Onwards and upwards: The development, piloting and validation of a new measure of academic tenacity- The Bolton Uni-Stride Scale (BUSS) by Kannangara, Chathurika Sewwandi, Allen, Rosie Elizabeth, Carson, Jerome Francis, Khan, Samia Zahraa Noor, Waugh, Gill, Kandadi, Kondal Reddy

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True Grit: How Important is the Concept of Grit for Education? A Narrative Literature Review by Allen, Rosie Elizabeth, Kannangara, Chathurika, Carson, Jerome

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Still worlds apart: flourishing in people with mental health problems by Allen, Rosie Elizabeth, Carson, Jerome, Merrifield, Bethany, Bush, Stacey

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Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans by Tuijnenburg, Paul, Jansen, Machiel H., Carss, Keren J., Baxendale, Helen, Chandra, Anita, Seneviratne, Suranjith L., Oksenhendler, Eric, Tool, Anton T.J., Whitehorn, Deborah, Turro, Ernest, Thaventhiran, James E., Kuijpers, Taco W., Adhya, Zoe, Anantharachagan, Ariharan, Arumugakani, Gururaj, Bacchelli, Chiara, Baxendale, Helen, Bibi, Shahnaz, Booth, Claire, Browning, Michael, Burns, Siobhan, Clifford, Hayley, Cooper, Nichola, Davies, Sophie, Devlin, Lisa, Edgar, David, Egner, William, Ghurye, Rohit, Gilmour, Kimberley, Goddard, Sarah, Gordins, Pavel, Hackett, Scott, Hague, Rosie, Hayman, Grant, Jolles, Stephen, Jones, Julie, Kelleher, Peter, Klein, Nigel, Kuijpers, Taco, Kumararatne, Dinakantha, Laffan, James, Lango Allen, Hana, Lear, Sara, Longhurst, Hilary, Maimaris, Jesmeen, McDermott, Elizabeth, Morrisson, Valerie, Nasir, Iman, Noorani, Sadia, Oksenhendler, Eric, Ponsford, Mark, Qasim, Waseem, Quinn, Ellen, Quinti, Isabella, Samarghitean, Crina, Savic, Sinisa, Seneviratne, Suranjith, Simeoni, Ilenia, Staples, Emily, Steele, Cathal, Thaventhiran, James, Thomas, Moira, Thrasher, Adrian, Worth, Austen, Yong, Patrick, Bradley, John, Hammerton, Tracey, Ouwehand, Willem, Raymond, F Lucy, Veltman, Marijke, Clements-Brod, Naomi, Davis, John, Dewhurst, Eleanor, Erwood, Marie, Frary, Amy, Linger, Rachel, Papadia, Sofia, Rehnstrom, Karola, Astle, William, Attwood, Antony, Bleda, Marta, Carss, Keren, Daugherty, Louise, Deevi, Sri, Graf, Stefan, Greene, Daniel, Halmagyi, Csaba, Matser, Vera, Meacham, Stuart, Megy, Karyn, Shamardina, Olga, Titterton, Catherine, Tuna, Salih, Turro, Ernest, von Ziegenweldt, Julie, Furnell, Abigail, Staines, Simon, Stephens, Jonathan, Whitehorn, Deborah, Watt, Christopher

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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations by Lorenzini, Tiziana, Fliegauf, Manfred, Klammer, Nils, Proietti, Michele, Bulashevska, Alla, Schejter, Yael D., Atschekzei, Faranaz, Stepensky, Polina, Pedroza, Luis A., van der Flier, Michiel, Martínez-Gallo, Mónica, Svec, Peter, Fischer, Ute, Ip, Winnie, Geha, Raif, Chou, Janet, Alosaimi, Mohammed, Weintraub, Lauren, Dos Santos Vilela, Maria Marluce, Holzinger, Dirk, Seidl, Maximilian, Lougaris, Vassilios, Plebani, Alessandro, Abolhassani, Hassan, Thaventhiran, James E., Warnatz, Klaus, Grimbacher, Bodo, Ashford, Sofie, Bacchelli, Chiara, Batista, Joana, Bibi, Shahnaz, Boardman, Barbara, Booth, Claire, Breen, Gerome, Burns, Siobhan O., Burren, Oliver S., Carss, Keren, Chambers, John, Cooper, Nichola, Davies, E.G., Dempster, John, Dewhurst, Eleanor F., Drewe, Elizabeth, Duarte, Daniel, Edgar, J. David M., Egner, William, El-Shanawany, Tariq, Erwood, Marie, Fox, James, Frontini, Mattia, Furnell, Abigail, Gaspar, H. Bobby, Gleadall, Nicholas S., Grigoriadou, Sofia, Hackett, Scott, Hague, Rosie, Haimel, Matthias, Hayman, Grant, Hu, Fengyuan, Huissoon, Aarnoud P., Jolles, Stephen, Kasanicki, Mary A., Kelleher, Peter, Klein, Nigel, Kreuzhuber, Roman, Kuijpers, Taco W., Kumararatne, Dinakantha, Allen, Hana Lango, Linger, Rachel, Lorenzo, Lorena E., Maimaris, Jesmeen, Martin, Jennifer, McDermott, Elizabeth M., Meacham, Stuart, Morrisson, Valerie, Nasir, Iman, Nejentsev, Sergey, Papadia, Sofia, Ponsford, Mark J., Quinn, Ellen, Quinti, Isabella, Rayner-Matthews, Paula J., Samani, Nilesh, Sanchis-Juan, Alba, Savic, Sinisa, Simpson, Michael A., Smith, Kenneth G.C., Thaventhiran, James E., Tilly, Tobias, Titterton, Catherine, Tuna, Salih, Urniaz, Rafal, von Ziegenweidt, Julie, Watt, Christopher, Welch, Steven B., Whitehorn, Deborah, Wood, Yvette, Workman, Sarita, Worth, Austen, Young, Timothy

