Using ‘next-generation’ sequencing in the identification of novel causes of inherited heart diseases by Hastings, R

Campylobacter genotypes from poultry transportation crates indicate a source of contamination and transmission. by Hastings, R, Colles, F, McCarthy, N, Maiden, M, Sheppard, S

Training Teachers to Deliver Mindfulness-Based Interventions: Learning from the UK Experience. by Crane, R, Kuyken, W, Hastings, R, Rothwell, N, Williams, J

Training Teachers to Deliver Mindfulness-Based Interventions: Learning from the UK Experience by Crane, R, Kuyken, W, Hastings, R, Rothwell, N, Williams, J

Competence in teaching mindfulness-based courses: concepts, development and assessment by Crane, R, Kuyken, W, Williams, J, Hastings, R, Cooper, L, Fennell, M

Development and validation of the mindfulness-based interventions - teaching assessment criteria (MBI:TAC). by Crane, R, Eames, C, Kuyken, W, Hastings, R, Williams, J, Bartley, T, Evans, A, Silverton, S, Soulsby, J, Surawy, C

Associations between school-level disadvantaged, bullying involvement and children's mental health by Badger, J, Zaneva, M, Hastings, R, Broome, M, Hayes, R, Patterson, P, Rose, N, Clarkson, S, Hutchings, J, Bowes, L

Phase 1 study of HSP90 inhibitor ganetespib with pemetrexed and cisplatin/carboplatin chemotherapy for pleural mesothelioma by Fennell, D, Danson, S, Forster, M, Talbot, D, Woll, P, Child, J, Ngai, Y, Farrelly, L, Hackshaw, A, Sharkey, A, Busacca, S, Hastings, R, Barnes, D, Nicolson, M, Taylor, P, Ahmed, S, Wheeler, G

The Early Positive Approaches to Support (E-PAtS) study: study protocol for a feasibility cluster randomised controlled trial of a group programme (E-PAtS) for family caregivers of... by Coulman, E, Hastings, R, Gore, N, Gillespie, D, McNamara, R, Petrou, S, Segrott, J, Bradshaw, J, Hood, K, Jahoda, A, Lindsay, G, Lugg-Widger, F, Robling, M, Shurlock, J, Totsika, V

A novel familial cardiac arrhythmia syndrome with widespread ST-segment depression by Bundgaard, H, Jøns, C, Lodder, EM, Izarzugaza, JMG, Pehrson, S, Tfelt-Hansen, J, Herrera, JA, Ahlberg, G, Olesen, MS, Holst, AG, Wellens, H, De Villiers, C, Hastings, R, Stuart, G, Brunak, S, Wilde, AAM, Watkins, H, Christensen, AH

Revolutionising genetic testing for Ataxias using Next Generation Sequencing (NGS) by Nemeth, A, Kwasniewska, A, Schnekenberg, R, Lise, S, Becker, E, Shanks, M, Cader, M, Talbot, K, de Silva, R, Fletcher, N, Hastings, R, Jayawant, S, Lunt, P, Morrisor, P, Worth, P, Tolmie, J, Packham, E, Seller, A, Ragoussis, J

Combination of Whole Genome Sequencing, Linkage and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy with Features of Left... by Hastings, R, de Villiers, C, Hooper, C, Ormondroyd, L, Pagnamenta, A, Lise, S, Salatino, S, Knight, S, Taylor, J, Thompson, K, Arnold, L, Chatziefthimiou, S, Konarev, P, Wilmanns, M, Ehler, E, Ghisleni, A, Gautel, M, Blair, E, Watkins, H, Gehmlich, K

Early positive approaches to support for families of young children with intellectual disability: the E-PAtS feasibility RCT by Coulman, E, Gore, N, Moody, G, Wright, M, Segrott, J, Gillespie, D, Petrou, S, Lugg-Widger, F, Kim, S, Bradshaw, J, McNamara, R, Jahoda, A, Lindsay, G, Shurlock, J, Totsika, V, Stanford, C, Flynn, S, Carter, A, Barlow, C, Hastings, R

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model by Németh, A, Jiannis Ragoussis, Kwasniewska, A, Lise, S, Schnekenberg, R, Becker, E, Bera, K, Shanks, M, Gregory, L, Buck, D, Cader, M, Talbot, K, de Silva, R, Fletcher, N, Hastings, R, Jayawant, S, Morrison, P, Worth, P, Taylor, M, Tolmie, J, O’Regan, M, Valentine, R, Packham, E, Evans, J, Seller, A

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model. by Németh, A, Kwasniewska, A, Lise, S, Parolin Schnekenberg, R, Becker, E, Bera, K, Shanks, M, Gregory, L, Buck, D, Zameel Cader, M, Talbot, K, de Silva, R, Fletcher, N, Hastings, R, Jayawant, S, Morrison, P, Worth, P, Taylor, M, Tolmie, J, O'Regan, M, Valentine, R, Packham, E, Evans, J, Seller, A, Ragoussis, J

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders. by Taylor, J, Martin, H, Lise, S, Broxholme, J, Cazier, J, Rimmer, A, Kanapin, A, Lunter, G, Fiddy, S, Allan, C, Aricescu, A, Attar, M, Babbs, C, Becq, J, Beeson, D, Bento, C, Bignell, P, Blair, E, Buckle, V, Bull, K, Cais, O, Cario, H, Chapel, H, Copley, R, Cornall, R, Craft, J, Dahan, K, Davenport, E, Dendrou, C, Devuyst, O, Fenwick, A, Flint, J, Fugger, L, Gilbert, R, Goriely, A, Green, A, Greger, I, Grocock, R, Gruszczyk, A, Hastings, R, Hatton, E, Higgs, D, Hill, A, Holmes, C, Howard, M, Hughes, L, Humburg, P, Johnson, D, Karpe, F, Kingsbury, Z, Kini, U, Knight, J, Krohn, J, Lamble, S, Langman, C, Lonie, L, Luck, J, McCarthy, D, McGowan, S, McMullin, M, Miller, K, Murray, L, Németh, A, Nesbit, A, Nutt, D, Ormondroyd, E, Oturai, A, Pagnamenta, A, Patel, S, Percy, M, Petousi, N, Piazza, P, Piret, S, Polanco-Echeverry, G, Popitsch, N, Powrie, F, Pugh, C, Quek, L, Robbins, P, Robson, K, Russo, A, Sahgal, N, van Schouwenburg, P, Schuh, A, Silverman, E, Simmons, A, Sørensen, P, Sweeney, E, Taylor, J, Thakker, R, Tomlinson, I, Trebes, A, Twigg, S, Uhlig, H, Vyas, P, Vyse, T, Wall, S, Watkins, H, Whyte, M, Witty, L, Wright, B, Yau, C, Buck, D, Humphray, S, Ratcliffe, P, Bell, J, Wilkie, A, Bentley, D, Donnelly, P, McVean, G