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Accelerated Epigenetic Ageing in Major Depressive Disorder

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.b.32150openalex-snapshot
On the outside, looking in: A review and evaluation of the comparability of blood and brain “‐omes”
inferredcites →https://doi.org/10.1002/da.20686openalex-snapshot
Depression gets old fast: do stress and depression accelerate cell aging?
inferredcites →https://doi.org/10.1002/wps.20128openalex-snapshot
Risks of all-cause and suicide mortality in mental disorders: a meta-review
inferredcites →https://doi.org/10.1016/j.envint.2016.12.024openalex-snapshot
Associations between long-term exposure to PM2.5 component species and blood DNA methylation age in the elderly: The VA normative aging study
inferredcites →https://doi.org/10.1016/j.jagp.2013.01.040openalex-snapshot
Anticipated Brain Molecular Aging in Major Depression
inferredcites →https://doi.org/10.1016/j.jpsychires.2016.01.015openalex-snapshot
Shortened telomere length in patients with depression: A meta-analytic study
inferredcites →https://doi.org/10.1016/j.molcel.2012.10.016openalex-snapshot
Genome-wide Methylation Profiles Reveal Quantitative Views of Human Aging Rates
inferredcites →https://doi.org/10.1016/j.psychres.2009.04.015openalex-snapshot
Depression and obesity: A meta-analysis of community-based studies
inferredcites →https://doi.org/10.1016/j.psyneuen.2015.09.020openalex-snapshot
Accelerated DNA methylation age: Associations with PTSD and neural integrity
inferredcites →https://doi.org/10.1016/s0140-6736(09)60318-4openalex-snapshot
Body-mass index and cause-specific mortality in 900 000 adults: collaborative analyses of 57 prospective studies
inferredcites →https://doi.org/10.1038/mp.2013.151openalex-snapshot
Major depressive disorder and accelerated cellular aging: results from a large psychiatric cohort study
inferredcites →https://doi.org/10.1038/mp.2015.86openalex-snapshot
Polygenic dissection of major depression clinical heterogeneity
inferredcites →https://doi.org/10.1038/nature14177openalex-snapshot
Genetic studies of body mass index yield new insights for obesity biology
inferredcites →https://doi.org/10.1038/ng.3211openalex-snapshot
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.3406openalex-snapshot
An atlas of genetic correlations across human diseases and traits
inferredcites →https://doi.org/10.1038/ng.3623openalex-snapshot
Identification of 15 genetic loci associated with risk of major depression in individuals of European descent
inferredcites →https://doi.org/10.1038/s41588-018-0090-3openalex-snapshot
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
inferredcites →https://doi.org/10.1038/tp.2016.207openalex-snapshot
Dissection of major depressive disorder using polygenic risk scores for schizophrenia in two independent cohorts
inferredcites →https://doi.org/10.1093/ije/dyi319openalex-snapshot
Cohort Profile: The Aberdeen Children of the 1950s Study
inferredcites →https://doi.org/10.1093/ije/dys084openalex-snapshot
Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness
inferredcites →https://doi.org/10.1097/psy.0000000000000356openalex-snapshot
The Association Between Psychiatric Disorders and Telomere Length: A Meta-Analysis Involving 14,827 Persons
inferredcites →https://doi.org/10.1111/acel.12349openalex-snapshot
DNA methylation and healthy human aging
inferredcites →https://doi.org/10.1111/j.1365-3016.2004.00552.xopenalex-snapshot
The AberdeenChildren of the 1950scohort study: background, methods and follow‐up information on a new resource for the study of life course and intergenerational influences on health
inferredcites →https://doi.org/10.1111/j.1365-3016.2004.00575.xopenalex-snapshot
The Walker Project: a longitudinal study of 48 000 children born 1952–1966 (aged 36–50 years in 2002) and their families
inferredcites →https://doi.org/10.1186/1471-2164-14-293openalex-snapshot
A data-driven approach to preprocessing Illumina 450K methylation array data
inferredcites →https://doi.org/10.1186/1471-2350-14-38openalex-snapshot
Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study
inferredcites →https://doi.org/10.1186/1471-2350-7-74openalex-snapshot
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability
inferredcites →https://doi.org/10.1186/gb-2012-13-10-r97openalex-snapshot
Aging effects on DNA methylation modules in human brain and blood tissue
inferredcites →https://doi.org/10.1186/gb-2013-14-10-r115openalex-snapshot
DNA methylation age of human tissues and cell types
inferredcites →https://doi.org/10.1186/s13059-015-0584-6openalex-snapshot
DNA methylation age of blood predicts all-cause mortality in later life
