Neurofibromatosis type 2 (NF2): a clinical and molecular review von Evans, D Gareth R

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Assessing Women at High Risk of Breast Cancer: A Review of Risk Assessment Models von Amir, Eitan, Freedman, Orit C., Seruga, Bostjan, Evans, D. Gareth

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Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome von Kratz, Christian P, Achatz, Maria Isabel, Brugières, Laurence, Frebourg, Thierry, Garber, Judy E, Greer, Mary-Louise C, Hansford, Jordan R, Janeway, Katherine A, Kohlmann, Wendy K, McGee, Rose, Mullighan, Charles G, Onel, Kenan, Pajtler, Kristian W, Pfister, Stefan M, Savage, Sharon A, Schiffman, Joshua D, Schneider, Katherine A, Strong, Louise C, Evans, D Gareth R, Wasserman, Jonathan D, Villani, Anita, Malkin, David

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Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers With Cancer Risk and Mortality von Domchek, Susan M, Friebel, Tara M, Singer, Christian F, Evans, D. Gareth, Lynch, Henry T, Isaacs, Claudine, Garber, Judy E, Neuhausen, Susan L, Matloff, Ellen, Eeles, Rosalind, Pichert, Gabriella, Van t’veer, Laura, Tung, Nadine, Weitzel, Jeffrey N, Couch, Fergus J, Rubinstein, Wendy S, Ganz, Patricia A, Daly, Mary B, Olopade, Olufunmilayo I, Tomlinson, Gail, Schildkraut, Joellen, Blum, Joanne L, Rebbeck, Timothy R

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Cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal Cancer Syndromes in Childhood von Achatz, Maria Isabel, Porter, Christopher C, Brugières, Laurence, Druker, Harriet, Frebourg, Thierry, Foulkes, William D, Kratz, Christian P, Kuiper, Roland P, Hansford, Jordan R, Hernandez, Hector Salvador, Nathanson, Katherine L, Kohlmann, Wendy K, Doros, Leslie, Onel, Kenan, Schneider, Kami Wolfe, Scollon, Sarah R, Tabori, Uri, Tomlinson, Gail E, Evans, D Gareth R, Plon, Sharon E

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Genetic predisposition to peripheral nerve neoplasia: diagnostic criteria and pathogenesis of neurofibromatoses, Carney complex, and related syndromes von Rodriguez, Fausto J., Stratakis, Constantine A., Evans, D. Gareth

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Choose and stay on one out of two paths: distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer von Ripperger, Tim, Evans, D Gareth, Malkin, David, Kratz, Christian P.

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The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes von Smith, Miriam J., Urquhart, Jill E., Harkness, Elaine F., Miles, Emma K., Bowers, Naomi L., Byers, Helen J., Bulman, Michael, Gokhale, Carolyn, Wallace, Andrew J., Newman, William G., Evans, D. Gareth

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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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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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Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria von Plotkin, Scott R., Blakeley, Jaishri O., Evans, D. Gareth, Hanemann, C. Oliver, Hulsebos, Theo J.M., Hunter-Schaedle, Kim, Kalpana, Ganjam V., Korf, Bruce, Messiaen, Ludwine, Papi, Laura, Ratner, Nancy, Sherman, Larry S., Smith, Miriam J., Stemmer-Rachamimov, Anat O., Vitte, Jeremie, Giovannini, Marco

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Toxicity profile of bevacizumab in the UK Neurofibromatosis type 2 cohort von Morris, Katrina A., Golding, John F., Blesing, Claire, Evans, D. Gareth, Ferner, Rosalie E., Foweraker, Karen, Halliday, Dorothy, Jena, Raj, McBain, Catherine, McCabe, Martin G., Swampillai, Angela, Warner, Nicola, Wilson, Shaun, Parry, Allyson, Afridi, Shazia K.

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Longitudinal evaluation of quality of life in 288 patients with neurofibromatosis 2 von Ferner, Rosalie E., Shaw, Adam, Evans, D. Gareth, McAleer, Dympna, Halliday, Dorothy, Parry, Allyson, Raymond, F. Lucy, Durie-Gair, Juliette, Hanemann, C. Oliver, Hornigold, Rachel, Axon, Patrick, Golding, John F.

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Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis von Smith, Miriam J., Wallace, Andrew J., Bowers, Naomi L., Rustad, Cecilie F., Woods, C. Geoff, Leschziner, Guy D., Ferner, Rosalie E., Evans, D. Gareth R.

