(Q37688994)

22 August 2017

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title

Child and adolescent psychiatric genetics (English)

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22 August 2017

2

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22 August 2017

4

Anke Hinney

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Johannes Hebebrand

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1

object named as

Johannes Hebebrand

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author name string

Benno G Schimmelmann

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3

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PubMed ID

20140632

22 August 2017

language of work or name

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6 February 2010

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European Child & Adolescent Psychiatry

22 August 2017

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22 August 2017

19

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22 August 2017

3

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22 August 2017

259-279

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https://scigraph.springernature.com/pub.10.1007/s00787-010-0091-y

22 August 2017

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cites work

Specification of the phenotype required for men with monoamine oxidase type A deficiency

1 reference

https://api.crossref.org/works/10.1007%2FS00787-010-0091-Y

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-010-0091-Y

Influence of the amyloid precursor protein locus on dementia in Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-010-0091-Y

A genome-wide survey of segmental duplications that mediate common human genetic variation of chromosomal architecture

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00787-010-0091-Y

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

12 December 2020

Common variants on chromosome 6p22.1 are associated with schizophrenia

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12 December 2020

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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12 December 2020

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression.

1 reference

12 December 2020

Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes

1 reference

12 December 2020

Genome-wide atlas of gene expression in the adult mouse brain

1 reference

12 December 2020

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

1 reference

12 December 2020

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

1 reference

12 December 2020

A genomic view of alternative splicing

1 reference

12 December 2020

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene

1 reference

12 December 2020

Mecp2-null mice provide new neuronal targets for Rett syndrome.

1 reference

12 December 2020

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

1 reference

12 December 2020

Genetic, environmental, and gender effects on individual differences in toddler expressive language

1 reference

12 December 2020

Molecular genetic aspects of attention-deficit/hyperactivity disorder

1 reference

12 December 2020

Many sequence variants affecting diversity of adult human height

1 reference

12 December 2020

A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

1 reference

12 December 2020

Breakthroughs in the search for dyslexia candidate genes

1 reference

12 December 2020

Identification of loci associated with schizophrenia by genome-wide association and follow-up

1 reference

12 December 2020

A twin study of anxiety-related behaviours in pre-school children.

1 reference

12 December 2020

Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies

1 reference

12 December 2020

Significance levels in complex inheritance

1 reference

12 December 2020

Recent segmental duplications in the human genome

1 reference

12 December 2020

Genetic influences on eating attitudes in a normal female twin population

1 reference

12 December 2020

The three-factor eating questionnaire to measure dietary restraint, disinhibition and hunger.

1 reference

12 December 2020

Meta-Analysis of Genome-wide Linkage Studies in BMI and Obesity*

1 reference

12 December 2020

Molecular Structure of Nucleic Acids: A Structure for Deoxyribose Nucleic Acid

1 reference

12 December 2020

The diploid genome sequence of an individual human

1 reference

12 December 2020

Therapeutic application of histone deacetylase inhibitors for central nervous system disorders

1 reference

12 December 2020

Eating behavior in the Old Order Amish: heritability analysis and a genome-wide linkage analysis.

1 reference

12 December 2020

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

1 reference

12 December 2020

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

1 reference

12 December 2020

Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study

1 reference

12 December 2020

Searching for genetic determinants in the new millennium

1 reference

12 December 2020

Breakthrough of the year. Human genetic variation

1 reference

12 December 2020

The eating attitudes test: psychometric features and clinical correlates

1 reference

12 December 2020

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 reference

12 December 2020

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

1 reference

12 December 2020

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

1 reference

12 December 2020

Genetics of autistic disorders: review and clinical implications

1 reference

12 December 2020

Study of somatic chromosomes from 9 mongoloid children

1 reference

12 December 2020

Genomewide association studies and human disease

1 reference

12 December 2020

A question of size: the eukaryotic proteome and the problems in defining it.

1 reference

12 December 2020

Genetics of developmental dyslexia

1 reference

12 December 2020

Delay in motor development of twins in Africa: a prospective cohort study

1 reference

12 December 2020

Heritability of the big five personality dimensions and their facets: a twin study

1 reference

12 December 2020

Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder

1 reference

12 December 2020

Finishing the euchromatic sequence of the human genome

1 reference

12 December 2020

Sequence variation and disease in the wake of the draft human genome

1 reference

12 December 2020

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

1 reference

12 December 2020

From monogenic to polygenic obesity: recent advances

1 reference

12 December 2020

Genetic counseling for psychiatric disorders

1 reference

12 December 2020

Neurofibromatosis type 1: new insights into neurocognitive issues

1 reference

12 December 2020

Mapping and sequencing of structural variation from eight human genomes

1 reference

12 December 2020

Childhood adversity, monoamine oxidase a genotype, and risk for conduct disorder

1 reference

12 December 2020

Genetic dissection of complex traits

1 reference

12 December 2020

Role of genotype in the cycle of violence in maltreated children

1 reference

12 December 2020

Role of brain-derived neurotrophic factor in eating disorders: recent findings and its pathophysiological implications.

