic Networks (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Amyotrophic Lateral Sclerosis Research (2 papers). The work is most often cited by research in Sensory Systems (205 citations), Genetics (447 citations), Endocrine and Autonomic Systems (63 citations), Molecular Biology (636 citations) and Small Animals (82 citations). Gemma F. Codner has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include Lydia Teboul, Adam Caulder, Shirley A. Ellis, Sara E. Wells, Joffrey Mianné, Marella F. T. R. De Bruijn, Joe R. Harman, Efrain Guzman, Vincent Frontera and Lucas V. Greder. Their work appears in journals such as Nature Communications, Human Molecular Genetics, Nature Genetics, The EMBO Journal and Methods.
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.