Kate Chandler
- Genetics top 2%
- Genomics and Rare Diseases 9
- Blood disorders and treatments 9
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 8
- Small Animals top 2%
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment 5
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- DNA Repair Mechanisms 6
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- Immunodeficiency and Autoimmune Disorders 6
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- Metabolism and Genetic Disorders 5
- Co-authors
- Holger A. VolkJill Clayton‐SmithAnnette WessmannGraeme C. BlackClare RusbridgeStefan MeyerRodolfo CappelloJuha Kolehmainen
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Kate Chandler
72 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 111
- Genetics 904
- Small Animals 143
- Cellular and Molecular Neuroscience 349
- Pediatrics, Perinatology and Child Health 319
- Psychiatry and Mental health 213
Countries citing papers authored by Kate Chandler
This map shows the geographic impact of Kate Chandler'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 Kate Chandler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kate Chandler more than expected).
Fields of papers citing papers by Kate Chandler
This network shows the impact of papers produced by Kate Chandler. 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 Kate Chandler. The network helps show where Kate Chandler may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Kate Chandler, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 0 | |
| 2 | 2021 | 2 | |
| 3 | 2019 | 12 | |
| 4 | 2017 | 30 | |
| 5 | 2015 | 19 | |
| 6 | 2015 | 21 | |
| 7 | 2014 | 38 | |
| 8 | 2011 | 40 | |
| 9 | 2010 | 7 | |
| 10 | 2010 | 3 | |
| 11 | 2010 | 1 | |
| 12 | 2009 | 16 | |
| 13 | 2009 | 43 | |
| 14 | 2008 | 65 | |
| 15 | 2005 | 6 | |
| 16 | 2004 | 69 | |
| 17 | 2003 | 249 | |
| 18 | 2003 | 100 | |
| 19 | 2000 | 113 | |
| 20 | Laparoscopic hernia repair: a preliminary report. | 1993 | 13 |
About Kate Chandler
Kate Chandler is a scholar working on Genetics, Clinical Biochemistry and Cellular and Molecular Neuroscience, having authored 73 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Blood disorders and treatments (9 papers), Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (8 papers), DNA Repair Mechanisms (6 papers), Immunodeficiency and Autoimmune Disorders (6 papers), Metabolism and Genetic Disorders (5 papers) and Epilepsy research and treatment (5 papers). The work is most often cited by research in Genetics (904 citations), Small Animals (143 citations) and Cellular and Molecular Neuroscience (349 citations). Kate Chandler has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Holger A. Volk, Jill Clayton‐Smith, Annette Wessmann, Graeme C. Black, Clare Rusbridge, Stefan Meyer, Rodolfo Cappello, Juha Kolehmainen, Reijo Norio and Mette Warburg.
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.