N. Simon Thomas

4.5k total citations
67 papers, 2.6k citations indexed

About

N. Simon Thomas is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N. Simon Thomas has authored 67 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Genetics, 26 papers in Molecular Biology and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N. Simon Thomas's work include Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (17 papers) and Genetic Syndromes and Imprinting (15 papers). N. Simon Thomas is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (17 papers) and Genetic Syndromes and Imprinting (15 papers). N. Simon Thomas collaborates with scholars based in United Kingdom, United States and Australia. N. Simon Thomas's co-authors include Marijcke W. M. Veltman, Patrick Bolton, Russell Thompson, Patricia A. Jacobs, David J. Bunyan, C.E. Browne, John A. Crolla, Siân E. Roberts, P. A. Jacobs and David Skuse and has published in prestigious journals such as Brain, American Journal of Respiratory and Critical Care Medicine and The American Journal of Human Genetics.

In The Last Decade

N. Simon Thomas

63 papers receiving 2.5k 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. Simon Thomas United Kingdom 30 2.0k 1.1k 502 434 332 67 2.6k
Karen Brøndum‐Nielsen Denmark 34 2.0k 1.0× 2.3k 2.0× 485 1.0× 514 1.2× 290 0.9× 137 4.1k
Damien Sanlaville France 33 2.2k 1.1× 1.6k 1.4× 585 1.2× 305 0.7× 385 1.2× 189 3.7k
S Gilgenkrantz France 26 1.6k 0.8× 1.5k 1.3× 276 0.5× 373 0.9× 272 0.8× 162 2.7k
Ute Moog Germany 29 1.7k 0.8× 1.3k 1.1× 257 0.5× 443 1.0× 215 0.6× 95 2.6k
Trilochan Sahoo United States 36 2.8k 1.4× 1.9k 1.6× 1.1k 2.3× 426 1.0× 381 1.1× 67 4.1k
R. Ellen Magenis United States 32 2.0k 1.0× 2.0k 1.8× 538 1.1× 205 0.5× 277 0.8× 71 3.7k
Tiziano Pramparo United States 27 1.2k 0.6× 1.7k 1.5× 219 0.4× 503 1.2× 201 0.6× 50 2.7k
Shivanand R. Patil United States 24 1.2k 0.6× 1.2k 1.0× 418 0.8× 150 0.3× 269 0.8× 77 2.2k
Christophe Philippe France 30 1.6k 0.8× 1.5k 1.3× 207 0.4× 309 0.7× 102 0.3× 77 2.7k
P Jalbert France 19 1.1k 0.6× 735 0.6× 360 0.7× 368 0.8× 263 0.8× 59 1.7k

Countries citing papers authored by N. Simon Thomas

Since Specialization
Citations

This map shows the geographic impact of N. Simon 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. Simon 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. Simon Thomas more than expected).

Fields of papers citing papers by N. Simon Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Simon Thomas

This figure shows the co-authorship network connecting the top 25 collaborators of N. Simon Thomas. A scholar is included among the top collaborators of N. Simon 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. Simon Thomas. N. Simon 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.
Watts, Laura, David J. Bunyan, Edoardo Giacopuzzi, et al.. (2024). FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6. Brain Communications. 6(5).
2.
Wheway, Gabrielle, Htoo A. Wai, Woolf T. Walker, et al.. (2024). Uplift of genetic diagnosis of rare respiratory disease using airway epithelium transcriptome analysis. Human Molecular Genetics. 34(2). 148–160.
3.
Wai, Htoo A., David J. Bunyan, N. Simon Thomas, et al.. (2024). Identification of diagnostic candidates in Mendelian disorders using an RNA sequencing-centric approach. Genome Medicine. 16(1). 110–110. 3 indexed citations
4.
Seaby, Eleanor G., N. Simon Thomas, David Hunt, et al.. (2023). A Panel-Agnostic Strategy ‘HiPPo’ Improves Diagnostic Efficiency in the UK Genomic Medicine Service. Healthcare. 11(24). 3179–3179.
5.
Wai, Htoo A., Tessy Thomas, David J. Bunyan, et al.. (2022). A systematic analysis of splicing variants identifies new diagnoses in the 100,000 Genomes Project. Genome Medicine. 14(1). 79–79. 20 indexed citations
6.
Barnicoat, Angela, Amaka C Offiah, Alistair Calder, et al.. (2021). AIFM1‐associated X‐linked spondylometaphyseal dysplasia with cerebral hypomyelination. American Journal of Medical Genetics Part A. 185(4). 1228–1235. 4 indexed citations
7.
Wai, Htoo A., Jenny Lord, Matthew Lyon, et al.. (2020). Blood RNA analysis can increase clinical diagnostic rate and resolve variants of uncertain significance. Genetics in Medicine. 22(6). 1005–1014. 103 indexed citations
8.
Thomas, N. Simon, et al.. (2020). Screening of a large Rubinstein–Taybi cohort identified many novel variants and emphasizes the importance of the CREBBP histone acetyltransferase domain. American Journal of Medical Genetics Part A. 182(11). 2508–2520. 8 indexed citations
9.
Barber, John, Jill A. Rosenfeld, Nicola Foulds, et al.. (2013). 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A. 161(3). 487–500. 33 indexed citations
10.
Thomas, N. Simon, et al.. (2012). Role of fecundity genes in prolificacy of small ruminants.. 10(3). 34–37. 8 indexed citations
11.
Barnicoat, Angela, Shuwen Huang, Viv Maloney, et al.. (2008). Transmitted duplication of 8p23.1–8p23.2 associated with speech delay, autism and learning difficulties. European Journal of Human Genetics. 17(1). 37–43. 61 indexed citations
12.
Gilling, Mette, Stefan Gesk, Reiner Siebert, et al.. (2006). Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans. The American Journal of Human Genetics. 78(5). 878–883. 30 indexed citations
13.
Thompson, Russell, Marijcke W. M. Veltman, N. Simon Thomas, et al.. (2005). Prader‐Willi syndrome: intellectual abilities and behavioural features by genetic subtype. Journal of Child Psychology and Psychiatry. 46(10). 1089–1096. 129 indexed citations
14.
Veltman, Marijcke W. M., Russell Thompson, Siân E. Roberts, et al.. (2004). Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders.. PubMed. 13(1). 42–50. 86 indexed citations
15.
Thomas, N. Simon, et al.. (2004). SHOX mutations in a family and a fetus with Langer mesomelic dwarfism. American Journal of Medical Genetics Part A. 128A(2). 179–184. 14 indexed citations
16.
Lachlan, Katherine, et al.. (2004). Functional disomy resulting from duplications of distal Xq in four unrelated patients. Human Genetics. 115(5). 399–408. 39 indexed citations
17.
Good, Catriona D., Kate Lawrence, N. Simon Thomas, et al.. (2003). Dosage‐sensitive X‐linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humans. Brain. 126(11). 2431–2446. 145 indexed citations
18.
Hassold, Terry, Lindsay C. Burrage, E. Ricky Chan, et al.. (2001). Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction. The American Journal of Human Genetics. 69(2). 434–439. 58 indexed citations
19.
Thomas, N. Simon, Jennifer Wilkinson, Píetro Lió, et al.. (2000). [Genetic factors involved in asthma and atopy. Studies in British families].. PubMed. 17(1 Pt 2). 177–82.
20.
Thomas, N. Simon, et al.. (2000). Linkage Analysis of Markers on Chromosome 11q13 with Asthma and Atopy in a United Kingdom Population. American Journal of Respiratory and Critical Care Medicine. 162(4). 1268–1272. 15 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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