(Q39785284)

14 September 2017

title

Evaluation of risk loci for schizophrenia derived from genome-wide association studies in a German population (English)

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genome-wide association study

14 September 2017

main subject

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5

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14 September 2017

2

A B Ekici

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14 September 2017

D Schanze

1

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14 September 2017

M Gawlik

series ordinal

3

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14 September 2017

B Pfuhlmann

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4

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14 September 2017

G Stöber

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6

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14 September 2017

publication date

13 January 2011

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American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

14 September 2017

published in

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14 September 2017

volume

156

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14 September 2017

issue

2

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14 September 2017

page(s)

198-203

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Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

14 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

OPCML is a broad tumor suppressor for multiple carcinomas and lymphomas with frequently epigenetic inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Estimation of significance thresholds for genomewide association scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Why Most Discovered True Associations Are Inflated

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

What will whole genome searches for susceptibility genes for common complex disease offer to clinical practice?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Best estimate of lifetime psychiatric diagnosis: a methodological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Association between Parkinson's disease and polymorphisms in the nNOS and iNOS genes in a community-based case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Association analysis for the CA repeat polymorphism of the neuronal nitric oxide synthase (NOS1) gene and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Psychiatric genetics gets a boost.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Multicenter linkage study of schizophrenia loci on chromosome 22q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

A neurologist's guide to genome-wide association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Expression of cellular adhesion molecule 'OPCML' is down-regulated in gliomas and other brain tumours.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Congruence of diagnoses 2 years after a first-admission diagnosis of psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

OPCML at 11q25 is epigenetically inactivated and has tumor-suppressor function in epithelial ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Allelic association of the neuronal nitric oxide synthase (NOS1) gene with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

New findings from genetic association studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.31156

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.31156

1 reference

release_cswz33wajjg65ashlavtnk3tgi

14 September 2017

Fatcat ID

0 references

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