Thomas Layman

437 citations
9 papers · 268 · h-index 9

Impact in

Papers in

    • Epigenetics and DNA Methylation 4
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
    • Genetics and Neurodevelopmental Disorders 1
    • Genetic Syndromes and Imprinting 1

Thomas Layman

9 papers receiving 265 citations

Peers

Thomas Layman
Comparison fields: 5 of 72
  • Biological Psychiatry 10
  • Developmental Neuroscience 12
  • Genetics 79
  • Emergency Medical Services 13
  • Molecular Biology 134
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Citations per field
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Citations per year

Countries citing papers authored by Thomas Layman

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Layman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Thomas Layman, 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 Thomas Layman Line = papers co-authored together Thomas Layman links everyone, so they are left out of the graph.

All Works

9 of 9 papers shown
#Work
1 201972
2 202168
3 199731
4 201724
5 202017
6 200916
7 201915
8 202114
9 202211

About Thomas Layman

Thomas Layman is a scholar working on Molecular Biology, Genetics, Plant Science, Infectious Diseases and General Health Professions, having authored 9 papers that have together received 268 indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Chromosomal and Genetic Variations (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Aortic Disease and Treatment Approaches (1 paper), Genetic Syndromes and Imprinting (1 paper), Aortic aneurysm repair treatments (1 paper) and Global Health Workforce Issues (1 paper). The work is most often cited by research in Biological Psychiatry (10 citations), Developmental Neuroscience (12 citations), Genetics (79 citations), Emergency Medical Services (13 citations) and Molecular Biology (134 citations). Thomas Layman has collaborated with scholars based in United States, Japan and Spain. Frequent co-authors include Soojin V. Yi, Paramita Chatterjee, Hyeonsoo Jeong, Stefano Berto, Noriyoshi Usui, Todd M. Preuss, Geneviève Konopka, Isabel Mendizabal, Kazuya Toriumi and Iksoo Huh. Their work appears in journals such as The Journal of Immunology, Surgical Clinics of North America, Genome Research, Molecular Ecology and Journal of Vascular Surgery.

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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