S. Quentin

发表

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.

F. Sigaux, J. Soulier, A. Baruchel, 2011, Blood.

Actinomycin D Targets NPM1c-Primed Mitochondria to Restore PML-Driven Senescence in AML Therapy

P. Bénit, T. Mak, J. Soulier, 2021, Cancer discovery.

First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

E. Pasmant, M. Vidaud, O. Farges, 2011, European Journal of Human Genetics.

Germline DDX41 mutations define a significant entity within adult MDS/AML patients.

J. Soulier, E. Clappier, H. Dombret, 2019, Blood.

Concurrent CDX2 cis-deregulation and UBTF::ATXN7L3 fusion define a novel high-risk subtype of B-cell ALL

F. Sigaux, J. Soulier, E. Clappier, 2022, Blood.

Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.

J. Soulier, E. Solary, P. Dessen, 2019, Blood.

Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma

J. Soulier, P. Rohrlich, C. Borg, 2014, Journal of Hematology & Oncology.

Insertion of an extra copy of Xq22.2 into 1p36 results in functional duplication of the PLP1 gene in a girl with classical Pelizaeus-Merzbacher disease

M. Elmaleh, O. Boespflug-Tanguy, J. Masliah-planchon, 2015, BMC Medical Genetics.

Exploration of nuclear body-enhanced sumoylation reveals that PML represses 2-cell features of embryonic stem cells

H. de Thé, R. González-Prieto, A. Vertegaal, 2022, Nature Communications.

Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission.

J. Soulier, J. Cayuela, H. Dombret, 2010, Blood.

Granulomonocytic progenitors are key target cells of azacytidine in higher risk myelodysplastic syndromes and acute myeloid leukemia

J. Soulier, E. Clappier, H. Dombret, 2018, Leukemia.

e- Blood Myelodysplasia and leukemia of Fanconi anemia are associated with a speciﬁc pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

F. Sigaux, J. Soulier, A. Baruchel, 2011 .

Copy-number analysis identified new prognostic marker in acute myeloid leukemia

J. Soulier, H. Dombret, B. Quesnel, 2017, Leukemia.

A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.

J. Soulier, E. Clappier, A. Baruchel, 2018, Blood.

Reversal of microRNA-150 silencing disadvantages crizotinib-resistant NPM-ALK(+) cell growth.

P. Brousset, S. Spicuglia, P. Ferrier, 2015, The Journal of clinical investigation.

FLT3-ITD impedes retinoic acid, but not arsenic, responses in murine acute promyelocytic leukemias.

S. Kogan, H. de Thé, C. Gaillard, 2019, Blood.

Unbiased in vivo exploration of nuclear bodies-enhanced sumoylation reveals that PML orchestrates embryonic stem cell fate

H. de Thé, R. González-Prieto, A. Vertegaal, 2021, bioRxiv.

Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.

E. Gilson, F. Sigaux, J. Soulier, 2023, Cell stem cell.

Meningioma progression in mice triggered by Nf2 and Cdkn2ab inactivation

A. Stemmer-Rachamimov, M. Giovannini, N. Karboul, 2013, Oncogene.

Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies

P. Gressens, A. Toutain, N. Chassaing, 2012, European Journal of Human Genetics.

Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly.

C. Fallet-Bianco, S. Gazal, A. Laquérriere, 2012, American journal of human genetics.

Deletion 6q Drives T-cell Leukemia Progression by Ribosome Modulation.

F. Sigaux, J. Soulier, E. Clappier, 2018, Cancer discovery.

Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies

B. Gilbert-Dussardier, M. Gonzalès, B. Grandchamp, 2011, Neuromuscular Disorders.

Clonal dominance is an adverse prognostic factor in acute myeloid leukemia treated with intensive chemotherapy

J. Soulier, E. Clappier, H. Dombret, 2020, Leukemia.

PAX5 P80R mutation identifies a novel subtype of B-cell precursor acute lymphoblastic leukemia with favorable outcome.

F. Sigaux, J. Soulier, E. Clappier, 2019, Blood.

Cullin7: a new gene involved in liver carcinogenesis related to metabolic syndrome

J. Soulier, V. Paradis, P. Bedossa, 2012, Gut.

Exploration of nuclear body-enhanced sumoylation reveals that PML represses 2-cell features of embryonic stem cells

H. de Thé, R. González-Prieto, A. Vertegaal, 2022, Nature Communications.

Association of TET2 Alterations with NPM1 Mutations and Prognostic Value in De Novo Acute Myeloid Leukemia (AML).

J. Soulier, J. Cayuela, H. Dombret, 2009 .

First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

E. Pasmant, M. Vidaud, O. Farges, 2011, European Journal of Human Genetics.

FLT3-ITD impedes retinoic acid, but not arsenic, responses in murine acute promyelocytic leukemias.

S. Kogan, H. de Thé, K. Rice, 2019, Blood.

BET inhibitors impair leukemic stem cell function only in defined oncogenic subgroups of acute myeloid leukaemias.

J. Soulier, E. Clappier, H. Dombret, 2019, Leukemia research.

Structural Basis of PML-RARA Oncoprotein Targeting by Arsenic Unravels a Cysteine Rheostat Controlling PML Body Assembly and Function

H. de Thé, M. Niwa-Kawakita, V. Lallemand-Breitenbach, 2023, Cancer discovery.