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Journal Articles

Cryptic insertion of KMT2A , a rare t(9;11) variant

Nada Assaf, Christine Terré

Blood (2021) 137 (13): 1843.

https://doi.org/10.1182/blood.2020010442

Published: 2021

Journal Articles

DIS3 Mutation in RUNX1-Mutated AML1 Confers a Highly Dismal Prognosis in AML By Repressing Sister Chromatid Cohesion

Christophe Desterke, PhD, Annelise Bennaceur-Griscelli, MD PhD, Ali G Turhan, MD PhD

Blood (2019) 134 (Supplement_1): 1454.

https://doi.org/10.1182/blood-2019-123352

Published: 2019

Journal Articles

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Claire Schwab, Eigil Kjeldsen, MD DMSc, Nyla A. Heerema, PhD, Andrew Carroll, PhD, Matthew Bashton, PhD, Sarra Ryan, PhD, Anthony V. Moorman, PhD, Stephen P. Hunger, MD, Mignon L. Loh, MD, Henrik Hasle, MD PhD, Christine J Harrison, PhD FRCPath

Blood (2017) 130 (Supplement 1): 3978.

https://doi.org/10.1182/blood.V130.Suppl_1.3978.3978

Published: 2017

Journal Articles

Telomere Length and Somatic Mutation in Aplastic Anemia- Correlation with Response to Treatement

Hee Sue Park, Si Nae Park, Kyoungok Im, Jung Ah Kim, Sang Mee Hwang, Dong Soon Lee

Blood (2016) 128 (22): 1504.

https://doi.org/10.1182/blood.V128.22.1504.1504

Published: 2016

Journal Articles

FANCA Fine-Tunes Chromosome Segregation By Controlling BUBR1 K250 Acetylation at the Kinetochores

Zahi Abdul Sater, Richa Sharma, MD, Elizabeth Sierra Potchanant, PhD, Ying He, Grzegorz Nalepa, MDPhD

Blood (2016) 128 (22): 1040.

https://doi.org/10.1182/blood.V128.22.1040.1040

Published: 2016

Journal Articles

Unfavorable Prognostic Impact of MYC Increased Copy Number (ICN) in Patients with Diffuse Large B-Cell and High-Grade Lymphoma Treated with Immuno-Chemotherapy (ICT)

Francesca Schieppati, MD, Simona Fisogni, MD, Piera Balzarini, PhD, Alessandro Re, MD, Luisa Lorenzi, MD, Daniela Dalceggio, MD, Angela Passi, MD, Chiara Cattaneo, MD, Fabio Facchetti, MD, Giuseppe Rossi, MD, Alessandra Tucci, MD

Blood (2016) 128 (22): 5295.

https://doi.org/10.1182/blood.V128.22.5295.5295

Published: 2016

Journal Articles

Selective Advantage of the Recurrent Isodicentric Chromosome 20 in Myeloid Disease

Justin B Schleede, PhD, Peter Papenhausen, PhD, Stuart Schwartz, PhD, Inder K. Gadi, PhD

Blood (2016) 128 (22): 5119.

https://doi.org/10.1182/blood.V128.22.5119.5119

Published: 2016

Journal Articles

Identification of PLZF-Dmrs in Hematopoiesis Highlight a Novel Role of PLZF As a Guardian of Hematopoietic Genome Integrity

Fabien Guidez, PhD, Laetitia Durand, Technician, Valerie Vidal, William Puszyk, PhD, David Grimwade, Ellen Solomon, Christine Chomienne, MD PhD

Blood (2014) 124 (21): 2904.

https://doi.org/10.1182/blood.V124.21.2904.2904

Published: 2014

Journal Articles

New Mutation in Chromosome 9 Associated with Familial Autosomal Recessive Macrothrombocytopenia

Shoshana Revel-Vilk, MD MSc, Ela Shai, PhD, Nivin Gashem, MSc, Esti Hyam, Galia Spectre, MD, Orly Elpeleg, MD, David Varon, MD

Blood (2014) 124 (21): 2776.

https://doi.org/10.1182/blood.V124.21.2776.2776

Published: 2014

Journal Articles

Passage-Dependent Cancerous Transformation Of Human Mesenchymal Stem Cell Of Adipose Origin During In Vitro Culture

Jung Ah Kim, MD, Qute Choi, MD, Kyong Ok Im, Ji Seok Kwon, Si Nae Park, Seon Young Kim, MD, Sang Mee Hwang, MD, Yeon-Mok Oh, MD, Dong Soon Lee, MD, PhD

Blood (2013) 122 (21): 4862.

https://doi.org/10.1182/blood.V122.21.4862.4862

Published: 2013

Journal Articles

Very High Risk CLL Characterized by a “Double Hit” Clone with Both 11q22 and 17p13 Deletion.

