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Searching for mammary analog secretory carcinoma of salivary gland among its mimics

Modern pathology, 2014-01, Vol.27 (1), p.30-37

2014

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Endoscopic ultrasound guided fine needle aspiration with fluorescence in situ hybridization analysis in 104 patients with pancreatic mass

Journal of gastroenterology and hepatology, 2014-08, Vol.29 (8), p.1654-1658

2014

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Comparison Between Integrated Genomic DNA/RNA Profiling and Fluorescence In Situ Hybridization in the Detection of MYC, BCL-2, and BCL-6 Gene Rearrangements in Large B-Cell Lymphomas

American journal of clinical pathology, 2020-02, Vol.153 (3), p.353-359

2020

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Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

PloS one, 2017-03, Vol.12 (3), p.e0169219-e0169219

2017

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Fractionated deep-inspiration breath-hold ZTE Compared with Free-breathing four-dimensional ZTE for detecting pulmonary nodules in oncological patients underwent PET/MRI

Scientific reports, 2021-09, Vol.11 (1), p.17636-17636, Article 17636

2021

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Gastric Mobility and Gastrointestinal Hormones in Older Patients with Sarcopenia

Nutrients, 2022-04, Vol.14 (9), p.1897

2022

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Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization

Human mutation, 2007-11, Vol.28 (11), p.1124-1132

2007

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Measurements of elemental iodine in soy sauces in Taiwan using a modified microplate method

Frontiers in endocrinology (Lausanne), 2023-03, Vol.14, p.1058695-1058695

2023

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A Case of AML Characterized by a Novel t(4;15)(q31;q22) Translocation That Confers a Growth-Stimulatory Response to Retinoid-Based Therapy

International journal of molecular sciences, 2017-07, Vol.18 (7), p.1492

2017

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Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region

American journal of medical genetics. Part A, 2012-09, Vol.158A (9), p.2139-2151

2012

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Molecular and genomic aberrations in Chlamydophila psittaci negative ocular adnexal marginal zone lymphomas

American journal of hematology, 2013-09, Vol.88 (9), p.730-735

2013

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EUS-FNA with rescue fluorescence in situ hybridization for the diagnosis of pancreatic carcinoma in patients with inconclusive on-site cytopathology results

Gastrointestinal endoscopy, 2011-09, Vol.74 (3), p.541-547

2011

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De novo acute myeloid leukemia with monocytoid blasts and erythrophagocytosis

Clinical case reports, 2014-12, Vol.2 (6), p.333-335

2014

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HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline

Breast cancer research and treatment, 2016-02, Vol.155 (3), p.457-462

2016

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A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System

Academic pathology, 2020, Vol.7, p.2374289520958200-2374289520958200, Article 2374289520958200

2020

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Innate Diversity of Adult Human Arterial Smooth Muscle Cells: Cloning of Distinct Subtypes From the Internal Thoracic Artery

Circulation research, 2001-09, Vol.89 (6), p.517-525

2001

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Companion diagnostic testing for targeted cancer therapies: an overview

Genetic testing and molecular biomarkers, 2013-07, Vol.17 (7), p.515

Fan, Yao-Shan

2013

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Comparative genome hybridization analysis of laser-capture microdissected in situ melanoma

Journal of cutaneous pathology, 2010-01, Vol.37 (1), p.3-7

2010

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Myeloid neoplasms with features intermediate between primary myelofibrosis and chronic myelomonocytic leukemia

Modern pathology, 2018-03, Vol.31 (3), p.429-441

2018

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Diagnostic application of cyclin D1 fluorescent in situ hybridization for histologically undetermined early lesions of acral melanoma in situ: A case series

Annals of diagnostic pathology, 2021-02, Vol.50, p.151681, Article 151681

2021

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Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?

Molecular cytogenetics, 2012-04, Vol.5 (1), p.18-18, Article 18

2012

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Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome

American journal of medical genetics. Part A, 2012-03, Vol.158A (3), p.547-552

2012

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Primary Mediastinal Large B-Cell Lymphoma With Translocations Involving BCL6 and MYC (Double-Hit Lymphoma)

American journal of clinical pathology, 2016-05, Vol.145 (5), p.710-716

2016

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DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome

Arthritis and rheumatism, 2013-08, Vol.65 (8), p.2183-2189

2013

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Searching for mammary analog secretory carcinoma of salivary gland among its mimics

Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar

Endoscopic ultrasound guided fine needle aspiration with fluorescence in situ hybridization analysis in 104 patients with pancreatic mass

Comparison Between Integrated Genomic DNA/RNA Profiling and Fluorescence In Situ Hybridization in the Detection of MYC, BCL-2, and BCL-6 Gene Rearrangements in Large B-Cell Lymphomas

Screening of deafness-causing DNA variants that are common in patients of European ancestry using a microarray-based approach

Fractionated deep-inspiration breath-hold ZTE Compared with Free-breathing four-dimensional ZTE for detecting pulmonary nodules in oncological patients underwent PET/MRI

Gastric Mobility and Gastrointestinal Hormones in Older Patients with Sarcopenia

Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization

Measurements of elemental iodine in soy sauces in Taiwan using a modified microplate method

A Case of AML Characterized by a Novel t(4;15)(q31;q22) Translocation That Confers a Growth-Stimulatory Response to Retinoid-Based Therapy

Genotype-phenotype analysis of 4q deletion syndrome: Proposal of a critical region

Molecular and genomic aberrations in Chlamydophila psittaci negative ocular adnexal marginal zone lymphomas

EUS-FNA with rescue fluorescence in situ hybridization for the diagnosis of pancreatic carcinoma in patients with inconclusive on-site cytopathology results

De novo acute myeloid leukemia with monocytoid blasts and erythrophagocytosis

HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline

A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System

Innate Diversity of Adult Human Arterial Smooth Muscle Cells: Cloning of Distinct Subtypes From the Internal Thoracic Artery

Companion diagnostic testing for targeted cancer therapies: an overview

Comparative genome hybridization analysis of laser-capture microdissected in situ melanoma

Myeloid neoplasms with features intermediate between primary myelofibrosis and chronic myelomonocytic leukemia

Diagnostic application of cyclin D1 fluorescent in situ hybridization for histologically undetermined early lesions of acral melanoma in situ: A case series

Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?

Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome

Primary Mediastinal Large B-Cell Lymphoma With Translocations Involving BCL6 and MYC (Double-Hit Lymphoma)

DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome

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