Matt Hurles

5.2k total citations
3 papers, 107 citations indexed

About

Matt Hurles is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Matt Hurles has authored 3 papers receiving a total of 107 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 1 paper in Genetics and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Matt Hurles's work include Genomics and Rare Diseases (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Neurological diseases and metabolism (1 paper). Matt Hurles is often cited by papers focused on Genomics and Rare Diseases (1 paper), Neurogenetic and Muscular Disorders Research (1 paper) and Neurological diseases and metabolism (1 paper). Matt Hurles collaborates with scholars based in United Kingdom, United States and Germany. Matt Hurles's co-authors include Barry A. Chioza, Saeed Al-Turki, Katy Barwick, Andrew H. Crosby, Jane Wright, Randy Blakely, Alicia M. Ruggiero, Ajith Nair, Mary M. Reilly and Katherine Dick and has published in prestigious journals such as The American Journal of Human Genetics and Neuromuscular Disorders.

In The Last Decade

Matt Hurles

3 papers receiving 104 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matt Hurles United Kingdom	2	51	32	26	20	17	3	107
Liena E. O. Elsayed Sudan	6	40 0.8×	53 1.7×	17 0.7×	22 1.1×	14 0.8×	14	108
Suad Alyamani Saudi Arabia	4	67 1.3×	35 1.1×	12 0.5×	22 1.1×	10 0.6×	8	118
Umer Javed Butt Germany	7	49 1.0×	15 0.5×	22 0.8×	18 0.9×	14 0.8×	11	153
Spencer Goodman United States	5	61 1.2×	21 0.7×	15 0.6×	7 0.3×	8 0.5×	7	105
Massimo Plumari Italy	5	107 2.1×	76 2.4×	16 0.6×	12 0.6×	27 1.6×	10	127
Eugenia Borgione Italy	8	81 1.6×	27 0.8×	8 0.3×	31 1.6×	22 1.3×	19	125
Selina Reich Germany	5	96 1.9×	37 1.2×	20 0.8×	24 1.2×	7 0.4×	8	127
Eline M. Hamilton Netherlands	6	173 3.4×	28 0.9×	40 1.5×	25 1.3×	15 0.9×	9	216
Inès Mademan Belgium	4	67 1.3×	49 1.5×	19 0.7×	5 0.3×	13 0.8×	4	109
Elham Alehabib Iran	9	114 2.2×	19 0.6×	24 0.9×	51 2.5×	11 0.6×	24	181

Countries citing papers authored by Matt Hurles

Since Specialization

Citations

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

Fields of papers citing papers by Matt Hurles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matt Hurles

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

All Works

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3 of 3 papers shown

1.

Whyte, Tamieka, Philip L. Beales, Daniel P. S. Osborn, et al.. (2014). G.P.154. Neuromuscular Disorders. 24(9-10). 847–848. 1 indexed citations

2.

Baple, Emma L., Reza Maroofian, Barry A. Chioza, et al.. (2013). Mutations in KPTN Cause Macrocephaly, Neurodevelopmental Delay, and Seizures. The American Journal of Human Genetics. 94(1). 87–94. 35 indexed citations

3.

Barwick, Katy, Jane Wright, Saeed Al-Turki, et al.. (2012). Defective Presynaptic Choline Transport Underlies Hereditary Motor Neuropathy. The American Journal of Human Genetics. 91(6). 1103–1107. 71 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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