Patricia T. Greipp, D.O., Stephanie A. Smoley, David S. Viswanatha, MD, Lori S. Frederick, BS, Ruchi G. Sharma, Kari G. Rabe, MS, Susan L Slager, PhD, Daniel L. Van Dyke, Ph.D., Neil E. Kay, MD, Tait D. Shanafelt, MD, Clive S. Zent, MD

Blood (2012) 120 (21): 2486.

https://doi.org/10.1182/blood.V120.21.2486.2486

Published: 2012

Journal Articles

Impact of Immunoglobulin Heavy Chain (IGH) Translocations In Chronic Lymphocytic Leukemia (CLL): Negative Effect on Patients with Isolated Deletion 13q Abnormality

Alina S. Gerrie, MD, FRCPC, Tanya L. Gillan, PhD, FCCMG, Helene Bruyere, MD, FCCMG, Mary Joyce Chan, BMLSc, Chinmay B. Dalal, MD, Cynthia L. Toze, MD, FRCPC

Blood (2010) 116 (21): 2434.

https://doi.org/10.1182/blood.V116.21.2434.2434

Published: 2010

Journal Articles

Searching for Amplification of Chromosome 5 Segments by Molecular Cytogenetics in 9 Myelodysplastic Syndromes/Acute Myeloid Leukemia (MDS)/(AML) Patients with Apparent Monosomy 5

Paolo Bernasconi, MD, Irene Dambruoso, Marina Boni, Rita Zappatore, Paola Maria Cavigliano, Ilaria Giardini, Marilena Caresa, Cesare Astori, Carlo Castagnola, Mario Lazzarino

Blood (2008) 112 (11): 4866.

https://doi.org/10.1182/blood.V112.11.4866.4866

Published: 2008

Journal Articles

Unfavourable Outcome and Heterogeneity of Partner Chromosomes in Chronic Lymphocytic Leukemia with 14q32/IGH Translocations.

Francesco Cavazzini, Jose A. Hernandez, Alessandro Gozzetti, Antonella Russo Rossi, Ruana Tiseo, Rossana Maffei, Antonella Bardi, Elisa Tammiso, Rosaria Crupi, Maria P. Lenoci, Roberto Marasca, Francesco Lauria, Giuseppe Torelli, Jesus M. Hernandez, Gian M. Rigolin, Antonio Cuneo

Blood (2007) 110 (11): 4686.

https://doi.org/10.1182/blood.V110.11.4686.4686

Published: 2007

Journal Articles

Analysis of MLL Amplification and 5q Deletions in AML/MDS Cell Lines Identifies Novel Targets.

Bjoern Schneider, Stefan Nagel, PhD, Maren Kaufmann, Hilmar Quentmeier, PhD, Yoshinobu Matsuo, PhD, Hans G. Drexler, MD, Roderick A.F. MacLeod, PhD

Blood (2006) 108 (11): 1424.

https://doi.org/10.1182/blood.V108.11.1424.1424

Published: 2006

Journal Articles

Genomic Composition of Howell-Jolly Bodies.

Nicole M. Gantt, Bob Walker, Y. Terry Lee, Yuan Jiang, Pamela Staker, Patricia A. Oneal, Natarajan V. Bhanu, Paul S. Meltzer, Jeffery L. Miller

Blood (2006) 108 (11): 1570.

https://doi.org/10.1182/blood.V108.11.1570.1570

Published: 2006

Journal Articles

Frequency, Hematopathology and Detection of a New Isodicentric Variant of Deletion 20q.

