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A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese

PLoS genetics, 2010-02, Vol.6 (2), p.e1000847-e1000847

2010

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Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence

Psychiatric genetics, 2019-08, Vol.29 (4), p.111-119

2019

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Source identification of HIV-1 transmission in three lawsuits Using Ultra-Deep pyrosequencing and phylogenetic analysis

Journal of microbiology, immunology and infection, 2021-08, Vol.54 (4), p.596-605

2021

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Effects of insomnia and non-vasomotor menopausal symptoms on coronary heart disease risk: a mendelian randomization study

Heliyon, 2023-02, Vol.9 (2), p.e13569, Article e13569

2023

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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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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Nature genetics, 1996-04, Vol.12 (4), p.431-435

1996

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On the use of multifactor dimensionality reduction (MDR) and classification and regression tree (CART) to identify haplotype–haplotype interactions in genetic studies

Genomics (San Diego, Calif.), 2011-02, Vol.97 (2), p.77-85

2011

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A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease

Translational research : the journal of laboratory and clinical medicine, 2013-06, Vol.161 (6), p.513-515

2013

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L-006 GENOME-WIDE SCAN FOR YOUNG-ONSET HYPERTENSION IN HAN CHINESE IN TAIWAN

Journal of hypertension, 2011-11, Vol.29 Suppl B, p.e36-e36

2011

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Han Chinese Cell and Genome Bank in Taiwan: Purpose, Design and Ethical Considerations

Human heredity, 2006, Vol.61 (1), p.27-30

2006

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Meta-analysis of effectiveness and safety of abciximab versus eptifibatide or tirofiban in percutaneous coronary intervention

The American journal of cardiology, 2001-03, Vol.87 (5), p.537-541

2001

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Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling

Human mutation, 2008-08, Vol.29 (8), p.1055-1062

2008

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Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Human molecular genetics, 2017-05, Vol.26 (9), p.1770-1784

2017

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Meta-analysis identifies common variants associated with body mass index in east Asians

Nature genetics, 2012-03, Vol.44 (3), p.307-311

2012

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Shared genomic segment analysis with equivalence testing

Genetic epidemiology, 2020-10, Vol.44 (7), p.741-747

2020

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Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families

World journal of gastroenterology : WJG, 2021-10, Vol.27 (37), p.6262-6276

2021

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Polymorphism Screening of PIP5K2A: A Candidate Gene for Chromosome 10p-Linked Psychiatric Disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2003-11, Vol.123B (1), p.50-58

2003

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Weight loss and metabolic improvements in obese patients undergoing gastric banding and gastric banded plication: A comparison

Nutrition (Burbank, Los Angeles County, Calif.), 2019-01, Vol.57, p.290-299

2019

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Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index

PloS one, 2012-07, Vol.7 (7), p.e40996-e40996

2012

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Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study

Virulence, 2021-12, Vol.12 (1), p.270-280

2021

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Methods for identifying differentially methylated regions for sequence- and array-based data

Briefings in functional genomics, 2016-11, Vol.15 (6), p.485-490

2016

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Extracellular Nicotinamide Phosphoribosyltransferase as a Surrogate Marker of Prominent Malignant Potential in Colonic Polyps: A 2-Year Prospective Study

Cancers, 2023-03, Vol.15 (6), p.1702

2023

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Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine-Altering Variants

Journal of the American Heart Association, 2023-11, Vol.12 (22), p.e032689

2023

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A non-threshold region-specific method for detecting rare variants in complex diseases

PloS one, 2017-11, Vol.12 (11), p.e0188566-e0188566

2017

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Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients

Frontiers in oncology, 2022-06, Vol.12, p.883437-883437

2022

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A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese

Determining population stratification and subgroup effects in association studies of rare genetic variants for nicotine dependence

Source identification of HIV-1 transmission in three lawsuits Using Ultra-Deep pyrosequencing and phylogenetic analysis

Effects of insomnia and non-vasomotor menopausal symptoms on coronary heart disease risk: a mendelian randomization study

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

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

On the use of multifactor dimensionality reduction (MDR) and classification and regression tree (CART) to identify haplotype–haplotype interactions in genetic studies

A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease

L-006 GENOME-WIDE SCAN FOR YOUNG-ONSET HYPERTENSION IN HAN CHINESE IN TAIWAN

Han Chinese Cell and Genome Bank in Taiwan: Purpose, Design and Ethical Considerations

Meta-analysis of effectiveness and safety of abciximab versus eptifibatide or tirofiban in percutaneous coronary intervention

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

Meta-analysis identifies common variants associated with body mass index in east Asians

Shared genomic segment analysis with equivalence testing

Hepatitis B virus persistent infection-related single nucleotide polymorphisms in HLA regions are associated with viral load in hepatoma families

Polymorphism Screening of PIP5K2A: A Candidate Gene for Chromosome 10p-Linked Psychiatric Disorders

Weight loss and metabolic improvements in obese patients undergoing gastric banding and gastric banded plication: A comparison

Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index

Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study

Methods for identifying differentially methylated regions for sequence- and array-based data

Extracellular Nicotinamide Phosphoribosyltransferase as a Surrogate Marker of Prominent Malignant Potential in Colonic Polyps: A 2-Year Prospective Study

Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine-Altering Variants

A non-threshold region-specific method for detecting rare variants in complex diseases

Patient-Derived Organoid Serves as a Platform for Personalized Chemotherapy in Advanced Colorectal Cancer Patients

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