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Browsing publications by Dr Pauline McCormack

Newcastle AuthorsTitleYearFull text
Dr Pauline McCormack
Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis (Genetics in Medicine, (2019), 10.1038/s41436-019-0579-x)2019
Dr Nina Hallowell
Dr Pauline McCormack
Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis2019
Dr Simon Woods
Dr Pauline McCormack
Professor Hanns Lochmuller
Professor Volker Straub
Improving the informed consent process in international collaborative rare disease research: Effective consent for effective research2016
Dr Pauline McCormack
Dr Simon Woods
New recommendation on biological materials could hamper muscular dystrophy research2016
Dr Pauline McCormack
Rare Disease, Big Data: the views of rare disease patients on systems for sharing data and biospecimens2016
Dr Pauline McCormack
Professor Hanns Lochmuller
'You should at least ask'. The expectations, hopes and fears of rare disease patients on large-scale data and biomaterial sharing for genomics research2016
Dr Pauline McCormack
Dr Simon Woods
Consent, collaboration and cures:the views of rare disease patients on systems for sharing data and biospecimens2015
Dr Pauline McCormack
Dr Simon Woods
Florian Schaefer
Professor Hanns Lochmuller
Professor Mats Hansson
et al.		International Charter of principles for sharing bio-specimens and data2015
Dr Matthias Wienroth
Dr Pauline McCormack
Professor Tom Joyce
Precaution, governance and the failure of medical implants: the ASR(TM) hip in the UK2014
Dr Pauline McCormack
Setting up strategies: patient inclusion in biobank and genomics research in Europe2014
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