Smith, R.G., Reichenberg, A., Kember, R.L., Buxbaum, J.D., Schalkwyk, L.C., Fernandes, C., and Mill, J. (In Press). Advanced paternal age is associated with altered DNA methylation at brain-expressed imprinted loci in inbred mice: implications for neuropsychiatric disease. Molecular Psychiatry.
Pidsley R., Fernandes C., Viana J., Paya-Cano JL., Liu L., Smith RG., Schalkwyk LC., Mill J (In Press). DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice. Mol Brain.
Pidsley, R., Dempster, E., Troakes, C., Al-Sarraj, S., and Mill, J. (2012). Epigenetic and genetic variation at the IGF2/H19 imprinting control region on 11p15.5 is associated with cerebellum weight. Epigenetics 7, 155-163.
Mizuno, K., Dempster, E., Mill, J., and Giese, K.P. (2012). Long-lasting regulation of hippocampal Bdnf gene transcription after contextual fear conditioning. Genes Brain Behav 11, 651-659.
Kember, R.L., Dempster, E.L., Lee, T.H., Schalkwyk, L.C., Mill, J., and Fernandes, C. (2012). Maternal separation is associated with strain-specific responses to stress and epigenetic alterations to Nr3c1, Avp, and Nr4a1 in mouse. Brain and behavior 2, 455-467.
Jeffries, A.R., Perfect, L.W., Ledderose, J., Schalkwyk, L.C., Bray, N.J., Mill, J., and Price, J. (2012). Stochastic choice of allelic expression in human neural stem cells. Stem cells 30, 1938-1947.
Heijmans, B.T., and Mill, J. (2012). Commentary: The seven plagues of epigenetic epidemiology. Int J Epidemiol 41, 74-78.
Dempster, E., Viana, J., Pidsley, R., and Mill, J. (2012). Epigenetic Studies of Schizophrenia: Progress, Predicaments, and Promises for the Future. Schizophr Bull.
Davies, M., Volta, M., Pidsley, R., Lunnon, K., Dixit, A., Lovestone, S., Coarfa, C., Harris, R.A., Milosavljevic, A., Troakes, C., et al. (2012). Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome Biol 13, R43.
Boks, M.P., de Jong, N.M., Kas, M.J., Vinkers, C.H., Fernandes, C., Kahn, R.S., Mill, J., and Ophoff, R.A. (2012). Current status and future prospects for epigenetic psychopharmacology. Epigenetics 7.
Bell, J.T., Tsai, P.C., Yang, T.P., Pidsley, R., Nisbet, J., Glass, D., Mangino, M., Zhai, G., Zhang, F., Valdes, A., et al. (2012). Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population. PLoS genetics 8, e1002629.
Wong, C.C., Mill, J., and Fernandes, C. (2011). Drugs and addiction: an introduction to epigenetics. Addiction 106, 480-489.
Wong, C.C., Caspi, A., Williams, B., Houts, R., Craig, I.W., and Mill, J. (2011). A longitudinal twin study of skewed X chromosome-inactivation. PLoS One 6, e17873.
Voineagu, I., Wang, X., Johnston, P., Lowe, J.K., Tian, Y., Horvath, S., Mill, J., Cantor, R.M., Blencowe, B.J., and Geschwind, D.H. (2011). Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature 474, 380-384.
Pidsley, R., and Mill, J. (2011). Epigenetic studies of psychosis: current findings, methodological approaches, and implications for postmortem research. Biol Psychiatry 69, 146-156.
Pidsley, R., and Mill, J. (2011). Research Highlights: epigenetic changes to serotonin receptor gene expression in schizophrenia and bipolar disorder. Epigenomics 3, 537-538.
Mill, J. (2011). Toward an integrated genetic and epigenetic approach to Alzheimer's disease. Neurobiology of aging 32, 1188-1191.
Kaminsky, Z., Tochigi, M., Jia, P., Pal, M., Mill, J., Kwan, A., Ioshikhes, I., Vincent, J.B., Kennedy, J.L., Strauss, J., et al. (2011). A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorder. Mol Psychiatry.
Engmann, O., Hortobagyi, T., Pidsley, R., Troakes, C., Bernstein, H.G., Kreutz, M.R., Mill, J., Nikolic, M., and Giese, K.P. (2011). Schizophrenia is associated with dysregulation of a Cdk5 activator that regulates synaptic protein expression and cognition. Brain 134, 2408-2421.
Dempster, E.L., Pidsley, R., Schalkwyk, L.C., Owens, S., Georgiades, A., Kane, F., Kalidindi, S., Picchioni, M., Kravariti, E., Toulopoulou, T., et al. (2011). Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder. Hum Mol Genet 20, 4786-4796.
Campbell, I.C., Mill, J., Uher, R., and Schmidt, U. (2011). Eating disorders, gene-environment interactions and epigenetics. Neurosci Biobehav Rev 35, 784-793.
