Matthew P. Conomos

11.0k citations
26 papers · 1.5k indexed · 1 hit paper · h-index 16
  • Genetics top 2%
    • Genetic Associations and Epidemiology 16
    • Genetic and phenotypic traits in livestock 5
    • Genetic Mapping and Diversity in Plants and Animals 5
    • BRCA gene mutations in cancer 3
    • Genomics and Rare Diseases 2
    • Gut microbiota and health 3
    • Gene expression and cancer classification 3
    • Epigenetics and DNA Methylation 2

Matthew P. Conomos

25 papers receiving 1.5k citations

Hit Papers

Principles and methods for transferring polygenic risk sc...1032023202620242025255075100

Peers

Matthew P. Conomos
Comparison fields: 5 of 128
  • Genetics 861
  • Molecular Biology 549
  • Physiology 177
  • Biological Psychiatry 16
  • Cancer Research 85
Replace Timothy A. Thornton with:
Timothy A. Thornton United States
Janis Wigginton United States
Hilary C. Martin United Kingdom
Doug Speed Denmark
María Cerezo Spain
Carl A. Anderson United Kingdom
М. И. Воевода Russia
Lukas Forer Austria
Nikunj Patel United States
Carolina Bonilla United Kingdom
Matthew P. Conomos relative to Timothy A. Thornton United States Timothy A. Thornton's profile →
Citations per field
00.5×1.5×1.8×
Timothy A. Thornton · 1×
Citations per year

Countries citing papers authored by Matthew P. Conomos

Since Specialization
Citations

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

Fields of papers citing papers by Matthew P. Conomos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew P. Conomos. 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 Matthew P. Conomos. The network helps show where Matthew P. Conomos may publish in the future.

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20250
2 20244
3
Principles and methods for transferring polygenic risk scores across global populationsbreakdown →
2023103
4 202249
5 202243
6 20218
7 202142
8 202015
9 201933
10 2019154
11 2018112
12 201782
13 201720
14 20164
15 2016221
16 2015188
17 201533
18 20146
19 201413
20
Attitudes of drivers towards organ donation.
19923

About Matthew P. Conomos

Matthew P. Conomos is a scholar working on Genetics, Biological Psychiatry and Periodontics, having authored 26 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (16 papers), Genetic and phenotypic traits in livestock (5 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers), BRCA gene mutations in cancer (3 papers), Gut microbiota and health (3 papers), Gene expression and cancer classification (3 papers), Genomics and Rare Diseases (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (861 citations), Molecular Biology (549 citations) and Physiology (177 citations). Matthew P. Conomos has collaborated with scholars based in United States, Australia and Singapore. Frequent co-authors include Timothy A. Thornton, Bruce S. Weir, Michael B. Miller, Alexander P. Reiner, Kenneth Rice, Stephanie M. Gogarten, Tamar Sofer, Cathy C. Laurie, Han Chen and Andrew T. Magis. Their work appears in journals such as Journal of Clinical Investigation, Bioinformatics and Nature Reviews Genetics.

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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