Cargando…

Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation

BACKGROUND: Cigarette smoking has severe adverse health consequences in adults and in the offspring of mothers who smoke during pregnancy. One of the most widely reported effects of smoking during pregnancy is reduced birth weight which is in turn associated with chronic disease in adulthood. Epigen...

Descripción completa

Detalles Bibliográficos
Autores principales:	Witt, Stephanie H., Frank, Josef, Gilles, Maria, Lang, Maren, Treutlein, Jens, Streit, Fabian, Wolf, Isabell A. C., Peus, Verena, Scharnholz, Barbara, Send, Tabea S., Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Dukal, Helene, Strohmaier, Jana, Sütterlin, Marc, Arloth, Janine, Laucht, Manfred, Nöthen, Markus M., Deuschle, Michael, Rietschel, Marcella
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5922319/ https://www.ncbi.nlm.nih.gov/pubmed/29695247 http://dx.doi.org/10.1186/s12864-018-4652-7

Ejemplares similares

Impact of prenatal stress on mother-infant dyadic behavior during the still-face paradigm
por: Wolf, Isabell Ann-Cathrin, et al.
Publicado: (2018)

New-born females show higher stress- and genotype-independent methylation of SLC6A4 than males
por: Dukal, Helene, et al.
Publicado: (2015)

Nightmare frequency in last trimester of pregnancy
por: Schredl, Michael, et al.
Publicado: (2016)

Response to the letter by Esteves et al.
por: Send, T. S., et al.
Publicado: (2018)

MORC1 exhibits cross-species differential methylation in association with early life stress as well as genome-wide association with MDD
por: Nieratschker, V, et al.
Publicado: (2014)

Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
por: Herrera-Rivero, Marisol, et al.
Publicado: (2020)

Investigation of manic and euthymic episodes identifies state- and trait-specific gene expression and STAB1 as a new candidate gene for bipolar disorder
por: Witt, S H, et al.
Publicado: (2014)

Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study
por: Krug, Axel, et al.
Publicado: (2020)

Epigenome-wide association study of alcohol use disorder in five brain regions
por: Zillich, Lea, et al.
Publicado: (2021)

Expert and self-assessment of lifetime symptoms and diagnosis of major depressive disorder in large-scale genetic studies in the general population: comparison of a clinical interview and a self-administered checklist
por: Martin, Jessica, et al.
Publicado: (2017)

Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
por: Henne, Sabrina Katrin, et al.
Publicado: (2023)

Response to therapeutic sleep deprivation: a naturalistic study of clinical and genetic factors and post-treatment depressive symptom trajectory
por: Trautmann, Nina, et al.
Publicado: (2018)

Analysis of Rare Variants in the Alcohol Dependence Candidate Gene GATA4
por: Degenhardt, Franziska, et al.
Publicado: (2016)

Glutamate concentration in the anterior cingulate cortex in alcohol dependence: association with alcohol withdrawal and exploration of contribution from glutamatergic candidate genes
por: Streit, Fabian, et al.
Publicado: (2018)

Associations between SNPs and immune-related circulating proteins in schizophrenia
por: Chan, Man K., et al.
Publicado: (2017)

Neurocognitive Endophenotypes of Schizophrenia and Bipolar Disorder and Possible Associations with FKBP Variant rs3800373
por: Memic, Amra, et al.
Publicado: (2018)

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum
por: Zillich, Lea, et al.
Publicado: (2022)

Exome sequencing in large, multiplex bipolar disorder families from Cuba
por: Maaser, Anna, et al.
Publicado: (2018)

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis
por: Treutlein, Jens, et al.
Publicado: (2017)

Evidence for increased genetic risk load for major depression in patients assigned to electroconvulsive therapy
por: Foo, Jerome C., et al.
Publicado: (2018)

Association of polygenic risk for schizophrenia with fast sleep spindle density depends on pro-cognitive variants
por: Schilling, Claudia, et al.
Publicado: (2022)

Dopamine Inactivation Efficacy Related to Functional DAT1 and COMT Variants Influences Motor Response Evaluation
por: Bender, Stephan, et al.
Publicado: (2012)

Time-Resolved Influences of Functional DAT1 and COMT Variants on Visual Perception and Post-Processing
por: Bender, Stephan, et al.
Publicado: (2012)

Sustained Immunoparalysis in Endotoxin-Tolerized Monocytic Cells
por: Weisheit, Christina K., et al.
Publicado: (2020)

Shared genetic etiology between alcohol dependence and major depressive disorder
por: Foo, Jerome C., et al.
Publicado: (2018)

Longitudinal transcriptome-wide gene expression analysis of sleep deprivation treatment shows involvement of circadian genes and immune pathways
por: Foo, Jerome C., et al.
Publicado: (2019)

Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
por: Henne, S. K., et al.
Publicado: (2021)

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
por: Andlauer, Till F. M., et al.
Publicado: (2019)

072 Covid-19 and male androgenetic alopecia: Systematic investigation of a potential epidemiological and genetic association
por: Henne, S.K., et al.
Publicado: (2021)

New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?
por: Nieratschker, Vanessa, et al.
Publicado: (2010)

Effect of the G72 (DAOA) putative risk haplotype on cognitive functions in healthy subjects
por: Jansen, Andreas, et al.
Publicado: (2009)

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients
por: Frank, J, et al.
Publicado: (2015)

Attitudes toward the right to autonomous decision‐making in psychiatric genetic testing: Controversial and context‐dependent
por: Strohmaier, Jana, et al.
Publicado: (2019)

New findings in the genetics of major psychoses
por: Nöthen, Markus M, et al.
Publicado: (2010)

Depression and bipolar disorder subtypes differ in their genetic correlations with biological rhythms
por: Sirignano, Lea, et al.
Publicado: (2022)

DNA methylation in cocaine use disorder–An epigenome-wide approach in the human prefrontal cortex
por: Poisel, Eric, et al.
Publicado: (2023)

Association of Locomotor Activity During Sleep Deprivation Treatment With Response
por: Foo, Jerome Clifford, et al.
Publicado: (2020)

Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families
por: Guzman-Parra, Jose, et al.
Publicado: (2021)

Genome-wide significant association between a ‘negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1
por: Meier, S, et al.
Publicado: (2012)

Expression profiling and bioinformatic analyses suggest new target genes and pathways for human hair follicle related microRNAs
por: Hochfeld, Lara M., et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_aptbr4kp3thhle2uqtjoo8h1va