Nigel Smith

545 total citations
11 papers, 409 citations indexed

About

Nigel Smith is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Nigel Smith has authored 11 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Nigel Smith's work include Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers) and Congenital limb and hand anomalies (2 papers). Nigel Smith is often cited by papers focused on Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers) and Congenital limb and hand anomalies (2 papers). Nigel Smith collaborates with scholars based in United Kingdom, Netherlands and United States. Nigel Smith's co-authors include Chris Denning, Lorraine Young, D. N. Anderson, Robert J. Thomas, Amit Chandra, David Williams, Helen Priddle, Cinzia Allegrucci, Tim Self and Christine L. Mummery and has published in prestigious journals such as Human Molecular Genetics, Biotechnology and Bioengineering and Reproductive BioMedicine Online.

In The Last Decade

Nigel Smith

11 papers receiving 387 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nigel Smith United Kingdom	8	337	144	86	76	30	11	409
Urielle Ullmann Belgium	6	306 0.9×	71 0.5×	40 0.5×	73 1.0×	26 0.9×	7	357
Tamar Dvash Israel	9	407 1.2×	59 0.4×	91 1.1×	50 0.7×	15 0.5×	9	469
Alexis Bosman Australia	10	329 1.0×	93 0.6×	33 0.4×	140 1.8×	19 0.6×	22	424
Erica C. Jonlin United States	7	471 1.4×	64 0.4×	96 1.1×	45 0.6×	38 1.3×	15	538
Yong Bin Park South Korea	6	303 0.9×	85 0.6×	34 0.4×	76 1.0×	6 0.2×	7	339
Man Tong China	8	655 1.9×	83 0.6×	105 1.2×	81 1.1×	62 2.1×	14	743
Yee Siang Lim Singapore	4	523 1.6×	73 0.5×	53 0.6×	47 0.6×	5 0.2×	6	554
Margot Van der Jeught Belgium	15	460 1.4×	71 0.5×	40 0.5×	43 0.6×	41 1.4×	25	517
Tushar Menon United States	7	407 1.2×	50 0.3×	106 1.2×	106 1.4×	10 0.3×	12	592

Countries citing papers authored by Nigel Smith

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Nigel Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Nigel Smith. A scholar is included among the top collaborators of Nigel Smith based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Nigel Smith. Nigel Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Dixit, Abhijit, Chirag Patel, Rachel Harrison, et al.. (2012). 17q12 microdeletion syndrome: Three patients illustrating the phenotypic spectrum. American Journal of Medical Genetics Part A. 158A(9). 2317–2321. 37 indexed citations

Priddle, Helen, Cinzia Allegrucci, Paul W. Burridge, et al.. (2010). Derivation and characterisation of the human embryonic stem cell lines, NOTT1 and NOTT2. In Vitro Cellular & Developmental Biology - Animal. 46(3-4). 367–375. 8 indexed citations

Thomas, Robert J., D. N. Anderson, Amit Chandra, et al.. (2008). Automated, scalable culture of human embryonic stem cells in feeder‐free conditions. Biotechnology and Bioengineering. 102(6). 1636–1644. 117 indexed citations

Allegrucci, Cinzia, Yue-Zhong Wu, Alexandra Thurston, et al.. (2007). Restriction landmark genome scanning identifies culture-induced DNA methylation instability in the human embryonic stem cell epigenome. Human Molecular Genetics. 16(10). 1253–1268. 117 indexed citations

Stolpe, Anja van de, Stieneke van den Brink, Dorien Ward‐van Oostwaard, et al.. (2005). Human embryonic stem cells: towards therapies for cardiac disease. Derivation of a Dutch human embryonic stem cell line. Reproductive BioMedicine Online. 11(4). 476–485. 19 indexed citations

Denning, Chris, Cinzia Allegrucci, Helen Priddle, et al.. (2005). Common culture conditions for maintenance and cardiomyocyte differentiation of the human embryonic stem cell lines, BG01 and HUES-7. The International Journal of Developmental Biology. 50(1). 27–37. 73 indexed citations

Martin, B., et al.. (1997). A magnetic colloid system for isolation of rare cells from blood for FISH analysis. Prenatal Diagnosis. 17(11). 1059–1066. 14 indexed citations

Morrison, P., Nigel Smith, Katherine Martin, & I D Young. (1997). Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation.. PubMed. 68(1). 50–3. 11 indexed citations

Morrison, P., et al.. (1997). Mosaic partial trisomy 17 due to a ring chromosome identified by fluorescence in situ hybridisation. American Journal of Medical Genetics. 68(1). 50–53. 7 indexed citations

10.

Walker, David, et al.. (1996). Inversion (14)(q11q32) in a patient with childhood T-cell acute lymphoblastic leukemia. Cancer Genetics and Cytogenetics. 88(1). 76–79. 2 indexed citations

11.

Terrett, Jonathan, Ruth Newbury‐Ecob, Nigel Smith, et al.. (1996). A translocation at 12q2 refines the interval containing the Holt-Oram syndrome 1 gene.. PubMed. 59(6). 1337–41. 4 indexed citations

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.

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