HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer

por Weeks, Alexia L., Wilson, Scott G., Ward, Lynley, Goldblatt, Jack, Hui, Jennie, Walsh, John P.
Publicado 2016

Reference exome data for a Northern Brazilian population

por Weeks, Alexia L., Francis, Richard W., Neri, Joao I. C. F., Costa, Nathaly M. C., Arrais, Nivea M. R., Lassmann, Timo, Blackwell, Jenefer M., Jeronimo, Selma M. B.
Publicado 2020

Reference exome data for Australian Aboriginal populations to support health-based research

por Weeks, Alexia L., D’Antoine, Heather A., McKinnon, Melita, Syn, Genevieve, Bessarab, Dawn, Brown, Ngiare, Tong, Steven Y. C., Reményi, Bo, Steer, Andrew, Gray, Lesley-Ann, Inouye, Michael, Carapetis, Jonathan R., Blackwell, Jenefer M., Lassmann, Timo
Publicado 2020

A flexible computational pipeline for research analyses of unsolved clinical exome cases

por Lassmann, Timo, Francis, Richard W., Weeks, Alexia, Tang, Dave, Jamieson, Sarra E., Broley, Stephanie, Dawkins, Hugh J. S., Dreyer, Lauren, Goldblatt, Jack, Groza, Tudor, Kamien, Benjamin, Kiraly-Borri, Cathy, McKenzie, Fiona, Murphy, Lesley, Pachter, Nicholas, Pathak, Gargi, Poulton, Cathryn, Samanek, Amanda, Skoss, Rachel, Slee, Jennie, Townshend, Sharron, Ward, Michelle, Baynam, Gareth S., Blackwell, Jenefer M.
Publicado 2020