Real time neutral beam power control on MAST by Homfray, David A., Benn, A., Ciric, D., Day, I., Dunkley, V., Keeling, D., Khilar, S., King, D., King, R., Kurutz, U., Payne, D., Simmonds, M., Stevenson, P., Tame, C.

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Refractory metals as structural materials for fusion high heat flux components by Hancock, David, Homfray, David, Porton, Michael, Todd, Iain, Wynne, Brad

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Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis by Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia

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Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination by Pearlman, Alexander, Loke, Johnny, Le Caignec, Cedric, White, Stefan, Chin, Lisa, Friedman, Andrew, Warr, Nicholas, Willan, John, Brauer, David, Farmer, Charles, Brooks, Eric, Oddoux, Carole, Riley, Bridget, Shajahan, Shahin, Camerino, Giovanna, Homfray, Tessa, Crosby, Andrew H., Couper, Jenny, David, Albert, Greenfield, Andy, Sinclair, Andrew, Ostrer, Harry

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Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis by Fotiou, Elisavet, Martin-Almedina, Silvia, Simpson, Michael A., Lin, Shin, Gordon, Kristiana, Brice, Glen, Atton, Giles, Jeffery, Iona, Rees, David C., Mignot, Cyril, Vogt, Julie, Homfray, Tessa, Snyder, Michael P., Rockson, Stanley G., Jeffery, Steve, Mortimer, Peter S., Mansour, Sahar, Ostergaard, Pia

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A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation by BARTOS, DANIEL C., ANDERSON, JEFFREY B., BASTIAENEN, RACHEL, JOHNSON, JONATHAN N., GOLLOB, MICHAEL H., TESTER, DAVID J., BURGESS, DON E., HOMFRAY, TESSA, BEHR, ELIJAH R., ACKERMAN, MICHAEL J., GUICHENEY, PASCALE, DELISLE, BRIAN P.

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NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses by Van Bergen, Nicole J, Guo, Yiran, Rankin, Julia, Paczia, Nicole, Becker-Kettern, Julia, Kremer, Laura S, Pyle, Angela, Conrotte, Jean-François, Ellaway, Carolyn, Procopis, Peter, Prelog, Kristina, Homfray, Tessa, Baptista, Júlia, Baple, Emma, Wakeling, Matthew, Massey, Sean, Kay, Daniel P, Shukla, Anju, Girisha, Katta M, Lewis, Leslie E S, Santra, Saikat, Power, Rachel, Daubeney, Piers, Montoya, Julio, Ruiz-Pesini, Eduardo, Kovacs-Nagy, Reka, Pritsch, Martin, Ahting, Uwe, Thorburn, David R, Prokisch, Holger, Taylor, Robert W, Christodoulou, John, Linster, Carole L, Ellard, Sian, Hakonarson, Hakon

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Exploring complex high heat flux geometries for fusion applications enabled by additive manufacturing by Hancock, David, Homfray, David, Porton, Michael, Todd, Iain, Wynne, Brad

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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy by Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.

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Consensus document on optimal management of patients with common arterial trunk by Hazekamp, Mark G, Barron, David J, Dangel, Joanna, Homfray, Tessa, Jongbloed, Monique R M, Voges, Inga

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The psychosocial impact of prostate cancer screening for BRCA1 and BRCA2 carriers by Brook, Mark N., Pope, Jennifer, Helfand, Brian T., Salinas, Monica, Buys, Saundra S., Davidson, Rosemarie, Side, Lucy, Cruellas, Mara, Ballestero, Eduard Perez, Hogben, Matthew, Saya, Sibel, Eyfjord, Jorunn, Falconer, Alison, Hamdy, Freddie C., Mitra, Anita, Wilson, Penny, Mitchell, Gillian, Shanley, Sue, Lam, Jimmy, Tucker, Katherine, Andrews, Lesley, Duffy, Jessica, Stricker, Phillip, Bowman, Michelle, Patel, Manish, Morton, Catherine, Susman, Rachel, Townshend, Sharron, Pachter, Nicholas, Gleeson, Margaret, Patterson, Briony, Swindle, Peter, Jeanjean, Marie, Tondering, Majbritt Kure, Schmutzler, Rita, Luedtke‐Heckenkamp, Kerstin, Herold, Natalie, Zastrow, S., Stefansdottir, Vigdis, Kowtal, Pradnya, Cahill, Aisling, Catanzaro, Mario, Sorrentino, Margherita, Asperen, Christi, Adank, Muriel A., Mæhle, Lovise, Hanslien, Eldbjørg, Maia, Sofia, Gonçalves, Nuno, Copakova, Lucia, Zgajnar, Janez, Ramón y Cajal, Teresa, Fisas, David, Hjälm‐Eriksson, Marie, George, Angela, Wiggins, Jennifer, Van As, Nicholas, Thompson, Alan, Ogden, Chris, Bulman, Barbara, Mercer, Catherine, Sands, Victoria, Stobie, Emma, Manalo, Merrie, Brice, Glen, Mencias, Mark, Potter, Alison, Thomas, Maggie, Adams, Lisa, Ashman, Sophie, Douglas, Fiona, Donaldson, Alan, Turnbull, Clare, Clowes, Virginia, Cummings, Carole, Bartlett, Marion, Adeoye, Toyin, Tidey, Lizzie, Howell, Alice, Hoffman, Jonathan, Islam, Farah, Poile, Charlotte, Johnstone, Anne, Woodward, Anthony, Cornford, Philip, Griffiths, Julie, Rubinstein, Wendy, Davis, John W., Yamamura, Yuko, Bout, C.A., Cornel, E.B., Fernandes, J.G., Jongen‐Huinink, M.M.G.J., Kil, P.J.M., Langbein, S.I., Meier, A.H.P., Naderi, N., Smits, G.A.H.J., Smorenburg, S., Vijverberg, P.

