PTCH2 is not a strong candidate gene for gorlin syndrome predisposition

por Smith, Miriam J., Evans, D. Gareth
Publicado 2021

Comparison of the frequency of loss‐of‐function LZTR1 variants between schwannomatosis patients and the general population

por Deng, Fanxuan, Evans, D. Gareth, Smith, Miriam J.
Publicado 2022

Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161

por Smith, Miriam J, Woodward, Emma R, Evans, D Gareth
Publicado 2023

Facial Skin Coloration Affects Perceived Health of Human Faces

por Stephen, Ian D., Law Smith, Miriam J., Stirrat, Michael R., Perrett, David I.
Publicado 2009

A mechanistic mathematical model of initiation and malignant transformation in sporadic vestibular schwannoma

por Paterson, Chay, Bozic, Ivana, Smith, Miriam J., Hoad, Xanthe, Evans, D. Gareth R.
Publicado 2022

Epithelial ovarian cancer risk: A review of the current genetic landscape

por Flaum, Nicola, Crosbie, Emma J., Edmondson, Richard J., Smith, Miriam J., Evans, Dafydd G.
Publicado 2019

Characterization of Age-Dependent and Progressive Cortical Neuronal Degeneration in Presenilin Conditional Mutant Mice

por Wines-Samuelson, Mary, Schulte, Eva C., Smith, Miriam J., Aoki, Chiye, Liu, Xinran, Kelleher, Raymond J., Shen, Jie
Publicado 2010

Targeting lung cancer screening to individuals at greatest risk: the role of genetic factors

por Lebrett, Mikey B, Crosbie, Emma J, Smith, Miriam J, Woodward, Emma R, Evans, D Gareth, Crosbie, Philip A J
Publicado 2021

Association between genetic polymorphisms and endometrial cancer risk: a systematic review

por Bafligil, Cemsel, Thompson, Deborah J, Lophatananon, Artitaya, Smith, Miriam J, Ryan, Neil AJ, Naqvi, Anie, Evans, D Gareth, Crosbie, Emma J
Publicado 2020

The spatial phenotype of genotypically distinct meningiomas demonstrate potential implications of the embryology of the meninges

por Fountain, Daniel M., Smith, Miriam J., O’Leary, Claire, Pathmanaban, Omar N., Roncaroli, Federico, Bobola, Nicoletta, King, Andrew T., Evans, Dafydd Gareth
Publicado 2020

Correction: The spatial phenotype of genotypically distinct meningiomas demonstrate potential implications of the embryology of the meninges

por Fountain, Daniel M., Smith, Miriam J., O’Leary, Claire, Pathmanaban, Omar N., Roncaroli, Federico, Bobola, Nicoletta, King, Andrew T., Evans, Dafydd Gareth
Publicado 2021

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

Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma

por Evans, D. Gareth, Messiaen, Ludwine M., Foulkes, William D., Irving, Rachel E. A., Murray, Alexandra J., Perez-Becerril, Cristina, Rivera, Barbara, McDonald-McGinn, Donna M., Stevenson, David A., Smith, Miriam J.
Publicado 2021

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

Pain correlates with germline mutation in schwannomatosis

por Jordan, Justin T., Smith, Miriam J., Walker, James A., Erdin, Serkan, Talkowski, Michael E., Merker, Vanessa L., Ramesh, Vijaya, Cai, Wenli, Harris, Gordon J., Bredella, Miriam A., Seijo, Marlon, Suuberg, Alessandra, Gusella, James F., Plotkin, Scott R.
Publicado 2018

A Dominantly Inherited 5′ UTR Variant Causing Methylation-Associated Silencing of BRCA1 as a Cause of Breast and Ovarian Cancer

por 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.
Publicado 2018

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

Familial unilateral vestibular schwannoma is rarely caused by inherited variants in the NF2 gene

por Evans, D. Gareth, Wallace, Andrew J., Hartley, Claire, Freeman, Simon R., Lloyd, Simon K., Thomas, Owen, Axon, Patrick, Hammerbeck‐Ward, Charlotte L., Pathmanaban, Omar, Rutherford, Scott A., Kellett, Mark, Laitt, Roger, King, Andrew T., Bischetsrieder, Jemma, Blakeley, Jaishri, Smith, Miriam J.
Publicado 2018