Search Results - Taylor, Georgia M.

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    Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study by Ibañez, Kristina, Polke, James, Hagelstrom, R Tanner, Dolzhenko, Egor, Pasko, Dorota, Thomas, Ellen Rachel Amy, Smith, Katherine R, McDonagh, Ellen M, Polychronopoulos, Dimitris, Chan, Georgia, Davison, James E, Festenstein, Richard, Fratta, Pietro, Giunti, Paola, Howard, Robin, Venkata, Laxmi, Laurá, Matilde, Morris, Huw, Robinson, Robert, Rosser, Elisabeth, Faravelli, Francesca, Schrag, Anette, Schott, Jonathan M, Wood, Nicholas W, Bourn, David, Eggleton, Kelly, Twiss, Philip, Almheiri, Ghareesa, Sheikh, Isabella, Vandrovcova, Jana, Brittain, Helen, Baple, Emma, Moutsianas, Loukas, Deshpande, Viraj, Perry, Denise L, Ajay, Subramanian S., Rajan, Vani, Oprych, Kathryn, Chinnery, Patrick F, Wilson, Gill, Ellard, Sian, Temple, I Karen, McMullan, Dom, Naresh, Kikkeri, Flinter, Frances A, Taylor, Jenny C, Greenhalgh, Lynn, Newman, William, Brennan, Paul, Sayer, John A, Raymond, F Lucy, Deans, Zandra C, Hill, Sue, Fowler, Tom, Scott, Richard H, Chinnery, Patrick F, Rendon, Augusto, Eberle, Michael A, Taft, Ryan J, Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boissiere, Jeanne M., Devereau, Andrew, Elgar, Greg, Foulger, Rebecca E., Furió-Tarí, Pedro, Hackett, Joanne, Hamblin, Angela, Holman, James, Hubbard, Tim J.P., Jones, Louise J., Kayikci, Melis, Lawson, Kay, Leigh, Sarah E.A., Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Mueller, Michael, Murugaesu, Nirupa, Odhams, Chris A., Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Riesgo-Ferreiro, Pablo, Ryten, Mina, Savage, Kevin, Sawant, Kushmita, Sieghart, Alexander, Smedley, Damian, Sosinsky, Alona, Spooner, William, Stevens, Helen E., Stuckey, Alexander, Sultana, Razvan, Tregidgo, Carolyn, Walsh, Emma, Watters, Sarah A., Williams, Eleanor, Zarowiecki, Magdalena

    Published in Lancet neurology
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    Asynchronous carbon sink saturation in African and Amazonian tropical forests by Hubau, Wannes, Lewis, Simon L., Phillips, Oliver L., Beeckman, Hans, Cuní-Sanchez, Aida, Daniels, Armandu K., Ewango, Corneille E. N., Fauset, Sophie, Mukinzi, Jacques M., Sheil, Douglas, Sonké, Bonaventure, Sullivan, Martin J. P., Sunderland, Terry C. H., Taedoumg, Hermann, Thomas, Sean C., White, Lee J. T., Abernethy, Katharine A., Adu-Bredu, Stephen, Amani, Christian A., Baker, Timothy R., Banin, Lindsay F., Baya, Fidèle, Begne, Serge K., Bennett, Amy C., Benedet, Fabrice, Bitariho, Robert, Bocko, Yannick E., Boeckx, Pascal, Boundja, Patrick, Brienen, Roel J. W., Brncic, Terry, Chezeaux, Eric, Chuyong, George B., Clark, Connie J., Collins, Murray, Comiskey, James A., Coomes, David A., Dargie, Greta C., de Haulleville, Thales, Kamdem, Marie Noel Djuikouo, Doucet, Jean-Louis, Esquivel-Muelbert, Adriane, Feldpausch, Ted R., Fofanah, Alusine, Foli, Ernest G., Gilpin, Martin, Gloor, Emanuel, Gonmadje, Christelle, Gourlet-Fleury, Sylvie, Hamilton, Alan C., Harris, David J., Hart, Terese B., Hockemba, Mireille B. N., Hladik, Annette, Jeffery, Kathryn J., Jucker, Tommaso, Yakusu, Emmanuel Kasongo, Kenfack, David, Koch, Alexander, Leal, Miguel E., Lindsell, Jeremy A., Lisingo, Janvier, Lopez-Gonzalez, Gabriela, Lovett, Jon C., Makana, Jean-Remy, Malhi, Yadvinder, Marshall, Andrew R., Martin, Jim, Martin, Emanuel H., Mbayu, Faustin M., Medjibe, Vincent P., Mihindou, Vianet, Mitchard, Edward T. A., Moore, Sam, Munishi, Pantaleo K. T., Bengone, Natacha Nssi, Ojo, Lucas, Ondo, Fidèle Evouna, Peh, Kelvin S.-H., Pickavance, Georgia C., Poulsen, Axel Dalberg, Poulsen, John R., Qie, Lan, Reitsma, Jan, Rovero, Francesco, Swaine, Michael D., Talbot, Joey, Taylor, David M., Thomas, Duncan W., Toirambe, Benjamin, Mukendi, John Tshibamba, Tuagben, Darlington, Umunay, Peter M., van der Heijden, Geertje M. F., Verbeeck, Hans, Vleminckx, Jason, Willcock, Simon, Wöll, Hannsjörg, Woods, John T., Zemagho, Lise

    Published in Nature (London)
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    Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study by Schon, Katherine R, Horvath, Rita, Wei, Wei, Calabrese, Claudia, Tucci, Arianna, Ibañez, Kristina, Ratnaike, Thiloka, Pitceathly, Robert D S, Bugiardini, Enrico, Quinlivan, Rosaline, Hanna, Michael G, Clement, Emma, Ashton, Emma, Sayer, John A, Brennan, Paul, Josifova, Dragana, Izatt, Louise, Fratter, Carl, Nesbitt, Victoria, Barrett, Timothy, McMullen, Dominic J, Smith, Audrey, Deshpande, Charulata, Smithson, Sarah F, Festenstein, Richard, Canham, Natalie, Caulfield, Mark, Houlden, Henry, Rahman, Shamima, Chinnery, Patrick F, Ambrose, John C, Arumugam, Prabhu, Bevers, Roel, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R, Brittain, Helen, Caulfield, Mark J, Chan, Georgia C, Elgar, Greg, Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J P, Jackson, Rob, Jones, Louise J, Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E A, Leong, Ivonne U S, Lopez, Javier F, Maleady-Crowe, Fiona, McEntegart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C, O’Donovan, Peter, Odhams, Chris A, Patch, Christine, Buonerimo Pereira, Mariana, Perez-Gil, Daniel, Pullinger, John, Rahim, Tahrima, Rendon, Augusto, Rogers, Tim, Savage, Kevin, Sawant, Kushmita, Scott, Richard H, Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C, Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R A, Thompson, Simon R, Tucci, Arianna, Welland, Matthew J, Williams, Eleanor, Witkowska, Katarzyna, Wood, Suzanne M

    Published in BMJ (Online)
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