ScholarWorks@Korea University: An, Joon Yong

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An, Joon Yong (안준용)

College of Health Sciences (School of Biosystems and Biomedical Sciences)

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Tel 02-3290-5646
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Autism spectrum disorder:3||Wholegenome sequencing:3||exome sequencing:3||autism spectrum disorder:3||Precision medicine:2||Neurodevelopment:2||Intellectual disability:2||neurodevelopment:2||systems biology:2||genomics:2||iron:1||brain development:1||neurological disorder:1||familial strabismus:1||multiomics analysis:1||fetal transition:1||mTOR:1||Locus discovery:1||Autism spectrum disorder (ASD):1||proteogenomics:1||Clinical improvement:1||haploinsufficient disorders:1||genetic association:1||Autism:1||Familial pattern:1||Congenital Anomalies:1||Multiomics integration:1||Proteomics:1||lipid peroxides:1||autism spectrum disorder (ASD):1||dorsolateral prefrontal cortex:1||prenatal eQTL:1||cell type:1||excitatoryinhibitory balance:1||Gene discovery:1||Voltagegated sodium channel:1||Kdm3b:1||Exome sequencing:1||functional genomics:1||structural anomaly:1||autism:1||cancer immunity:1||Mass spectrometry proteomics:1||Multiomics:1||ferroptosis:1||CNS:1||gene pathway:1||BrainVar:1||liability:1||Whole exome sequencing:1||cancer research:1||Congenital fibrosis of extraocular muscles:1||karyotype:1||microarray:1||prenatal:1||firsttier:1||CP: Neuroscience:1||CRISPRi:1||Phenotypic diversity:1||Whole Genome Sequencing:1||Genetic Variant:1||Cancer subtype:1||strabismus genetics:1||autism spectrum disorders:1||PsychENCODE:1||excitatory neurons:1||inhibitory neurons:1||Isoform:1||Splicing:1||Epileptic encephalopathy:1||Hippocampus:1||noncoding genome:1||Sex differences:1||Clustering methods:1||Exon 5A:1||Seizures:1||proteomics:1||structural variant:1||chromatin:1||rare variant:1||genetics in psychiatry:1||tandem repeat:1||whole genome sequencing:1||N<sup>6</sup>methyladenosine:1||Cancer heterogeneity:1||Proteogenomics:1||strabismus genes:1||LOC101926933 RP11298I3.1 AL132780.1 ENSG00000257285:1||Developmental delay:1||Exon 5N:1||Infantile esotropia:1||Neurodevelopmental outcome:1||computational genomics:1||autism disease genetics:1||genome sequencing:1||CP: Genomics:1||mouse brain development:1||regulatory noncoding variant:1||biological psychiatry:1||Polygenic burden:1||YTHDF proteins:1||Multiomics subtype:1||Proteomic subtype:1||DLPFC:1||RHEBL1:1||Cerebellum:1||multiomics approach:1||Strabismus:1||Ultraviolet irradiation:1||diagnostic:1||convergence:1||transcriptional regulators:1||wholegenome sequencing:1||Rare Disease:1||Population genetics:1||Genomic subtype:1||Kinasemediated signaling pathway:1||strabismus genomic analyses:1||wholeexome sequencing:1||cytoskeleton:1||genetics:1||Optokinetic response (OKR):1||Histone modification:1||Wholeexome sequencing:1||Microglia dysfunction:1||gene regulation:1||neural development:1||human fetal development:1||Cortex:1||Gene expression:1||RNAseq:1||Sex difference:1||gastric cancer:1||interferonγ signaling:1||Biobank:1||Integration methods:1||Molecular subtype:1||Phosphoproteomics:1||

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