1 reference

12 December 2020

Estimate of human gene number provided by genome-wide analysis using Tetraodon nigroviridis DNA sequence

1 reference

12 December 2020

ADHD: strategies to unravel its genetic architecture

1 reference

12 December 2020

Genotype and psychological phenotype in tuberous sclerosis

1 reference

12 December 2020

Genetic analysis of motor milestones attainment in early childhood

1 reference

12 December 2020

Molecular genetics of attention-deficit/hyperactivity disorder: an overview

1 reference

12 December 2020

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

12 December 2020

Epigenetic differences arise during the lifetime of monozygotic twins

1 reference

12 December 2020

Mutation analysis of methyl-CpG binding protein family genes in autistic patients

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

1 reference

12 December 2020

Eating disorders: the current status of molecular genetic research

1 reference

12 December 2020

Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche

1 reference

12 December 2020

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

1 reference

12 December 2020

Large-scale copy number polymorphism in the human genome

1 reference

12 December 2020

"A gene for...": the nature of gene action in psychiatric disorders

1 reference

12 December 2020

The Tridimensional Personality Questionnaire: U.S. Normative Data

1 reference

12 December 2020

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

1 reference

12 December 2020

Neuropathology of Rett syndrome

1 reference

12 December 2020

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

12 December 2020

Recent advances in MeCP2 structure and function

1 reference

12 December 2020

Genetic variation in LIN28B is associated with the timing of puberty

1 reference

12 December 2020

Progress in genome-wide association studies of human height.

1 reference

12 December 2020

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement

1 reference

12 December 2020

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 reference

12 December 2020

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

1 reference

12 December 2020

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

12 December 2020

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

1 reference

12 December 2020

Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism

1 reference

12 December 2020

Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

1 reference

12 December 2020

On a unusual brain atrophy syndrome in hyperammonemia in childhood

1 reference

12 December 2020

Polygenic obesity in humans

1 reference

12 December 2020

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

12 December 2020

What is known about autism: genes, brain, and behavior

1 reference

12 December 2020

Identification of the breast cancer susceptibility gene BRCA2

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Analysis of multilocus models of association

1 reference

12 December 2020

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

1 reference

12 December 2020

Birth of 'human-specific' genes during primate evolution

1 reference

12 December 2020

Genetic and environmental influences on conduct disorder: symptom, domain and full-scale analyses.

1 reference

12 December 2020

Sequence variants in SLITRK1 are associated with Tourette's syndrome

1 reference

12 December 2020

Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases

1 reference

12 December 2020

The future of genetic studies of complex human diseases

1 reference

12 December 2020

Evolution of the tumor suppressor BRCA1 locus in primates: implications for cancer predisposition.

1 reference

12 December 2020

A HapMap harvest of insights into the genetics of common disease

1 reference

12 December 2020

The story of Rett syndrome: from clinic to neurobiology

1 reference

12 December 2020

Common variants conferring risk of schizophrenia

1 reference

12 December 2020

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

1 reference

12 December 2020

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

1 reference

12 December 2020

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

1 reference

12 December 2020

Initial sequencing and comparative analysis of the mouse genome

1 reference

12 December 2020

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

1 reference

12 December 2020

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

1 reference

12 December 2020

Use of unlinked genetic markers to detect population stratification in association studies.

1 reference

12 December 2020

Genetics of early-onset obsessive-compulsive disorder

1 reference

12 December 2020

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

1 reference

12 December 2020

Common genetic variants on 5p14.1 associate with autism spectrum disorders

1 reference

12 December 2020

Genetic and environmental contributions to the Child Behavior Checklist Obsessive-Compulsive Scale: a cross-cultural twin study

1 reference

12 December 2020

The diploid genome sequence of an Asian individual

1 reference

12 December 2020

Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis

1 reference

12 December 2020

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

1 reference

12 December 2020

Lesch-Nyhan disease: from mechanism to model and back again

1 reference

12 December 2020

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

12 December 2020

EST comparison indicates 38% of human mRNAs contain possible alternative splice forms.

1 reference

12 December 2020

What can genome-wide association studies tell us about the genetics of common disease?

1 reference

12 December 2020

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

1 reference

12 December 2020

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 reference

12 December 2020

The Sequence of the Human Genome

1 reference

12 December 2020

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

1 reference

12 December 2020

The PAH gene, phenylketonuria, and a paradigm shift

1 reference

12 December 2020

Copy-number variations associated with neuropsychiatric conditions

1 reference

12 December 2020

The genetics of enuresis: a review

1 reference

12 December 2020

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

1 reference

12 December 2020

Widespread evidence for non-additive genetic variation in Cloninger's and Eysenck's personality dimensions using a twin plus sibling design

1 reference

12 December 2020

Frequent alternative splicing of human genes

1 reference

12 December 2020

Discovery and modeling of transcriptional regulatory regions

1 reference

12 December 2020

Signals and their transduction pathways regulating alternative splicing: a new dimension of the human genome

1 reference

12 December 2020

Genetic epidemiology of major depression: review and meta-analysis

1 reference

12 December 2020

1 reference

12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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12 December 2020

Leptin regulates striatal regions and human eating behavior

1 reference

12 December 2020

Psychiatric genetics: progress amid controversy

1 reference

12 December 2020

Phenotypic and measurement influences on heritability estimates in childhood ADHD.

1 reference

12 December 2020

Detecting recent positive selection in the human genome from haplotype structure

1 reference

12 December 2020

A genetic risk factor for periodic limb movements in sleep

1 reference

12 December 2020

Genome sequencing in microfabricated high-density picolitre reactors

1 reference

12 December 2020

Comparative evolutionary genomics of androgen-binding protein genes

1 reference

12 December 2020

How to use an article about genetic association: B: Are the results of the study valid?

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 reference

12 December 2020

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

1 reference

12 December 2020

Finding genes in child psychology and psychiatry: when are we going to be there?

1 reference

12 December 2020

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

1 reference

12 December 2020

Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibiotics

1 reference

12 December 2020

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism

1 reference

12 December 2020

Genetic and environmental influences on obsessional traits and symptoms

1 reference

12 December 2020

Family, twin, and adoption studies of bipolar disorder

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

1 reference

12 December 2020

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

1 reference

12 December 2020

10.1007/S00787-010-0091-Y

Identifiers

DOI

1 reference

22 August 2017

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PubMed ID

20140632