Timothy Read

947 citations
11 papers · 175 · h-index 7

Impact in

    • Genetic Associations and Epidemiology
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Cancer-related molecular mechanisms research

Papers in

    • RNA and protein synthesis mechanisms 2
    • Genomics and Chromatin Dynamics 2
    • RNA Research and Splicing 2
    • Genetic Associations and Epidemiology 4
    • Genomic variations and chromosomal abnormalities 2
    • Connective tissue disorders research 1

Timothy Read

11 papers receiving 169 citations

Peers

Timothy Read
Comparison fields: 5 of 48
  • Genetics 56
  • Cancer Research 27
  • Molecular Biology 114
  • Biological Psychiatry 3
  • Psychiatry and Mental health 12
Replace Mark E. Wadsworth with:
Mark E. Wadsworth United States
Christopher C Park United States
Arkadiy K. Golov Russia
Stephanie K. Jones United States
Véronique Damagnez France
Jennifer Parla United States
Fernanda T. Bellucco Brazil
Natàlia Padilla Spain
Angela Shone United Kingdom
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Citations per field
00.5×1.5×
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Citations per year

Countries citing papers authored by Timothy Read

Since Specialization
Citations

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

Fields of papers citing papers by Timothy Read

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 201873
2 199532
3 200615
4 199412
5 199512
6 20168
7 20228
8 19896
9 20144
10 20243
11 19992

About Timothy Read

Timothy Read is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Clinical Psychology and Ecology, Evolution, Behavior and Systematics, having authored 11 papers that have together received 175 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (4 papers), RNA and protein synthesis mechanisms (2 papers), Autism Spectrum Disorder Research (2 papers), Genomics and Chromatin Dynamics (2 papers), RNA Research and Splicing (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Plant and animal studies (1 paper) and Connective tissue disorders research (1 paper). The work is most often cited by research in Genetics (56 citations), Cancer Research (27 citations), Molecular Biology (114 citations), Biological Psychiatry (3 citations) and Psychiatry and Mental health (12 citations). Timothy Read has collaborated with scholars based in United States, United Kingdom and Iceland. Frequent co-authors include Robin D. Dowell, Jonathan D. Rubin, Mary A. Allen, Joseph Azofeifa, David W. Ussery, David Curtis, Hannes Pétursson, Jon Brynjolfsson, Gursharan Kalsi and P. Murphy. Their work appears in journals such as Psychiatric Genetics, The American Naturalist, Schizophrenia Bulletin, PLoS Genetics and Genome Research.

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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