Alison Gardner
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
Papers in
- Genetics 19
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 4
- Neurogenetic and Muscular Disorders Research 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 3
- Co-authors
- Jozef Gécz (18 shared papers)Gabriel Kremmidiotis (6 shared papers)John C. Mulley (3 shared papers)Mark Corbett (9 shared papers)David F. Callen (5 shared papers)Samuel F. Berkovic (5 shared papers)Leanne M. Dibbens (3 shared papers)Joanna Crawford (3 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)The American Journal of Human Genetics (4 papers)npj Genomic Medicine (2 papers)Molecular Psychiatry (2 papers)Genomics (2 papers)
- Partner nations
- AustraliaUnited StatesNetherlands
In The Last Decade
Alison Gardner
30 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 94
- Psychiatry and Mental health 307
- Genetics 521
- Clinical Biochemistry 82
- Cellular and Molecular Neuroscience 214
- Molecular Biology 746
Countries citing papers authored by Alison Gardner
This map shows the geographic impact of Alison Gardner'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 Alison Gardner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alison Gardner more than expected).
Fields of papers citing papers by Alison Gardner
This network shows the impact of papers produced by Alison Gardner. 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 Alison Gardner. The network helps show where Alison Gardner may publish in the future.
Co-authors
The 25 scholars most cited alongside Alison Gardner, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 284 | |
| 2 | 1998 | 202 | |
| 3 | 1996 | 161 | |
| 4 | 2015 | 158 | |
| 5 | 2004 | 124 | |
| 6 | 2008 | 97 | |
| 7 | 2011 | 88 | |
| 8 | 2010 | 88 | |
| 9 | 2012 | 75 | |
| 10 | CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3. | 2002 | 53 |
| 11 | 2012 | 42 | |
| 12 | 2002 | 41 | |
| 13 | 2001 | 40 | |
| 14 | 2018 | 30 | |
| 15 | 2016 | 28 | |
| 16 | 2021 | 23 | |
| 17 | 2018 | 22 | |
| 18 | 2013 | 17 | |
| 19 | 2019 | 16 | |
| 20 | 2015 | 13 |
About Alison Gardner
Alison Gardner is a scholar working on Genetics, Molecular Biology, Genetics, Cellular and Molecular Neuroscience and Oncology, having authored 30 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Congenital heart defects research (3 papers), Antifungal resistance and susceptibility (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Psychiatry and Mental health (307 citations), Genetics (521 citations), Clinical Biochemistry (82 citations), Cellular and Molecular Neuroscience (214 citations) and Molecular Biology (746 citations). Alison Gardner has collaborated with scholars based in Australia, United States and Netherlands. Frequent co-authors include Jozef Gécz, Gabriel Kremmidiotis, John C. Mulley, Mark Corbett, David F. Callen, Samuel F. Berkovic, Leanne M. Dibbens, Joanna Crawford, Ingrid E. Scheffer and Alastair H. MacLennan. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, npj Genomic Medicine, Molecular Psychiatry and Genomics.
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.