Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Browse by Current Cardiff authors

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Number of items: 14.

Girardi, Fabio, Barnes, Daniel R., Barrowdale, Daniel, Frost, Debra, Brady, Angela F., Miller, Claire, Henderson, Alex, Donaldson, Alan, Murray, Alex, Brewer, Carole, Pottinger, Caroline, Evans, D. Gareth, Eccles, Diana, Lalloo, Fiona, Gregory, Helen, Cook, Jackie, Eason, Jacqueline, Adlard, Julian, Barwell, Julian, Ong, Kai Ren, Walker, Lisa, Izatt, Louise, Side, Lucy E., Kennedy, M John, Tischkowitz, Marc, Rogers, Mark T., Porteous, Mary E., Morrison, Patrick J., Eeles, Ros, Davidson, Rosemarie, Snape, Katie, Easton, Douglas F. and Antoniou, Antonis C. 2018. Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study. Genetics in Medicine 10.1038/gim.2018.44
file

Rogers, Mark F., Shihab, Hashem A., Mort, Matthew, Cooper, David, Gaunt, Tom R. and Campbell, Colin 2018. FATHMM-XF: accurate prediction of pathogenic point mutations via extended features. Bioinformatics 34 (3) , pp. 511-513. 10.1093/bioinformatics/btx536
file

Wood, Libby, Cordts, Isabell, Atalaia, Antonio, Marini-Bettolo, Chiara, Maddison, Paul, Phillips, Margaret, Roberts, Mark, Rogers, Mark, Hammans, Simon, Straub, Volker, Petty, Richard, Orrell, Richard, Monckton, Darren G., Nikolenko, Nikoletta, Jimenez-Moreno, Aura Cecilia, Thompson, Rachel, Hilton-Jones, David, Turner, Chris and Lochmüller, Hanns 2017. The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research. Journal of Neurology 264 (5) , pp. 979-988. 10.1007/s00415-017-8483-2

Lemmers, R. J. L. F., Goeman, J. J., van der Vliet, P. J., van Nieuwenhuizen, M. P., Balog, J., Vos-Versteeg, M., Camano, P., Ramos Arroyo, M. A., Jerico, I., Rogers, Mark, Miller, D. G., Upadhyaya, Meena, Verschuuren, J. J. G. M., Lopez de Munain Arregui, A., van Engelen, B. G. M., Padberg, G. W., Sacconi, S., Tawil, R., Tapscott, S. J., Bakker, B. and van der Maarel, S. M. 2015. Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2. Human Molecular Genetics 24 (3) , pp. 659-669. 10.1093/hmg/ddu486

Winston, Jincy, Duerden, Laura, Mort, Matthew, Frayling, Ian, Rogers, Mark and Upadhyaya, Meena 2015. Identification of two novel SMCHD1 sequence variants in families with FSHD-like muscular dystrophy. European Journal of Human Genetics 23 (1) , pp. 67-71. 10.1038/ejhg.2014.58

Witt, J., Elwyn, G., Wood, Fiona Claire, Rogers, Mark, Menon, U. and Brain, Katherine Emma 2014. Adapting the Coping in Deliberation (CODE) framework: A multi-method approach in the context of familial ovarian cancer risk management. Patient Education and Counseling 97 (2) , pp. 200-220. 10.1016/j.pec.2014.07.004

