Gastrointestinal Stromal Tumours (GISTs) with KRAS Mutation: A Rare but Important Subset of GISTs

por Mullen, Dorinda, Vajpeyi, Rajkumar, Capo-Chichi, Jose-Mario, Nowak, Klaudia, Wong, Newton, Chetty, Runjan
Publicado 2023

Molecular characterization of AML‐MRC reveals TP53 mutation as an adverse prognostic factor irrespective of MRC‐defining criteria, TP53 allelic state, or TP53 variant allele...

por Zhao, Davidson, Eladl, Entsar, Zarif, Mojgan, Capo‐Chichi, José‐Mario, Schuh, Andre, Atenafu, Eshetu, Minden, Mark, Chang, Hong
Publicado 2022

SmMIP-tools: a computational toolset for processing and analysis of single-molecule molecular inversion probes-derived data

por Medeiros, Jessie J F, Capo-Chichi, Jose-Mario, Shlush, Liran I, Dick, John E, Arruda, Andrea, Minden, Mark D, Abelson, Sagi
Publicado 2022

TP53 Mutations in AML Patients Are Associated with Dismal Clinical Outcome Irrespective of Frontline Induction Regimen and Allogeneic Hematopoietic Cell Transplantation

por Zhao, Davidson, Zarif, Mojgan, Zhou, Qianghua, Capo-Chichi, José-Mario, Schuh, Andre, Minden, Mark D., Atenafu, Eshetu G., Kumar, Rajat, Chang, Hong
Publicado 2023

Heterogenous loss of mismatch repair (MMR) protein expression: a challenge for immunohistochemical interpretation and microsatellite instability (MSI) evaluation

por McCarthy, Aoife J, Capo‐Chichi, Jose‐Mario, Spence, Tara, Grenier, Sylvie, Stockley, Tracy, Kamel‐Reid, Suzanne, Serra, Stefano, Sabatini, Peter, Chetty, Runjan
Publicado 2018

P1040: FACTORS ASSOCIATED WITH THROMBOSIS IN MYELOFIBROSIS

por Bankar, Aniket, Gupta, Gopila, Cheung, Verna, Claudio, Jaime O., Arruda, Andrea, Tsui, Hubert, Capo-Chichi, Jose-Mario, Sibai, Hassan, Davidson, Marta, Maze, Dawn, Gupta, Vikas
Publicado 2023

The Impairment of MAGMAS Function in Human Is Responsible for a Severe Skeletal Dysplasia

por Mehawej, Cybel, Delahodde, Agnès, Legeai-Mallet, Laurence, Delague, Valérie, Kaci, Nabil, Desvignes, Jean-Pierre, Kibar, Zoha, Capo-Chichi, José-Mario, Chouery, Eliane, Munnich, Arnold, Cormier-Daire, Valérie, Mégarbané, André
Publicado 2014

Cardiovascular Disease Among Patients With AML and CHIP-Related Mutations

por Calvillo-Argüelles, Oscar, Schoffel, Alice, Capo-Chichi, José-Mario, Abdel-Qadir, Husam, Schuh, Andre, Carrillo-Estrada, Montserrat, Liu, Shiying, Gupta, Vikas, Schimmer, Aaron D., Yee, Karen, Shlush, Liran I., Natarajan, Pradeep, Thavendiranathan, Paaladinesh
Publicado 2022

Single cell proteogenomic sequencing identifies a relapse‐fated AML subclone carrying FLT3‐ITD with CN‐LOH at chr13q

por Kim, TaeHyung, Lee, Hyewon, Capo‐Chichi, Jose‐Mario, Chang, Myung Hee, Yoo, Young Seok, Basi, Gurbaksh, Ketela, Troy, Smith, Adam C., Tierens, Anne, Zhang, Zhaolei, Minden, Mark D., Kim, Dennis Dong Hwan
Publicado 2022

Biallelic disruption of DDX41 activity is associated with distinct genomic and immunophenotypic hallmarks in acute leukemia

por Tierens, Anne, Kagotho, Elizabeth, Shinriki, Satoru, Seto, Andrew, Smith, Adam C., Care, Melanie, Maze, Dawn, Sibai, Hassan, Yee, Karen W., Schuh, Andre C., Kim, Dennis Dong Hwan, Gupta, Vikas, Minden, Mark D., Matsui, Hirotaka, Capo-Chichi, José-Mario
Publicado 2023

Association of frailty with clinical outcomes in myelofibrosis: a retrospective cohort study

por Bankar, Aniket, Alibhai, Shabbir, Smith, Elliot, Yang, Dongyang, Malik, Sarah, Cheung, Verna, Siddiq, Nancy, Claudio, Jaime, Arruda, Andrea, Tsui, Hubert, Capo‐Chichi, Jose‐Mario, Kennedy, James A., McNamara, Caroline, Sibai, Hassan, Maze, Dawn, Xu, Wei, Gupta, Vikas
Publicado 2021

P421: TARGETED DISRUPTION OF HUMAN FLT3 ERADICATES LEUKEMIC STEM CELLS WITHOUT HARMING HEALTHY HEMATOPOIETIC STEM CELLS

por Araújo, Joana, Wagenblast, Elvin, Voisin, Veronique, Mcleod, Jessica, Gan, Olga, Jin, Liqing, Mitchell, Amanda, Gratton, Blaise, Cutting, Sarah, Arruda, Andrea, Doedens, Monica, Capo-Chichi, Jose-Mario, Minden, Mark, Sobrinho-Simões, Manuel, Pinto-Do-Ó, Perpétua, Lechman, Eric, Dick, John
Publicado 2023

De Novo Mutations in Moderate or Severe Intellectual Disability

por Hamdan, Fadi F., Srour, Myriam, Capo-Chichi, Jose-Mario, Daoud, Hussein, Nassif, Christina, Patry, Lysanne, Massicotte, Christine, Ambalavanan, Amirthagowri, Spiegelman, Dan, Diallo, Ousmane, Henrion, Edouard, Dionne-Laporte, Alexandre, Fougerat, Anne, Pshezhetsky, Alexey V., Venkateswaran, Sunita, Rouleau, Guy A., Michaud, Jacques L.
Publicado 2014

Clinical and molecular correlates of JAK-inhibitor therapy failure in myelofibrosis: long-term data from a molecularly annotated cohort

por England, James T., McNamara, Caroline J., Kennedy, James A., Capo-Chichi, Jose-Mario, Huang, Jingyue, Arruda, Andrea, Nye, Taylor, Cheung, Verna, Claudio, Jaime O., Maze, Dawn, Sibai, Hassan, Tierens, Anne, Tsui, Hubert, Bankar, Aniket, Xu, Wei, Stockley, Tracy, Gupta, Vikas
Publicado 2022

Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

por Brue, Thierry, Quentien, Marie-Hélène, Khetchoumian, Konstantin, Bensa, Marco, Capo-Chichi, José-Mario, Delemer, Brigitte, Balsalobre, Aurelio, Nassif, Christina, Papadimitriou, Dimitris T, Pagnier, Anne, Hasselmann, Caroline, Patry, Lysanne, Schwartzentruber, Jeremy, Souchon, Pierre-François, Takayasu, Shinobu, Enjalbert, Alain, Van Vliet, Guy, Majewski, Jacek, Drouin, Jacques, Samuels, Mark E
Publicado 2014