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Correction: Quantitative background parenchymal enhancement and fibro-glandular density at breast MRI: Association with BRCA status by Goodburn, Rosie, Kousi, Evanthia, Sanders, Clarrissa, Macdonald, Alison, Scurr, Erica, Bunce, Catey, Khabra, Komel, Reddy, Mamatha, Wilkinson, Louise, O’Flynn, Elizabeth, Allen, Steven, Schmidt, Maria Angélica

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Quantitative background parenchymal enhancement and fibro-glandular density at breast MRI: Association with BRCA status by Goodburn, Rosie, Kousi, Evanthia, Sanders, Clarrissa, Macdonald, Alison, Scurr, Erica, Bunce, Catey, Khabra, Komel, Reddy, Mamatha, Wilkinson, Louise, O’Flynn, Elizabeth, Allen, Steven, Schmidt, Maria Angélica

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Designing meditation for doctor well-being: can ‘Om’ help obstetrics and gynaecology doctors? by Allen, Rosie, Robinson, Andrew, Allen, Shelley, Nathan, Elizabeth, Coghlan, Edwina, Leung, Yee

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Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma by Minskaia, Ekaterina, Maimaris, Jesmeen, Jenkins, Persephone, Albuquerque, Adriana S., Hong, Ying, Eleftheriou, Despina, Gilmour, Kimberly C., Grace, Richard, Moreira, Fernando, Grimbacher, Bodo, Morris, Emma C., Burns, Siobhan O.

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Practical challenges for functional validation of STAT1 gain of function genetic variants by Albuquerque, Adriana S, Maimaris, Jesmeen, McKenna, Alexander J, Lambourne, Jonathan, Moreira, Fernando, Workman, Sarita, Megy, Karyn, Simeoni, Ilenia, Lango Allen, Hana, Morris, Emma C, Burns, Siobhan O

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An automated approach for the optimised estimation of breast density with Dixon methods by Goodburn, Rosie, Kousi, Evanthia, Macdonald, Alison, Morgan, Veronica, Scurr, Erica, Reddy, Mamatha, Wilkinson, Louise, O'Flynn, Elizabeth, Pope, Romney, Allen, Steven, Schmidt, Maria Angélica

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Loss‐of‐function mutations in CSF3R cause moderate neutropenia with fully mature neutrophils: two novel pedigrees by Sprenkeler, Evelien G. G., Tool, Anton T. J., Kreft, Iris C., Alphen, Floris P. J., Seneviratne, Suranjith L., Maimaris, Jesmeen, Luqmani, Asad, Leeuwen, Karin, Bruggen, Robin, Burns, Siobhan O., Kuijpers, Taco W.

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Making co-enrolment feasible for randomised controlled trials in paediatric intensive care by Harron, Katie, Lee, Twin, Ball, Tracy, Mok, Quen, Gamble, Carrol, Macrae, Duncan, Gilbert, Ruth

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Task-specific training in Huntington disease: a randomized controlled feasibility trial by Quinn, Lori, Debono, Katy, Dawes, Helen, Rosser, Anne Elizabeth, Nemeth, Andrea H, Rickards, Hugh, Tabrizi, Sarah J, Quarrell, Oliver, Trender-Gerhard, Iris, Kelson, Mark J, Townson, Julia, Busse, Monica

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