VHL, the story of a tumour suppressor gene von Gossage, Lucy, Eisen, Tim, Maher, Eamonn R.

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Hereditary renal cell carcinoma syndromes: diagnosis, surveillance and management von Maher, Eamonn R.

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Familial Kidney Cancer: Implications of New Syndromes and Molecular Insights von Carlo, Maria I., Hakimi, A. Ari, Stewart, Grant D., Bratslavsky, Gennady, Brugarolas, James, Chen, Ying-Bei, Linehan, W. Marston, Maher, Eamonn R., Merino, Maria J., Offit, Kenneth, Reuter, Victor E., Shuch, Brian, Coleman, Jonathan A.

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Genomics and epigenomics of renal cell carcinoma von Maher, Eamonn R

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The Deubiquitinase OTULIN Is an Essential Negative Regulator of Inflammation and Autoimmunity von Damgaard, Rune Busk, Walker, Jennifer A., Marco-Casanova, Paola, Morgan, Neil V., Titheradge, Hannah L., Elliott, Paul R., McHale, Duncan, Maher, Eamonn R., McKenzie, Andrew N.J., Komander, David

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Genomic imprinting disorders: lessons on how genome, epigenome and environment interact von Monk, David, Mackay, Deborah J. G., Eggermann, Thomas, Maher, Eamonn R., Riccio, Andrea

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Wilms tumour resulting from paternal transmission of a TRIM28 pathogenic variant-A first report von Whitworth, James, Armstrong, Ruth, Maher, Eamonn R

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Hypoxia, Hypoxia-inducible Transcription Factors, and Renal Cancer von Schödel, Johannes, Grampp, Steffen, Maher, Eamonn R, Moch, Holger, Ratcliffe, Peter J, Russo, Paul, Mole, David R

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Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment von Menko, Fred H., Maher, Eamonn R., Schmidt, Laura S., Middelton, Lindsay A., Aittomäki, Kristiina, Tomlinson, Ian, Richard, Stéphane, Linehan, W. Marston

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The genetics of phaeochromocytoma: using clinical features to guide genetic testing von JAFRI, Mariam, MAHER, Eamonn R

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von Hippel-Lindau disease: A clinical and scientific review von Maher, Eamonn R, Neumann, Hartmut PH, Richard, Stéphane

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Characteristics, aetiology and implications for management of multiple primary renal tumours: a systematic review von Zhang, Huairen, Andreou, Avgi, Bhatt, Rupesh, Whitworth, James, Yngvadottir, Bryndis, Maher, Eamonn R

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Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome) von Meyer, Esther, Lim, Derek, Pasha, Shanaz, Tee, Louise J, Rahman, Fatimah, Yates, John R W, Woods, C Geoffrey, Reik, Wolf, Maher, Eamonn R

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OTULIN deficiency in ORAS causes cell type‐specific LUBAC degradation, dysregulated TNF signalling and cell death von Damgaard, Rune Busk, Elliott, Paul R, Swatek, Kirby N, Maher, Eamonn R, Stepensky, Polina, Elpeleg, Orly, Komander, David, Berkun, Yackov

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Genetic stratification of inherited and sporadic phaeochromocytoma and paraganglioma: implications for precision medicine von Casey, Ruth, Neumann, Hartmut P H, Maher, Eamonn R

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Causes and Consequences of Multi-Locus Imprinting Disturbances in Humans von Sanchez-Delgado, Marta, Riccio, Andrea, Eggermann, Thomas, Maher, Eamonn R, Lapunzina, Pablo, Mackay, Deborah, Monk, David

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Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: risks of breast/ovarian cancer quoted should reflect the cancer bur... von Evans, D Gareth, Shenton, Andrew, Woodward, Emma, Lalloo, Fiona, Howell, Anthony, Maher, Eamonn R

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Von Hippel-Lindau Disease: Genetics and Role of Genetic Counseling in a Multiple Neoplasia Syndrome von Nielsen, Sarah M, Rhodes, Lindsay, Blanco, Ignacio, Chung, Wendy K, Eng, Charis, Maher, Eamonn R, Richard, Stéphane, Giles, Rachel H

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Fumarate is an epigenetic modifier that elicits epithelial-to-mesenchymal transition von Sciacovelli, Marco, Gonçalves, Emanuel, Johnson, Timothy Isaac, Zecchini, Vincent Roberto, da Costa, Ana Sofia Henriques, Gaude, Edoardo, Drubbel, Alizee Vercauteren, Theobald, Sebastian Julian, Abbo, Sandra Riekje, Tran, Maxine Gia Binh, Rajeeve, Vinothini, Cardaci, Simone, Foster, Sarah, Yun, Haiyang, Cutillas, Pedro, Warren, Anne, Gnanapragasam, Vincent, Gottlieb, Eyal, Franze, Kristian, Huntly, Brian, Maher, Eamonn Richard, Maxwell, Patrick Henry, Saez-Rodriguez, Julio, Frezza, Christian

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Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups von Maas, Saskia M., Vansenne, Fleur, Kadouch, Daniel J. M., Ibrahim, Abdulla, Bliek, Jet, Hopman, Saskia, Mannens, Marcel M., Merks, Johannes H. M., Maher, Eamonn R., Hennekam, Raoul C.

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