On the public citation graph

The role of rare copy number variants in depression

https://doi.org/10.1101/378307
0 signed · 37 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/ajmg.b.32034openalex-snapshot
Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample
inferredcites →https://doi.org/10.1016/j.biopsych.2013.07.022openalex-snapshot
The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay
inferredcites →https://doi.org/10.1016/j.biopsych.2013.10.028openalex-snapshot
Rare Copy Number Variation in Treatment-Resistant Major Depressive Disorder
inferredcites →https://doi.org/10.1016/j.biopsych.2015.02.025openalex-snapshot
Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder
inferredcites →https://doi.org/10.1016/j.biopsych.2016.08.014openalex-snapshot
Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
inferredcites →https://doi.org/10.1016/j.euroneuro.2018.07.005openalex-snapshot
COPY NUMBER VARIATION AND NEURODEVELOPMENTAL PROBLEMS IN FEMALES AND MALES IN THE GENERAL POPULATION
inferredcites →https://doi.org/10.1016/j.genhosppsych.2007.06.002openalex-snapshot
Major depression in individuals with chronic medical disorders: prevalence, correlates and association with health resource utilization, lost productivity and functional disability
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/10.1016/s0165-0327(98)00131-1openalex-snapshot
Gender differences in the prevalence of depression: a survey in primary care
inferredcites →https://doi.org/10.1038/mp.2011.144openalex-snapshot
Genome-wide association analysis of copy number variation in recurrent depressive disorder
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/nature12818openalex-snapshot
CNVs conferring risk of autism or schizophrenia affect cognition in controls
inferredcites →https://doi.org/10.1038/ng.3092openalex-snapshot
Refining analyses of copy number variation identifies specific genes associated with developmental delay
inferredcites →https://doi.org/10.1038/ng.909openalex-snapshot
A copy number variation morbidity map of developmental delay
inferredcites →https://doi.org/10.1038/s41467-018-03819-3openalex-snapshot
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
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/srep25986openalex-snapshot
Gender differences in CNV burden do not confound schizophrenia CNV associations
inferredcites →https://doi.org/10.1038/tpj.2013.51openalex-snapshot
Copy number variants and therapeutic response to antidepressant medication in major depressive disorder
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/aje/kwf182openalex-snapshot
Socioeconomic Inequalities in Depression: A Meta-Analysis
inferredcites →https://doi.org/10.1093/hmg/ddt540openalex-snapshot
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
inferredcites →https://doi.org/10.1093/schbul/sbn135openalex-snapshot
Psychiatric Comorbidities and Schizophrenia
inferredcites →https://doi.org/10.1101/gr.6861907openalex-snapshot
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
inferredcites →https://doi.org/10.1176/appi.ajp.2011.11060822openalex-snapshot
Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3
inferredcites →https://doi.org/10.1186/s12875-015-0329-3openalex-snapshot
Multiple physical and mental health comorbidity in adults with intellectual disabilities: population-based cross-sectional analysis
inferredcites →https://doi.org/10.1192/bjp.181.3.208openalex-snapshot
Duration of major depressive episodes in the general population: Results from the Netherlands Mental Health Survey and Incidence Study (NEMESIS)
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.1002334openalex-snapshot
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
inferredcites →https://doi.org/10.1371/journal.pone.0015463openalex-snapshot
Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
inferredcites →https://doi.org/10.1371/journal.pone.0046315openalex-snapshot
Copy Number Variation in Subjects with Major Depressive Disorder Who Attempted Suicide
inferredcites →https://doi.org/10.1371/journal.pone.0075362openalex-snapshot
Prevalence and Characteristics of Probable Major Depression and Bipolar Disorder within UK Biobank: Cross-Sectional Study of 172,751 Participants
inferredcites →https://doi.org/10.18637/jss.v048.i02openalex-snapshot
lavaan : An R Package for Structural Equation Modeling
inferredcites →https://doi.org/10.2147/jmdh.s104807openalex-snapshot
Information bias in health research: definition, pitfalls, and adjustment methods

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-981-33-6044-0_12openalex-snapshot
Genetic Architecture of Depression: Where Do We Stand Now?
inferred← citeshttps://doi.org/10.1016/j.neuron.2019.03.022openalex-snapshot
Uncovering the Genetic Architecture of Major Depression
inferred← citeshttps://doi.org/10.1101/583468openalex-snapshot
Genetic association study of psychotic experiences in UK Biobank
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.