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Unraveling the genomic underpinnings of unbalanced MYC break-apart FISH results using whole genome sequencing analysis.
- Published in:
- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00967-8
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- Publication type:
- Article
Prospective evaluation of genome sequencing to compare conventional cytogenetics in acute myeloid leukemia.
- Published in:
- Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00908-5
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- Publication type:
- Article
High-grade B-cell lymphoma with a quadruple-hit genetic profile including concurrent MYC, BCL2, BCL6, and CCND1 gene rearrangements.
- Published in:
- Laboratory Medicine, 2024, v. 5, n. 5, p. 649, doi. 10.1093/labmed/lmae017
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- Publication type:
- Article
Novel USP25::PDGFRA Gene Fusion in a 78 Year Old Patient with a Myeloid Neoplasm.
- Published in:
- Laboratory Medicine, 2022, v. 53, n. 5, p. e134, doi. 10.1093/labmed/lmac010
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- Publication type:
- Article
Detection of a Cryptic KMT2A/AFDN Gene Fusion [ins(6;11)(q27;q23q23)] in a Pediatric Patient with Newly Diagnosed Acute Myeloid Leukemia.
- Published in:
- Laboratory Medicine, 2022, v. 53, n. 4, p. e95, doi. 10.1093/labmed/lmab109
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- Publication type:
- Article
Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia.
- Published in:
- Laboratory Medicine, 2022, v. 53, n. 4, p. e87, doi. 10.1093/labmed/lmab105
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- Publication type:
- Article
Concomitant 11p15.4-p15.5 Duplication and Terminal 22q13.33 Deletion in a Patient with Features of Beckwith-Wiedemann Syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170, n. 12, p. 3348, doi. 10.1002/ajmg.a.37939
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- Publication type:
- Article
Elucidating discrepant results in a prenatal diagnosis of 48,XXY,+18 (Edwards and Klinefelter syndromes).
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 11, p. 2855, doi. 10.1002/ajmg.a.37250
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- Publication type:
- Article
Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 5, p. 1047, doi. 10.1002/ajmg.a.36839
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- Publication type:
- Article
Absence of skeletal anomalies in siblings with a maternally inherited 12q13.13-q13.2 microdeletion partially involving the HOXC gene cluster.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 810, doi. 10.1002/ajmg.a.36359
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- Publication type:
- Article
Familial microduplication of 17q23.1-q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 2, p. 364, doi. 10.1002/ajmg.a.36238
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- Publication type:
- Article
Comparative study of therapy‐related and de novo adult b‐cell acute lymphoblastic leukaemia.
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- British Journal of Haematology, 2022, v. 196, n. 4, p. 963, doi. 10.1111/bjh.17906
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- Publication type:
- Article
B-cell acute lymphoblastic leukemia in an elderly man with plasma cell myeloma and long-term exposure to thalidomide and lenalidomide: a case report and literature review.
- Published in:
- 2019
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- Publication type:
- journal article
Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 710, doi. 10.1002/gcc.23084
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- Publication type:
- Article
Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 10, p. 629, doi. 10.1002/gcc.23070
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- Publication type:
- Article
Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 10, p. 678, doi. 10.1002/gcc.22977
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- Publication type:
- Article
Identification of a novel KMT2A/GIMAP8 gene fusion in a pediatric patient with acute undifferentiated leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 2, p. 108, doi. 10.1002/gcc.22902
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- Publication type:
- Article
Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2020, v. 59, n. 7, p. 422, doi. 10.1002/gcc.22842
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- Publication type:
- Article
A near‐haploid clone harboring a BCR/ABL1 gene fusion in an adult patient with newly diagnosed B‐lymphoblastic leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 665, doi. 10.1002/gcc.22744
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- Publication type:
- Article
Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 567, doi. 10.1002/gcc.22741
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- Publication type:
- Article
KMT2A (MLL) rearrangements observed in pediatric/young adult T‐lymphoblastic leukemia/lymphoma: A 10‐year review from a single cytogenetic laboratory.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 11, p. 541, doi. 10.1002/gcc.22666
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- Publication type:
- Article
Spurious CD34 expression in B‐cell lymphoma due to nonspecific binding to PerCP‐Cy5.5 fluorochrome conjugates: A rare phenomenon and a diagnostic pitfall.
- Published in:
- Cytometry. Part B, 2022, v. 102, n. 4, p. 326, doi. 10.1002/cyto.b.22079
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- Publication type:
- Article
Comprehensive morphologic characterization of bone marrow biopsy findings in a large cohort of patients with VEXAS syndrome: A single-institution longitudinal study of 111 bone marrow samples from 52 patients.
- Published in:
- American Journal of Clinical Pathology, 2024, v. 161, n. 6, p. 609, doi. 10.1093/ajcp/aqad186
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- Publication type:
- Article
Recurrent Chromosomal Abnormalities in Tissues Involved by Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma.
- Published in:
- American Journal of Clinical Pathology, 2022, v. 157, n. 2, p. 286, doi. 10.1093/ajcp/aqab128
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- Publication type:
- Article
The Utilization of Chromosomal Microarray Technologies for Hematologic NeoplasmsAn ACLPS Critical Review.
