Jean Soulier

发表

Genome-wide DNA profiling of marginal zone lymphomas identifies subtype-specific lesions with an impact on the clinical outcome.

Francesco Bertoni, Ivo Kwee, Govind Bhagat, 2011, Blood.

PHF6 mutations in T-cell acute lymphoblastic leukemia

Rob Pieters, Raul Rabadan, Frank Speleman, 2010, Nature Genetics.

A NOTCH1-driven MYC enhancer promotes T cell development, transformation and acute lymphoblastic leukemia

Teresa Palomero, Carlos Cordon-Cardo, Alberto Ambesi-Impiombato, 2014, Nature Medicine.

Erratum: NOTCH1 directly regulates c-MYC and activates a feed-forward-loop transcriptional network promoting leukemic cell growth (Proceedings of the National Academy of Sciences of the United States of America (2006) 103, 48, (18261-18266) DOI: 10.1073/pnas.0606108103)

Andrew P. Weng, Jon C. Aster, Andrea Califano, 2007 .

Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia

Stein Aerts, Gert Hulselmans, Jan Cools, 2012, Nature Genetics.

Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

Jérôme Larghero, Kenneth Cornetta, Philippe Leboulch, 2010, Nature.

The TLX1 oncogene drives aneuploidy in T-cell transformation

Andrea Califano, Frank Speleman, Susana Raimondi, 2010, Nature Medicine.

Bone marrow microenvironment in fanconi anemia: a prospective functional study in a cohort of fanconi anemia patients.

Jérôme Larghero, Christine Chomienne, Valérie Vanneaux, 2010, Stem cells and development.

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.

Ying Wang, Christopher C. Porter, Anna L. Brown, 2019, Blood advances.