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Measurable residual disease monitoring provides insufficient lead-time to prevent morphologic relapse in the majority of patients with core-binding factor acute myeloid leukemia

Haematologica (Roma), 2021-01, Vol.106 (1), p.56-63

2021

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Upfront Next Generation Sequencing in Non-Small Cell Lung Cancer

Current oncology (Toronto), 2022-06, Vol.29 (7), p.4428-4437

2022

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Inter-Laboratory Comparison of Chronic Myeloid Leukemia Minimal Residual Disease Monitoring

The Journal of molecular diagnostics : JMD, 2007, Vol.9 (4), p.421-430

2007

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Lung transplantation complicated by graft-versus-host disease and confounded by incidental transfusion-associated macrochimerism

Transfusion (Philadelphia, Pa.), 2008-10, Vol.48 (10), p.2190-2196

2008

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Concurrent hyperdiploid acute myeloid leukemia and trisomy 12+ chronic lymphocytic leukemia

EJHaem, 2024-10, Vol.5 (5), p.1082-1083

2024

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Radar plots facilitate differential diagnosis of acute promyelocytic leukemia and NPM1+ acute myeloid leukemia by flow cytometry

Cytometry. Part B, Clinical cytometry, 2021-07, Vol.100 (4), p.409-420

2021

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AML with CEBPA mutations: A comparison of ICC and WHO-HAEM5 criteria in patients with 20% or more blasts

Leukemia research, 2023-11, Vol.134, p.107376-107376, Article 107376

2023

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Impact on turnaround times (TAT) among non-squamous non-small cell lung cancer (NSCLC) patients across three time periods with varying biomarker testing techniques

Journal of clinical oncology, 2023-06, Vol.41 (16_suppl), p.9085-9085

2023

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Sample Features Associated with Success Rates in Population-Based EGFR Mutation Testing

Journal of thoracic oncology, 2014-07, Vol.9 (7), p.947-956

2014

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A real-world analysis of clinical outcomes in AML with myelodysplasia-related changes: a comparison of ICC and WHO-HAEM5 criteria

Blood advances, 2024-04, Vol.8 (7), p.1760-1771

2024

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Primary Marginal Zone Lymphoma of the Subcutis Associated With Panniculitis and Fat Necrosis

American journal of clinical pathology, 2015-08, Vol.144 (2), p.341-346

2015

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Mixed Fields on RHD Typing As an Indicator of Malignancy-Associated Loss of Heterozygosity on Chromosome 1p in Myeloid Neoplasm

Blood, 2014-12, Vol.124 (21), p.5105-5105

2014

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Abstract 4713: High-throughput multiplex Sequenom MassARRAY clinical diagnostic assay for the identification of actionable genetic variants in hematologic malignancies

Cancer research (Chicago, Ill.), 2014-10, Vol.74 (19_Supplement), p.4713-4713

2014

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Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

Human molecular genetics, 2001-12, Vol.10 (26), p.2989-3000

2001

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Mixed fields on RhD typing as an indication of loss of heterozygosity on chromosome 1p in acute myeloid leukemia

Leukemia & lymphoma, 2015-07, Vol.56 (7), p.2196-2199

2015

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Benchmarking population-based EGFR mutation testing in nonsquamous non-small cell lung cancer

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.e19032-e19032

2013

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Inter-Laboratory Comparison of Chronic Myeloid Leukemia Minimal Residual Disease Monitoring: Summary and Recommendations

The Journal of molecular diagnostics : JMD, 2007-09, Vol.9 (4), p.421-430

2007

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Genetic determinants of extracellular magnesium concentration: Analysis of multiple candidate genes, and evidence for association with the estrogen receptor α ( ESR1) locus

Clinica chimica acta, 2009-11, Vol.409 (1), p.28-32

2009

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Recurrent Familial Hypocalcemia Due to Germline Mosaicism for an Activating Mutation of the Calcium-Sensing Receptor Gene

The journal of clinical endocrinology and metabolism, 2003-08, Vol.88 (8), p.3674-3681

2003

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Overproduction of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells

Wei, Cuihong

1994

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Overexpression of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells

Somatic cell and molecular genetics, 1993-07, Vol.19 (4), p.321-330

1993

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Transcriptional regulation of the asparagine synthetase gene in Chinese hamster ovary cells

Wei, Cuihong

1999

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Mixed fields on RhD typing as an indication of loss of heterozygosity on chromosome 1p in acute myeloid leukemia

Leukemia & lymphoma, 2015, Vol.56 (7), p.2196-2199

2015

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Monitoring of Minimal Residual Hematologic Disease

Cell and Tissue Based Molecular Pathology: A Volume in the Foundations in Diagnostic Pathology Series, 2009, p.135-144

First Edition, 2009

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Chapter 14 - Monitoring of Minimal Residual Hematologic Disease

Cell and Tissue Based Molecular Pathology, p.135-144

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Measurable residual disease monitoring provides insufficient lead-time to prevent morphologic relapse in the majority of patients with core-binding factor acute myeloid leukemia

Upfront Next Generation Sequencing in Non-Small Cell Lung Cancer

Inter-Laboratory Comparison of Chronic Myeloid Leukemia Minimal Residual Disease Monitoring

Lung transplantation complicated by graft-versus-host disease and confounded by incidental transfusion-associated macrochimerism

Concurrent hyperdiploid acute myeloid leukemia and trisomy 12+ chronic lymphocytic leukemia

Radar plots facilitate differential diagnosis of acute promyelocytic leukemia and NPM1+ acute myeloid leukemia by flow cytometry

AML with CEBPA mutations: A comparison of ICC and WHO-HAEM5 criteria in patients with 20% or more blasts

Impact on turnaround times (TAT) among non-squamous non-small cell lung cancer (NSCLC) patients across three time periods with varying biomarker testing techniques

Sample Features Associated with Success Rates in Population-Based EGFR Mutation Testing

A real-world analysis of clinical outcomes in AML with myelodysplasia-related changes: a comparison of ICC and WHO-HAEM5 criteria

Primary Marginal Zone Lymphoma of the Subcutis Associated With Panniculitis and Fat Necrosis

Mixed Fields on RHD Typing As an Indicator of Malignancy-Associated Loss of Heterozygosity on Chromosome 1p in Myeloid Neoplasm

Abstract 4713: High-throughput multiplex Sequenom MassARRAY clinical diagnostic assay for the identification of actionable genetic variants in hematologic malignancies

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1

Mixed fields on RhD typing as an indication of loss of heterozygosity on chromosome 1p in acute myeloid leukemia

Benchmarking population-based EGFR mutation testing in nonsquamous non-small cell lung cancer

Inter-Laboratory Comparison of Chronic Myeloid Leukemia Minimal Residual Disease Monitoring: Summary and Recommendations

Genetic determinants of extracellular magnesium concentration: Analysis of multiple candidate genes, and evidence for association with the estrogen receptor α ( ESR1) locus

Recurrent Familial Hypocalcemia Due to Germline Mosaicism for an Activating Mutation of the Calcium-Sensing Receptor Gene

Overproduction of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells

Overexpression of asparagine synthetase in albizziin-resistant murine diploid embryonic stem cells

Transcriptional regulation of the asparagine synthetase gene in Chinese hamster ovary cells

Mixed fields on RhD typing as an indication of loss of heterozygosity on chromosome 1p in acute myeloid leukemia

Monitoring of Minimal Residual Hematologic Disease

Chapter 14 - Monitoring of Minimal Residual Hematologic Disease

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