On the public citation graph

Using three-dimensional regulatory chromatin interactions from adult and fetal cortex to interpret genetic results for psychiatric disorders and cognitive traits

https://doi.org/10.1101/406330
0 signed · 176 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archpsyc.60.12.1187openalex-snapshot
Schizophrenia as a Complex Trait
inferredcites →https://doi.org/10.1002/0471250953.bi1112s47openalex-snapshot
BEDTools: The Swiss‐Army Tool for Genome Feature Analysis
inferredcites →https://doi.org/10.1016/j.ajhg.2017.06.005openalex-snapshot
10 Years of GWAS Discovery: Biology, Function, and Translation
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.12.004openalex-snapshot
Discovering genome regulation with 3C and 3C-related technologies
inferredcites →https://doi.org/10.1016/j.cell.2013.03.035openalex-snapshot
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
inferredcites →https://doi.org/10.1016/j.cell.2013.09.053openalex-snapshot
Super-Enhancers in the Control of Cell Identity and Disease
inferredcites →https://doi.org/10.1016/j.cell.2017.05.038openalex-snapshot
An Expanded View of Complex Traits: From Polygenic to Omnigenic
inferredcites →https://doi.org/10.1016/j.cell.2018.05.051openalex-snapshot
Common Disease Is More Complex Than Implied by the Core Gene Omnigenic Model
inferredcites →https://doi.org/10.1016/j.cell.2019.01.015openalex-snapshot
Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders
inferredcites →https://doi.org/10.1016/j.cell.2019.12.036openalex-snapshot
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
inferredcites →https://doi.org/10.1016/j.celrep.2014.10.015openalex-snapshot
A Role for Noncoding Variation in Schizophrenia
inferredcites →https://doi.org/10.1016/j.celrep.2016.10.061openalex-snapshot
A Compendium of Chromatin Contact Maps Reveals Spatially Active Regions in the Human Genome
inferredcites →https://doi.org/10.1016/j.schres.2016.01.039openalex-snapshot
Understanding the genetic liability to schizophrenia through the neuroepigenome
inferredcites →https://doi.org/10.1016/j.tig.2016.01.003openalex-snapshot
Breaking TADs: How Alterations of Chromatin Domains Result in Disease
inferredcites →https://doi.org/10.1038/mp.2014.40openalex-snapshot
Copy number variation in schizophrenia in Sweden
inferredcites →https://doi.org/10.1038/nature07239openalex-snapshot
Rare chromosomal deletions and duplications increase risk of schizophrenia
inferredcites →https://doi.org/10.1038/nature09298openalex-snapshot
Integrating common and rare genetic variation in diverse human populations
inferredcites →https://doi.org/10.1038/nature11049openalex-snapshot
Spatial partitioning of the regulatory landscape of the X-inactivation centre
inferredcites →https://doi.org/10.1038/nature11082openalex-snapshot
Topological domains in mammalian genomes identified by analysis of chromatin interactions
inferredcites →https://doi.org/10.1038/nature12644openalex-snapshot
A high-resolution map of the three-dimensional chromatin interactome in human cells
inferredcites →https://doi.org/10.1038/nature13138openalex-snapshot
Obesity-associated variants within FTO form long-range functional connections with IRX3
inferredcites →https://doi.org/10.1038/nature14450openalex-snapshot
Condensin-driven remodelling of X chromosome topology during dosage compensation
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature15394openalex-snapshot
An integrated map of structural variation in 2,504 human genomes
inferredcites →https://doi.org/10.1038/nature16549openalex-snapshot
Schizophrenia risk from complex variation of complement component 4
inferredcites →https://doi.org/10.1038/nature18642openalex-snapshot
The genetic architecture of type 2 diabetes
inferredcites →https://doi.org/10.1038/nature19847openalex-snapshot
Chromosome conformation elucidates regulatory relationships in developing human brain
inferredcites →https://doi.org/10.1038/nature24277openalex-snapshot
Genetic effects on gene expression across human tissues
inferredcites →https://doi.org/10.1038/nbt.1630openalex-snapshot
GREAT improves functional interpretation of cis-regulatory regions
inferredcites →https://doi.org/10.1038/ncomms6890openalex-snapshot
