Joon-Yong An

Dr. An is an Associate Professor in the Department of Biosystem and Biomedical Science at Korea University.

He is a human geneticist whose research focuses on the genetic architecture of autism spectrum disorder (ASD) and other neurodevelopmental conditions. His group investigates how genetic variants contribute to the etiology and phenotypic heterogeneity of ASD through large-scale whole-genome sequencing and multi-omics integration. The team combines population-scale genomics with single-cell and epigenomic resources to delineate the cell-type and temporal specificity of neuropsychiatric risk genes and to uncover the molecular mechanisms underlying brain development.

Dr. An’s research advances cross-ancestry genetic discovery by integrating Korean ASD cohorts with international datasets, expanding the understanding of ASD beyond European-centric studies. His laboratory also develops computational frameworks for noncoding variant association and applies integrative analyses of genomic, transcriptomic, and epigenomic data to connect genetic variation with neural function and clinical outcomes.

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Professional Experience

2022-Present, Associate Professor, Korea University
2019-2022, Assistant Professor, Korea University
2015-2019, Postdoctoral Scholar, UCSF

Education & Training

2015-2019 Postdoctoral Fellow, University of California, San Francisco.
2012-2016 Ph.D., Neuroscience, University of Queensland, Australia
2010-2011 M.Sc., Molecular Biology, University of Queensland, Australia
2005-2010 B.Sc., Molecular Biotechnology, Konkuk University, South Korea

Awards

2025 Seoktap Research Award (석탑연구상), Korea University
2024 Rising Star Award, Korea Genome Organization
2024 Green Ribbon Lecture Award, Korean Society for Molecular and Cellular Biology
2023 Young Scientist Award, Korea Society of Bioinformatics
2022 Young Scientist Travel Award, The Japan Neuroscience Society
2020 Young Scientist Travel Award, The Japan Neuroscience Society
2019 Young Investigator Research Award, International Society for Autism Research

Academic Service

2022-present, Editorial Board, eLife
2021-present, Editorial Board, Molecular Brain
2021-present, Editorial Board, Experimental and Molecular Medicine
2021-present, Editorial Board, Molecules and Cells
2024-Present, Editorial Board, BMC Genomics & Informatics
2024-Present, Committee Member, Data Sharing and Utilization Committee, Korea National Institute of Health (질병관리청 보건의료연구자원정보센터 데이터 공개·활용위원회, 전문위원)
2024-Present, Review Board, Advanced Biotechnology Division, National Research Foundation of Korea (한국연구재단 첨단바이오 분과, 전문위원)
2022-Present, Planning Committee Member, Division of Future Medicine, Korea Disease Control and Prevention Agency (질병관리청 국립보건연구원 미래의료연구부, 기획위원)
2024-2025, Committee Member, Bio·Health Data Platform Council, Ministry of Science and ICT (과학기술정보통신부 바이오·헬스 데이터플랫폼 협의체 전문위원)
2022-2024, Committee Member, Digital Health Subcommittee, Health Policy Review Committee, Ministry of Health and Welfare (보건복지부 보건의료정책심의위원회 디지털헬스 분과, 전문위원)
2020-2023, Planning Commissioner, National Project of Bio Big Data, South Korea (국가통합바이오빅데이터 구축 사업, 총괄기획위원)
2021-Present, Grant Review Panel, Israel Science Foundation
2020-Present, Grant Review Panel, Wellcome Trust Foundation
2024-Present, Grant Review Panel, UK Research and Innovation
Ad hoc peer reviewer: Biological Psychiatry, BMC Genomics, Experimental and Molecular Medicine, eLife, JAMA, JAMA Psychiatry, Molecular Autism, Molecular Psychiatry, Nature Communications, PLOS Genetics, Translational Psychiatry

