UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 140

Sortiert nach

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

BMC medical genetics, 2014-01, Vol.15 (1), p.2-2, Article 2

2014

Volltextzugriff (PDF)

Genetic association, mutation screening, and functional analysis of a Kozak sequence variant in the metabotropic glutamate receptor 3 gene in bipolar disorder

JAMA psychiatry (Chicago, Ill.), 2013-06, Vol.70 (6), p.591

2013

Volltextzugriff (PDF)

A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder

Pharmacogenetics and genomics, 2007-08, Vol.17 (8), p.605-617

2007

Volltextzugriff (PDF)

Genetics of attention-deficit hyperactivity disorder (ADHD)

Neuropharmacology, 2009-12, Vol.57 (7), p.590-600

2009

Volltextzugriff (PDF)

Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome

Molecular genetics and genomics : MGG, 2007-01, Vol.277 (1), p.71-81

2007

Volltextzugriff (PDF)

Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-06, Vol.165B (4), p.373-380

2014

Volltextzugriff (PDF)

Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-03, Vol.156B (2), p.177-187

2011

Volltextzugriff (PDF)

Support of association between BRD1 and both schizophrenia and bipolar affective disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-03, Vol.153B (2), p.582-591

2010

Volltextzugriff (PDF)

Three-dimensional textural analysis of brain images reveals distributed grey-matter abnormalities in schizophrenia

European radiology, 2010-04, Vol.20 (4), p.941-948

2010

Volltextzugriff (PDF)

Genetic variant analysis of the putative regulatory regions of the LRRC7 gene in bipolar disorder

Psychiatric genetics, 2016-04, Vol.26 (2), p.99-100

2016

Volltextzugriff (PDF)

The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis

Psychiatric genetics, 2013-08, Vol.23 (4), p.153-162

2013

Volltextzugriff (PDF)

Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition

Nature communications, 2013-11, Vol.4 (1), p.2816, Article 2816

2013

Volltextzugriff (PDF)

A Genetic Association Study of Chromosome 11q22-24 in Two Different Samples Implicates the FXYD6 Gene, Encoding Phosphohippolin, in Susceptibility to Schizophrenia

American journal of human genetics, 2007-04, Vol.80 (4), p.664-672

2007

Volltextzugriff (PDF)

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

Psychiatric genetics, 2011-02, Vol.21 (1), p.1-4

2011

Volltextzugriff (PDF)

A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia

Psychiatric genetics, 2012-06, Vol.22 (3), p.150-151

2012

Volltextzugriff (PDF)

No evidence for excess runs of homozygosity in bipolar disorder

Psychiatric genetics, 2009-08, Vol.19 (4), p.165-170

2009

Volltextzugriff (PDF)

Mutation screening of X-chromosomal neuroligin genes: No mutations in 196 autism probands

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-08, Vol.129B (1), p.82-84

2004

Volltextzugriff (PDF)

Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia

Behavioral and brain functions, 2009-07, Vol.5 (1), p.28-28, Article 28

2009

Volltextzugriff (PDF)

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

Archives of general psychiatry, 2006-08, Vol.63 (8), p.844

2006

Volltextzugriff (PDF)

Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample

Biological psychiatry (1969), 2006-01, Vol.59 (2), p.195-197

2006

Volltextzugriff (PDF)

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

American journal of human genetics, 2014-12, Vol.95 (6), p.744-753

2014

Volltextzugriff (PDF)

Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-08, Vol.137B (1), p.17-19

2005

Volltextzugriff (PDF)

Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

American journal of human genetics, 2001-03, Vol.68 (3), p.661-673

2001

Volltextzugriff (PDF)

1 – 25 von 140

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(131)
Mit Volltextzugriff
(118)

Publikationsform

Artikel
(139)
Buchkapitel
(1)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(120)
Humans
(117)
Life Sciences & Biomedicine
(103)
Schizophrenia
(57)
Genetics & Heredity
(56)
Schizophrenia - Genetics
(53)
Male
(51)
Biological And Medical Sciences
(50)
Female
(49)
Medical Sciences
(46)
Psychiatry
(44)
Psychology. Psychoanalysis. Psychiatry
(38)
Psychopathology. Psychiatry
(37)
Adult And Adolescent Clinical Studies
(34)
Genetic Predisposition To Disease
(33)
Genome-Wide Association Study
(33)
Neurosciences
(32)
Alleles
(30)
Medicin Och Hälsovetenskap
(30)
Neurosciences & Neurology
(30)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1

Genetic association, mutation screening, and functional analysis of a Kozak sequence variant in the metabotropic glutamate receptor 3 gene in bipolar disorder

A microarray gene expression study of the molecular pharmacology of lithium carbonate on mouse brain mRNA to understand the neurobiology of mood stabilization and treatment of bipolar affective disorder

Genetics of attention-deficit hyperactivity disorder (ADHD)

Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome

Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome

Genetic association and sequencing of the insulin-like growth factor 1 gene in bipolar affective disorder

Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population

Support of association between BRD1 and both schizophrenia and bipolar affective disorder

Three-dimensional textural analysis of brain images reveals distributed grey-matter abnormalities in schizophrenia

Genetic variant analysis of the putative regulatory regions of the LRRC7 gene in bipolar disorder

The effect of clozapine on mRNA expression for genes encoding G protein-coupled receptors and the protein components of clathrin-mediated endocytosis

Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition

A Genetic Association Study of Chromosome 11q22-24 in Two Different Samples Implicates the FXYD6 Gene, Encoding Phosphohippolin, in Susceptibility to Schizophrenia

Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia

No evidence for excess runs of homozygosity in bipolar disorder

Mutation screening of X-chromosomal neuroligin genes: No mutations in 196 autism probands

Evidence for genetic susceptibility to the alcohol dependence syndrome from the thiamine transporter 2 gene solute carrier SLC19A3

Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia

Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

Direct genomic PCR sequencing of the high affinity thiamine transporter (SLC19A2) gene identifies three genetic variants in Wernicke Korsakoff syndrome (WKS)

Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

Suchergebnisse filtern