# Eamonn R. Maher

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/eamonn-r-maher/

## Facts

| Field | Value |
| --- | --- |
| Citations | 68,661 |
| Field | Epigenetics and DNA Methylation |
| h-index | 135 |
| i10-index | 479 |
| Last Known Institution | Aston University |
| OpenAlex ID | https://openalex.org/A5056034710 |
| ORCID iD | 0000-0002-6226-6918 |
| Works | 847 |

## Researcher papers

Showing 12 of 20.

- [The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis](https://scholariq.org/papers/the-tumour-suppressor-protein-vhl-targets-hypoxia-inducible-factors-for-oxygen/)
- [Identification of the von Hippel-Lindau Disease Tumor Suppressor Gene](https://scholariq.org/papers/identification-of-the-von-hippel-lindau-disease-tumor-suppressor-gene/)
- [Hypoxia Inducible Factor-α Binding and Ubiquitylation by the von Hippel-Lindau Tumor Suppressor Protein](https://scholariq.org/papers/hypoxia-inducible-factor-binding-and-ubiquitylation-by-the-von-hippel-lindau/)
- [Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial](https://scholariq.org/papers/long-term-effect-of-aspirin-on-cancer-risk-in-carriers-of-hereditary-colorectal/)
- [Clinical Features and Natural History of von Hippel-Lindau Disease](https://scholariq.org/papers/clinical-features-and-natural-history-of-von-hippel-lindau-disease/)
- [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](https://scholariq.org/papers/mutations-in-a-novel-gene-lead-to-kidney-tumors-lung-wall-defects-and-benign/)
- [VHL, the story of a tumour suppressor gene](https://scholariq.org/papers/vhl-the-story-of-a-tumour-suppressor-gene/)
- [von Hippel–Lindau disease: A clinical and scientific review](https://scholariq.org/papers/von-hippel-lindau-disease-a-clinical-and-scientific-review/)
- [Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study](https://scholariq.org/papers/prenatal-exome-sequencing-analysis-in-fetal-structural-anomalies-detected-by/)
- [Von Hippel-Lindau disease: a genetic study.](https://scholariq.org/papers/von-hippel-lindau-disease-a-genetic-study/)
- [Whole-genome sequencing of patients with rare diseases in a national health system](https://scholariq.org/papers/whole-genome-sequencing-of-patients-with-rare-diseases-in-a-national-health/)
- [TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum](https://scholariq.org/papers/ttc21b-contributes-both-causal-and-modifying-alleles-across-the-ciliopathy/)

## Researcher topics

- [Epigenetics and DNA Methylation](https://scholariq.org/topics/epigenetics-and-dna-methylation/)
- [Cancer, Hypoxia, and Metabolism](https://scholariq.org/topics/cancer-hypoxia-and-metabolism/)
- [Renal cell carcinoma treatment](https://scholariq.org/topics/renal-cell-carcinoma-treatment/)
- [Adrenal and Paraganglionic Tumors](https://scholariq.org/topics/adrenal-and-paraganglionic-tumors/)
- [Genetic Syndromes and Imprinting](https://scholariq.org/topics/genetic-syndromes-and-imprinting/)

## Researcher university

- [Aston University](https://scholariq.org/institutions/aston-university/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.