Genomic imprinting and the social brain

Por Isles, Anthony R, Davies, William, Wilkinson, Lawrence S
Publicado em 2006

Methods of epigenome editing for probing the function of genomic imprinting

Por Rienecker, Kira DA, Hill, Matthew J, Isles, Anthony R
Publicado no Epigenomics (2016)

Territorial Behavior and Social Stability in the Mouse Require Correct Expression of Imprinted Cdkn1c

Por McNamara, Gráinne I., John, Rosalind M., Isles, Anthony R.
Publicado no Front Behav Neurosci (2018)

A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice.

Por Isles, Anthony R, Baum, Michael J, Ma, Dan, Szeto, Abigail, Keverne, Eric B, Allen, Nicholas D
Publicado em 2002

No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci

Por Escott-Price, Valentina, Kirov, George, Rees, Elliott, Isles, Anthony R., Owen, Michael J., O’Donovan, Michael C.
Publicado no PLoS One (2015)

Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader–Willi syndrome

Por Davies, Jennifer R., Humby, Trevor, Dwyer, Dominic M., Garfield, Alastair S., Furby, Hannah, Wilkinson, Lawrence S., Wells, Timothy, Isles, Anthony R.
Publicado no Eur J Neurosci (2015)

Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT(2C) receptor mediated appetite

Por Garfield, Alastair S., Davies, Jennifer R., Burke, Luke K., Furby, Hannah V., Wilkinson, Lawrence S., Heisler, Lora K., Isles, Anthony R.
Publicado no Mol Brain (2016)

Imprinted Nesp55 Influences Behavioral Reactivity to Novel Environments

Por Plagge, Antonius, Isles, Anthony R., Gordon, Emma, Humby, Trevor, Dean, Wendy, Gritsch, Sabine, Fischer-Colbrie, Reiner, Wilkinson, Lawrence S., Kelsey, Gavin
Publicado em 2005

Impulsive Choice in Mice Lacking Paternal Expression of Grb10 Suggests Intragenomic Conflict in Behavior

Por Dent, Claire L., Humby, Trevor, Lewis, Katie, Ward, Andrew, Fischer-Colbrie, Reiner, Wilkinson, Lawrence S., Wilkins, Jon F., Isles, Anthony R.
Publicado no Genetics (2018)

Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT(2C)R-mediated behaviour

Por Doe, Christine M., Relkovic, Dinko, Garfield, Alastair S., Dalley, Jeffrey W., Theobald, David E.H., Humby, Trevor, Wilkinson, Lawrence S., Isles, Anthony R.
Publicado em 2009

Paradoxical leanness in the imprinting-centre deletion mouse model for Prader–Willi syndrome

Por Golding, David M, Rees, Daniel J, Davies, Jennifer R, Relkovic, Dinko, Furby, Hannah V, Guschina, Irina A, Hopkins, Anna L, Davies, Jeffrey S, Resnick, James L, Isles, Anthony R, Wells, Timothy
Publicado no J Endocrinol (2016)

Distinct physiological and behavioural functions for parental alleles of imprinted Grb10

Por Garfield, Alastair S., Cowley, Michael, Smith, Florentia M., Moorwood, Kim, Stewart-Cox, Joanne E., Gilroy, Kerry, Baker, Sian, Xia, Jing, Dalley, Jeffrey W., Hurst, Laurence D., Wilkinson, Lawrence S., Isles, Anthony R., Ward, Andrew
Publicado em 2011

Developmental Programming Mediated by Complementary Roles of Imprinted Grb10 in Mother and Pup

Por Cowley, Michael, Garfield, Alastair S., Madon-Simon, Marta, Charalambous, Marika, Clarkson, Richard W., Smalley, Matthew J., Kendrick, Howard, Isles, Anthony R., Parry, Aled J., Carney, Sara, Oakey, Rebecca J., Heisler, Lora K., Moorwood, Kim, Wolf, Jason B., Ward, Andrew
Publicado em 2014

Analysis of copy number variations at 15 schizophrenia-associated loci

Por Rees, Elliott, Walters, James T. R., Georgieva, Lyudmila, Isles, Anthony R., Chambert, Kimberly D., Richards, Alexander L., Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J., Kirov, George
Publicado em 2014

Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders

Por Isles, Anthony R., Ingason, Andrés, Lowther, Chelsea, Walters, James, Gawlick, Micha, Stöber, Gerald, Rees, Elliott, Martin, Joanna, Little, Rosie B., Potter, Harry, Georgieva, Lyudmila, Pizzo, Lucilla, Ozaki, Norio, Aleksic, Branko, Kushima, Itaru, Ikeda, Masashi, Iwata, Nakao, Levinson, Douglas F., Gejman, Pablo V., Shi, Jianxin, Sanders, Alan R., Duan, Jubao, Willis, Joseph, Sisodiya, Sanjay, Costain, Gregory, Werge, Thomas M., Degenhardt, Franziska, Giegling, Ina, Rujescu, Dan, Hreidarsson, Stefan J., Saemundsen, Evald, Ahn, Joo Wook, Ogilvie, Caroline, Girirajan, Santhosh D., Stefansson, Hreinn, Stefansson, Kari, O’Donovan, Michael C., Owen, Michael J., Bassett, Anne, Kirov, George
Publicado no PLoS Genet (2016)

Maternally Derived Microduplications at 15q11-q13: Implication of Imprinted Genes in Psychotic Illness

Por Ingason, Andrés, Kirov, George, Giegling, Ina, Hansen, Thomas, Isles, Anthony R., Jakobsen, Klaus D., Kristinsson, Kari T., le Roux, Louise, Gustafsson, Omar, Craddock, Nick, Möller, Hans-Jürgen, McQuillin, Andrew, Muglia, Pierandrea, Cichon, Sven, Rietschel, Marcella, Ophoff, Roel A., Djurovic, Srdjan, Andreassen, Ole A., Pietiläinen, Olli P.H., Peltonen, Leena, Dempster, Emma, Collier, David A., St. Clair, David, Rasmussen, Henrik B., Glenthøj, Birte Y., Kiemeney, Lambertus A., Franke, Barbara, Tosato, Sarah, Bonetto, Chiara, Saemundsen, Evald, Hreidarsson, Stefán J., Nöthen, Markus M., Gurling, Hugh, O’Donovan, Michael C., Owen, Michael J., Sigurdsson, Engilbert, Petursson, Hannes, Stefansson, Hreinn, Rujescu, Dan, Stefansson, Kari, Werge, Thomas
Publicado em 2011