Sequence variants in the genes for the interleukin-23 receptor (IL23R) and its ligand (IL12B) confer protection against psoriasis
CAPON, Francesca, DI MEGLIO, Paola, LANCHBURY, Jerry, BARKER, Jonathan N, TREMBATH, Richard C, NESTLE, Frank O, SZAUB, Joanna, PRESCOTT, Natalie J, DUNSTER, Christina, BAUMBER, Laura, TIMMS, Kirsten, GUTIN, Alexander, ABKEVIC, Victor, BURDEN, A. David
Published in Human genetics (01.09.2007)
Published in Human genetics (01.09.2007)
Get full text
Journal Article
Sequence variants in the genes for the interleukin-23 receptor
Capon, Francesca, Di Meglio, Paola, Szaub, Joanna, Prescott, Natalie J, Dunster, Christina, Baumber, Laura, Timms, Kirsten
Published in Human genetics (01.09.2007)
Published in Human genetics (01.09.2007)
Get full text
Journal Article
Corrigendum: Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R, Raymond, F Lucy, Gottlob, Irene
Published in Nature genetics (01.07.2011)
Published in Nature genetics (01.07.2011)
Get full text
Journal Article
Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R, Raymond, F Lucy, Gottlob, Irene
Published in Nature genetics (28.06.2011)
Published in Nature genetics (28.06.2011)
Get full text
Journal Article
Correction: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus
Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R, Raymond, F Lucy, Gottlob, Irene
Published in Nature genetics (2011)
Published in Nature genetics (2011)
Get full text
Journal Article
Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing
ALDRED, Micheala A, BAUMBER, Laura, HILL, Alison, SCHWALBE, Edward C, GOH, Kai, KARWATOWSKI, Wojciech, TREMBATH, Richard C
Published in Human genetics (01.10.2004)
Published in Human genetics (01.10.2004)
Get full text
Journal Article
A novel locus for Meckel-Gruber syndrome, MKS3, maps to chromosome 8q24
MORGAN, Neil V, GISSEN, Paul, TREMBATH, Richard C, MAHER, Eamonn R, JOHNSON, Colin A, SAGHIRA MALIK SHARIF, BAUMBER, Laura, SUTHERLAND, Joan, KELLY, Deirdre A, AMINU, Kingi, BENNETT, Christopher P, WOODS, C. Geoffrey, MUELLER, Robert F
Published in Human genetics (01.10.2002)
Published in Human genetics (01.10.2002)
Get full text
Journal Article