Eamonn R. Maher

67.6k citations

423 papers · 32.5k indexed · 8 hit papers · h-index 94

Impact in

Cancer Research top 0.02%
- Cancer, Hypoxia, and Metabolism
Molecular Biology top 0.05%
- Epigenetics and DNA Methylation
- Renal and related cancers
- RNA modifications and cancer

Papers in

Cancer Research 120
- Cancer, Hypoxia, and Metabolism 90
Genetics 124
- Genetic Syndromes and Imprinting 57

Co-authors: Farida Latif Peter J. Ratcliffe Steven C. Clifford Patrick H. Maxwell Christopher W. Pugh Gin-Wen Chang Matthew E. Cockman Michael S. Wiesener
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 Kingdom United States Germany

In The Last Decade

Eamonn R. Maher

415 papers receiving 31.8k citations

Hit Papers

8 papers align trajectories log scale

Genomic imprinting disorders: lessons on how genome, epigenome and environment interact 2019 · 252 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2019 Nature Reviews Genetics
2015 European Urology
2014 Nature reviews. Cancer
2002 Cancer Cell
2002 Cancer Cell
2000 Journal of Biological Chemistry
1999 Nature
1990 QJM

Peers

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

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.

Border = papers with Eamonn R. Maher Line = papers co-authored together Eamonn R. Maher links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Paediatric research sets new standards for therapy in paediatric and adult cholestasis The Lancet Child & Adolescent Health ·Muhamad Ripai, Eamonn R. Maher, Déirdre Kelly	2023	9
2	HIRA loss transforms FH -deficient cells Science Advances ·Lorea Valcárcel-Jiménez, Zipporah Rini Benher, Cissy Yong, Christina Schmidt, Ming Yang, TU Xingmin, Victoria Harle, Victoria Offord, Kim Wong, A. Martín Ruiz, Alyson Speed, 裴仲晓, Maxine Tran, Eamonn R. Maher, Grant D. Stewart, Sakari Vanharanta, David J. Adams, Christian Frezza	2022	9
3	Isolated‐ and Beckwith‐Wiedemann syndrome related‐ lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals Clinical Genetics ·春李, Editors EUROPEAN ENCOUNTERS, Ataf Sabir, Nae-Yeou Jih, Jie Zheng, Rachel L. Jones, Ferenc. aut Vicko, Т Л Кобалия, William Reardon, Ruth Richardson, 藤原靖, Eamonn R. Maher	2021	9
4	A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours European Journal of Human Genetics ·R C Miller, Derek Lim, Paul D.P. Pharoah, Eamonn R. Maher, Stefan J. Marciniak	2021	15
5	Mitochondria in health and disease The biomedical & life sciences collection. ·Eamonn R. Maher	2020	8
6	Ensuring that COVID-19 research is inclusive: guidance from the NIHR INCLUDE project BMJ Open ·Miles D. Witham, Eleanor Anderson, Camille Carroll, Paul Dark, Freddy Abad Célleri, Alistair S. Hall, Izaskun Vergara R., Eamonn R. Maher, Rebecca Maier, Gail Mountain, Gary Nestor, John T. O’Brien, YU Jun-feng, James Wason, Lynn Rochester	2020	25
7	Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumab Seminars in Oncology ·Ruth Casey, Olivier Giger, Ian Seetho, Alison Marker, Jin-Guo Liu, Louise H. Boyle, Mark Gurnell, Ashley Shaw, Marc Tischkowitz, Eamonn R. Maher, Krishna Chatterjee, Tobias Janowitz, George Mells, Pippa Corrie, Benjamin Challis	2018	23
8	Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2 American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Mark R. Morris, Dewi Astuti, Eamonn R. Maher	2013	34
9	Genome-Wide DNA Methylation Profiling of CpG Islands in Breast Cancer Identifies Novel Genes Associated with Tumorigenicity Cancer Research ·Victoria Hill, Christopher J. Ricketts, Ivan Bièche, Sophie Vacher, Dean Gentle, Cheryl Lewis, Eamonn R. Maher, Farida Latif	2011	126
10	A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis Cancer Prevention Research ·John Burn, D. Timothy Bishop, Pamela Chapman, Faye Elliott, Lucio Bertario, Malcolm G. Dunlop, Diana Eccles, Anthony E. Ellis, D. Gareth Evans, Riccardo Fodde, Eamonn R. Maher, Gabriela Möslein, Hans F. A. Vasen, Pilar Rodríguez Maestu, Robin Phillips, Steffen Bülow, John C. Mathers	2011	151
