The proportion of endometrial tumours associated with Lynch syndrome (PETALS): A prospective cross-sectional study von Ryan, Neil A. J., McMahon, Raymond, Tobi, Simon, Snowsill, Tristan, Esquibel, Shona, Wallace, Andrew J., Bunstone, Sancha, Bowers, Naomi, Mosneag, Ioana E., Kitson, Sarah J., O’Flynn, Helena, Ramchander, Neal C., Sivalingam, Vanitha N., Frayling, Ian M., Bolton, James, McVey, Rhona J., Evans, D. Gareth, Crosbie, Emma J.

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A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer von Evans, D.Gareth R., van Veen, Elke M., Byers, Helen J., Wallace, Andrew J., Ellingford, Jamie M., Beaman, Glenda, Santoyo-Lopez, Javier, Aitman, Timothy J., Eccles, Diana M., Lalloo, Fiona I., Smith, Miriam J., Newman, William G.

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A Land Plant-Specific Transcription Factor Directly Enhances Transcription of a Pathogenic Noncoding RNA Template by DNA-Dependent RNA Polymerase II von Wang, Ying, Qu, Jie, Ji, Shaoyi, Wallace, Andrew J., Wu, Jian, Li, Yi, Gopalan, Venkat, Ding, Biao

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New challenges for BRCA testing: a view from the diagnostic laboratory von Wallace, Andrew J

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Germline SMARCE1 mutations predispose to both spinal and cranial clear cell meningiomas von Smith, Miriam J, Wallace, Andrew J, Bennett, Chris, Hasselblatt, Martin, Elert-Dobkowska, Ewelina, Evans, Linton T, Hickey, William F, van Hoff, Jack, Bauer, David, Lee, Amy, Hevner, Robert F, Beetz, Christian, du Plessis, Daniel, Kilday, John-Paul, Newman, William G, Evans, D Gareth

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Clinical and molecular predictors of mortality in neurofibromatosis 2: a UK national analysis of 1192 patients von Hexter, Adam, Jones, Adrian, Joe, Harry, Heap, Laura, Smith, Miriam J, Wallace, Andrew J, Halliday, Dorothy, Parry, Allyson, Taylor, Amy, Raymond, Lucy, Shaw, Adam, Afridi, Shazia, Obholzer, Rupert, Axon, Patrick, King, Andrew T, Friedman, Jan M, Evans, D Gareth R

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New challenges for BRCA testing: a view from the diagnostic laboratory von Wallace, Andrew J

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Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis von Smith, Miriam J., Wallace, Andrew J., Bowers, Naomi L., Rustad, Cecilie F., Woods, C. Geoff, Leschziner, Guy D., Ferner, Rosalie E., Evans, D. Gareth R.

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Predictors of the Risk of Mortality in Neurofibromatosis 2 von Baser, Michael E., Friedman, J.M., Aeschliman, Dana, Joe, Harry, Wallace, Andrew J., Ramsden, Richard T., Evans, D. Gareth R.

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Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1-related schwannomatosis von Smith, Miriam J, Bowers, Naomi L, Bulman, Michael, Gokhale, Carolyn, Wallace, Andrew J, King, Andrew T, Lloyd, Simon K.L, Rutherford, Scott A, Hammerbeck-Ward, Charlotte L, Freeman, Simon R, Evans, D Gareth

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30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes von Woodward, Emma R, Green, Kate, Burghel, George J, Bulman, Michael, Clancy, Tara, Lalloo, Fiona, Schlecht, Helene, Wallace, Andrew J, Evans, D Gareth

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The utility of TP53 and PIK3CA mutations as prognostic biomarkers in salivary adenoid cystic carcinoma von Adderley, Helen, Rack, Samuel, Hapuarachi, Brindley, Feeney, Laura, Morgan, David, Hussell, Tracy, Wallace, Andrew J, Betts, Guy, Hodgson, Clare, Harrington, Kevin, Metcalf, Robert

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Multi-Maintenance Olaparib Therapy in Relapsed, Germline BRCA1/2-Mutant High-Grade Serous Ovarian Cancer (MOLTO): A Phase II Trial von Morgan, Robert D, Clamp, Andrew R, White, Daniel J, Price, Marcus, Burghel, George J, Ryder, W David J, Mahmood, Reem D, Murphy, Alexander D, Hasan, Jurjees, Mitchell, Claire L, Salih, Zena, Wheeler, Chelsey, Buckley, Emma, Truelove, Joanna, King, Georgia, Ainaoui, Yasmina, Bhaskar, Sanjeev S, Shaw, Joseph, Evans, D Gareth R, Kilerci, Bedirhan, Pearce, Simon P, Brady, Gerard, Dive, Caroline, O'Connor, James P B, Wallace, Andrew J, Rothwell, Dominic G, Edmondson, Richard J, Jayson, Gordon C

