APOE, CETP and LPL genes show strong association with lipid levels in Greek children()

por Smart, M.C., Dedoussis, G., Louizou, E., Yannakoulia, M., Drenos, F., Papoutsakis, C., Maniatis, N., Humphries, S.E., Talmud, P.J.
Publicado 2010

Utility of genetic and non-genetic risk factors in prediction of type 2 diabetes: Whitehall II prospective cohort study

por Talmud, Philippa J, Hingorani, Aroon D, Cooper, Jackie A, Marmot, Michael G, Brunner, Eric J, Kumari, Meena, Kivimäki, Mika, Humphries, Steve E
Publicado 2010

Post-GWAS methodologies for localisation of functional non-coding variants: ANGPTL3

por Oldoni, Federico, Palmen, Jutta, Giambartolomei, Claudia, Howard, Philip, Drenos, Fotios, Plagnol, Vincent, Humphries, Steve E., Talmud, Philippa J., Smith, Andrew J.P.
Publicado 2016

Demonstration of the Presence of the “Deleted” MIR122 Gene in HepG2 Cells

por Hamad, Ibrahim A. Y., Fei, Yue, Kalea, Anastasia Z., Yin, Dan, Smith, Andrew J. P., Palmen, Jutta, Humphries, Steve E., Talmud, Philippa J., Walker, Ann P.
Publicado 2015

Functional Analysis of Two PLA2G2A Variants Associated with Secretory Phospholipase A2-IIA Levels

por Exeter, Holly J., Folkersen, Lasse, Palmen, Jutta, Franco-Cereceda, Anders, Cooper, Jackie A., Kalea, Anastasia Z., Hooft, Ferdinand van’t, Eriksson, Per, Humphries, Steve E., Talmud, Philippa J.
Publicado 2012

It's not just the mitral valve - abnormal motion of the whole aorto-mitral apparatus occurs in both overt and subclinical hypertrophic cardiomyopathy

por Obianyo, Chinwe, Captur, Gaby, Syrris, Petros, Lopes, Luis, Patel, Vimal, Reant, Patricia, Mirabel, Mariana, Manisty, Charlotte, Bassett, Paul, Sado, Daniel, Talmud, Phillippa, Elliott, Perry M, Moon, James C
Publicado 2016

Effect of the PPARG2 Pro12Ala Polymorphism on Associations of Physical Activity and Sedentary Time with Markers of Insulin Sensitivity in Those with an Elevated Risk of Type 2 Diab...

por Yates, Thomas, Davies, Melanie J., Henson, Joseph, Edwardson, Charlotte, Webb, David, Bodicoat, Danielle H., Webb, M’Balu, Howard, Philip, Cooper, Jackie A., Humphries, Steve E., Khunti, Kamlesh, Talmud, Philippa
Publicado 2015

Use of Allele-Specific FAIRE to Determine Functional Regulatory Polymorphism Using Large-Scale Genotyping Arrays

por Smith, Andrew J. P., Howard, Philip, Shah, Sonia, Eriksson, Per, Stender, Stefan, Giambartolomei, Claudia, Folkersen, Lasse, Tybjærg-Hansen, Anne, Kumari, Meena, Palmen, Jutta, Hingorani, Aroon D., Talmud, Philippa J., Humphries, Steve E.
Publicado 2012

The Impact of Focused Gene Ontology Curation of Specific Mammalian Systems

por Alam-Faruque, Yasmin, Huntley, Rachael P., Khodiyar, Varsha K., Camon, Evelyn B., Dimmer, Emily C., Sawford, Tony, Martin, Maria J., O'Donovan, Claire, Talmud, Philippa J., Scambler, Peter, Apweiler, Rolf, Lovering, Ruth C.
Publicado 2011

ANGPTL4 variants E40K and T266M are associated with lower fasting triglyceride levels in Non-Hispanic White Americans from the Look AHEAD Clinical Trial

por Smart-Halajko, Melissa C, Kelley-Hedgepeth, Alyson, Montefusco, Maria Claudia, Cooper, Jackie A, Kopin, Alan, McCaffrey, Jeanne M, Balasubramanyam, Ashok, Pownall, Henry J, Nathan, David M, Peter, Inga, Talmud, Philippa J, Huggins, Gordon S
Publicado 2011

Cholesteryl Ester Transfer Protein (CETP) Polymorphisms Affect mRNA Splicing, HDL Levels, and Sex-Dependent Cardiovascular Risk

por Papp, Audrey C., Pinsonneault, Julia K., Wang, Danxin, Newman, Leslie C., Gong, Yan, Johnson, Julie A., Pepine, Carl J., Kumari, Meena, Hingorani, Aroon D., Talmud, Philippa J., Shah, Sonia, Humphries, Steve E., Sadee, Wolfgang
Publicado 2012

Genetic variation within IL18 is associated with insulin levels, insulin resistance and postprandial measures()

por Smart, M.C., Dedoussis, G., Yiannakouris, N., Grisoni, M.L., Dror, G.K., Yannakoulia, M., Papoutsakis, C., Louizou, E., Mantzoros, C.S., Melistas, L., Kontogianni, M.D., Cooper, J.A., Humphries, S.E., Talmud, P.J.
Publicado 2011

