On the public citation graph

Association between schizophrenia and both loss of function and missense mutations in paralog conserved sites of voltage-gated sodium channels

https://doi.org/10.1101/246850
0 signed · 50 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/jamapsychiatry.2016.1831openalex-snapshot
Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia
inferredcites →https://doi.org/10.1002/0471142905.hg0725s87openalex-snapshot
Interpreting de novo Variation in Human Disease Using denovolyzeR
inferredcites →https://doi.org/10.1002/ajmg.b.32560openalex-snapshot
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia
inferredcites →https://doi.org/10.1002/mpr.1352openalex-snapshot
Genetic Risk and Outcome of Psychosis (GROUP), a multi site longitudinal cohort study focused on gene–environment interaction: objectives, sample characteristics, recruitment and assessment methods
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.neuron.2014.04.043openalex-snapshot
Loss-of-Function Variants in Schizophrenia Risk and SETD1A as a Candidate Susceptibility Gene
inferredcites →https://doi.org/10.1016/j.neuron.2015.04.022openalex-snapshot
Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia
inferredcites →https://doi.org/10.1016/j.neuropharm.2017.09.018openalex-snapshot
Voltage-gated sodium channel β subunits: The power outside the pore in brain development and disease
inferredcites →https://doi.org/10.1038/ejhg.2015.218openalex-snapshot
De novo variants in sporadic cases of childhood onset schizophrenia
inferredcites →https://doi.org/10.1038/mp.2011.154openalex-snapshot
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
inferredcites →https://doi.org/10.1038/mp.2014.29openalex-snapshot
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
inferredcites →https://doi.org/10.1038/nature05911openalex-snapshot
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
inferredcites →https://doi.org/10.1038/nature12929openalex-snapshot
De novo mutations in schizophrenia implicate synaptic networks
inferredcites →https://doi.org/10.1038/nature12975openalex-snapshot
A polygenic burden of rare disruptive mutations in schizophrenia
inferredcites →https://doi.org/10.1038/nature13595openalex-snapshot
Biological insights from 108 schizophrenia-associated genetic loci
inferredcites →https://doi.org/10.1038/nature14135openalex-snapshot
Large-scale discovery of novel genetic causes of developmental disorders
inferredcites →https://doi.org/10.1038/nature19057openalex-snapshot
Analysis of protein-coding genetic variation in 60,706 humans
inferredcites →https://doi.org/10.1038/ng.1108openalex-snapshot
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
inferredcites →https://doi.org/10.1038/ng.2303openalex-snapshot
Exome sequencing and the genetic basis of complex traits
inferredcites →https://doi.org/10.1038/ng.2446openalex-snapshot
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia
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.2892openalex-snapshot
A general framework for estimating the relative pathogenicity of human genetic variants
inferredcites →https://doi.org/10.1038/ng.3050openalex-snapshot
A framework for the interpretation of de novo mutation in human disease
inferredcites →https://doi.org/10.1038/ng.3725openalex-snapshot
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
inferredcites →https://doi.org/10.1038/ng.3894openalex-snapshot
Truncating mutations in RBM12 are associated with psychosis
inferredcites →https://doi.org/10.1038/ng.3903openalex-snapshot
The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/ng.886openalex-snapshot
Increased exonic de novo mutation rate in individuals with schizophrenia
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.4402openalex-snapshot
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
inferredcites →https://doi.org/10.1038/nn.4404openalex-snapshot
Ultra-rare disruptive and damaging mutations influence educational attainment in the general population
inferredcites →https://doi.org/10.1038/nrg3240openalex-snapshot
Genetic architectures of psychiatric disorders: the emerging picture and its implications
inferredcites →https://doi.org/10.1038/nrg3241openalex-snapshot
De novo mutations in human genetic disease
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/srep18209openalex-snapshot
Increased co-expression of genes harboring the damaging de novo mutations in Chinese schizophrenic patients during prenatal development
inferredcites →https://doi.org/10.1038/tp.2015.99openalex-snapshot
Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia
inferredcites →https://doi.org/10.1093/bioinformatics/19.1.149openalex-snapshot
Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btq559openalex-snapshot
Robust relationship inference in genome-wide association studies
inferredcites →https://doi.org/10.1093/brain/aws225openalex-snapshot
Neurological perspectives on voltage-gated sodium channels
inferredcites →https://doi.org/10.1093/ije/dyi183openalex-snapshot
Cohort profile: 1958 British birth cohort (National Child Development Study)
inferredcites →https://doi.org/10.1093/ije/dyl310openalex-snapshot
Life-course influences on health in British adults: effects of socio-economic position in childhood and adulthood
inferredcites →https://doi.org/10.1101/159780openalex-snapshot
Gene family information facilitates variant interpretation and identification of disease-associated genes
inferredcites →https://doi.org/10.1101/gr.107524.110openalex-snapshot
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
inferredcites →https://doi.org/10.1186/s12864-015-1796-6openalex-snapshot
Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling
inferredcites →https://doi.org/10.1192/bjp.bp.113.131052openalex-snapshot
Analysis of copy number variations at 15 schizophrenia-associated loci
inferredcites →https://doi.org/10.1371/journal.pgen.0020190openalex-snapshot
Population Structure and Eigenanalysis
inferredcites →https://doi.org/10.1371/journal.pone.0112745openalex-snapshot
Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s40263-022-00935-zopenalex-snapshot
Progress and Pitfalls in Developing Agents to Treat Neurocognitive Deficits Associated with Schizophrenia
inferred← citeshttps://doi.org/10.1038/s41467-019-11874-7openalex-snapshot
Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits
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.