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Functional Enhancers Shape Extrachromosomal Oncogene Amplifications

Cell, 2019-11, Vol.179 (6), p.1330-1341.e13

2019

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Genetic aspects of human prion diseases

Frontiers in neurology, 2022-10, Vol.13, p.1003056-1003056

2022

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Aggressive Lymphoplasmacytic Neoplasm With an Unusual In-frame Deletion of MYD88 Associated With TRAF3 and TP53 Mutations and Complex Karyotype

International journal of surgical pathology, 2024-02, Vol.32 (1), p.5-10

2024

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Philadelphia chromosome-positive T-cell acute lymphoblastic leukemia: a case report

Journal of international medical research, 2024-02, Vol.52 (2), p.3000605231156757-3000605231156757

2024

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Integrative genomic and transcriptomic analysis identified candidate genes implicated in the pathogenesis of hepatosplenic T-cell lymphoma

PloS one, 2014-07, Vol.9 (7), p.e102977-e102977

2014

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Identification of a Cancer-Predisposing Germline POT1 p.Ile49Metfs7 Variant by Targeted Sequencing of a Splenic Marginal Zone Lymphoma

Genes, 2022-03, Vol.13 (4), p.591

2022

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P576: Recalibration of scoring metrics to assess the pathogenicity of constitutional copy number variants (CNVs)

Genetics in Medicine Open, 2024, Vol.2, p.101482

2024

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Transcription Factor NF-κB Differentially Regulates Death Receptor 5 Expression Involving Histone Deacetylase 1

Molecular and Cellular Biology, 2005-07, Vol.25 (13), p.5404-5416

2005

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Utility of a column-free cell sorting system for separation of plasma cells in multiple myeloma FISH testing in clinical laboratories

International journal of hematology, 2012-03, Vol.95 (3), p.274-281

2012

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Lifting the Limit: Updated ISSCR Guidance for Lab-Grown Human Embryos

Clinical chemistry (Baltimore, Md.), 2022-05, Vol.68 (5), p.738-738

2022

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NEK2 Induces Drug Resistance Mainly through Activation of Efflux Drug Pumps and Is Associated with Poor Prognosis in Myeloma and Other Cancers

Cancer cell, 2013-01, Vol.23 (1), p.48-62

2013

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Detecting atypical anomalies by non-invasive prenatal screening in advanced maternal age vs. sonographically abnormal pregnancies

American journal of obstetrics and gynecology, 2022-01, Vol.226 (1), p.S682-S682

2022

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Analysis of Racial Differences in the Incidence of a Targetable Biomarker, t(11;14), in Patients with Multiple Myeloma

Blood, 2020-11, Vol.136 (Supplement 1), p.1-2

2020

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eP366: A comprehensive study of E200K genetic Creutzfeldt Jakob disease cases; effects of codon 129 polymorphism

Genetics in medicine, 2022-03, Vol.24 (3), p.S230-S231

2022

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Novel molecular aberrations and pathologic findings in a tubulocystic variant of renal cell carcinoma

Indian journal of pathology & microbiology, 2013-10, Vol.56 (4), p.428-433

2013

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Triploid dizygotic twin pregnancy: elucidating meiotic error using STR marker and chromosomal SNP microarray data

Molecular genetics and metabolism, 2021-04, Vol.132, p.S259-S260

2021

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eP401 - Triploid dizygotic twin pregnancy: elucidating meiotic error using STR marker and chromosomal SNP microarray data

Molecular genetics and metabolism, 2021-04, Vol.132, p.S259-S260

2021

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ZBTB16::RARA variant acute promyelocytic leukemia (vAPL) treated with gemtuzumab ozogamicin (GO) with unique pathology and genetic findings

British journal of haematology, 2023-09, Vol.202 (6), p.1077-1078

2023

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A multicolour flow cytometric assay for c-MYC protein in B-cell lymphoma

