Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Lorraine, Cowley"'
Autor:
Danya F. Vears, Joel T. Minion, Stephanie J. Roberts, James Cummings, Mavis Machirori, Mwenza Blell, Isabelle Budin-Ljøsne, Lorraine Cowley, Stephanie O. M. Dyke, Clara Gaff, Robert Green, Alison Hall, Amber L. Johns, Bartha M. Knoppers, Stephanie Mulrine, Christine Patch, Eva Winkler, Madeleine J. Murtagh
Publikováno v:
PLoS ONE, Vol 16, Iss 11 (2021)
Despite the plethora of empirical studies conducted to date, debate continues about whether and to what extent results should be returned to participants of genomic research. We aimed to systematically review the empirical literature exploring stakeh
Externí odkaz:
https://doaj.org/article/08013997ec0e494496b417420b999001
Autor:
Madeleine J. Murtagh, Mwenza T. Blell, Olly W. Butters, Lorraine Cowley, Edward S. Dove, Alissa Goodman, Rebecca L. Griggs, Alison Hall, Nina Hallowell, Meena Kumari, Massimo Mangino, Barbara Maughan, Melinda C. Mills, Joel T. Minion, Tom Murphy, Gillian Prior, Matthew Suderman, Susan M. Ring, Nina T. Rogers, Stephanie J. Roberts, Catherine Van der Straeten, Will Viney, Deborah Wiltshire, Andrew Wong, Neil Walker, Paul R. Burton
Publikováno v:
Human Genomics, Vol 12, Iss 1, Pp 1-12 (2018)
Abstract Background Genomic and biosocial research data about individuals is rapidly proliferating, bringing the potential for novel opportunities for data integration and use. The scale, pace and novelty of these applications raise a number of urgen
Externí odkaz:
https://doaj.org/article/733decf5a9504990937c04bf2531d84a
Autor:
Mari Jones, Lorraine Cowley
Publikováno v:
OBM Genetics. 4:1-18
This paper explores views of healthcare professionals (HCPs) in genetics and foetal medicine settings on offering pre-natal diagnosis (PND) for adult onset cancer susceptibility (AOCS) genes. Study participants came from different disciplinary backgr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26f9f1467d5f32db7c1d46a837b4097b
https://doi.org/10.21926/obm.genet.2002108
https://doi.org/10.21926/obm.genet.2002108
Autor:
Mavis Machirori, James Cummings, Alison Hall, Eva C. Winkler, Joel T. Minion, Lorraine Cowley, Christine Patch, Stephanie O. M. Dyke, Stephanie J. Roberts, Isabelle Budin-Ljøsne, Mwenza Blell, Stephanie Mulrine, Robert C. Green, Madeleine J. Murtagh, Danya F. Vears, Bartha Maria Knoppers, Clara Gaff, Amber L. Johns
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 11 (2021)
PLoS ONE, Vol 16, Iss 11, p e0258646 (2021)
PLOS ONE
PLoS ONE, Vol 16, Iss 11 (2021)
PLoS ONE, Vol 16, Iss 11, p e0258646 (2021)
PLOS ONE
Despite the plethora of empirical studies conducted to date, debate continues about whether and to what extent results should be returned to participants of genomic research. We aimed to systematically review the empirical literature exploring stakeh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e65b2235622883e7ddc6741bfdc77270
https://eprints.gla.ac.uk/258636/1/258636.pdf
https://eprints.gla.ac.uk/258636/1/258636.pdf
Autor:
Laura, Powell, Eric, Olinger, Sarah, Wedderburn, Vijayalakshmi Salem, Ramakumaran, Usha, Kini, Jill, Clayton-Smith, Simon C, Ramsden, Sarah J, Rice, Miguel, Barroso-Gil, Ian, Wilson, Lorraine, Cowley, Sally, Johnson, Elizabeth, Harris, Tara, Montgomery, Marta, Bertoli, Eugen, Boltshauser, John A, Sayer
Publikováno v:
Brain Communications
Paediatric neurology syndromes are a broad and complex group of conditions with a large spectrum of clinical phenotypes. Joubert syndrome is a genetically heterogeneous neurological ciliopathy syndrome with molar tooth sign as the neuroimaging hallma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f73dfcfef91e4ec8be8f3f7a99094043
https://pubmed.ncbi.nlm.nih.gov/34423300
https://pubmed.ncbi.nlm.nih.gov/34423300
Autor:
Sarah Wedderburn, Miguel Barroso-Gil, Laura Powell, Lorraine Cowley, Jill Clayton-Smith, John A. Sayer, Eric Olinger, Ian D. Wilson, Marta Bertoli, Eugen Boltshauser, Simon C Ramsden, Tara Montgomery, Sarah J. Rice, Usha Kini, Elizabeth Harris, Vijayalakshmi Salem Ramakumaran, Sally Johnson
Publikováno v:
Brain Communications. 3
Paediatric neurology syndromes are a broad and complex group of conditions with a large spectrum of clinical phenotypes. Joubert syndrome is a genetically heterogeneous neurological ciliopathy syndrome with molar tooth sign as the neuroimaging hallma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::719f50fc5b79f896741b31a28c7f76b8
https://doi.org/10.1093/braincomms/fcab163
https://doi.org/10.1093/braincomms/fcab163
Autor:
Lorraine Cowley
Publikováno v:
What About the Family?
The context of this case study, based on empirical qualitative research, is genetic testing for cancer susceptibility. Within genetics, information may have shared significance for family members, but not everyone necessarily has the same desire to k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39dfc1df67cd56018f6a755c805dba85
https://doi.org/10.1093/med/9780190624880.003.0005
https://doi.org/10.1093/med/9780190624880.003.0005
Publikováno v:
Genetic Transparency? Ethical and Social Implications of Next Generation Human Genomics and Genetic Medicine ISBN: 9789004311893
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31449fb8181323c8d449f7cf39905b8e
https://doi.org/10.1163/9789004311893_009
https://doi.org/10.1163/9789004311893_009
Autor:
Angus John Clarke, Penny Guilbert, Lorraine Cowley, Van Tran, Anna Middleton, Rhona MacLeod, Alison Clarke
Publikováno v:
Journal of Genetic Counseling. 16:127-142
The Association of Genetic Nurses and Counsellors (AGNC) is the professional organisation which represents genetic counsellors and genetic nurses in the United Kingdom (UK) and Eire. The AGNC recognises that genetic counselling supervision is instrum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fbaff188636a0523f80d227a18132db
https://doi.org/10.1007/s10897-006-9065-0
https://doi.org/10.1007/s10897-006-9065-0
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 9, Iss Suppl 1, p P6 (2011)
Hereditary Cancer in Clinical Practice
Europe PubMed Central
Hereditary Cancer in Clinical Practice
Europe PubMed Central
Results Choice in genetic testing and research does not appear to be the key value for participants in this study; instead they are influenced by a sense of responsibility [3]. Choice for them is an important right, one exercised by other family memb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1896077e93aeb30bdc502e0eba610a08
https://doaj.org/article/abd09e8e003346c99731be5cc27c729d
https://doaj.org/article/abd09e8e003346c99731be5cc27c729d