4.1 Review

Animal Models of Psychiatric Disorders That Reflect Human Copy Number Variation

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Editorial Material Neurosciences

Placental Source for 5-HT that Tunes Fetal Brain Development

Alexandre Bonnin et al.

NEUROPSYCHOPHARMACOLOGY (2012)

Article Psychology, Developmental

Anxiety and Sensory Over-Responsivity in Toddlers with Autism Spectrum Disorders: Bidirectional Effects Across Time

Shulamite A. Green et al.

JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)

Article Clinical Neurology

Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother

Marina Michelson et al.

EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY (2011)

Review Behavioral Sciences

Comparative immunogenetics of autism and schizophrenia

B. J. Crespi et al.

GENES BRAIN AND BEHAVIOR (2011)

Article Developmental Biology

The 22q11.2 microdeletion: Fifteen years of insights into the genetic and neural complexity of psychiatric disorders

Liam J. Drew et al.

INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE (2011)

Article Clinical Neurology

The neurobiology of mouse models syntenic to human chromosome 15q

Toru Takumi

JOURNAL OF NEURODEVELOPMENTAL DISORDERS (2011)

Article Multidisciplinary Sciences

A transient placental source of serotonin for the fetal forebrain

Alexandre Bonnin et al.

NATURE (2011)

Article Pediatrics

Modeling Autistic Features in Animals

Paul H. Patterson

PEDIATRIC RESEARCH (2011)

Article Multidisciplinary Sciences

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism

Guy Horev et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Article Multidisciplinary Sciences

Impaired hippocampal-prefrontal synchrony in a genetic mouse model of schizophrenia

Torfi Sigurdsson et al.

NATURE (2010)

Review Neurosciences

Behavioural phenotyping assays for mouse models of autism

Jill L. Silverman et al.

NATURE REVIEWS NEUROSCIENCE (2010)

Review Neurosciences

22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia

Maria Karayiorgou et al.

NATURE REVIEWS NEUROSCIENCE (2010)

Review Neurosciences

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

Amber Hogart et al.

NEUROBIOLOGY OF DISEASE (2010)

Article Clinical Neurology

Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome

Vandana Shashi et al.

PSYCHIATRY RESEARCH-NEUROIMAGING (2010)

Article Genetics & Heredity

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

Helen V. Firth et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2009)

Article Medicine, Research & Experimental

Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice

Hong Hua Li et al.

EMBO MOLECULAR MEDICINE (2009)

Article Clinical Neurology

Analysis of prepulse inhibition in mouse lines overexpressing 22q11.2 orthologues

Kimberly L. Stark et al.

INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY (2009)

Review Nursing

Review of the Evidence for Treatment of Children with Autism with Selective Serotonin Reuptake Inhibitors

Lis West et al.

JOURNAL FOR SPECIALISTS IN PEDIATRIC NURSING (2009)

Article Genetics & Heredity

Microduplications of 16p11.2 are associated with schizophrenia

Shane E. McCarthy et al.

NATURE GENETICS (2009)

Article Multidisciplinary Sciences

Association and Mutation Analyses of 16p11.2 Autism Candidate Genes

Ravinesh A. Kumar et al.

PLOS ONE (2009)

Article Multidisciplinary Sciences

Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

Daniel W. Meechan et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)

Review Genetics & Heredity

Copy-number variants in neurodevelopmental disorders: promises and challenges

Alison K. Merikangas et al.

TRENDS IN GENETICS (2009)

Article Genetics & Heredity

Structural variation of chromosomes in autism spectrum disorder

Christian R. Marshall et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Review Clinical Neurology

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome

Doron Gothelf et al.

DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2008)

Article Genetics & Heredity

Strong association of de novo copy number mutations with sporadic schizophrenia

Bin Xu et al.

NATURE GENETICS (2008)

Article Genetics & Heredity

Integrated detection and population-genetic analysis of SNPs and copy number variation

Steven A. McCarroll et al.

NATURE GENETICS (2008)

Review Genetics & Heredity

Timeline - Trends in large-scale mouse mutagenesis: from genetics to functional genomics

Yoichi Gondo

NATURE REVIEWS GENETICS (2008)

Article Medicine, General & Internal

Association between microdeletion and microduplication at 16p11.2 and autism

Lauren A. Weiss et al.

NEW ENGLAND JOURNAL OF MEDICINE (2008)

Review Medicine, General & Internal

Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes

Lisa J. Kobrynski et al.

LANCET (2007)

Article Neurosciences

Mapping cortical thickness in children with 22q11.2 deletions

Carrie E. Bearden et al.

CEREBRAL CORTEX (2007)

Article Genetics & Heredity

Methods and strategies for analyzing copy number variation using DNA microarrays

Nigel P. Carter

NATURE GENETICS (2007)

Article Multidisciplinary Sciences

Global variation in copy number in the human genome

Richard Redon et al.

NATURE (2006)

Article Neurosciences

Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome

Joel P. Bish et al.

NEUROSCIENCE LETTERS (2006)

Article Multidisciplinary Sciences

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans:: Implications for 22q11 deletion syndrome

Richard Paylor et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Psychology, Developmental

Temporal lobe anatomy and psychiatric symptoms in velocardiofacial syndrome (22q11.2 deletion syndrome)

WR Kates et al.

JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY (2006)

Article Genetics & Heredity

Angelman syndrome 2005: Updated consensus for diagnostic criteria

CA Williams et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)

Article Psychology, Developmental

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: A case and family study

MWM Veltman et al.

JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2005)

Article Genetics & Heredity

Detection of large-scale variation in the human genome

AJ Iafrate et al.

NATURE GENETICS (2004)

Article Genetics & Heredity

Mutagenic insertion and chromosome engineering resource (MICER)

DJ Adams et al.

NATURE GENETICS (2004)

Article Multidisciplinary Sciences

Large-scale copy number polymorphism in the human genome

J Sebat et al.

SCIENCE (2004)

Article Genetics & Heredity

Autism in Angelman syndrome: implications for autism research

SU Peters et al.

CLINICAL GENETICS (2004)

Article Biochemistry & Molecular Biology

Radiation-induced genomic instability and its implications for radiation carcinogenesis

L Huang et al.

ONCOGENE (2003)

Article Biochemistry & Molecular Biology

TBX1 is responsible for cardiovascular defects in Velo-Cardio-Facial/DiGeorge syndrome

S Merscher et al.

Article Multidisciplinary Sciences

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

J Cavaillé et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)

Article Biochemistry & Molecular Biology

The 22q11 deletion syndromes

PJ Scambler

HUMAN MOLECULAR GENETICS (2000)

Article Biochemistry & Molecular Biology

A genetic screen for novel behavioral mutations in mice

DM Sayah et al.

MOLECULAR PSYCHIATRY (2000)

Article Psychiatry

Children and adolescents with velocardiofacial syndrome: A volumetric MRI study

S Eliez et al.

AMERICAN JOURNAL OF PSYCHIATRY (2000)

Article Education, Special

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes

E Roof et al.

JOURNAL OF INTELLECTUAL DISABILITY RESEARCH (2000)