Psychiatric genetics: progress amid controversy (Q28284253)

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9 January 2020

review article

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title

Psychiatric genetics: progress amid controversy (English)

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9 January 2020

1

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9 January 2020

author name string

Melvin G McInnis

series ordinal

2

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9 January 2020

Sebastian Zöllner

series ordinal

3

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9 January 2020

language of work or name

English

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publication date

1 July 2008

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9 January 2020

published in

Nature Reviews Genetics

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9 January 2020

volume

9

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9 January 2020

issue

7

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9 January 2020

page(s)

527-540

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The genetic basis of complex human behaviors

9 January 2020

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Evidence of positive selection acting at the human dopamine receptor D4 gene locus

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High prevalence of rare dopamine receptor D4 alleles in children diagnosed with attention-deficit hyperactivity disorder

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Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

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Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

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Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

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No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics

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Neuregulin 1 genotype and schizophrenia

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A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

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Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

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Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

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Efficacy assessment of SNP sets for genome-wide disease association studies

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Power to detect risk alleles using genome-wide tag SNP panels

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

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Whole-genome association study of bipolar disorder

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Genomewide association for schizophrenia in the CATIE study: results of stage 1

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Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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Neurobiology of schizophrenia

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Association mapping in structured populations

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Undetected genotyping errors cause apparent overtransmission of common alleles in the transmission/disequilibrium test

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Spurious genetic associations.

31 March 2020

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Meta-analyses of genetic studies on major depressive disorder

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Molecular mechanisms of schizophrenia

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Molecular genetics of bipolar disorder

31 March 2020

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Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology

31 March 2020

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Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

31 March 2020

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Neuronal and non-neuronal functions of the AP-3 sorting machinery

31 March 2020

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Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

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Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia

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31 March 2020

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The PDE4B gene confers sex-specific protection against schizophrenia.

31 March 2020

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31 March 2020

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31 March 2020

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NRG2381

2 references

Consolidated OpenCitations Corpus – April 2017

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Dimensions Publication ID

9 January 2020

1010506183

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Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

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