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Plos One|April 27, 2012
MicroRNA genes and their target 3'-untranslated regions are infrequently somatically mutated in ovarian cancersGeorgina L Ryland, Jennifer L Bearfoot, Maria A Doyle, et al.
Ejhaem|November 29, 2023
Persistence of UBTF tandem duplications in remission in acute myeloid leukaemiaSean Harrop, Phillip C Nguyen, David Byrne, et al.
Scientific Reports|February 10, 2017
Multiplexed transcriptome analysis to detect ALK, ROS1 and RET rearrangements in lung cancerToni-Maree Rogers, Gisela Mir Arnau, Georgina L Ryland, et al.
Oncotarget|December 15, 2018
Frequent activating STAT3 mutations and novel recurrent genomic abnormalities detected in breast implant-associated anaplastic large cell lymphomaPiers Blombery, Ella Thompson, Georgina L Ryland, et al.
BMC Medical Genomics|August 2, 2015
Loss of heterozygosity: what is it good for?Georgina L Ryland, Maria A Doyle, David Goode, et al.
Genome Medicine|August 11, 2015
Mutational landscape of mucinous ovarian carcinoma and its neoplastic precursorsGeorgina L Ryland, Sally M Hunter, Maria A Doyle, et al.
Human Mutation|October 13, 2011
Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patientsElla R Thompson, Samantha E Boyle, Julie Johnson, et al.
Scientific Reports|April 25, 2019
CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencingJohn F Markham, Satwica Yerneni, Georgina L Ryland, et al.
Scientific Reports|June 25, 2020
Publisher Correction: CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencingJohn F Markham, Satwica Yerneni, Georgina L Ryland, et al.
Plos Genetics|October 3, 2012
Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility allelesElla R Thompson, Maria A Doyle, Georgina L Ryland, et al.
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