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SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients

Leukemia, 2012-05, Vol.26 (5), p.1135-1137

2012

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Prognostic significance of ASXL1 mutation types and allele burden in myelofibrosis

Leukemia, 2018-03, Vol.32 (3), p.837-839

2018

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Core-binding factor acute myeloid leukemia: long-term outcome of 70 patients uniformly treated with “7+3”

Blood cancer journal (New York), 2022-04, Vol.12 (4), p.55-55, Article 55

2022

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Application of current prognostic models for primary myelofibrosis in the setting of post-polycythemia vera or post-essential thrombocythemia myelofibrosis

Leukemia, 2017-12, Vol.31 (12), p.2851-2852

2017

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Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Blood cancer journal (New York), 2016-04, Vol.6 (4), p.e414-e414

2016

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Novel FISH probes designed to detect IGK-MYC and IGL-MYC rearrangements in b-cell lineage malignancy identify a new breakpoint cluster region designated BVR2

Leukemia, 2006-10, Vol.20 (10), p.1790-1799

2006

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Predictors of survival in WHO-defined hypereosinophilic syndrome and idiopathic hypereosinophilia and the role of next-generation sequencing

Leukemia, 2016-09, Vol.30 (9), p.1924-1926

2016

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U2AF1 mutations in primary myelofibrosis are strongly associated with anemia and thrombocytopenia despite clustering with JAK2V617F and normal karyotype

Leukemia, 2014-02, Vol.28 (2), p.431-433

2014

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Vascular events and risk factors for thrombosis in refractory anemia with ring sideroblasts and thrombocytosis

Leukemia, 2016-11, Vol.30 (11), p.2273-2275

2016

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Mutational analysis of candidate tumor-associated genes in acute megakaryoblastic leukemia

Leukemia, 2009-11, Vol.23 (11), p.2159-2160

2009

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Bone marrow JAK2V617F allele burden and clinical correlates in polycythemia vera

Leukemia, 2007-09, Vol.21 (9), p.2074-2075

2007

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Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Blood cancer journal (New York), 2016-04, Vol.6 (4), p.e415-e415

2016

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Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Blood cancer journal (New York), 2015-02, Vol.5 (2), p.e280-e280

2015

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Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes

Leukemia, 2013-10, Vol.27 (10), p.2112

2013

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Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Blood cancer journal (New York), 2016-05, Vol.6 (5), p.e416-e416

2016

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Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

American journal of clinical pathology, 2021-10, Vol.156 (Supplement_1), p.S100-S101

2021

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The factor IX gene as a model for analysis of human germline mutations: an update

Human molecular genetics, 1996-01, Vol.5 (Supplement-1), p.1505-1514

1996

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The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene

American journal of human genetics, 1994-05, Vol.54 (5), p.831-835

1994

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The rates and patterns of deletions in the human factor IX gene

American journal of human genetics, 1994-02, Vol.54 (2), p.201-213

1994

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Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization

Genetics in medicine, 2011-06, Vol.13 (6), p.545-552

2011

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Anaplastic astroblastoma-sarcoma in neurofibromatosis Type 1

Clinical neuropathology, 2010-09, Vol.29 (5), p.289-296

2010

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Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization

Genetics in medicine, 2011-07, Vol.13 (7), p.667-675

2011

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Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemia

Leukemia, 2005-01, Vol.19 (1), p.126-131

2005

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Oncocytic choroid plexus carcinoma: case report

Clinical neuropathology, 2010-01, Vol.29 (1), p.14-20

2010

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A postulated mechanism for deletions with inversions

American journal of human genetics, 1993-05, Vol.52 (5), p.1016-1018

1993

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SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients

Prognostic significance of ASXL1 mutation types and allele burden in myelofibrosis

Core-binding factor acute myeloid leukemia: long-term outcome of 70 patients uniformly treated with “7+3”

Application of current prognostic models for primary myelofibrosis in the setting of post-polycythemia vera or post-essential thrombocythemia myelofibrosis

Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Novel FISH probes designed to detect IGK-MYC and IGL-MYC rearrangements in b-cell lineage malignancy identify a new breakpoint cluster region designated BVR2

Predictors of survival in WHO-defined hypereosinophilic syndrome and idiopathic hypereosinophilia and the role of next-generation sequencing

U2AF1 mutations in primary myelofibrosis are strongly associated with anemia and thrombocytopenia despite clustering with JAK2V617F and normal karyotype

Vascular events and risk factors for thrombosis in refractory anemia with ring sideroblasts and thrombocytosis

Mutational analysis of candidate tumor-associated genes in acute megakaryoblastic leukemia

Bone marrow JAK2V617F allele burden and clinical correlates in polycythemia vera

Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes

Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

The factor IX gene as a model for analysis of human germline mutations: an update

The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene

The rates and patterns of deletions in the human factor IX gene

Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization

Anaplastic astroblastoma-sarcoma in neurofibromatosis Type 1

Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization

Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemia

Oncocytic choroid plexus carcinoma: case report

A postulated mechanism for deletions with inversions

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