Nigel Smith
Impact in
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- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- Epigenetics and DNA Methylation
- Renal and related cancers
- Congenital heart defects research
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- 3D Printing in Biomedical Research
Papers in
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- Pluripotent Stem Cells Research 5
- CRISPR and Genetic Engineering 4
- Congenital heart defects research 2
- Advanced biosensing and bioanalysis techniques 1
- Genetics 3
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Chris Denning (5 shared papers)Lorraine Young (4 shared papers)D. N. Anderson (2 shared papers)Amit Chandra (1 shared paper)Robert J. Thomas (1 shared paper)David Williams (1 shared paper)Cinzia Allegrucci (3 shared papers)Helen Priddle (3 shared papers)
- Journals
- Reproductive BioMedicine Online (1 paper)Biotechnology and Bioengineering (1 paper)The International Journal of Developmental Biology (1 paper)In Vitro Cellular & Developmental Biology - Animal (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- United KingdomNetherlandsUnited States
In The Last Decade
Nigel Smith
11 papers receiving 387 citations
Peers
Comparison fields: 5 of 52
- Molecular Biology 337
- Biomedical Engineering 144
- Genetics 86
- Genetics 27
- Developmental Neuroscience 8
Countries citing papers authored by Nigel Smith
This map shows the geographic impact of Nigel 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 Nigel Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nigel Smith more than expected).
Fields of papers citing papers by Nigel Smith
This network shows the impact of papers produced by Nigel 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 Nigel Smith. The network helps show where Nigel Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Nigel 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
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 117 | |
| 2 | 2007 | 117 | |
| 3 | 2005 | 73 | |
| 4 | 2012 | 37 | |
| 5 | 2005 | 19 | |
| 6 | 1997 | 14 | |
| 7 | Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation. | 1997 | 11 |
| 8 | 2010 | 8 | |
| 9 | 1997 | 7 | |
| 10 | A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene. | 1996 | 4 |
| 11 | 1996 | 2 |
About Nigel Smith
Nigel Smith is a scholar working on Molecular Biology, Genetics, Surgery, Cellular and Molecular Neuroscience and Developmental Biology, having authored 11 papers that have together received 409 indexed citations. Recurring topics across this work include Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers), Hereditary Neurological Disorders (2 papers), Tissue Engineering and Regenerative Medicine (2 papers), Congenital heart defects research (2 papers), Congenital limb and hand anomalies (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Advanced biosensing and bioanalysis techniques (1 paper). The work is most often cited by research in Molecular Biology (337 citations), Biomedical Engineering (144 citations), Genetics (86 citations), Genetics (27 citations) and Developmental Neuroscience (8 citations). Nigel Smith has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Chris Denning, Lorraine Young, D. N. Anderson, Amit Chandra, Robert J. Thomas, David Williams, Cinzia Allegrucci, Helen Priddle, Christine L. Mummery and Dorien Ward‐van Oostwaard. Their work appears in journals such as Reproductive BioMedicine Online, Biotechnology and Bioengineering, The International Journal of Developmental Biology, In Vitro Cellular & Developmental Biology - Animal and Human Molecular 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.