On the public citation graph
Comparative genetic architectures of schizophrenia in East Asian and European populations
0 signed · 96 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/art.39589openalex-snapshot
Effects of Complement C4 Gene Copy Number Variations, Size Dichotomy, and C4A Deficiency on Genetic Risk and Clinical Presentation of Systemic Lupus Erythematosus in East Asian Populations
inferredcites →https://doi.org/10.1002/gepi.21614openalex-snapshot
A Better Coefficient of Determination for Genetic Profile Analysis
inferredcites →https://doi.org/10.1002/gepi.21906openalex-snapshot
Explicit Modeling of Ancestry Improves Polygenic Risk Scores and BLUP Prediction
inferredcites →https://doi.org/10.1002/gepi.22083openalex-snapshot
Multiethnic polygenic risk scores improve risk prediction in diverse populations
inferredcites →https://doi.org/10.1016/j.ajhg.2015.06.007openalex-snapshot
Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies
inferredcites →https://doi.org/10.1016/j.ajhg.2015.11.003openalex-snapshot
SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation
inferredcites →https://doi.org/10.1016/j.ajhg.2016.05.001openalex-snapshot
Transethnic Genetic-Correlation Estimates from Summary Statistics
inferredcites →https://doi.org/10.1016/j.ajhg.2017.03.004openalex-snapshot
Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations
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.cell.2013.01.035openalex-snapshot
Identifying Recent Adaptations in Large-Scale Genomic Data
inferredcites →https://doi.org/10.1016/j.cell.2013.06.049openalex-snapshot
Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network
inferredcites →https://doi.org/10.1016/j.pneurobio.2015.09.002openalex-snapshot
Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders
inferredcites →https://doi.org/10.1016/s0140-6736(12)62129-1openalex-snapshot
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
inferredcites →https://doi.org/10.1017/s0264180100000904openalex-snapshot
Schizophrenia: manifestations, incidence and course in different cultures A World Health Organization Ten-Country Study
inferredcites →https://doi.org/10.1038/hdy.2015.42openalex-snapshot
Properties of different selection signature statistics and a new strategy for combining them
inferredcites →https://doi.org/10.1038/mp.2012.21openalex-snapshot
A mega-analysis of genome-wide association studies for major depressive disorder
inferredcites →https://doi.org/10.1038/mp.2013.187openalex-snapshot
A genome-wide association study of anorexia nervosa
inferredcites →https://doi.org/10.1038/mp.2015.98openalex-snapshot
High-throughput sequencing of the synaptome in major depressive disorder
inferredcites →https://doi.org/10.1038/mp.2016.212openalex-snapshot
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population
inferredcites →https://doi.org/10.1038/mp.2016.45openalex-snapshot
Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151)
inferredcites →https://doi.org/10.1038/mp.2017.153openalex-snapshot
Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117)
inferredcites →https://doi.org/10.1038/nature06250openalex-snapshot
Genome-wide detection and characterization of positive selection in human populations
inferredcites →https://doi.org/10.1038/nature08185openalex-snapshot
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
inferredcites →https://doi.org/10.1038/nature10405openalex-snapshot
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
inferredcites →https://doi.org/10.1038/nature10530openalex-snapshot
A high-resolution map of human evolutionary constraint using 29 mammals
inferredcites →https://doi.org/10.1038/nature13425openalex-snapshot
A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes
inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot
Biological insights from 108 schizophrenia-associated genetic loci
inferredcites →https://doi.org/10.1038/nature13835openalex-snapshot
Genetic and epigenetic fine mapping of causal autoimmune disease variants
inferredcites →https://doi.org/10.1038/nature14659openalex-snapshot
Sparse whole-genome sequencing identifies two loci for major depressive disorder
inferredcites →https://doi.org/10.1038/nature15393openalex-snapshot
