Kath Smith
Impact in
- Molecular Biology top 5%
- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- Renal and related cancers
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Mesenchymal stem cell research
Papers in
- Genetics 13
- Genomic variations and chromosomal abnormalities 9
- Genetics and Neurodevelopmental Disorders 4
- Congenital Ear and Nasal Anomalies 4
- Genomics and Rare Diseases 3
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- Pluripotent Stem Cells Research 4
- Congenital heart defects research 4
- CRISPR and Genetic Engineering 4
- Renal and related cancers 2
- Co-authors
- Peter W. Andrews (4 shared papers)Edna L. Maltby (3 shared papers)H. D. M. Moore (2 shared papers)Jonathan S. Draper (2 shared papers)Paul J. Gokhale (2 shared papers)James A. Thomson (1 shared paper)Lorraine F. Meisner (1 shared paper)Thomas P. Zwaka (1 shared paper)
- Journals
- Nature Biotechnology (2 papers)European Journal of Medical Genetics (1 paper)Journal of Psychosomatic Research (1 paper)Human Molecular Genetics (1 paper)AlterNative An International Journal of Indigenous Peoples (1 paper)
- Partner nations
- United KingdomUnited StatesAustria
In The Last Decade
Kath Smith
23 papers receiving 1.7k citations
Kath Smith's Hit Papers
Peers
Comparison fields: 5 of 85
- Molecular Biology 1.4k
- Genetics 137
- Developmental Neuroscience 49
- Genetics 347
- Biomedical Engineering 321
Countries citing papers authored by Kath Smith
This map shows the geographic impact of Kath Smith'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 Kath Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kath Smith more than expected).
Fields of papers citing papers by Kath Smith
This network shows the impact of papers produced by Kath Smith. 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 Kath Smith. The network helps show where Kath Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Kath Smith, 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 | Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells Hit paper breakdown → | 2003 | 759 |
| 2 | 2007 | 481 | |
| 3 | 2005 | 222 | |
| 4 | 2011 | 65 | |
| 5 | 2003 | 55 | |
| 6 | 1988 | 24 | |
| 7 | 2018 | 23 | |
| 8 | 2015 | 21 | |
| 9 | 2011 | 18 | |
| 10 | 2015 | 17 | |
| 11 | 2019 | 17 | |
| 12 | 2015 | 17 | |
| 13 | 2012 | 17 | |
| 14 | 2018 | 11 | |
| 15 | 2018 | 9 | |
| 16 | 2016 | 6 | |
| 17 | 2015 | 5 | |
| 18 | 2015 | 4 | |
| 19 | 2017 | 3 | |
| 20 | 2014 | 3 |
About Kath Smith
Kath Smith is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pathology and Forensic Medicine, having authored 24 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (4 papers), Pluripotent Stem Cells Research (4 papers), Congenital heart defects research (4 papers), Congenital Ear and Nasal Anomalies (4 papers), CRISPR and Genetic Engineering (4 papers), Genomics and Rare Diseases (3 papers) and Renal and related cancers (2 papers). The work is most often cited by research in Molecular Biology (1.4k citations), Genetics (137 citations), Developmental Neuroscience (49 citations), Genetics (347 citations) and Biomedical Engineering (321 citations). Kath Smith has collaborated with scholars based in United Kingdom, United States and Austria. Frequent co-authors include Peter W. Andrews, Edna L. Maltby, H. D. M. Moore, Jonathan S. Draper, Paul J. Gokhale, James A. Thomson, Lorraine F. Meisner, Thomas P. Zwaka, Julie A. Johnson and Hazel M. Holden. Their work appears in journals such as Nature Biotechnology, European Journal of Medical Genetics, Journal of Psychosomatic Research, Human Molecular Genetics and AlterNative An International Journal of Indigenous Peoples.
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.