Cargando…

Hypomethylation of FAM63B in bipolar disorder patients

Bipolar disorder (BD) and schizophrenia (SZ) are known to share common genetic and psychosocial risk factors. A recent epigenome-wide association study performed on blood samples from SZ patients found significant hypomethylation of FAM63B in exon 9. Here, we used iPLEX-based methylation analysis to...

Descripción completa

Detalles Bibliográficos
Autores principales:	Starnawska, Anna, Demontis, Ditte, McQuillin, Andrew, O’Brien, Niamh L., Staunstrup, Nicklas H., Mors, Ole, Nielsen, Anders L., Børglum, Anders D., Nyegaard, Mette
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2016
Materias:	Short Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865008/ https://www.ncbi.nlm.nih.gov/pubmed/27175219 http://dx.doi.org/10.1186/s13148-016-0221-6

Ejemplares similares

Genome-wide DNA methylation profiling with MeDIP-seq using archived dried blood spots
por: Staunstrup, Nicklas H., et al.
Publicado: (2016)

CACNA1C hypermethylation is associated with bipolar disorder
por: Starnawska, A, et al.
Publicado: (2016)

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins
por: Starnawska, Anna, et al.
Publicado: (2017)

Whole-exome sequencing of individuals from an isolated population implicates rare risk variants in bipolar disorder
por: Lescai, F, et al.
Publicado: (2017)

DNA methylation of the KLK8 gene in depression symptomatology
por: Starnawska, Anna, et al.
Publicado: (2021)

Genetic variation in the miR‐708 gene and its binding targets in bipolar disorder
por: Fiorentino, Alessia, et al.
Publicado: (2016)

Role of DNA Methylation in Mediating Genetic Risk of Psychiatric Disorders
por: Starnawska, Anna, et al.
Publicado: (2021)

Identification of the BRD1 interaction network and its impact on mental disorder risk
por: Fryland, Tue, et al.
Publicado: (2016)

Epigenome-wide association study of depression symptomatology in elderly monozygotic twins
por: Starnawska, A., et al.
Publicado: (2019)

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq
por: Rajkumar, Anto P., et al.
Publicado: (2015)

Analysis of ANK3 and CACNA1C variants identified in bipolar disorder whole genome sequence data
por: Fiorentino, Alessia, et al.
Publicado: (2014)

Antidepressant medication during pregnancy and epigenetic changes in umbilical cord blood: a systematic review
por: Viuff, Anne-Cathrine F., et al.
Publicado: (2016)

Association of rare variation in the glutamate receptor gene SLC1A2 with susceptibility to bipolar disorder and schizophrenia
por: Fiorentino, Alessia, et al.
Publicado: (2015)

Genome-wide scans using archived neonatal dried blood spot samples
por: Hollegaard, Mads V, et al.
Publicado: (2009)

Allelic Association, DNA Resequencing and Copy Number Variation at the Metabotropic Glutamate Receptor GRM7 Gene Locus in Bipolar Disorder
por: Kandaswamy, Radhika, et al.
Publicado: (2014)

Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder
por: O'Brien, N.L., et al.
Publicado: (2018)

No association of polymorphisms in the serotonin transporter gene with thermal pain sensation in healthy individuals
por: Schaldemose, Ellen Lund, et al.
Publicado: (2014)

A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment
por: Nyegaard, Mette, et al.
Publicado: (2015)

Circulating miRNAs as Potential Biomarkers for Patient Stratification in Bipolar Disorder: A Combined Review and Data Mining Approach
por: Clausen, Alexandra R., et al.
Publicado: (2022)

Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples
por: Esteller-Cucala, Paula, et al.
Publicado: (2020)

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source
por: Hollegaard, Mads V, et al.
Publicado: (2011)

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele
por: Dyrvig, Mads, et al.
Publicado: (2017)

An introduction to seismic interpretation
por: McQuillin, Robert
Publicado: (1979)

Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy
por: Verhoef, Ellen, et al.
Publicado: (2021)

Medical abortion with mifepristone and home administration of misoprostol up to 63 days’ gestation
por: Løkeland, Mette, et al.
Publicado: (2014)

CtIP Mutations Cause Seckel and Jawad Syndromes
por: Qvist, Per, et al.
Publicado: (2011)

Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia
por: Al Eissa, Mariam M., et al.
Publicado: (2017)

Polymorphism in Serotonin Receptor 3B Is Associated with Pain Catastrophizing
por: Horjales-Araujo, Emilia, et al.
Publicado: (2013)

Working memory and reaction time variability mediate the relationship between polygenic risk and ADHD traits in a general population sample
por: Moses, Mia, et al.
Publicado: (2022)

Application of immunofluorescence technique to clinical virology
por: GARDNER, P.S., et al.
Publicado: (1980)

Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Markers
por: Marcheco-Teruel, Beatriz, et al.
Publicado: (2014)

Polygenic risk score, psychosocial environment and the risk of attention-deficit/hyperactivity disorder
por: Østergaard, Søren D., et al.
Publicado: (2020)

DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD
por: Nissen, Judith Becker, et al.
Publicado: (2016)

Investigating causality between liability to ADHD and substance use, and liability to substance use and ADHD risk, using Mendelian randomization
por: Treur, Jorien L., et al.
Publicado: (2019)

F67. NEUROCOGNITION IN 7-YEAR-OLD CHILDREN OF PARENTS WITH SCHIZOPHRENIA OR BIPOLAR DISORDER
por: Hemager, Nicoline, et al.
Publicado: (2018)

Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder
por: Pineda-Cirera, Laura, et al.
Publicado: (2019)

Genetic assortative mating for schizophrenia and bipolar disorder
por: Jefsen, Oskar Hougaard, et al.
Publicado: (2022)

PS63. The choice of medication for patients with bipolar disorder
por: Hwang, HyunChan, et al.
Publicado: (2016)

The effects of emergency government cash transfers on beliefs and behaviours during the COVID pandemic: Evidence from Brazil()
por: de Leon, Fernanda L. Lopez, et al.
Publicado: (2023)

M56. ASSORTATIVE MATING IN SCHIZOPHRENIA AND BIPOLAR DISORDER: A NATIONWIDE COHORT STUDY EXPLORING THE CHARACTERISTICS OF INDIVIDUALS WHO HAVE CHILDREN BY PARTNERS WITH SCHIZOPHRENIA OR BIPOLAR DISORDER
por: Greve, Aja, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_rsp6cfoti2atr33nr4oerqgfdj