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Journal Articles

CD371-positive pediatric B-cell acute lymphoblastic leukemia: propensity to lineage switch and slow early response to treatment

Blood (2024) 143 (17): 1738–1751.

https://doi.org/10.1182/blood.2023021952

Published: 2024

Includes: Supplemental data

Journal Articles

Nanopore Cas9-Targeted Long-Read Sequencing - a Fast and Flexible Diagnostic Tool for the Identification of B-Cell Acute Lymphoblastic Leukemia Associated Gene Rearrangements

Kathrin Liszt, Maximilian von der Linde, Dagmar Schinnerl, Karin Nebral, Sabine Strehl, Andishe Attarbaschi, Oskar A. Haas, Stefan Koehrer

Blood (2023) 142 (Supplement 1): 2984.

https://doi.org/10.1182/blood-2023-178519

Published: 2023

Journal Articles

Somatic and Germline Cohesin Genes Alterations in Pediatric Acute Lymphoblastic Leukemia

Blood (2023) 142 (Supplement 1): 1600.

https://doi.org/10.1182/blood-2023-189244

Published: 2023

Journal Articles

ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells

Blood (2022) 139 (3): 399–412.

https://doi.org/10.1182/blood.2020010405

Published: 2022

Includes: Supplemental data

Journal Articles

NUTM1 -Rearranged Infant and Pediatric B Cell Precursor Acute Lymphoblastic Leukemia: A Good Prognostic Subtype Identified in a Collaborative International Study

Blood (2020) 136 (Supplement 1): 25–26.

https://doi.org/10.1182/blood-2020-139376

Published: 2020

Journal Articles

A Comprehensive FISH- and Array-Based Diagnostic Screeningstrategy for the Assessment of Clinically Relevant Genetic Parameters: A Prospective Analysis of 205 Childhood ALL Cases

Oskar A. Haas, MD, Karin Nebral, PhD, Sabrina Haslinger, BSc, Andrea Inthal, PhD, Margit König, Sabine Strehl, PhD, Renate Panzer-Grümayer, MD, Andishe Attarbaschi, MD, Georg Mann, MD

Blood (2018) 132 (Supplement 1): 4082.

https://doi.org/10.1182/blood-2018-99-115761

Published: 2018

Journal Articles

The role of the Janus-faced transcription factor PAX5-JAK2 in acute lymphoblastic leukemia

Dagmar Schinnerl, Klaus Fortschegger, Maximilian Kauer, João R. M. Marchante, Reinhard Kofler, Monique L. Den Boer, Sabine Strehl

Blood (2015) 125 (8): 1282–1291.

https://doi.org/10.1182/blood-2014-04-570960

Published: 2015

Includes: Supplemental data

Journal Articles

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/ MLL -rearranged AML patients: results of an international study

Blood (2011) 117 (26): 7102–7111.

https://doi.org/10.1182/blood-2010-12-328302

Published: 2011

Includes: Supplemental data

Journal Articles

ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling

Lilian Kuster, Reinhard Grausenburger, Gerhard Fuka, Ulrike Kaindl, Gerd Krapf, Andrea Inthal, Georg Mann, Maximilian Kauer, Johannes Rainer, Reinhard Kofler, Andrew Hall, Markus Metzler, Lüder Hinrich Meyer, Claus Meyer, Jochen Harbott, Rolf Marschalek, Sabine Strehl, Oskar A. Haas, Renate Panzer-Grümayer

Blood (2011) 117 (9): 2658–2667.

https://doi.org/10.1182/blood-2010-03-275347

Published: 2011

Includes: Supplemental data

Journal Articles

Clinical Impact of Additional Cytogenetic Aberrations and Complex Karyotype In Pediatric 11q23/ MLL -Rearranged AML: Results from an International Retrospective Study

Blood (2010) 116 (21): 762.

https://doi.org/10.1182/blood.V116.21.762.762

Published: 2010

Journal Articles

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2 : a report from the International BFM Study Group

Blood (2010) 115 (5): 1006–1017.

https://doi.org/10.1182/blood-2009-08-235408

Published: 2010

Includes: Supplemental data

Journal Articles

DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.

Blood (2009) 114 (22): 11.

https://doi.org/10.1182/blood.V114.22.11.11

Published: 2009

Journal Articles

Novel prognostic subgroups in childhood 11q23/ MLL -rearranged acute myeloid leukemia: results of an international retrospective study

Blood (2009) 114 (12): 2489–2496.

https://doi.org/10.1182/blood-2009-04-215152

Published: 2009

Includes: Supplemental data

Journal Articles

Sequential Order of Genetic Events in NUP214-ABL1 Positive T-Cell Leukemia.

Markus Pisecker, Lisa Arzt, Margit König, Reinhard Ullmann, Sabine Strehl

Blood (2008) 112 (11): 2054.

https://doi.org/10.1182/blood.V112.11.2054.2054

Published: 2008

Journal Articles

Juxtaposition of the BCL11B Gene to a Novel Region at 17q by a t(14;17)(q32;Q21) in Childhood T-Cell Lymphoblastic Lymphoma.

