Resultados da pesquisa - Wheeler, Eleanor

Quantitative trait association in parent offspring trios: Extension of case/pseudocontrol method and comparison of prospective and retrospective approaches Por Wheeler, Eleanor, Cordell, Heather J

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Genetic aetiology of glycaemic traits: approaches and insights Por Wheeler, Eleanor, Marenne, Gaëlle, Barroso, Inês

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Linkage analysis of GAW14 simulated data: comparison of multimarker, multipoint, and conditional approaches Por Barber, Mathew J, Wheeler, Eleanor, Cordell, Heather J

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Proteogenomic links to human metabolic diseases Por Koprulu, Mine, Carrasco-Zanini, Julia, Wheeler, Eleanor, Lockhart, Sam, Kerrison, Nicola D., Wareham, Nicholas J., Pietzner, Maik, Langenberg, Claudia

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A Bayesian Approach to the Overlap Analysis of Epidemiologically Linked Traits Por Asimit, Jennifer L., Panoutsopoulou, Kalliope, Wheeler, Eleanor, Berndt, Sonja I., Cordell, Heather J., Morris, Andrew P., Zeggini, Eleftheria, Barroso, Inês

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Development and validation of a metabolite score for red meat intake: an observational cohort study and randomized controlled dietary intervention Por Li, Chunxiao, Imamura, Fumiaki, Wedekind, Roland, Stewart, Isobel D, Pietzner, Maik, Wheeler, Eleanor, Forouhi, Nita G, Langenberg, Claudia, Scalbert, Augustin, Wareham, Nicholas J

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Synergistic insights into human health from aptamer- and antibody-based proteomic profiling Por Pietzner, Maik, Wheeler, Eleanor, Carrasco-Zanini, Julia, Kerrison, Nicola D., Oerton, Erin, Koprulu, Mine, Luan, Jian’an, Hingorani, Aroon D., Williams, Steve A., Wareham, Nicholas J., Langenberg, Claudia

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Meta-analysis investigating the role of interleukin-6 mediated inflammation in type 2 diabetes Por Bowker, Nicholas, Shah, Rupal L., Sharp, Stephen J., Luan, Jian'an, Stewart, Isobel D., Wheeler, Eleanor, Ferreira, Manuel A.R., Baras, Aris, Wareham, Nicholas J., Langenberg, Claudia, Lotta, Luca A.

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Lung cancer in Europe: The way forward Por Racovita, Monica, Wheeler, Eleanor, Wait, Suzanne, Bancroft, Dani, Eastabrook, Rowan, Albreht, Tit, Baird, Anne-Marie, Jassem, Jacek, McNamara, Aoife, Novello, Silvia, Radu-Loghin, Cornel, van Meerbeeck, Jan P.

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Mendelian Randomization Analysis of Hemoglobin A(1c) as a Risk Factor for Coronary Artery Disease Por Leong, Aaron, Chen, Ji, Wheeler, Eleanor, Hivert, Marie-France, Liu, Ching-Ti, Merino, Jordi, Dupuis, Josée, Tai, E Shyong, Rotter, Jerome I., Florez, Jose C., Barroso, Inês, Meigs, James B.

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Evaluating the Role of LPIN1 Variation in Insulin Resistance, Body Weight, and Human Lipodystrophy in U.K. Populations Por Fawcett, Katherine A., Grimsey, Neil, Loos, Ruth J.F., Wheeler, Eleanor, Daly, Allan, Soos, Maria, Semple, Robert, Syddall, Holly, Cooper, Cyrus, Siniossoglou, Symeon, O'Rahilly, Stephen, Wareham, Nicholas J., Barroso, Inês

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Genetic architecture of human thinness compared to severe obesity Por Riveros-McKay, Fernando, Mistry, Vanisha, Bounds, Rebecca, Hendricks, Audrey, Keogh, Julia M., Thomas, Hannah, Henning, Elana, Corbin, Laura J., O’Rahilly, Stephen, Zeggini, Eleftheria, Wheeler, Eleanor, Barroso, Inês, Farooqi, I. Sadaf

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The influence of rare variants in circulating metabolic biomarkers Por Riveros-Mckay, Fernando, Oliver-Williams, Clare, Karthikeyan, Savita, Walter, Klaudia, Kundu, Kousik, Ouwehand, Willem H., Roberts, David, Di Angelantonio, Emanuele, Soranzo, Nicole, Danesh, John, Wheeler, Eleanor, Zeggini, Eleftheria, Butterworth, Adam S., Barroso, Inês

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Proteomic signatures for identification of impaired glucose tolerance Por Carrasco-Zanini, Julia, Pietzner, Maik, Lindbohm, Joni V, Wheeler, Eleanor, Oerton, Erin, Kerrison, Nicola, Simpson, Missy, Westacott, Matthew, Drolet, Dan, Kivimaki, Mika, Ostroff, Rachel, Williams, Stephen A, Wareham, Nicholas J, Langenberg, Claudia

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GIGYF1 loss of function is associated with clonal mosaicism and adverse metabolic health Por Zhao, Yajie, Stankovic, Stasa, Koprulu, Mine, Wheeler, Eleanor, Day, Felix R., Lango Allen, Hana, Kerrison, Nicola D., Pietzner, Maik, Loh, Po-Ru, Wareham, Nicholas J., Langenberg, Claudia, Ong, Ken K., Perry, John R. B.

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Mapping the serum proteome to neurological diseases using whole genome sequencing Por Png, Grace, Barysenka, Andrei, Repetto, Linda, Navarro, Pau, Shen, Xia, Pietzner, Maik, Wheeler, Eleanor, Wareham, Nicholas J., Langenberg, Claudia, Tsafantakis, Emmanouil, Karaleftheri, Maria, Dedoussis, George, Mälarstig, Anders, Wilson, James F., Gilly, Arthur, Zeggini, Eleftheria

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Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways Por Soranzo, Nicole, Sanna, Serena, Wheeler, Eleanor, Gieger, Christian, Radke, Dörte, Dupuis, Josée, Bouatia-Naji, Nabila, Langenberg, Claudia, Prokopenko, Inga, Stolerman, Elliot, Sandhu, Manjinder S., Heeney, Matthew M., Devaney, Joseph M., Reilly, Muredach P., Ricketts, Sally L.

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Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity Por Wheeler, Eleanor, Huang, Ni, Bochukova, Elena, Keogh, Julia M., Lindsay, Sarah, Garg, Sumedha, Henning, Elana, Blackburn, Hannah, Loos, Ruth J.F., Wareham, Nick J, O’Rahilly, Stephen, Hurles, Matthew E., Barroso, Inês, Farooqi, I. Sadaf

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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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Genetically Predicted Glucose-Dependent Insulinotropic Polypeptide (GIP) Levels and Cardiovascular Disease Risk Are Driven by Distinct Causal Variants in the GIPR Region Por Bowker, Nicholas, Hansford, Robert, Burgess, Stephen, Foley, Christopher N., Auyeung, Victoria P.W., Erzurumluoglu, A. Mesut, Stewart, Isobel D., Wheeler, Eleanor, Pietzner, Maik, Gribble, Fiona, Reimann, Frank, Bhatnagar, Pallav, Coghlan, Matthew P., Wareham, Nicholas J., Langenberg, Claudia

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