Nigel M. Smith
Impact in
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- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- Epigenetics and DNA Methylation
- Renal and related cancers
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- 3D Printing in Biomedical Research
Papers in
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- Congenital limb and hand anomalies 2
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- Pluripotent Stem Cells Research 5
- CRISPR and Genetic Engineering 4
- Congenital heart defects research 2
- Co-authors
- Chris N. Denning (5 shared papers)Lorraine E. Young (4 shared papers)D. N. Anderson (2 shared papers)Amit Chandra (1 shared paper)David J. Williams (1 shared paper)Robert James Thomas (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 M. Smith
11 papers receiving 411 citations
Peers
Comparison fields: 5 of 55
- Molecular Biology 347
- Biomedical Engineering 156
- Genetics 30
- Genetics 76
- Developmental Neuroscience 8
Countries citing papers authored by Nigel M. Smith
This map shows the geographic impact of Nigel M. 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 M. 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 M. Smith more than expected).
Fields of papers citing papers by Nigel M. Smith
This network shows the impact of papers produced by Nigel M. 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 M. Smith. The network helps show where Nigel M. Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Nigel M. 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 | 134 | |
| 2 | 2007 | 130 | |
| 3 | 2005 | 76 | |
| 4 | 2012 | 38 | |
| 5 | 2005 | 18 | |
| 6 | 1997 | 14 | |
| 7 | Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation. | 1997 | 12 |
| 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 | 3 |
About Nigel M. Smith
Nigel M. Smith is a scholar working on Developmental Biology, Molecular Biology, Cancer Research, Genetics and Cellular and Molecular Neuroscience, having authored 11 papers that have together received 444 indexed citations. Recurring topics across this work include Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers), Congenital limb and hand anomalies (2 papers), Congenital heart defects research (2 papers), Hereditary Neurological Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Tissue Engineering and Regenerative Medicine (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Molecular Biology (347 citations), Biomedical Engineering (156 citations), Genetics (30 citations), Genetics (76 citations) and Developmental Neuroscience (8 citations). Nigel M. Smith has collaborated with scholars based in United Kingdom, Netherlands and United States. Frequent co-authors include Chris N. Denning, Lorraine E. Young, D. N. Anderson, Amit Chandra, David J. Williams, Robert James Thomas, 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.