Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes
- Creator: Biankin, Andrew V. , Waddell, Nicola , Kassahn, Karin S. , Gingras, Marie-Claude , Muthuswamy, Lakshmi B. , Johns, Amber L. , Miller, David K. , Wilson, Peter J. , Patch, Ann-Marie , Wu, Jianmin , Chang, David K. , Cowley, Mark J. , Gardiner, Brooke B. , Song, Sarah , Harliwong, Ivon , Idrisoglu, Senel , Nourse, Craig , Nourbakhsh, Ehsan , Manning, Suzanne , Wani, Shivangi , Scarlett, Christopher J.
- Resource Type: journal article
- Date: 2012
Histomolecular phenotypes and outcome in adenocarcinoma of the ampulla of Vater
- Creator: Chang, David K. , Jamieson, Nigel B. , Nagrial, Adnan M. , Chantrill, Lorraine A. , Chin, Venessa T. , Pinho, Andreia V. , Rooman, Ilse , Cowley, Mark J. , Wu, Jianmin , Mead, R. Scott , Colvin, Emily K. , Samra, Jaswinder S. , Johns, Amber L. , Corbo, Vincenzo , Bassi, Claudio , Falconi, Massimo , Lawlor, Rita T. , Crippa, Stefano , Sperandio, Nicola , Bersani, Samantha , Dickson, Euan J. , Mohamed, Mohamed A. A. , Oien, Karin A. , Scarlett, Christopher J. , Foulis, Alan K. , Musgrove, Elizabeth A. , Sutherland, Robert L. , Kench, James G. , Carter, C. Ross , Gill, Anthony J. , Scarpa, Aldo , McKay, Colin J. , Biankin, Andrew V. , Pajic, Marina , Chou, Angela , Pinese, Mark , Humphris, Jeremy L. , Jones, Marc D. , Toon, Christopher
- Resource Type: journal article
- Date: 2013
Clinical and pathologic features of familial pancreatic cancer
- Creator: Humphris, Jeremy L. , Johns, Amber L. , Mead, R. Scott , Gill, Anthony J. , Samra, Jaswinder S. , Kench, James G. , Musgrove, Elizabeth A. , Tucker, Katherine M. , Spigelman, Allan D. , Waddell, Nic , Grimmond, Sean M. , Biankin, Andrew V. Biankin , Simpson, Skye H. , Australian Pancreatic Cancer Genome Initiative, , Cowley, Mark J. , Pajic, Marina , Chang, David K. , Nagrial, Adnan M. , Chin, Venessa T. , Chantrill, Lorraine A. , Pinese, Mark
- Resource Type: journal article
- Date: 2014
A recurrent De Novo nonsense variant in ZSWIM6 results in severe intellectual disability without frontonasal or limb malformations
- Creator: Palmer, Elizabeth E. , Kumar, Raman , Oufadem, Myriam , Lalani, Seema R. , Lewis, Andrea M. , Xia, Fan , Tam, Allison , Webster, Richard , Brammah, Susan , Filippini, Francesca , Pollard, John , Spies, Judy , Gordon, Christopher T. , Minoche, Andre E. , Cowley, Mark J. , Risen, Sarah , Powell-Hamilton, Nina N. , Tusi, Jessica E. , Immken, LaDonna , Nagakura, Honey , Bole-Feysot, Christine , Nitschké, Patrick , Garrigue, Alexandrine , Shaw, Marie , de Saint Basile, Geneviève , Kivuva, Emma , Scott, Richard H. , Rendon, Augusto , Munnich, Arnold , Newman, William , Kerr, Bronwyn , Besmond, Claude , Rosenfeld, Jill A. , Amiel, Jeanne , Hubert, Laurence , Field, Michael , Gecz, Jozef , Carroll, Renee , Rio, Marlène , Murray, Lucinda , Leffler, Melanie , Dudding-Byth, Tracy
- Resource Type: journal article
- Date: 2017
Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy
- Creator: Bagnall, Richard D. , Ingles, Jodie , Berman, Yemima , Ronan, Anne , Fatkin, Diane , Semsarian, Christopher , Dinger, Marcel E. , Cowley, Mark J. , Ross, Samantha Barratt , Minoche, André E. , Lal, Sean , Turner, Christian , Colley, Alison , Rajagopalan, Sulekha
- Resource Type: journal article
- Date: 2018
Precision oncology in surgery: patient selection for operable pancreatic cancer
- Creator: Dreyer, Stephan B. , Pinese, Mark , Jamieson, Nigel B. , Scarlett, Christopher J. , Colvin, Emily K. , Pajic, Marina , Johns, Amber L. , Humphris, Jeremy L. , Wu, Jianmin , Cowley, Mark J. , Chou, Angela , Nagrial, Adnan M. , Chantrill, Lorraine , Chin, Venessa T. , Jones, Marc D. , Moran-Jones, Kim , Carter, Christopher Ross , Dickson, Euan J. , Samra, Jaswinder S. , Merrett, Neil D. , Gill, Anthony J. , Kench, JG , Duthie, F , Miller, DK , Cooke, S , Aust, D , Knösel, T , Rümmele, P , Grützmann, R , Pilarsky, C , Nguyen, NQ , Musgrove, EA , Bailey, PJ , McKay, CJ , Biankin, AV , Chang, DK , Australian Pancreatic Cancer Genome Initiative , Glasgow Precision Oncology Laboratory
- Resource Type: journal article
- Date: 2020
Different types of disease-causing noncoding variants revealed by genomic and gene expression analyses in families with X-linked intellectual disability
- Creator: Field, Michael J. , Kumar, Raman , Gardner, Alison E. , Sullivan, Patricia , Ha, Thuong T. , Schwartz, Charles E. , Cowley, Mark J. , Dinger, Marcel E. , Palmer, Elizabeth E. , Christie, Louise , Shaw, Marie , Roscioli, Tony , Hackett, Anna , Gecz, Jozef , Corbett, MA , Kayumi, Sayaka , Shoubridge, Cheryl A. , Ewans, Lisa J. , Ivancevic, Atma M. , Dudding-Byth, Tracy , Carroll, Renée , Kroes, Thessa
- Resource Type: journal article
- Date: 2021