A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

Tekijä Garg, Paras, Jadhav, Bharati, Rodriguez, Oscar L., Patel, Nihir, Martin-Trujillo, Alejandro, Jain, Miten, Metsu, Sofie, Olsen, Hugh, Paten, Benedict, Ritz, Beate, Kooy, R. Frank, Gecz, Jozef, Sharp, Andrew J.
Julkaisussa Am J Hum Genet (2020)

FRA2A Is a CGG Repeat Expansion Associated with Silencing of AFF3

Tekijä Metsu, Sofie, Rooms, Liesbeth, Rainger, Jacqueline, Taylor, Martin S., Bengani, Hemant, Wilson, David I., Chilamakuri, Chandra Sekhar Reddy, Morrison, Harris, Vandeweyer, Geert, Reyniers, Edwin, Douglas, Evelyn, Thompson, Geoffrey, Haan, Eric, Gecz, Jozef, FitzPatrick, David R., Kooy, R. Frank
Julkaistu 2014

Multidisciplinary molecular tumour board: a tool to improve clinical practice and selection accrual for clinical trials in patients with cancer

Tekijä Rolfo, Christian, Manca, Paolo, Salgado, Roberto, Van Dam, Peter, Dendooven, Amelie, Machado Coelho, Andreia, Ferri Gandia, Jose, Rutten, Annemie, Lybaert, Willem, Vermeij, Joanna, Gevaert, Thomas, Weyn, Christine, Lefebure, Anneke, Metsu, Sofie, Van Laere, Steven, Peeters, Marc, Pauwels, Patrick
Julkaisussa ESMO Open (2018)