Usability assessment of Versius, a new robot-assisted surgical device for use in minimal access surgery von Haig, Fiona, Medeiros, Ana Cristina Barbosa, Chitty, Karen, Slack, Mark

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Promises, pitfalls and practicalities of prenatal whole exome sequencing von Best, Sunayna, Wou, Karen, Vora, Neeta, Van der Veyver, Ignatia B., Wapner, Ronald, Chitty, Lyn S.

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis von Blayney, Gillian V, Laffan, Eoghan, Jacob, Preethi A, Baptiste, Caitlin D, Gabriel, Heinz, Sparks, Teresa N, Yaron, Yuval, Norton, Mary E, Diderich, Karin, Wang, Yiming, Chong, Karen, Chitayat, David, Saini, Neelam, Aggarwal, Shagun, Pauta, Montse, Borrell, Antoni, Gilmore, Kelly, Chandler, Natalie J, Allen, Stephanie, Vora, Neeta, Noor, Abdul, Monaghan, Caitriona, Kilby, Mark D, Wapner, Ronald J, Chitty, Lyn S, Mone, Fionnuala

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Clinical utility of prenatal SNP microarray by clinical indication von Tan, Brian, Woodward, Karen, Tracey Edwards, Sarah Nickerson, Weston, Kathryn, Chionh, Amanda, Warren, Hayley, Taylor, Fiona, Chitty, Kenneth, Azmanov, Dimitar

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants von Chawner, Samuel J.R.A, Doherty, Joanne L, Anney, Richard J. L, Antshel, Kevin M, Bearden, Carrie E, Bernier, Raphael, Chung, Wendy K, Clements, Caitlin C, Curran, Sarah R, Cuturilo, Goran, Fiksinski, Ania M, Gallagher, Louise, Goin-Kochel, Robin P, Gur, Raquel E, Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R, Kushan, Leila, Maillard, Anne M, McDonald-McGinn, Donna M, Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T, Green-Snyder, LeeAnne, Vorstman, Jacob A, Wenger, Tara L, Hall, Jeremy, Owen, Michael J, van den Bree, Marianne B.M

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A Multicenter Evaluation of the Seraph 100 Microbind Affinity Blood Filter for the Treatment of Severe COVID-19 von Chitty, Stephen A, Mobbs, Sarah, Rifkin, Brian S, Stogner, Steven W, Lewis, Michael S, Betancourt, Jaime, DellaVolpe, Jeffrey, Abouzahr, Fadi, Wilhelm, Andrew M, Szerlip, Harold M, Parikh, Amay, Gaeta, Robert M, Rivera, Ian, Park, Caroline, Levi, Benjamin, Anesi, George L, Alcover, Karl C, Arnold, Thomas B, Howard, Jeffrey T, Sharma, Kumar, Pratt, Kathleen P, Stewart, Ian J, Chung, Kevin K

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‘We have been in lockdown since he was born’: a mixed methods exploration of the experiences of families caring for children with intellectual disability during the COVID-19 pandem... von Wolstencroft, Jeanne, Hull, Laura, Warner, Lauren, Akhtar, Tooba Nadeem, Mandy, William, Skuse, David, Baker, Kate, Dewhurst, Eleanor, Lafont, Amy, Lucy Raymond, F, Shirley, Terry, Tilley, Hayley, Timur, Husne, Titterton, Catherine, Walker, Neil, Wallwork, Sarah, Wicks, Francesca, Ye, Zheng, Erwood, Marie, Andrews, Sophie, Birch, Philippa, Bowen, Samantha, Bradley, Karen, Challenger, Aimee, Chawner, Samuel, Cuthbert, Andrew, Hall, Jeremy, Holmans, Peter, Law, Sarah, Lewis, Nicola, Morrison, Sinead, Moss, Hayley, Owen, Michael, Ray, Sinead, Sopp, Matthew, Tong, Molly, Bree, Marianne van den, Coscini, Nadia, Davies, Sarah, Denaxas, Spiros, Denyer, Hayley, Fatih, Nasrtullah, Juj, Manoj, Kerry, Ellie, Lucock, Anna, Printzlau, Frida, Srinivasan, Ramya, Walker, Susan, Watkins, Alice, Searle, Beverly, Pelling, Anna, Dean, John, Robertson, Lisa, Alan, Denise Williams, Lucy, Donaldson, Procter, Annie, Berg, Jonathan, Lampe, Anne, Rankin, Julia, Joss, Shelagh, Chitty, Lyn, Flinter, Frances, Holder, Muriel, Kraus, Alison, Barwell, Julian, Vasudevan, Pradeep, Weber, Astrid, Newman, William, Splitt, Miranda, Clowes, Virginia, Dijk, Fleur van, Harrison, Rachel, Kini, Usha, Quarrell, Oliver, Baralle, Diana, Mansour, Sahar, Crow, Yanick

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Dominantly inherited syndrome comprising partially absent eye muscles, hydrocephaly, skeletal abnormalities, and a distinctive facial phenotype von Chitty, Lyn S., McCrimmon, Rory, Temple, I. Karen, Russell-Eggitt, Isobel M., Baraitser, Michael

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Process and apparatus for reproducible production of non-uniform product distributions von CHITTY, ALTON L, OEHLBECK, DOUGLAS L, HENRY, MARIAN S, POND, KAREN L, DARRON, WARD K

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