Funding

2025–2030 Identification of sex-specific genetic factors in autism using DNA methylation and genomic imprinting, Mid-career Researcher Program, National Research Foundation of Korea (PI), DNA 메틸레이션 및 유전체 각인을 활용한 자폐 성별 특이적 유전인자 규명 연구, 중견연구자지원사업, 한국연구재단
2025–2028 Development of proteogenomics framework for predicting anticancer drug resistance, Korea–US Joint Cancer Research Program, National Cancer Center (PI), 인산화 단백체-유전체 통합 분석을 통한 항암제 내성 예측 및 인포매틱스 기술 개발, 한미암공동연구사업, 국립암센터
2024–2028 Development of analytic framework for long-read sequencing and improving rare disease diagnostic yield, Korean National Research Centre in Bioinformatics, Korea Research Institute of Bioscience and Biotechnology (CI), 롱리드 시퀀싱 기반 한국인 전장유전체 변이분석 방법론 개발 및 희귀질환 진단률 향상, 국가생명연구자원정보센터, 한국생명공학연구원
2024–2028 Mapping immune–neural networks using a human brain organoid, Global Collaborative Research Program, Ministry of Health and Welfare (CI), 인간신경오가노이드 패널을 이용한 면역-신경 네트워크 지도 작성, 글로벌연구협력지원사업, 보건복지부
2024–2027 AI models for diagnosing neurodevelopmental disorders and discovering new biomarkers, Bio & Medical Technology Development Program, National Research Foundation of Korea (CI), 빅데이터 기반 신경발달장애 진단 AI 모델 개발 및 신규 바이오마커 발굴, 바이오·의료기술개발사업, 한국연구재단
2022–2024 Characterization and regulation of neuronal diversity in the fear–anxiety network, Bio & Medical Technology Development Program, National Research Foundation of Korea (CI), 공포-불안 네트워크를 구성하는 신경세포 다양성 규명 및 조절, 바이오·의료기술개발사업, 한국연구재단
2022–2024 Development of analytical methods for structural and noncoding variants causing dementia in the Korean population using whole-genome data, Dementia Overcoming Research & Development Program (PI), 전장유전체 기반 한국인 치매 유발 구조변이 및 비암호화 유전변이 분석 및 유전연관성 규명 방법 개발, 치매극복연구개발사업단
2022–2023 Analysis of autism-causing structural variants in the Korean population and development of genetic association methods using whole-genome sequencing, Inseong Foundation, Korea University (PI), 전장유전체 기반 한국인 자폐 원인 구조변이 분석 및 유전연관성 규명 방법 개발, 고려대학교 인성재단
2021–2025 Development of gene-based diagnostic technologies in Korean families with autism spectrum disorder, Bio & Medical Technology Development Program, National Research Foundation of Korea (CI), 한국인 자폐스펙트럼장애 가족에서 유전자기반 진단 기술 개발, 바이오·의료기술개발사업, 한국연구재단
2021–2024 Active Transition T Cell Tolerance Research Laboratory, Basic Research Laboratory Program, National Research Foundation of Korea (CI), 능동전환 T세포관용 연구실, 기초연구실지원사업, 한국연구재단
2020–2025 Development of categorical association methods for studying noncoding mutations and identifying pathogenic enhancer mutations underlying neurodevelopmental disorders, Young Investigator Program, National Research Foundation of Korea (PI), Noncoding mutation 연구를 위한 범주형 연관성 방법론 개발 및 신경발달장애 원인 pathogenic enhancer mutation 규명, 신진연구자지원사업, 한국연구재단
2020–2021 Identification and validation of novel molecular targets and pathways related to autism using mouse models, Brain Research Program, National Research Foundation of Korea (CI), 생쥐 모델을 이용한 자폐증 관련 신규표적분자, 경로 발굴 및 검증, 뇌과학원천기술개발사업, 한국연구재단
2020–2021 Analysis of cellular composition and disease relevance in the subthalamic nucleus using single-cell transcriptomic data, Brain Research Program, National Research Foundation of Korea (PI), 단일세포 전사체 기반 하 시상핵의 세포 조성 및 뇌질환 연관성 분석, 뇌과학원천기술개발사업, 한국연구재단
2019–2024 Development of intelligent informatics technologies and infrastructure for multi-omics–based precision medicine, Bio & Medical Technology Development Program, National Research Foundation of Korea (CI), 다중오믹스 기반 정밀의료를 위한 지능형 인포매틱스 기술 개발 및 기반 구축, 바이오·의료기술개발사업, 한국연구재단
2018–2019 Post-Doctoral Fellowship, Autism Science Foundation & FamilieSCN2A Foundation (PI)

