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Number of items: 8.

Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, GROUP Investigators, Han, Jun, Morgan, Joanne, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Golimbat, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2020. De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia. Nature Neuroscience 23 (2) , pp. 179-184. 10.1038/s41593-019-0565-2
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Pardinas, Antonio F. ORCID: https://orcid.org/0000-0001-6845-7590, GERAD Consortium, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew J. ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda, Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nichols G., McIntosh, Andrew M., Plomin, Robert P., Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Eeben A., Als, Thomas P., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bocker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Giørtz Pedersenu, Marianne, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Søholm Hansen, Christine, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael J ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Williams, Julie ORCID: https://orcid.org/0000-0002-4069-0259 and CRESTAR Consortium 2018. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nature Genetics 50 , pp. 381-389. 10.1038/s41588-018-0059-2
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Pardinas, Antonio ORCID: https://orcid.org/0000-0001-6845-7590, Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Ripke, Stephan, Carrera, Noa ORCID: https://orcid.org/0000-0003-0739-0382, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L. ORCID: https://orcid.org/0000-0002-8990-0958, Han, Jun, Hubbard, Leon, Lynham, Amy ORCID: https://orcid.org/0000-0002-3189-6888, Mantripragada, Kiran ORCID: https://orcid.org/0000-0003-2070-8105, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, MacCabe, James H., McCarroll, Stephen A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Consortium, Collier, David A., Rujescu, Dan, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Owen, Michael ORCID: https://orcid.org/0000-0003-4798-0862, O'Donovan, Michael ORCID: https://orcid.org/0000-0001-7073-2379 and Walters, James ORCID: https://orcid.org/0000-0002-6980-4053 2016. Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection. [Online]. bioRxiv. Available at: http://dx.doi.org/10.1101/068593
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Han, Jun, Walters, James ORCID: https://orcid.org/0000-0002-6980-4053, Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Escott-Price, Valentina ORCID: https://orcid.org/0000-0003-1784-5483, Owen, Michael John ORCID: https://orcid.org/0000-0003-4798-0862, Holmans, Peter Alan ORCID: https://orcid.org/0000-0003-0870-9412, O'Donovan, Michael Conlon ORCID: https://orcid.org/0000-0001-7073-2379 and Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222 2016. Gender differences in CNV burden do not confound schizophrenia CNV associations. Scientific Reports 6 , 25986. 10.1038/srep25986
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Lee, J. M., Wheeler, V. C., Chao, M. J., Vonsattel, P., Pinto, R. M., Lucente, D., Abu-Elmeel, K., Ramos, E. M., Mysore, J. S., Gillis, T., MacDonald, M. E., Gusella, J. F., Harold, D., Stone, T. C. ORCID: https://orcid.org/0000-0003-4591-9611, Escott-Price, V. ORCID: https://orcid.org/0000-0003-1784-5483, Han, J., Vedernikov, A., Holmans, P. A. ORCID: https://orcid.org/0000-0003-0870-9412, Jones, L. ORCID: https://orcid.org/0000-0002-3007-4612, Kwak, S., Mahmoudi, M., Orth, M., Landwehmeyer, G. B., Paulsen, J. S., Dorsey, R., Shoulson, I. and Myers, R. H. 2015. Identification of genetic factors that modify clinical onset of Huntington's disease. Cell 162 (3) , pp. 516-526. 10.1016/j.cell.2015.07.003

Pocklington, Andrew ORCID: https://orcid.org/0000-0002-2137-0452, Rees, Elliott ORCID: https://orcid.org/0000-0002-6168-9222, Walters, James T. R. ORCID: https://orcid.org/0000-0002-6980-4053, Han, Jun, Kavanagh, David H., Chambert, Kimberly D., Holmans, Peter ORCID: https://orcid.org/0000-0003-0870-9412, Moran, Jennifer L., McCarroll, Steven A., Kirov, George ORCID: https://orcid.org/0000-0002-3427-3950, O'Donovan, Michael C. ORCID: https://orcid.org/0000-0001-7073-2379 and Owen, Michael J. ORCID: https://orcid.org/0000-0003-4798-0862 2015. Novel findings from CNVs implicate inhibitory and excitatory signaling complexes in schizophrenia. Neuron 86 (5) , pp. 1203-1214. 10.1016/j.neuron.2015.04.022
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Soler, Cedric, Han, Jun and Taylor, Michael Victor ORCID: https://orcid.org/0000-0003-1351-939X 2012. The conserved transcription factor Mef2 has multiple roles in adult Drosophila musculature formation. Development 139 (7) , pp. 1270-1275. 10.1242/dev.077875

Elgar, S. J., Han, Jun and Taylor, Michael Victor ORCID: https://orcid.org/0000-0003-1351-939X 2008. mef2 activity levels differentially regulate gene expression during Drosophila muscle development. Proceedings of the National Academy of Sciences of the United States of America 105 (3) , pp. 918-923. 10.1073/pnas.0711255105

This list was generated on Wed Apr 24 10:11:39 2024 BST.


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