Výsledky vyhledávání - Gwilliam, Rhian

A genotype calling algorithm for the Illumina BeadArray platform Autor Teo, Yik Y., Inouye, Michael, Small, Kerrin S., Gwilliam, Rhian, Deloukas, Panagiotis, Kwiatkowski, Dominic P., Clark, Taane G.

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Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion Autor Bonaglia, Maria Clara, Giorda, Roberto, Beri, Silvana, Bigoni, Stefania, Sensi, Alberto, Baroncini, Anna, Capucci, Antonella, De Agostini, Cristina, Gwilliam, Rhian, Deloukas, Panos, Dunham, Ian, Zuffardi, Orsetta

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Molecular analysis of the VSX1 gene in familial keratoconus Autor Liskova, Petra, Ebenezer, Neil D., Hysi, Pirro G., Gwilliam, Rhian, El-Ashry, Mohamed F., Moodaley, Lalitha C., Hau, Scott, Twa, Michael, Tuft, Stephen J., Bhatacharya, Shomi S.

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High Prevalence of Posterior Polymorphous Corneal Dystrophy in the Czech Republic; Linkage Disequilibrium Mapping and Dating an Ancestral Mutation Autor Liskova, Petra, Gwilliam, Rhian, Filipec, Martin, Jirsova, Katerina, Reinstein Merjava, Stanislava, Deloukas, Panos, Webb, Tom R., Bhattacharya, Shomi S., Ebenezer, Neil D., Morris, Alex G., Hardcastle, Alison J.

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Novel Mutations in the ZEB1 Gene Identified in Czech and British Patients With Posterior Polymorphous Corneal Dystrophy Autor Liskova, Petra, Tuft, Stephen J., Gwilliam, Rhian, Ebenezer, Neil D., Jirsova, Katerina, Prescott, Quincy, Martincova, Radka, Pretorius, Marike, Sinclair, Neil, Boase, David L., Jeffrey, Margaret J., Deloukas, Panos, Hardcastle, Alison J., Filipec, Martin, Bhattacharya, Shomi S.

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High-Resolution Landmark Framework for the Sequence-Ready Mapping of Xq23–q26.1 Autor Steingruber, Helen E., Dunham, Andrew, Coffey, Alison J., Clegg, Sheila M., Howell, Gareth R., Maslen, Gareth L., Scott, Carol E., Gwilliam, Rhian, Hunt, Paul J., Sotheran, Elizabeth C., Huckle, Elizabeth J., Hunt, Sarah E., Dhami, Pawandeep, Soderlund, Cari, Leversha, Margaret A., Bentley, David R., Ross, Mark T.

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IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease Autor Tremelling, Mark, Cummings, Fraser, Fisher, Sheila A., Mansfield, John, Gwilliam, Rhian, Keniry, Andrew, Nimmo, Elaine R., Drummond, Hazel, Onnie, Clive M., Prescott, Natalie J., Sanderson, Jeremy, Bredin, Francesca, Berzuini, Carlo, Forbes, Alastair, Lewis, Cathryn M., Cardon, Lon, Deloukas, Panos, Jewell, Derek, Mathew, Christopher G., Parkes, Miles, Satsangi, Jack

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Observational study on variability between biobanks in the estimation of DNA concentration Autor Brown, Jay, Donev, Alexander N, Aslanidis, Charalampos, Bracegirdle, Pippa, Dixon, Katherine P, Foedinger, Manuela, Gwilliam, Rhian, Hardy, Matthew, Illig, Thomas, Ke, Xiayi, Krinka, Dagni, Lagerberg, Camilla, Laiho, Päivi, Lewis, David H, McArdle, Wendy, Patton, Simon, Ring, Susan M, Schmitz, Gerd, Stevens, Helen, Tybring, Gunnel, Wichmann, H Erich, Ollier, William ER, Yuille, Martin A

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Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease Autor Combarros, Onofre, van Duijn, Cornelia M, Hammond, Naomi, Belbin, Olivia, Arias-Vásquez, Alejandro, Cortina-Borja, Mario, Lehmann, Michael G, Aulchenko, Yurii S, Schuur, Maaike, Kölsch, Heike, Heun, Reinhard, Wilcock, Gordon K, Brown, Kristelle, Kehoe, Patrick G, Harrison, Rachel, Coto, Eliecer, Alvarez, Victoria, Deloukas, Panos, Mateo, Ignacio, Gwilliam, Rhian, Morgan, Kevin, Warden, Donald R, Smith, A David, Lehmann, Donald J