Biological interpretation of genome-wide association studies using predicted gene functions
inferredcites →https://doi.org/10.1038/ng.2711openalex-snapshot
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
inferredcites →https://doi.org/10.1038/ng.2742openalex-snapshot
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
inferredcites →https://doi.org/10.1038/ng.3211openalex-snapshot
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3285openalex-snapshot
Meta-analysis of the heritability of human traits based on fifty years of twin studies
inferredcites →https://doi.org/10.1038/ng.3404openalex-snapshot
Partitioning heritability by functional annotation using genome-wide association summary statistics
inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot
An atlas of genetic correlations across human diseases and traits
inferredcites →https://doi.org/10.1038/ng.3894openalex-snapshot
Truncating mutations in RBM12 are associated with psychosis
inferredcites →https://doi.org/10.1038/ng.403openalex-snapshot
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nmeth.2688openalex-snapshot
Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position
inferredcites →https://doi.org/10.1038/nmeth.3542openalex-snapshot
ChIPmentation: fast, robust, low-input ChIP-seq for histones and transcription factors
inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot
Salmon provides fast and bias-aware quantification of transcript expression
inferredcites →https://doi.org/10.1038/nn.4267openalex-snapshot
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
inferredcites →https://doi.org/10.1038/nn.4399openalex-snapshot
Gene expression elucidates functional impact of polygenic risk for schizophrenia
inferredcites →https://doi.org/10.1038/nn.4402openalex-snapshot
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
inferredcites →https://doi.org/10.1038/nrg.2016.112openalex-snapshot
Organization and function of the 3D genome
inferredcites →https://doi.org/10.1038/nrg.2016.147openalex-snapshot
Erratum: Organization and function of the 3D genome
inferredcites →https://doi.org/10.1038/nrg.2016.161openalex-snapshot
Deciphering non-coding variation with 3D epigenomics
inferredcites →https://doi.org/10.1038/nrg.2016.29openalex-snapshot
The statistical properties of gene-set analysis
inferredcites →https://doi.org/10.1038/nrg2611openalex-snapshot
Genetics in geographically structured populations: defining, estimating and interpreting FST
inferredcites →https://doi.org/10.1038/nrm.2016.104openalex-snapshot
Genome-wide mapping and analysis of chromosome architecture
inferredcites →https://doi.org/10.1038/nrm.2016.126openalex-snapshot
Long non-coding RNAs: spatial amplifiers that control nuclear structure and gene expression
inferredcites →https://doi.org/10.1038/nrm.2016.138openalex-snapshot
Regulation of disease-associated gene expression in the 3D genome
inferredcites →https://doi.org/10.1038/nrm.2016.151openalex-snapshot
Mapping the 3D genome: Aiming for consilience
inferredcites →https://doi.org/10.1038/nrn.2016.124openalex-snapshot
Spatial genome organization and cognition
inferredcites →https://doi.org/10.1038/s41467-018-05379-yopenalex-snapshot
Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia
inferredcites →https://doi.org/10.1038/s41588-018-0059-2openalex-snapshot
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
inferredcites →https://doi.org/10.1038/s41588-018-0081-4openalex-snapshot
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types
inferredcites →https://doi.org/10.1038/s41588-018-0129-5openalex-snapshot
Genetic identification of brain cell types underlying schizophrenia
inferredcites →https://doi.org/10.1038/s41588-018-0152-6openalex-snapshot
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
inferredcites →https://doi.org/10.1038/s41593-018-0253-7openalex-snapshot
A histone acetylome-wide association study of Alzheimer’s disease identifies disease-associated H3K27ac differences in the entorhinal cortex
inferredcites →https://doi.org/10.1056/nejmp0806284openalex-snapshot
Common Genetic Variation and Human Traits
inferredcites →https://doi.org/10.1086/427926openalex-snapshot
Ethnicity and Human Genetic Linkage Maps
inferredcites →https://doi.org/10.1086/514346openalex-snapshot
