Chiea Chuen Khor
Khor, Chiea Chuen
VIAF ID: 45155767400627761923 (Personal)
Permalink: http://viaf.org/viaf/45155767400627761923
Preferred Forms
- 100 0 _ ‡a Chiea Chuen Khor
- 100 1 _ ‡a Khor, Chiea Chuen
4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | |
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area | |
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium | |
A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration. | |
Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia | |
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population | |
Genome-wide expression profiling identifies type 1 interferon response pathways in active tuberculosis | |
Genome-wide linkage and association mapping identify susceptibility alleles in ABCC4 for Kawasaki disease. | |
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia | |
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | |
Genotype-phenotype correlation analysis for three primary angle closure glaucoma-associated genetic polymorphisms | |
Genotyping methods to analyse polymorphisms in Toll-like receptors and disease. | |
Glaucoma Genetics: Recent Advances and Future Directions. | |
Global gene expression profiling identifies new therapeutic targets in acute Kawasaki disease | |
Hepatocyte growth factor and retinal arteriolar diameter in Singapore Chinese | |
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis | |
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy | |
Host-pathogen interactions revealed by human genome-wide surveys | |
A hybrid framework for genome wide epistasis discovery | |
iCall: a genotype-calling algorithm for rare, low-frequency and common variants on the Illumina exome array. | |
Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations | |
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. | |
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy | |
Identification of type 2 diabetes loci in 433,540 East Asian individuals | |
IkappaB genetic polymorphisms and invasive pneumococcal disease | |
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. | |
Impact of measurement error on testing genetic association with quantitative traits. | |
Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing | |
Interaction Between Peroxisome Proliferator Activated Receptor δ and Epithelial Membrane Protein 2 Polymorphisms Influences HDL-C Levels in the Chinese Population. | |
An intronic FTO variant rs16952570 confers protection against thiopurine-induced myelotoxicities in multiethnic Asian IBD patients | |
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development | |
Keratoconus-susceptibility gene identification by corneal thickness genome-wide association study and artificial intelligence IBM Watson | |
Lack of association between primary angle-closure glaucoma susceptibility loci and the ocular biometric parameters anterior chamber depth and axial length. | |
Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size | |
Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium | |
Leprosy and the adaptation of human toll-like receptor 1. | |
Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease. | |
Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies | |
LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets | |
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility | |
Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema | |
Mapping the genetic diversity of HLA haplotypes in the Japanese populations | |
mcr-1 in Multidrug-Resistant blaKPC-2-Producing Clinical Enterobacteriaceae Isolates in Singapore | |
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error | |
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline | |
A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy | |
Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions | |
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters | |
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians | |
Mutational spectrum of Barrett's stem cells suggests paths to initiation of a precancerous lesion | |
Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies | |
Neonatal genetics of gene expression reveal potential origins of autoimmune and allergic disease risk | |
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. | |
A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias. | |
Patient-based transcriptome-wide analysis identify interferon and ubiquination pathways as potential predictors of influenza A disease severity | |
Pharmacogenetics of irinotecan, doxorubicin and docetaxel transporters in Asian and Caucasian cancer patients: a comparative review. | |
Pharmacogenetics of UGT1A4, UGT2B7 and UGT2B15 and Their Influence on Tamoxifen Disposition in Asian Breast Cancer Patients | |
Polypoidal choroidal vasculopathy and systemic lupus erythematosus | |
Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. | |
PTPN22 and invasive bacterial disease | |
Replication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility | |
Reply to ”Analysis of association of the TIRAP (MAL) S180L variant and tuberculosis in three populations” | |
Revealing the molecular signatures of host-pathogen interactions. | |
rs4711751 and rs1999930 are not associated with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in the Chinese population. | |
Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms | |
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls | |
SgD-CNV, a database for common and rare copy number variants in three Asian populations | |
Shared pathways to infectious disease susceptibility? | |
Strategies for identifying the genetic basis of dyslipidemia: genome-wide association studies vs. the resequencing of extremes. | |
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry | |
Support for TGFB1 as a Susceptibility Gene for High Myopia in Individuals of Chinese Descent | |
Targeted next-generation sequencing to diagnose disorders of HDL cholesterol. | |
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities | |
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation | |
Variation at HLA-DRB1 is associated with resistance to enteric fever | |
Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphoma | |
Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations | |
Whole-genome reconstruction and mutational signatures in gastric cancer. | |
Whole-Genome Sequencing Analysis of Serially Isolated Multi-Drug and Extensively Drug Resistant Mycobacterium tuberculosis from Thai Patients |