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Joon-Yong An · SciRah

Researcher profile · Semantic Scholar

Joon-Yong An

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Joon-Yong An — researcher profile on SciRah

h-index: 22
Works: 50
Citations: 4,722

Most-cited papers

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
Joon-Yong An, K. Lin, Lingxue Zhu, D. Werling +31 more
2018Science298 citations Open access
Semantic Scholar
Opposing effects on NaV1.2 function underlie differences between SCN2A variants observed in individuals with autism spectrum disorder or infantile seizures
Roy Ben-Shalom, Caroline M. Keeshen, Kiara N. Berríos, Joon-Yong An +2 more
2017Biological Psychiatry268 citations Open access
Semantic Scholar
An analytical framework for whole genome sequence association studies and its implications for autism spectrum disorder
D. Werling, H. Brand, Joon-Yong An, M. Stone +43 more
2018Nature Genetics257 citations Open access
Semantic Scholar
Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system
A. Cristino, SM Williams, Z. Hawi, Joon-Yong An +4 more
2014Molecular Psychiatry225 citations Open access
Semantic Scholar
Integrative Multi-Omics Approaches in Cancer Research: From Biological Networks to Clinical Subtypes
Yong Jin Heo, Chanwoong Hwa, Gang-Hee Lee, Jae-Min Park +1 more
2021Molecules and Cells196 citations Open access
Semantic Scholar
Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome
Ryan L. Collins, H. Brand, C. Redin, C. Hanscom +26 more
2017Genome Biology186 citations Open access
Semantic Scholar
Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex
D. Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An +29 more
2019bioRxiv137 citations Open access
Semantic Scholar
Whole Genome Sequencing in Psychiatric Disorders: the WGSPD Consortium
Stephan J Sanders, B. Neale, Hai-Liang Huang, D. Werling +24 more
2017Nature Neuroscience125 citations Open access
Semantic Scholar
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
Benxia Hu, H. Won, Won Mah, Royce B. Park +152 more
2021Nature Communications91 citations Open access
Semantic Scholar
Towards a molecular characterization of autism spectrum disorders: an exome sequencing and systems approach
Joon-Yong An, A. Cristino, Qiongyi Zhao, J. Edson +7 more
2014Translational Psychiatry79 citations Open access
Semantic Scholar
An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder
Sarah M Williams, Joon-Yong An, J. Edson, M. Watts +6 more
2019Molecular Psychiatry71 citations Open access
Semantic Scholar
Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies.
Leejee Choi, Joon-Yong An
2021Neuroscience and Biobehavioral Reviews61 citations Open access
Semantic Scholar
Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +153 more
2018bioRxiv60 citations Open access
Semantic Scholar
Genetic heterogeneity in autism: from single gene to a pathway perspective
Joon-Yong An, C. Claudianos
2016bioRxiv59 citations Open access
Semantic Scholar
High-throughput characterization of the role of non-B DNA motifs on promoter function
I. Georgakopoulos-Soares, Jesús Victorino, Guillermo E. Parada, V. Agarwal +11 more
2022Cell Genomics58 citations Open access
Semantic Scholar
Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain
Lindsay Liang, Siavash Fazel Darbandi, Sirisha Pochareddy, Forrest O. Gulden +9 more
2021Genome Medicine55 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +41 more
2023American Journal of Human Genetics54 citations Open access
Semantic Scholar
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis
Wooyoung Eric Jang, Ji Hwan Park, Gaeun Park, G. Bang +8 more
2022Molecular Psychiatry48 citations Open access
Semantic Scholar
Revealing the brain's molecular architecture.
A. Ashley-Koch, Gregory E. Crawford, M. Garrett, Ling-Yun Song +149 more
2018Science48 citations Open access
Semantic Scholar
Ferroptosis-Related Genes in Neurodevelopment and Central Nervous System
Soo-Whee Kim, Yujin Kim, S. Kim, Joon-Yong An
2021Biology40 citations Open access
Semantic Scholar
CRISPR screens identify a novel combination treatment targeting BCL-XL and WNT signaling for KRAS/BRAF-mutated colorectal cancers
H. Jung, Yumi Oh, Deukchae Na, Seoyeon Min +11 more
2021Oncogene25 citations
Semantic Scholar
Augmentation of the RNA m6A reader signature is associated with poor survival by enhancing cell proliferation and EMT across cancer types
Jaeik Oh, Chanwoong Hwa, Dongjun Jang, Seungjae Shin +9 more
2022Experimental and Molecular Medicine20 citations Open access
Semantic Scholar
A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo
Tomas Lagunas, Stephen P. Plassmeyer, A. Fischer, Ryan Z. Friedman +11 more
2021bioRxiv20 citations Open access
Semantic Scholar
Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder
Il Bin Kim, Taeyeop Lee, Junehawk Lee, Jonghun Kim +16 more
2022Molecular Psychiatry18 citations
Semantic Scholar
Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers
Özgür Genç, Joon-Yong An, R. Fetter, Yelena D Kulik +3 more
2020eLife17 citations Open access
Semantic Scholar
Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families
D. Werling, H. Brand, Joon-Yong An, M. Stone +41 more
2017bioRxiv16 citations Open access
Semantic Scholar
Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays
Justin Koesterich, Joon-Yong An, Fumitaka Inoue, Ajuni Sohota +3 more
2023International Journal of Molecular Sciences15 citations Open access
Semantic Scholar
National human genome projects: an update and an agenda
Joon-Yong An
2017Epidemiology and Health14 citations Open access
Semantic Scholar
Chronic skin ultraviolet irradiation induces transcriptomic changes associated with microglial dysfunction in the hippocampus
Kyeonghee Yoon, Yujin Kim, Yidan Cui, Jungeun Ji +5 more
2022Molecular Brain12 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +41 more
2020bioRxiv12 citations Open access
Semantic Scholar
ANO1 regulates the maintenance of stemness in glioblastoma stem cells by stabilizing EGFRvIII
Hee-Jin Kim, Jeong-Yub Kim, Chan-Woong Jung, Young-Sun Lee +6 more
2021Oncogene11 citations
Semantic Scholar
Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis
Joon-Yong An, J. Jung, Leejee Choi, E. Wieben +1 more
2021Genes7 citations Open access
Semantic Scholar
Kdm3b haploinsufficiency impairs the consolidation of cerebellum-dependent motor memory in mice
Yong Gyu Kim, Myeong Seong Bak, Ahbin Kim, Yujin Kim +7 more
2021Molecular Brain7 citations Open access
Semantic Scholar
Spatio-Temporal Roles of ASD-Associated Variants in Human Brain Development
Yujin Kim, Joon-Yong An
2020Genes7 citations Open access
Semantic Scholar
LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES
D. Werling, H. Brand, Joon-Yong An, M. Stone +11 more
2019European Neuropsychopharmacology6 citations Open access
Semantic Scholar
Appreciating the Popula Commentary BiolPsy tion-wide Impact of Copy Number Variants on Cognition
Joon-Yong An, Stephan J Sanders
20174 citations
Semantic Scholar
Brief Report: Risk Variants Could Inform Early Neurodevelopmental Outcome in Children with Developmental Disabilities
Taeyeop Lee, Hyeji Lee, S. Kim, K. Park +2 more
2022Journal of Autism and Developmental Disorders3 citations
Semantic Scholar
Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse neocortex
Lindsay Liang, S. Darbandi, Sirisha Pochareddy, Forrest O. Gulden +9 more
2020bioRxiv2 citations Open access
Semantic Scholar
Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders
Chelsea Lowther, E. Valkanas, J. Giordano, Harold Wang +32 more
20202 citations
Semantic Scholar
Autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
Siavash Fazel Darbandi, Joon-Yong An, Kenneth J. Lim, Nicholas F. Page +7 more
2023bioRxiv1 citations Open access
Semantic Scholar
Homeostatic Plasticity Commonly Fails at the Intersection of Autism-Gene Mutations and a Novel Class of Common Phenotypic Modifier
Özgür Genç, Joon-Yong An, R. Fetter, Yelena D Kulik +3 more
2020bioRxiv1 citations Open access
Semantic Scholar
29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX
D. Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An +11 more
2019European Neuropsychopharmacology1 citations
Semantic Scholar
Assessing Long-Term Stored Tissues for Multi-Omics Data Quality and Proteogenomics Suitability
K. J. Song, Minsuh Kim, Yong Jin Heo, Kyung-Cho Cho +14 more
2024bioRxiv0 citations Open access
Semantic Scholar
1.62 Early Neurodevelopmental Trajectory in Children With Developmental Disabilities Could Be Predicted by Risk Variants
Taeyeop Lee, Hyeji Lee, S. Kim, K. Park +2 more
2022Journal of the American Academy of Child & Adolescent Psychiatry0 citations
Semantic Scholar
INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING
Joon-Yong An, K. Lin, Lingxue Zhu, D. Werling +11 more
2019European Neuropsychopharmacology0 citations
Semantic Scholar
Whole-Genome Sequencing to Detect Rare Noncoding Variants in Autism Spectrum Disorder
Joon-Yong An
20180 citations
Semantic Scholar
National human genome projects
Joon-Yong An
20170 citations
Semantic Scholar
Identification and characterization of genetic variants in an Australian autism spectrum disorder cohort
Joon-Yong An
20160 citations
Semantic Scholar
PS207. Integrated systems analysis of serum proteome profiles of individual drug responses in MDD patients
Hyun Jeong Lee, Min Young Lee, Kyung-Cho Cho, Joon-Yong An +4 more
2016International Journal of Neuropsychopharmacology0 citations Open access
Semantic Scholar

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