Mendelian Inheritance in Man and Its Online Version, OMIM
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/bts570openalex-snapshot
HiCNorm: removing biases in Hi-C data via Poisson regression
inferredcites →https://doi.org/10.1093/bioinformatics/btv650openalex-snapshot
A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data
inferredcites →https://doi.org/10.1093/bioinformatics/btw240openalex-snapshot
FastHiC: a fast and accurate algorithm to detect long-range chromosomal interactions from Hi-C data
inferredcites →https://doi.org/10.1093/genetics/166.2.835openalex-snapshot
Molecular and Comparative Genetics of Mental Retardation
inferredcites →https://doi.org/10.1093/hmg/ddi232openalex-snapshot
Factors influencing recombination frequency and distribution in a human meiotic crossover hotspot
inferredcites →https://doi.org/10.1093/molbev/msx154openalex-snapshot
Soft Sweeps Are the Dominant Mode of Adaptation in the Human Genome
inferredcites →https://doi.org/10.1093/nar/gkt1188openalex-snapshot
1000 Genomes Selection Browser 1.0: a genome browser dedicated to signatures of natural selection in modern humans
inferredcites →https://doi.org/10.1101/245688openalex-snapshot
Easy Hi-C: A simple efficient protocol for 3D genome mapping in small cell populations
inferredcites →https://doi.org/10.1101/272245openalex-snapshot
Most regulatory interactions are not in linkage disequilibrium
inferredcites →https://doi.org/10.1101/gr.160374.113openalex-snapshot
Statistical confidence estimation for Hi-C data reveals regulatory chromatin contacts
inferredcites →https://doi.org/10.1101/gr.232488.117openalex-snapshot
An atlas of chromatin accessibility in the adult human brain
inferredcites →https://doi.org/10.1101/gr.238022.118openalex-snapshot
Most chromatin interactions are not in linkage disequilibrium
inferredcites →https://doi.org/10.1111/j.1558-5646.1984.tb05657.xopenalex-snapshot
ESTIMATING F -STATISTICS FOR THE ANALYSIS OF POPULATION STRUCTURE
inferredcites →https://doi.org/10.1126/science.1117196openalex-snapshot
A Fine-Scale Map of Recombination Rates and Hotspots Across the Human Genome
inferredcites →https://doi.org/10.1126/science.1152850openalex-snapshot
Gene Regulation in the Third Dimension
inferredcites →https://doi.org/10.1126/science.1181369openalex-snapshot
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
inferredcites →https://doi.org/10.1126/science.1188021openalex-snapshot
A Draft Sequence of the Neandertal Genome
inferredcites →https://doi.org/10.1126/science.aag0776openalex-snapshot
Detection of human adaptation during the past 2000 years
inferredcites →https://doi.org/10.1126/science.aap8757openalex-snapshot
Analysis of shared heritability in common disorders of the brain
inferredcites →https://doi.org/10.1126/science.aat7615openalex-snapshot
Integrative functional genomic analysis of human brain development and neuropsychiatric risks
inferredcites →https://doi.org/10.1126/science.aat8464openalex-snapshot
Comprehensive functional genomic resource and integrative model for the human brain
inferredcites →https://doi.org/10.1128/mcb.01384-09openalex-snapshot
Upregulation of c- MYC in cis through a Large Chromatin Loop Linked to a Cancer Risk-Associated Single-Nucleotide Polymorphism in Colorectal Cancer Cells
inferredcites →https://doi.org/10.1146/annurev-cellbio-100616-060531openalex-snapshot
The Three-Dimensional Organization of Mammalian Genomes
inferredcites →https://doi.org/10.1146/annurev-genet-111212-133526openalex-snapshot
Detecting Natural Selection in Genomic Data
inferredcites →https://doi.org/10.1176/appi.ajp.2014.14040516openalex-snapshot
IQ and Schizophrenia in a Swedish National Sample: Their Causal Relationship and the Interaction of IQ With Genetic Risk
inferredcites →https://doi.org/10.1176/appi.ajp.2017.17030283openalex-snapshot
Psychiatric Genomics: An Update and an Agenda
inferredcites →https://doi.org/10.1186/1471-2105-9-559openalex-snapshot
WGCNA: an R package for weighted correlation network analysis
inferredcites →https://doi.org/10.1186/gb-2008-9-9-r137openalex-snapshot
Model-based Analysis of ChIP-Seq (MACS)
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1186/s13059-018-1567-1openalex-snapshot