Sabine Strehl, PhD, Margit König, Katharina Spath, Markus Pisecker, MSc, Georg Mann, MD

Blood (2007) 110 (11): 4130.

https://doi.org/10.1182/blood.V110.11.4130.4130

Published: 2007

Journal Articles

Collaboration between Activating Mutations in JAK2 and Trisomy 21 in the Acute Lymphoblastic Leukemias of Down Syndrome (DS).

Blood (2007) 110 (11): LB6.

https://doi.org/10.1182/blood.V110.11.LB6.lb6

Published: 2007

Journal Articles

A Novel Fusion between ETV6 and NCOA2 Defines a New Entity of Acute Leukemia with Co-Expression of T-Cell and Myeloid Markers.

Sabine Strehl, Karin Nebral, Margit König, Jochen Harbott, Bella Bielorai, Stephanie Struski, Shai Izraeli, Oskar A. Haas

Blood (2006) 108 (11): 804.

https://doi.org/10.1182/blood.V108.11.804.804

Published: 2006

Journal Articles

Topoisomerase (DNA) II Beta 180 kDa TOP2B ) - A New NUP98 Fusion Partner.

Sabine Strehl, PhD, Karin Nebral, MSc, Helmut H. Schmidt, MD, Oskar A. Haas, MD

Blood (2005) 106 (11): 2849.

https://doi.org/10.1182/blood.V106.11.2849.2849

Published: 2005

Journal Articles

Treatment Response and Outcome in Childhood t(1;19)/ TCF3-PBX1 Positive Acute Lymphoblastic Leukemia: A Report from the Austrian BFM Group.

Leo Kager, MD, Thomas Lion, MD, PhD, Andishe Attarbaschi, MD, Margit Koenig, PhD, Sabine Strehl, PhD, Oskar A. Haas, MD, Michael N. Dworzak, MD, Martin Schrappe, MD, PhD, Helmut Gadner, MD, Georg Mann, MD

Blood (2005) 106 (11): 1458.

https://doi.org/10.1182/blood.V106.11.1458.1458

Published: 2005

Journal Articles

A DNA-Based RQ-PCR Screening Assay for the Identification of Cases with RUNX1 Copy Number Changes in Childhood B Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL).

Oskar A. Haas, MD, Anne Moritz, MS, Martin Stanulla, MD, Margit Koenig, Sylvia Roettgers, PhD, Carsten Reichelt, PhD, Jochen Harbott, PhD, Sabine Strehl, PhD, Martin Schrappe, MD

Blood (2005) 106 (11): 90.

https://doi.org/10.1182/blood.V106.11.90.90

Published: 2005

NARROW

CD371-positive pediatric B-cell acute lymphoblastic leukemia: propensity to lineage switch and slow early response to treatment

Nanopore Cas9-Targeted Long-Read Sequencing - a Fast and Flexible Diagnostic Tool for the Identification of B-Cell Acute Lymphoblastic Leukemia Associated Gene Rearrangements

Somatic and Germline Cohesin Genes Alterations in Pediatric Acute Lymphoblastic Leukemia

ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells

NUTM1 -Rearranged Infant and Pediatric B Cell Precursor Acute Lymphoblastic Leukemia: A Good Prognostic Subtype Identified in a Collaborative International Study

A Comprehensive FISH- and Array-Based Diagnostic Screeningstrategy for the Assessment of Clinically Relevant Genetic Parameters: A Prospective Analysis of 205 Childhood ALL Cases

The role of the Janus-faced transcription factor PAX5-JAK2 in acute lymphoblastic leukemia

Prognostic significance of additional cytogenetic aberrations in 733 de novo pediatric 11q23/ MLL -rearranged AML patients: results of an international study

ETV6/RUNX1-positive relapses evolve from an ancestral clone and frequently acquire deletions of genes implicated in glucocorticoid signaling

Clinical Impact of Additional Cytogenetic Aberrations and Complex Karyotype In Pediatric 11q23/ MLL -Rearranged AML: Results from an International Retrospective Study

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2 : a report from the International BFM Study Group

DOWN'S Syndrome Acute Lymphoblastic LEUKEMIA: A HIGHLY Heterogeneous DISEASE DRIVEN by an Aberrant CRLF2/JAK2 Cooperation – A REPORT FROM the Ibfm-STUDY GROUP.

Novel prognostic subgroups in childhood 11q23/ MLL -rearranged acute myeloid leukemia: results of an international retrospective study

Sequential Order of Genetic Events in NUP214-ABL1 Positive T-Cell Leukemia.

Juxtaposition of the BCL11B Gene to a Novel Region at 17q by a t(14;17)(q32;Q21) in Childhood T-Cell Lymphoblastic Lymphoma.

Collaboration between Activating Mutations in JAK2 and Trisomy 21 in the Acute Lymphoblastic Leukemias of Down Syndrome (DS).

A Novel Fusion between ETV6 and NCOA2 Defines a New Entity of Acute Leukemia with Co-Expression of T-Cell and Myeloid Markers.

Topoisomerase (DNA) II Beta 180 kDa TOP2B ) - A New NUP98 Fusion Partner.

Treatment Response and Outcome in Childhood t(1;19)/ TCF3-PBX1 Positive Acute Lymphoblastic Leukemia: A Report from the Austrian BFM Group.

A DNA-Based RQ-PCR Screening Assay for the Identification of Cases with RUNX1 Copy Number Changes in Childhood B Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL).

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American Society of Hematology

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American Society of Hematology

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