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Author Details

Sek Won Kong
Boston Children's Hospital, Seoul National University, Seoul National University Hospital
0000-0003-4877-7567
2003
81
36
PMIDPaper TitleJournal TitlePublished Year
36672888ADGR: Admixture-Informed Differential Gene Regulation.Genes (Basel)2023
38012303Centrosome clustering control in osteoclasts through CCR5-mediated signaling.Sci Rep2023
37544204Association between Neuroligin-1 polymorphism and plasma glutamine levels in individuals with autism spectrum disorder.EBioMedicine2023
37645766Broadcasters, receivers, functional groups of metabolites and the link to heart failure progression using polygenic factors.Res Sq2023
34687147Inhibition of mevalonate metabolism by statins augments the immunoregulatory phenotype of vascular endothelial cells and inhibits the costimulation of CD4<sup>+</sup> T cells.Am J Transplant2022
36482414Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort.Hum Genomics2022
36153334Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder.Transl Psychiatry2022
35913450Evolution of multiple omics approaches to define pathophysiology of pediatric acute respiratory distress syndrome.Elife2022
32249310GenoPheno: cataloging large-scale phenotypic and next-generation sequencing data within human datasets.Brief Bioinform2021
33595856Genetic variation analyses indicate conserved SARS-CoV-2-host interaction and varied genetic adaptation in immune response factors in modern human evolution.Dev Growth Differ2021
33568650Two macrophages, osteoclasts and microglia: from development to pleiotropy.Bone Res2021
35028569Plasma metabolomics of autism spectrum disorder and influence of shared components in proband families.Exposome2021
34475249Increased Prevalence of Familial Autoimmune Disease in Children With Opsoclonus-Myoclonus Syndrome.Neurol Neuroimmunol Neuroinflamm2021
34016036WEScover: selection between clinical whole exome sequencing and gene panel testing.BMC Bioinformatics2021
32914305A two-step gas chromatography-tandem mass spectrometry method for measurement of multiple environmental pollutants in human plasma.Environ Sci Pollut Res Int2021
32402162Personalized iPSC-Derived Dopamine Progenitor Cells for Parkinson's Disease.N Engl J Med2020
31691385The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.Hum Mutat2020
31714896Human autologous iPSC-derived dopaminergic progenitors restore motor function in Parkinson's disease models.J Clin Invest2020
31797630Assessment of coverage for endogenous metabolites and exogenous chemical compounds using an untargeted metabolomics platform.Pac Symp Biocomput2020
32858233A survey of genetic variants in SARS-CoV-2 interacting domains of ACE2, TMPRSS2 and TLR3/7/8 across populations.Infect Genet Evol2020
30520558Solving for X: Evidence for sex-specific autism biomarkers across multiple transcriptomic studies.Am J Med Genet B Neuropsychiatr Genet2019
29969188DEPTOR modulates activation responses in CD4<sup>+</sup> T cells and enhances immunoregulation following transplantation.Am J Transplant2019
31590408An Improved Prediction Model for Ovarian Cancer Using Urinary Biomarkers and a Novel Validation Strategy.Int J Mol Sci2019
31326977Highly differentiated cytotoxic T cells in inclusion body myositis.Brain2019
31541025T Cell-Specific Adaptor Protein Regulates Mitochondrial Function and CD4<sup>+</sup> T Regulatory Cell Activity In Vivo following Transplantation.J Immunol2019
31618209Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel disease.PLoS One2019
30858925Co-inhibitory T cell receptor KLRG1: human cancer expression and efficacy of neutralization in murine cancer models.Oncotarget2019
30824715Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings.Sci Rep2019
29653250Pluripotent stem cell-based therapy for Parkinson's disease: Current status and future prospects.Prog Neurobiol2018
29789557Measuring coverage and accuracy of whole-exome sequencing in clinical context.Genet Med2018
27862943Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined-samples mega-analysis.Am J Med Genet B Neuropsychiatr Genet2017
