H. Won
Molecular Biology · Nature Genetics · 2012–2019
A researcher in the Science corpus: 10 papers; trusts 3 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 309 citations into it
- Genetics — 299 citations into it
- Cognitive Neuroscience — 109 citations into it
Whom H. Won trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from H. Won's perspective
Ordered by how strongly the researchers H. Won trusts endorse each paper. Same corpus, a different order for every researcher.
- Spatiotemporal gene expression trajectories reveal developmental hierarchies of the human cortex (Science)
- Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci (Neuron)
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (Nature)
- Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism (Cell)
- A gene-based association method for mapping traits using reference transcriptome data (Nature Genetics)
- Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia (Nature Neuroscience)
- Regional differences in synaptogenesis in human cerebral cortex
- Spatiotemporal transcriptome of the human brain
- De Novo Gene Disruptions in Children on the Autistic Spectrum (Neuron)
- Statistical significance for genomewide studies (Proceedings of the National Academy of Sciences of the United States of America)
Their papers
- Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism (2013) — 1,012 citations
- Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder (2018) — 1,134 citations
- Advancing the understanding of autism disease mechanisms through genetics (2016) — 765 citations
- Comprehensive functional genomic resource and integrative model for the human brain (2018) — 946 citations
- Integrative functional genomic analysis of human brain development and neuropsychiatric risks (2018) — 740 citations
- Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
- Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection (2018) — 1,432 citations
- De novo mutations in regulatory elements in neurodevelopmental disorders (2018) — 234 citations
- Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
- Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function (2012) — 669 citations