Chiea Chuen Khor


Ontology type: schema:Person     


Person Info

NAME

Chiea Chuen

SURNAME

Khor

Publications in SciGraph latest 50 shown

  • 2019-12 Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases in NATURE COMMUNICATIONS
  • 2018-12 Novel mutation G324C in WNT1 mapped in a large Pakistani family with severe recessively inherited Osteogenesis Imperfecta in JOURNAL OF BIOMEDICAL SCIENCE
  • 2018-12 Gene-diet interaction effects on BMI levels in the Singapore Chinese population in NUTRITION JOURNAL
  • 2018-12 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases in NATURE COMMUNICATIONS
  • 2018-11 Whole exome sequencing identifies recessive germline mutations in FAM160A1 in familial NK/T cell lymphoma in BLOOD CANCER JOURNAL
  • 2018-10-31 Replication and Meta-analysis of the Association between BDNF Val66Met Polymorphism and Cognitive Impairment in Patients Receiving Chemotherapy in MOLECULAR NEUROBIOLOGY
  • 2018-06 Current Development in Genome Wide Association Studies of Glaucoma in CURRENT OPHTHALMOLOGY REPORTS
  • 2018-06 Frequent transmission of the Mycobacterium tuberculosis Beijing lineage and positive selection for the EsxW Beijing variant in Vietnam in NATURE GENETICS
  • 2018-01-23 Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12-19 Sequence data and association statistics from 12,940 type 2 diabetes cases and controls in SCIENTIFIC DATA
  • 2017-12 Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians in JOURNAL OF HUMAN GENETICS
  • 2017-12 ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development in SCIENTIFIC REPORTS
  • 2017-12 Identification and in silico characterization of a novel p.P208PfsX1 mutation in V-ATPase a3 subunit associated with autosomal recessive osteopetrosis in a Pakistani family in BMC MEDICAL GENETICS
  • 2017-12 A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration in SCIENTIFIC REPORTS
  • 2017-12 Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study in NATURE COMMUNICATIONS
  • 2017-12 Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia in SCIENTIFIC REPORTS
  • 2017-12 Exome chip meta-analysis identifies novel loci and East Asian–specific coding variants that contribute to lipid levels and coronary artery disease in NATURE GENETICS
  • 2017-12 Genetic variants of MICB and PLCE1 and associations with the laboratory features of dengue in BMC INFECTIOUS DISEASES
  • 2017-12 Evaluation of plasma brain-derived neurotrophic factor levels and self-perceived cognitive impairment post-chemotherapy: a longitudinal study in BMC CANCER
  • 2017-07 Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci in NATURE GENETICS
  • 2017-05-23 Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1 in NATURE COMMUNICATIONS
  • 2017-04 Characterising private and shared signatures of positive selection in 37 Asian populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-02-27 The spatial organization of intra-tumour heterogeneity and evolutionary trajectories of metastases in hepatocellular carcinoma in NATURE COMMUNICATIONS
  • 2017 Genome-Wide Association Studies of Glaucoma in ADVANCES IN VISION RESEARCH, VOLUME I
  • 2016-12 Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies in SCIENTIFIC REPORTS
  • 2016-11 Mapping the genetic diversity of HLA haplotypes in the Japanese populations in SCIENTIFIC REPORTS
  • 2016-10 Pharmacogenetics of UGT1A4, UGT2B7 and UGT2B15 and Their Influence on Tamoxifen Disposition in Asian Breast Cancer Patients in CLINICAL PHARMACOKINETICS
  • 2016-09 Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium in SCIENTIFIC REPORTS
  • 2016-08 The genetic architecture of type 2 diabetes in NATURE
  • 2016-06 A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy in NATURE GENETICS
  • 2016-05 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma in NATURE GENETICS
  • 2016-04 Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-03-29 Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error in NATURE COMMUNICATIONS
  • 2016-02 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma in NATURE GENETICS
  • 2016-01-19 Mutational spectrum of Barrett’s stem cells suggests paths to initiation of a precancerous lesion in NATURE COMMUNICATIONS
  • 2015-12 Identification of new susceptibility loci for IgA nephropathy in Han Chinese in NATURE COMMUNICATIONS
  • 2015-12 New loci and coding variants confer risk for age-related macular degeneration in East Asians in NATURE COMMUNICATIONS
  • 2015-12 Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia in NATURE COMMUNICATIONS
  • 2015-12 Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians in NATURE COMMUNICATIONS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-12 Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations in NATURE COMMUNICATIONS
  • 2015-11 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population in GENES & NUTRITION
  • 2015-11 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation in NATURE GENETICS
  • 2015-06 Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome in NATURE GENETICS
  • 2015-06 Cloning and variation of ground state intestinal stem cells in NATURE
  • 2015-05 Sensitive detection of chromatin-altering polymorphisms reveals autoimmune disease mechanisms in NATURE METHODS
  • 2015-04 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome in NATURE GENETICS
  • 2015-03 Genes in FSGS: Diagnostic and Management Strategies in Children in CURRENT PEDIATRICS REPORTS
  • 2015-02 Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium in HUMAN GENETICS
  • 2014-12 Characterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India in BMC GENETICS
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