Chromosome Aberrations Determined by FISH in Radiation Workers from the Sellafield Nuclear Facility von Tawn, E. Janet, Curwen, Gillian B., Jonas, Patricia, Gillies, Michael, Hodgson, Leanne, Cadwell, Kevin K.

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The Characterization and Transmissibility of Chromosome Aberrations Induced in Peripheral Blood Lymphocytes by In Vitro α-Particle Radiation von Tawn, E. Janet, Whitehouse, Caroline A., De Ruyck, Kim, Hodgson, Leanne, Vandenbulcke, Katia, Thierens, Hubert

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome von Heron, Sarah E., Grinton, Bronwyn E., Kivity, Sara, Afawi, Zaid, Zuberi, Sameer M., Hughes, James N., Pridmore, Clair, Hodgson, Bree L., Iona, Xenia, Sadleir, Lynette G., Pelekanos, James, Herlenius, Eric, Goldberg-Stern, Hadassa, Bassan, Haim, Haan, Eric, Korczyn, Amos D., Gardner, Alison E., Corbett, Mark A., Gécz, Jozef, Thomas, Paul Q., Mulley, John C., Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.

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Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy von Ricos, Michael G., Hodgson, Bree L., Pippucci, Tommaso, Saidin, Akzam, Ong, Yeh Sze, Heron, Sarah E., Licchetta, Laura, Bisulli, Francesca, Bayly, Marta A., Hughes, James, Baldassari, Sara, Palombo, Flavia, Santucci, Margherita, Meletti, Stefano, Berkovic, Samuel F., Rubboli, Guido, Thomas, Paul Q., Scheffer, Ingrid E., Tinuper, Paolo, Geoghegan, Joel, Schreiber, Andreas W., Dibbens, Leanne M.

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Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations von Scheffer, Ingrid E., Heron, Sarah E., Regan, Brigid M., Mandelstam, Simone, Crompton, Douglas E., Hodgson, Bree L., Licchetta, Laura, Provini, Federica, Bisulli, Francesca, Vadlamudi, Lata, Gecz, Jozef, Connelly, Alan, Tinuper, Paolo, Ricos, Michael G., Berkovic, Samuel F., Dibbens, Leanne M.

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GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome von Carvill, Gemma L, Weckhuysen, Sarah, McMahon, Jacinta M, Hartmann, Corinna, Møller, Rikke S, Hjalgrim, Helle, Cook, Joseph, Geraghty, Eileen, O’Roak, Brian J, Petrou, Steve, Clarke, Alison, Gill, Deepak, Sadleir, Lynette G, Muhle, Hiltrud, von Spiczak, Sarah, Nikanorova, Marina, Hodgson, Bree L, Gazina, Elena V, Suls, Arvid, Shendure, Jay, Dibbens, Leanne M, De Jonghe, Peter, Helbig, Ingo, Berkovic, Samuel F, Scheffer, Ingrid E, Mefford, Heather C

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Mutations in DEPDC5 cause familial focal epilepsy with variable foci von Dibbens, Leanne M, de Vries, Boukje, Donatello, Simona, Heron, Sarah E, Hodgson, Bree L, Chintawar, Satyan, Crompton, Douglas E, Hughes, James N, Bellows, Susannah T, Klein, Karl Martin, Callenbach, Petra M C, Corbett, Mark A, Gardner, Alison E, Kivity, Sara, Iona, Xenia, Regan, Brigid M, Weller, Claudia M, Crimmins, Denis, O'Brien, Terence J, Guerrero-López, Rosa, Mulley, John C, Dubeau, Francois, Licchetta, Laura, Bisulli, Francesca, Cossette, Patrick, Thomas, Paul Q, Gecz, Jozef, Serratosa, Jose, Brouwer, Oebele F, Andermann, Frederick, Andermann, Eva, van den Maagdenberg, Arn M J M, Pandolfo, Massimo, Berkovic, Samuel F, Scheffer, Ingrid E