Expression quantitative trait loci in the developing human brain and their enrichment in neuropsychiatric disorders
inferredcites →https://doi.org/10.1186/s13073-017-0497-yopenalex-snapshot
Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders
inferredcites →https://doi.org/10.1192/bjp.bp.106.025585openalex-snapshot
Schizophrenia: a common disease caused by multiple rare alleles
inferredcites →https://doi.org/10.1192/bjp.bp.107.044461openalex-snapshot
Intellectual disability co-occurring with schizophrenia and other psychiatric illness: population-based study
inferredcites →https://doi.org/10.12688/f1000research.7563.1openalex-snapshot
Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences
inferredcites →https://doi.org/10.12688/f1000research.7563.2openalex-snapshot
Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences
inferredcites →https://doi.org/10.1371/journal.pbio.0040072openalex-snapshot
A Map of Recent Positive Selection in the Human Genome
inferredcites →https://doi.org/10.1371/journal.pbio.1001046openalex-snapshot
A User's Guide to the Encyclopedia of DNA Elements (ENCODE)
inferredcites →https://doi.org/10.1371/journal.pgen.1004412openalex-snapshot
A Population Genetic Signal of Polygenic Adaptation
inferredcites →https://doi.org/10.1371/journal.pone.0043227openalex-snapshot
Quantitative Analysis of Focused A-To-I RNA Editing Sites by Ultra-High-Throughput Sequencing in Psychiatric Disorders
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/alz.14461openalex-snapshot
Sex‐stratified genome‐wide meta‐analysis identifies novel loci for cognitive decline in older adults
inferred← citeshttps://doi.org/10.1002/ana.26094openalex-snapshot
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-819602-1.00002-4openalex-snapshot
Schizophrenia genomics
inferred← citeshttps://doi.org/10.1016/j.ajhg.2021.01.009openalex-snapshot
HiC-ACT: improved detection of chromatin interactions from Hi-C data via aggregated Cauchy test
inferred← citeshttps://doi.org/10.1016/j.biopsych.2020.05.022openalex-snapshot
Emerging Methods and Resources for Biological Interrogation of Neuropsychiatric Polygenic Signal
inferred← citeshttps://doi.org/10.1016/j.biopsych.2020.06.033openalex-snapshot
Parsing the Functional Impact of Noncoding Genetic Variants in the Brain Epigenome
inferred← citeshttps://doi.org/10.1016/j.csbj.2020.12.026openalex-snapshot
FIREcaller: Detecting frequently interacting regions from Hi-C data
inferred← citeshttps://doi.org/10.1016/j.jad.2022.04.097openalex-snapshot
Characterizing the polygenic overlaps of bipolar disorder subtypes with schizophrenia and major depressive disorder
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100581openalex-snapshot
Super hotspots and super coldspots in the repair of UV-induced DNA damage in the human genome
inferred← citeshttps://doi.org/10.1016/j.jgg.2021.06.017openalex-snapshot
3D genome organization in the central nervous system, implications for neuropsychological disorders
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.12.024openalex-snapshot
SATB2 organizes the 3D genome architecture of cognition in cortical neurons
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.03.022openalex-snapshot
Uncovering the Genetic Architecture of Major Depression
inferred← citeshttps://doi.org/10.1016/j.neuron.2024.04.009openalex-snapshot
A systems biology-based identification and in vivo functional screening of Alzheimer’s disease risk genes reveal modulators of memory function
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2023.110785openalex-snapshot
Unrevealing the shared genetic mechanisms underlying C-reactive protein and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.psychres.2022.114795openalex-snapshot
Comprehensive analysis of shared genetic loci between hippocampal volume and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.xgen.2022.100140openalex-snapshot
Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities
inferred← citeshttps://doi.org/10.1016/j.xhgg.2021.100036openalex-snapshot
MUNIn: A statistical framework for identifying long-range chromatin interactions from multiple samples
inferred← citeshttps://doi.org/10.1038/s41380-022-01857-4openalex-snapshot
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
