Resultados da busca - Gwilliam, Rhian

A genotype calling algorithm for the Illumina BeadArray platform por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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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