Treffer 1 - 20 von 41 für Suche 'Wheeler, Jonathan Simon', Suchdauer: 1,39s Treffer weiter einschränken
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    Establishing a Core Outcome Set for Peritoneal Dialysis: Report of the SONG-PD (Standardized Outcomes in Nephrology–Peritoneal Dialysis) Consensus Workshop von Manera, Karine E., Johnson, David W., Craig, Jonathan C., Shen, Jenny I., Gutman, Talia, Wang, Angela Yee-Moon, Brown, Edwina A., Brunier, Gillian, Dong, Jie, Dunning, Tony, Mehrotra, Rajnish, Naicker, Saraladevi, Pecoits-Filho, Roberto, Wilkie, Martin, Tong, Allison, Cueto Manzano, Alfonso, Abu Alfa, Ali, Neu, Alicia, Tong, Allison, Bernier-Jean, Amelie, Kelly, Amy, Figueiredo, Ana, Matus, Andrea, Viecelli, Andrea, Ju, Angela, Wang, Angela Yee-Moon, Saxena, Anjali, Nadeau-Fredette, Annie-Claire, Teixeira-Pinto, Armando, Mendelson, Asher, Kelly, Ayano, Goh, Bak Leong, Sautenet, Benedicte, Manns, Braden, Hemmelgarn, Brenda, Robinson, Bruce, Hanson, Camilla, Cheung, Catherine, Guha, Chandana, Logeman, Charlotte, Szeto, Cheuk-Chun, Rutherford, Claudia, Schwartz, Daniel, Sumpton, Daniel, Brown, Edwina, O’Lone, Emma, Au, Eric, Goffin, Eric, Abraham, Georgi, Brunier, Gillian, Germino, Greg, Hurst, Helen, Kawanishi, Hideki, Htay, Htay, Yap, Hui Kim, Teitelbaum, Isaac, Shen, Jenny, Dong, Jie, Neumann, Joanna, Bargman, Joanne, Morelle, Johann, Kilonzo, Kajiru Gad, Manera, Karine, Azukaitis, Karolis, Krishnan, Mahesh, Schreiber, Martin, Wilkie, Martin, Oliver, Matthew, Sanabria, Mauricio Rafael, Lichodziejewska-Niemierko, Monika, Verdin, Nancy, Mann, Neelam, Boudville, Neil, Scholes-Robertson, Nicole, Blake, Peter, Nourse, Peter, Tugwell, Peter, Li, Philip Kam-Tao, Mehrotra, Rajnish, McGee, Richard, Quinn, Robert, Pecoits-Filho, Roberto, Crowe, Sally, Anumudu, Samaya, Bernays, Sarah, Naicker, Sarala, Wilson, Scott, Teo, Sharon, Davies, Simon, Sweety, Soheli Ahmed, Gutman, Talia, Toffelmire, Ted, Jassal, Vanita, da Silva, Viviane Calice, Van Biesen, Wim, Winkelmayer, Wolfgang, Ito, Yasuhiko, Cho, Yeoungjee, Kim, Yong-Lim, Butt, Zeeshan


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    A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing von Alioto, Tyler S., Buchhalter, Ivo, Derdak, Sophia, Hutter, Barbara, Eldridge, Matthew D., Hovig, Eivind, Heisler, Lawrence E., Beck, Timothy A., Simpson, Jared T., Tonon, Laurie, Sertier, Anne-Sophie, Patch, Ann-Marie, Jäger, Natalie, Ginsbach, Philip, Drews, Ruben, Paramasivam, Nagarajan, Kabbe, Rolf, Chotewutmontri, Sasithorn, Diessl, Nicolle, Previti, Christopher, Schmidt, Sabine, Brors, Benedikt, Feuerbach, Lars, Heinold, Michael, Gröbner, Susanne, Korshunov, Andrey, Tarpey, Patrick S., Butler, Adam P., Hinton, Jonathan, Jones, David, Menzies, Andrew, Raine, Keiran, Shepherd, Rebecca, Stebbings, Lucy, Teague, Jon W., Ribeca, Paolo, Giner, Francesc Castro, Beltran, Sergi, Raineri, Emanuele, Dabad, Marc, Heath, Simon C., Gut, Marta, Denroche, Robert E., Harding, Nicholas J., Yamaguchi, Takafumi N., Fujimoto, Akihiro, Nakagawa, Hidewaki, Quesada, Víctor, Valdés-Mas, Rafael, Nakken, Sigve, Vodák, Daniel, Bower, Lawrence, Lynch, Andrew G., Anderson, Charlotte L., Waddell, Nicola, Pearson, John V., Grimmond, Sean M., Peto, Myron, Spellman, Paul, He, Minghui, Kandoth, Cyriac, Lee, Semin, Zhang, John, Létourneau, Louis, Ma, Singer, Seth, Sahil, Torrents, David, Xi, Liu, Wheeler, David A., López-Otín, Carlos, Campo, Elías, Campbell, Peter J., Boutros, Paul C., Puente, Xose S., Gerhard, Daniela S., Pfister, Stefan M., McPherson, John D., Hudson, Thomas J., Schlesner, Matthias, Lichter, Peter, Eils, Roland, Jones, David T. W., Gut, Ivo G.

