Multilocus Inherited Neoplasia Allele Syndrome (MINAS): an update

por McGuigan, Anthony, Whitworth, James, Andreou, Avgi, Hearn, Timothy, Tischkowitz, Marc, Maher, Eamonn R.
Publicado 2022

Elongin C (ELOC/TCEB1)-associated von Hippel–Lindau disease

por Andreou, Avgi, Yngvadottir, Bryndis, Bassaganyas, Laia, Clark, Graeme, Martin, Ezequiel, Whitworth, James, Cornish, Alex J, Houlston, Richard S, Rich, Philip, Egan, Catherine, Hodgson, Shirley V, Warren, Anne Y, Snape, Katie, Maher, Eamonn R
Publicado 2022

Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases

por Yngvadottir, Bryndis, Andreou, Avgi, Bassaganyas, Laia, Larionov, Alexey, Cornish, Alex J, Chubb, Daniel, Saunders, Charlie N, Smith, Philip S, Zhang, Huairen, Cole, Yasemin, Research Consortium, Genomics England, Larkin, James, Browning, Lisa, Turajlic, Samra, Litchfield, Kevin, Houlston, Richard S, Maher, Eamonn R
Publicado 2022

Seventh BHD international symposium: recent scientific and clinical advancement

por Woodford, Mark R., Andreou, Avgi, Baba, Masaya, van de Beek, Irma, Di Malta, Chiara, Glykofridis, Iris, Grimes, Hannah, Henske, Elizabeth P., Iliopoulos, Othon, Kurihara, Masatoshi, Lazor, Romain, Linehan, W. Marston, Matsumoto, Kenki, Marciniak, Stefan J., Namba, Yukiko, Pause, Arnim, Rajan, Neil, Ray, Anindita, Schmidt, Laura S., Shi, Wei, Steinlein, Ortrud K., Thierauf, Julia, Zoncu, Roberto, Webb, Anna, Mollapour, Mehdi
Publicado 2022