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Number of items: 11.

McVeigh, Terri Patricia, Donnelly, Deirdre, Al Shehhi, Maryam, Jones, Elizabeth A., Murray, Alexandra, Wedderburn, Sarah, Porteous, Mary and Lynch, Sally Ann 2019. Towards establishing consistency in triage in a tertiary specialty. European Journal of Human Genetics 27 , pp. 547-555. 10.1038/s41431-018-0322-0
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Brunstrom, Kate, Murray, Alexandra and McAllister, Marion 2016. Experiences of women who underwent predictive BRCA 1/2 mutation testing before the age of 30. Journal of Genetic Counselling 25 (1) , pp. 90-100. 10.1007/s10897-015-9845-5

Shipman, Hannah Elizabeth, Arribas-Ayllon, Michael, Murray, Alexandra and Gaff, Clara Louise 2014. On the limits of genetic responsibility: Communication and consent for tumour testing for Lynch syndrome. Communication & Medicine 10 (3) , pp. 225-235. 10.1558/cam.v10i3.225

Phelps, Ceri, Bennett, Paul, Hood, Kerenza, Brain, Katherine Emma and Murray, Alexandra 2013. A self-help coping intervention can reduce anxiety and avoidant health behaviours whilst waiting for cancer genetic risk information: results of a phase III randomised trial. Psycho-Oncology 22 (4) , pp. 837-844. 10.1002/pon.3072

Bennett, P., Phelps, C., Hilgart, Jennifer, Hood, Kerenza, Brain, Katherine Emma and Murray, Alexandra 2012. Concerns and coping during cancer genetic risk assessment. Psycho-Oncology 21 (6) , pp. 611-617. 10.1002/pon.1938

Renton, Alan E., Majounie, Elisa, Waite, Adrian James, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James William, Murray, Alexandra, Pearson, Justin Peter, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek J., Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel Melville, Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw Rees, Tienari, Pentti J. and Traynor, Bryan J. 2011. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72 (2) , pp. 257-268. 10.1016/j.neuron.2011.09.010

Iredale, Rachel, Mundy, Lisa, Marsden, Debbie and Murray, Alexandra 2011. Patient involvement at the Cancer Genetics Service for Wales: meeting the long-term information and support needs of people at risk of inherited cancer. Patient Education and Counseling 84 (2) , pp. 280-281. 10.1016/j.pec.2011.03.004

Pearson, Justin P., Williams, Nigel Melville, Majounie, Elisa, Waite, Adrian James, Stott, Jennifer, Newsway, Victoria, Murray, Alexandra, Hernandez, Dena, Guerreiro, Rita, Singleton, Andrew B., Neal, James William and Morris, Huw Rees 2011. Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p. Journal of Neurology 258 (4) , pp. 647-655. 10.1007/s00415-010-5815-x

Hilgart, Jennifer, Phelps, C., Bennett, Paul, Hood, Kerenza, Brain, Katherine Emma and Murray, Alexandra 2010. "I have always believed I was at high risk..." The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of free-text questionnaire comments. Familial Cancer 9 (3) , pp. 469-477. 10.1007/s10689-010-9324-y

Jones, Wendy, Emmerson, L., Myring, J., Palmer-Smith, S., Frayling, Ian Martin and Murray, Alexandra 2009. Using the Wijnen Score to triage for mismatch repair gene analysis :a review of MSI negative results in Wales [Abstract]. Journal of Medical Genetics 46 (Supp.) , S111.

Murray, Alexandra, Keegan, C., Gaff, C., Myring, J., Palmer-Smith, S., Butler, R., Rogers, M. and Frayling, Ian Martin 2008. Do the Cancer Genetics Service for Wales guidelines for selecting patients for tumour testing appropriately identify Lynch syndrome families? [Abstract]. Journal of Medical Genetics 45 (Supp.) , S119.

This list was generated on Thu Jun 27 08:11:04 2019 BST.