M. Roberts

513 total citations
7 papers, 310 citations indexed

About

M. Roberts is a scholar working on Molecular Biology, Epidemiology and Clinical Biochemistry. According to data from OpenAlex, M. Roberts has authored 7 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Epidemiology and 3 papers in Clinical Biochemistry. Recurrent topics in M. Roberts's work include Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Rare Diseases (1 paper). M. Roberts is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Rare Diseases (1 paper). M. Roberts collaborates with scholars based in United Kingdom, Germany and Australia. M. Roberts's co-authors include E. G. V. Evans, R. E. Warren, David W. Denning, Thomas R. Rogers, David W. Warnock, C Kibbler, Malcolm Richardson, Douglass M. Turnbull, E. Martoni and Debbie Hicks and has published in prestigious journals such as Neurology, Human Molecular Genetics and British Journal of Dermatology.

In The Last Decade

M. Roberts

7 papers receiving 300 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Roberts United Kingdom	7	122	100	89	65	50	7	310
Makiko Yamada Japan	13	236 1.9×	45 0.5×	53 0.6×	26 0.4×	52 1.0×	26	401
Wanyu Zhang China	11	131 1.1×	58 0.6×	30 0.3×	10 0.2×	22 0.4×	46	434
Jessica S. Hook United States	14	122 1.0×	57 0.6×	45 0.5×	7 0.1×	39 0.8×	22	381
Mathilde Lefebvre France	8	207 1.7×	29 0.3×	43 0.5×	67 1.0×	136 2.7×	18	400
Qiujiang Du Canada	10	134 1.1×	75 0.8×	38 0.4×	6 0.1×	45 0.9×	11	308
Mitsuo Toyoshima Japan	9	78 0.6×	30 0.3×	62 0.7×	43 0.7×	43 0.9×	24	253
Guoguo Yi China	11	120 1.0×	32 0.3×	17 0.2×	27 0.4×	14 0.3×	29	345
Xingguang Ye China	11	92 0.8×	40 0.4×	32 0.4×	8 0.1×	64 1.3×	25	296
Frances V. Sjaastad United States	11	133 1.1×	137 1.4×	39 0.4×	9 0.1×	18 0.4×	15	465
Anna Waśkiel‐Burnat Poland	17	173 1.4×	139 1.4×	52 0.6×	4 0.1×	83 1.7×	52	840

Countries citing papers authored by M. Roberts

Since Specialization

Citations

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

Fields of papers citing papers by M. Roberts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Roberts

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

All Works

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7 of 7 papers shown

1.

Gorman, Gráinne S., Gerald Pfeffer, Helen Griffin, et al.. (2014). Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated With Spinocerebellar Ataxia Type 28. JAMA Neurology. 72(1). 106–106. 33 indexed citations

2.

Hicks, Debbie, S.H. Laval, James J. Collins, et al.. (2013). Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy. Human Molecular Genetics. 23(9). 2353–2363. 81 indexed citations

3.

Alston, Charlotte L., Andrew M. Schaefer, Nicola Solaroli, et al.. (2013). Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions. Neurology. 81(23). 2051–2053. 17 indexed citations

4.

Stewart, Joanna D., Stephen Tennant, Heather Powell, et al.. (2009). Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children. Journal of Medical Genetics. 46(3). 209–214. 39 indexed citations

5.

Gorman, Gráinne S., et al.. (2009). Clinical Reasoning: Blurred vision and dancing feet. Neurology. 72(18). e86–90. 9 indexed citations

6.

Denning, David W., E. G. V. Evans, C Kibbler, et al.. (1997). Guidelines for the investigation of invasive fungal infections in haematological malignancy and solid organ transplantation. European Journal of Clinical Microbiology & Infectious Diseases. 16(6). 424–436. 124 indexed citations

7.

Butterfield, W. J. H., et al.. (1987). Sensitivities of Pityrosporum sp. to selected commercial shampoos. British Journal of Dermatology. 116(2). 233–235. 7 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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