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Over-expression of AURKA, SKA3 and DSN1 contributes to colorectal adenoma to carcinoma progression

Oncotarget, 2016-07, Vol.7 (29), p.45803-45818

2016

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High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan

Scientific reports, 2017-09, Vol.7 (1), p.11919-10, Article 11919

2017

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High Frequency of Epidermal Growth Factor Receptor Mutations with Complex Patterns in Non–Small Cell Lung Cancers Related to Gefitinib Responsiveness in Taiwan

Clinical cancer research, 2004-12, Vol.10 (24), p.8195-8203

2004

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Mutation in the Tyrosine Kinase Domain of Epidermal Growth Factor Receptor Is a Predictive and Prognostic Factor for Gefitinib Treatment in Patients with Non–Small Cell Lung Cancer

Clinical cancer research, 2005-05, Vol.11 (10), p.3750-3757

2005

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Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma

PLoS genetics, 2016-05, Vol.12 (5), p.e1006051-e1006051

2016

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Epidemiologic clues to SARS origin in China

Emerging infectious diseases, 2004-06, Vol.10 (6), p.1030-1037

2004

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A new oncolytic adenoviral vector carrying dual tumour suppressor genes shows potent anti‐tumour effect

Journal of cellular and molecular medicine, 2012-06, Vol.16 (6), p.1298-1309

2012

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The analgesic efficacy of subcostal transversus abdominis plane block with Mercedes incision

BMC anesthesiology, 2018-04, Vol.18 (1), p.36-36, Article 36

2018

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Plasma decorin predicts the presence of esophageal squamous cell carcinoma

International journal of cancer, 2010-11, Vol.127 (9), p.2138-2146

2010

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Embryo morphologic quality in relation to the metabolic and cognitive development of singletons conceived by in vitro fertilization and intracytoplasmic sperm injection: a matched cohort study

American journal of obstetrics and gynecology, 2022-09, Vol.227 (3), p.479.e1-479.e23

2022

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Usefulness of Severe Cardiac Sympathetic Dysfunction to Predict the Occurrence of Rapid Atrial Fibrillation in Patients With Wolff-Parkinson-White Syndrome

The American journal of cardiology, 2013-09, Vol.112 (5), p.688-693

2013

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A combination of P wave electrocardiography and plasma brain natriuretic peptide level for predicting the progression to persistent atrial fibrillation: comparisons of sympathetic activity and left atrial size

Journal of interventional cardiac electrophysiology, 2013-11, Vol.38 (2), p.79-84

2013

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Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan

Journal of biomedical science, 2011-06, Vol.18 (1), p.36-36, Article 36

2011

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Association Between Left and Right Atrial Remodeling With Atrial Fibrillation Recurrence After Pulmonary Vein Catheter Ablation in Patients With Paroxysmal Atrial Fibrillation: A Pilot Study

Circulation. Cardiovascular imaging, 2011-09, Vol.4 (5), p.524-531

2011

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Cardiac sympathetic nerve abnormality predicts ventricular tachyarrhythmic events in patients without conventional risk of sudden death

European Journal of Nuclear Medicine, 2008-11, Vol.35 (11), p.2066-2073

2008

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Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2‐13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high‐density oligonucleotide array‐a recognizable syndrome

American journal of medical genetics. Part A, 2010-09, Vol.152A (9), p.2365-2371

2010

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Iodine-123 mIBG Imaging for Predicting the Development of Atrial Fibrillation

JACC. Cardiovascular imaging, 2011-01, Vol.4 (1), p.78-86

2011

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Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

Human molecular genetics, 2009-12, Vol.18 (24), p.4781-4790

2009

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Activation of RAS/ERK alone is insufficient to inhibit RXRα function and deplete retinoic acid in hepatocytes

Biochemical and biophysical research communications, 2014-09, Vol.452 (3), p.801-807

2014

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Regional calcified plaque score evaluated by multidetector computed tomography for predicting the addition of rotational atherectomy during percutaneous coronary intervention

Journal of cardiovascular computed tomography, 2016-05, Vol.10 (3), p.221-228

2016

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The Significance of Cardiac Sympathetic Nervous System Abnormality in the Long-Term Prognosis of Patients with a History of Ventricular Tachyarrhythmia

Journal of Nuclear Medicine, 2009-01, Vol.50 (1), p.61-67

2009

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Type II Collagen Gene Variants and Inherited Osteonecrosis of the Femoral Head

The New England journal of medicine, 2005-06, Vol.352 (22), p.2294-2301

2005

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De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay

Gene, 2014-01, Vol.533 (1), p.78-85

2014

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Coronary Arterial Plaque Characterized by Multislice Computed Tomography Predicts Complications Following Coronary Intervention

International Heart Journal, 2007, Vol.48(1), pp.25-33

2007

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Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia

Journal of neuroimmunology, 2010-04, Vol.221 (1), p.101-106

2010

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Over-expression of AURKA, SKA3 and DSN1 contributes to colorectal adenoma to carcinoma progression

High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan

High Frequency of Epidermal Growth Factor Receptor Mutations with Complex Patterns in Non–Small Cell Lung Cancers Related to Gefitinib Responsiveness in Taiwan

Mutation in the Tyrosine Kinase Domain of Epidermal Growth Factor Receptor Is a Predictive and Prognostic Factor for Gefitinib Treatment in Patients with Non–Small Cell Lung Cancer

Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma

Epidemiologic clues to SARS origin in China

A new oncolytic adenoviral vector carrying dual tumour suppressor genes shows potent anti‐tumour effect

The analgesic efficacy of subcostal transversus abdominis plane block with Mercedes incision

Plasma decorin predicts the presence of esophageal squamous cell carcinoma

Embryo morphologic quality in relation to the metabolic and cognitive development of singletons conceived by in vitro fertilization and intracytoplasmic sperm injection: a matched cohort study

Usefulness of Severe Cardiac Sympathetic Dysfunction to Predict the Occurrence of Rapid Atrial Fibrillation in Patients With Wolff-Parkinson-White Syndrome

A combination of P wave electrocardiography and plasma brain natriuretic peptide level for predicting the progression to persistent atrial fibrillation: comparisons of sympathetic activity and left atrial size

Molecular profile and copy number analysis of sporadic colorectal cancer in Taiwan

Association Between Left and Right Atrial Remodeling With Atrial Fibrillation Recurrence After Pulmonary Vein Catheter Ablation in Patients With Paroxysmal Atrial Fibrillation: A Pilot Study

Cardiac sympathetic nerve abnormality predicts ventricular tachyarrhythmic events in patients without conventional risk of sudden death

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2‐13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high‐density oligonucleotide array‐a recognizable syndrome

Iodine-123 mIBG Imaging for Predicting the Development of Atrial Fibrillation

Chromosomal and genetic alterations in human hepatocellular adenomas associated with type Ia glycogen storage disease

Activation of RAS/ERK alone is insufficient to inhibit RXRα function and deplete retinoic acid in hepatocytes

Regional calcified plaque score evaluated by multidetector computed tomography for predicting the addition of rotational atherectomy during percutaneous coronary intervention

The Significance of Cardiac Sympathetic Nervous System Abnormality in the Long-Term Prognosis of Patients with a History of Ventricular Tachyarrhythmia

Type II Collagen Gene Variants and Inherited Osteonecrosis of the Femoral Head

De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay

Coronary Arterial Plaque Characterized by Multislice Computed Tomography Predicts Complications Following Coronary Intervention

Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia

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