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Models of Peer Support to Remediate Post-Intensive Care Syndrome: A Report Developed by the Society of Critical Care Medicine Thrive International Peer Support Collaborative von McPeake, Joanne, Hirshberg, Eliotte L., Christie, Leeann M., Drumright, Kelly, Haines, Kimberley, Hough, Catherine L., Meyer, Joel, Wade, Dorothy, Andrews, Adair, Bakhru, Rita, Bates, Samantha, Barwise, John A., Bastarache, Julie, Beesley, Sarah J., Boehm, Leanne M., Brown, Sheryl, Clay, Alison S., Firshman, Penelope, Greenberg, Steven, Harris, Wendy, Hill, Christopher, Hodgson, Carol, Holdsworth, Clare, Hope, Aluko A., Hopkins, Ramona O., Howell, David C. J., Janssen, Anna, Jackson, James C., Johnson, Annie, Kross, Erin K., Lamas, Daniela, MacLeod-Smith, Belinda, Mandel, Ruth, Marshall, John, Mikkelsen, Mark E., Nackino, Megan, Quasim, Tara, Sevin, Carla M., Slack, Andrew, Spurr, Rachel, Still, Mary, Thompson, Carol, Weinhouse, Gerald, Wilcox, M. Elizabeth, Iwashyna, Theodore J.

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Platelet rich plasma injection for acute Achilles tendon rupture: PATH-2 randomised, placebo controlled, superiority trial von Keene, David J, Alsousou, Joseph, Harrison, Paul, Hulley, Philippa, Wagland, Susan, Parsons, Scott R, Thompson, Jacqueline Y, O’Connor, Heather M, Schlüssel, Michael Maia, Dutton, Susan J, Lamb, Sarah E, Willett, Keith

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Tomato Brown Rugose Fruit Virus: Survival and Disinfection Efficacy on Common Glasshouse Surfaces von Skelton, Anna, Frew, Leanne, Ward, Richard, Hodgson, Rachel, Forde, Stephen, McDonough, Sam, Webster, Gemma, Chisnall, Kiera, Mynett, Mary, Buxton-Kirk, Adam, Fowkes, Aimee R, Weekes, Rebecca, Fox, Adrian

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Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis von Berkovic, Samuel F., Dibbens, Leanne M., Oshlack, Alicia, Silver, Jeremy D., Katerelos, Marina, Vears, Danya F., Lüllmann-Rauch, Renate, Blanz, Judith, Zhang, Ke Wei, Stankovich, Jim, Kalnins, Renate M., Dowling, John P., Andermann, Eva, Andermann, Frederick, Faldini, Enrico, D'Hooge, Rudi, Vadlamudi, Lata, Macdonell, Richard A., Hodgson, Bree L., Bayly, Marta A., Savige, Judy, Mulley, John C., Smyth, Gordon K., Power, David A., Saftig, Paul, Bahlo, Melanie

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Augmented currents of an HCN2 variant in patients with febrile seizure syndromes von Dibbens, Leanne M., Reid, Christopher A., Hodgson, Bree, Thomas, Evan A., Phillips, Alison M., Gazina, Elena, Cromer, Brett A., Clarke, Alison L., Baram, Tallie Z., Scheffer, Ingrid E., Berkovic, Samuel F., Petrou, Steven

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GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies von Dibbens, Leanne M., Feng, Hua-Jun, Richards, Michaella C., Harkin, Louise A., Hodgson, Bree L., Scott, Darren, Jenkins, Misty, Petrou, Steven, Sutherland, Grant R., Scheffer, Ingrid E., Berkovic, Samuel F., Macdonald, Robert L., Mulley, John C.

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Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome von Mulley, John C., Hodgson, Bree, McMahon, Jacinta M., Iona, Xenia, Bellows, Susannah, Mullen, Saul A, Farrell, Kevin, Mackay, Mark, Sadleir, Lynette, Bleasel, Andrew, Gill, Deepak, Webster, Richard, Wirrell, Elaine C., Harbord, Michael, Sisodiya, Sanyjay, Andermann, Eva, Kivity, Sara, Berkovic, Samuel F., Scheffer, Ingrid E., Dibbens, Leanne M.

