Matthew F. Hunter

3.3k citations
35 papers · 478 indexed · h-index 13
Topics
Genetics and Neurodevelopmental Disorders (12 papers)Genomics and Rare Diseases (10 papers)Genomic variations and chromosomal abnormalities (8 papers)

In The Last Decade

Matthew F. Hunter

33 papers receiving 471 citations

Peers

Matthew F. Hunter
Comparison fields: 5 of 69
  • Genetics 273
  • Molecular Biology 225
  • Cognitive Neuroscience 105
  • Sensory Systems 51
  • Pediatrics, Perinatology and Child Health 49
Replace Brian P. Perry with:
Brian P. Perry United States
Dean Phelan Australia
Tiia Reimand Estonia
Bella Davidov Israel
Katherine O. Welch United States
Dinah Yaeger United States
Antonia Paula Marques‐de‐Faria Brazil
С.А. Федорова Russia
Virginia W. Norris United States
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Citations per field
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Citations per year

Countries citing papers authored by Matthew F. Hunter

Since Specialization
Citations

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

Fields of papers citing papers by Matthew F. Hunter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew F. Hunter

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

All Works

20 of 20 papers shown
#WorkIndexed citations
1 1
2 0
3 6
4 12
5 2
6 8
7 12
8 10
9 14
10 11
11 6
12 3
13 13
14 20
15 7
16 4
17 67
18 25
19 21
20 3

About Matthew F. Hunter

Matthew F. Hunter is a scholar working on Genetics, Sensory Systems and Cognitive Neuroscience, having authored 35 papers that have together received 478 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (10 papers) and Genomic variations and chromosomal abnormalities (8 papers). The work is most often cited by research in Sensory Systems (51 citations), Genetics (273 citations) and Otorhinolaryngology (25 citations). Matthew F. Hunter has collaborated with scholars based in Australia, United States and New Zealand. Frequent co-authors include Sebastian Lunke, David J. Amor, Zornitza Stark, Tiong Yang Tan, Trent Burgess, Clara Gaff, David R. Thorburn, Melissa Martyn, Alison Yeung and Susan M. White. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

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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