Mill, Jonathan
Jonathan Mill
VIAF ID: 172301052 (Personal)
Permalink: http://viaf.org/viaf/172301052
Preferred Forms
- 100 0 _ ‡a Jonathan Mill
- 100 1 _ ‡a Mill, Jonathan
-
- 100 1 _ ‡a Mill, Jonathan
-
- 100 1 _ ‡a Mill, Jonathan
-
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
---|---|
Brain, behavior and epigenetics, 2011: | |
Erratum: Prenatal maternal immune activation causes epigenetic differences in adolescent mouse brain | |
Establishing a generalized polyepigenetic biomarker for tobacco smoking | |
Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene. | |
Exposure to violence during childhood is associated with telomere erosion from 5 to 10 years of age: a longitudinal study | |
Family-based association study between brain-derived neurotrophic factor gene polymorphisms and attention deficit hyperactivity disorder in UK and Taiwanese samples. | |
Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing | |
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood | |
Functional effects of a tandem duplication polymorphism in the 5'flanking region of the DRD4 gene | |
Genetic architecture of epigenetic and neuronal ageing rates in human brain regions | |
Genetic risk variants for brain disorders are enriched in cortical H3K27ac domains | |
Genetic variants near MLST8 and DHX57 affect the epigenetic age of the cerebellum | |
Genetic variation at 16q24.2 is associated with small vessel stroke | |
Genetics and the geography of health, behaviour and attainment. | |
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. | |
Genome-wide DNA methylation levels and altered cortisol stress reactivity following childhood trauma in humans | |
Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion | |
Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging | |
Guidance for DNA methylation studies: statistical insights from the Illumina EPIC array | |
Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD. | |
Histone Acetylome-wide Association Study of Autism Spectrum Disorder. | |
Home-cage activity in heterogeneous stock (HS) mice as a model of baseline activity. | |
Hypermethylation in the ZBTB20 gene is associated with major depressive disorder | |
Increased DNA methylation near TREM2 is consistently seen in the superior temporal gyrus in Alzheimer's disease brain | |
Independent Methylome-Wide Association Studies of Schizophrenia Detect Consistent Case-Control Differences | |
Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene | |
Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus | |
Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism | |
Is treatment-resistant schizophrenia categorically distinct from treatment-responsive schizophrenia? a systematic review. | |
Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes | |
Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burden | |
Leveraging DNA methylation quantitative trait loci to characterize the relationship between methylomic variation, gene expression and complex traits | |
Long-lasting regulation of hippocampal Bdnf gene transcription after contextual fear conditioning. | |
Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder | |
Longitudinal investigation of DNA methylation changes preceding adolescent psychotic experiences | |
A longitudinal twin study of skewed X chromosome-inactivation | |
Mapping epigenetic changes to the host cell genome induced by Burkholderia pseudomallei reveals pathogen-specific and pathogen-generic signatures of infection | |
Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders | |
Methylation age acceleration does not predict mortality in schizophrenia | |
Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci | |
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits | |
Methylomic analysis of salivary DNA in childhood ADHD identifies altered DNA methylation in VIPR2. | |
Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease | |
Methylomic profiling of cortex samples from completed suicide cases implicates a role for PSORS1C3 in major depression and suicide | |
Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia | |
The mitochondrial epigenome: a role in Alzheimer's disease? | |
Molecular studies of major depressive disorder: the epigenetic perspective | |
A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorder. | |
Mutation screen and association analysis of the glucocorticoid receptor gene (NR3C1) in childhood-onset mood disorders (COMD). | |
Non-neuronal expression of SARS-CoV-2 entry genes in the olfactory system suggests mechanisms underlying COVID-19-associated anosmia | |
Paternal Age Alters Social Development in Offspring | |
Peripheral DNA methylation, cognitive decline and brain aging: pilot findings from the Whitehall II imaging study | |
Pleiotropic Effects of Trait-Associated Genetic Variation on DNA Methylation: Utility for Refining GWAS Loci. | |
Prediction of heterogeneity in intelligence and adult prognosis by genetic polymorphisms in the dopamine system among children with attention-deficit/hyperactivity disorder: evidence from 2 birth cohorts. | |
Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet. | |
Profiling DNA methylation from small amounts of genomic DNA starting material: efficient sodium bisulfite conversion and subsequent whole-genome amplification | |
Profiling Regulatory Variation in the Brain: Methods for Exploring the Neuronal Epigenome. | |
QTL association analysis of the DRD4 exon 3 VNTR polymorphism in a population sample of children screened with a parent rating scale for ADHD symptoms. | |
The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression | |
Quantitative promoter DNA methylation analysis of four candidate genes in anorexia nervosa: a pilot study. | |
Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue | |
Rodent models: utility for candidate gene studies in human attention-deficit hyperactivity disorder (ADHD). | |
Role of genotype in the cycle of violence in maltreated children | |
Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions | |
Schizophrenia is associated with dysregulation of a Cdk5 activator that regulates synaptic protein expression and cognition | |
Severe psychosocial deprivation in early childhood is associated with increased DNA methylation across a region spanning the transcription start site of CYP2E1. | |
Sex-specific transcription and DNA methylation profiles of reproductive and epigenetic associated genes in the gonads and livers of breeding zebrafish. | |
Sleep quality and diurnal preference in a sample of young adults: associations with 5HTTLPR, PER3, and CLOCK 3111. | |
Socioeconomic Position and DNA Methylation Age Acceleration Across the Life Course | |
SORL1 and SIRT1 mRNA expression and promoter methylation levels in aging and Alzheimer's Disease. | |
Stochastic choice of allelic expression in human neural stem cells | |
Stress-induced gene expression and behavior are controlled by DNA methylation and methyl donor availability in the dentate gyrus | |
Tissue-specific patterns of allelically-skewed DNA methylation | |
Toward an integrated genetic and epigenetic approach to Alzheimer's disease | |
Trajectories leading to autism spectrum disorders are affected by paternal age: findings from two nationally representative twin studies. | |
Transcriptomic analysis of autistic brain reveals convergent molecular pathology | |
Transcriptomic changes in the frontal cortex associated with paternal age. | |
Transient expression analysis of allelic variants of a VNTR in the dopamine transporter gene (DAT1) | |
Variation in 5-hydroxymethylcytosine across human cortex and cerebellum. | |
Whole genome amplification of sodium bisulfite-treated DNA allows the accurate estimate of methylated cytosine density in limited DNA resources. |