Intervention planning for Antibiotic Review Kit (ARK): a digital and behavioural intervention to safely review and reduce antibiotic prescriptions in acute and general medicine von Santillo, M, Sivyer, K, Krusche, A, Mowbray, F, Jones, N, Peto, T E A, Walker, A S, Llewelyn, M J, Yardley, L

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British Thoracic Society Quality Standards for acute non-invasive ventilation in adults von Davies, Michael, Allen, Martin, Bentley, Andrew, Bourke, Stephen C, Creagh-Brown, Ben, D’Oliveiro, Rachel, Glossop, Alastair, Gray, Alasdair, Jacobs, Phillip, Mahadeva, Ravi, Moses, Rachael, Setchfield, Ian

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Systems Leadership Enablement of Collaborative Healthcare Practices von Solman, Annette, Manley, Kim, Christie, Jane, Setchfield, Ian

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Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls von Soemedi, Rachel, Topf, Ana, Wilson, Ian J., Darlay, Rebecca, Rahman, Thahira, Glen, Elise, Hall, Darroch, Huang, Ni, Bentham, Jamie, Bhattacharya, Shoumo, Cosgrove, Catherine, Brook, J. David, Granados-Riveron, Javier, Setchfield, Kerry, Bu'Lock, Frances, Thornborough, Chris, Devriendt, Koenraad, Breckpot, Jeroen, Hofbeck, Michael, Lathrop, Mark, Rauch, Anita, Blue, Gillian M., Winlaw, David S., Hurles, Matthew, Santibanez-Koref, Mauro, Cordell, Heather J., Goodship, Judith A., Keavney, Bernard D.

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Phenotype-Specific Effect of Chromosome 1q21.1 Rearrangements and GJA5 Duplications in 2436 Congenital Heart Disease Patients and 6760 Controls von Soemedi, Rachel, Topf, Ana, Wilson, Ian J, Darlay, Rebecca, Rahman, Thahira, Glen, Elise, Hall, Darroch, Huang, Ni, Bentham, Jamie, Bhattacharya, Shoumo, Cosgrove, Catherine, Brook, J. David, Granados-Riveron, Javier, Setchfield, Kerry, Bulock, Frances, Thornborough, Chris, Devriendt, Koenraad, Breckpot, Jeroen, Hofbeck, Michael, Lathrop, Mark, Rauch, Anita, Blue, Gillian M, Winlaw, David S, Hurles, Matthew, Santibanez-Koref, Mauro, Cordell, Heather J, Goodship, Judith A, Keavney, Bernard D

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Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot von Cordell, Heather J, Töpf, Ana, Mamasoula, Chrysovalanto, Postma, Alex V, Bentham, Jamie, Zelenika, Diana, Heath, Simon, Blue, Gillian, Cosgrove, Catherine, Granados Riveron, Javier, Darlay, Rebecca, Soemedi, Rachel, Wilson, Ian J, Ayers, Kristin L, Rahman, Thahira J, Hall, Darroch, Mulder, Barbara J.M, Zwinderman, Aelko H, van Engelen, Klaartje, Brook, J. David, Setchfield, Kerry, Bu'lock, Frances A, Thornborough, Chris, O'Sullivan, John, Stuart, A. Graham, Parsons, Jonathan, Bhattacharya, Shoumo, Winlaw, David, Mital, Seema, Gewillig, Marc, Breckpot, Jeroen, Devriendt, Koenraad, Moorman, Antoon F.M, Rauch, Anita, Lathrop, G. Mark, Keavney, Bernard D, Goodship, Judith A

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Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease von Soemedi, Rachel, Wilson, Ian J, Bentham, Jamie, Darlay, Rebecca, Töpf, Ana, Zelenika, Diana, Cosgrove, Catherine, Setchfield, Kerry, Thornborough, Chris, Granados-Riveron, Javier, Blue, Gillian M, Breckpot, Jeroen, Hellens, Stephen, Zwolinkski, Simon, Glen, Elise, Mamasoula, Chrysovalanto, Rahman, Thahira J, Hall, Darroch, Rauch, Anita, Devriendt, Koenraad, Gewillig, Marc, O'Sullivan, John, Winlaw, David S, Bu'lock, Frances, Brook, J David, Bhattacharya, Shoumo, Lathrop, Mark, Santibanez-Koref, Mauro, Cordell, Heather J, Goodship, Judith A

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Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease von Soemedi, Rachel, Wilson, Ian J, Bentham, Jamie, Darlay, Rebecca, Töpf, Ana, Zelenika, Diana, Cosgrove, Catherine, Setchfield, Kerry, Thornborough, Chris, Granados-Riveron, Javier, Blue, Gillian M, Breckpot, Jeroen, Hellens, Stephen, Zwolinkski, Simon, Glen, Elise, Mamasoula, Chrysovalanto, Rahman, Thahira J, Hall, Darroch, Rauch, Anita, Devriendt, Koenraad, Gewillig, Marc, O' Sullivan, John, Winlaw, David S, Bu'lock, Frances, Brook, J. David, Bhattacharya, Shoumo, Lathrop, Mark, Santibanez-Koref, Mauro, Cordell, Heather J, Goodship, Judith A, Keavney, Bernard D

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Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls von Soemedi, Rachel, Topf, Ana, Wilson, Ian J, Darlay, Rebecca, Rahman, Thahira, Glen, Elise, Hall, Darroch, Huang, Ni, Bentham, Jamie, Bhattacharya, Shoumo, Cosgrove, Catherine, Brook, J David, Granados-Riveron, Javier, Setchfield, Kerry, Bu'lock, Frances, Thornborough, Chris, Devriendt, Koenraad, Breckpot, Jeroen, Hofbeck, Michael, Lathrop, Mark, Rauch, Anita, Blue, Gillian M, Winlaw, David S, Hurles, Matthew, Santibanez-Koref, Mauro, Cordell, Heather J, Goodship, Judith A, Keavney, Bernard D

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Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot von Cordell, Heather J, Töpf, Ana, Mamasoula, Chrysovalanto, Postma, Alex V, Bentham, Jamie, Zelenika, Diana, Heath, Simon, Blue, Gillian, Cosgrove, Catherine, Granados Riveron, Javier, Darlay, Rebecca, Soemedi, Rachel, Wilson, Ian J, Ayers, Kristin L, Rahman, Thahira J, Hall, Darroch, Mulder, Barbara J M, Zwinderman, Aelko H, van Engelen, Klaartje, Brook, J David, Setchfield, Kerry, Bu'Lock, Frances A, Thornborough, Chris, O'Sullivan, John, Stuart, A Graham, Parsons, Jonathan, Bhattacharya, Shoumo, Winlaw, David, Mital, Seema, Gewillig, Marc, Breckpot, Jeroen, Devriendt, Koen, Moorman, Antoon F M, Rauch, Anita, Lathrop, G Mark, Keavney, Bernard D, Goodship, Judith A

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