PRAME protein expression in DICER1‐related tumours

por Thorner, Paul S, Chong, Anne‐Sophie, Nadaf, Javad, Benlimame, Naciba, Marrano, Paula, Chami, Rose, Fu, Lili, Foulkes, William D
Publicado 2022

PRAME protein expression in DICER1‐related tumours

por Thorner, Paul S, Chong, Anne‐Sophie, Nadaf, Javad, Benlimame, Naciba, Marrano, Paula, Chami, Rose, Fu, Lili, Foulkes, William D
Publicado 2022

DICER1 platform domain missense variants inhibit miRNA biogenesis and lead to tumor susceptibility

por Pelletier, Dylan, Chong, Anne-Laure, Wu, Mona, Witkowski, Leora, Albert, Sophie, Sabbaghian, Nelly, Fabian, Marc R, Foulkes, William D
Publicado 2023

Blending oxytocin and dopamine with everyday creativity

por Chong, Anne, Tolomeo, Serenella, Xiong, Yue, Angeles, Dario, Cheung, Mike, Becker, Benjamin, Lai, Poh San, Lei, Zhen, Malavasi, Fabio, Tang, Qianzi, Chew, Soo Hong, Ebstein, Richard P.
Publicado 2021

Genomic characterization of DICER1-associated neoplasms uncovers molecular classes

por Kommoss, Felix K. F., Chong, Anne-Sophie, Chong, Anne-Laure, Pfaff, Elke, Jones, David T. W., Hiemcke-Jiwa, Laura S., Kester, Lennart A., Flucke, Uta, Gessler, Manfred, Schrimpf, Daniel, Sahm, Felix, Clarke, Blaise A., Stewart, Colin J. R., Wang, Yemin, Gilks, C. Blake, Kommoss, Friedrich, Huntsman, David G., Schüller, Ulrich, Koelsche, Christian, McCluggage, W. Glenn, von Deimling, Andreas, Foulkes, William D.
Publicado 2023

Common clonal origin of chronic myelomonocytic leukemia and B-cell acute lymphoblastic leukemia in a patient with a germline CHEK2 variant

por Bazinet, Alexandre, Heath, John, Chong, Anne-Sophie, Simo-Cheyou, Estelle R., Worme, Samantha, Rivera Polo, Barbara, Foulkes, William D., Caplan, Stephen, Johnson, Nathalie A., Orthwein, Alexandre, Mercier, François E.
Publicado 2021

Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis

por Apellaniz-Ruiz, Maria, Sabbaghian, Nelly, Chong, Anne-Laure, de Kock, Leanne, Cetinkaya, Semra, Bayramoğlu, Elvan, Dinjens, Winand N. M., McCluggage, W. Glenn, Wagner, Anja, Yilmaz, Aslihan Arasli, Foulkes, William D.
Publicado 2023

Poorly differentiated thyroid carcinoma of childhood and adolescence: A distinct entity characterized by DICER1 mutations

por Chernock, Rebecca D, Rivera, Barbara, Borrelli, Nicla, Hill, D. Ashley, Fahiminiya, Somayyeh, Shah, Tasha, Chong, Anne-Sophie, Aqil, Barina, Mehrad, Mitra, Giordano, Thomas J, Sheridan, Rachel, Rutter, Meilan M, Dehner, Louis P., Foulkes, William D., Nikiforov, Yuri E
Publicado 2020

RARE-22. GERMLINE PATHOGENIC VARIANT c.1552G>A;p.E518K IN DGCR8 CONFERS SUSCEPTIBILITY FOR SCHWANNOMATOSIS AND THYROID TUMORS

por Chong, Anne-Sophie, Nadaf, Javad, Grau, Elia, Apellaniz-Ruiz, Maria, Fahiminiya, Somayyeh, Saskin, Avi, Han, HyeRim, Turcotte, Robert, Muchantef, Karl, Thomas, Christian, Wagener, Rabea, Bassenden, Angelia, Mete, Ozgur, Pusztaszeri, Marc, Paulus, Werner, Berghuis, Albert, Siebert, Reiner, Albrecht, Steffen, Hasselblatt, Martin, Lazaro, Conxi, Teule, Alexander, Fabian, Marc, Brunet, Joan, Foulkes, William, Rivera, Barbara
Publicado 2020

A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes

por Gallon, Richard, Mühlegger, Barbara, Wenzel, Sören‐Sebastian, Sheth, Harsh, Hayes, Christine, Aretz, Stefan, Dahan, Karin, Foulkes, William, Kratz, Christian P., Ripperger, Tim, Azizi, Amedeo A., Baris Feldman, Hagit, Chong, Anne‐Laure, Demirsoy, Ugur, Florkin, Benoît, Imschweiler, Thomas, Januszkiewicz‐Lewandowska, Danuta, Lobitz, Stephan, Nathrath, Michaela, Pander, Hans‐Jürgen, Perez‐Alonso, Vanesa, Perne, Claudia, Ragab, Iman, Rosenbaum, Thorsten, Rueda, Daniel, Seidel, Markus G., Suerink, Manon, Taeubner, Julia, Zimmermann, Stefanie‐Yvonne, Zschocke, Johannes, Borthwick, Gillian M., Burn, John, Jackson, Michael S., Santibanez‐Koref, Mauro, Wimmer, Katharina
Publicado 2019