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Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population

https://doi.org/10.1086/345442
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What this work says

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

inferredcites →https://doi.org/10.1002/(sici)1096-8628(19961122)67:6<580::aid-ajmg11>3.0.co;2-popenalex-snapshot
Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19980710)81:4<282::aid-ajmg2>3.0.co;2-wopenalex-snapshot
NIMH genetics initiative millennium schizophrenia consortium: Linkage analysis of African-American pedigrees
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19980907)81:5<364::aid-ajmg4>3.0.co;2-topenalex-snapshot
A genome-wide search for schizophrenia susceptibility genes
inferredcites →https://doi.org/10.1002/ajmg.10538openalex-snapshot
Genome‐wide scan for linkage to schizophrenia in a Spanish‐origin cohort from Costa Rica
inferredcites →https://doi.org/10.1002/ajmg.1320600316openalex-snapshot
Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes
inferredcites →https://doi.org/10.1016/s0166-4328(99)00175-8openalex-snapshot
Heregulin, but not ErbB2 or ErbB3, heterozygous mutant mice exhibit hyperactivity in multiple behavioral tasks
inferredcites →https://doi.org/10.1038/1734openalex-snapshot
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21
inferredcites →https://doi.org/10.1038/37795openalex-snapshot
Neuregulin-β induces expression of an NMDA-receptor subunit
inferredcites →https://doi.org/10.1038/sj.mp.4001051openalex-snapshot
Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes
inferredcites →https://doi.org/10.1073/pnas.041394098openalex-snapshot
β-Neuregulin-1 is required for the in vivo development of functional Ca 2+ -activated K + channels in parasympathetic neurons
inferredcites →https://doi.org/10.1073/pnas.070042497openalex-snapshot
The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses
inferredcites →https://doi.org/10.1086/302560openalex-snapshot
Candidate-Gene Association Studies of Schizophrenia
inferredcites →https://doi.org/10.1086/302566openalex-snapshot
Transmission/Disequilibrium Tests for Extended Marker Haplotypes
inferredcites →https://doi.org/10.1086/302579openalex-snapshot
Linkage of Familial Schizophrenia to Chromosome 13q32
inferredcites →https://doi.org/10.1086/318785openalex-snapshot
mtDNA and the Islands of the North Atlantic: Estimating the Proportions of Norse and Gaelic Ancestry
inferredcites →https://doi.org/10.1086/318788openalex-snapshot
Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23
inferredcites →https://doi.org/10.1086/319506openalex-snapshot
Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements
inferredcites →https://doi.org/10.1086/339252openalex-snapshot
Localization of a Susceptibility Gene for Common Forms of Stroke to 5q12
inferredcites →https://doi.org/10.1086/341291openalex-snapshot
Presence of Large Deletions in Kindreds with Autism
inferredcites →https://doi.org/10.1086/342734openalex-snapshot
Neuregulin 1 and Susceptibility to Schizophrenia
inferredcites →https://doi.org/10.1093/acrefore/9780199975839.013.104openalex-snapshot
Diagnostic and Statistical Manual of Mental Disorders
inferredcites →https://doi.org/10.1093/oxfordjournals.jhered.a111613openalex-snapshot
HAPLO: A Program Using the EM Algorithm to Estimate the Frequencies of Multi-site Haplotypes
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040269openalex-snapshot
Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.
