Resultados de procura - Payne, Felicity

A two-stage inter-rater approach for enrichment testing of variants associated with multiple traits por Asimit, Jennifer L, Payne, Felicity, Morris, Andrew P, Cordell, Heather J, Barroso, Inês

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Disease-associated DNA methylation signatures in esophageal biopsies of children diagnosed with Eosinophilic Esophagitis por Strisciuglio, Caterina, Payne, Felicity, Nayak, Komal, Andreozzi, Marialuisa, Vitale, Alessandra, Miele, Erasmo, Zilbauer, Matthias

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Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden por Renström, Frida, Payne, Felicity, Nordström, Anna, Brito, Ema C., Rolandsson, Olov, Hallmans, Göran, Barroso, Ines, Nordström, Peter, Franks, Paul W.

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The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion por Rocha, Nuno, Payne, Felicity, Huang-Doran, Isabel, Sleigh, Alison, Fawcett, Katherine, Adams, Claire, Stears, Anna, Saudek, Vladimir, O’Rahilly, Stephen, Barroso, Inês, Semple, Robert K.

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The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes por Cooper, Jason D, Smyth, Deborah J, Bailey, Rebecca, Payne, Felicity, Downes, Kate, Godfrey, Lisa M, Masters, Jennifer, Zeitels, Lauren R, Vella, Adrian, Walker, Neil M, Todd, John A

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Polymorphism discovery and association analyses of the interferon genes in type 1 diabetes por Morris, Gerard AJ, Lowe, Christopher E, Cooper, Jason D, Payne, Felicity, Vella, Adrian, Godfrey, Lisa, Hulme, John S, Walker, Neil M, Healy, Barry C, Lam, Alex C, Lyons, Paul A, Todd, John A

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Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance por Payne, Felicity, Colnaghi, Rita, Rocha, Nuno, Seth, Asha, Harris, Julie, Carpenter, Gillian, Bottomley, William E., Wheeler, Eleanor, Wong, Stephen, Saudek, Vladimir, Savage, David, O’Rahilly, Stephen, Carel, Jean-Claude, Barroso, Inês, O’Driscoll, Mark, Semple, Robert

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Transcription and DNA Methylation Patterns of Blood-Derived CD8(+) T Cells Are Associated With Age and Inflammatory Bowel Disease But Do Not Predict Prognosis por Gasparetto, Marco, Payne, Felicity, Nayak, Komal, Kraiczy, Judith, Glemas, Claire, Philip-McKenzie, Yosef, Ross, Alexander, Edgar, Rachel D., Zerbino, Daniel R., Salvestrini, Camilla, Torrente, Franco, Ventham, Nicholas T., Kalla, Rahul, Satsangi, Jack, Sarkies, Peter, Heuschkel, Robert, Zilbauer, Matthias

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Analysis of polymorphisms in 16 genes in type 1 diabetes that have been associated with other immune-mediated diseases por Smyth, Deborah J, Howson, Joanna MM, Payne, Felicity, Maier, Lisa M, Bailey, Rebecca, Holland, Kieran, Lowe, Christopher E, Cooper, Jason D, Hulme, John S, Vella, Adrian, Dahlman, Ingrid, Lam, Alex C, Nutland, Sarah, Walker, Neil M, Twells, Rebecca CJ, Todd, John A

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Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease por Payne, Felicity, Lim, Koini, Girousse, Amandine, Brown, Rebecca J., Kory, Nora, Robbins, Ann, Xue, Yali, Sleigh, Alison, Cochran, Elaine, Adams, Claire, Dev Borman, Arundhati, Russel-Jones, David, Gorden, Phillip, Semple, Robert K., Saudek, Vladimir, O’Rahilly, Stephen, Walther, Tobias C., Barroso, Inês, Savage, David B.

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Development of an integrated genome informatics, data management and workflow infrastructure: A toolbox for the study of complex disease genetics por Burren, Oliver S, Healy, Barry C, Lam, Alex C, Schuilenburg, Helen, Dolman, Geoffrey E, Everett, Vincent H, Laneri, Davide, Nutland, Sarah, Rance, Helen E, Payne, Felicity, Smyth, Deborah, Lowe, Chris, Barratt, Bryan J, Twells, Rebecca CJ, Rainbow, Daniel B, Wicker, Linda S, Todd, John A, Walker, Neil M, Smink, Luc J

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Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription por Marenne, Gaëlle, Hendricks, Audrey E., Perdikari, Aliki, Bounds, Rebecca, Payne, Felicity, Keogh, Julia M., Lelliott, Christopher J., Henning, Elana, Pathan, Saad, Ashford, Sofie, Bochukova, Elena G., Mistry, Vanisha, Daly, Allan, Hayward, Caroline, Wareham, Nicholas J., O’Rahilly, Stephen, Langenberg, Claudia, Wheeler, Eleanor, Zeggini, Eleftheria, Farooqi, I. Sadaf, Barroso, Inês

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Sequencing and association analysis of the type 1 diabetes – linked region on chromosome 10p12-q11 por Nejentsev, Sergey, Smink, Luc J, Smyth, Deborah, Bailey, Rebecca, Lowe, Christopher E, Payne, Felicity, Masters, Jennifer, Godfrey, Lisa, Lam, Alex, Burren, Oliver, Stevens, Helen, Nutland, Sarah, Walker, Neil M, Smith, Anne, Twells, Rebecca, Barratt, Bryan J, Wright, Charmain, French, Lisa, Chen, Yuan, Deloukas, Panagiotis, Rogers, Jane, Dunham, Ian, Todd, John A

