Matthew Hayden

2.3k total citations · 2 hit papers
5 papers, 1.4k citations indexed

About

Matthew Hayden is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Matthew Hayden has authored 5 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Matthew Hayden's work include RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Rare Diseases (2 papers). Matthew Hayden is often cited by papers focused on RNA modifications and cancer (4 papers), RNA and protein synthesis mechanisms (3 papers) and Genomics and Rare Diseases (2 papers). Matthew Hayden collaborates with scholars based in United Kingdom, France and China. Matthew Hayden's co-authors include D.N. Cooper, Matthew Mort, Edward V. Ball, Sally Heywood, Andrew D. Phillips, Peter D. Stenson, Michelle Hussain, David Millar, Luı́sa Azevedo and Matthew D. C. Neville and has published in prestigious journals such as Genome Research, Human Mutation and Human Genetics.

In The Last Decade

Matthew Hayden

5 papers receiving 1.4k citations

Hit Papers

2 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.

The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies

2017 921 citations Peter D. Stenson, Matthew Mort et al. Human Genetics profile →
The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting

2020 410 citations Peter D. Stenson, Matthew Mort et al. Human Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Matthew Hayden United Kingdom	5	826	511	104	97	97	5	1.4k
Sally Heywood United Kingdom	4	798 1.0×	504 1.0×	102 1.0×	96 1.0×	91 0.9×	8	1.4k
Michelle Hussain United Kingdom	4	565 0.7×	356 0.7×	66 0.6×	66 0.7×	62 0.6×	6	966
Xueqiu Jian United States	11	940 1.1×	753 1.5×	58 0.6×	60 0.6×	232 2.4×	17	1.5k
Tawfeg Ben‐Omran Qatar	25	608 0.7×	348 0.7×	105 1.0×	48 0.5×	88 0.9×	62	1.4k
Fuyuki Miya Japan	19	509 0.6×	299 0.6×	99 1.0×	50 0.5×	76 0.8×	84	1.0k
Joshua L. Deignan United States	18	685 0.8×	753 1.5×	53 0.5×	67 0.7×	289 3.0×	32	1.6k
Elisabetta Flex Italy	21	941 1.1×	239 0.5×	159 1.5×	35 0.4×	45 0.5×	39	1.3k
Chandree L. Beaulieu Canada	20	645 0.8×	459 0.9×	74 0.7×	24 0.2×	93 1.0×	33	1.1k
Laurence Duprez Belgium	16	1.2k 1.4×	330 0.6×	97 0.9×	46 0.5×	88 0.9×	17	2.3k
Sarah L. Sawyer Canada	15	589 0.7×	486 1.0×	42 0.4×	28 0.3×	80 0.8×	37	1.0k

Countries citing papers authored by Matthew Hayden

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Hayden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Hayden

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

All Works

Sort: Min cites: Since: Top N: Style:

5 of 5 papers shown

1.

Neville, Matthew D. C., Narendra Kumar Meena, Matthew Hayden, et al.. (2021). A platform for curated products from novel open reading frames prompts reinterpretation of disease variants. Genome Research. 31(2). 327–336. 16 indexed citations

2.

Chen, Jian‐Min, Jin‐Huan Lin, Emmanuelle Masson, et al.. (2020). The Experimentally Obtained Functional Impact Assessments of 5' Splice Site GT>GC Variants Differ Markedly from Those Predicted. Current Genomics. 21(1). 56–66. 13 indexed citations

3.

Lin, Jin‐Huan, Emmanuelle Masson, Arnaud Boulling, et al.. (2020). 5′ splice site GC>GT and GT>GC variants differ markedly in terms of their functionality and pathogenicity. Human Mutation. 41(8). 1358–1364. 5 indexed citations

4.

Stenson, Peter D., Matthew Mort, Edward V. Ball, et al.. (2020). The Human Gene Mutation Database (HGMD®): optimizing its use in a clinical diagnostic or research setting. Human Genetics. 139(10). 1197–1207. 410 indexed citations breakdown →

5.

Stenson, Peter D., Matthew Mort, Edward V. Ball, et al.. (2017). The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies. Human Genetics. 136(6). 665–677. 921 indexed citations breakdown →

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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