inferredcites →https://doi.org/10.1101/gr.9.5.492openalex-snapshot
Fluorescence Polarization in Homogeneous Nucleic Acid Analysis
inferredcites →https://doi.org/10.1111/j.2517-6161.1977.tb01600.xopenalex-snapshot
Maximum Likelihood from Incomplete Data Via the EM Algorithm
inferredcites →https://doi.org/10.1146/annurev.neuro.20.1.429openalex-snapshot
ARIA: A Neuromuscular Junction Neuregulin
inferredcites →https://doi.org/10.1176/ajp.153.12.1534openalex-snapshot
Evidence for a schizophrenia vulnerability locus on chromosome 8p in the Irish Study of High-Density Schizophrenia Families
inferredcites →https://doi.org/10.1523/jneurosci.19-24-10757.1999openalex-snapshot
Neuregulin Induces GABAAReceptor Subunit Expression and Neurite Outgrowth in Cerebellar Granule Cells

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4613876openalex-extracted
inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2009.82openalex-snapshot
Support for NRG1 as a Susceptibility Factor for Schizophrenia in a Northern Swedish Isolated Population
inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2010.117openalex-snapshot
Biological Validation of Increased Schizophrenia Risk With NRG1, ERBB4, and AKT1 Epistasis via Functional Neuroimaging in Healthy Controls
inferred← citeshttps://doi.org/10.1001/archpsyc.61.4.336openalex-snapshot
Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1)
inferred← citeshttps://doi.org/10.1001/archpsyc.62.6.642openalex-snapshot
Operation of the Schizophrenia Susceptibility Gene, Neuregulin 1, Across Traditional Diagnostic Boundaries to Increase Risk for Bipolar Disorder
inferred← citeshttps://doi.org/10.1001/archpsyc.63.8.844openalex-snapshot
Genetic Association and Brain Morphology Studies and the Chromosome 8p22 Pericentriolar Material 1 (PCM1) Gene in Susceptibility to Schizophrenia
inferred← citeshttps://doi.org/10.1001/archpsyc.65.3.345openalex-snapshot
Genome-Wide Association for Methamphetamine Dependence
inferred← citeshttps://doi.org/10.1001/archpsyc.65.4.378openalex-snapshot
Dysfunctional Neural Plasticity in Patients With Schizophrenia
inferred← citeshttps://doi.org/10.1002/047001153x.g202204openalex-snapshot
Haplotype mapping
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005180.pub2openalex-snapshot
de CODE and Iceland: A Critique
inferred← citeshttps://doi.org/10.1002/9780470015902.a0006270openalex-snapshot
deCODE: A Genealogical Approach to Human Genetics in Iceland
inferred← citeshttps://doi.org/10.1002/9780470041000.cedt050openalex-snapshot
Prospects for Genomics—Derived Drugs: New Approaches and Impact on Pharmaceutical Pipelines
inferred← citeshttps://doi.org/10.1002/9780470101001.hcn031openalex-snapshot
Molecular Genetics of Schizophrenia
inferred← citeshttps://doi.org/10.1002/9780470101001.hcn032openalex-snapshot
Postmortem Brain Studies: Focus on Susceptibility Genes in Schizophrenia
inferred← citeshttps://doi.org/10.1002/9780470978672.ch4openalex-snapshot
The Genetics of Schizophrenia
inferred← citeshttps://doi.org/10.1002/9781444327298.ch12openalex-snapshot
Classical Genetic Studies of Schizophrenia
inferred← citeshttps://doi.org/10.1002/9783527619672.ch37openalex-snapshot
Emerging Treatments for Depression: Beyond the Monoamine Hypothesis
inferred← citeshttps://doi.org/10.1002/ajmg.b.20074openalex-snapshot
Interleukin‐1β (IL‐1β) gene and increased risk for the depressive symptom‐dimension in schizophrenia spectrum disorders
inferred← citeshttps://doi.org/10.1002/ajmg.b.20175openalex-snapshot
Association of the HOPA12bp allele with a large X‐chromosome haplotype and positive symptom schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.30099openalex-snapshot
Fine mapping of a region on chromosome 8p gives evidence for a QTL contributing to individual differences in an anxiety‐related personality trait: TPQ harm avoidance
inferred← citeshttps://doi.org/10.1002/ajmg.b.30209openalex-snapshot
Linkage and association of schizophrenia with genetic variations in the locus of neuregulin 1 in Korean population
inferred← citeshttps://doi.org/10.1002/ajmg.b.30219openalex-snapshot
Neuregulin‐1 polymorphism in late onset Alzheimer's disease families with psychoses
inferred← citeshttps://doi.org/10.1002/ajmg.b.30236openalex-snapshot
Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.30242openalex-snapshot
Analysis of polymorphisms in AT‐rich domains of neuregulin 1 gene in schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.30274openalex-snapshot
Genetic association between schizophrenia and the DISC1 gene in the Scottish population
inferred← citeshttps://doi.org/10.1002/ajmg.b.30275openalex-snapshot
The involvement of ErbB4 with schizophrenia: Association and expression studies
inferred← citeshttps://doi.org/10.1002/ajmg.b.30306openalex-snapshot
Association study of CHRFAM7A copy number and 2bp deletion polymorphisms with schizophrenia and bipolar affective disorder
inferred← citeshttps://doi.org/10.1002/ajmg.b.30511openalex-snapshot
Family‐based association study of neuregulin‐1 gene and psychosis in a Spanish sample
inferred← citeshttps://doi.org/10.1002/ajmg.b.30549openalex-snapshot
Prediction of psychosis onset in Alzheimer disease: The role of depression symptom severity and the HTR2A T102C polymorphism
inferred← citeshttps://doi.org/10.1002/ajmg.b.30727openalex-snapshot
The neuregulin 1 promoter polymorphism rs6994992 is not associated with chronic schizophrenia or neurocognition
inferred← citeshttps://doi.org/10.1002/ajmg.b.30895openalex-snapshot
Family‐based association study of Neuregulin 1 with psychotic bipolar disorder
inferred← citeshttps://doi.org/10.1002/ajmg.b.30965openalex-snapshot
NRG1 gene in recurrent major depression: No association in a large‐scale case–control association study
inferred← citeshttps://doi.org/10.1002/ajmg.b.31115openalex-snapshot
EGR3 as a potential susceptibility gene for schizophrenia in Korea
inferred← citeshttps://doi.org/10.1002/ajmg.b.31154openalex-snapshot
Linkage and association on 8p21.2-p21.1 in schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.32045openalex-snapshot
Association study of neuregulin 1 gene polymorphisms with auditory p300 in schizophrenia
inferred← citeshttps://doi.org/10.1002/ajmg.b.32206openalex-snapshot
Effects of neuregulin‐1 genetic variation and depression symptom severity on longitudinal patterns of psychotic symptoms in primary care attendees
inferred← citeshttps://doi.org/10.1002/ajmg.b.32428openalex-snapshot
Genetic association between NRG1 and schizophrenia, major depressive disorder, bipolar disorder in Han Chinese population
inferred← citeshttps://doi.org/10.1002/ajmg.b.32573openalex-snapshot
Association study of NDST3 gene for schizophrenia, bipolar disorder, major depressive disorder in the Han Chinese population
inferred← citeshttps://doi.org/10.1002/art.11037openalex-snapshot
High‐throughput single‐nucleotide polymorphism analysis of the IL1RN locus in patients with ankylosing spondylitis by matrix‐assisted laser desorption ionization‐time‐of‐flight mass spectrometry
inferred← citeshttps://doi.org/10.1002/cne.20016openalex-snapshot
Neuregulin‐2 is developmentally regulated and targeted to dendrites of central neurons
inferred← citeshttps://doi.org/10.1002/ddr.10367openalex-snapshot
Role of pharmacogenomics in drug development
inferred← citeshttps://doi.org/10.1002/gepi.20126openalex-snapshot
Comparison of methods incorporating quantitative covariates into affected sib pair linkage analysis
inferred← citeshttps://doi.org/10.1002/gepi.20432openalex-snapshot
A novel method for haplotype clustering and visualization
inferred← citeshttps://doi.org/10.1002/hbm.20761openalex-snapshot
Genetic variation in the schizophrenia‐risk gene neuregulin 1 correlates with brain activation and impaired speech production in a verbal fluency task in healthy individuals
inferred← citeshttps://doi.org/10.1002/hbm.20818openalex-snapshot
Genetic variation in neuregulin1 is associated with differences in prefrontal engagement in children
inferred← citeshttps://doi.org/10.1002/hipo.10185openalex-snapshot
Neuregulin1 downregulates postsynaptic GABAa receptors at the hippocampal inhibitory synapse
inferred← citeshttps://doi.org/10.1002/humu.20369openalex-snapshot
Major affective disorders and schizophrenia: a common molecular signature?
inferred← citeshttps://doi.org/10.1002/jcla.23187openalex-snapshot
Genetic variation in NRG 1 gene and risk of post‐traumatic stress disorders in patients with hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/mgg3.169openalex-snapshot
Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations
inferred← citeshttps://doi.org/10.1002/stem.3447openalex-snapshot
A Protein-Centric View of in Vitro Biological Model Systems for Schizophrenia
inferred← citeshttps://doi.org/10.1002/stem.762openalex-snapshot
Concise Review: The Promise of Human Induced Pluripotent Stem Cell-Based Studies of Schizophrenia
inferred← citeshttps://doi.org/10.1007/3-211-29109-1_6openalex-snapshot
Aktuelle Aspekte genetischer Forschung bei Schizophrenie
inferred← citeshttps://doi.org/10.1007/3-211-29109-1_8openalex-snapshot
Schizophrenie, Entzündung und glutamaterge Neurotransmission: ein pathophysiologisches Modell
inferred← citeshttps://doi.org/10.1007/3-540-29048-6_15openalex-snapshot
Neurogenetik und die Genetik des Verhaltens
inferred← citeshttps://doi.org/10.1007/3-540-30887-3_7openalex-snapshot
Schizophrenie und verwandte Störungen — Neurobiologie
inferred← citeshttps://doi.org/10.1007/7854_2011_183openalex-snapshot
Schizophrenia Genes: On the Matter of Their Convergence
inferred← citeshttps://doi.org/10.1007/82_2010_82openalex-snapshot
The Neurodevelopmental Implications of PI3K Signaling
inferred← citeshttps://doi.org/10.1007/978-0-387-30410-6_6openalex-snapshot
Neuregulin 1 and Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-0-387-74351-6_8openalex-snapshot
Alterations in Hippocampal Function in Schizophrenia: its Genetic Associations and Systems Implications
inferred← citeshttps://doi.org/10.1007/978-0-387-76727-7_5openalex-snapshot
Models of Human Behavior: Talking to the Animals
inferred← citeshttps://doi.org/10.1007/978-0-387-79251-4openalex-snapshot
Biomarkers for Psychiatric Disorders
inferred← citeshttps://doi.org/10.1007/978-0-387-79251-4_18openalex-snapshot
DNA Biomarkers for Pharmacogenomics and Personalized Medicine
inferred← citeshttps://doi.org/10.1007/978-0-387-79251-4_2openalex-snapshot
Biomarkers in Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-1-4419-7197-5_13openalex-snapshot
Genetic Studies of Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-1-4939-2528-5_29openalex-snapshot
Genetics of Psychiatric Disorders
inferred← citeshttps://doi.org/10.1007/978-1-59745-252-6_29openalex-snapshot
Genetics of Psychiatric Disorders
inferred← citeshttps://doi.org/10.1007/978-1-59745-499-5_4openalex-snapshot
Genetic Regulation of the Variation in Pubertal Timing
inferred← citeshttps://doi.org/10.1007/978-1-60327-139-4_9openalex-snapshot
Interaction Between Physical Activity and Genetic Factors in Complex Metabolic Disease
inferred← citeshttps://doi.org/10.1007/978-3-211-92215-6_6openalex-snapshot
Gemeinsame Risikogene von affektiven und schizophrenen Erkrankungen
inferred← citeshttps://doi.org/10.1007/978-3-211-92215-6_9openalex-snapshot
Neue Ergebnisse in der genetischen Forschung bei schizophrenen Psychosen
inferred← citeshttps://doi.org/10.1007/978-3-540-33129-2_4openalex-snapshot
Genetik psychischer Störungen
inferred← citeshttps://doi.org/10.1007/978-3-540-85383-1_2openalex-snapshot
Dissecting the Molecular Causes of Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-3-642-03637-8_5openalex-snapshot
Genetik bei psychischen Erkrankungen
inferred← citeshttps://doi.org/10.1007/978-3-642-45028-0_5-1openalex-snapshot
Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen
inferred← citeshttps://doi.org/10.1007/978-3-642-45028-0_5-2openalex-snapshot
Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen
inferred← citeshttps://doi.org/10.1007/978-3-662-44817-5_14openalex-snapshot
Verhaltens- und Neurogenetik
inferred← citeshttps://doi.org/10.1007/978-3-662-49295-6_5openalex-snapshot
Genetik und Gen-Umwelt-Interaktionen bei psychischen Erkrankungen
inferred← citeshttps://doi.org/10.1007/978-3-662-60909-5_14openalex-snapshot
Verhaltens- und Neurogenetik
inferred← citeshttps://doi.org/10.1007/978-3-662-70328-1_14openalex-snapshot
Verhaltens- und Neurogenetik
inferred← citeshttps://doi.org/10.1007/978-3-7091-0623-5_6openalex-snapshot
Neuentwicklungen in der Erforschung der Genetik der Schizophrenie
inferred← citeshttps://doi.org/10.1007/978-3-7091-0932-8_22openalex-snapshot
Synaptic Dysfunction in Schizophrenia
inferred← citeshttps://doi.org/10.1007/978-3-7985-1953-4_15openalex-snapshot
Searching for inherited causes for schizophrenia: has progress been made?
