Allele-specific methylation in the human genome: Implications for genetic studies of complex disease

Por Meaburn, Emma L, Schalkwyk, Leonard C, Mill, Jonathan
Publicado em 2010

Gene set enrichment; a problem of pathways

Por Davies, Matthew N., Meaburn, Emma L., Schalkwyk, Leonard C.
Publicado em 2010

Reading and Generalist Genes

Por Haworth, Claire M A, Meaburn, Emma L, Harlaar, Nicole, Plomin, Robert
Publicado em 2007

Assessing Individual Differences in Genome-Wide Gene Expression in Human Whole Blood: Reliability Over Four Hours and Stability Over 10 Months

Por Meaburn, Emma L., Fernandes, Cathy, Craig, Ian W., Plomin, Robert, Schalkwyk, Leonard C.
Publicado em 2009

Common DNA Markers Can Account for More Than Half of the Genetic Influence on Cognitive Abilities

Por Plomin, Robert, Haworth, Claire M. A., Meaburn, Emma L., Price, Thomas S., Davis, Oliver S. P.
Publicado em 2013

Allelic Skewing of DNA Methylation Is Widespread across the Genome

Por Schalkwyk, Leonard C., Meaburn, Emma L., Smith, Rebecca, Dempster, Emma L., Jeffries, Aaron R., Davies, Matthew N., Plomin, Robert, Mill, Jonathan
Publicado em 2010

Genetics of Callous-Unemotional Behavior in Children

Por Viding, Essi, Price, Thomas S., Jaffee, Sara R., Trzaskowski, Maciej, Davis, Oliver S. P., Meaburn, Emma L., Haworth, Claire M. A., Plomin, Robert
Publicado em 2013

Correction: Genetics of Callous-Unemotional Behavior in Children

Por Viding, Essi, Price, Thomas S., Jaffee, Sara R., Trzaskowski, Maciej, Davis, Oliver S. P., Meaburn, Emma L., Haworth, Claire M. A., Plomin, Robert
Publicado em 2013

Are Genetic Risk Factors for Psychosis Also Associated with Dimension-Specific Psychotic Experiences in Adolescence?

Por Sieradzka, Dominika, Power, Robert A., Freeman, Daniel, Cardno, Alastair G., McGuire, Philip, Plomin, Robert, Meaburn, Emma L., Dudbridge, Frank, Ronald, Angelica
Publicado em 2014

A Three-Stage Genome-Wide Association Study of General Cognitive Ability: Hunting the Small Effects

Por Davis, Oliver S. P., Butcher, Lee M., Docherty, Sophia J., Meaburn, Emma L., Curtis, Charles J. C., Simpson, Michael A., Schalkwyk, Leonard C., Plomin, Robert
Publicado em 2010

First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood

Por Trzaskowski, Maciej, Eley, Thalia C., Davis, Oliver S. P., Doherty, Sophia J., Hanscombe, Ken B., Meaburn, Emma L., Haworth, Claire M. A., Price, Thomas, Plomin, Robert
Publicado em 2013

Correction: First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood

Por Trzaskowski, Maciej, Eley, Thalia C., Davis, Oliver S. P., Doherty, Sophia J., Hanscombe, Ken B., Meaburn, Emma L., Haworth, Claire M. A., Price, Thomas, Plomin, Robert
Publicado em 2013

Tissue-specific patterns of allelically-skewed DNA methylation

Por Marzi, Sarah J., Meaburn, Emma L., Dempster, Emma L., Lunnon, Katie, Paya-Cano, Jose L., Smith, Rebecca G., Volta, Manuela, Troakes, Claire, Schalkwyk, Leonard C., Mill, Jonathan
Publicado no Epigenetics (2016)

Genome-Wide Association Study of Receptive Language Ability of 12-Year-Olds

Por Harlaar, Nicole, Meaburn, Emma L., Hayiou-Thomas, Marianna E., Davis, Oliver S. P., Docherty, Sophia, Hanscombe, Ken B., Haworth, Claire M. A., Price, Thomas S., Trzaskowski, Maciej, Dale, Philip S., Plomin, Robert
Publicado em 2014

Common variation near ROBO2 is associated with expressive vocabulary in infancy

Por St Pourcain, Beate, Cents, Rolieke A.M., Whitehouse, Andrew J.O., Haworth, Claire M.A., Davis, Oliver S.P., O’Reilly, Paul F., Roulstone, Susan, Wren, Yvonne, Ang, Qi W., Velders, Fleur P., Evans, David M., Kemp, John P., Warrington, Nicole M., Miller, Laura, Timpson, Nicholas J., Ring, Susan M., Verhulst, Frank C., Hofman, Albert, Rivadeneira, Fernando, Meaburn, Emma L., Price, Thomas S., Dale, Philip S., Pillas, Demetris, Yliherva, Anneli, Rodriguez, Alina, Golding, Jean, Jaddoe, Vincent W.V., Jarvelin, Marjo-Riitta, Plomin, Robert, Pennell, Craig E., Tiemeier, Henning, Davey Smith, George
Publicado em 2014

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Por Davis, Oliver S. P., Band, Gavin, Pirinen, Matti, Haworth, Claire M. A., Meaburn, Emma L., Kovas, Yulia, Harlaar, Nicole, Docherty, Sophia J., Hanscombe, Ken B., Trzaskowski, Maciej, Curtis, Charles J. C., Strange, Amy, Freeman, Colin, Bellenguez, Céline, Su, Zhan, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A. Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Dale, Philip S., Petrill, Stephen A., Schalkwyk, Leonard S., Craig, Ian W., Lewis, Cathryn M., Price, Thomas S., Donnelly, Peter, Plomin, Robert, Spencer, Chris C. A.
Publicado em 2014