RNA variant assessment using transactivation and transdifferentiation
Nicolas-Martinez, Emmylou C., Robinson, Olivia, Pflueger, Christian, Gardner, Alison, Corbett, Mark A., Ritchie, Tarin, Kroes, Thessa, van Eyk, Clare L., Scheffer, Ingrid E., Hildebrand, Michael S., Barnier, Jean-Vianney, Rousseau, Véronique, Genevieve, David, Haushalter, Virginie, Piton, Amélie, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Nambot, Sophie, Isidor, Bertrand, Grigg, John, Gonzalez, Tina, Ghedia, Sondhya, Marchant, Rhett G., Bournazos, Adam, Wong, Wui-Kwan, Webster, Richard I., Evesson, Frances J., Jones, Kristi J., Azmanov, Dimitar N., Barnett, Christopher P., Barry, Simon C., Baynam, Gareth, Berkovic, Samuel F., Christodoulou, John, Coman, David J., Cooper, Sandra, Corbett, Mark A., Delatycki, Martin, Dudding, Tracy E., Fletcher, Sue, Gardner, Alison E., Gecz, Jozef, Higgins, Megan J., Hildebrand, Michael S., Jolly, Lachlan A., Lister, Ryan, McGaughran, Julie, Pflueger, Christian, Poulton, Cathryn, Roscioli, Tony, Hamish S. Scott, Ingrid Scheffer, Sinclair, Andrew H., Spurdle, Amanda B., Tan, Tiong Y., van Eyk, Clare L., Voineagu, Irina, Cooper, Sandra T., Lister, Ryan, Gecz, Jozef, Jolly, Lachlan A.
Published in American journal of human genetics (08.08.2024)
Published in American journal of human genetics (08.08.2024)
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Journal Article
RNA variant assessment using transactivation and transdifferentiation
Nicolas-Martinez, Emmylou C, Robinson, Olivia, Pflueger, Christian, Gardner, Alison, Corbett, Mark A, Ritchie, Tarin, Kroes, Thessa, van Eyk, Clare L, Scheffer, Ingrid E, Hildebrand, Michael S, Barnier, Jean-Vianney, Rousseau, Véronique, Genevieve, David, Haushalter, Virginie, Piton, Amélie, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Nambot, Sophie, Isidor, Bertrand, Grigg, John, Gonzalez, Tina, Ghedia, Sondhya, Marchant, Rhett G, Bournazos, Adam, Wong, Wui-Kwan, Webster, Richard I, Evesson, Frances J, Jones, Kristi J, Azmanov, Dimitar N, Barnett, Christopher P, Barry, Simon C, Baynam, Gareth, Berkovic, Samuel F, Christodoulou, John, Coman, David J, Cooper, Sandra T, Delatycki, Martin, Dudding, Tracy E, Fletcher, Sue, Gardner, Alison E, Gecz, Jozef, Higgins, Megan J, Jolly, Lachlan A, Lister, Ryan, Mcgaughran, Julie, Pflueger, Christian, Poulton, Cathryn, Roscioli, Tony, Scheffer, Ingrid, Scott, Hamish S., Sinclair, Andrew H, Spurdle, Amanda B, Tan, Tiong Y, Voineagu, Irina, Gecz, Jozef, Jolly, Lachlan A
Published in American journal of human genetics (25.07.2024)
Published in American journal of human genetics (25.07.2024)
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Journal Article
The clinical utility and costs of whole-genome sequencing to detect cancer susceptibility variants—a multi-site prospective cohort study
Davidson, Aimee L, Dressel, Uwe, Norris, Sarah, Canson, Daffodil M, Glubb, Dylan M, Fortuno, Cristina, Hollway, Georgina E, Parsons, Michael T, Vidgen, Miranda E, Holmes, Oliver, Koufariotis, Lambros T, Lakis, Vanessa, Leonard, Conrad, Wood, Scott, Xu, Qinying, McCart Reed, Amy E, Pickett, Hilda A, Al-Shinnag, Mohammad K, Austin, Rachel L, Burke, Jo, Cops, Elisa J, Nichols, Cassandra B, Goodwin, Annabel, Harris, Marion T, Higgins, Megan J, Ip, Emilia L, Kiraly-Borri, Catherine, Lau, Chiyan, Mansour, Julia L, Millward, Michael W, Monnik, Melissa J, Pachter, Nicholas S, Ragunathan, Abiramy, Susman, Rachel D, Townshend, Sharron L, Trainer, Alison H, Troth, Simon L, Tucker, Katherine M, Wallis, Mathew J, Walsh, Maie, Williams, Rachel A, Winship, Ingrid M, Newell, Felicity, Tudini, Emma, Pearson, John V, Poplawski, Nicola K, Mar Fan, Helen G, James, Paul A, Spurdle, Amanda B, Waddell, Nicola, Ward, Robyn L
Published in Genome medicine (19.09.2023)
Published in Genome medicine (19.09.2023)
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