Localisation of glycine receptors in the human forebrain, brainstem, and cervical spinal cord: an immunohistochemical review

by Kristin Baer, Henry J Waldvogel, Richard L M Faull, Mark I Rees, Mark I Rees
Published 2009-11-01

A critical role for glycine transporters in hyperexcitability disorders

by Robert J Harvey, Eloisa Carta, Brian R Pearce, Seo-Kyung Chung, Stéphane Supplisson, Mark I Rees, Mark I Rees, Kirsten Harvey
Published 2008-03-01

Data safe havens to combine health and genomic data: benefits and challenges

by Kerina H Jones, Arron S Lacey, Brian L Perkins, Mark I Rees
Published 2017-04-01

The glycinergic system in human startle disease: a genetic screening approach

by Jeff S Davies, Seo-Kyung Chung, Rhys H Thomas, Angela Robinson, Carrie L Hammond, Jonathan G L Mullins, Eloisa Carta, Brian R Pearce, Kirsten Harvey, Robert J Harvey, Mark I Rees, Mark I Rees
Published 2010-03-01

Obtaining structured clinical data from unstructured data using natural language processing software

by Arron S Lacey, Beata Fonferko-Shadrach, Ronan A Lyons, Mike P Kerr, David V Ford, Mark I Rees, Owen W Pickrell
Published 2017-04-01

Idiopathic Intracranial Hypertension in Wales

by Huw Strafford, Latif Miah, Beata Fonferko-Shadrach, Joe Hollinghurst, Mark I Rees, Inder Sawhney, Savvas Hadjikoutis, Rob Powell, Arron Lacey, Arron Lacey
Published 2020-12-01

Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene

by Jennifer L. Gill, Deborah Capper, Jean-François Vanbellinghen, Seo-Kyung Chung, Robert J. Higgins, Mark I. Rees, G. Diane Shelton, Robert J. Harvey
Published 2011-07-01

Codifying unstructured data: A Natural Language Processing approach to extract rich data from clinical letters

by Arron Lacey, Jane Lyons, Ashley Akbari, Samantha L Turner, Angharad M Walters, Beata Fonferko-Shadrach, Owen Pickrell, Mark I Rees, Ronan A Lyons, David V Ford, Rod M Middleton
Published 2017-04-01

Molecular investigation of TBP allele length:

by Suzanne J. Reid, Mark I. Rees, Willeke M.C. van Roon-Mom, A.Lesley Jones, Marcy E. MacDonald, Greg Sutherland, Matthew J. During, Richard L.M. Faull, Michael J. Owen, Mike Dragunow, Russell G. Snell
Published 2003-06-01

Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease

by Victoria M. James, Anna Bode, Seo-Kyung Chung, Jennifer L. Gill, Maartje Nielsen, Frances M. Cowan, Mihailo Vujic, Rhys H. Thomas, Mark I. Rees, Kirsten Harvey, Angelo Keramidas, Maya Topf, Ieke Ginjaar, Joseph W. Lynch, Robert J. Harvey
Published 2013-04-01

A Novel GABRG2 mutation, p.R136*, in a family with GEFS+ and extended phenotypes

by Ann J. Johnston, Jing-Qiong Kang, Wangzhen Shen, William O. Pickrell, Thomas D. Cushion, Jeffrey S. Davies, Kristin Baer, Jonathan G.L. Mullins, Carrie L. Hammond, Seo-Kyung Chung, Rhys H. Thomas, Cathy White, Phil E.M. Smith, Robert L. Macdonald, Mark I. Rees
Published 2014-04-01

Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy

by Costin Leu, Simona Balestrini, Bridget Maher, Laura Hernández-Hernández, Padhraig Gormley, Eija Hämäläinen, Kristin Heggeli, Natasha Schoeler, Jan Novy, Joseph Willis, Vincent Plagnol, Rachael Ellis, Eleanor Reavey, Mary O'Regan, William O. Pickrell, Rhys H. Thomas, Seo-Kyung Chung, Norman Delanty, Jacinta M. McMahon, Stephen Malone, Lynette G. Sadleir, Samuel F. Berkovic, Lina Nashef, Sameer M. Zuberi, Mark I. Rees, Gianpiero L. Cavalleri, Josemir W. Sander, Elaine Hughes, J. Helen Cross, Ingrid E. Scheffer, Aarno Palotie, Sanjay M. Sisodiya
Published 2015-09-01