Eamonn R. Maher
Impact in
- Cancer Research top 0.02%
- Cancer, Hypoxia, and Metabolism
- Genetics top 0.05%
- Genetic Syndromes and Imprinting
Papers in
-
- Epigenetics and DNA Methylation 98
- Renal and related cancers 50
- Cancer-related gene regulation 27
- Genetics 109
- Genetic Syndromes and Imprinting 57
- Co-authors
- Peter J. Ratcliffe (8 shared papers)Farida Latif (78 shared papers)Steven C. Clifford (8 shared papers)Patrick H. Maxwell (7 shared papers)Christopher W. Pugh (4 shared papers)Gin-Wen Chang (2 shared papers)Matthew E. Cockman (2 shared papers)Michael S. Wiesener (8 shared papers)
- Journals
- Journal of Medical Genetics (31 papers)Human Molecular Genetics (23 papers)Oncogene (22 papers)The American Journal of Human Genetics (11 papers)European Journal of Human Genetics (11 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Eamonn R. Maher
418 papers receiving 32.1k citations
Eamonn R. Maher's Hit Papers
Peers
Comparison fields: 5 of 171
- Cancer Research 10.6k
- Genetics 6.9k
- Molecular Biology 16.9k
- Pulmonary and Respiratory Medicine 5.5k
- Pediatrics, Perinatology and Child Health 3.1k
Countries citing papers authored by Eamonn R. Maher
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
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-authors
The 25 scholars most cited alongside Eamonn R. Maher, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 425 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis Hit paper breakdown → | 1999 | 4182 |
| 2 | Hypoxia Inducible Factor-α Binding and Ubiquitylation by the von Hippel-Lindau Tumor Suppressor Protein Hit paper breakdown → | 2000 | 892 |
| 3 | Clinical Features and Natural History of von Hippel-Lindau Disease Hit paper breakdown → | 1990 | 679 |
| 4 | Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome Hit paper breakdown → | 2002 | 647 |
| 5 | VHL, the story of a tumour suppressor gene Hit paper breakdown → | 2014 | 566 |
| 6 | 2011 | 426 | |
| 7 | 1991 | 415 | |
| 8 | HIF activation identifies early lesions in VHL kidneys Hit paper breakdown → | 2002 | 398 |
| 9 | 2009 | 371 | |
| 10 | 1999 | 341 | |
| 11 | 2001 | 336 | |
| 12 | 2003 | 307 | |
| 13 | Hypoxia, Hypoxia-inducible Transcription Factors, and Renal Cancer Hit paper breakdown → | 2015 | 286 |
| 14 | 2005 | 275 | |
| 15 | 1994 | 265 | |
| 16 | Constitutive activation of hypoxia-inducible genes related to overexpression of hypoxia-inducible factor-1alpha in clear cell renal carcinomas. | 2001 | 263 |
| 17 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact Hit paper breakdown → | 2019 | 259 |
| 18 | 1999 | 250 | |
| 19 | 2008 | 248 | |
| 20 | 2016 | 237 |
About Eamonn R. Maher
Eamonn R. Maher is a scholar working on Molecular Biology, Genetics, Cancer Research, Pulmonary and Respiratory Medicine and Surgery, having authored 425 papers that have together received 32.8k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (98 papers), Cancer, Hypoxia, and Metabolism (84 papers), Genetic Syndromes and Imprinting (57 papers), Renal cell carcinoma treatment (54 papers), Renal and related cancers (50 papers), Adrenal and Paraganglionic Tumors (43 papers), Prenatal Screening and Diagnostics (33 papers) and Cancer-related gene regulation (27 papers). The work is most often cited by research in Cancer Research (10.6k citations), Genetics (6.9k citations), Molecular Biology (16.9k citations), Pulmonary and Respiratory Medicine (5.5k citations) and Pediatrics, Perinatology and Child Health (3.1k citations). Eamonn R. Maher has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Peter J. Ratcliffe, Farida Latif, Steven C. Clifford, Patrick H. Maxwell, Christopher W. Pugh, Gin-Wen Chang, Matthew E. Cockman, Michael S. Wiesener, Charles C. Wykoff and Wolf Reik. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Oncogene, The American Journal of Human Genetics and European Journal of Human Genetics.
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.