(Q51877526)

15 April 2018

title

A glimmer of light for neuropsychiatric disorders (English)

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15 April 2018

author name string

Steven E Hyman

series ordinal

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15 April 2018

language of work or name

English

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publication date

1 October 2008

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15 April 2018

published in

Nature

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15 April 2018

volume

455

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15 April 2018

issue

7215

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15 April 2018

page(s)

890-893

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15 April 2018

Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Prevalence and treatment of mental disorders, 1990 to 2003

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

The familial aggregation of common psychiatric and substance use disorders in the National Comorbidity Survey: A family history study

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

The genetics of schizophrenia and bipolar disorder: dissecting psychosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Can neuroscience be integrated into the DSM-V?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

The genetics of autistic disorders and its clinical relevance: a review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Will the genomics revolution revolutionize psychiatry?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genomic Priorities and Public Health

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

A Swedish National Twin Study of Lifetime Major Depression

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

A hundred years of Alzheimer's disease research

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Association within a family of a balanced autosomal translocation with major mental illness

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

From Darwin's finches to canaries in the coal mine--mining the genome for new biology

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

EGFR antagonists in cancer treatment

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Disruption of two novel genes by a translocation co-segregating with schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Identification of loci associated with schizophrenia by genome-wide association and follow-up

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

The story of Rett syndrome: from clinic to neurobiology

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genotype and psychological phenotype in tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Chromosome 22 deletion syndrome and schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Autism as a paradigmatic complex genetic disorder

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genome-Wide Association Studies in Alzheimer Disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genetics of Parkinson disease: paradigm shifts and future prospects.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Genetics of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Strong association of de novo copy number mutations with sporadic schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Rare chromosomal deletions and duplications increase risk of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Identifying autism loci and genes by tracing recent shared ancestry

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Animal models of Alzheimer's disease and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Modelling brain diseases in mice: the challenges of design and analysis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Bipolar affective disorders linked to DNA markers on chromosome 11

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07454

7 January 2021

Identifiers

DOI

10.1038/NATURE07454

1 reference

15 April 2018

Dimensions Publication ID

1050129273

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1 reference

15 April 2018