Andrea Byrnes

5.7k total citations · 1 hit paper
8 papers, 786 citations indexed

About

Andrea Byrnes is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Andrea Byrnes has authored 8 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Psychiatry and Mental health. Recurrent topics in Andrea Byrnes's work include Genetic Associations and Epidemiology (3 papers), Genomics and Rare Diseases (1 paper) and RNA modifications and cancer (1 paper). Andrea Byrnes is often cited by papers focused on Genetic Associations and Epidemiology (3 papers), Genomics and Rare Diseases (1 paper) and RNA modifications and cancer (1 paper). Andrea Byrnes collaborates with scholars based in United States, Sweden and Switzerland. Andrea Byrnes's 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 and has published in prestigious journals such as Nature, Bioinformatics and PLoS ONE.

In The Last Decade

Andrea Byrnes

7 papers receiving 779 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Landscape of X chromosome inactivation across human tissues

2017 665 citations Taru Tukiainen, Alexandra–Chloé Villani et al. Nature profile →

Peers

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

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8 of 8 papers shown

#	Work	Indexed citations
1	Photoaffinity enabled transcriptome-wide identification of splice modulating small molecule–RNA binding events in native cells 2025 ·RSC Chemical Biology ·(unknown), (unknown), (unknown), (unknown), Fan Lin, Lynn M. McGregor, Andrew Krueger, Nicole Renaud, Andrea Byrnes, Jason R. Thomas	0
2	Landscape of X chromosome inactivation across human tissues breakdown → 2017 ·Nature ·Taru Tukiainen, Alexandra–Chloé Villani, Angela Yen, Manuel A. Rivas, Jamie L. Marshall, Rahul Satija, Matthew Aguirre, Laura D. Gauthier, Mark Fleharty, Andrew Kirby, Beryl B. Cummings, Stephane E. Castel, Konrad J. Karczewski, François Aguet, Andrea Byrnes, Tuuli Lappalainen, Aviv Regev, Kristin Ardlie, Nir Hacohen, Daniel G. MacArthur	665
3	P1‐227: Comparative and combined accuracies of objective versus subjective screening instruments in distinguishing Alzheimer's disease, mild cognitive impairment, and age‐related cognitive decline 2015 ·Alzheimer s & Dementia ·Todd M. Solomon, (unknown), Andrea Byrnes, Cynthia Murphy, Paul R. Solomon	6
4	Likelihood-based complex trait association testing for arbitrary depth sequencing data 2015 ·Bioinformatics ·Yan Song, Shuai Yuan, Zheng Xu, (unknown), Bo Zhang, Guolian Kang, Andrea Byrnes, Yun Li	3
5	The Value of Statistical or Bioinformatics Annotation for Rare Variant Association With Quantitative Trait 2013 ·Genetic Epidemiology ·Andrea Byrnes, Michael C. Wu, Fred A. Wright, Mingyao Li, Yun Li	14
6	To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests 2011 ·The American Journal of Human Genetics ·Yun Li, Andrea Byrnes, Mingyao Li	2
7	To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests 2010 ·The American Journal of Human Genetics ·Yun Li, Andrea Byrnes, Mingyao Li	78
8	Gene Expression in Peripheral Blood Leukocytes in Monozygotic Twins Discordant for Chronic Fatigue: No Evidence of a Biomarker 2009 ·PLoS ONE ·Andrea Byrnes, (unknown), Karin Dahlman‐Wright, Birgitta Evengård, Fred A. Wright, Nancy L. Pedersen, Patrick F. Sullivan	18

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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