Public Engagement and Outreach

2023/7/27, KSMCB Kyeongam Bio Youth Camp, Understanding female autism through DNA
2024/3/16, Brain Awareness Week Event, Human brain development through the lens of single-cell atlas
2024/7/12, 3rd Autism Expo, Genetic Studies in Autism: What Does Genetic Research Mean?
2025/04/06, Paradise Foundation, Genetics and Autism
2025/05/19, Special Education for Teachers (Dankook University), Genetics of Autism
2025/09/17, Gwangseong Haneulbit School, Genetics of Autism

Education Workshop

2019/12/14, Precision Medicine Education Workshop (Korea University College of Medicine), Whole genome sequencing analysis towards genetic architecture of human disorders
2021/10/2, Swiss School of Management, Understanding Genetic Model and Quantitative Nature of Human Genetics
2020/10/31, Precision Medicine Education Workshop (Korea University College of Medicine), Whole genome sequencing analysis towards genetic architecture of human disorders
2021/2/17, Bioinformatics & Machine Learning Workshop for Life Scientists (Korean Society for Bioinformatics), Whole genome sequencing analyses to understand the genetic architecture of human disorders
2021/5/12, Gangwon Precision Medicine Industry Program, A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2022/10/11, Hongneung Innopolis Digital Healthcare, Genome-Wide Approaches for Understanding Genetic Architecture
2022/11/18, 21st Genetics Training Course (Samsung Medical Center), Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2021/8/21, Fellowship Education Workshop (Korean Society for Schizophrenia Research), Understanding Genetic Model and Quantitative Nature of Human Genetics
2021/11/13, Precision Medicine Education Workshop (Korea University College of Medicine), Whole genome sequencing analysis towards genetic architecture of human disorders
2022/2/22, Bioinformatics & Machine Learning Workshop for Life Scientists (Korean Society for Bioinformatics), Introduction of Hail for Whole Genome Sequencing Analysis
2022/11/12, Precision Medicine Education Workshop (Korea University College of Medicine), Whole genome sequencing analysis towards genetic architecture of human disorders
2022/11/15, Artificial Intelligence Training Course (Korea Pharmaceutical and Bio-Pharma Manufacturers Association), Introduction to whole genome sequencing genetic association methodology and genetic architecture
2023/3/23, Precision Medicine Education Workshop (Seoul National University Bundang Hospital), GWAS basics and hands-on training
2023/8/18, LAIDD Workshop, LAIDD Workshop presentation
2023/8/26, Fellowship Education Workshop (Korean Society for Schizophrenia Research), Whole genome sequencing analysis towards genetic architecture of schizophrenia
2023/9/23, Korean Bioinformation Center, Introductory Course for Getting Started with Bioinformatics
2023/11/11, Precision Medicine Education Workshop (Seoul National University Bundang Hospital), Genome-Wide Approaches for Understanding Genetic Architecture
2024/3/13, Education Workshop (Precision Medicine Center, Seoul National University Bundang Hospital), Introduction to Genome-Wide Association Studies
2024/7/22, 18th Asian Institute in Statistical Genetics and Genomics, Introduction to Genetics

