UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

Molecular psychiatry, 2017-12, Vol.22 (12), p.1664-1672

2017

Volltextzugriff (PDF)

A double hit implicates DIAPH3 as an autism risk gene

Molecular psychiatry, 2011-04, Vol.16 (4), p.442-451

2011

Volltextzugriff (PDF)

Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study

Schizophrenia research, 2017-10, Vol.188, p.59-62

2017

Volltextzugriff (PDF)

Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses

Pharmacopsychiatry, 2015-09, Vol.48 (6), p.219-220

2015

Volltextzugriff (PDF)

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

Journal of intellectual disability research, 2015-09, Vol.59 (9), p.803-815

2015

Volltextzugriff (PDF)

Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research

Cytogenetic and genome research, 2011-12, Vol.135 (3-4), p.174-202

2011

Volltextzugriff (PDF)

A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome

Journal of intellectual disability research, 2024-10

2024

Volltextzugriff (PDF)

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia

Psychological medicine, 2019-04, Vol.49 (6), p.1047-1054

2019

Volltextzugriff (PDF)

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome

Clinical genetics, 2016-11, Vol.90 (5), p.420-427

2016

Volltextzugriff (PDF)

Detailed analysis of 22q11.2 with a high density MLPA probe set

Human mutation, 2008-03, Vol.29 (3), p.433-440

2008

Volltextzugriff (PDF)

Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: A matched control study

American journal of medical genetics. Part A, 2007-03, Vol.143A (6), p.574-580

2007

Volltextzugriff (PDF)

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

Molecular psychiatry, 2006-01, Vol.11 (1), p.18-28

2006

Volltextzugriff (PDF)

Individual common variants exert weak effects on the risk for autism spectrum disorderspi

Human molecular genetics, 2012-11, Vol.21 (21), p.4781-4792

2012

Volltextzugriff (PDF)

Guidelines on genetic testing in psychiatry: an overview

Tijdschrift voor psychiatrie, 2022-01, Vol.64 (5), p.278-285

2022

Volltextzugriff (PDF)

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

Human mutation, 2006-08, Vol.27 (8), p.814-821

2006

Volltextzugriff (PDF)

Overview of cytogenetic regions of interest (CROIs) associated with the autism phenotype across the human genome

Molecular psychiatry, 2006-01, Vol.11 (1), p.1-1

2006

Volltextzugriff (PDF)

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

Molecular psychiatry, 2006-01, Vol.11 (1), p.1-28

2006

Volltextzugriff (PDF)

A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome

Nederlands tijdschrift voor geneeskunde, 2002-10, Vol.146 (43), p.2033

2002

Volltextzugriff (PDF)

Autism genetics: opportunities and challenges for clinical translation

Nature reviews. Genetics, 2017-06, Vol.18 (6), p.362-376

2017

Volltextzugriff (PDF)

22q11.2 deletion syndrome

Nature reviews. Disease primers, 2015-11, Vol.1 (1), p.15071-15071, Article 15071

2015

Volltextzugriff (PDF)

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

Current psychiatry reports, 2021-03, Vol.23 (3), p.13-13, Article 13

2021

Volltextzugriff (PDF)

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome

American journal of medical genetics. Part A, 2018-10, Vol.176 (10), p.2182-2191

2018

Volltextzugriff (PDF)

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model

Psychological medicine, 2022-10, Vol.52 (14), p.3184-3192

2022

Volltextzugriff (PDF)

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

Schizophrenia research, 2013-01, Vol.143 (1), p.55-59

2013

Volltextzugriff (PDF)

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism

Neurogenetics, 2011-11, Vol.12 (4), p.315-323

2011

Volltextzugriff (PDF)

1 – 25 von 170

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(156)
Mit Volltextzugriff
(149)

Publikationsform

Artikel
(169)
Buchkapitel
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

A double hit implicates DIAPH3 as an autism risk gene

Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study

Pharmacological treatment of 22q11.2 deletion syndrome-related psychoses

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

Genome Arrays for the Detection of Copy Number Variations in Idiopathic Mental Retardation, Idiopathic Generalized Epilepsy and Neuropsychiatric Disorders: Lessons for Diagnostic Workflow and Research

A comprehensive overview of neuropsychiatric symptoms in adolescents with 22q11.2 deletion syndrome

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome

Detailed analysis of 22q11.2 with a high density MLPA probe set

Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: A matched control study

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

Individual common variants exert weak effects on the risk for autism spectrum disorderspi

Guidelines on genetic testing in psychiatry: an overview

MLPA: a rapid, reliable, and sensitive method for detection and analysis of abnormalities of 22q

Overview of cytogenetic regions of interest (CROIs) associated with the autism phenotype across the human genome

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

A bifid uvula in a patient with schizophrenia as a sign of 22q11 deletion syndrome

Autism genetics: opportunities and challenges for clinical translation

22q11.2 deletion syndrome

Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome

Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model

Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism

Suchergebnisse filtern