Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder (Q36120530)

12 August 2017

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder (English)

1 reference

12 August 2017

1 reference

1 reference

Sven Cichon

0 references

Marcella Rietschel

series ordinal

object named as

Marcella Rietschel

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Francis J McMahon

0 references

Markus M Nöthen

0 references

Andrew B Singleton

1 reference

12 August 2017

Thomas G Schulze

1 reference

12 August 2017

Michael A Nalls

1 reference

12 August 2017

Nirmala Akula

1 reference

12 August 2017

René Breuer

1 reference

12 August 2017

Franziska A Degenhardt

1 reference

12 August 2017

Jo Steele

1 reference

PMC publication ID

3406228

12 August 2017

Bipolar Genome Study

series ordinal

1 reference

12 August 2017

9 March 2012

1 reference

World Journal of Biological Psychiatry

12 August 2017

1 reference

12 August 2017

1 reference

12 August 2017

1 reference

12 August 2017

200-208

1 reference

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Hundreds of variants clustered in genomic loci and biological pathways affect human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Common SNPs explain a large proportion of the heritability for human height

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genetics and genomics of ankylosing spondylitis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genetic research into bipolar disorder: the need for a research framework that integrates sophisticated molecular biology and clinically informed phenotype characterization

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Common variants on chromosome 6p22.1 are associated with schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genome-wide association study of bipolar disorder in European American and African American individuals

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genome-based prediction of common diseases: methodological considerations for future research

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Clinical risk factors, DNA variants, and the development of type 2 diabetes

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Predicting unobserved phenotypes for complex traits from whole-genome SNP data

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Prediction of individual genetic risk to disease from genome-wide association studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

PLINK: a tool set for whole-genome association and population-based linkage analyses

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Computer-assisted phenotype characterization for genetic research in psychiatry

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Evidence for shared susceptibility in bipolar disorder and schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Are schizophrenic and bipolar disorders related? A review of family and molecular studies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

A polygenic theory of schizophrenia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

A controlled family study of chronic psychoses. Schizophrenia and schizoaffective disorder

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Depression and Parkinson's disease: a review

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Value of genetic profiling for the prediction of coronary heart disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3406228

GRR: graphical representation of relationship errors

23 September 2018

1 reference

PubMed

12 December 2020

Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

Genomewide SNP assay reveals mutations underlying Parkinson disease

1 reference

PubMed

12 December 2020

10.3109/15622975.2012.662282

Identifiers

DOI

1 reference

12 August 2017

1 reference

PMC publication ID

3406228

12 August 2017

PubMed publication ID

22404658

1 reference

PMC publication ID

3406228