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Establishment and genomic characterization of a sporadic malignant peripheral nerve sheath tumor cell line

Scientific reports, 2021-03, Vol.11 (1), p.5690-5690, Article 5690

2021

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P596: Diagnostic challenges and phenotypic variations in chimeric genome-wide maternal and paternal uniparental disomy: A prenatal and postnatal perspective

Genetics in Medicine Open, 2024, Vol.2, p.101502, Article 101502

2024

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Chromothripsis in Two Patients With Renal Cell Carcinoma: A Case Series

Clinical genitourinary cancer, 2017-02, Vol.15 (1), p.e137-e143

2017

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First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination

Pediatric and developmental pathology, 2018-11, Vol.21 (6), p.561-567

2018

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Expression of renal cell markers and detection of 3p loss links endolymphatic sac tumor to renal cell carcinoma and warrants careful evaluation to avoid diagnostic pitfalls

Acta neuropathologica communications, 2018-10, Vol.6 (1), p.107-107, Article 107

2018

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Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients

Cancer genetics, 2014-06, Vol.207 (6), p.286-286

2014

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Reversal of activation of human myofibroblast-like cells by culture on a basement membrane-like substrate

Journal of hepatology, 2002-08, Vol.37 (2), p.214-221

2002

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Expression of oncostatin M and its receptors in normal and cirrhotic human liver

Journal of hepatology, 2005-11, Vol.43 (5), p.893-900

2005

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Amplified Allelic Imbalance – A Genetic Signature of Malignant Peripheral Nerve Sheath Tumors (MPNST)

Cancer genetics, 2015-06, Vol.208 (6), p.358-358

2015

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2. Distinct genetic signature of a high risk AML subgroup with ERG amplification

Cancer genetics, 2018-10, Vol.226-227, p.36-37

2018

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Clinical Utility of Chromosomal Microarray in Establishing Clonality and High Risk Features in Patients with Richter Transformation

Blood, 2019-11, Vol.134 (Supplement_1), p.1736-1736

2019

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Title: SNP Microarray Reveals Predicted Outcomes of a Novel High Risk AML Subgroup with ERG Amplification

Blood, 2019-11, Vol.134 (Supplement_1), p.2737-2737

2019

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1. Microdeletion 13q12.2 in B cell acute lymphoblastic leukemia: Little but important

Cancer genetics, 2022-11, Vol.268-269, p.1

2022

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Novel high–risk acute myeloid leukemia subgroup with ERG amplification and Biallelic loss of TP53

Cancer genetics, 2023-04, Vol.272-273, p.23-28

2023

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17. One test to rule them all? The utility of nanopore sequencing for variant detection in hematological malignancies

Cancer genetics, 2020-06, Vol.244, p.7-7

2020

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35 - Chromosomal Microarray in the Era of Next Generation Sequencing: Still Going Strong and Making a Difference in Patient Care. Cases from Medical University of South Carolina

Cancer genetics, 2016-06, Vol.209 (6), p.296-296

2016

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Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia

Genes chromosomes & cancer, 2020-07, Vol.59 (7), p.422-427

2020

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64 - Copy Numbers and Much More: Multifaceted Impact of SNP Microarrays in Cancer Diagnostics

Cancer genetics, 2017-08, Vol.214-215, p.52-52

2017

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Copy Numbers and Much More: Multifaceted Impact of SNP Microarrays in Cancer Diagnostics

Cancer genetics, 2017-08, Vol.214, p.52-52

2017

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78. Identification of a non-productive KMT2A rearrangement in B-ALL with apparent concurrent ETV6::RUNX1 and KMT2A fusions

Cancer genetics, 2022-11, Vol.268-269, p.25-26

2022

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63. Near-haploidization molecularly defines giant cell glioblastoma

Cancer genetics, 2020-06, Vol.244, p.24-24

2020

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Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL

Leukemia & lymphoma, 2022-07, Vol.63 (9), p.2243-2246

2022

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2. Giant cell glioblastoma with massive loss of heterozygosity: A new molecularly defined subtype

Cancer genetics, 2021-04, Vol.252-253, p.S1-S1

2021

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Clinical utility of chromosomal microarray in establishing clonality and high risk features in patients with Richter transformation

Cancer genetics, 2022-01, Vol.260-261, p.18-22

2022

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Chromosomal Microarray in the Era of Next Generation Sequencing: Still Going Strong and Making a Difference in Patient Care. Cases from Medical University of South Carolina

Cancer genetics, 2016-06, Vol.209 (6), p.296-296

2016

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Establishment and genomic characterization of a sporadic malignant peripheral nerve sheath tumor cell line

P596: Diagnostic challenges and phenotypic variations in chimeric genome-wide maternal and paternal uniparental disomy: A prenatal and postnatal perspective

Chromothripsis in Two Patients With Renal Cell Carcinoma: A Case Series

First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination

Expression of renal cell markers and detection of 3p loss links endolymphatic sac tumor to renal cell carcinoma and warrants careful evaluation to avoid diagnostic pitfalls

Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients

Reversal of activation of human myofibroblast-like cells by culture on a basement membrane-like substrate

Expression of oncostatin M and its receptors in normal and cirrhotic human liver

Amplified Allelic Imbalance – A Genetic Signature of Malignant Peripheral Nerve Sheath Tumors (MPNST)

2. Distinct genetic signature of a high risk AML subgroup with ERG amplification

Clinical Utility of Chromosomal Microarray in Establishing Clonality and High Risk Features in Patients with Richter Transformation

Title: SNP Microarray Reveals Predicted Outcomes of a Novel High Risk AML Subgroup with ERG Amplification

1. Microdeletion 13q12.2 in B cell acute lymphoblastic leukemia: Little but important

Novel high–risk acute myeloid leukemia subgroup with ERG amplification and Biallelic loss of TP53

17. One test to rule them all? The utility of nanopore sequencing for variant detection in hematological malignancies

35 - Chromosomal Microarray in the Era of Next Generation Sequencing: Still Going Strong and Making a Difference in Patient Care. Cases from Medical University of South Carolina

Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia

64 - Copy Numbers and Much More: Multifaceted Impact of SNP Microarrays in Cancer Diagnostics

Copy Numbers and Much More: Multifaceted Impact of SNP Microarrays in Cancer Diagnostics

78. Identification of a non-productive KMT2A rearrangement in B-ALL with apparent concurrent ETV6::RUNX1 and KMT2A fusions

63. Near-haploidization molecularly defines giant cell glioblastoma

Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL

2. Giant cell glioblastoma with massive loss of heterozygosity: A new molecularly defined subtype

Clinical utility of chromosomal microarray in establishing clonality and high risk features in patients with Richter transformation

Chromosomal Microarray in the Era of Next Generation Sequencing: Still Going Strong and Making a Difference in Patient Care. Cases from Medical University of South Carolina

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