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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A distinctive, low‐grade oncocytic fumarate hydratase‐deficient renal cell carcinoma, morphologically reminiscent of succinate dehydrogenase‐deficient renal cell carcinoma von Smith, Steven C, Sirohi, Deepika, Ohe, Chisato, McHugh, Jonathan B, Hornick, Jason L, Kalariya, Jigna, Karia, Sushil, Snape, Katie, Hodgson, Shirley V, Cani, Andi K, Hovelson, Daniel, Luthringer, Daniel J, Martignoni, Guido, Chen, Ying‐Bei, Tomlins, Scott A, Mehra, Rohit, Amin, Mahul B

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Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study von Movahedi, Mohammad, Bishop, D Timothy, Macrae, Finlay, Mecklin, Jukka-Pekka, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diana, Evans, D Gareth, Maher, Eamonn R, Bertario, Lucio, Bisgaard, Marie-Luise, Dunlop, Malcolm G, Ho, Judy W C, Hodgson, Shirley V, Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J, Murday, Victoria, Ramesar, Raj S, Side, Lucy, Scott, Rodney J, Thomas, Huw J W, Vasen, Hans F, Burn, John, Mathers, John C

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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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Disruption of the Fanconi anemia-BRCA pathway in cisplatin-sensitive ovarian tumors von D'Andrea, Alan D, Taniguchi, Toshiyasu, Tischkowitz, Marc, Ameziane, Najim, Hodgson, Shirley V, Mathew, Christopher G, Joenje, Hans, Mok, Samuel C

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Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, p... von Burn, John, Sheth, Harsh, Elliott, Faye, Reed, Lynn, Macrae, Finlay, Mecklin, Jukka-Pekka, Möslein, Gabriela, McRonald, Fiona E, Bertario, Lucio, Evans, D Gareth, Gerdes, Anne-Marie, Ho, Judy W C, Lindblom, Annika, Morrison, Patrick J, Rashbass, Jem, Ramesar, Raj, Seppälä, Toni, Thomas, Huw J W, Pylvänäinen, Kirsi, Borthwick, Gillian M, Mathers, John C, Bishop, D Timothy, Boussioutas, Alex, Brewer, Carole, Cook, Jackie, Eccles, Diana, Ellis, Anthony, Hodgson, Shirley V, Lubinski, Jan, Maher, Eamonn R, Porteous, Mary EM, Sampson, Julian, Scott, Rodney J, Side, Lucy

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Mutational Analysis of the Adaptor Protein 2 Sigma Subunit (AP2S1) Gene: Search for Autosomal Dominant Hypocalcemia Type 3 (ADH3) von Rogers, Angela, Nesbit, M. Andrew, Hannan, Fadil M, Howles, Sarah A, Gorvin, Caroline M, Cranston, Treena, Allgrove, Jeremy, Bevan, John S, Bano, Gul, Brain, Caroline, Datta, Vipan, Grossman, Ashley B, Hodgson, Shirley V, Izatt, Louise, Millar-Jones, Lynne, Pearce, Simon H, Robertson, Lisa, Selby, Peter L, Shine, Brian, Snape, Katie, Warner, Justin, Thakker, Rajesh V

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Familial Non-VHL Clear Cell (Conventional) Renal Cell Carcinoma: Clinical Features, Segregation Analysis, and Mutation Analysis of FLCN von WOODWARD, Emma R, RICKETTS, Christopher, ESCUDIER, Bernard, LATIF, Farida, RICHARD, Stéphane, MAHERL, Eamonn R, KILLICK, Pip, GAD, Sophie, MORRIS, M. R, KAVALIER, Fred, HODGSON, Shirleyv, GIRAUD, Sophie, BRESSAC-DE PAILLERETS, Brigitte, CHAPMAN, Cyril

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Whole-genome sequencing in health care von Van El, Carla G, Cornel, Martina C, Borry, Pascal, Hastings, Ros J, Fellmann, Florence, Hodgson, Shirley V, Howard, Heidi C, Cambon-thomsen, Anne, Knoppers, Bartha M, Meijers-heijboer, Hanne, Scheffer, Hans, Tranebjaerg, Lisbeth, Dondorp, Wybo, De Wert, Guido Mwr

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Loss of expression and promoter methylation of SLIT2 are associated with sessile serrated adenoma formation von Beggs, Andrew D, Jones, Angela, Shepherd, Neil, Arnaout, Abed, Finlayson, Caroline, Abulafi, A Muti, Morton, Dion G, Matthews, Glenn M, Hodgson, Shirley V, Tomlinson, Ian P M

