Using Openly Accessible Resources to Strengthen Causal Inference in Epigenetic Epidemiology of Neurodevelopment and Mental Health

por Walton, Esther, Relton, Caroline L., Caramaschi, Doretta
Publicado 2019

Epigenetics applied to child and adolescent mental health: Progress, challenges and opportunities

por Cecil, Charlotte A. M., Neumann, Alexander, Walton, Esther
Publicado 2022

Emotion processing differences mediate the link between sex and autistic traits in young adulthood

por Livingston, Lucy A., Waldren, Lucy H., Walton, Esther, Shah, Punit
Publicado 2022

Examining the possible causal relationship between lung function, COPD and Alzheimer’s disease: a Mendelian randomisation study

por Higbee, Daniel, Granell, Raquel, Walton, Esther, Korologou-Linden, Roxanna, Davey Smith, George, Dodd, James
Publicado 2021

The impact of early adversity and education on genetic and brain morphological predictors of cognitive ability

por Corley, Emma, Fahey, Laura, Fitzgerald, Joan, Holleran, Laurena, Walton, Esther, Morris, Derek W., Donohoe, Gary
Publicado 2023

A systematic review of neuroimaging epigenetic research: calling for an increased focus on development

por Walton, Esther, Baltramonaityte, Vilte, Calhoun, Vince, Heijmans, Bastiaan T., Thompson, Paul M., Cecil, Charlotte A. M.
Publicado 2023

Identifying risk factors involved in the common versus specific liabilities to substance use: A genetically informed approach

por Iob, Eleonora, Schoeler, Tabea, Cecil, Charlotte M., Walton, Esther, McQuillin, Andrew, Pingault, Jean‐Baptiste
Publicado 2020

Epigenetic profiling of ADHD symptoms trajectories: A prospective, methylome-wide study

por Walton, Esther, Pingault, Jean-Baptiste, Cecil, Charlotte AM, Gaunt, Tom R., Relton, Caroline, Mill, Jonathan, Barker, Edward D.
Publicado 2016

Epigenome-wide contributions to individual differences in childhood phenotypes: a GREML approach

por Neumann, Alexander, Pingault, Jean-Baptiste, Felix, Janine F., Jaddoe, Vincent W. V., Tiemeier, Henning, Cecil, Charlotte, Walton, Esther
Publicado 2022

Epigenome-wide association study of seizures in childhood and adolescence

por Caramaschi, Doretta, Hatcher, Charlie, Mulder, Rosa H., Felix, Janine F., Cecil, Charlotte A. M., Relton, Caroline L., Walton, Esther
Publicado 2020

A cross-disorder PRS-pheWAS of 5 major psychiatric disorders in UK Biobank

por Leppert, Beate, Millard, Louise A. C., Riglin, Lucy, Davey Smith, George, Thapar, Anita, Tilling, Kate, Walton, Esther, Stergiakouli, Evie
Publicado 2020

Longitudinal epigenetic predictors of amygdala:hippocampus volume ratio

por Walton, Esther, Cecil, Charlotte A.M., Suderman, Matthew, Liu, Jingyu, Turner, Jessica A., Calhoun, Vince, Ehrlich, Stefan, Relton, Caroline L., Barker, Edward D.
Publicado 2017

Prenatal unhealthy diet, insulin‐like growth factor 2 gene (IGF2) methylation, and attention deficit hyperactivity disorder symptoms in youth with early‐onset conduct problems

por Rijlaarsdam, Jolien, Cecil, Charlotte A.M., Walton, Esther, Mesirow, Maurissa S.C., Relton, Caroline L., Gaunt, Tom R., McArdle, Wendy, Barker, Edward D.
Publicado 2016

A multivariate genome-wide association study of psycho-cardiometabolic multimorbidity

por Baltramonaityte, Vilte, Pingault, Jean-Baptiste, Cecil, Charlotte A. M., Choudhary, Priyanka, Järvelin, Marjo-Riitta, Penninx, Brenda W. J. H., Felix, Janine, Sebert, Sylvain, Milaneschi, Yuri, Walton, Esther
Publicado 2023

Sensitive Periods for the Effect of Childhood Adversity on DNA Methylation: Updated Results From a Prospective, Longitudinal Study

por Lussier, Alexandre A., Zhu, Yiwen, Smith, Brooke J., Simpkin, Andrew J., Smith, Andrew D.A.C., Suderman, Matthew J., Walton, Esther, Relton, Caroline L., Ressler, Kerry J., Dunn, Erin C.
Publicado 2022

The Impact of Genome-Wide Supported Schizophrenia Risk Variants in the Neurogranin Gene on Brain Structure and Function

por Walton, Esther, Geisler, Daniel, Hass, Johanna, Liu, Jingyu, Turner, Jessica, Yendiki, Anastasia, Smolka, Michael N., Ho, Beng-Choon, Manoach, Dara S., Gollub, Randy L., Roessner, Veit, Calhoun, Vince D., Ehrlich, Stefan
Publicado 2013

Epigenomics of being bullied: changes in DNA methylation following bullying exposure

por Mulder, Rosa H., Walton, Esther, Neumann, Alexander, Houtepen, Lotte C., Felix, Janine F., Bakermans-Kranenburg, Marian J., Suderman, Matthew, Tiemeier, Henning, van IJzendoorn, Marinus H., Relton, Caroline L., Cecil, Charlotte A. M.
Publicado 2020

A Methylome‐Wide Association Study of Trajectories of Oppositional Defiant Behaviors and Biological Overlap With Attention Deficit Hyperactivity Disorder

por Barker, Edward D., Walton, Esther, Cecil, Charlotte A.M., Rowe, Richard, Jaffee, Sara R., Maughan, Barbara, O'Connor, Thomas G., Stringaris, Argyris, Meehan, Alan J., McArdle, Wendy, Relton, Caroline L., Gaunt, Tom R.
Publicado 2017

A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype

por Hass, Johanna, Walton, Esther, Kirsten, Holger, Liu, Jingyu, Priebe, Lutz, Wolf, Christiane, Karbalai, Nazanin, Gollub, Randy, White, Tonya, Roessner, Veit, Müller, Kathrin U., Paus, Tomas, Smolka, Michael N., Schumann, Gunter, Scholz, Markus, Cichon, Sven, Calhoun, Vince, Ehrlich, Stefan
Publicado 2013

Population neuroimaging: generation of a comprehensive data resource within the ALSPAC pregnancy and birth cohort

por Sharp, Tamsin H., McBride, Nancy S., Howell, Amy E., Evans, C. John, Jones, Derek K., Perry, Gavin, Dimitriadis, Stavros I., Lancaster, Thomas M., Zuccolo, Luisa, Relton, Caroline, Matthews, Sarah M., Breeze, Thomas, David, Anthony S., Drakesmith, Mark, Linden, David E. J., Paus, Tomas, Walton, Esther
Publicado 2020