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361 results on '"Chiea Chuen Khor"'

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151. A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

152. Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy

153. Neonatal genetics of gene expression reveal the origins of autoimmune and allergic disease risk

154. Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

155. The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome

156. Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye

157. Utility of genetic and non-genetic risk factors in predicting coronary heart disease in Singaporean Chinese

158. Pharmacogenetics of irinotecan, doxorubicin and docetaxel transporters in Asian and Caucasian cancer patients: a comparative review

159. Interaction Between Peroxisome Proliferator Activated Receptor δ and Epithelial Membrane Protein 2 Polymorphisms Influences HDL-C Levels in the Chinese Population

160. The genetic architecture of type 2 diabetes

161. Glaucoma Genetics

162. Linking a genome-wide association study signal to aLRRK2coding variant in Parkinson's disease

163. Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta

164. Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphoma

165. Predictive Genes for the Prognosis of Central Serous Chorioretinopathy

166. A Novel Homozygous Frameshift Variant in

167. Large-scale whole-genome sequencing of three diverse Asian populations in Singapore

168. Gene-diet interaction effects on BMI levels in the Singapore Chinese population

169. Joint ancestry and association test indicate two distinct pathogenic pathways involved in classical dengue fever and dengue shock syndrome

170. A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

171. Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

172. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

173. WHOLE-GENOME SEQUENCING REVEALS IMMUNOTHERAPEUTIC OPTIONS FOR NATURAL-KILLER/T CELL LYMPHOMA PATIENTS

174. ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma

175. Evaluation of plasma brain-derived neurotrophic factor levels and self-perceived cognitive impairment post-chemotherapy: a longitudinal study

176. Genes in FSGS: Diagnostic and Management Strategies in Children

177. Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility

178. A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration

179. Genetic variants of MICB and PLCE1 and associations with the laboratory features of dengue

180. Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis

181. Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function

182. ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development

183. Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1

184. ADP ribosyl-cyclases (CD38/CD157), social skills and friendship

185. Genome-Wide Association Studies of Glaucoma

186. Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma

187. CMPK1 and RBP3 are associated with corneal curvature in Asian populations

188. Multiple Nonglycemic Genomic Loci Are Newly Associated With Blood Level of Glycated Hemoglobin in East Asians

189. Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations

190. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

191. Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

192. Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore

193. Fish and marine fatty acids intakes, theFADSgenotypes and long-term weight gain: a prospective cohort study

194. Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization

196. Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies

197. Coding Variants at Hexa-allelic Amino Acid 13 of HLA-DRB1 Explain Independent SNP Associations with Follicular Lymphoma Risk

198. Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size

199. Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

200. Social, health and ocular factors associated with primary open-angle glaucoma amongst Chinese Singaporeans

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