Eamonn R. Maher

2.7k total citations · 2 hit papers
8 papers, 2.0k citations indexed

About

Eamonn R. Maher is a scholar working on Cancer Research, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Eamonn R. Maher has authored 8 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cancer Research, 5 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Eamonn R. Maher's work include Cancer, Hypoxia, and Metabolism (6 papers), Epigenetics and DNA Methylation (4 papers) and Cancer-related Molecular Pathways (2 papers). Eamonn R. Maher is often cited by papers focused on Cancer, Hypoxia, and Metabolism (6 papers), Epigenetics and DNA Methylation (4 papers) and Cancer-related Molecular Pathways (2 papers). Eamonn R. Maher collaborates with scholars based in United Kingdom, United States and Netherlands. Eamonn R. Maher's co-authors include William G. Kaelin, Charis Eng, Ashraf Dallol, Emad George, Farida Latif, Dewi Astuti, Fiona Douglas, Patricia L. M. Dahia, Keith Foster and Malcolm A. Ferguson-Smith and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Medicine.

In The Last Decade

Eamonn R. Maher

8 papers receiving 2.0k citations

Hit Papers

Gene Mutations in the Succinate Dehydrogenase Subunit SDH... 1997 2026 2006 2016 2001 1997 250 500 750
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.

  1. Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma
    2001 840 citations Dewi Astuti, Farida Latif et al. The American Journal of Human Genetics profile →
  2. von Hippel-Lindau Disease
    1997 395 citations Eamonn R. Maher, William G. Kaelin Medicine profile →

Peers

Eamonn R. Maher
Dewi Astuti United Kingdom
Diana E. Benn Australia
Virpi Launonen Finland
Karine Perlemoine France
Outi Vierimaa Finland
Amanda Prowse United Kingdom
Fernande René-Corail France
Trisha Dwight Australia
Armelle Logié United Kingdom
Esther Korpershoek Netherlands
Dewi Astuti United Kingdom
Eamonn R. Maher
Citations per year, relative to Eamonn R. Maher Eamonn R. Maher (= 1×) peers Dewi Astuti

Countries citing papers authored by Eamonn R. Maher

Since Specialization
Citations

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

Fields of papers citing papers by Eamonn R. Maher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eamonn R. Maher. 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 Eamonn R. Maher. The network helps show where Eamonn R. Maher may publish in the future.

Co-authorship network of co-authors of Eamonn R. Maher

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

All Works

8 of 8 papers shown
1.
Clifford, Steven C. & Eamonn R. Maher. (2001). von Hippel-Lindau disease: Clinical and molecular perspectives. Advances in cancer research. 82. 85–105. 73 indexed citations
2.
Astuti, Dewi, Farida Latif, Ashraf Dallol, et al.. (2001). Gene Mutations in the Succinate Dehydrogenase Subunit SDHB Cause Susceptibility to Familial Pheochromocytoma and to Familial Paraganglioma. The American Journal of Human Genetics. 69(1). 49–54. 840 indexed citations breakdown →
3.
Buchberger, Alexander, et al.. (2000). Comparative Sequence Analysis of the VHL Tumor Suppressor Gene. Genomics. 65(3). 253–265. 49 indexed citations
4.
5.
Maher, Eamonn R. & William G. Kaelin. (1997). von Hippel-Lindau Disease. Medicine. 76(6). 381–391. 395 indexed citations breakdown →
6.
Foster, Keith, Amanda Prowse, Anke van den Berg, et al.. (1994). Somatic mutations of the von Hippel — Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma. Human Molecular Genetics. 3(12). 2169–2173. 307 indexed citations
7.
Richards, Frances M., Paul A. Crossey, Keith Foster, et al.. (1994). Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene. Human Molecular Genetics. 3(4). 595–598. 61 indexed citations
8.
Crossey, Paul A., Keith Foster, Amanda Prowse, et al.. (1994). Identification of intragenic mutations in the Von Hippel — Lindau disease tumour suppressor gene andcorrelation with disease phenotype. Human Molecular Genetics. 3(8). 1303–1308. 304 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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