Výsledky vyhledávání - Wheeler, Eleanor

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

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

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

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Proteogenomic links to human metabolic diseases Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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