about
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopiaNine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorGene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP ConsortiaThe genetic architecture of type 2 diabetesInsights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencingCharacterizing the genetic differences between two distinct migrant groups from Indo-European and Dravidian speaking populations in India.Common variants in major histocompatibility complex region and TCF4 gene are significantly associated with schizophrenia in Han Chinese.Common variants in the BCL9 gene conferring risk of schizophrenia.Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.Pathways-driven sparse regression identifies pathways and genes associated with high-density lipoprotein cholesterol in two Asian cohortsMeta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel lociDeep whole-genome sequencing of 100 southeast Asian Malays.Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.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.Genetic variation in CDH13 is associated with lower plasma adiponectin levels but greater adiponectin sensitivity in East Asian populations.Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies.A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure lociImpact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.Differential dependence on DNA ligase of type II restriction enzymes: a practical way toward ligase-free DNA automaton.Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies.A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore.CMPK1 and RBP3 are associated with corneal curvature in Asian populations.Analysis of association between common SNPs in ErbB4 and bipolar affective disorder, major depressive disorder and schizophrenia in the Han Chinese population.Common SNPs in CSF2RB are associated with major depression and schizophrenia in the Chinese Han population.Gold nanoparticles for high-throughput genotyping of long-range haplotypes.Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populationsMeta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataractCommon SNPs and haplotypes in DGKH are associated with bipolar disorder and schizophrenia in the Chinese Han population
P50
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P50
description
onderzoeker
@nl
researcher ORCID: 0000-0002-1422-4641
@en
name
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
Peng Chen
@sl
type
label
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
Peng Chen
@sl
prefLabel
Peng Chen
@en
Peng Chen
@es
Peng Chen
@nl
Peng Chen
@sl
P106
P1153
50761072700
P21
P31
P496
0000-0002-1422-4641