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The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project Autor Combarros, Onofre, Warden, Donald R, Hammond, Naomi, Cortina-Borja, Mario, Belbin, Olivia, Lehmann, Michael G, Wilcock, Gordon K, Brown, Kristelle, Kehoe, Patrick G, Barber, Rachel, Coto, Eliecer, Alvarez, Victoria, Deloukas, Panos, Gwilliam, Rhian, Heun, Reinhard, Kölsch, Heike, Mateo, Ignacio, Oulhaj, Abderrahim, Arias-Vásquez, Alejandro, Schuur, Maaike, Aulchenko, Yurii S, Ikram, M Arfan, Breteler, Monique M, van Duijn, Cornelia M, Morgan, Kevin, Smith, A David, Lehmann, Donald J

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 Autor van Heel, David A, Franke, Lude, Hunt, Karen A, Gwilliam, Rhian, Zhernakova, Alexandra, Inouye, Mike, Wapenaar, Martin C, Barnardo, Martin CNM, Bethel, Graeme, Holmes, Geoffrey KT, Feighery, Con, Jewell, Derek, Kelleher, Dermot, Kumar, Parveen, Travis, Simon, Walters, Julian RF, Sanders, David S, Howdle, Peter, Swift, Jill, Playford, Raymond J, McLaren, William M, Mearin, M Luisa, Mulder, Chris J, McManus, Ross, McGinnis, Ralph, Cardon, Lon R, Deloukas, Panos, Wijmenga, Cisca

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Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression Autor Almlöf, Jonas Carlsson, Lundmark, Per, Lundmark, Anders, Ge, Bing, Maouche, Seraya, Göring, Harald H. H., Liljedahl, Ulrika, Enström, Camilla, Brocheton, Jessy, Proust, Carole, Godefroy, Tiphaine, Sambrook, Jennifer G., Jolley, Jennifer, Crisp-Hihn, Abigail, Foad, Nicola, Lloyd-Jones, Heather, Stephens, Jonathan, Gwilliam, Rhian, Rice, Catherine M., Hengstenberg, Christian, Samani, Nilesh J., Erdmann, Jeanette, Schunkert, Heribert, Pastinen, Tomi, Deloukas, Panos, Goodall, Alison H., Ouwehand, Willem H., Cambien, François, Syvänen, Ann-Christine

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Population Genetic Analysis of Plasmodium falciparum Parasites Using a Customized Illumina GoldenGate Genotyping Assay Autor Campino, Susana, Auburn, Sarah, Kivinen, Katja, Zongo, Issaka, Ouedraogo, Jean-Bosco, Mangano, Valentina, Djimde, Abdoulaye, Doumbo, Ogobara K., Kiara, Steven M., Nzila, Alexis, Borrmann, Steffen, Marsh, Kevin, Michon, Pascal, Mueller, Ivo, Siba, Peter, Jiang, Hongying, Su, Xin-Zhuan, Amaratunga, Chanaki, Socheat, Duong, Fairhurst, Rick M., Imwong, Mallika, Anderson, Timothy, Nosten, François, White, Nicholas J., Gwilliam, Rhian, Deloukas, Panos, MacInnis, Bronwyn, Newbold, Christopher I., Rockett, Kirk, Clark, Taane G., Kwiatkowski, Dominic P.

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Investigation of Crohn’s Disease Risk Loci in Ulcerative Colitis Further Defines Their Molecular Relationship Autor ANDERSON, CARL A., MASSEY, DUNECAN C. O., BARRETT, JEFFREY C., PRESCOTT, NATALIE J., TREMELLING, MARK, FISHER, SHEILA A., GWILLIAM, RHIAN, JACOB, JEMIMA, NIMMO, ELAINE R., DRUMMOND, HAZEL, LEES, CHARLIE W., ONNIE, CLIVE M., HANSON, CATHERINE, BLASZCZYK, KATARZYNA, RAVINDRARAJAH, RADHI, HUNT, SARAH, VARMA, DHIRAJ, HAMMOND, NAOMI, LEWIS, GREGORY, ATTLESEY, HEATHER, WATKINS, NICK, OUWEHAND, WILLEM, STRACHAN, DAVID, MCARDLE, WENDY, LEWIS, CATHRYN M., LOBO, ALAN, SANDERSON, JEREMY, JEWELL, DEREK P., DELOUKAS, PANOS, MANSFIELD, JOHN C., MATHEW, CHRISTOPHER G., SATSANGI, JACK, PARKES, MILES

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Linkage Disequilibrium Mapping of the Replicated Type 2 Diabetes Linkage Signal on Chromosome 1q Autor Prokopenko, Inga, Zeggini, Eleftheria, Hanson, Robert L., Mitchell, Braxton D., Rayner, N. William, Akan, Pelin, Baier, Leslie, Das, Swapan K., Elliott, Katherine S., Fu, Mao, Frayling, Timothy M., Groves, Christopher J., Gwilliam, Rhian, Scott, Laura J., Voight, Benjamin F., Hattersley, Andrew T., Hu, Cheng, Morris, Andrew D., Ng, Maggie, Palmer, Colin N.A., Tello-Ruiz, Marcela, Vaxillaire, Martine, Wang, Cong-rong, Stein, Lincoln, Chan, Juliana, Jia, Weiping, Froguel, Philippe, Elbein, Steven C., Deloukas, Panos, Bogardus, Clifton, Shuldiner, Alan R., McCarthy, Mark I.