inferred← citeshttps://doi.org/10.1038/s41398-020-0765-2openalex-snapshot
Genetic overlap between psychotic experiences in the community across age and with psychiatric disorders
inferred← citeshttps://doi.org/10.1038/s41398-021-01436-1openalex-snapshot
Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene
inferred← citeshttps://doi.org/10.1038/s41467-019-10945-zopenalex-snapshot
Non-coding variability at the APOE locus contributes to the Alzheimer’s risk
inferred← citeshttps://doi.org/10.1038/s41467-020-15707-wopenalex-snapshot
Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia
inferred← citeshttps://doi.org/10.1038/s41467-020-20851-4openalex-snapshot
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries
inferred← citeshttps://doi.org/10.1038/s41467-023-38480-yopenalex-snapshot
The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism
inferred← citeshttps://doi.org/10.1038/s41467-024-44842-xopenalex-snapshot
Genetic architecture distinguishes tinnitus from hearing loss
inferred← citeshttps://doi.org/10.1038/s41467-024-55635-7openalex-snapshot
Multi-omic spatial effects on high-resolution AI-derived retinal thickness
inferred← citeshttps://doi.org/10.1038/s41467-025-63236-1openalex-snapshot
Sex-stratified genome-wide association meta-analysis of major depressive disorder
inferred← citeshttps://doi.org/10.1038/s41525-021-00225-5openalex-snapshot
Association between genes regulating neural pathways for quantitative traits of speech and language disorders
inferred← citeshttps://doi.org/10.1038/s41562-021-01069-wopenalex-snapshot
The genetic architecture of structural left–right asymmetry of the human brain
inferred← citeshttps://doi.org/10.1038/s41562-026-02476-7openalex-snapshot
Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestry
inferred← citeshttps://doi.org/10.1038/s41588-019-0439-2openalex-snapshot
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa
inferred← citeshttps://doi.org/10.1038/s41588-022-01039-6openalex-snapshot
Common variants contribute to intrinsic human brain functional networks
inferred← citeshttps://doi.org/10.1038/s41588-024-01707-9openalex-snapshot
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
inferred← citeshttps://doi.org/10.1038/s41598-022-22218-9openalex-snapshot
Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK
inferred← citeshttps://doi.org/10.1038/s44220-025-00475-7openalex-snapshot
The overlapping genetic architecture of psychiatric disorders and cortical brain structure
inferred← citeshttps://doi.org/10.1073/pnas.2200638119openalex-snapshot
Using neuroimaging genomics to investigate the evolution of human brain structure
inferred← citeshttps://doi.org/10.1073/pnas.2214834120openalex-snapshot
Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness
inferred← citeshttps://doi.org/10.1093/bfgp/elab024openalex-snapshot
Review of multi-omics data resources and integrative analysis for human brain disorders
inferred← citeshttps://doi.org/10.1093/bib/bbae096openalex-snapshot
scENCORE: leveraging single-cell epigenetic data to predict chromatin conformation using graph embedding
inferred← citeshttps://doi.org/10.1093/cercor/bhae078openalex-snapshot
Neuroimaging genomics as a window into the evolution of human sulcal organization
inferred← citeshttps://doi.org/10.1101/2020.04.16.045369openalex-snapshot
Nucleotide excision repair hotspots and coldspots of UV-induced DNA damage in the human genome
inferred← citeshttps://doi.org/10.1101/2020.04.22.054825openalex-snapshot
Combining multivariate genomic approaches to elucidate the comorbidity between ASD and ADHD
inferred← citeshttps://doi.org/10.1101/2020.07.27.222364openalex-snapshot
Statistical model integrating interactions into genotype-phenotype association mapping: an application to reveal 3D-genetic basis underlying Autism
inferred← citeshttps://doi.org/10.1101/2020.07.30.229914openalex-snapshot
Common variants contribute to intrinsic human brain functional networks
inferred← citeshttps://doi.org/10.1101/2021.10.13.21261078openalex-snapshot
Genome-wide association study identifies new locus associated with OCD
inferred← citeshttps://doi.org/10.1101/2022.11.11.516161openalex-snapshot
Cell adhesion molecules play subclass-specific roles in electrophysiological response and Schizophrenia risk