Conference Talk

2019/5/11, Korean Society for Medical and Biological Engineering, An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
2019/10/16, 2019 Asian Transplantation Week International Conference, Lesson from large-scale genomic studies and research consortia
2020/7/29, The 43rd Annual Meeting of the Japan Neuroscience Society, Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex
2020/8/20, BIOINFO Annual Conference of Korean Society for Bioinformatics, Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex
2020/10/15, The 29th International KOGO Annual Conference, De novo variants in developmental disorders: Lessons from large-scale whole genome and exome sequencing studies
2020/11/19, Korea-Finland Joint Symposium, An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
2021/1/19, 2nd Single-Cell Division Meeting (Korean Society for Biochemistry and Molecular Biology), Single-cell study on SCN2A
2021/2/2, The 17th Korea Genome Organization Winter Symposium, Integrative multi-omics approaches decipher molecular and clinical subtypes underlying lung cancers
2021/10/8, International Conference of the Genetics Society of Korea, Noncoding mutations associated with autism spectrum disorder from whole genome sequence analysis
2021/10/28, BIOINFO Annual Conference of Korean Society for Bioinformatics, Category-wide association for whole genome sequencing and regulatory noncoding mutations in autism spectrum disorder
2022/2/9, The 18th Korea Genome Organization Winter Symposium, Genetic Architecture of Autism Spectrum Disorder from the Korean ASD-WGS cohort
2022/3/8, Regional Meeting (Gyeonggi Branch, Korean Dermatological Association), Genome-Wide Approaches for Understanding Genetic Architecture
2022/5/12, Korean Genome Symposium (Korea National Institute for Bioethics Policy), Whole-Genome Analysis of Autism Spectrum Disorder Genetics in the Korean Population
2022/5/25, Korean Society for Biochemistry and Molecular Biology (KSBMB) International Conference 2022, Shared gene regulation in autism-associated transcriptional regulators in neurodevelopment
2022/7/3, The 45th Annual Meeting of the Japan Neuroscience Society, Identification of regulatory noncoding mutations associated with autism spectrum disorder
2022/9/29, Korean Society for Molecular and Cellular Biology International Conference, Shared gene regulation in Autism-associated Transcriptional regulators in Neurodevelopment
2022/10/19, BIOINFO Annual Conference of Korean Society for Bioinformatics, AI in whole genome sequencing: Variant prediction and Interpretation
2022/12/8, Yilian Medical Life Science Forum (Yonsei University College of Medicine), Single-cell transcriptomic analysis revealed oligodendrocyte alteration in autism-associated gene SCN2A
2023/2/3, The 19th Korea Genome Organization Winter Symposium, Whole genome sequencing analysis identifies the genetic architecture underlying sex bias in autism spectrum disorder
2023/2/19, The 12th Cognition Sleep Mood and Stress (COSMOS) Symposium, Whole genome sequencing-based genetic architecture study of Korean autism families
2023/3/24, Korean Society of Neuromuscular Disorders, Genome-Wide Approaches for Understanding Genetic Architecture
2023/5/7, INSAR Annual Meeting 2023, WGS identifies genetic architecture underlying female protective effect in ASD
2023/5/11, BIO KOREA 2023, UK Biobank Current status & future directions
2023/9/16, International Cancer Proteogenome Consortium (ICPC) Regional Meeting (Seoul), Presentation on cancer proteomics and WGS
2023/10/13, The 32nd International KOGO Annual Conference, To be sparse, or not to be, that is the question: Scalable VCF for a biobank-scale WGS project
2023/11/10, Korean Society for Diagnostic Genetics, Genome-Wide Approaches for Understanding Genetic Architecture
2024/1/18, The Korean Human Proteome Organization Winter Workshop, Proteogenomics of intractable lung cancers
2024/2/7, KSMCB Winter Conference 2024, Genetic Architecture underlying Female Protective Effect in Autism
2024/5/16, AWS Summit 2024, Large-scale genomic research with AWS
2024/7/4, Neurodevelopment Division Meeting (KSMCB), An integrative single-cell atlas to explore the cellular and temporal specificity of neurological disorder genes during human brain development
2024/8/12, KSBMB-BIKO Meeting, Large-scale whole genome analysis to explore tandem repeats in human disorders
2024/10/26, K-BioX AI/BI Session, Whole-Genome Analysis of Autism Spectrum Disorder Genetics in the Korean Population
2024/10, The 2nd Conference on Gene- and Cell-Based Biopharmaceuticals, AI Approaches for Identifying Risk Genetic Variants in Neurodevelopmental Disorders
2024/11/9, Annual Conference The Korean Association for Persons with Autism, Autism and Genetics: Insights from Large-Scale Genomic Studies
2024/11/14, Bio Future Forum 2024, Bio Big Data: From Observation to Prediction and Inference