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Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies Autor Nolte, Ilja M., Wallace, Chris, Newhouse, Stephen J., Waggott, Daryl, Fu, Jingyuan, Soranzo, Nicole, Gwilliam, Rhian, Deloukas, Panos, Savelieva, Irina, Zheng, Dongling, Dalageorgou, Chrysoula, Farrall, Martin, Samani, Nilesh J., Connell, John, Brown, Morris, Dominiczak, Anna, Lathrop, Mark, Zeggini, Eleftheria, Wain, Louise V., Newton-Cheh, Christopher, Eijgelsheim, Mark, Rice, Kenneth, de Bakker, Paul I. W., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Asselbergs, Folkert W., Spector, Tim D., Carter, Nicholas D., Jeffery, Steve, Tobin, Martin, Caulfield, Mark, Snieder, Harold, Paterson, Andrew D., Munroe, Patricia B., Jamshidi, Yalda

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Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn’s disease Autor Fisher, Sheila A, Tremelling, Mark, Anderson, Carl A, Gwilliam, Rhian, Bumpstead, Suzannah, Prescott, Natalie J, Nimmo, Elaine R, Massey, Dunecan, Berzuini, Carlo, Johnson, Christopher, Barrett, Jeffrey C, Cummings, Fraser R, Drummond, Hazel, Lees, Charlie W, Onnie, Clive M, Hanson, Catherine E, Blaszczyk, Katarzyna, Inouye, Mike, Ewels, Philip, Ravindrarajah, Radhi, Keniry, Andrew, Hunt, Sarah, Carter, Martyn, Watkins, Nick, Ouwehand, Willem, Lewis, Cathryn M, Cardon, Lon, Lobo, Alan, Forbes, Alastair, Sanderson, Jeremy, Jewell, Derek P, Mansfield, John C, Deloukas, Panos, Mathew, Christopher G, Parkes, Miles, Satsangi, Jack

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Meta-Analysis of Genome-Wide Scans for Human Adult Stature Identifies Novel Loci and Associations with Measures of Skeletal Frame Size Autor Soranzo, Nicole, Rivadeneira, Fernando, Chinappen-Horsley, Usha, Malkina, Ida, Richards, J. Brent, Hammond, Naomi, Stolk, Lisette, Nica, Alexandra, Inouye, Michael, Hofman, Albert, Stephens, Jonathan, Wheeler, Eleanor, Arp, Pascal, Gwilliam, Rhian, Jhamai, P. Mila, Potter, Simon, Chaney, Amy, Ghori, Mohammed J. R., Ravindrarajah, Radhi, Ermakov, Sergey, Estrada, Karol, Pols, Huibert A. P., Williams, Frances M., McArdle, Wendy L., van Meurs, Joyce B., Loos, Ruth J. F., Dermitzakis, Emmanouil T., Ahmadi, Kourosh R., Hart, Deborah J., Ouwehand, Willem H., Wareham, Nicholas J., Barroso, Inês, Sandhu, Manjinder S., Strachan, David P., Livshits, Gregory, Spector, Timothy D., Uitterlinden, André G., Deloukas, Panos

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Novel celiac disease genetic determinants related to the immune response Autor Hunt, Karen A, Zhernakova, Alexandra, Turner, Graham, Heap, Graham A.R., Franke, Lude, Bruinenberg, Marcel, Romanos, Jihane, Dinesen, Lotte C., Ryan, Anthony W, Panesar, Davinder, Gwilliam, Rhian, Takeuchi, Fumihiko, McLaren, William M, Holmes, Geoffrey KT, Howdle, Peter D, Walters, Julian RF, Sanders, David S, Playford, Raymond J, Trynka, Gosia, Mulder, Chris JJ, Mearin, M Luisa, Verbeek, Wieke HM, Trimble, Valerie, Stevens, Fiona M, O’Morain, Colm, Kennedy, Nicholas P, Kelleher, Dermot, Pennington, Daniel J, Strachan, David P, McArdle, Wendy L, Mein, Charles A, Wapenaar, Martin C, Deloukas, Panos, McGinnis, Ralph, McManus, Ross, Wijmenga, Cisca, van Heel, David A

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Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1 Autor Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A.W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., McPherson, Ruth, Folkersen, Lasse, Franco-Cereceda, Anders, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicolas, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjærg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J.

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