Lista de obras -

162. Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.

artículo científico publicado en 2017

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Accuracy of CNV Detection from GWAS Data ⬇️

artículo científico publicado el 13 de enero de 2011

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees

artículo científico publicado en 2002

Association study of Wnt signaling pathway genes in bipolar disorder

artículo científico publicado en 2008

Association study of serotonin pathway genes in attempted suicide

artículo científico publicado en 2011

Attempted Suicide in Bipolar Disorder Pedigrees: Evidence for Linkage to 2p12

article

Auditory steady-state EEG response across the schizo-bipolar spectrum

scientific article published on 09 May 2019

Biotyping in psychosis: using multiple computational approaches with one data set

scientific article published on 26 September 2020

Brain gray matter network organization in psychotic disorders

artículo científico publicado en 2019

Case-control association study of TGOLN2 in attempted suicide

artículo científico publicado en 2010

Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder

scientific article published on 16 November 2018

Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm

artículo científico publicado en 2008

Common and rare variants of DAOA in bipolar disorder

artículo científico publicado en 2009

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

artículo científico publicado en 2011

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin

artículo científico publicado en 2012

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

artículo científico publicado en 2008

Familial aggregation of postpartum mood symptoms in bipolar disorder pedigrees

artículo científico publicado en 2008

Family-based association study of Neuregulin 1 with psychotic bipolar disorder

artículo científico publicado en 2009

GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size

scientific article published on 17 February 2020

Genetic Analysis of Deep Phenotyping Projects in Common Disorders

Genetic analysis of deep phenotyping projects in common disorders

artículo científico publicado en 2017

Genetic and childhood trauma interaction effect on age of onset in bipolar disorder: An exploratory analysis

artículo científico publicado en 2015

Genetic control of individual differences in gene-specific methylation in human brain.

artículo científico publicado en 2010

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

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

artículo científico publicado en 2003

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X.

artículo científico publicado en 2003

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: chromosomes 4, 7, 9, 18, 19, 20, and 21.

artículo científico publicado en 2003

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

scientific journal article

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

article

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

artículo científico publicado en 2008

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

artículo científico publicado en 2003

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

artículo científico publicado en 2012

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

artículo científico publicado en 2003

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

article

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

artículo científico publicado en 2011

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

artículo científico publicado en 1997

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

article

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

artículo científico publicado en 2004

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

artículo científico publicado en 2004

Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33.

artículo científico publicado en 2007

Multivariate relationships between peripheral inflammatory marker subtypes and cognitive and brain structural measures in psychosis

scientific article published on 15 October 2020

NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis

artículo científico publicado en 2019

Neurotransmission and bipolar disorder: a systematic family-based association study

artículo científico publicado en 2008

Rare variants in neuronal excitability genes influence risk for bipolar disorder

artículo científico publicado en 2015

Removing batch effects in analysis of expression microarray data: an evaluation of six batch adjustment methods

artículo científico publicado en 2011

Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.

artículo científico publicado en 2018

The Pharmacogenomics of Bipolar Disorder study (PGBD): identification of genes for lithium response in a prospective sample

artículo científico publicado en 2016

The association between lithium use and neurocognitive performance in patients with bipolar disorder

artículo científico publicado en 2020

The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders

artículo científico publicado en 2018

VEGFA GENE variation influences hallucinations and frontotemporal morphology in psychotic disorders: a B-SNIP study

article

Lista de obras de

162. Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Accuracy of CNV Detection from GWAS Data ⬇️

Analysis of shared heritability in common disorders of the brain

Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees

Association study of Wnt signaling pathway genes in bipolar disorder

Association study of serotonin pathway genes in attempted suicide

Attempted Suicide in Bipolar Disorder Pedigrees: Evidence for Linkage to 2p12

Auditory steady-state EEG response across the schizo-bipolar spectrum

Biotyping in psychosis: using multiple computational approaches with one data set

Brain gray matter network organization in psychotic disorders

Case-control association study of TGOLN2 in attempted suicide

Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder

Clock genes may influence bipolar disorder susceptibility and dysfunctional circadian rhythm

Common and rare variants of DAOA in bipolar disorder

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

Familial aggregation of postpartum mood symptoms in bipolar disorder pedigrees

Family-based association study of Neuregulin 1 with psychotic bipolar disorder

GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size

Genetic Analysis of Deep Phenotyping Projects in Common Disorders

Genetic analysis of deep phenotyping projects in common disorders

Genetic and childhood trauma interaction effect on age of onset in bipolar disorder: An exploratory analysis

Genetic control of individual differences in gene-specific methylation in human brain.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X.

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: chromosomes 4, 7, 9, 18, 19, 20, and 21.

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33.

Multivariate relationships between peripheral inflammatory marker subtypes and cognitive and brain structural measures in psychosis

NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis

Neurotransmission and bipolar disorder: a systematic family-based association study

Rare variants in neuronal excitability genes influence risk for bipolar disorder

Removing batch effects in analysis of expression microarray data: an evaluation of six batch adjustment methods

Shared Genetic Risk of Schizophrenia and Gray Matter Reduction in 6p22.1.

The Pharmacogenomics of Bipolar Disorder study (PGBD): identification of genes for lithium response in a prospective sample

The association between lithium use and neurocognitive performance in patients with bipolar disorder

The transcription factor POU3F2 regulates a gene coexpression network in brain tissue from patients with psychiatric disorders

VEGFA GENE variation influences hallucinations and frontotemporal morphology in psychotic disorders: a B-SNIP study