A global reference for human genetic variation
inferredcites →https://doi.org/10.1038/nature16549openalex-snapshot
Schizophrenia risk from complex variation of complement component 4
inferredcites →https://doi.org/10.1038/nature17671openalex-snapshot
Genome-wide association study identifies 74 loci associated with educational attainment
inferredcites →https://doi.org/10.1038/nature22969openalex-snapshot
Fine-mapping inflammatory bowel disease loci to single-variant resolution
inferredcites →https://doi.org/10.1038/ncomms10206openalex-snapshot
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese
inferredcites →https://doi.org/10.1038/ng.2354openalex-snapshot
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
inferredcites →https://doi.org/10.1038/ng.2435openalex-snapshot
Bayesian refinement of association signals for 14 loci in 3 common diseases
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.3211openalex-snapshot
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3359openalex-snapshot
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations
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.3437openalex-snapshot
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
inferredcites →https://doi.org/10.1038/ng.3552openalex-snapshot
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
inferredcites →https://doi.org/10.1038/ng.3598openalex-snapshot
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
inferredcites →https://doi.org/10.1038/ng.3973openalex-snapshot
Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia
inferredcites →https://doi.org/10.1038/ng.943openalex-snapshot
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
inferredcites →https://doi.org/10.1038/ng.979openalex-snapshot
Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2
inferredcites →https://doi.org/10.1038/ng.980openalex-snapshot
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia
inferredcites →https://doi.org/10.1038/ng1847openalex-snapshot
Principal components analysis corrects for stratification in genome-wide association studies
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/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/s41588-018-0090-3openalex-snapshot
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
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/s41588-018-0269-7openalex-snapshot
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
inferredcites →https://doi.org/10.1053/j.gastro.2016.06.051openalex-snapshot
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn’s Disease and Human Gut Microbiome Composition
inferredcites →https://doi.org/10.1086/519795openalex-snapshot
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btq340openalex-snapshot
METAL: fast and efficient meta-analysis of genomewide association scans
inferredcites →https://doi.org/10.1093/bioinformatics/btr260openalex-snapshot
Molecular signatures database (MSigDB) 3.0
inferredcites →https://doi.org/10.1093/bioinformatics/bts115openalex-snapshot
rehh : an R package to detect footprints of selection in genome-wide SNP data from haplotype structure
inferredcites →https://doi.org/10.1093/nar/gkw865openalex-snapshot
denovo-db: a compendium of humande novovariants
inferredcites →https://doi.org/10.1093/schbul/sbi052openalex-snapshot
Variations in the Incidence of Schizophrenia: Data Versus Dogma
inferredcites →https://doi.org/10.1101/048991openalex-snapshot
Analysis of Shared Heritability in Common Disorders of the Brain
inferredcites →https://doi.org/10.1101/129312openalex-snapshot
Base-specific mutational intolerance near splice-sites clarifies role of non-essential splice nucleotides
inferredcites →https://doi.org/10.1101/141986openalex-snapshot
Evaluation of Chromatin Accessibility in Prefrontal Cortex of Schizophrenia Cases and Controls
inferredcites →https://doi.org/10.1101/245506openalex-snapshot
Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
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.1183863openalex-snapshot
A Composite of Multiple Signals Distinguishes Causal Variants in Regions of Positive Selection
inferredcites →https://doi.org/10.1126/science.182.4118.1275openalex-snapshot
Flexible System for the Diagnosis of Schizophrenia: Report from the WHO International Pilot Study of Schizophrenia