- Published in:
- American Journal of Clinical Pathology, 2018, v. 150, n. 5, p. 375, doi. 10.1093/ajcp/aqy076
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- Publication type:
- Article
The Utilization of Chromosomal Microarray Technologies for Hematologic Neoplasms: An ACLPS Critical Review.
- Published in:
- 2018
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- Publication type:
- journal article
Evaluation of a microarray-based genotyping assay for the rapid detection of cytochrome P450 2C19 *2 and *3 polymorphisms from whole blood using nanoparticle probes.
- Published in:
- 2011
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- Publication type:
- journal article
Cover Image.
- Published in:
- 2019
- By:
- Publication type:
- Cover Art
Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia.
- Published in:
- European Journal of Haematology, 2019, v. 102, n. 1, p. 87, doi. 10.1111/ejh.13179
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- Publication type:
- Article
Leukemic phase and CSF involvement of diffuse large B‐cell lymphoma with a complex karyotype including a <italic>TP53</italic> deletion.
- Published in:
- Clinical Case Reports, 2018, v. 6, n. 1, p. 235, doi. 10.1002/ccr3.1250
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- Publication type:
- Article
Fluorescence in‐situ hybridisation for TP63 rearrangements in T cell lymphomas: single‐site experience of 470 patients and implications for clinical testing.
- Published in:
- Histopathology, 2020, v. 76, n. 3, p. 481, doi. 10.1111/his.14005
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- Publication type:
- Article
Detection of an MN1::ETV6 Gene Fusion in a Case of Acute Myeloid Leukemia with Erythroid Differentiation: A Case Report and Review of the Literature.
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- 2023
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- Publication type:
- Case Study
Acute Myeloid Leukemia in an Infant with t(8;19)(p11.2;q13) Translocation: Case Report and a Review of the Literature.
- Published in:
- Case Reports in Hematology, 2019, p. 1, doi. 10.1155/2019/4198415
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- Publication type:
- Article
Dual Primary IGH Translocations in Multiple Myeloma: A Novel Finding.
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2021, v. 21, n. 9, p. e710, doi. 10.1016/j.clml.2021.05.001
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- Publication type:
- Article
Whole Genome Mate-pair Sequencing of Plasma Cell Neoplasm as a Novel Diagnostic Strategy: A Case of Unrecognized t(2;11) Structural Variation.
- Published in:
- 2019
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- Publication type:
- journal article
MYC break-apart FISH probe set reveals frequent unbalanced patterns of uncertain significance when evaluating aggressive B-cell lymphoma.
- Published in:
- 2021
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- Publication type:
- Letter
Identification of adult Philadelphia-like acute lymphoblastic leukemia using a FISH‐based algorithm distinguishes prognostic groups and outcomes.
- Published in:
- 2021
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- Publication type:
- Letter
Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma.
- Published in:
- Blood Cancer Journal, 2019, v. 9, n. 12, p. 1, doi. 10.1038/s41408-019-0255-z
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- Publication type:
- Article
Characterization of TCF3 rearrangements in pediatric B-lymphoblastic leukemia/lymphoma by mate-pair sequencing (MPseq) identifies complex genomic rearrangements and a novel TCF3/TEF gene fusion.
- Published in:
- Blood Cancer Journal, 2019, v. 9, n. 10, p. N.PAG, doi. 10.1038/s41408-019-0239-z
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- Publication type:
- Article
Clinical utility of fluorescence in situ hybridization‐based diagnosis of BCR‐ABL1 like (Philadelphia chromosome like) B‐acute lymphoblastic leukemia.
- Published in:
- American Journal of Hematology, 2020, v. 95, n. 3, p. E68, doi. 10.1002/ajh.25729
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- Publication type:
- Article
Mosaic Trisomy 9p in a Patient with Mild Dysmorphic Features and Normal Intelligence.
- Published in:
- Journal of the Association of Genetic Technologists, 2017, v. 43, n. 2, p. 56
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- Publication type:
- Article
Seizure Disorder in a Patient with a 5.09 Mb 7q11.23-q21.11 Microdeletion Including the MAGI2 Gene.
- Published in:
- 2014
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- Publication type:
- Case Study
Circulating Breast Carcinoma Cells Mimicking Therapy-Related Acute Myeloid Leukemia: A Potential Cytogenetic and Flow Cytometry Pitfall.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
A TRIP11:: FLT3 gene fusion in a patient with myeloid/lymphoid neoplasm with eosinophilia and tyrosine kinase gene fusions: a case report and review of the literature.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2023, v. 9, n. 1, p. 1, doi. 10.1101/mcs.a006243
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- Publication type:
- Article
The Complexities of Defining a Complex Karyotype in Hematological Malignancies: A Need for Standardization?
- Published in:
- Acta Haematologica, 2017, v. 138, n. 1, p. 65, doi. 10.1159/000477894
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- Publication type:
- Article
Two Distinct BCL2 Rearrangements, Each Observed in 2 Independent Subclones, Evolving from a Founder Clone with Trisomy 12 in a Unique Case of Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2021, v. 145, n. 2, p. 176, doi. 10.5858/arpa.2020-0089-CP
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- Publication type:
- Article