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Phenotypic profiling with a living biobank of primary rhabdomyosarcoma unravels disease heterogeneity and AKT sensitivity

Nature communications, 2020-09, Vol.11 (1), p.4629-4629, Article 4629

2020

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Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups

Cancer, 2016-12, Vol.122 (24), p.3821-3830

2016

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True Donor Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation: Diagnostic and Therapeutic Considerations-Brief Report

Current oncology (Toronto), 2024-04, Vol.31 (4), p.2067-2075

2024

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Histological and molecular characterization of TFEB-rearranged renal cell carcinomas

Virchows Archiv : an international journal of pathology, 2019-05, Vol.474 (5), p.625-631

2019

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Mutational patterns in therapy-related acute lymphoblastic leukemia subgroups: one step closer to unveiling the genetic odyssey

Leukemia & lymphoma, 2024-05, Vol.65 (6), p.1-815

2024

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Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia

Genes chromosomes & cancer, 2020-04, Vol.59 (4), p.268-274

2020

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Microarray‐based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype

British journal of haematology, 2019-01, Vol.184 (2), p.282-287

2019

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CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.936-943

2020

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The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia

Blood, 2008-05, Vol.111 (9), p.4668-4680

2008

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Ex vivo drug response heterogeneity reveals personalized therapeutic strategies for patients with multiple myeloma

Nature cancer, 2023-05, Vol.4 (5), p.734-753

2023

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Long-term transfusion independence in del(5q) MDS patients after short term therapy with lenalidomide: 2 new cases

Leukemia research, 2012-05, Vol.36 (5), p.656-657

2012

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Molecular Characterization of TMPRSS2-ERG Gene Fusion in the NCI-H660 Prostate Cancer Cell Line: A New Perspective for an Old Model

Neoplasia (New York, N.Y.), 2007-03, Vol.9 (3), p.200,IN3-206,IN3

2007

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Hotspots for Copy Number Variation in Chimpanzees and Humans

Proceedings of the National Academy of Sciences - PNAS, 2006-05, Vol.103 (21), p.8006-8011

2006

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Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray‐based comparative genomic hybridization

British journal of haematology, 2004-08, Vol.126 (4), p.495-500

2004

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Successful Combination of Sequential Gene Therapy and Rescue Allo-HSCT in Two Children with X-CGD - Importance of Timing

Current gene therapy, 2015-01, Vol.15 (4), p.416-427

2015

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Detecting copy number variation in the human genome using comparative genomic hybridization

BioTechniques, 2006-10, Vol.41 (4), p.385-392

2006

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Targeted therapeutic approach for an anaplastic thyroid cancer in vitro and in vivo

Cancer science, 2008-09, Vol.99 (9), p.1847-1852

2008

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A New t(7;9)(p12;q34) Involving NOTCH1 and IKZF1 in Pediatric T-Cell Lymphoblastic Lymphoma

Blood, 2023-11, Vol.142 (Supplement 1), p.5734-5734

2023

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Double hit, triple hit—look for it

Blood, 2013-03, Vol.121 (13), p.2383-2383

2013

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Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

Nature medicine, 2021-10, Vol.27 (10), p.1806-1817

2021

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Myoepithelial Carcinoma of Soft Tissue With an EWSR1-KLF15 Gene Fusion in an Infant

Pediatric and developmental pathology, 2021-08, Vol.24 (4), p.371-377

2021

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Phenotypic profiling with a living biobank of primary rhabdomyosarcoma unravels disease heterogeneity and AKT sensitivity

Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups

True Donor Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation: Diagnostic and Therapeutic Considerations-Brief Report

Histological and molecular characterization of TFEB-rearranged renal cell carcinomas

Mutational patterns in therapy-related acute lymphoblastic leukemia subgroups: one step closer to unveiling the genetic odyssey

Detection of rare reciprocal RUNX1 rearrangements by next‐generation sequencing in acute myeloid leukemia

Microarray‐based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype

Targeting receptor kinases by a novel indolinone derivative in multiple myeloma: abrogation of stroma-derived interleukin-6 secretion and induction of apoptosis in cytogenetically defined subgroups

CRISPR-Directed Therapeutic Correction at the NCF1 Locus Is Challenged by Frequent Incidence of Chromosomal Deletions

The recurrent SET-NUP214 fusion as a new HOXA activation mechanism in pediatric T-cell acute lymphoblastic leukemia

Ex vivo drug response heterogeneity reveals personalized therapeutic strategies for patients with multiple myeloma

Long-term transfusion independence in del(5q) MDS patients after short term therapy with lenalidomide: 2 new cases

Molecular Characterization of TMPRSS2-ERG Gene Fusion in the NCI-H660 Prostate Cancer Cell Line: A New Perspective for an Old Model

Hotspots for Copy Number Variation in Chimpanzees and Humans

Double Induction Containing Either Two Courses or One Course of High-Dose Cytarabine Plus Mitoxantrone and Postremission Therapy by Either Autologous Stem-Cell Transplantation or by Prolonged Maintenance for Acute Myeloid Leukemia

Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray‐based comparative genomic hybridization

Successful Combination of Sequential Gene Therapy and Rescue Allo-HSCT in Two Children with X-CGD - Importance of Timing

Detecting copy number variation in the human genome using comparative genomic hybridization

Targeted therapeutic approach for an anaplastic thyroid cancer in vitro and in vivo

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

A New t(7;9)(p12;q34) Involving NOTCH1 and IKZF1 in Pediatric T-Cell Lymphoblastic Lymphoma

Double hit, triple hit—look for it

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

Myoepithelial Carcinoma of Soft Tissue With an EWSR1-KLF15 Gene Fusion in an Infant

Ex vivo drug response profiling detects recurrent sensitivity patterns in drug-resistant acute lymphoblastic leukemia

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