about
Development of heart valves requires Gata4 expression in endothelial-derived cellsThe MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicineIntegration of heterogeneous expression data sets extends the role of the retinol pathway in diabetes and insulin resistance.Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.Cytosolic 5'-nucleotidase 1A autoimmunity in sporadic inclusion body myositis.Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart.Gata4 is required for maintenance of postnatal cardiac function and protection from pressure overload-induced heart failureksRepo: a generalized platform for computational drug repositioningMitf is a master regulator of the v-ATPase, forming a control module for cellular homeostasis with v-ATPase and TORC1.Summarizing polygenic risks for complex diseases in a clinical whole-genome reportAnalysis of the Otd-dependent transcriptome supports the evolutionary conservation of CRX/OTX/OTD functions in flies and vertebratesType I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.Absence of evidence for increase in risk for autism or attention-deficit hyperactivity disorder following antidepressant exposure during pregnancy: a replication study.Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders.Learning a Comorbidity-Driven Taxonomy of Pediatric Pulmonary Hypertension.A model-driven methodology for exploring complex disease comorbidities applied to autism spectrum disorder and inflammatory bowel diseaseBlood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined-samples mega-analysis.Altered vulnerability to asthma at various levels of ambient Benzo[a]Pyrene by CTLA4, STAT4 and CYP2E1 polymorphisms.Mouse cardiac surgery: comprehensive techniques for the generation of mouse models of human diseases and their application for genomic studies.Pluripotent stem cell-based therapy for Parkinson's disease: Current status and future prospects.Measuring coverage and accuracy of whole-exome sequencing in clinical contextComparative analysis of whole-genome sequencing pipelines to minimize false negative findingsSolving for X: Evidence for sex-specific autism biomarkers across multiple transcriptomic studiesCo-inhibitory T cell receptor KLRG1: human cancer expression and efficacy of neutralization in murine cancer modelsThe insulin-like growth factor 1 receptor induces physiological heart growth via the phosphoinositide 3-kinase(p110alpha) pathwayAltered microRNA expression in human heart diseaseRelationship between disease activity and type 1 interferon- and other cytokine-inducible gene expression in blood in dermatomyositis and polymyositisI148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver diseaseDEPTOR modulates activation responses in CD4+ T cells and enhances immunoregulation following transplantationT Cell-Specific Adaptor Protein Regulates Mitochondrial Function and CD4+ T Regulatory Cell Activity In Vivo following TransplantationThe Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry compositionCorrection: The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning systemThe Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0003-4877-7567
@en
name
Sek Won Kong
@ast
Sek Won Kong
@en
Sek Won Kong
@es
Sek Won Kong
@nl
type
label
Sek Won Kong
@ast
Sek Won Kong
@en
Sek Won Kong
@es
Sek Won Kong
@nl
prefLabel
Sek Won Kong
@ast
Sek Won Kong
@en
Sek Won Kong
@es
Sek Won Kong
@nl
P106
P31
P496
0000-0003-4877-7567