UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 201

Sortiert nach

Cognitive performance among carriers of pathogenic copy number variants: Analysis of 152,000 UK Biobank subjects

Biological psychiatry (1969), 2017-07, Vol.82 (2), p.103-110

2017

Volltextzugriff (PDF)

Translating insights from neuropsychiatric genetics and genomics for precision psychiatry

Genome medicine, 2020-04, Vol.12 (1), p.43-43, Article 43

2020

Volltextzugriff (PDF)

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

Molecular psychiatry, 2020-04, Vol.25 (4), p.854-862

2020

Volltextzugriff (PDF)

De novo mutations in schizophrenia implicate synaptic networks

Nature (London), 2014-02, Vol.506 (7487), p.179-184

2014

Volltextzugriff (PDF)

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

Progress in neurobiology, 2015-11, Vol.134, p.36-54

2015

Volltextzugriff (PDF)

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

British journal of psychiatry, 2019-05, Vol.214 (5), p.297-304

2019

Volltextzugriff (PDF)

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

Journal of medical genetics, 2019-03, Vol.56 (3), p.131

2019

Volltextzugriff (PDF)

Analysis of copy number variations at 15 schizophrenia-associated loci

British journal of psychiatry, 2014-02, Vol.204 (2), p.108-114

2014

Volltextzugriff (PDF)

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

Biological psychiatry (1969), 2014-03, Vol.75 (5), p.378-385

2014

Volltextzugriff (PDF)

A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia

Human molecular genetics, 2020-01, Vol.29 (1), p.159-167

2020

Volltextzugriff (PDF)

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

Nature communications, 2021-09, Vol.12 (1), p.5353-5353, Article 5353

2021

Volltextzugriff (PDF)

Clinical indicators of treatment-resistant psychosis

British journal of psychiatry, 2020-05, Vol.216 (5), p.259-266

2020

Volltextzugriff (PDF)

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Neuron (Cambridge, Mass.), 2015-06, Vol.86 (5), p.1203-1214

2015

Volltextzugriff (PDF)

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

BMC genomics, 2018-12, Vol.19 (1), p.867-9, Article 867

2018

Volltextzugriff (PDF)

The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis

International journal of molecular sciences, 2024-01, Vol.25 (2), p.946

2024

Volltextzugriff (PDF)

Copy number variation and neuropsychiatric illness

Current opinion in genetics & development, 2021-06, Vol.68, p.57-63

2021

Volltextzugriff (PDF)

De novo CNVs in bipolar affective disorder and schizophrenia

Human molecular genetics, 2014-12, Vol.23 (24), p.6677-6683

2014

Volltextzugriff (PDF)

De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants

Biological psychiatry (1969), 2011-12, Vol.70 (12), p.1109-1114

2011

Volltextzugriff (PDF)

Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

Nature communications, 2022-01, Vol.13 (1), p.27-27, Article 27

2022

Volltextzugriff (PDF)

Characterization of Single Gene Copy Number Variants in Schizophrenia

Biological psychiatry (1969), 2020-04, Vol.87 (8), p.736-744

2020

Volltextzugriff (PDF)

Developing a novel tonsillitis pathway to reduce pressures on front-door services: A multi-phase quality improvement project in a large UK teaching hospital

Surgery in practice and science, 2023-09, Vol.14, p.100214, Article 100214

2023

Volltextzugriff (PDF)

Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia

Biological psychiatry global open science, 2024-09, Vol.4 (5), p.100345, Article 100345

2024

Volltextzugriff (PDF)

What a psychiatrist needs to know about copy number variants

BJPsych advances, 2015-05, Vol.21 (3), p.157-163

2015

Volltextzugriff (PDF)

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

PloS one, 2015-12, Vol.10 (12), p.e0144172-e0144172

2015

Volltextzugriff (PDF)

83. DAMAGING RARE CODING VARIANTS IDENTIFIED BY EXOME SEQUENCING ARE ASSOCIATED WITH REDUCED COGNITIVE FUNCTION IN SCHIZOPHRENIA

European neuropsychopharmacology, 2021-10, Vol.51, p.e85-e85

2021

Volltextzugriff (PDF)

1 – 25 von 201

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(191)
Mit Volltextzugriff
(178)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Englisch
(201)
Japanisch
(32)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Cognitive performance among carriers of pathogenic copy number variants: Analysis of 152,000 UK Biobank subjects

Translating insights from neuropsychiatric genetics and genomics for precision psychiatry

Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank

De novo mutations in schizophrenia implicate synaptic networks

Genetic disruption of voltage-gated calcium channels in psychiatric and neurological disorders

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank

Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank

Analysis of copy number variations at 15 schizophrenia-associated loci

The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay

A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations

Clinical indicators of treatment-resistant psychosis

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Effects of pathogenic CNVs on physical traits in participants of the UK Biobank

The Association of Hippocampal Long-Term Potentiation-Induced Gene Expression with Genetic Risk for Psychosis

Copy number variation and neuropsychiatric illness

De novo CNVs in bipolar affective disorder and schizophrenia

De Novo Rates and Selection of Schizophrenia-Associated Copy Number Variants

Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants

Characterization of Single Gene Copy Number Variants in Schizophrenia

Developing a novel tonsillitis pathway to reduce pressures on front-door services: A multi-phase quality improvement project in a large UK teaching hospital

Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia

What a psychiatrist needs to know about copy number variants

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

83. DAMAGING RARE CODING VARIANTS IDENTIFIED BY EXOME SEQUENCING ARE ASSOCIATED WITH REDUCED COGNITIVE FUNCTION IN SCHIZOPHRENIA

Suchergebnisse filtern