Gareth Highnam

1.9k total citations
10 papers, 582 citations indexed

About

Gareth Highnam is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Gareth Highnam has authored 10 papers receiving a total of 582 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Plant Science. Recurrent topics in Gareth Highnam's work include Genomics and Phylogenetic Studies (6 papers), RNA and protein synthesis mechanisms (3 papers) and Chromosomal and Genetic Variations (2 papers). Gareth Highnam is often cited by papers focused on Genomics and Phylogenetic Studies (6 papers), RNA and protein synthesis mechanisms (3 papers) and Chromosomal and Genetic Variations (2 papers). Gareth Highnam collaborates with scholars based in United States, Switzerland and Spain. Gareth Highnam's co-authors include David Mittelman, Melissa Gymrek, Yaniv Erlich, Thomas Willems, Andrew J. Sharp, Christopher T. Franck, Audrey Guilmatre, Ricky S. Joshi, Javier Quilez and Paras Garg and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Methods.

In The Last Decade

Gareth Highnam

10 papers receiving 569 citations

Peers

Gareth Highnam

MB

GENET

CMN

PS

CR

William Spooner United Kingdom

M Braun Germany

Colleen Davis United States

Simon Brent United Kingdom

Isaac Ho United States

Etienne Raimondeau United Kingdom

Jürgen Dönitz Germany

Vidhya Narayanan United States

Sharona Shleizer-Burko United States

Kerrie Nichol Edamura Canada

William Spooner United Kingdom

Gareth Highnam

625 ×1.5

MB

242 ×0.8

GENET

15 ×0.2

CMN

161 ×1.7

PS

57 ×1.2

CR

Citations per year, relative to Gareth Highnam Gareth Highnam (= 1×) peers William Spooner

Countries citing papers authored by Gareth Highnam

Since Specialization

Citations

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

Fields of papers citing papers by Gareth Highnam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gareth Highnam

This figure shows the co-authorship network connecting the top 25 collaborators of Gareth Highnam. A scholar is included among the top collaborators of Gareth Highnam 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 Gareth Highnam. Gareth Highnam is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Quilez, Javier, Audrey Guilmatre, Paras Garg, et al.. (2016). Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans. Nucleic Acids Research. 44(8). 3750–3762. 100 indexed citations

2.

Zook, Justin M., et al.. (2015). An analytical framework for optimizing variant discovery from personal genomes. Nature Methods. 6. 2 indexed citations

3.

Highnam, Gareth, et al.. (2015). An analytical framework for optimizing variant discovery from personal genomes. Nature Communications. 6(1). 6275–6275. 66 indexed citations

4.

Sonay, Tugce Bilgin, Tiago Carvalho, Mark D. Robinson, et al.. (2015). Tandem repeat variation in human and great ape populations and its impact on gene expression divergence. Genome Research. 25(11). 1591–1599. 56 indexed citations

5.

Goodyear, Andrew, Iona L. Bartek, Allison K. Stewart, et al.. (2015). A Burkholderia pseudomallei Colony Variant Necessary for Gastric Colonization. mBio. 6(1). 19 indexed citations

6.

Willems, Thomas, Melissa Gymrek, Gareth Highnam, David Mittelman, & Yaniv Erlich. (2014). The landscape of human STR variation. Genome Research. 24(11). 1894–1904. 176 indexed citations

7.

Guilmatre, Audrey, Gareth Highnam, Christelle Borel, David Mittelman, & Andrew J. Sharp. (2013). Rapid Multiplexed Genotyping of Simple Tandem Repeats using Capture and High-Throughput Sequencing. Human Mutation. 34(9). 1304–1311. 17 indexed citations

8.

Ward, R. Matthew, Robert Schmieder, Gareth Highnam, & David Mittelman. (2013). Big data challenges and opportunities in high-throughput sequencing. 1(1). 29–34. 28 indexed citations

9.

Highnam, Gareth & David Mittelman. (2012). Personal genomes and precision medicine. Genome Biology. 13(12). 324–324. 9 indexed citations

10.

Highnam, Gareth, et al.. (2012). Accurate human microsatellite genotypes from high-throughput resequencing data using informed error profiles. Nucleic Acids Research. 41(1). e32–e32. 109 indexed citations

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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