Stephanie R. Fink, Stephanie A. Smoley, Sarah F. Paternoster, Kimberly J. Stockero, Lai P. Nguyen, Phuong L. Nguyen, M.D., Curtis A. Hanson, M.D., Gordon W. Dewald, Ph.D.

Blood (2006) 108 (11): 4843.

https://doi.org/10.1182/blood.V108.11.4843.4843

Published: 2006

Journal Articles

Familial Myelodysplastic Syndromes with Centromere Instability of Chromosome 1 Origin.

Klas Raaschou-Jensen, MD, Mette Klarskov Andersen, MD,PhD, Bendt Nielsen, MD,PhD, Eigil Kjeldsen, MD,PhD, Lars Kjeldsen, MD,PhD

Blood (2006) 108 (11): 4855.

https://doi.org/10.1182/blood.V108.11.4855.4855

Published: 2006

Journal Articles

Mapping of Genes That Control the Antibody Response to Human FVIII in Mice.

Jay Nelson Lozier, MD, PhD, Pei Zhang, MD

Blood (2005) 106 (11): 1888.

https://doi.org/10.1182/blood.V106.11.1888.1888

Published: 2005

Journal Articles

Cryptic MLL , AF10 , ARMC3 Rearrangement in Secondary AML Creates ARMC3-MLL Fusion That Disrupts Gene Encoding Armadillo Repeats Similar to Major Cancer Genes.

Giuseppe Germano, PhD, Blaine W. Robinson, PhD, Carolyn A. Felix, MD

Blood (2005) 106 (11): 4345.

https://doi.org/10.1182/blood.V106.11.4345.4345

Published: 2005

NARROW

Cryptic insertion of KMT2A , a rare t(9;11) variant

DIS3 Mutation in RUNX1-Mutated AML1 Confers a Highly Dismal Prognosis in AML By Repressing Sister Chromatid Cohesion

Constitutional Ring Chromosome 21 Predisposes to Acute Lymphoblastic Leukaemia (ALL) with iAMP21

Telomere Length and Somatic Mutation in Aplastic Anemia- Correlation with Response to Treatement

FANCA Fine-Tunes Chromosome Segregation By Controlling BUBR1 K250 Acetylation at the Kinetochores

Unfavorable Prognostic Impact of MYC Increased Copy Number (ICN) in Patients with Diffuse Large B-Cell and High-Grade Lymphoma Treated with Immuno-Chemotherapy (ICT)

Selective Advantage of the Recurrent Isodicentric Chromosome 20 in Myeloid Disease

Identification of PLZF-Dmrs in Hematopoiesis Highlight a Novel Role of PLZF As a Guardian of Hematopoietic Genome Integrity

New Mutation in Chromosome 9 Associated with Familial Autosomal Recessive Macrothrombocytopenia

Passage-Dependent Cancerous Transformation Of Human Mesenchymal Stem Cell Of Adipose Origin During In Vitro Culture

Very High Risk CLL Characterized by a “Double Hit” Clone with Both 11q22 and 17p13 Deletion.

Impact of Immunoglobulin Heavy Chain (IGH) Translocations In Chronic Lymphocytic Leukemia (CLL): Negative Effect on Patients with Isolated Deletion 13q Abnormality

Searching for Amplification of Chromosome 5 Segments by Molecular Cytogenetics in 9 Myelodysplastic Syndromes/Acute Myeloid Leukemia (MDS)/(AML) Patients with Apparent Monosomy 5

Unfavourable Outcome and Heterogeneity of Partner Chromosomes in Chronic Lymphocytic Leukemia with 14q32/IGH Translocations.

Analysis of MLL Amplification and 5q Deletions in AML/MDS Cell Lines Identifies Novel Targets.

Genomic Composition of Howell-Jolly Bodies.

Frequency, Hematopathology and Detection of a New Isodicentric Variant of Deletion 20q.

Familial Myelodysplastic Syndromes with Centromere Instability of Chromosome 1 Origin.

Mapping of Genes That Control the Antibody Response to Human FVIII in Mice.

Cryptic MLL , AF10 , ARMC3 Rearrangement in Secondary AML Creates ARMC3-MLL Fusion That Disrupts Gene Encoding Armadillo Repeats Similar to Major Cancer Genes.

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American Society of Hematology

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American Society of Hematology

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