Screening of potential novel candidate genes in schwannomatosis patients

por Perez‐Becerril, Cristina, Wallace, Andrew J., Schlecht, Helene, Bowers, Naomi L., Smith, Philip T., Gokhale, Carolyn, Eaton, Helen, Charlton, Chris, Robinson, Rachel, Charlton, Ruth S., Evans, D. Gareth, Smith, Miriam J.
Publicado 2022

Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in BRCA1, BRCA2, and TP53 Genes in Women with Very Early-Onset (<36 Years) Breast Cancer

por Hyder, Zerin, Harkness, Elaine F., Woodward, Emma R., Bowers, Naomi L., Pereira, Marta, Wallace, Andrew J., Howell, Sacha J., Howell, Anthony, Lalloo, Fiona, Newman, William G., Smith, Miriam J., Evans, D Gareth
Publicado 2020

Re‐evaluation of missense variant classifications in NF2

por Sadler, Katherine V., Rowlands, Charlie F., Smith, Philip T., Hartley, Claire L., Bowers, Naomi L., Roberts, Nicola Y., Harris, Jade L., Wallace, Andrew J., Evans, D. Gareth, Messiaen, Ludwine M., Smith, Miriam J.
Publicado 2022

Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior BRCA1/2 Probability

por Evans, D. Gareth, van Veen, Elke M., Woodward, Emma R., Harkness, Elaine F., Ellingford, Jamie M., Bowers, Naomi L., Wallace, Andrew J., Howell, Sacha J., Howell, Anthony, Lalloo, Fiona, Newman, William G., Smith, Miriam J.
Publicado 2021

Extended gene panel testing in lobular breast cancer

por van Veen, Elke M., Evans, D. Gareth, Harkness, Elaine F., Byers, Helen J., Ellingford, Jamie M., Woodward, Emma R., Bowers, Naomi L., Wallace, Andrew J., Howell, Sacha J., Howell, Anthony, Lalloo, Fiona, Newman, William G., Smith, Miriam J.
Publicado 2021

Clinical utility of testing for PALB2 and CHEK2 c.1100delC in breast and ovarian cancer

por Woodward, Emma R., van Veen, Elke M., Forde, Claire, Harkness, Elaine F., Byers, Helen J., Ellingford, Jamie M., Burghel, George J., Schlech, Helene, Bowers, Naomi L., Wallace, Andrew J., Howell, Sacha J., Howell, Anthony, Lalloo, Fiona, Newman, William G., Smith, Miriam J., Gareth Evans, D.
Publicado 2021

High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer

por Evans, D Gareth, van Veen, Elke Maria, Byers, Helen J, Evans, Sarah J, Burghel, George J, Woodward, Emma Roisin, Harkness, Elaine F, Eccles, Diana M, Greville-Haygate, Stephanie L, Ellingford, Jamie M, Bowers, Naomi L, Pereira, Marta, Wallace, Andrew J, Howell, Sasha J, Howell, Anthony, Lalloo, Fiona, Newman, William G, Smith, Miriam Jane
Publicado 2022

Implementation of Multigene Germline and Parallel Somatic Genetic Testing in Epithelial Ovarian Cancer: SIGNPOST Study

por Chandrasekaran, Dhivya, Sobocan, Monika, Blyuss, Oleg, Miller, Rowan E., Evans, Olivia, Crusz, Shanthini M., Mills-Baldock, Tina, Sun, Li, Hammond, Rory F. L., Gaba, Faiza, Jenkins, Lucy A., Ahmed, Munaza, Kumar, Ajith, Jeyarajah, Arjun, Lawrence, Alexandra C., Brockbank, Elly, Phadnis, Saurabh, Quigley, Mary, El Khouly, Fatima, Wuntakal, Rekha, Faruqi, Asma, Trevisan, Giorgia, Casey, Laura, Burghel, George J., Schlecht, Helene, Bulman, Michael, Smith, Philip, Bowers, Naomi L., Legood, Rosa, Lockley, Michelle, Wallace, Andrew, Singh, Naveena, Evans, D. Gareth, Manchanda, Ranjit
Publicado 2021