inferred← citeshttps://doi.org/10.1007/978-4-431-53945-2_6openalex-snapshot
Impaired Neurogenesis as a Risk Factor for Schizophrenia and Related Mental Diseases
inferred← citeshttps://doi.org/10.1007/978-90-481-2298-1_4openalex-snapshot
Molecular Genetics of Schizophrenia: Focus on Symptom Dimensions
inferred← citeshttps://doi.org/10.1007/978-90-481-8553-5_19openalex-snapshot
Inhibition of Glycine Transporter-1 Improves the Functional Outcome of Schizophrenia
inferred← citeshttps://doi.org/10.1007/bf02879896openalex-snapshot
Neuregulin-1 genotype moderates the association between job strain and early atherosclerosis in young men
inferred← citeshttps://doi.org/10.1007/bf03033242openalex-snapshot
Schizophrenia as an inflammation-mediated dysbalance of glutamatergic neurotransmission
inferred← citeshttps://doi.org/10.1007/bf03033484openalex-snapshot
Are some genetic risk factors common to schizophrenia, bipolar disorder and depression? evidence fromDISC1, GRIK4 andNRG1
inferred← citeshttps://doi.org/10.1007/bf03033897openalex-snapshot
Comorbidity implications in brain disease: Neuronal substrates of symptom profiles
inferred← citeshttps://doi.org/10.1007/bf03033899openalex-snapshot
Genetic variation and shared biological susceptibility underlying comorbidity in neuropsychiatry
inferred← citeshttps://doi.org/10.1007/s00213-003-1502-2openalex-snapshot
Ethical issues in psychiatric genetics research: points to consider
inferred← citeshttps://doi.org/10.1007/s00213-006-0482-4openalex-snapshot
Family and case–control association study of the tumor necrosis factor-alpha (TNF-α) gene with schizophrenia and response to antipsychotic medication
inferred← citeshttps://doi.org/10.1007/s00213-013-3003-2openalex-snapshot
Neuregulin-1 signalling and antipsychotic treatment
inferred← citeshttps://doi.org/10.1007/s00335-004-2427-8openalex-snapshot
Fine mapping of a major locus on Chromosome 10 for exploratory and fear-like behavior in mice
inferred← citeshttps://doi.org/10.1007/s00406-005-0583-9openalex-snapshot
Genetic models of schizophrenia and bipolar disorder
inferred← citeshttps://doi.org/10.1007/s00406-007-0756-9openalex-snapshot
Interleukin-1 beta gene polymorphism and its interactions with neuregulin-1 gene polymorphism are associated with schizophrenia
inferred← citeshttps://doi.org/10.1007/s00406-008-0837-4openalex-snapshot
Neuregulin 1 ICE-single nucleotide polymorphism in first episode schizophrenia correlates with cerebral activation in fronto-temporal areas
inferred← citeshttps://doi.org/10.1007/s00406-008-5019-xopenalex-snapshot
Impact of neuregulin-1 on the pathophysiology of schizophrenia in human post-mortem studies
inferred← citeshttps://doi.org/10.1007/s00406-009-0017-1openalex-snapshot
Gene expression of NMDA receptor subunits in the cerebellum of elderly patients with schizophrenia
inferred← citeshttps://doi.org/10.1007/s00406-009-0024-2openalex-snapshot
Cannabis and psychosis/schizophrenia: human studies
inferred← citeshttps://doi.org/10.1007/s00406-009-0032-2openalex-snapshot
Neuregulin-1 genotypes and eye movements in schizophrenia
inferred← citeshttps://doi.org/10.1007/s00426-022-01649-zopenalex-snapshot
The molecular genetic basis of creativity: a mini review and perspectives
inferred← citeshttps://doi.org/10.1007/s00429-008-0181-5openalex-snapshot
Age-related changes in the expression of schizophrenia susceptibility genes in the human prefrontal cortex
inferred← citeshttps://doi.org/10.1007/s00429-009-0219-3openalex-snapshot
Further immunohistochemical characterization of BRD1 a new susceptibility gene for schizophrenia and bipolar affective disorder
inferred← citeshttps://doi.org/10.1007/s00508-004-0256-0openalex-snapshot
In search of susceptibility genes for schizophrenia
inferred← citeshttps://doi.org/10.1007/s00702-008-0182-9openalex-snapshot
Neuregulin 1 and age of onset in the major psychoses
inferred← citeshttps://doi.org/10.1007/s10038-008-0332-9openalex-snapshot
Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese population
inferred← citeshttps://doi.org/10.1007/s10519-009-9317-5openalex-snapshot
Influence of Neuregulin1 Genotype on Neural Substrate of Perceptual Matching in Children
inferred← citeshttps://doi.org/10.1007/s11033-010-0606-0openalex-snapshot
Potential role of Neuregulin 1 and TNF-alpha (−308) polymorphism in schizophrenia patients visiting hospitals in Lahore, Pakistan
inferred← citeshttps://doi.org/10.1007/s11055-012-9692-xopenalex-snapshot
Association between Polymorphism of the Neuregulin Gene (NRG1) and Cognitive Functions in Schizophrenia Patients and Healthy Subjects
inferred← citeshttps://doi.org/10.1007/s11689-009-9017-8openalex-snapshot
Deficient NRG1-ERBB signaling alters social approach: relevance to genetic mouse models of schizophrenia
inferred← citeshttps://doi.org/10.1007/s11845-007-0004-3openalex-snapshot
Unravelling the genome: a review of molecular genetic research in schizophrenia
inferred← citeshttps://doi.org/10.1007/s11897-013-0176-2openalex-snapshot
Neuregulin as a Heart Failure Therapy and Mediator of Reverse Remodeling
inferred← citeshttps://doi.org/10.1007/s11920-003-0028-yopenalex-snapshot
Linkage and association studies of schizophrenia
inferred← citeshttps://doi.org/10.1007/s11920-004-0081-1openalex-snapshot
The genes for schizophrenia: Finally a breakthrough?