Invited Seminar

2019/3/19, Department Seminar (School of Biological Sciences, Seoul National University), Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
2019/3/20, Grand Rounds (Korea University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/3/22, Grand Rounds (Samsung Medical Center), Developmentally and genetically regulated gene expression patterns in human prefrontal cortex
2019/3/27, College Seminar (Health Sciences, Korea University), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/4/16, Neurology Grand Rounds (Hanyang University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/4/25, Psychiatry Grand Rounds (Seoul National University Bundang Hospital), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/5/10, Department Seminar (Biological Systems, Sookmyung Women’s University), Identification of noncoding mutations associated with autism spectrum disorders
2019/5/10, Department Seminar (Biomedical Engineering, Kangwon National University), Identification of noncoding mutations associated with autism spectrum disorders
2019/9/4, Institute Seminar (KIST Brain Science Institute), Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex
2019/9/5, The 28th International KOGO Annual Conference, Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
2019/9/10, Department Seminar (Molecular and Life Science, Hanyang University), Identification of noncoding mutations associated with autism spectrum disorders
2019/10/23, College Seminar (Pharmacy, Chung-Ang University), Lessons from 7,600 whole genome and 35,000 exome sequencing analysis of autism spectrum disorders
2019/10/31, Department Seminar (Graduate School of Medical Science and Engineering, KAIST), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/12/3, Institute Seminar (Korea National Institute of Health), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/12/9, Department Seminar (Preventive Medicine, Yonsei University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2019/12/12, Center Seminar (Samsung Genome Center, Samsung Medical Center), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/3/6, Korean Bioinformation Center, A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/3/27, Department Seminar (Biomedical Engineering, Kangwon National University), R & co-expression network analysis
2020/4/24, Department Seminar (Korea University College of Medicine), Re-visiting Mendel, Galton and Fisher in the era of large-scale genomic research collaborations
2020/6/3, Department Seminar (Brain and Cognitive Sciences, DGIST), Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex
2020/6/10, Graduate Seminar Series (Samsung Advanced Institute for Health Sciences & Technology), Understanding the genetic architecture of human disorders
2020/6/12, Department Seminar (School of Life Sciences, Korea University), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/6/17, Center Seminar (Center for Cognition and Sociality, IBS), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/8/27, Department Seminar (School of Biological Sciences, Seoul National University), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/9/10, Graduate Seminar (Catholic University of Korea), Re-visiting Mendel, Galton and Fisher in the era of Large-scale genomic research collaborations
2020/9/15, Department Seminar (Biological Sciences, Hanyang University), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/9/22, Graduate Seminar (New Biology, DGIST), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/10/6, Department Seminar (Biological Sciences, UNIST), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2020/10/14, Psychiatry Grand Rounds (Seoul National University Bundang Hospital), Genetic Architecture of Autism Spectrum Disorders
2020/11/20, Korea Disease Control and Prevention Agency, Introduction to genomic analysis with Hail
2021/3/17, Grand Rounds (Korea University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/4/13, Neurology Grand Rounds (Seoul National University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/4/16, DNALink, Hail seminar
2021/4/30, Department Seminar (School of Biological Sciences, Seoul National University), Genome-Wide Association Study methodology for understanding genetic architecture
2021/5/11, Psychiatry Grand Rounds (Samsung Medical Center), Recent progress in psychiatric genomics: From single genes to the complete genetic architecture
2021/5/26, Ground Rounds (Hanim Precision Medicine Center, Severance Hospital), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/6/9, Molecular Pathology Study Group (The Korean Society of Pathologists), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/7/30, Neurology Grand Rounds (Samsung Medical Center), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/7/30, Grand Rounds (CHA University College of Medicine), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/8/28, Department Seminar (Biomedical Science and Engineering, GIST), A priori and null in autism genetics: Lesson from 7,600 whole genome and 35,000 exome sequencing data
2021/9/28, Grand Rounds (Seoul National University College of Medicine), Polygenic risk score analysis of Korean ASD-WGS cohort
