Search Results - Annett, Robert G.

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    Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders by Gillentine, Madelyn A, Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N, De Vries, Bert B A, Vissers, Lisenka E L M, Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A, Bhat, Gifty, Cobian, Katherine, Bird, Lynne M, Friedman, Jennifer, Wright, Meredith S, Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K, White, Kerry M, Elpeleg, Orly, Berger, Itai, Espineli, Edward J, Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjærsgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L Manace, Mckee, Shane, Mirzaa, Ghayda M, Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E H, van Gassen, Koen L I, Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K, Nowakowski, Tomasz, Bernier, Raphael A, Eichler, Evan E

    Published in Genome medicine
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    The impact of viral mutations on recognition by SARS-CoV-2 specific T cells by Shah, Dhruv, Mentzer, Alexander J., Aanensen, David M., Adams, Helen, Alcolea-Medina, Adela, Ash, Amy, Atkinson, Laura, Balcazar, Carlos E., Bayzid, Nadua, Bicknell, Kelly, Byott, Matthew, Carabelli, Alessandro M., Chappell, Joseph G., Clarke, Phillip, Cogger, Benjamin J., Cook, Kate F., Coombes, Jason, Curran, Tanya, Davies, Robert M., Dey, Jayasree, Dobie, Donald, Edwards, Sue, Erkiert, Michelle J., Fairley, Derek J., Fanaie, Arezou, Fina, Laia, Fragakis, Mireille, Freeman, Timothy M., George, Ryan P., Goudarzi, Salman, Gutierrez, Bernardo, Hassan-Ibrahim, Mohammed O., Jackson, Leigh M., John, Michaela, Kay, Sally, Kraemer, Moritz U.G., Livett, Rich, Mack, Andrew, McClure, Patrick C., McCrone, J.T., McManus, Georgina M., McNally, Alan, Mondani, Matteo, Moses, Samuel, Nebbia, Gaia, Parmar, Surendra, Pritchard, David T., Pugh, Georgia, Quick, Joshua, Rainbow, Lucille, Rajatileka, Shavanthi, Rey, Sara, Richter, Alex, Robinson, Esther, Scher, Emily, Shah, Divya, Sheridan, Liz A., Wastnedge, Elizabeth, Watkins, Joanne, Whitehead, Mark, Whitwham, Andrew, Williams, Lesley-Anne, Zhang, Peijun, Bach, Benjamin, Barclay, Wendy S., Griffin, Julian L., Horby, Peter W., Khoo, Saye, Mentzer, Alexander J., Stuart, David, Tedder, Richard S., Roberts, Stephanie, Lee, James, Scott-Brown, James, Shaw, Victoria, Ahmed, Katie A., Brennan, Benjamin, Cox, Helen, Garcia-Dorival, Isabel, Lant, Suzannah, Penrice-Randal, Rebekah, Morrice, Kirstie, Bari, Shahedal, Drummond, Andrew, Garg, Sanjeev, Gkrania-Klotsas, Effrossyni, Godden, Jo, Goldsmith, Arthur, Hartshorn, Stuart, Lillie, Patrick, Lyttle, Mark, O'Shea, Matthew K., Pais, Mark, Post, Frank, Richardson, Neil, Sharma, Anil, Spittle, Nick, Stambach, Tom, Waddy, Sam, Whitehouse, Tony

    Published in iScience
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