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Insulin resistance uncoupled from dyslipidemia due to C-terminal PIK3R1 mutations por Huang-Doran, Isabel, Tomlinson, Patsy, Payne, Felicity, Gast, Alexandra, Sleigh, Alison, Bottomley, William, Harris, Julie, Daly, Allan, Rocha, Nuno, Rudge, Simon, Clark, Jonathan, Kwok, Albert, Romeo, Stefano, McCann, Emma, Müksch, Barbara, Dattani, Mehul, Zucchini, Stefano, Wakelam, Michael, Foukas, Lazaros C., Savage, David B., Murphy, Rinki, O’Rahilly, Stephen, Barroso, Inês, Semple, Robert K.

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Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes por Bonnefond, Amélie, Clément, Nathalie, Fawcett, Katherine, Yengo, Loïc, Vaillant, Emmanuel, Guillaume, Jean-Luc, Dechaume, Aurélie, Payne, Felicity, Roussel, Ronan, Czernichow, Sébastien, Hercberg, Serge, Hadjadj, Samy, Balkau, Beverley, Marre, Michel, Lantieri, Olivier, Langenberg, Claudia, Bouatia-Naji, Nabila, Charpentier, Guillaume, Vaxillaire, Martine, Rocheleau, Ghislain, Wareham, Nicholas J., Sladek, Robert, McCarthy, Mark I., Dina, Christian, Barroso, Inês, Jockers, Ralf, Froguel, Philippe

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Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase por Leiter, Sarah M, Parker, Victoria E R, Welters, Alena, Knox, Rachel, Rocha, Nuno, Clark, Graeme, Payne, Felicity, Lotta, Luca, Harris, Julie, Guerrero-Fernández, Julio, González-Casado, Isabel, García-Miñaur, Sixto, Gordo, Gema, Wareham, Nick, Martínez-Glez, Víctor, Allison, Michael, O’Rahilly, Stephen, Barroso, Inês, Meissner, Thomas, Davies, Susan, Hussain, Khalid, Temple, Karen, Barreda-Bonis, Ana-Coral, Kummer, Sebastian, Semple, Robert K

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Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes por Maier, Lisa M, Smyth, Deborah J, Vella, Adrian, Payne, Felicity, Cooper, Jason D, Pask, Rebecca, Lowe, Christopher, Hulme, John, Smink, Luc J, Fraser, Heather, Moule, Carolyn, Hunter, Kara M, Chamberlain, Giselle, Walker, Neil, Nutland, Sarah, Undlien, Dag E, Rønningen, Kjersti S, Guja, Cristian, Ionescu-Tîrgovişte, Constantin, Savage, David A, Strachan, David P, Peterson, Laurence B, Todd, John A, Wicker, Linda S, Twells, Rebecca C

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Mosaic Overgrowth with Fibroadipose Hyperplasia is Caused by Somatic Activating Mutations in PIK3CA por Lindhurst, Marjorie J, Parker, Victoria ER, Payne, Felicity, Sapp, Julie C, Rudge, Simon, Harris, Julie, Witkowski, Alison M, Zhang, Qifeng, Groeneveld, Matthijs P, Scott, Carol E, Daly, Allan, Huson, Susan M, Tosi, Laura L, Cunningham, Michael L, Darling, Thomas N, Geer, Joseph, Gucev, Zoran, Sutton, V. Reid, Tziotzios, Christos, Dixon, Adrian K, Helliwell, Timothy, O’Rahilly, Stephen, Savage, David B, Wakelam, Michael JO, Barroso, Inês, Biesecker, Leslie G, Semple, Robert K

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Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression por Rocha, Nuno, Bulger, David A, Frontini, Andrea, Titheradge, Hannah, Gribsholt, Sigrid Bjerge, Knox, Rachel, Page, Matthew, Harris, Julie, Payne, Felicity, Adams, Claire, Sleigh, Alison, Crawford, John, Gjesing, Anette Prior, Bork-Jensen, Jette, Pedersen, Oluf, Barroso, Inês, Hansen, Torben, Cox, Helen, Reilly, Mary, Rossor, Alex, Brown, Rebecca J, Taylor, Simeon I, McHale, Duncan, Armstrong, Martin, Oral, Elif A, Saudek, Vladimir, O’Rahilly, Stephen, Maher, Eamonn R, Richelsen, Bjørn, Savage, David B, Semple, Robert K

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Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations por Salanti, Georgia, Southam, Lorraine, Altshuler, David, Ardlie, Kristin, Barroso, Inês, Boehnke, Michael, Cornelis, Marilyn C., Frayling, Timothy M., Grallert, Harald, Grarup, Niels, Groop, Leif, Hansen, Torben, Hattersley, Andrew T., Hu, Frank B., Hveem, Kristian, Illig, Thomas, Kuusisto, Johanna, Laakso, Markku, Langenberg, Claudia, Lyssenko, Valeriya, McCarthy, Mark I., Morris, Andrew, Morris, Andrew D., Palmer, Colin N. A., Payne, Felicity, Platou, Carl G. P., Scott, Laura J., Voight, Benjamin F., Wareham, Nicholas J., Zeggini, Eleftheria, Ioannidis, John P. A.

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