Barros, M., Dempster, E.L., Illott, N., Chabrawi, S., Maior, R.S., Tomaz, C., De Souza Silva, M.A., Huston, J.P., Mill, J., and Muller, C.P. (2011). Decreased methylation of the NK3 receptor coding gene (TACR3) after cocaine-induced place preference in marmoset monkeys. Addict Biol.
Wong, C.C., Caspi, A., Williams, B., Craig, I.W., Houts, R., Ambler, A., Moffitt, T.E., and Mill, J. (2010). A longitudinal study of epigenetic variation in twins. Epigenetics 5, 516-526.
Schalkwyk, L.C., Meaburn, E.L., Smith, R., Dempster, E.L., Jeffries, A.R., Davies, M.N., Plomin, R., and Mill, J. (2010). Allelic skewing of DNA methylation is widespread across the genome. Am J Hum Genet 86, 196-212.
Pidsley, R., Dempster, E.L., and Mill, J. (2010). Brain weight in males is correlated with DNA methylation at IGF2. Mol Psychiatry 15, 880-881.
Meaburn, E.L., Schalkwyk, L.C., and Mill, J. (2010). Allele-specific methylation in the human genome: implications for genetic studies of complex disease. Epigenetics 5, 578-582.
Lundstrom, S., Haworth, C.M., Carlstrom, E., Gillberg, C., Mill, J., Rastam, M., Hultman, C.M., Ronald, A., Anckarsater, H., Plomin, R., et al. (2010). Trajectories leading to autism spectrum disorders are affected by paternal age: findings from two nationally representative twin studies. J Child Psychol Psychiatry 51, 850-856.
Docherty, S.J., Davis, O.S., Haworth, C.M., Plomin, R., and Mill, J. (2010). DNA methylation profiling using bisulfite-based epityping of pooled genomic DNA. Methods 52, 255-258.
Bell, C.G., Finer, S., Lindgren, C.M., Wilson, G.A., Rakyan, V.K., Teschendorff, A.E., Akan, P., Stupka, E., Down, T.A., Prokopenko, I., et al. (2010). Integrated Genetic and Epigenetic Analysis Identifies Haplotype-Specific Methylation in the FTO Type 2 Diabetes and Obesity Susceptibility Locus. PLoS One 5.
Smith, R.G., Kember, R.L., Mill, J., Fernandes, C., Schalkwyk, L.C., Buxbaum, J.D., and Reichenberg, A. (2009). Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: a mouse model. PLoS One 4, e8456.
Rutten, B.P., and Mill, J. (2009). Epigenetic mediation of environmental influences in major psychotic disorders. Schizophr Bull 35, 1045-1056.
Reichenberg, A., Mill, J., and MacCabe, J.H. (2009). Epigenetics, genomic mutations and cognitive function. Cogn Neuropsychiatry 14, 377-390.
Mill, J., and Petronis, A. (2009). Profiling DNA methylation from small amounts of genomic DNA starting material: efficient sodium bisulfite conversion and subsequent whole-genome amplification. Methods Mol Biol 507, 371-381.
Docherty, S.J., Davis, O.S., Haworth, C.M., Plomin, R., and Mill, J. (2009). Bisulfite-based epityping on pooled genomic DNA provides an accurate estimate of average group DNA methylation. Epigenetics Chromatin 2, 3.
Mill, J., Tang, T., Kaminsky, Z., Khare, T., Yazdanpanah, S., Bouchard, L., Jia, P., Assadzadeh, A., Flanagan, J., Schumacher, A., et al. (2008). Epigenomic profiling reveals DNA-methylation changes associated with major psychosis. Am J Hum Genet 82, 696-711.
Mill, J., and Petronis, A. (2008). Pre- and peri-natal environmental risks for attention-deficit hyperactivity disorder (ADHD): the potential role of epigenetic processes in mediating susceptibility. J Child Psychol Psychiatry 49, 1020-1030.
Mill, J., and Petronis, A. (2007). Molecular studies of major depressive disorder: the epigenetic perspective. Mol Psychiatry 12, 799-814.
Mill, J., Yazdanpanah, S., Guckel, E., Ziegler, S., Kaminsky, Z., and Petronis, A. (2006). Whole genome amplification of sodium bisulfite-treated DNA allows the accurate estimate of methylated cytosine density in limited DNA resources. Biotechniques 41, 603-607.
Mill, J., Dempster, E., Caspi, A., Williams, B., Moffitt, T., and Craig, I. (2006). Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-O-methyltransferase (COMT) gene. Am J Med Genet B Neuropsychiatr Genet 141B, 421-425.
Dempster, E.L., Mill, J., Craig, I.W., and Collier, D.A. (2006). The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression. BMC Med Genet 7, 10.