inferred← citeshttps://doi.org/10.1007/s11920-005-0012-9openalex-snapshot
Meta-analysis in psychiatric genetics
inferred← citeshttps://doi.org/10.1007/s11920-008-0029-yopenalex-snapshot
Genomic structural variation and schizophrenia
inferred← citeshttps://doi.org/10.1007/s11922-004-0032-7openalex-snapshot
The genes for schizophrenia: Finally a breakthrough?
inferred← citeshttps://doi.org/10.1007/s12017-014-8323-9openalex-snapshot
No Association Between NRG1 and ErbB4 Genes and Psychopathological Symptoms of Schizophrenia
inferred← citeshttps://doi.org/10.1007/s12031-011-9619-yopenalex-snapshot
Lack of Associations of Neuregulin 1 Variations with Schizophrenia and Smooth Pursuit Eye Movement Abnormality in a Korean Population
inferred← citeshttps://doi.org/10.1007/s12041-011-0112-8openalex-snapshot
Positive association between NTNG1 and schizophrenia in Chinese Han population
inferred← citeshttps://doi.org/10.1007/s40429-013-0006-3openalex-snapshot
Genetics and Smoking
inferred← citeshttps://doi.org/10.1016/b978-0-12-373861-5.00008-4openalex-snapshot
Developing New Drugs for Schizophrenia: From Animals to the Clinic
inferred← citeshttps://doi.org/10.1016/b978-0-12-394309-5.00002-xopenalex-snapshot
Functional Diversity of Actin Cytoskeleton in Neurons and its Regulation by Tropomyosin
inferred← citeshttps://doi.org/10.1016/b978-0-12-394596-9.00012-3openalex-snapshot
Animal Models of Schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-800981-9.00020-1openalex-snapshot
Modeling Gene–Environment Interaction in Schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-800981-9.00026-2openalex-snapshot
Dimensions of GSK3 Monoamine-Related Intracellular Signaling in Schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.65836-1openalex-snapshot
Excitotoxicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-801829-3.00028-8openalex-snapshot
Modeling Schizophrenia in Animals
inferred← citeshttps://doi.org/10.1016/b978-0-12-803592-4.00107-3openalex-snapshot
Human Puberty: Physiology, Progression, and Genetic Regulation of Variation in Onset
inferred← citeshttps://doi.org/10.1016/b978-0-12-812215-0.00008-xopenalex-snapshot
Epigenetics in Neurobehavioral Disease
inferred← citeshttps://doi.org/10.1016/b978-0-444-52002-9.00003-6openalex-snapshot
Human genetics of schizophrenia
inferred← citeshttps://doi.org/10.1016/b978-0-444-63327-9.00016-3openalex-snapshot
Changes in Plasticity Across the Lifespan
inferred← citeshttps://doi.org/10.1016/b978-0-7020-3137-3.00015-2openalex-snapshot
Schizophrenia and related disorders
inferred← citeshttps://doi.org/10.1016/b978-0-7020-3397-1.00019-7openalex-snapshot
Schizophrenia and related disorders
inferred← citeshttps://doi.org/10.1016/b978-008088783-8.00065-6openalex-snapshot
Human Puberty: Physiology, Progression, and Genetic Regulation of Variation in Onset
inferred← citeshttps://doi.org/10.1016/b978-012160281-9/50003-7openalex-snapshot
Neuregulins
inferred← citeshttps://doi.org/10.1016/bs.adgen.2015.09.001openalex-snapshot
Decoding Advances in Psychiatric Genetics
inferred← citeshttps://doi.org/10.1016/bs.mie.2014.10.008openalex-snapshot
Sleep and Circadian Rhythm Disruption and Recognition Memory in Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.ajhg.2008.01.008openalex-snapshot
Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis
inferred← citeshttps://doi.org/10.1016/j.ajp.2020.102363openalex-snapshot
Impact of NRG1 HapICE gene variants on digit ratio and dermatoglyphic measures in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.ajpath.2025.03.012openalex-snapshot
Multiple Roles for Neuregulins and Their v-Erb-B2 Avian Erythroblastic Leukemia Viral Oncogene Homolog Receptors in Neurodegenerative Disease Pathogenesis and Therapy
inferred← citeshttps://doi.org/10.1016/j.applanim.2026.107172openalex-snapshot
Genetic determinants and polygenic architecture of canine aggression
inferred← citeshttps://doi.org/10.1016/j.arr.2023.101988openalex-snapshot
BACE1-dependent metabolism of neuregulin 1: Bridging the gap in explaining the occurrence of schizophrenia-like symptoms in Alzheimer's disease with psychosis?
