N S Thomas

1.3k total citations
31 papers, 768 citations indexed

About

N S Thomas is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, N S Thomas has authored 31 papers receiving a total of 768 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 16 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in N S Thomas's work include dental development and anomalies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). N S Thomas is often cited by papers focused on dental development and anomalies (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). N S Thomas collaborates with scholars based in United Kingdom, United States and Germany. N S Thomas's co-authors include Peter N. Goodfellow, Paul J. Goodfellow, S. M. Darling, Peter S. Harper, Angus Clarke, Keith Roberts, M. Sarfarazi, J. Zonana, Hywel Williams and Meena Upadhyaya and has published in prestigious journals such as Science, Human Molecular Genetics and The Journal of Pediatrics.

In The Last Decade

N S Thomas

30 papers receiving 748 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N S Thomas United Kingdom 15 580 257 95 80 76 31 768
Jacqueline Siegel‐Bartelt Canada 8 820 1.4× 477 1.9× 44 0.5× 38 0.5× 33 0.4× 10 1.1k
Astrid Golla Germany 15 317 0.5× 333 1.3× 84 0.9× 143 1.8× 47 0.6× 25 806
Cornelia Leimeister Germany 13 1.0k 1.8× 213 0.8× 105 1.1× 20 0.3× 72 0.9× 13 1.1k
Branko Latinkic United Kingdom 19 1.1k 2.0× 231 0.9× 110 1.2× 40 0.5× 23 0.3× 28 1.3k
Yves Lacassie United States 18 475 0.8× 425 1.7× 93 1.0× 39 0.5× 14 0.2× 70 952
Ken Arita Japan 17 375 0.6× 184 0.7× 326 3.4× 99 1.2× 78 1.0× 31 804
Luís Garcia Alonso Brazil 17 541 0.9× 621 2.4× 107 1.1× 74 0.9× 21 0.3× 56 1.1k
Kouji Narahara Japan 18 509 0.9× 500 1.9× 38 0.4× 41 0.5× 19 0.3× 52 877
Rita Gardella Italy 16 373 0.6× 479 1.9× 265 2.8× 56 0.7× 16 0.2× 32 968
Yolande van Bever Netherlands 18 297 0.5× 441 1.7× 39 0.4× 56 0.7× 61 0.8× 46 871

Countries citing papers authored by N S Thomas

Since Specialization
Citations

This map shows the geographic impact of N S Thomas'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 N S Thomas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N S Thomas more than expected).

Fields of papers citing papers by N S Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N S Thomas. 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 N S Thomas. The network helps show where N S Thomas may publish in the future.

Co-authorship network of co-authors of N S Thomas

This figure shows the co-authorship network connecting the top 25 collaborators of N S Thomas. A scholar is included among the top collaborators of N S Thomas 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 N S Thomas. N S Thomas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Spurlock, Gillian, Ellen Bennett, Nadia Chuzhanova, et al.. (2009). SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype. Journal of Medical Genetics. 46(7). 431–437. 58 indexed citations
2.
Cockwell, Annette E., et al.. (2005). Molecular investigation of a dicentric 13;17 chromosome found in a 21-week gestation fetus with multiple congenital abnormalities. Cytogenetic and Genome Research. 112(1-2). 166–169. 2 indexed citations
3.
Bunyan, David J., et al.. (2003). Importance of mutation screening in 'false-positive' MLPA cases. 30(6). 422–5.
4.
Ferguson, Betsy, et al.. (1998). Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications.. Journal of Medical Genetics. 35(2). 112–115. 29 indexed citations
5.
Laporte, Jocelyn, Petra Kioschis, Annemarie Poustka, et al.. (1996). Deletions in Xq28 in Two Boys with Myotubular Myopathy and Abnormal Genital Development Define a New Contiguous Gene Syndrome in a 430 kb Region. Human Molecular Genetics. 5(1). 139–143. 57 indexed citations
6.
Thomas, N S, J. Zonana, Kathryn J.P. Davies, et al.. (1993). Characterisation of molecular DNA rearrangements within the Xq12 – q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA). Human Molecular Genetics. 2(10). 1679–1685. 10 indexed citations
7.
Clarke, Angus, David Bradley, Kathleen M. Gillespie, et al.. (1992). Fragile X mental retardation and the iduronate sulphatase locus: Testing laird's model of Fra(X) inheritance. American Journal of Medical Genetics. 43(1-2). 299–306. 10 indexed citations
8.
Aldred, Michael J., P J Crawford, N S Thomas, et al.. (1992). Genetic heterogeneity in X-linked amelogenesis imperfecta. Genomics. 14(3). 567–573. 58 indexed citations
9.
Upadhyaya, Meena, Robert A. Smith, N S Thomas, Andrew Norman, & P.S. Harper. (1990). Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA. Clinical Genetics. 37(6). 456–462. 15 indexed citations
10.
Zonana, Jonathan, Albert Schinzel, Meena Upadhyaya, et al.. (1990). Prenatal diagnosis of X‐linked hypohidrotic ectodermal dysplasia by linkage analysis. American Journal of Medical Genetics. 35(1). 132–135. 14 indexed citations
11.
12.
Norman, Andrew, Meena Upadhyaya, N S Thomas, Keith Roberts, & Peter S. Harper. (1989). Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.. Journal of Medical Genetics. 26(9). 565–571. 4 indexed citations
13.
Zonana, J., Angus Clarke, N S Thomas, et al.. (1988). Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group). Journal of Medical Genetics. 25(4). 274–283. 3 indexed citations
14.
Zonana, Jonathan, Selwyn H. Roberts, N S Thomas, & Peter S. Harper. (1988). Recognition andreanalysis ofacell line froma manifesting female withX linked hypohidrotic ectodermal dysplasia andanX;autosome balanced translocation. 2 indexed citations
15.
Clarke, Alan R., M. Sarfarazi, N S Thomas, Keith Roberts, & Peter S. Harper. (1987). X-linked hypohidrotic ectodermal dysplasia: DNA probe linkage analysis and gene localization. Human Genetics. 75(4). 378–380. 24 indexed citations
16.
Brook, J. David, Duncan J. Shaw, N S Thomas, et al.. (1986). Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids. Cytogenetic and Genome Research. 41(1). 30–37. 26 indexed citations
17.
18.
Thomas, N S, Hywel Williams, Louis J. Elsas, et al.. (1986). Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.. Journal of Medical Genetics. 23(6). 596–598. 36 indexed citations
19.
Goodfellow, Paul J., S. M. Darling, N S Thomas, & Peter N. Goodfellow. (1986). A Pseudoautosomal Gene in Man. Science. 234(4777). 740–743. 176 indexed citations
20.
Upadhyaya, Meena, Peter S. Harper, Bharat Jasani, et al.. (1984). DNA and enzyme studies on chorionic villi for use in antenatal diagnosis. Clinica Chimica Acta. 140(1). 39–46. 12 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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