(Q36786517)

16 August 2017

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title

Molecular studies of major depressive disorder: the epigenetic perspective (English)

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major depressive disorder

16 August 2017

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1

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16 August 2017

A Petronis

2

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PubMed ID

17420765

16 August 2017

language of work or name

English

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publication date

10 April 2007

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16 August 2017

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16 August 2017

12

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16 August 2017

9

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16 August 2017

799-814

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https://scigraph.springernature.com/pub.10.1038/sj.mp.4001992

16 August 2017

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7 January 2021

Major Depressive Disorder in a Community-Based Twin Sample: Are There Different Genetic and Environmental Contributions for Men and Women?

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Genetic risk factors for major depression in men and women: similar or different heritabilities and same or partly distinct genes?

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Comorbid psychiatric disorders in depressed outpatients: demographic and clinical features.

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7 January 2021

Dissecting the genetic etiology of major depressive disorder using linkage analysis

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7 January 2021

Predisposition Locus for Major Depression at Chromosome 12q22-12q23.2

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7 January 2021

Serotonin brain circuits involved in major depression and suicide

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7 January 2021

Meta-analysis of serotonin transporter polymorphisms and affective disorders

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Haplotype analysis reveals tryptophan hydroxylase (TPH) 1 gene variants associated with major depression

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample.

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7 January 2021

Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

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7 January 2021

Genetic association between the phospholipase A2 gene and unipolar affective disorder: a multicentre case???control study

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7 January 2021

Polymorphisms of the glucocorticoid receptor gene and major depression

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7 January 2021

Evidence for a combined genetic effect of the 5-HT(1A) receptor and serotonin transporter genes in the clinical outcome of major depressive patients treated with citalopram

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7 January 2021

The genetics of depression: a review

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7 January 2021

Psychosocial risk factors for depressive disorders in late life

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7 January 2021

A population-based twin study of lifetime major depression in men and women

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7 January 2021

Nonshared environment: a theoretical, methodological, and quantitative review

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7 January 2021

Sources of human psychological differences: the Minnesota Study of Twins Reared Apart

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7 January 2021

Genetic and environmental influences on human psychological differences

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7 January 2021

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7 January 2021

A twin study of recent life events and difficulties

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7 January 2021

Stressful life events and genetic liability to major depression: genetic control of exposure to the environment?

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7 January 2021

Urban-rural mental health differences in Great Britain: findings from the National Morbidity Survey

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7 January 2021

Rural-urban differences in the prevalence of major depression and associated impairment

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Choice of Residential Location: Chance, Family Influences, or Genes?

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7 January 2021

The interaction of stressful life events and a serotonin transporter polymorphism in the prediction of episodes of major depression: a replication

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7 January 2021

Life events, first depression onset and the serotonin transporter gene

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Strategy for investigating interactions between measured genes and measured environments

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Exploring and explaining epigenetic effects.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Translating the Histone Code

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

DNA methylation in health and disease

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Fidelity of the methylation pattern and its variation in the genome.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Inherited epigenetic variation--revisiting soft inheritance

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes

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7 January 2021

The fundamental role of epigenetic events in cancer

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7 January 2021

Phenotypic differences in genetically identical organisms: the epigenetic perspective.

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Genetic or epigenetic difference causing discordance between monozygotic twins as a clue to molecular basis of mental disorders

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetic differences arise during the lifetime of monozygotic twins

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https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Metastable epialleles in mammals

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

The origin of schizophrenia: genetic thesis, epigenetic antithesis, and resolving synthesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetics and the Environment

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Early nutrition, epigenetic changes at transposons and imprinted genes, and enhanced susceptibility to adult chronic diseases

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Psychostimulant alters expression of DNA methyltransferase mRNA in the rat brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetic programming by maternal behavior

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

A Swedish National Twin Study of Lifetime Major Depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Sex-specific association between bipolar affective disorder in women and GPR50, an X-linked orphan G protein-coupled receptor

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Sex differences in affective disorder: genetic transmission

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

The genetic basis for sex differences in human behaviour: role of the sex chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

X inactivation as a source of behavioural differences in monozygotic female twins.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

X-inactivation profile reveals extensive variability in X-linked gene expression in females

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Genome-wide linkage survey for genetic loci that influence the development of depressive disorders in families with recurrent, early-onset, major depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Increased acetylation of histones at an early stage of oestradiol-mediated gene activation in the liver of immature chicks

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Histone acetylation decreased by estradiol in the MCF-7 human mammary cancer cell line

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Sexually dimorphic DNA demethylation in the promoter of the Slp (sex-limited protein) gene in mouse liver

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Genomic sequencing reveals a positive correlation between the kinetics of strand-specific DNA demethylation of the overlapping estradiol/glucocorticoid-receptor binding sites and the rate of avian vitellogenin mRNA synthesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Analysis of polymorphisms in the olfactory G-protein Golf in major depression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Association of the human kainate receptor GluR7 gene (GRIK3) with recurrent major depressive disorder

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Imprinted gene expression in the brain

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Sensitive flow cytometric analysis reveals a novel type of parent-of-origin effect in the mouse genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetic heterogeneity at imprinted loci in normal populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Identification of cis- and trans-acting factors possibly modifying the risk of epimutations on chromosome 15

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Allele C-specific methylation of the 5-HT2A receptor gene: evidence for correlation with its expression and expression of DNA methylase DNMT1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Intra- and interindividual epigenetic variation in human germ cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Cytosine methylation: quantitation by automated genomic sequencing and GENESCAN analysis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Whole genome amplification of sodium bisulfite-treated DNA allows the accurate estimate of methylated cytosine density in limited DNA resources.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Investigating stem cells in human colon by using methylation patterns

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Microarray-based DNA methylation profiling: technology and applications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Microarray-based methylation analysis using dual-color fluorescence hybridization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Microarrays in brain research: the good, the bad and the ugly.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Epigenetic characterization of the early embryo with a chromatin immunoprecipitation protocol applicable to small cell populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Chromatin immunoprecipitation in postmortem brain.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

In psychosis, cortical interneurons overexpress DNA-methyltransferase 1

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Gene expression profiling in the post-mortem human brain--no cause for dismay.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Loss of IGF2 imprinting: a potential marker of colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Germline epimutation of MLH1 in individuals with multiple cancers.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Future potential of the Human Epigenome Project

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

DNA methylation profiling of human chromosomes 6, 20 and 22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Hypothesis: comparisons of inter- and intra-individual variations can substitute for twin studies in drug research

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4001992

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4001992

1 reference

16 August 2017

1 reference

PubMed ID

17420765