inferred← citeshttps://doi.org/10.1016/j.bbadis.2004.06.023openalex-snapshot
A high proportion of polymorphisms in the promoters of brain expressed genes influences transcriptional activity
inferred← citeshttps://doi.org/10.1016/j.bbi.2009.04.004openalex-snapshot
Neonatal infection with neurotropic influenza A virus affects working memory and expression of type III Nrg1 in adult mice
inferred← citeshttps://doi.org/10.1016/j.bbi.2009.08.012openalex-snapshot
Neuregulin-1, the fetal endothelium, and brain damage in preterm newborns
inferred← citeshttps://doi.org/10.1016/j.bbr.2009.04.010openalex-snapshot
Animal models of gene–environment interactions in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.bbr.2011.05.008openalex-snapshot
Sex-specific neuroendocrine and behavioral phenotypes in hypomorphic Type II Neuregulin 1 rats
inferred← citeshttps://doi.org/10.1016/j.bbr.2018.03.026openalex-snapshot
Schizophrenia-relevant behaviours of female mice overexpressing neuregulin 1 type III
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.06.031openalex-snapshot
Evaluating the role of the alpha-7 nicotinic acetylcholine receptor in the pathophysiology and treatment of schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2003.11.002openalex-snapshot
Support for RGS4 as a susceptibility gene for schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2004.01.014openalex-snapshot
Identification of PIK3C3 promoter variant associated with bipolar disorder and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2004.02.025openalex-snapshot
Reduced frontal white matter integrity in Early-Onset schizophrenia: a preliminary study
inferred← citeshttps://doi.org/10.1016/j.biopsych.2005.01.005openalex-snapshot
Principles of Haplotype Mapping and Potential Applications to Attention-Deficit/Hyperactivity Disorder
inferred← citeshttps://doi.org/10.1016/j.biopsych.2005.04.006openalex-snapshot
Evidence for a Relationship Between Genetic Variants at the Brain-Derived Neurotrophic Factor (BDNF) Locus and Major Depression
inferred← citeshttps://doi.org/10.1016/j.biopsych.2005.11.002openalex-snapshot
Neuregulin 1 and Schizophrenia: Genetics, Gene Expression, and Neurobiology
inferred← citeshttps://doi.org/10.1016/j.biopsych.2006.02.015openalex-snapshot
Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples
inferred← citeshttps://doi.org/10.1016/j.biopsych.2006.02.024openalex-snapshot
Genetic Mouse Models of Schizophrenia: From Hypothesis-Based To Susceptibility Gene-Based Models
inferred← citeshttps://doi.org/10.1016/j.biopsych.2006.03.017openalex-snapshot
A Novel Missense Mutation in the Transmembrane Domain of Neuregulin 1 is Associated with Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2006.04.018openalex-snapshot
A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci
inferred← citeshttps://doi.org/10.1016/j.biopsych.2008.01.003openalex-snapshot
The Role of the Cerebellum in Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2008.03.025openalex-snapshot
Support for Neuregulin 1 as a Susceptibility Gene for Bipolar Disorder and Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biopsych.2008.07.012openalex-snapshot
Neuregulin 3 Genetic Variations and Susceptibility to Schizophrenia in a Chinese Population
inferred← citeshttps://doi.org/10.1016/j.biopsych.2013.01.020openalex-snapshot
Focal Adhesion Dynamics Are Altered in Schizophrenia
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2007.11.003openalex-snapshot
Agrin and neuregulin, expanding roles and implications for therapeutics
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.07.065openalex-snapshot
Neuregulin 1 transgenic mice display reduced mismatch negativity, contextual fear conditioning and social interactions
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2010.04.011openalex-snapshot
Neuregulin 1–erbB4 pathway in schizophrenia: From genes to an interactome
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2005.11.006openalex-snapshot
Neuregulins: Versatile growth and differentiation factors in nervous system development and human disease
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2006.09.001openalex-snapshot
Early brain development disruption from NMDA receptor hypofunction: Relevance to schizophrenia
inferred← citeshttps://doi.org/10.1016/j.brs.2011.06.003openalex-snapshot
A randomized controlled trial of sequentially bilateral prefrontal cortex repetitive transcranial magnetic stimulation in the treatment of negative symptoms in schizophrenia
inferred← citeshttps://doi.org/10.1016/j.brs.2015.01.404openalex-snapshot
Consensus Paper: Probing Homeostatic Plasticity of Human Cortex With Non-invasive Transcranial Brain Stimulation
inferred← citeshttps://doi.org/10.1016/j.brs.2015.06.016openalex-snapshot
Erratum to “Consensus Paper: Probing Homeostatic Plasticity of Human Cortex With Non-invasive Transcranial Brain Stimulation”. Brain Stimulation 8 (2015) 442–454
inferred← citeshttps://doi.org/10.1016/j.brs.2015.06.017openalex-snapshot
Consensus Paper: Probing Homeostatic Plasticity of Human Cortex With Non-invasive Transcranial Brain Stimulation
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2006.01.009openalex-snapshot
Analysis of GABRB2 association with schizophrenia in German population with DNA sequencing and one-label extension method for SNP genotyping
inferred← citeshttps://doi.org/10.1016/j.ejphar.2003.08.105openalex-snapshot
The genetics of schizophrenia: glutamate not dopamine?