2022/4/15, Graduate Seminar Series in Bioengineering (Seoul National University College of Medicine), Whole-Genome Analysis of Autism Spectrum Disorder Genetics in the Korean Population
2022/4/28, Griffith Institute for Drug Discovery Seminar (Griffith University, Australia), Shared gene regulation in autism-associated transcriptional regulators in neurodevelopment
2022/5/16, GenomeInsight, Cloud computing and genomic research
2022/7/26, Pusan National University, Genetic Architecture of Autism Spectrum Disorders
2022/8/16, Department Seminar (Medical Science, Korea University), Shared gene regulation in Autism-associated Transcriptional regulators in Neurodevelopment
2022/10/13, Lecture (Modern Biology, Chungbuk National University), History of research on disease-causing gene discovery: From the perspective of genetic architecture
2022/10/14, Graduate Seminar (Department of Biology, Kyung Hee University), Whole genome sequencing study on genetic architecture of autism spectrum disorder
2022/10/14, Future Medicine Special Lecture (Konkuk University Hospital), Whole genome sequencing study on genetic architecture of autism spectrum disorder
2022/11/15, Korea Disease Control and Prevention Agency, Cloud computing and genomic research
2022/12/8, Department Seminar (Interdisciplinary Program in Bioinformatics, Seoul National University), An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
2022/12/8, Pathology Grand Rounds (Asan Medical Center), Cancer genomics research using multi-omics
2022/12/9, Translational Research Institute (Asan Medical Center), Multiomics approaches reveal NSCLC subtypes associated with metastasis and tumor microenvironment
2023/3/30, Medical and Bio Special Lecture (Ajou University College of Medicine), Genome-Wide Approaches for Understanding Genetic Architecture
2023/4/4, Grand Rounds (Korea University College of Medicine), Genome-Wide Approaches for Understanding Genetic Architecture
2023/4/12, Graduate Seminar Series in Bioengineering (Seoul National University College of Medicine), Multiomics approaches reveal NSCLC subtypes
2023/4/18, Korea University College of Medicine, Genome-Wide Approaches for Understanding Genetic Architecture
2023/4/26, Department Seminar (Brain and Cognitive Sciences, DGIST), Integrative multi-omics analyses to find noncoding mutations associated with ASD
2023/5/16, Department Seminar (Biological Sciences, KAIST), WGS analysis toward ASD genetic architecture (Korean ASD-WGS progress)
2023/5/16, Department Seminar (Graduate School of Medical Science and Engineering, KAIST), Introduction to basic concepts of Hail
2023/5/18, Department Seminar (Biological Sciences, Sungkyunkwan University), Whole genome sequencing analysis towards genetic architecture of ASD
2023/5/26, Gaesin Medical Conference (Chungbuk National University), Single-cell atlas-based genomic analysis of neurological disorders
2023/9/8, Department Seminar (Biological Systems, Sookmyung Women’s University), Whole genome sequencing analysis towards genetic architecture of autism
2023/9/13, Department Seminar (Psychiatry, Seoul National University Hospital), Lecture on ASD and developmental disorder genomics
2023/9/25, Psychiatry Grand Rounds (Seoul National University Bundang Hospital), Presentation on ASD/WGS research
2023/10/5, Department Seminar (Systems Biology, Yonsei University), Scalable VCF for a biobank-scale WGS project
2023/11/22, Department Seminar (Anatomy, Yonsei University College of Medicine), Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2024/1/17, Department Seminar (Life Sciences, POSTECH), Whole genome sequencing analysis towards genetic architecture of autism
2024/1/30, Grand Rounds (Korea University College of Medicine), Sex-bias in autism and large-scale genomic analysis
2024/3/16, SPARKing Knowledge 2024, Whole-Genome Analysis of Autism Spectrum Disorder Genetics in the Korean Population
2024/3/19, Department Seminar (Biological Sciences, Konkuk University), Whole Genome Sequencing Analysis Identifies Genetic Architecture underlying Female Protective Effect in Autism
2024/3/22, Department Seminar (Biological Sciences, Dongguk University), Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2024/4/16, Illumina User Meeting, Whole genome sequencing analyses to understand the genetic architecture of Korean autism families
2024/4/30, Department Seminar (Brain and Cognitive Sciences, Seoul National University), Genomic and transcriptomic research on Alzheimer’s disease
2024/5/9, Department Seminar (Biomedical Science, Soongsil University), Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2024/5/20, Theragen Bio, Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2024/6/4, Department Seminar (Biological Sciences, UNIST), Whole genome sequencing analysis towards genetic architecture of autism spectrum disorder
2024/8/2, National Cancer Center, Pan-cancer Proteogenomic Landscape of Whole-Genome Doubling
2024/9/19, Disease Study Society, Whole-Genome Analysis of Autism Spectrum Disorder Genetics in the Korean Population
2024/10/21, Graduate Seminar Series (Samsung Advanced Institute for Health Sciences & Technology), Introduction to Multi-Omics Analysis