Journal of clinical pathology, 2018-10, Vol.71 (10), p.906

2018

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IGJ and SPATS2L immunohistochemistry sensitively and specifically identify BCR::ABL1+ and BCR::ABL1-like B-acute lymphoblastic leukaemia

British journal of haematology, 2024-01, Vol.204 (1), p.229-239

2024

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A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques

Acta neuropathologica, 2023-07, Vol.146 (1), p.121-143

2023

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Mucin 4 protein is expressed in B-acute lymphoblastic leukemia and is restricted to BCR::ABL1-positive and BCR::ABL-like subtypes

Human pathology, 2023-06, Vol.136, p.75-83

2023

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Correction: A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques

Acta neuropathologica, 2023-07, Vol.146 (1), p.167-170

2023

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Impact of an alternative chromosome 17 probe and the 2013 American Society of Clinical Oncology and College of American Pathologists guidelines on fluorescence in situ hybridization for the determination of HER2 gene amplification in breast cancer

Cancer, 2017-06, Vol.123 (12), p.2230-2239

2017

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Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)

Cancer genetics, 2019-01, Vol.230, p.28-36

2019

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Functional Enhancers Shape Extrachromosomal Oncogene Amplifications

Genetic aspects of human prion diseases

Aggressive Lymphoplasmacytic Neoplasm With an Unusual In-frame Deletion of MYD88 Associated With TRAF3 and TP53 Mutations and Complex Karyotype

Philadelphia chromosome-positive T-cell acute lymphoblastic leukemia: a case report

Integrative genomic and transcriptomic analysis identified candidate genes implicated in the pathogenesis of hepatosplenic T-cell lymphoma

Identification of a Cancer-Predisposing Germline POT1 p.Ile49Metfs7 Variant by Targeted Sequencing of a Splenic Marginal Zone Lymphoma

P576: Recalibration of scoring metrics to assess the pathogenicity of constitutional copy number variants (CNVs)

Transcription Factor NF-κB Differentially Regulates Death Receptor 5 Expression Involving Histone Deacetylase 1

Utility of a column-free cell sorting system for separation of plasma cells in multiple myeloma FISH testing in clinical laboratories

Lifting the Limit: Updated ISSCR Guidance for Lab-Grown Human Embryos

NEK2 Induces Drug Resistance Mainly through Activation of Efflux Drug Pumps and Is Associated with Poor Prognosis in Myeloma and Other Cancers

Detecting atypical anomalies by non-invasive prenatal screening in advanced maternal age vs. sonographically abnormal pregnancies

Analysis of Racial Differences in the Incidence of a Targetable Biomarker, t(11;14), in Patients with Multiple Myeloma

eP366: A comprehensive study of E200K genetic Creutzfeldt Jakob disease cases; effects of codon 129 polymorphism

Novel molecular aberrations and pathologic findings in a tubulocystic variant of renal cell carcinoma

Triploid dizygotic twin pregnancy: elucidating meiotic error using STR marker and chromosomal SNP microarray data

eP401 - Triploid dizygotic twin pregnancy: elucidating meiotic error using STR marker and chromosomal SNP microarray data

ZBTB16::RARA variant acute promyelocytic leukemia (vAPL) treated with gemtuzumab ozogamicin (GO) with unique pathology and genetic findings

A multicolour flow cytometric assay for c-MYC protein in B-cell lymphoma

IGJ and SPATS2L immunohistochemistry sensitively and specifically identify BCR::ABL1+ and BCR::ABL1-like B-acute lymphoblastic leukaemia

A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques

Mucin 4 protein is expressed in B-acute lymphoblastic leukemia and is restricted to BCR::ABL1-positive and BCR::ABL-like subtypes

Correction: A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques

Impact of an alternative chromosome 17 probe and the 2013 American Society of Clinical Oncology and College of American Pathologists guidelines on fluorescence in situ hybridization for the determination of HER2 gene amplification in breast cancer

Molecular and pathologic characterization of AML with double Inv(3)(q21q26.2)

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