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Mosaic structural variation in children with developmental disorders by King, Daniel A, Jones, Wendy D, Crow, Yanick J, Dominiczak, Anna F, Foster, Nicola A, Gaunt, Tom R, Harris, Jade, Hellens, Stephen W, Homfray, Tessa, Innes, Josie, Jones, Elizabeth A, Joss, Shelagh, Kulkarni, Abhijit, Mansour, Sahar, Morris, Andrew D, Parker, Michael J, Porteous, David J, Shihab, Hashem A, Smith, Blair H, Tatton-Brown, Katrina, Tolmie, John L, Trzaskowski, Maciej, Vasudevan, Pradeep C, Wakeling, Emma, Wright, Michael, Plomin, Robert, Timpson, Nicholas J, Hurles, Matthew E

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Consensus document on optimal management of patients with common arterial trunk by Hazekamp, Mark G, Barron, David J, Dangel, Joanna, Homfray, Tessa, Jongbloed, Monique R M, Voges, Inga

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Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia by Connell, Fiona, Kalidas, Kamini, Ostergaard, Pia, Brice, Glen, Homfray, Tessa, Roberts, Lesley, Bunyan, David J, Mitton, Sally, Mansour, Sahar, Mortimer, Peter, Jeffery, Steve

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The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants by Tatton-Brown, Katrina, Zachariou, Anna, Loveday, Chey, Renwick, Anthony, Mahamdallie, Shazia, Aksglaede, Lise, Baralle, Diana, Barge-Schaapveld, Daniela, Blyth, Moira, Bouma, Mieke, Breckpot, Jeroen, Crabb, Beau, Dabir, Tabib, Cormier-Daire, Valerie, Fauth, Christine, Fisher, Richard, Gener, Blanca, Goudie, David, Homfray, Tessa, Hunter, Matthew, Jorgensen, Agnete, Kant, Sarina G, Kirally-Borri, Cathy, Koolen, David, Kumar, Ajith, Labilloy, Anatalia, Lees, Melissa, Marcelis, Carlo, Mercer, Catherine, Mignot, Cyril, Miller, Kathryn, Neas, Katherine, Newbury-Ecob, Ruth, Pilz, Daniela T, Posmyk, Renata, Prada, Carlos, Ramsey, Keri, Randolph, Linda M, Selicorni, Angelo, Shears, Deborah, Suri, Mohnish, Temple, I Karen, Turnpenny, Peter, Val Maldergem, Lionel, Varghese, Vinod, Veenstra-Knol, Hermine E, Yachelevich, Naomi, Yates, Laura, Rahman, Nazneen

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Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities by Bateman, Mark S., Collinson, Morag N., Bunyan, David J., Collins, Amanda L., Duncan, Philippa, Firth, Rachel, Harrison, Victoria, Homfray, Tessa, Huang, Shuwen, Kirk, Beth, Lachlan, Katherine L., Maloney, Viv K., Barber, John C. K.

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NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses by Van Bergen, Nicole J, Guo, Yiran, Rankin, Julia, Paczia, Nicole, Becker-Kettern, Julia, Kremer, Laura S, Pyle, Angela, Conrotte, Jean-François, Ellaway, Carolyn, Procopis, Peter, Prelog, Kristina, Homfray, Tessa, Baptista, Júlia, Baple, Emma, Wakeling, Matthew, Massey, Sean, Kay, Daniel P, Shukla, Anju, Girisha, Katta M, Lewis, Leslie E S, Santra, Saikat, Power, Rachel, Daubeney, Piers, Montoya, Julio, Ruiz-Pesini, Eduardo, Kovacs-Nagy, Reka, Pritsch, Martin, Ahting, Uwe, Thorburn, David R, Prokisch, Holger, Taylor, Robert W, Christodoulou, John, Linster, Carole L, Ellard, Sian, Hakonarson, Hakon

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Gene-gene interactions in breast cancer susceptibility by Turnbull, Clare, Seal, Sheila, Renwick, Anthony, Warren-Perry, Margaret, Hughes, Deborah, Elliott, Anna, Pernet, David, Peock, Susan, Adlard, Julian W., Barwell, Julian, Berg, Jonathan, Brady, Angela F., Brewer, Carole, Brice, Glen, Chapman, Cyril, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Douglas, Fiona, Greenhalgh, Lynn, Henderson, Alex, Izatt, Louise, Kumar, Ajith, Lalloo, Fiona, Miedzybrodzka, Zosia, Morrison, Patrick J, Paterson, Joan, Porteous, Mary, Rogers, Mark T., Shanley, Susan, Walker, Lisa, Ahmed, Munaza, Eccles, Diana, Evans, D. Gareth, Donnelly, Peter, Easton, Douglas F., Stratton, Michael R., Rahman, Nazneen

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Telomere length shows no association with BRCA1 and BRCA2 mutation status by Killick, Emma, Tymrakiewicz, Malgorzata, Cieza-Borrella, Clara, Smith, Paula, Thompson, Deborah J, Pooley, Karen A, Easton, Doug F, Bancroft, Elizabeth, Page, Elizabeth, Leongamornlert, Daniel, Kote-Jarai, Zsofia, Eeles, Rosalind A

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Abstract 18901: Direct Evidence that a KCNQ1 Mutation is Linked to Familial Early-onset Atrial Fibrillation by Bartos, Daniel C, Anderson, Jeffrey B, Bastiaenen, Rachel, Johnson, Jonathan N, Gollob, Michael H, Tester, David J, Burgess, Don E, Homfray, Tessa, Behr, Elijah R, Ackerman, Michael J, Guicheney, Pascale, Delisle, Brian P

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