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Incidence of mosaicism in 1055 de novo NF2 cases: much higher than previous estimates with high utility of next-generation sequencing von Evans, D. Gareth, Hartley, Claire L., Smith, Philip T., King, Andrew T., Bowers, Naomi L., Tobi, Simon, Wallace, Andrew J., Perry, Mary, Anup, Raji, Lloyd, Simon K. W., Rutherford, Scott A., Hammerbeck-Ward, Charlotte, Pathmanaban, Omar N., Stapleton, Emma, Freeman, Simon R., Kellett, Mark, Halliday, Dorothy, Parry, Allyson, Gair, Juliette J., Axon, Patrick, Laitt, Roger, Thomas, Owen, Afridi, Shazia K., Obholzer, Rupert, Duff, Chris, Stivaros, Stavros M., Vassallo, Grace, Harkness, Elaine F., Smith, Miriam J.

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Mainstreaming germline BRCA1/2 testing in non-mucinous epithelial ovarian cancer in the North West of England von Flaum, Nicola, Morgan, Robert D, Burghel, George J, Bulman, Michael, Clamp, Andrew R, Hasan, Jurjees, Mitchell, Claire L, Badea, Doina, Moon, Sarah, Hogg, Martin, Hadjiyiannakis, Dennis, Clancy, Tara, Schlecht, Helene, Woodward, Emma R, Crosbie, Emma J, Edmondson, Richard J, Wallace, Andrew J, Jayson, Gordon C, Lalloo, Fiona I, Harkness, Elaine F, Evans, D Gareth R

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BRCA1/2 in non-mucinous epithelial ovarian cancer: tumour with or without germline testing? von Morgan, Robert D., Burghel, George J., Flaum, Nicola, Bulman, Michael, Smith, Philip, Clamp, Andrew R., Hasan, Jurjees, Mitchell, Claire L., Salih, Zena, Woodward, Emma R., Lalloo, Fiona, Crosbie, Emma J., Edmondson, Richard J., Wallace, Andrew J., Jayson, Gordon C., Evans, D. Gareth R.

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Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer von Morgan, Robert D, Burghel, George J, Flaum, Nicola, Bulman, Michael, Smith, Philip, Clamp, Andrew R, Hasan, Jurjees, Mitchell, Claire, Salih, Zena, Woodward, Emma R, Lalloo, Fiona, Shaw, Joseph, Desai, Sudha, Crosbie, Emma J, Edmondson, Richard J, Schlecht, Helene, Wallace, Andrew J, Jayson, Gordon C, Evans, D Gareth R

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Early Adaptation of Colorectal Cancer Cells to the Peritoneal Cavity Is Associated with Activation of "Stemness" Programs and Local Inflammation von Barriuso, Jorge, Nagaraju, Raghavendar T, Belgamwar, Shreya, Chakrabarty, Bipasha, Burghel, George J, Schlecht, Helene, Foster, Lucy, Kilgour, Elaine, Wallace, Andrew J, Braun, Michael, Dive, Caroline, Evans, D Gareth, Bristow, Robert G, Saunders, Mark P, O'Dwyer, Sarah T, Aziz, Omer

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HNRNPA1 promotes recognition of splice site decoys by U2AF2 in vivo von Howard, Jonathan M, Lin, Hai, Wallace, Andrew J, Kim, Garam, Draper, Jolene M, Haeussler, Maximilian, Katzman, Sol, Toloue, Masoud, Liu, Yunlong, Sanford, Jeremy R

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Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK) von Loong, Lucy, Garrett, Alice, Allen, Sophie, Choi, Subin, Durkie, Miranda, Callaway, Alison, Drummond, James, Burghel, George J, Robinson, Rachel, Torr, Beth, Berry, Ian R, Wallace, Andrew J, Eccles, Diana M, Ellard, Sian, Baple, Emma, Evans, D Gareth, Woodward, Emma R, Kulkarni, Anjana, Lalloo, Fiona, Tischkowitz, Marc, Lucassen, Anneke, Hanson, Helen, Turnbull, Clare

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