29244735Development of the Precision Link Biobank at Boston Children's Hospital: Challenges and Opportunities.J Pers Med2017
28807506Altered vulnerability to asthma at various levels of ambient Benzo[a]Pyrene by CTLA4, STAT4 and CYP2E1 polymorphisms.Environ Pollut2017
28611076Learning a Comorbidity-Driven Taxonomy of Pediatric Pulmonary Hypertension.Circ Res2017
28822752Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders.Cell Syst2017
26731445Absence of evidence for increase in risk for autism or attention-deficit hyperactivity disorder following antidepressant exposure during pregnancy: a replication study.Transl Psychiatry2016
27522000A model-driven methodology for exploring complex disease comorbidities applied to autism spectrum disorder and inflammatory bowel disease.J Biomed Inform2016
26860211ksRepo: a generalized platform for computational drug repositioning.BMC Bioinformatics2016
25341114Summarizing polygenic risks for complex diseases in a clinical whole-genome report.Genet Med2015
26357316An Efficient Search Algorithm for Finding Genomic-Range Overlaps Based on the Maximum Range Length.IEEE/ACM Trans Comput Biol Bioinform2015
26697163Gene expression analysis in Fmr1KO mice identifies an immunological signature in brain tissue and mGluR5-related signaling in primary neuronal cultures.Mol Autism2015
26092939Mitf is a master regulator of the v-ATPase, forming a control module for cellular homeostasis with v-ATPase and TORC1.J Cell Sci2015
26148225I148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver disease.Liver Int2015
24478219Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline.Hum Mutat2014
24829188Reducing false-positive incidental findings with ensemble genotyping and logistic regression based variant filtering methods.Hum Mutat2014
24564913Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.Mol Autism2014
24645908The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.Trials2014
23596012Cytosolic 5'-nucleotidase 1A autoimmunity in sporadic inclusion body myositis.Ann Neurol2013
24063311Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.BMC Med Genomics2013
23625158Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.Neurogenetics2013
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Collaborators

Children's Hospital Boston
Co-authored papers 21
Co-authored papers 20
Harvard Medical School
Co-authored papers 19
Boston Children's Hospital, Harvard Medical School
Co-authored papers 11
Massachusetts General Hospital
Co-authored papers 10
Boston Children's Hospital
Co-authored papers 9
Soongsil University
Co-authored papers 8
Harvard Medical School
Co-authored papers 7
Boston Children's Hospital
Co-authored papers 6
Brigham Women's Hospital, Harvard Medical School
Co-authored papers 6
University of British Columbia
Co-authored papers 6
Brigham and Women's Hospital Department of Neurology, and Harvard Medical School
Co-authored papers 5
Beth Israel Deaconess Medical Center.
Co-authored papers 5
Stanford University School of Medicine
Co-authored papers 4
College of Plant Science and Technology, Huazhong Agricultural University
Co-authored papers 4
VA Boston Healthcare System
Co-authored papers 4
Hanyang University Hospital
Co-authored papers 4
Centro de Investigacion Biomedica en Red en Epidemiologia y Salud Publica (CIBERESP)
Co-authored papers 4
Boston Children's Hospital and Harvard Medical School
Co-authored papers 4
Tokyo Medical and Dental University Hospital
Co-authored papers 4
Samsung Medical Center, Sungkyunkwan University School of Medicine
Co-authored papers 4
Beth Israel Deaconess Medical Center, Harvard Medical School
Co-authored papers 4
Medical University of Graz
Co-authored papers 4
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
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Brigham and Women's Hospital, Harvard Medical School
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Beth Israel Deaconess Medical Center
Co-authored papers 3
Co-authored papers 3
Clinical Biomarkers Laboratory, Emory University
Co-authored papers 3
Boston Children's Hospital
Co-authored papers 3
Emory University Department of Human Genetics Atlanta Georgia 30322.
Co-authored papers 3