inferredcites →https://doi.org/10.1172/jci90896openalex-snapshot
Hepatic metal ion transporter ZIP8 regulates manganese homeostasis and manganese-dependent enzyme activity
inferredcites →https://doi.org/10.1186/1744-9081-3-65openalex-snapshot
A lesson not learned: allele misassignment
inferredcites →https://doi.org/10.1186/s12863-016-0387-0openalex-snapshot
Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans
inferredcites →https://doi.org/10.1186/s13073-014-0091-5openalex-snapshot
Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations
inferredcites →https://doi.org/10.1192/bjp.bp.110.082065openalex-snapshot
Cross-national clinical and functional remission rates: Worldwide Schizophrenia Outpatient Health Outcomes (W-SOHO) study
inferredcites →https://doi.org/10.1192/bjp.bp.110.090845openalex-snapshot
Differential outcome of schizophrenia: where we are and where we would like to be
inferredcites →https://doi.org/10.1371/journal.pcbi.1004219openalex-snapshot
MAGMA: Generalized Gene-Set Analysis of GWAS Data
inferredcites →https://doi.org/10.1371/journal.pgen.1000471openalex-snapshot
Widespread Genomic Signatures of Natural Selection in Hominid Evolution
inferredcites →https://doi.org/10.1371/journal.pgen.1004234openalex-snapshot
A General Approach for Haplotype Phasing across the Full Spectrum of Relatedness
inferredcites →https://doi.org/10.1371/journal.pgen.1006340openalex-snapshot
The Strength of Selection against Neanderthal Introgression
inferredcites →https://doi.org/10.1371/journal.pone.0007969openalex-snapshot
How Many Genetic Variants Remain to Be Discovered?
inferredcites →https://doi.org/10.1371/journal.pone.0062376openalex-snapshot
Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6
inferredcites →https://doi.org/10.31887/dcns.2010.12.3/sstiloopenalex-snapshot
The epidemology of schizophrenia: replacing dogma with knowledge
inferredcites →https://doi.org/10.4149/gpb_2014037openalex-snapshot
Emerging evidence for specific neuronal functions of auxiliary calcium channel α2δ subunits
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-030-28703-0_6openalex-snapshot
Sequencing and Mapping IBD Genes to Individual Causative Variants and Their Clinical Relevance
inferred← citeshttps://doi.org/10.1007/s40142-019-0159-zopenalex-snapshot
GWAS and Beyond: Using Omics Approaches to Interpret SNP Associations
inferred← citeshttps://doi.org/10.1016/j.gene.2021.145824openalex-snapshot
A role for zinc transporter gene SLC39A12 in the nervous system and beyond
inferred← citeshttps://doi.org/10.1016/j.psychres.2024.116080openalex-snapshot
Psychiatric polygenic risk scores: Experience, hope for utility, and concerns among child and adolescent psychiatrists
inferred← citeshttps://doi.org/10.1038/s41467-021-21049-yopenalex-snapshot
Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups
inferred← citeshttps://doi.org/10.1038/s41588-019-0379-xopenalex-snapshot
Clinical use of current polygenic risk scores may exacerbate health disparities
inferred← citeshttps://doi.org/10.1093/hmg/ddz187openalex-snapshot
Towards clinical utility of polygenic risk scores
inferred← citeshttps://doi.org/10.1093/med/9780197640654.003.0012openalex-snapshot
Genetics of Schizophrenia
inferred← citeshttps://doi.org/10.1093/med/9780198735588.003.0004openalex-snapshot
Psychosis across persons 3: Genes, biology, and neurodevelopment
inferred← citeshttps://doi.org/10.1101/2020.02.21.959510openalex-snapshot
In silico integration of thousands of epigenetic datasets into 707 cell type regulatory annotations improves the trans-ethnic portability of polygenic risk scores
inferred← citeshttps://doi.org/10.1186/s12881-019-0757-3openalex-snapshot
Association between polymorphisms in the GRIN1 gene 5′ regulatory region and schizophrenia in a northern Han Chinese population and haplotype effects on protein expression in vitro
inferred← citeshttps://doi.org/10.1214/23-aoas1747openalex-snapshot
Targeting underrepresented populations in precision medicine: A federated transfer learning approach
inferred← citeshttps://doi.org/10.7717/peerj-cs.3039openalex-snapshot
A review of methods and software for polygenic risk score analysis
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.