inferredcites →https://doi.org/10.1186/s13148-016-0228-zopenalex-snapshot
Epigenetic age acceleration predicts cancer, cardiovascular, and all-cause mortality in a German case cohort
inferredcites →https://doi.org/10.1186/s13148-016-0301-7openalex-snapshot
Obesity accelerates epigenetic aging in middle-aged but not in elderly individuals
inferredcites →https://doi.org/10.12688/f1000research.4680.2openalex-snapshot
shinyMethyl: interactive quality control of Illumina 450k DNA methylation arrays in R
inferredcites →https://doi.org/10.18632/aging.101020openalex-snapshot
DNA methylation-based measures of biological age: meta-analysis predicting time to death
inferredcites →https://doi.org/10.2217/epi-2016-0179openalex-snapshot
Aging, exceptional longevity and comparisons of the Hannum and Horvath epigenetic clocks
inferredcites →https://doi.org/10.31887/dcns.2011.13.1/owolkowitzopenalex-snapshot
Of sound mind and body: depression, disease, and accelerated aging
inferredcites →https://doi.org/10.31887/dcns.2013.15.1/esibilleopenalex-snapshot
Molecular aging of the brain, neuroplasticity, and vulnerability to depression and other brain-related disorders

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.pnpbp.2019.109805openalex-snapshot
Accelerated extrinsic epigenetic aging and increased natural killer cells in blood of suicide completers
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2026.111632openalex-snapshot
Accelerated aging in psychiatric disorders: evidence from epigenetic clocks
inferred← citeshttps://doi.org/10.1016/j.psychres.2018.09.001openalex-snapshot
Epigenetic age analysis of brain in major depressive disorder
inferred← citeshttps://doi.org/10.1016/j.psychres.2023.115103openalex-snapshot
Epigenetic clock analysis reveals increased plasma cystatin C levels based on DNA methylation in major depressive disorder
inferred← citeshttps://doi.org/10.1017/s0033291724001570openalex-snapshot
Lagged effects of childhood depressive symptoms on adult epigenetic aging
inferred← citeshttps://doi.org/10.1038/s41380-020-0754-0openalex-snapshot
Brain aging in major depressive disorder: results from the ENIGMA major depressive disorder working group
inferred← citeshttps://doi.org/10.1038/s41398-020-0813-yopenalex-snapshot
Decelerated epigenetic aging associated with mood stabilizers in the blood of patients with bipolar disorder
inferred← citeshttps://doi.org/10.1038/s41398-022-02198-0openalex-snapshot
Dimensions of childhood adversity differentially affect biological aging in major depression
inferred← citeshttps://doi.org/10.1038/s41514-023-00117-1openalex-snapshot
Accelerated epigenetic aging and decreased natural killer cells based on DNA methylation in patients with untreated major depressive disorder
inferred← citeshttps://doi.org/10.1093/gerona/glag083openalex-snapshot
Monocyte epigenetic age acceleration is linked to non-somatic depressive symptoms in women with and without HIV
inferred← citeshttps://doi.org/10.1101/2020.11.24.20237156openalex-snapshot
Associations between alcohol use and accelerated biological ageing
inferred← citeshttps://doi.org/10.1101/2021.12.17.21267979openalex-snapshot
‘Inflammaging’ in Major Depressive Disorder: Associations between markers of inflammation and brain ageing in depression across two large community-based cohorts
inferred← citeshttps://doi.org/10.1111/acer.14532openalex-snapshot
Epigenetic Clock Analysis in Children With Fetal Alcohol Spectrum Disorder
inferred← citeshttps://doi.org/10.1111/bdi.12876openalex-snapshot
Accelerated hippocampal biological aging in bipolar disorder
inferred← citeshttps://doi.org/10.1177/25168657221109781openalex-snapshot
Associations Between DNA Methylation Age Acceleration, Depressive Symptoms, and Cardiometabolic Traits in African American Mothers From the InterGEN Study
inferred← citeshttps://doi.org/10.1371/journal.pone.0263478openalex-snapshot
Epigenetic clock analysis and increased plasminogen activator inhibitor-1 in high-functioning autism spectrum disorder
inferred← citeshttps://doi.org/10.3389/fcell.2022.1051556openalex-snapshot
Associations between epigenetic aging and childhood peer victimization, depression, and suicidal ideation in adolescence and adulthood: A study of two population-based samples
inferred← citeshttps://doi.org/10.3390/brainsci11111376openalex-snapshot
Reduction in Epigenetic Age Acceleration Is Related to Empathy in Mothers with Neglectful Caregiving
inferred← citeshttps://doi.org/10.3390/ijms26041738openalex-snapshot
An Update on Neuroaging on Earth and in Spaceflight
inferred← citeshttps://doi.org/10.7554/elife.59479openalex-snapshot
An integrative study of five biological clocks in somatic and mental health
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