11	Therapeutic Targeting the Loss of the Birt-Hogg-Dubé Suppressor Gene Molecular Cancer Therapeutics ·Xiaohong Lü, Wenbin Wei, Janine Fenton, Michael S. Nahorski, Anny Vitória Ribeiro Silva, Anne Reiman, Bruce Cords, Zsuzsanna Nagy, Farida Latif, Eamonn R. Maher	2011	15
12	Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy) Gastroenterology ·Jane Hartley, Nicholas C. Zachos, Ban B. Dawood, Mark Donowitz, Julia Forman, R. J. Pollitt, Neil V. Morgan, Louise Tee, Paul Gissen, Walter H.A. Kahr, A. S. Knisely, Steve P. Watson, David Chitayat, I W Booth, Sue Protheroe, 時男園田, Esther de Vries, Déirdre Kelly, Eamonn R. Maher	2010	96
13	Analysis of VHL Gene Alterations and their Relationship to Clinical Parameters in Sporadic Conventional Renal Cell Carcinoma Clinical Cancer Research ·Cordeiro Foto e Vídeo, Rachel A. Craven, D. Cohen, Claire Taylor, Christopher Booth, Patricia Harnden, David A. Cairns, Dewi Astuti, Walter M. Gregory, Eamonn R. Maher, Margaret A. Knowles, Adrian Joyce, Peter J. Selby, Rosamonde E. Banks	2009	137
14	Depletion of the Ras Association Domain Family 1, Isoform A–Associated Novel Microtubule-Associated Protein, C19ORF5/MAP1S, Causes Mitotic Abnormalities Cancer Research ·Ashraf Dallol, Wendy N. Cooper, Fahd Al‐Mulla, Angelo Agathanggelou, Eamonn R. Maher, Farida Latif	2007	42
15	Genetic and Epigenetic Analysis of von Hippel-Lindau ( VHL ) Gene Alterations and Relationship with Clinical Variables in Sporadic Renal Cancer Cancer Research ·Rosamonde E. Banks, Prasanna Tirukonda, Claire Taylor, Nick Hornigold, Dewi Astuti, D. Cohen, Eamonn R. Maher, Anthea J. Stanley, Patricia Harnden, Adrian Joyce, Margaret A. Knowles, Peter J. Selby	2006	214
16	Involvement of the RASSF1A Tumor Suppressor Gene in Controlling Cell Migration Cancer Research ·Ashraf Dallol, Angelo Agathanggelou, Stella Tommasi, Gerd P. Pfeifer, Eamonn R. Maher, Farida Latif	2005	76
17	Tumor Suppressor Activity and Epigenetic Inactivation of Hepatocyte Growth Factor Activator Inhibitor Type 2/SPINT2 in Papillary and Clear Cell Renal Cell Carcinoma Cancer Research ·Mark R. Morris, Dean Gentle, Mahera Abdulrahman, Esther N. Maina, Kunal Gupta, Rosamonde E. Banks, Michael S. Wiesener, Takeshi Kishida, Masahiro Yao, Bin Tean Teh, Farida Latif, Eamonn R. Maher	2005	95
18	Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations Human Genetics ·Tim Forshew, Colin A. Johnson, Shagufta Khaliq, Shanaz Pasha, Catherine Willis, V. N. Udodov, Louise Tee, Sevgi Sevil Özgan M s rc, Richard C. Trembath, S. Qasim Mehdi, Anthony T. Moore, Eamonn R. Maher	2005	66
19	Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas Endocrine Related Cancer ·S. Sumanth Kori, Dewi Astuti, Dean Gentle, Wendy N. Cooper, Alberto Cascón, Daniel Catchpoole, Mercedes Robledo, Hartmut P.H. Neumann, Farida Latif, Eamonn R. Maher	2005	55
20	Detailed genetic and physical mapping of tumor suppressor loci on chromosome 3p in ovarian cancer. PubMed ·SajanZ Ahmad, Sergio Marchini, Janet S. Rader, Alonso Martínez, Donia Macartney‐Coxson, Massimo Broggini, Maria Cristina Morelli, Giuseppe Barbanti‐Brodano, Eamonn R. Maher, Farida Latif	1999	48

About Eamonn R. Maher

Eamonn R. Maher is a scholar working on Cancer Research, Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health and Pathology and Forensic Medicine, having authored 423 papers that have together received 32.5k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (114 papers), Cancer, Hypoxia, and Metabolism (90 papers), Renal and related cancers (59 papers), Genetic Syndromes and Imprinting (57 papers), Renal cell carcinoma treatment (56 papers), Prenatal Screening and Diagnostics (49 papers), Adrenal and Paraganglionic Tumors (44 papers) and Cancer-related gene regulation (31 papers). The work is most often cited by research in Cancer Research (11.8k citations), Molecular Biology (19.4k citations), Genetics (7.8k citations), Pulmonary and Respiratory Medicine (6.2k citations) and Pediatrics, Perinatology and Child Health (3.7k citations). Eamonn R. Maher has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Farida Latif, Peter J. Ratcliffe, 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.

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