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Detection of tomato brown rugose fruit virus is influenced by infection at different growth stages and sampling from different plant parts von Skelton, Anna, van Gemert, Jerom, Fowkes, Aimee, Frew, Leanne, Alraiss, Kinda, Hodgson, Rachel, Cressey, Jessica, Barnhoorn, Ruud, Macarthur, Roy, Stijger, Ineke, Verbeek, Martin, van der Vlugt, Rene, Koenraadt, Harrie, Roenhorst, Annelien, Botermans, Marleen, Fox, Adrian

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Early versus delayed weight-bearing following operatively treated ankle fracture (WAX): a non-inferiority, multicentre, randomised controlled trial von Bretherton, Christopher Patrick, Achten, Juul, Jogarah, Vidoushee, Petrou, Stavros, Peckham, Nicholas, Achana, Felix, Appelbe, Duncan, Kearney, Rebecca, Claireux, Harry, Bell, Philip, Griffin, Xavier L, McAndrew, Andrew, Jacobs, Neal, Forder, Justin, Hester, Thomas, Cross, Charlotte, Bateman, Tony, Kieffer, Will, Barton, Tristan, Walter, Richard, Savva, Nick, Marsland, Daniel, Rose, Barry, Beech, Zine, Koc, Togay, Armstead, Bethany, Ollivere, Ben, Diamond, Owen, Teoh, Kar, Magill, Paul, Mangwani, Jitendra, Hodgson, Paul, Ray, Robbie, Dhinsa, Baljinder, Majeed, Haroon, Wong-Chung, John, Young, Jonathan, Lagare, Agnes, Soogumbur, Akash, Morozova, Albina, Hunt, Alexander, Adamson, Amanda, Dempster, Angie, McCormack, Ann, Arif, Azra, Vye, Charlotte, Dojode, Chetan, Brown, Chloe, Haines, Christina, To, Christopher, Brennan, Ciaran, Winson, Dan, McGough, Elizabeth, Jessup-Dunton, Ellen, Bintcliffe, Fiona, Thompson, Fiona, Omogra, Gabriel, Scott, Georgia, Samuel, Helen, Fraig, Hossam, Burokiene, Ina, Odysseos-Beaumont, Isabel, Rand, James, Edkins, Janet, Barrett-Lee, Joe, McFall, John, Wahed, Karim, Herbert, Kate, Death, Kelly, Beddard, Laura, Dupley, Leanne, Bryce, Leeann, Wright, Lianne, Bailey, Lucy, Maling, Lucy, Raad, Marjan, Morris, Matt, Williams, Matthew, Labidi, May, Holmes, Natalie, Staines, Nikki, Matthews, Paul A, McCormac, Philip, Easow, Rashmi, Matthews, Scott, Kapoor, Smriti, Harris, Sophie, Wagland, Susan, Cobb, Timothy, White, Tracey

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Sildenafil citrate therapy for severe early‐onset intrauterine growth restriction von von Dadelszen, P, Dwinnell, S, Magee, LA, Carleton, BC, Gruslin, A, Lee, B, Lim, KI, Liston, RM, Miller, SP, Rurak, D, Sherlock, RL, Skoll, MA, Wareing, MM, Baker, PN

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Epilepsy and mental retardation limited to females: an under-recognized disorder von Scheffer, Ingrid E., Turner, Samantha J., Dibbens, Leanne M., Bayly, Marta A., Friend, Kathryn, Hodgson, Bree, Burrows, Linda, Shaw, Marie, Wei, Chen, Ullmann, Reinhard, Ropers, Hans-Hilger, Szepetowski, Pierre, Haan, Eric, Mazarib, Aziz, Afawi, Zaid, Neufeld, Miriam Y., Andrews, P. Ian, Wallace, Geoffrey, Kivity, Sara, Lev, Dorit, Lerman-Sagie, Tally, Derry, Christopher P., Korczyn, Amos D., Gecz, Jozef, Mulley, John C., Berkovic, Samuel F.

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Thriving in a Male-Dominated Workplace (HBR Women at Work Series) von Review, Harvard Business, Abrams, Stacey, Hodgson, Lara, Grenny, Joseph, King, Michelle P

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Autosomal dominant vasovagal syncope: Clinical features and linkage to chromosome 15q26 von KLEIN, Karl Martin, BROMHEAD, Catherine J, SCHEFFER, Ingrid E, DIBBENS, Leanne M, BAHLO, Melanie, BERKOVIC, Samuel F, SMITH, Katherine R, O'CALLAGHAN, Christopher J, CORCORAN, Susan J, HERON, Sarah E, IONA, Xenia, HODGSON, Bree L, MCMAHON, Jacinta M, LAWRENCE, Kate M

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