inferred← citeshttps://doi.org/10.1016/j.ejphar.2004.07.031openalex-snapshot
Advances in pharmacogenomics and individualized drug therapy: exciting challenges that lie ahead
inferred← citeshttps://doi.org/10.1016/j.ejpsy.2019.12.004openalex-snapshot
Neuregulin1 gene variants as a biomarker for cognitive impairments in patients with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.eurpsy.2008.03.004openalex-snapshot
Genetic variation in the schizophrenia-risk gene neuregulin1 correlates with personality traits in healthy individuals
inferred← citeshttps://doi.org/10.1016/j.gde.2004.04.005openalex-snapshot
Why genetic investigation of psychiatric disorders is so difficult
inferred← citeshttps://doi.org/10.1016/j.gene.2004.07.029openalex-snapshot
Multiple novel transcription initiation sites for NRG1
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147285openalex-snapshot
Correlation of rs35753505 polymorphism in Neuregulin 1 gene with psychopathology and intelligence of people with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e30193openalex-snapshot
Associations among plasma markers for N-methyl-d-aspartate receptor hypofunction, redox dysregulation, and insufficient myelination in patients with schizophrenia
inferred← citeshttps://doi.org/10.1016/j.ijpsycho.2016.09.010openalex-snapshot
Genome-wide association study of working memory brain activation
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2007.02.005openalex-snapshot
Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2008.01.009openalex-snapshot
Neuregulin-1 haplotype HAPICE is associated with lower hippocampal volumes in schizophrenic patients and in non-affected family members
inferred← citeshttps://doi.org/10.1016/j.mcn.2004.01.013openalex-snapshot
Disrupted in Schizophrenia 1 (DISC1) is a multicompartmentalized protein that predominantly localizes to mitochondria
inferred← citeshttps://doi.org/10.1016/j.mcn.2004.08.001openalex-snapshot
Neuregulin-1β induces neurite extension and arborization in cultured hippocampal neurons
inferred← citeshttps://doi.org/10.1016/j.mcn.2006.12.001openalex-snapshot
Novel regional and developmental NMDA receptor expression patterns uncovered in NR2C subunit-β-galactosidase knock-in mice
inferred← citeshttps://doi.org/10.1016/j.mehy.2003.11.026openalex-snapshot
Intrathecal therapy with trastuzumab may be beneficial in cases of refractory schizophrenia
inferred← citeshttps://doi.org/10.1016/j.mgene.2017.12.008openalex-snapshot
Association of Neuregulin-1 gene polymorphisms with neuro-cognitive features of schizophrenia patients from South India: A pilot study
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2005.01.006openalex-snapshot
Genetic association studies of complex traits: design and analysis issues
inferred← citeshttps://doi.org/10.1016/j.nbd.2011.01.025openalex-snapshot
Mitochondria, oligodendrocytes and inflammation in bipolar disorder: Evidence from transcriptome studies points to intriguing parallels with multiple sclerosis
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2009.11.022openalex-snapshot
Genetics and intermediate phenotypes of the schizophrenia—bipolar disorder boundary
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2015.10.014openalex-snapshot
Sex differences in animal models of schizophrenia shed light on the underlying pathophysiology
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2019.08.019openalex-snapshot
Translating preclinical findings in clinically relevant new antipsychotic targets: focus on the glutamatergic postsynaptic density. Implications for treatment resistant schizophrenia
inferred← citeshttps://doi.org/10.1016/j.neulet.2004.05.027openalex-snapshot
Case-control and family-based association studies between the neuregulin 1 (Arg38Gln) polymorphism and schizophrenia
inferred← citeshttps://doi.org/10.1016/j.neulet.2004.05.063openalex-snapshot
Lack of a genetic association between the frizzled-3 gene and schizophrenia in a British population
inferred← citeshttps://doi.org/10.1016/j.neulet.2005.11.015openalex-snapshot
Supportive evidence for neuregulin 1 as a susceptibility gene for schizophrenia in a Japanese population
inferred← citeshttps://doi.org/10.1016/j.neulet.2010.04.056openalex-snapshot
Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder
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