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Recent developments in neurofibromatoses and RASopathies: Management, diagnosis and current and future therapeutic avenues von Rauen, Katherine A., Huson, Susan M., Burkitt-Wright, Emma, Evans, D. Gareth, Farschtschi, Said, Ferner, Rosalie E., Gutmann, David H., Hanemann, C. Oliver, Kerr, Bronwyn, Legius, Eric, Parada, Luis F., Patton, Michael, Peltonen, Juha, Ratner, Nancy, Riccardi, Vincent M., van der Vaart, Thijs, Vikkula, Miikka, Viskochil, David H., Zenker, Martin, Upadhyaya, Meena

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Sex bias in autism spectrum disorder in neurofibromatosis type 1 von Garg, Shruti, Heuvelman, Hein, Huson, Susan, Tobin, Hannah, Green, Jonathan

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Gene-gene interactions in breast cancer susceptibility von Turnbull, Clare, Seal, Sheila, Renwick, Anthony, Warren-Perry, Margaret, Hughes, Deborah, Elliott, Anna, Pernet, David, Peock, Susan, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J, Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Ahmed, Munaza, Eccles, Diana, Evans, D. Gareth, Donnelly, Peter, Easton, Douglas F., Stratton, Michael R., Rahman, Nazneen

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Mammographic density and breast cancer risk in BRCA1 and BRCA2 mutation carriers von MITCHELL, Gillian, ANTONIOU, Antonis C, ECCLES, Diana, DOUGLAS, Fiona, PATERSON, Joan, HODGSON, Shirley, IZATT, Louise, COLE, Trevor, BURGESS, Lucy, EELES, Ros, EASTON, Douglas F, WARREN, Ruth, PEOCK, Susan, BROWN, Judith, DAVIES, Russell, MATTISON, Jenny, COOK, Margaret, WARSI, Iqbal, EVANS, D. Gareth

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Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes von REBBECK, Timothy R, MITRA, Nandita, OLOPADE, Olufunmilayo I, WEITZEL, Jeffrey N, LYNCH, Henry T, SNYDER, Carrie L, GARBER, Judy E, ANTONIOU, Antonis C, PEOCK, Susan, GARETH EVANS, D, PATERSON, Joan, KENNEDY, M. John, DOMCHEK, Susan M, DONALDSON, Alan, DORKINS, Huw, EASTON, Douglas F, RUBINSTEIN, Wendy S, DALY, Mary B, ISAACS, Claudine, NEVANLINNA, Heli, COUCH, Fergus J, ANDRULIS, Irene L, FREIDMAN, Eitan, FEI WAN, LAITMAN, Yael, GANZ, Patricia A, TOMLINSON, Gail E, NEUHAUSEN, Susan L, NAROD, Steven A, PHELAN, Catherine M, GREENBERG, Roger, NATHANSON, Katherine L, FRIEBEL, Tara M, TRAN, Teo V, SINGER, Christian F, TEA, Muy-Kheng Maria, BLUM, Joanne L, TUNG, Nadine

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A genome wide linkage search for breast cancer susceptibility genes von Smith, Paula, McGuffog, Lesley, Easton, Douglas F., Mann, Graham J., Pupo, Gulietta M., Newman, Beth, Chenevix-Trench, Georgia, Szabo, Csilla, Southey, Melissa, Renard, Hélène, Odefrey, Fabrice, Lynch, Henry, Stoppa-Lyonnet, Dominique, Couch, Fergus, Hopper, John L., Giles, Graham G., McCredie, Margaret R. E., Buys, Saundra, Andrulis, Irene, Senie, Ruby, Goldgar, David E., Oldenburg, Rogier, Kroeze-Jansema, Karin, Kraan, Jaennelle, Meijers-Heijboer, Hanne, Klijn, Jan G. M., van Asperen, Christi, van Leeuwen, Inge, Vasen, Hans F. A., Cornelisse, Cees J., Devilee, Peter, Baskcomb, Linda, Seal, Sheila, Barfoot, Rita, Mangion, Jon, Hall, Anita, Edkins, Sarah, Rapley, Elizabeth, Wooster, Richard, Chang-Claude, Jenny, Eccles, Diana, Evans, D. Gareth, Futreal, P. Andrew, Nathanson, Katherine L., Weber, Barbara L., Rahman, Nazneen, Stratton, Michael R.

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