Key health outcomes for children and young people with neurodisability: qualitative research with young people and parents

por Allard, Amanda, Fellowes, Andrew, Shilling, Valerie, Janssens, Astrid, Beresford, Bryony, Morris, Christopher
Publicado 2014

Canary: an atomic pipeline for clinical amplicon assays

por Doig, Kenneth D., Ellul, Jason, Fellowes, Andrew, Thompson, Ella R., Ryland, Georgina, Blombery, Piers, Papenfuss, Anthony T., Fox, Stephen B.
Publicado 2017

Findings from precision oncology in the clinic: rare, novel variants are a significant contributor to scaling molecular diagnostics

por Doig, Kenneth D., Love, Christopher G., Conway, Thomas, Seleznev, Andrei, Ma, David, Fellowes, Andrew, Blombery, Piers, Fox, Stephen B.
Publicado 2022

SDH-deficient renal cell carcinoma associated with biallelic mutation in succinate dehydrogenase A: comprehensive genetic profiling and its relation to therapy response

por McEvoy, Christopher R., Koe, Lisa, Choong, David Y., Leong, Huei San, Xu, Huiling, Karikios, Deme, Plew, Jeffrey D., Prall, Owen W., Fellowes, Andrew P., Fox, Stephen B.
Publicado 2018

Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures

por Morris, Christopher, Janssens, Astrid, Shilling, Valerie, Allard, Amanda, Fellowes, Andrew, Tomlinson, Richard, Williams, Jane, Thompson Coon, Jo, Rogers, Morwenna, Beresford, Bryony, Green, Colin, Jenkinson, Crispin, Tennant, Alan, Logan, Stuart
Publicado 2015

Multiplexed transcriptome analysis to detect ALK, ROS1 and RET rearrangements in lung cancer

por Rogers, Toni-Maree, Arnau, Gisela Mir, Ryland, Georgina L., Huang, Stephen, Lira, Maruja E., Emmanuel, Yvette, Perez, Omar D., Irwin, Darryl, Fellowes, Andrew P., Wong, Stephen Q., Fox, Stephen B.
Publicado 2017

Towards a shared vision for measureable and meaningful health outcomes for children and young people with neurodisability: qualitative research, Delphi survey, systematic review, a...

por Morris, Christopher, Janssens, Astrid, Allard, Amanda, Thompson Coon, Joanne, Shilling, Valerie, Tomlinson, Richard, Williams, Jane, Fellowes, Andrew, Rogers, Morwenna, Allen, Karen, Beresford, Bryony, Green, Colin, Jenkinson, Crispin, Tennant, Alan, Logan, Stuart
Publicado 2015

Six-year experience of Australia’s first dedicated cancer of unknown primary clinic

por van Mourik, Arielle, Tonkin-Hill, Gina, O’Farrell, John, Waller, Shohei, Tan, Lavinia, Tothill, Richard W., Bowtell, David, Fox, Stephen, Fellowes, Andrew, Fedele, Clare, Schofield, Penelope, Sivakumaran, Tharani, Wong, Hui-Li, Mileshkin, Linda
Publicado 2023

CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing

por Markham, John F., Yerneni, Satwica, Ryland, Georgina L., Leong, Huei San, Fellowes, Andrew, Thompson, Ella R., De Silva, Wasanthi, Kumar, Amit, Lupat, Richard, Li, Jason, Ellul, Jason, Fox, Stephen, Dickinson, Michael, Papenfuss, Anthony T., Blombery, Piers
Publicado 2019

Publisher Correction: CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing

por Markham, John F., Yerneni, Satwica, Ryland, Georgina L., Leong, Huei San, Fellowes, Andrew, Thompson, Ella R., De Silva, Wasanthi, Kumar, Amit, Lupat, Richard, Li, Jason, Ellul, Jason, Fox, Stephen, Dickinson, Michael, Papenfuss, Anthony T., Blombery, Piers
Publicado 2020

Clinical implications of prospective genomic profiling of metastatic breast cancer patients

por van Geelen, Courtney T., Savas, Peter, Teo, Zhi Ling, Luen, Stephen J., Weng, Chen-Fang, Ko, Yi-An, Kuykhoven, Keilly S., Caramia, Franco, Salgado, Roberto, Francis, Prudence A., Dawson, Sarah-Jane, Fox, Stephen B., Fellowes, Andrew, Loi, Sherene
Publicado 2020

Correction to: Clinical implications of prospective genomic profiling of metastatic breast cancer patients

por van Geelen, Courtney T., Savas, Peter, Teo, Zhi Ling, Luen, Stephen J., Weng, Chen-Fang, Ko, Yi-An, Kuykhoven, Keilly S., Caramia, Franco, Salgado, Roberto, Francis, Prudence A., Dawson, Sarah-Jane, Fox, Stephen B., Fellowes, Andrew, Loi, Sherene
Publicado 2022

PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories

por Doig, Kenneth D., Fellowes, Andrew, Bell, Anthony H., Seleznev, Andrei, Ma, David, Ellul, Jason, Li, Jason, Doyle, Maria A., Thompson, Ella R., Kumar, Amit, Lara, Luis, Vedururu, Ravikiran, Reid, Gareth, Conway, Thomas, Papenfuss, Anthony T., Fox, Stephen B.
Publicado 2017

Sequence artefacts in a prospective series of formalin-fixed tumours tested for mutations in hotspot regions by massively parallel sequencing

por Wong, Stephen Q, Li, Jason, Tan, Angela Y-C, Vedururu, Ravikiran, Pang, Jia-Min B, Do, Hongdo, Ellul, Jason, Doig, Ken, Bell, Anthony, MacArthur, Grant A, Fox, Stephen B, Thomas, David M, Fellowes, Andrew, Parisot, John P, Dobrovic, Alexander
Publicado 2014

“Cancer 2015”: A Prospective, Population-Based Cancer Cohort—Phase 1: Feasibility of Genomics-Guided Precision Medicine in the Clinic

por Parisot, John P., Thorne, Heather, Fellowes, Andrew, Doig, Ken, Lucas, Mark, McNeil, John J., Doble, Brett, Dobrovic, Alexander, John, Thomas, James, Paul A., Lipton, Lara, Ashley, David, Hayes, Theresa, McMurrick, Paul, Richardson, Gary, Lorgelly, Paula, Fox, Stephen B., Thomas, David M.
Publicado 2015

Development and interlaboratory evaluation of a NIST Reference Material RM 8366 for EGFR and MET gene copy number measurements

por He, Hua-Jun, Das, Biswajit, Cleveland, Megan H., Chen, Li, Camalier, Corinne E., Liu, Liang-Chun, Norman, Kara L., Fellowes, Andrew P., McEvoy, Christopher R., Lund, Steve P., Almeida, Jamie, Steffen, Carolyn R., Karlovich, Chris, Williams, P. Mickey, Cole, Kenneth D.
Publicado 2019

Breast cancer metastasis to gynaecological organs: a clinico‐pathological and molecular profiling study

por Kutasovic, Jamie R, McCart Reed, Amy E, Males, Renique, Sim, Sarah, Saunus, Jodi M, Dalley, Andrew, McEvoy, Christopher R, Dedina, Liana, Miller, Gregory, Peyton, Stephen, Reid, Lynne, Lal, Samir, Niland, Colleen, Ferguson, Kaltin, Fellowes, Andrew P, Al‐Ejeh, Fares, Lakhani, Sunil R, Cummings, Margaret C, Simpson, Peter T
Publicado 2018

Immune and genomic biomarkers of immunotherapy response in cancer of unknown primary

por Posner, Atara, Sivakumaran, Tharani, Pattison, Andrew, Etemadmoghadam, Dariush, Thio, Niko, Wood, Colin, Fisher, Krista, Webb, Samantha, DeFazio, Anna, Wilcken, Nicholas, Gao, Bo, Karapetis, Christos S, Singh, Madhu, Collins, Ian M, Richardson, Gary, Steer, Christopher, Warren, Mark, Karanth, Narayan, Fellowes, Andrew, Fox, Stephen B, Hicks, Rodney J, Schofield, Penelope, Bowtell, David, Prall, Owen W J, Tothill, Richard William, Mileshkin, Linda
Publicado 2023

A Matched Molecular and Clinical Analysis of the Epithelioid Haemangioendothelioma Cohort in the Stafford Fox Rare Cancer Program and Contextual Literature Review

por Abdelmogod, Arwa, Papadopoulos, Lia, Riordan, Stephen, Wong, Melvin, Weltman, Martin, Lim, Ratana, McEvoy, Christopher, Fellowes, Andrew, Fox, Stephen, Bedő, Justin, Penington, Jocelyn, Pham, Kym, Hofmann, Oliver, Vissers, Joseph H. A., Grimmond, Sean, Ratnayake, Gayanie, Christie, Michael, Mitchell, Catherine, Murray, William K., McClymont, Kelly, Luk, Peter, Papenfuss, Anthony T., Kee, Damien, Scott, Clare L., Goldstein, David, Barker, Holly E.
Publicado 2023

One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation

por Lincoln, Stephen E., Hambuch, Tina, Zook, Justin M., Bristow, Sara L., Hatchell, Kathryn, Truty, Rebecca, Kennemer, Michael, Shirts, Brian H., Fellowes, Andrew, Chowdhury, Shimul, Klee, Eric W., Mahamdallie, Shazia, Cleveland, Megan H., Vallone, Peter M., Ding, Yan, Seal, Sheila, DeSilva, Wasanthi, Tomson, Farol L., Huang, Catherine, Garlick, Russell K., Rahman, Nazneen, Salit, Marc, Kingsmore, Stephen F., Ferber, Matthew J., Aradhya, Swaroop, Nussbaum, Robert L.
Publicado 2021