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Number of items: 9.

Davies, Rachel, Price Tate, Rachel and Taverner, Nicola V. 2024. What next for “counseling” in genetic counseling training: A co‐production workshop exploring how CBT and ACT approaches can contribute to the genetic counseling toolkit. Journal of Genetic Counseling 10.1002/jgc4.1868
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Davies, Rachel, Price Tate, Rachel and Taverner, Nicola V. 2024. What next for “counseling” in genetic counseling training: A reflection on how CBT and ACT approaches can contribute to the genetic counseling toolkit. Journal of Genetic Counseling 10.1002/jgc4.1873
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Kay, Alison and Taverner, Nicola 2023. Adoptees’ views and experiences of direct-to-consumer (DTC) genomic testing: an exploratory interview study from the UK. Journal of Community Genetics 14 , pp. 149-162. 10.1007/s12687-022-00622-y
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Jezkova, Jana, Shaw, Sophie, Taverner, Nicola V. and Williams, Hywel J. ORCID: https://orcid.org/0000-0001-7758-0312 2022. Rapid genome sequencing for pediatrics. Human Mutation: Variation, Informatics and Disease 43 (11) , pp. 1507-1518. 10.1002/humu.24466
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Middleton, Anna, Taverner, Nicola, Moreton, Natalie, Rizzo, Roberta, Houghton, Catherine, Watt, Catherine, Horton, Esther, Levene, Sara, Leonard, Phil, Melville, Athalie, Ellis, Somya, Tripathi, Vishakha, Patch, Christine and Jenkins, Elaine 2022. The genetic counsellor role in the United Kingdom. European Journal of Human Genetics 31 , pp. 13-15. 10.1038/s41431-022-01212-9
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Middleton, Anna ORCID: https://orcid.org/0000-0003-3103-8098, Taverner, Nicola, Houghton, Catherine, Smithson, Sarah, Balasubramanian, Meena and Elmslie, Frances 2022. Scope of professional roles for genetic counsellors and clinical geneticists in the United Kingdom. European Journal of Human Genetics 31 (1) , pp. 9-12. 10.1038/s41431-022-01214-7
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Dearing, Audrey and Taverner, Nicola 2017. Mainstreaming genetics in palliative care: barriers and suggestions for clinical genetic services. Journal of Community Genetics 9 , pp. 243-256. 10.1007/s12687-017-0345-1
Item availability restricted.
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Baig, Sheharyar, Strong, Mark, Rosser, Elizabeth, Taverner, Nicola, Glew, Ruth, Miedzybrodzka, Zosia, Clarke, Angus, Craufurd, David and Quarrell, Oliver 2016. 22 Years of predictive testing for Huntington’s disease: the experience of the UK Huntington’s Prediction Consortium. European Journal of Human Genetics 24 , pp. 1396-1402. 10.1038/ejhg.2016.36

Baig, Sheharyar S., Strong, Mark, Rosser, Elisabeth, Taverner, Nicola, Glew, Ruth, Miedzybrodzka, Zosia, Clarke, Angus John ORCID: https://orcid.org/0000-0002-1200-9286, Craufurd, David, UK Huntington’s Disease Prediction Consortium and Quarrell, Oliver W. 2016. 22 years of predictive testing for Huntington's disease: the experience of the UK Huntington's Prediction Consortium. European Journal of Human Genetics 24 , pp. 1396-1402. 10.1038/ejhg.2016.36
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This list was generated on Thu Mar 28 11:05:04 2024 GMT.