Simon Thomas

1.8k citations
8 papers · 961 · 1 hit paper · h-index 7

Impact in

  • Genetics top 10%
    • Genetic Syndromes and Imprinting
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Spectroscopy and Chemometric Analyses

Papers in

    • Genetic Syndromes and Imprinting 4
    • Genetics and Neurodevelopmental Disorders 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
    • Epigenetics and DNA Methylation 2
    • Genomics and Chromatin Dynamics 1
    • RNA regulation and disease 1

Simon Thomas

8 papers receiving 929 citations

Simon Thomas's Hit Papers

Cross-validation pitfalls when selecting and assessing regression and classification models 2014 · 724 citations
7240+4+8Years since publication200400600

Peers

Simon Thomas
Comparison fields: 5 of 169
  • Genetics 213
  • Analytical Chemistry 62
  • Health Informatics 8
  • Biophysics 30
  • Pediatrics, Perinatology and Child Health 86
Replace Burcu F. Darst with:
Burcu F. Darst United States
Ljubomir Buturović United States
Lewis Moffat United Kingdom
Andrius Vabalas United Kingdom
Benjamin Hofner Germany
Iakov I. Davydov Switzerland
Trang T. Le United States
Juliane Siebourg‐Polster Switzerland
Ping Huang China
Li-Yu Hu Taiwan
Simon Thomas relative to Burcu F. Darst United States Burcu F. Darst's profile →
Citations per field
00.5×
Burcu F. Darst · 1×
Citations per year

Countries citing papers authored by Simon Thomas

Since Specialization
Citations

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

Fields of papers citing papers by Simon Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Simon Thomas, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Simon Thomas Line = papers co-authored together Simon Thomas links everyone, so they are left out of the graph.

All Works

8 of 8 papers shown
#Work
1
Cross-validation pitfalls when selecting and assessing regression and classification models
Hit paper breakdown →
2014724
2 200277
3 200272
4 200232
5 200525
6 200318
7 202110
8
Chromosome aberrations and mutations in nature.
19603

About Simon Thomas

Simon Thomas is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience and Infectious Diseases, having authored 8 papers that have together received 961 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Epigenetics and DNA Methylation (2 papers), Autism Spectrum Disorder Research (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Genomics and Chromatin Dynamics (1 paper) and RNA regulation and disease (1 paper). The work is most often cited by research in Genetics (213 citations), Analytical Chemistry (62 citations), Health Informatics (8 citations), Biophysics (30 citations) and Pediatrics, Perinatology and Child Health (86 citations). Simon Thomas has collaborated with scholars based in United Kingdom, Italy and Singapore. Frequent co-authors include Damjan Krstajić, Ljubomir Buturović, David E. Leahy, Nicholas R. Dennis, Patricia A. Jacobs, Siân E. Roberts, Annette E. Cockwell, Bronwyn Kerr, Andrew Fisher and I. Karen Temple. Their work appears in journals such as Human Genetics, Mammalian Genome, Current Science, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and RNA.

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.

Explore authors with similar magnitude of impact