Alexa Kidd
Impact in
- Cell Biology top 5%
- Microtubule and mitosis dynamics
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
-
- Muscle Physiology and Disorders 3
- ATP Synthase and ATPases Research 2
- Genetics 9
- Neurogenetic and Muscular Disorders Research 5
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 2
- Co-authors
- Nora Shannon (1 shared paper)John Tolmie (1 shared paper)Sandra Hanks (1 shared paper)David Fitzpatrick (1 shared paper)Helen V. Firth (1 shared paper)Nazneen Rahman (1 shared paper)Kim Coleman (1 shared paper)Alexandre Irrthum (1 shared paper)
- Journals
- Nature Genetics (1 paper)British Journal of Haematology (1 paper)European Journal of Human Genetics (1 paper)Journal of Neuromuscular Diseases (1 paper)European Journal of Medical Genetics (1 paper)
- Partner nations
- New ZealandUnited StatesUnited Kingdom
In The Last Decade
Alexa Kidd
24 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 74
- Cell Biology 305
- Genetics 327
- Cancer Research 150
- Molecular Biology 663
- Neurology 127
Countries citing papers authored by Alexa Kidd
This map shows the geographic impact of Alexa Kidd'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 Alexa Kidd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexa Kidd more than expected).
Fields of papers citing papers by Alexa Kidd
This network shows the impact of papers produced by Alexa Kidd. 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 Alexa Kidd. The network helps show where Alexa Kidd may publish in the future.
Co-authors
The 25 scholars most cited alongside Alexa Kidd, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2004 | 444 | |
| 2 | 2010 | 105 | |
| 3 | 2001 | 78 | |
| 4 | 2006 | 73 | |
| 5 | 2004 | 66 | |
| 6 | 2011 | 54 | |
| 7 | 2009 | 43 | |
| 8 | 2007 | 34 | |
| 9 | 2003 | 26 | |
| 10 | 2014 | 22 | |
| 11 | 2012 | 20 | |
| 12 | 2010 | 19 | |
| 13 | Myotonic dystrophy in Otago, New Zealand. | 2006 | 17 |
| 14 | 2021 | 17 | |
| 15 | Genetic testing in New Zealand: the role of the general practitioner. | 2004 | 12 |
| 16 | 2004 | 12 | |
| 17 | 2017 | 6 | |
| 18 | Suspected adverse reactions to medicines during 1989. | 1990 | 5 |
| 19 | 2014 | 3 | |
| 20 | 2021 | 2 |
About Alexa Kidd
Alexa Kidd is a scholar working on Molecular Biology, Genetics, Genetics, Neurology and Cellular and Molecular Neuroscience, having authored 24 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Muscle Physiology and Disorders (3 papers), Metabolism and Genetic Disorders (2 papers), ATP Synthase and ATPases Research (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers), BRCA gene mutations in cancer (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Cell Biology (305 citations), Genetics (327 citations), Cancer Research (150 citations), Molecular Biology (663 citations) and Neurology (127 citations). Alexa Kidd has collaborated with scholars based in New Zealand, United States and United Kingdom. Frequent co-authors include Nora Shannon, John Tolmie, Sandra Hanks, David Fitzpatrick, Helen V. Firth, Nazneen Rahman, Kim Coleman, Alexandre Irrthum, K Méhes and John Swansbury. Their work appears in journals such as Nature Genetics, British Journal of Haematology, European Journal of Human Genetics, Journal of Neuromuscular Diseases and European Journal of Medical Genetics.
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.