Kath Smith
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Molecular Biology top 5%
- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- Renal and related cancers
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 5
- Congenital Ear and Nasal Anomalies 4
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- CRISPR and Genetic Engineering 4
- Pluripotent Stem Cells Research 4
- Congenital heart defects research 4
- Co-authors
- Peter W. Andrews (4 shared papers)Edna L. Maltby (3 shared papers)H. D. M. Moore (2 shared papers)Paul J. Gokhale (2 shared papers)Jonathan S. Draper (2 shared papers)James Alexander Thomson (1 shared paper)Lorraine F. Meisner (1 shared paper)Thomas P. Zwaka (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Genetics in Medicine (2 papers)Nature Biotechnology (2 papers)Journal of Medical Genetics (2 papers)Microscopy and Microanalysis (1 paper)
- Partner nations
- United KingdomUnited StatesEstonia
In The Last Decade
Kath Smith
34 papers receiving 2.6k citations
Kath Smith's Hit Papers
Peers
Comparison fields: 5 of 110
- Genetics 881
- Molecular Biology 1.9k
- Genetics 171
- Developmental Neuroscience 59
- Psychiatry and Mental health 119
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 36 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 | 839 |
| 2 | 2007 | 530 | |
| 3 | 2009 | 260 | |
| 4 | 2005 | 242 | |
| 5 | 2017 | 207 | |
| 6 | 2017 | 111 | |
| 7 | 2018 | 91 | |
| 8 | 2011 | 83 | |
| 9 | 2019 | 62 | |
| 10 | 2003 | 55 | |
| 11 | 2019 | 50 | |
| 12 | 2018 | 27 | |
| 13 | 1988 | 26 | |
| 14 | 2012 | 24 | |
| 15 | 2013 | 22 | |
| 16 | 2015 | 22 | |
| 17 | 2015 | 22 | |
| 18 | 2011 | 19 | |
| 19 | 2015 | 18 | |
| 20 | 2019 | 17 |
About Kath Smith
Kath Smith is a scholar working on Genetics, Genetics, Molecular Biology, Psychiatry and Mental health and Pathology and Forensic Medicine, having authored 36 papers that have together received 2.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genomics and Rare Diseases (5 papers), CRISPR and Genetic Engineering (4 papers), Pluripotent Stem Cells Research (4 papers), Congenital Ear and Nasal Anomalies (4 papers), Congenital heart defects research (4 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (881 citations), Molecular Biology (1.9k citations), Genetics (171 citations), Developmental Neuroscience (59 citations) and Psychiatry and Mental health (119 citations). Kath Smith has collaborated with scholars based in United Kingdom, United States and Estonia. Frequent co-authors include Peter W. Andrews, Edna L. Maltby, H. D. M. Moore, Paul J. Gokhale, Jonathan S. Draper, James Alexander Thomson, Lorraine F. Meisner, Thomas P. Zwaka, Julie Ann Johnson and Paul Roy Heath. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Nature Biotechnology, Journal of Medical Genetics and Microscopy and Microanalysis.
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.