Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective (Q38153341)

29 August 2017

Taiwan Schizophrenia Linkage Study: lessons learned from endophenotype-based genome-wide linkage scans and perspective (English)

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29 August 2017

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29 August 2017

1 October 2013

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

29 August 2017

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29 August 2017

162B

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29 August 2017

7

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29 August 2017

636-647

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Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

29 August 2017

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Linkage analysis in the next-generation sequencing era

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Morbidity risk of psychiatric disorders among the first degree relatives of schizophrenia patients in Taiwan.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Impaired flush response to niacin skin patch among schizophrenia patients and their nonpsychotic relatives: the effect of genetic loading.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Sustained attention deficits as markers of genetic susceptibility to schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Performance of the Continuous Performance Test among community samples.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Sustained attention deficit and schizotypal personality features in nonpsychotic relatives of schizophrenic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic and environmental influences on the Wisconsin Card Sorting Test performance in healthy adolescents: a twin/sibling study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The schizophrenia prodrome: treatment and high-risk perspectives.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Prodromes and precursors: epidemiologic data for primary prevention of disorders with slow onset

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Relationship between positive and negative symptoms of schizophrenia and schizotypal symptoms in nonpsychotic relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Comparative gene expression analysis of blood and brain provides concurrent validation of SELENBP1 up-regulation in schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Further evidence for dementia of the prefrontal type in schizophrenia? A controlled study of teaching the Wisconsin Card Sorting Test.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The endophenotype concept in psychiatry: etymology and strategic intentions

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic Theorizing and Schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

An overview of relations among causal modelling methods

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Taiwan schizophrenia linkage study: the field study

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The Structured Interview for Schizotypy (SIS): a preliminary report

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

MicroRNA expression aberration as potential peripheral blood biomarkers for schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Executive/attentional performance and measures of schizotypy in patients with schizophrenia and in their nonpsychotic first-degree relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

A genome-wide quantitative trait loci scan of neurocognitive performances in families with schizophrenia.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

A genome-wide linkage scan for distinct subsets of schizophrenia characterized by age at onset and neurocognitive deficits

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

A genome-wide quantitative linkage scan of niacin skin flush response in families with schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Performance on the Wisconsin Card Sorting Test among adolescents in Taiwan: norms, factorial structure, and relation to schizotypy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic and environmental influences on schizotypy among adolescents in Taiwan: a multivariate twin/sibling analysis.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Familial aggregation in skin flush response to niacin patch among schizophrenic patients and their nonpsychotic relatives

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Effects of atypical neuroleptics on sustained attention deficits in schizophrenia: a trial of risperidone versus haloperidol

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

No association of G72 and D-amino acid oxidase genes with schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

More evidence supports the association of PPP3CC with schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

A HapMap harvest of insights into the genetics of common disease

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Finding the missing heritability of complex diseases

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The niacin skin flush abnormality in schizophrenia: a quantitative dose-response study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Identification of skin as a major site of prostaglandin D2 release following oral administration of niacin in humans

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Modifier genes in mice and humans

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Diagnostic interview for genetic studies. Rationale, unique features, and training. NIMH Genetics Initiative

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Surrogate endpoints in clinical trials: definition and operational criteria

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Linkage and associated studies of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The future of genetic studies of complex human diseases

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

The genetic architecture of schizophrenia: new mutations and emerging paradigms

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Maneuvering in the complex path from genotype to phenotype

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

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

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Tests of executive functions in first-degree relatives of schizophrenic patients: a meta-analysis

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Schizophrenia: genes and environment

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Heterogeneity of schizophrenia. Conceptual models and analytic strategies

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

More severe sustained attention deficits in nonpsychotic siblings of multiplex schizophrenia families than in those of simplex ones.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Genome Scan of Han Chinese Schizophrenia Families From Taiwan: Confirmation of Linkage to 10q22.3

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

Evaluation ofRGS4 as a candidate gene for schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32166

No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32166

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32166

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29 August 2017

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PubMed ID

24132895