inferred← citeshttps://doi.org/10.1101/2022.12.20.521277openalex-snapshot
DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network
inferred← citeshttps://doi.org/10.1101/2023.06.02.23290906openalex-snapshot
Combined GWAS and single cell transcriptomics uncover the underlying genes and cell types in disorders of gut-brain interaction
inferred← citeshttps://doi.org/10.1101/2024.07.24.24310923openalex-snapshot
Uncovering the multivariate genetic architecture of frailty with genomic structural equation modelling
inferred← citeshttps://doi.org/10.1101/603134openalex-snapshot
Multivariate GWAS of psychiatric disorders and their cardinal symptoms reveal two dimensions of cross-cutting genetic liabilities
inferred← citeshttps://doi.org/10.1101/619288openalex-snapshot
FIREcaller: Detecting Frequently Interacting Regions from Hi-C Data
inferred← citeshttps://doi.org/10.1101/842872openalex-snapshot
Transcriptome-wide association analysis of 211 neuroimaging traits identifies new genes for brain structures and yields insights into the gene-level pleiotropy with other complex traits
inferred← citeshttps://doi.org/10.1111/jcpp.13479openalex-snapshot
Combining multivariate genomic approaches to elucidate the comorbidity between autism spectrum disorder and attention deficit hyperactivity disorder
inferred← citeshttps://doi.org/10.1126/sciadv.add2870openalex-snapshot
Genetic architecture of the white matter connectome of the human brain
inferred← citeshttps://doi.org/10.1126/science.aay6690openalex-snapshot
The genetic architecture of the human cerebral cortex
inferred← citeshttps://doi.org/10.1172/jci.insight.170068openalex-snapshot
Multiancestry sex-stratified genomic associations with HIV viral load and controller status from the ICGH
inferred← citeshttps://doi.org/10.1177/2470547020924844openalex-snapshot
Heterogeneity and Polygenicity in Psychiatric Disorders: A Genome-Wide Perspective
inferred← citeshttps://doi.org/10.1186/s11689-022-09429-xopenalex-snapshot
Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm
inferred← citeshttps://doi.org/10.1186/s13073-020-0715-xopenalex-snapshot
A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons
inferred← citeshttps://doi.org/10.1186/s13073-023-01158-7openalex-snapshot
Ultra-low-coverage genome-wide association study—insights into gestational age using 17,844 embryo samples with preimplantation genetic testing
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010102openalex-snapshot
THUNDER: A reference-free deconvolution method to infer cell type proportions from bulk Hi-C data
inferred← citeshttps://doi.org/10.18699/bgrs/sb-2022-056openalex-snapshot
Maps of chromatin conformation in the cerebral cortex
inferred← citeshttps://doi.org/10.18699/sbb-2022-056openalex-snapshot
Maps of chromatin conformation in the cerebral cortex
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2399024/v1openalex-snapshot
DeepGWAS: Enhance GWAS Signals for Neuropsychiatric Disorders via Deep Neural Network
inferred← citeshttps://doi.org/10.3390/genes13010106openalex-snapshot
Adolescent Verbal Memory as a Psychosis Endophenotype: A Genome-Wide Association Study in an Ancestrally Diverse Sample
inferred← citeshttps://doi.org/10.3390/genes13040586openalex-snapshot
Understanding Regulatory Mechanisms of Brain Function and Disease through 3D Genome Organization
inferred← citeshttps://doi.org/10.3390/ijms22147612openalex-snapshot
Chromatin Profiling Techniques: Exploring the Chromatin Environment and Its Contributions to Complex Traits
inferred← citeshttps://doi.org/10.3390/ijms24021428openalex-snapshot
Molecular Landscape of Tourette’s Disorder
inferred← citeshttps://doi.org/10.3390/ijms26083578openalex-snapshot
GWAS by Subtraction to Disentangle RBD Genetic Background from α-Synucleinopathies
inferred← citeshttps://doi.org/10.3390/ijms26146940openalex-snapshot
APOE Genotype-Stratified Meta-Analysis of Cognitive Decline Reveals Novel Loci for Language and Global Cognitive Function in Older Adults
inferred← citeshttps://doi.org/10.34133/cbsystems.0451openalex-snapshot
Hemispheric Asymmetry in the Genetic Overlap between Schizophrenia and White Matter Microstructure
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.