Couch, F, Wang, X, McGuffog, L, Lee, A, Olswold, C, Kuchenbaecker, K, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O, Lee, A, Bacot, F, Vincent, D, Hogervorst, F, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Investigators, k, Radice, P, Schmutzler, R, Domchek, S, Piedmonte, M, Singer, C, Friedman, E, Thomassen, M, Hansen, T, Neuhausen, S, Szabo, C, Blanco, I, Greene, M, Karlan, B, Garber, J, Phelan, C, Weitzel, J, Montagna, M, Olah, E, Andrulis, I, Godwin, A, Yannoukakos, D, Goldgar, D, Caldes, T, Nevanlinna, H, Osorio, A, Terry, M, Daly, M, van Rensburg, E, Hamann, U, Ramus, S, Ewart Toland, A, Caligo, M, Olopade, O, Tung, N, Claes, K, Beattie, M, Southey, M, Imyanitov, E, Tischkowitz, M, Janavicius, R, John, E, Kwong, A, Diez, O, Balmaña, J, Barkardottir, R, Arun, A, Rennert, G, Teo, H, Ganz, P, Campbell, I, van der Hout, A, van Deurzen, C, Seynaeve, C, Gómez Garcia, E, van Leeuwen, F, Meijers-Heijboer, H, Gills, J, Ausems, M, Blok, M, Ligtenberg, M, Rookus, M, Devilee, P, Verhoef, S, van Os, T, Wijneb, J, Frost, D, Ellis, S, Fineberg, E, Platte, R, Evans, D, Izatt, L, Eeles, R, Adlard, J, Eccles, D, Cook, J, Brewer, C, Douglas, F, Hodgson, S, Morrison, P, Side, L, Donaldson, A, Houghton, C, Rogers, Mark, Dorkins, H, Eason, J, Gregory, H, McCann, E, Murray, A, Calender, A, Hardouin, A, Berthet, P, Delnatte, C, Nogues, C, Lasset, C, Houdayer, C, Leroux, D, Rouleau, E, Prieur, F, Damiola, F, Sobol, H, Coupier, I, Venat-Bouvet, L, Castera, L, Gauthier-Villars, M, Léone, M, Pujol, P, Mazoyer, S, Bignon, Y, Zlowocka-Perlowska, E, Gronwald, J, Lubinski, J, Durda, K, Jaworska, K, Huzarski, T, Spurdle, A, Viel, A, Peissel, B, Bonanni, B, Melloni, G, Ottini, L, Papi, L, Varesco, L, Tibiletti, M, Peterlongo, P, Volorio, S, Manoukian, S, Pensotti, V, Arnold, N, Engel, C, Deissler, H, Gadzicki, D, Gehrig, A, Kast, K, Rhiem, K, Meindl, A, Niederacher, D, Ditsch, N, Plendl, H, Preisler-Adams, S, Engert, S, Sutter, C, Varon-Mateeva, R, Wappenschmidt, B, Weber, B, Arver, B, Stenmark-Askmalm, M, Loman, N, Rosenquist, R, Einbeigi, Z, Nathanson, K, Rebbeck, T, Blank, S, Cohn, D, Rodriguez, G, Small, L, Friedlander, M, Bae-Jump, V, Fink-Retter, A, Rappaport, C, Gschwantler-Kaulich, D, Pfeiler, G, Tea, M, Lindor, N, Kaufman, B, Shimon Paluch, S, Laitman, Y, Skytte, A, Gerdes, A, Pedersen, I, Moeller, S, Kruse, T, Jensen, U, Vijai, J, Sarrel, K, Robson, M, Kauff, N, Mulligan, A, Glendon, G, Ozcelik, H, Ejlertsen, B, Nielsen, F, Jønson, L, Andersen, M, Ding, Y, Steele, L, Foretova, L, Teule, A, Lazaro, C, Brunet, J, Pujana, M, Mai, P, Loud, J, Walsh, C, Lester, J, Orsulic, S, Narod, S, Herzog, J, Sand, S, Tognazzo, S, Agata, S, Vaszko, T, Weaver, J, Stavropoulou, A, Buys, S, Romero, A, de la Hoya, M, Aittomäki, K, Muranen, T, Duran, M, Chung, W, Lasa, A, Dorfling, C, Miron, A, Benitez, J, Senter, L, Huo, D, Chan, S, Sokolenko, A, Chiquette, J, Tihomirova, L, Friebel, T, Agnarsson, B, Lu, K, Lejbkowicz, F, James, P, Hall, P, Dunning, A, Tessier, D, Cunningham, J, Slager, S, Wang, C, Hart, S, Stevens, K, Simard, J, Pastinen, T, Pankratz, V, Offit, K, Easton, D, Chenevix-Trench, G and Antoniou, A. 2013. Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. PLoS Genetics 9 (3) , e1003212. 10.1371/journal.pgen.1003212
file

Brain, Katherine Emma, Lifford, Kate Joanna, Fraser, Lindsay, Rosenthal, Adam N., Rogers, Mark, Lancastle, Deborah, Phelps, Ceri, Watson, Eila K., Clements, Alison and Menon, Usha 2012. Psychological outcomes of familial ovarian cancer screening: No evidence of long-term harm. Gynecologic Oncology 127 (3) , pp. 556-563. 10.1016/j.ygyno.2012.08.034

Lifford, Kate Joanna, Fraser, Lindsay, Rosenthal, Adam N., Rogers, Mark, Lancastle, Deborah, Phelps, Ceri, Watson, Eila K., Clements, Alison, Iredale, Rachel, Jacobs, Ian, Menon, Usha and Brain, Katherine Emma 2012. Withdrawal from familial ovarian cancer screening for surgery: Findings from a psychological evaluation study (PsyFOCS). Gynecologic Oncology 124 (1) , pp. 158-163. 10.1016/j.ygyno.2011.09.015

Gaff, C. L., Rogers, Mark and Frayling, Ian Martin 2007. Genetic counselling and consent for tumour testing in HNPCC. Clinical Genetics 71 (5) , pp. 400-405. 10.1111/j.1399-0004.2007.00779.x

Gaff, C. L., Rogers, Mark and Frayling, Ian 2006. Variability and inequity in testing of somatic tissue for hereditary cancer: a survey of UK clinical practice. Clinical Genetics 70 (4) , pp. 312-319. 10.1111/j.1399-0004.2006.00676.x

Wiles, Charles Mark, Busse, Monica, Sampson, Catherine Mary Anne, Rogers, Mark, Fenton-May, Jane Mary and Van Deursen, Robert William Martin 2005. Falls and stumbles in myotonic dystrophy. Journal of Neurology, Neurosurgery and Psychiatry 77 (3) , pp. 393-396. 10.1136/jnnp.2005.066258
file

Wiles, Charles Mark, Busse, Monica, Sampson, C. M, Rogers, Mark, Fenton-May, Jane Mary and Van Deursen, Robert William Martin 2005. Falls in myotonic dystrophy.(Abstract). Journal of Neurology, Neurosurgery and Psychiatry 76 (9) , p. 1315.

Brain, Katherine Emma, Sivell, Stephanie, Bennert, Kristina, Howell, Lucy, France, L., Jordan, S., Rogers, Mark, Gray, Jonathon and Sampson, Julian Roy 2005. An exploratory comparison of genetic counselling protocols for HNPCC predictive testing. Clinical Genetics 68 (3) , pp. 255-261. 10.1111/j.1399-0004.2005.00491.x

This list was generated on Fri Aug 17 03:40:20 2018 BST.