Andrea Byrnes

5.7k citations
8 papers · 786 indexed · 1 hit paper · h-index 5
Topics
Genetic Associations and Epidemiology (3 papers)Genomics and Rare Diseases (1 paper)RNA modifications and cancer (1 paper)

In The Last Decade

Andrea Byrnes

7 papers receiving 779 citations

Hit Papers

Landscape of X chromosome inactivation across human tissues20172026202020232017200400600

Peers

Andrea Byrnes
Comparison fields: 5 of 85
  • Genetics 390
  • Molecular Biology 318
  • Immunology 103
  • Infectious Diseases 98
  • Public Health, Environmental and Occupational Health 80
Replace Mark Fleharty with:
Mark Fleharty United States
Matthew Aguirre United States
Elior Rahmani United States
P. Saccucci Italy
Antoine De Pauw France
Fabiana B. Kohlrausch Brazil
Fabio Spreafico Italy
Elizabeth McPherson United States
Charles E. Breeze United Kingdom
Shijie Zheng China
Andrea Byrnes relative to Mark Fleharty United States Mark Fleharty's profile →
Citations per field
00.5×
Mark Fleharty · 1×
Citations per year

Countries citing papers authored by Andrea Byrnes

Since Specialization
Citations

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

Fields of papers citing papers by Andrea Byrnes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Byrnes

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Byrnes. A scholar is included among the top collaborators of Andrea Byrnes based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrea Byrnes. Andrea Byrnes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
#WorkIndexed citations
1 0
2
Landscape of X chromosome inactivation across human tissuesbreakdown →
665
3 6
4 3
5 14
6 2
7 78
8 18

About Andrea Byrnes

Andrea Byrnes is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology, having authored 8 papers that have together received 786 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Genomics and Rare Diseases (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (390 citations), Obstetrics and Gynecology (48 citations) and Infectious Diseases (98 citations). Andrea Byrnes has collaborated with scholars based in United States, Sweden and Switzerland. Frequent co-authors include Alexandra–Chloé Villani, Rahul Satija, Laura D. Gauthier, Aviv Regev, Jamie L. Marshall, Mark Fleharty, Manuel A. Rivas, Matthew Aguirre, Andrew Kirby and Stephane E. Castel. Their work appears in journals such as Nature, Bioinformatics and PLoS ONE.

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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