检索结果 - Wheeler, Eleanor

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

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

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

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Proteogenomic links to human metabolic diseases 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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