| # | Title | Journal | Year | Citations |
|---|
| 1 | The landscape of cancer genes and mutational processes in breast cancer | Nature | 2012 | 1,535 |
| 2 | A Genome-Wide Association Study Identifies Susceptibility Variants for Type 2 Diabetes in Han Chinese | PLoS Genetics | 2010 | 301 |
| 3 | Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease | Nature Immunology | 2011 | 248 |
| 4 | Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1 | PLoS Genetics | 2013 | 118 |
| 5 | A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease | Human Genetics | 2011 | 79 |
| 6 | Smoking and Genetic Risk Variation Across Populations of European, Asian, and African American Ancestry—A Meta‐Analysis of Chromosome 15q25 | Genetic Epidemiology | 2012 | 69 |
| 7 | A Single Nucleotide Polymorphism Fine Mapping Study of Chromosome 1q42.1 Reveals the Vulnerability Genes for Schizophrenia, GNPAT and DISC1: Association with Impairment of Sustained Attention | Biological Psychiatry | 2006 | 64 |
| 8 | Neuregulin 1 gene and variations in perceptual aberration of schizotypal personality in adolescents | Psychological Medicine | 2005 | 59 |
| 9 | More evidence supports the association of PPP3CC with schizophrenia | Molecular Psychiatry | 2007 | 57 |
| 10 | RASD2, MYH9, and CACNG2 Genes at Chromosome 22q12 Associated with the Subgroup of Schizophrenia with Non-Deficit in Sustained Attention and Executive Function | Biological Psychiatry | 2008 | 51 |
| 11 | No association of G72 and d-amino acid oxidase genes with schizophrenia | Schizophrenia Research | 2006 | 49 |
| 12 | Determinants of Human Adipose Tissue Gene Expression: Impact of Diet, Sex, Metabolic Status, and Cis Genetic Regulation | PLoS Genetics | 2012 | 48 |
| 13 | PrimerZ: streamlined primer design for promoters, exons and human SNPs | Nucleic Acids Research | 2007 | 45 |
| 14 | Genetic variation in the nuclear factor κB pathway in relation to susceptibility to rheumatoid arthritis | Annals of the Rheumatic Diseases | 2009 | 40 |
| 15 | Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p | Genes, Brain and Behavior | 2009 | 34 |
| 16 | Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population | Psychiatric Genetics | 2006 | 33 |
| 17 | Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits | Diabetes | 2012 | 31 |
| 18 | Plasma decorin predicts the presence of esophageal squamous cell carcinoma | International Journal of Cancer | 2010 | 27 |
| 19 | Recessive MYPN mutations cause cap myopathy with occasional nemaline rods | Annals of Neurology | 2017 | 27 |
| 20 | A novel locus for autosomal recessive spastic ataxia on chromosome 17p | Human Genetics | 2007 | 26 |
| 21 | Acculturation, psychiatric comorbidity and posttraumatic stress disorder in a Taiwanese aboriginal population | Social Psychiatry and Psychiatric Epidemiology | 2009 | 20 |
| 22 | Garlic Accelerates Red Blood Cell Turnover and Splenic Erythropoietic Gene Expression in Mice: Evidence for Erythropoietin-Independent Erythropoiesis | PLoS ONE | 2010 | 19 |
| 23 | New Adjustment Factors and Sample Size Calculation in a DNA-Pooling Experiment With Preferential Amplification | Genetics | 2005 | 18 |
| 24 | Evaluation ofRGS4 as a candidate gene for schizophrenia | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2006 | 16 |
| 25 | Functional analysis of novel SNPs and mutations in human and mouse genomes | BMC Bioinformatics | 2008 | 16 |
| 26 | Exhaustive methylation analysis revealed uneven profiles of methylation atIGF2/ICR1/H1911p15 loci in Russell Silver syndrome | Journal of Medical Genetics | 2015 | 16 |
| 27 | No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families | Schizophrenia Research | 2007 | 15 |
| 28 | Novel susceptibility genes associated with diabetic cataract in a Taiwanese population | Ophthalmic Genetics | 2013 | 14 |
| 29 | Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities | Genetics in Medicine | 2021 | 14 |
| 30 | Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical description | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | 2007 | 13 |
| 31 | Selective loss of a LAP1 isoform causes a muscle-specific nuclear envelopathy | Neurogenetics | 2021 | 3 |
