Brett Thomas

11.2k citations
9 papers · 9.1k · 2 hit papers · h-index 8

Impact in

  • Genetics top 0.5%
    • Genomics and Rare Diseases
    • Genetic Associations and Epidemiology
    • Genetics and Neurodevelopmental Disorders
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Metabolism and Genetic Disorders

Papers in

    • Genomics and Rare Diseases 4
    • Muscle Physiology and Disorders 2
    • Bioinformatics and Genomic Networks 1

Brett Thomas

9 papers receiving 9k citations

Brett Thomas's Hit Papers

Analysis of protein-coding genetic variation in 60,706 humans 2016 · 7.9k citations
7.9k0+3+6Years since publication2.5k5k7.5k

Peers

Brett Thomas
Comparison fields: 5 of 119
  • Genetics 4k
  • Clinical Biochemistry 219
  • Molecular Biology 1.9k
  • Cancer Research 387
  • Developmental Biology 48
Replace Joanne Berghout with:
Joanne Berghout United States
Nicole A. Deflaux United States
Eleanor G. Seaby United Kingdom
Clicerio González United States
Eleina M. England United States
Colin N. A. Palmer United States
Sam Novod United States
Kristen M. Connolly United States
Kristen M. Laricchia United States
Diane Kaplan United States
Brett Thomas relative to Joanne Berghout United States Joanne Berghout's profile →
Citations per field
00.5×1.5×
Joanne Berghout · 1×
Citations per year

Countries citing papers authored by Brett Thomas

Since Specialization
Citations

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

Fields of papers citing papers by Brett Thomas

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

9 of 9 papers shown
#Work
1
Analysis of protein-coding genetic variation in 60,706 humans
Hit paper breakdown →
20167891
2
The ExAC browser: displaying reference data information from over 60 000 exomes
Hit paper breakdown →
2016575
3 2012187
4 2014174
5 201498
6 201568
7 201358
8 201527
9 20207

About Brett Thomas

Brett Thomas is a scholar working on Genetics, Molecular Biology, Ophthalmology, Reproductive Medicine and Rheumatology, having authored 9 papers that have together received 9.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Muscle Physiology and Disorders (2 papers), Bioinformatics and Genomic Networks (1 paper), Glycogen Storage Diseases and Myoclonus (1 paper), Cardiomyopathy and Myosin Studies (1 paper), Lysosomal Storage Disorders Research (1 paper), Retinal Diseases and Treatments (1 paper) and Reproductive Biology and Fertility (1 paper). The work is most often cited by research in Genetics (4k citations), Clinical Biochemistry (219 citations), Molecular Biology (1.9k citations), Cancer Research (387 citations) and Developmental Biology (48 citations). Brett Thomas has collaborated with scholars based in United States, Australia and United Kingdom. Frequent co-authors include Mark Daly, Daniel G. MacArthur, David Kavanagh, Colm T. O’Dushlaine, Shaun Purcell, Konrad J. Karczewski, Matthew Solomonson, Douglas M. Ruderfer, Monkol Lek and Kaitlin E. Samocha. Their work appears in journals such as Journal of Clinical Investigation, Human Molecular Genetics, The Journal of Clinical Endocrinology & Metabolism, Nucleic Acids Research and Nature.

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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