IRS1 gene variants, dysglycaemic metabolic changes and type-2 diabetes risk

por Yiannakouris, N., Cooper, J.A., Shah, S., Drenos, F., Ireland, H.A., Stephens, J.W., Li, K.-W., Elkeles, R., Godsland, I.F., Kivimaki, M., Hingorani, A.D., Kumari, M., Talmud, P.J., Humphries, S.E.
Publicado 2012

Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies

por Talmud, P. J., Cooper, J. A., Gaunt, T., Holmes, M. V., Shah, S., Palmen, J., Drenos, F., Shah, T., Kumari, M., Kivimaki, M., Whittaker, J., Lawlor, D. A., Day, I. N., Hingorani, A. D., Casas, J. P., Humphries, S. E.
Publicado 2011

Association of TERC and OBFC1 Haplotypes with Mean Leukocyte Telomere Length and Risk for Coronary Heart Disease

por Maubaret, Cécilia G., Salpea, Klelia D., Romanoski, Casey E., Folkersen, Lasse, Cooper, Jackie A., Stephanou, Coralea, Wah Li, Ka, Palmen, Jutta, Hamsten, Anders, Neil, Andrew, Stephens, Jeffrey W., Lusis, Aldons J., Eriksson, Per, Talmud, Philippa J., Humphries, Steve E.
Publicado 2013

Association of a sequence variant in DAB2IP with coronary heart disease

por Harrison, Seamus C., Cooper, Jackie A., Li, Kawah, Talmud, Phillipa J., Sofat, Reecha, Stephens, Jeffery W., Hamsten, Anders, Sanders, Julie, Montgomery, Hugh, Neil, Andrew, Humphries, Steve E., Juhan-Vague, Irène, Margaglione, Maurizio, di Minno, Giovanni, Yudkin, John, Tremoli, Elena, Naoumova, Rossi, Thompson, Gil, Seed, Mary, Durrington, Paul, Miller, Paul, Betteridge, John
Publicado 2012

Marginal role for 53 common genetic variants in cardiovascular disease prediction

por Morris, Richard W, Cooper, Jackie A, Shah, Tina, Wong, Andrew, Drenos, Fotios, Engmann, Jorgen, McLachlan, Stela, Jefferis, Barbara, Dale, Caroline, Hardy, Rebecca, Kuh, Diana, Ben-Shlomo, Yoav, Wannamethee, S Goya, Whincup, Peter H, Casas, Juan-Pablo, Kivimaki, Mika, Kumari, Meena, Talmud, Philippa J, Price, Jacqueline F, Dudbridge, Frank, Hingorani, Aroon D, Humphries, Steve E
Publicado 2016

Improving Interpretation of Cardiac Phenotypes and Enhancing Discovery With Expanded Knowledge in the Gene Ontology

por Lovering, Ruth C., Roncaglia, Paola, Howe, Douglas G., Laulederkind, Stanley J.F., Khodiyar, Varsha K., Berardini, Tanya Z., Tweedie, Susan, Foulger, Rebecca E., Osumi-Sutherland, David, Campbell, Nancy H., Huntley, Rachael P., Talmud, Philippa J., Blake, Judith A., Breckenridge, Ross, Riley, Paul R., Lambiase, Pier D., Elliott, Perry M., Clapp, Lucie, Tinker, Andrew, Hill, David P.
Publicado 2018

D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile

por Valleix, Sophie, Verona, Guglielmo, Jourde-Chiche, Noémie, Nédelec, Brigitte, Mangione, P. Patrizia, Bridoux, Frank, Mangé, Alain, Dogan, Ahmet, Goujon, Jean-Michel, Lhomme, Marie, Dauteuille, Carolane, Chabert, Michèle, Porcari, Riccardo, Waudby, Christopher A., Relini, Annalisa, Talmud, Philippa J., Kovrov, Oleg, Olivecrona, Gunilla, Stoppini, Monica, Christodoulou, John, Hawkins, Philip N., Grateau, Gilles, Delpech, Marc, Kontush, Anatol, Gillmore, Julian D., Kalopissis, Athina D., Bellotti, Vittorio
Publicado 2016

A systematic review and meta-analysis of 130,000 individuals shows smoking does not modify the association of APOE genotype on risk of coronary heart disease

por Holmes, Michael V., Frikke-Schmidt, Ruth, Melis, Daniela, Luben, Robert, Asselbergs, Folkert W., Boer, Jolanda M.A., Cooper, Jackie, Palmen, Jutta, Horvat, Pia, Engmann, Jorgen, Li, Ka-Wah, Onland-Moret, N. Charlotte, Hofker, Marten H., Kumari, Meena, Keating, Brendan J., Hubacek, Jaroslav A., Adamkova, Vera, Kubinova, Ruzena, Bobak, Martin, Khaw, Kay-Tee, Nordestgaard, Børge G., Wareham, Nick, Humphries, Steve E., Langenberg, Claudia, Tybjaerg-Hansen, Anne, Talmud, Philippa J.
Publicado 2014