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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Corrigendum: 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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Correction: Corrigendum: 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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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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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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von Hippel-Lindau disease: A clinical and scientific review von MAHER, Eamonn R, NEUMANN, Hartmut Ph, RICHARD, Stephane

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Health and population effects of rare gene knockouts in adult humans with related parents von Narasimhan, Vagheesh M., Hunt, Karen A., Mason, Dan, Baker, Christopher L., Karczewski, Konrad J., Barnes, Michael R., Barnett, Anthony H., Bates, Chris, Bellary, Srikanth, Bockett, Nicholas A., Giorda, Kristina, Griffiths, Christopher J., Hemingway, Harry, Jia, Zhilong, Kelly, M. Ann, Khawaja, Hajrah A., Lek, Monkol, McCarthy, Shane, McEachan, Rosie, O'Donnell-Luria, Anne, Paigen, Kenneth, Parisinos, Constantinos A., Sheridan, Eamonn, Southgate, Laura, Tee, Louise, Thomas, Mark, Xue, Yali, Schnall-Levin, Michael, Petkov, Petko M., Tyler-Smith, Chris, Maher, Eamonn R., Trembath, Richard C., MacArthur, Daniel G., Wright, John, Durbin, Richard, van Heel, David A.

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Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes von Narasimhan, Vagheesh M., Rahbari, Raheleh, Scally, Aylwyn, Wuster, Arthur, Mason, Dan, Xue, Yali, Wright, John, Trembath, Richard C., Maher, Eamonn R., van Heel, David A., Auton, Adam, Hurles, Matthew E., Tyler-Smith, Chris, Durbin, Richard

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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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Elongin C (ELOC/TCEB1)-associated von Hippel–Lindau disease von Andreou, Avgi, Yngvadottir, Bryndis, Bassaganyas, Laia, Clark, Graeme, Martin, Ezequiel, Whitworth, James, Cornish, Alex J, Houlston, Richard S, Rich, Philip, Egan, Catherine, Hodgson, Shirley V, Warren, Anne Y, Snape, Katie, Maher, Eamonn R

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Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility von Astuti, Dewi, Morris, Mark R, Cooper, Wendy N, Staals, Raymond H J, Wake, Naomi C, Fews, Graham A, Gill, Harmeet, Gentle, Dean, Shuib, Salwati, Ricketts, Christopher J, Cole, Trevor, van Essen, Anthonie J, van Lingen, Richard A, Neri, Giovanni, Opitz, John M, Rump, Patrick, Stolte-Dijkstra, Irene, Müller, Ferenc, Pruijn, Ger J M, Latif, Farida, Maher, Eamonn R

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Germline FH Mutations Presenting With Pheochromocytoma von Clark, Graeme R, Sciacovelli, Marco, Gaude, Edoardo, Walsh, Diana M, Kirby, Gail, Simpson, Michael A, Trembath, Richard C, Berg, Jonathan N, Woodward, Emma R, Kinning, Esther, Morrison, Patrick J, Frezza, Christian, Maher, Eamonn R

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Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease von Morgan, Neil V, Morris, Mark R, Cangul, Hakan, Gleeson, Diane, Straatman-Iwanowska, Anna, Davies, Nicholas, Keenan, Stephen, Pasha, Shanaz, Rahman, Fatimah, Gentle, Dean, Vreeswijk, Maaike P G, Devilee, Peter, Knowles, Margaret A, Ceylaner, Serdar, Trembath, Richard C, Dalence, Carlos, Kismet, Erol, Köseoğlu, Vedat, Rossbach, Hans-Christoph, Gissen, Paul, Tannahill, David, Maher, Eamonn R

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Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases von Yngvadottir, Bryndis, Andreou, Avgi, Bassaganyas, Laia, Larionov, Alexey, Cornish, Alex J, Chubb, Daniel, Saunders, Charlie N, Smith, Philip S, Zhang, Huairen, Cole, Yasemin, Research Consortium, Genomics England, Larkin, James, Browning, Lisa, Turajlic, Samra, Litchfield, Kevin, Houlston, Richard S, Maher, Eamonn R

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A genome-wide screen identifies frequently methylated genes in haematological and epithelial cancers von Dunwell, Thomas, Hesson, Luke, Rauch, Tibor A, Wang, Lihui, Clark, Richard E, Dallol, Ashraf, Gentle, Dean, Catchpoole, Daniel, Maher, Eamonn R, Pfeifer, Gerd P, Latif, Farida

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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas von Palles, Claire, Cazier, Jean-Baptiste, Howarth, Kimberley M, Domingo, Enric, Jones, Angela M, Broderick, Peter, Kemp, Zoe, Spain, Sarah L, Guarino, Estrella, Salguero, Israel, Sherborne, Amy, Chubb, Daniel, Carvajal-Carmona, Luis G, Ma, Yusanne, Kaur, Kulvinder, Dobbins, Sara, Barclay, Ella, Gorman, Maggie, Martin, Lynn, Kovac, Michal B, Humphray, Sean, Lucassen, Anneke, Holmes, Christopher C, Bentley, David, Donnelly, Peter, Taylor, Jenny, Petridis, Christos, Roylance, Rebecca, Sawyer, Elinor J, Kerr, David J, Clark, Susan, Grimes, Jonathan, Kearsey, Stephen E, Thomas, Huw J W, McVean, Gilean, Houlston, Richard S, Tomlinson, Ian

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A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma von Rattenberry, Eleanor, Vialard, Lindsey, Yeung, Anna, Bair, Hayley, McKay, Kirsten, Jafri, Mariam, Canham, Natalie, Cole, Trevor R, Denes, Judit, Hodgson, Shirley V, Irving, Richard, Izatt, Louise, Korbonits, Márta, Kumar, Ajith V, Lalloo, Fiona, Morrison, Patrick J, Woodward, Emma R, Macdonald, Fiona, Wallis, Yvonne, Maher, Eamonn R

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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von Hippel-Lindau Disease: an Update von Maher, Eamonn R, Sandford, Richard N

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Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies von Southgate, Laura, Machado, Rajiv D., Snape, Katie M., Primeau, Martin, Dafou, Dimitra, Ruddy, Deborah M., Branney, Peter A., Fisher, Malcolm, Lee, Grace J., Simpson, Michael A., He, Yi, Bradshaw, Teisha Y., Blaumeiser, Bettina, Winship, William S., Reardon, Willie, Maher, Eamonn R., FitzPatrick, David R., Wuyts, Wim, Zenker, Martin, Lamarche-Vane, Nathalie, Trembath, Richard C.

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