    Veröffentlicht in Nature communications

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    Red cell transfusion in outpatients with myelodysplastic syndromes: a feasibility and exploratory randomised trial von Killick, Sally, Karakantza, Marina, Hodge, Renate L., Hopkins, Valerie, Deary, Alison J., Callum, Jeannie, Lin, Yulia, Wood, Erica M., Buckstein, Rena, Wallis, Louise, Rabbi, Taslima, Serrano, Monica, Williams, Rachel, Watson, Lucy, Woods, Lois, Clarke, Christine, Sternberg, Alex, Owen, Tim, Meakin, Sue, Lake, Donna, Culligan, Dominic, Johannesson, Nicola, Taylor, Gordon, Tomlinson, Jill, Shaw, Ann, Ratcliffe, Maria, Lamacchia, Mariella, Duncan, Caroline, Untiveros, Paraskevi, Olaiya, Adetomilola, Preston, Gavin, Lawrie, Alastair, Robertson, Charlotte, Onyeakazi, Uzunma, Radia, Rohini, Stainthorp, Katherine, Mc Connell, Steward, Langton, Catherine, Howcroft, Clare, Saddiq, Ismail, Byrne, Jennifer, Lindsey‐Hill, Jo, Badder, Denise, Pol, Raj, Bancroft, Rachel, Springett, Sally, Gray, Louisa, Friesen, Heather, Wardle, Katrin, Murthy, Vidhya, Kishore, Bhuvan, Mayer, Georgina, Nikolousis, Emmanouil, Lovell, Richard, Kartsios, Charalampos, Lumley, Matthew, Khawaja, Jahanzeb, Murray, Duncan, Milligan, Donald, Dhani, Sundip, Schumacher, Anne, Enstone, Rosemarie, Boal, Lauren, Latter, Ruth, Birt, Mark, Watts, Emily, Charlton, Andrew, Forsyth, Hazel, Lennard, Anne, Robinson, Kate, Grand, Effie, Cullis, Jonathan, Collins, Freya, Tudgay, Saffron, Salisbury, Sarah, Mathew, Siju, Tipler, Nicole, Stobie, Emma, Tribbeck, Michele, Hebballi, Sangam, Millar, Christopher, Lala, Jai, Chmeil, Jo, Hufton, Lianne, Dawson, Sarah, Buyck, Hubertus, Hayden, Jina, Baluwala, Israel, Wheeler, Matthew, Miles, Rebecca, Blakemore, Maureen, Hargreaves, Ann, Hayden, Gina, Mo, Allison, Uhe, Micheleine, Indran, Tishya, Wong, Jonathan, Pearson, Sharon, Parker, Jane, Player, Matthew

    Veröffentlicht in British journal of haematology

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    De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder von Mirzaa, Ghayda M., Chong, Jessica X., Piton, Amélie, Popp, Bernt, Foss, Kimberly, Guo, Hui, Harripaul, Ricardo, Xia, Kun, Scheck, Joshua, Aldinger, Kimberly A., Sajan, Samin A., Tang, Sha, Bonneau, Dominique, Beck, Anita, White, Janson, Mahida, Sonal, Harris, Jacqueline, Smith-Hicks, Constance, Hoyer, Juliane, Zweier, Christiane, Reis, André, Thiel, Christian T., Jamra, Rami Abou, Zeid, Natasha, Yang, Amy, Farach, Laura S., Walsh, Laurence, Payne, Katelyn, Rohena, Luis, Velinov, Milen, Ziegler, Alban, Schaefer, Elise, Gatinois, Vincent, Geneviève, David, Simon, Marleen E.H., Kohler, Jennefer, Rotenberg, Joshua, Wheeler, Patricia, Larson, Austin, Ernst, Michelle E., Akman, Cigdem I., Westman, Rachel, Blanchet, Patricia, Schillaci, Lori-Anne, Vincent-Delorme, Catherine, Gripp, Karen W., Mattioli, Francesca, Guyader, Gwenaël Le, Gerard, Bénédicte, Mathieu-Dramard, Michèle, Morin, Gilles, Sasanfar, Roksana, Ayub, Muhammad, Vasli, Nasim, Yang, Sandra, Person, Rick, Monaghan, Kristin G., Nickerson, Deborah A., van Binsbergen, Ellen, Enns, Gregory M., Dries, Annika M., Rowe, Leah J., Tsai, Anne C.H., Svihovec, Shayna, Friedman, Jennifer, Agha, Zehra, Qamar, Raheel, Rodan, Lance H., Martinez-Agosto, Julian, Ockeloen, Charlotte W., Vincent, Marie, Sunderland, William James, Bernstein, Jonathan A., Eichler, Evan E., Vincent, John B., Bamshad, Michael J.

    Veröffentlicht in Genetics in medicine

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