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Peutz–Jeghers syndrome: a systematic review and recommendations for management von Beggs, A D, Latchford, A R, Vasen, H F A, Moslein, G, Alonso, A, Aretz, S, Bertario, L, Blanco, I, Bülow, S, Burn, J, Capella, G, Colas, C, Friedl, W, Møller, P, Hes, F J, Järvinen, H, Mecklin, J-P, Nagengast, F M, Parc, Y, Phillips, R K S, Hyer, W, Ponz de Leon, M, Renkonen-Sinisalo, L, Sampson, J R, Stormorken, A, Tejpar, S, Thomas, H J W, Wijnen, J T, Clark, S K, Hodgson, S V

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Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD von Ricketts, Christopher J, Forman, Julia R, Rattenberry, Eleanor, Bradshaw, Nicola, Lalloo, Fiona, Izatt, Louise, Cole, Trevor R, Armstrong, Ruth, Kumar, V.K. Ajith, Morrison, Patrick J, Atkinson, A. Brew, Douglas, Fiona, Ball, Steve G, Cook, Jackie, Srirangalingam, Umasuthan, Killick, Pip, Kirby, Gail, Aylwin, Simon, Woodward, Emma R, Evans, D. Gareth R, Hodgson, Shirley V, Murday, Vicky, Chew, Shern L, Connell, John M, Blundell, Tom L, MacDonald, Fiona, Maher, Eamonn R

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Cancer incidence in relatives of British Fanconi Anaemia patients von Tischkowitz, Marc, Easton, Douglas F, Ball, Jan, Hodgson, Shirley V, Mathew, Christopher G

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Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility von Astuti, Dewi, Hart-Holden, Niki, Latif, Farida, Lalloo, Fiona, Black, Graeme C., Lim, Caron, Moran, Anthony, Grossman, Ashley B., Hodgson, Shirley V., Freemont, Anthony, Ramsden, Richard, Eng, Charis, Evans, D. Gareth R., Maher, Eamonn R.

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Whole-genome methylation analysis of benign and malignant colorectal tumours von Beggs, Andrew D, Jones, Angela, El-Bahwary, Mona, Abulafi, Muti, Hodgson, Shirley V, Tomlinson, Ian PM

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Refining the relation between 'first hits' and 'second hits' at the APC locus: the 'loose fit' model and evidence for differences in somatic mutation spectra among patients von CRABTREE, Michael, SIEBER, Oliver M, LIPTON, Lara, HODGSON, Shirley V, LAMLUM, Hanan, THOMAS, Hunu J. W, NEALE, Kay, PHILLIPS, Robin K. S, HEINIMANN, Karl, TOMLINSON, Ian P. M

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Multiple Colorectal Adenomas, Classic Adenomatous Polyposis, and Germ-Line Mutations in MYH von Sieber, Oliver M, Lipton, Lara, Crabtree, Michael, Heinimann, Karl, Fidalgo, Paulo, Phillips, Robin K.S, Bisgaard, Marie-Luise, Orntoft, Torben F, Aaltonen, Lauri A, Hodgson, Shirley V, Thomas, Huw J.W, Tomlinson, Ian P.M

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Cancer risk and genotype–phenotype correlations in PTEN hamartoma tumor syndrome von Nieuwenhuis, Marry H., Kets, C. Marleen, Murphy-Ryan, Maureen, Yntema, Helger G., Evans, D. Gareth, Colas, Chrystelle, Møller, Pal, Hes, Frederik J., Hodgson, Shirley V., Olderode-Berends, Maran J. W., Aretz, Stefan, Heinimann, Karl, Gómez García, Encarna B., Douglas, Fiona, Spigelman, Allan, Timshel, Susanne, Lindor, Noralane M., Vasen, Hans F. A.

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Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma von Jafri, Mariam, Whitworth, James, Rattenberry, Eleanor, Vialard, Lindsey, Kilby, Gail, Kumar, Ajith V., Izatt, Louise, Lalloo, Fiona, Brennan, Paul, Cook, Jackie, Morrison, Patrick J., Canham, Natalie, Armstrong, Ruth, Brewer, Carole, Tomkins, Susan, Donaldson, Alan, Barwell, Julian, Cole, Trevor R., Atkinson, A. Brew, Aylwin, Simon, Ball, Steve G., Srirangalingam, Umasuthan, Chew, Shern L., Evans, Dafydd Gareth R, Hodgson, Shirley V., Irving, Richard, Woodward, Emma, Macdonald, Fiona, Maher, Eamonn R.

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Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC) von Geary, Johanne, Sasieni, Peter, Houlston, Richard, Izatt, Louise, Eeles, Ros, Payne, Stewart J., Fisher, Samantha, Hodgson, Shirley V.

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