about
Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association studyGenome-wide association study identifies five new susceptibility loci for primary angle closure glaucomaX-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentCISH and susceptibility to infectious diseasesFunctional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal diseaseWhole-Genome Sequencing Analysis of Serially Isolated Multi-Drug and Extensively Drug Resistant Mycobacterium tuberculosis from Thai PatientsA Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosisLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityGenome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosyGenome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibilityGenome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.The genetic architecture of type 2 diabetesGenotyping methods to analyse polymorphisms in Toll-like receptors and disease.High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis.CD209 genetic polymorphism and tuberculosis disease.Mannose-binding lectin genotypes: lack of association with susceptibility to thoracic empyema.Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencingLeprosy and the adaptation of human toll-like receptor 1.Whole-genome reconstruction and mutational signatures in gastric cancer.Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy.Characterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India.Shared pathways to infectious disease susceptibility?Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast sizeLack of association between primary angle-closure glaucoma susceptibility loci and the ocular biometric parameters anterior chamber depth and axial length.Genotype-phenotype correlation analysis for three primary angle closure glaucoma-associated genetic polymorphisms.Genome-wide expression profiling identifies type 1 interferon response pathways in active tuberculosis.Patient-based transcriptome-wide analysis identify interferon and ubiquination pathways as potential predictors of influenza A disease severity.Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.IkappaB genetic polymorphisms and invasive pneumococcal disease.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.Genetic variants of MICB and PLCE1 and associations with non-severe dengueReplication and meta-analysis of GWAS identified susceptibility loci in Kawasaki disease confirm the importance of B lymphoid tyrosine kinase (BLK) in disease susceptibility.New loci and coding variants confer risk for age-related macular degeneration in East Asians.ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma.Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel locirs4711751 and rs1999930 are not associated with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in the Chinese population.Identification of new susceptibility loci for IgA nephropathy in Han Chinese.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Chiea Chuen Khor
@ast
Chiea Chuen Khor
@en
Chiea Chuen Khor
@es
Chiea Chuen Khor
@nl
Chiea Chuen Khor
@sl
type
label
Chiea Chuen Khor
@ast
Chiea Chuen Khor
@en
Chiea Chuen Khor
@es
Chiea Chuen Khor
@nl
Chiea Chuen Khor
@sl
altLabel
Chiea-Chuen Khor
@en
prefLabel
Chiea Chuen Khor
@ast
Chiea Chuen Khor
@en
Chiea Chuen Khor
@es
Chiea Chuen Khor
@nl
Chiea Chuen Khor
@sl
P106
P1153
13404065800
P31
P496
0000-0002-1128-4729