Search Results - "Sorli, J. V."

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    Association between the APOA2 promoter polymorphism and body weight in Mediterranean and Asian populations: replication of a gene–saturated fat interaction by Corella, D, Tai, E.S, Sorlí, J.V, Chew, S.K, Coltell, O, Sotos-Prieto, M, García-Rios, A, Estruch, R, Ordovas, J.M

    Published in International Journal of Obesity (01-05-2011)
    “…Objective: The APOA2 gene has been associated with obesity and insulin resistance (IR) in animal and human studies with controversial results. We have reported…”
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    Education modulates the association of the FTO rs9939609 polymorphism with body mass index and obesity risk in the Mediterranean population by Corella, D, Carrasco, P, Sorlí, J.V, Coltell, O, Ortega-Azorín, C, Guillén, M, González, J.I, Sáiz, C, Estruch, R, Ordovas, J.M

    “…Abstract Objective To define whether the rs9939609 FTO (fat mass and obesity associated) single nucleotide polymorphism (SNP) is associated with anthropometric…”
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    Non-targeted metabolomic biomarkers and metabotypes of type 2 diabetes: A cross-sectional study of PREDIMED trial participants by Urpi-Sarda, M., Almanza-Aguilera, E., Llorach, R., Vázquez-Fresno, R., Estruch, R., Corella, D., Sorli, J.V., Carmona, F., Sanchez-Pla, A., Salas-Salvadó, J., Andres-Lacueva, C.

    Published in Diabetes & metabolism (01-04-2019)
    “…To characterize the urinary metabolomic fingerprint and multi-metabolite signature associated with type 2 diabetes (T2D), and to classify the population into…”
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    Polymorphisms of the Renin-Angiotensin System Influence Height in Normotensive Women in a Spanish Population by Chaves, F. J., Corella, D., Sorli, J. V., Marin-Garcia, P., Guillen, M., Redon, J.

    “…The objective of this study was to analyze the influence of the polymorphisms G-6A of the angiotensinogen gene, insertion/deletion (I/D) of the…”
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    Genetic variation at the perilipin (PLIN) locus is associated with obesity-related phenotypes in White women by Qi, L, Corella, D, Sorlí, JV, Portolés, O, Shen, H, Coltell, O, Godoy, D, Greenberg, AS, Ordovas, JM

    Published in Clinical genetics (01-10-2004)
    “…Perilipin coats intracellular lipid droplets and modulates adipocyte lipolysis. We have evaluated the association between several polymorphisms at the…”
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    The 1258 G>A polymorphism in the neuropeptide Y gene is associated with greater alcohol consumption in a Mediterranean population by Francès, F, Guillen, M, Verdú, F, Portolés, O, Castelló, A, Sorlí, J.V, Corella, D

    Published in Alcohol (Fayetteville, N.Y.) (01-03-2011)
    “…Abstract Neuropeptide Y (NPY) is a neurotransmitter widely distributed in the central nervous system. Several studies have demonstrated that increases of NPY…”
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    Coffee and tea consumption in a high cardiovascular risk Mediterranean population by Sotos-Prieto, M, Carrasco, P, Sorlí, J V, Guillén, M, Guillém-Sáiz, P, Quiles, L, Corella, D

    “…Coffee and tea consumption recommendations for a healthy diet have been changing in recent years as it has increased the level of evidence on their benefits…”
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    Caffeinated coffee consumption and risk of atrial fibrillation in two Spanish cohorts by Bazal, P, Gea, A, Navarro, A M, Salas-Salvadó, J, Corella, D, Alonso-Gómez, A, Fitó, M, Muñoz-Bravo, C, Estruch, R, Fiol, M, Lapetra, J, Serra-Majem, L, Ros, E, Rekondo, J, Muñoz, M A, Basora, J, Sorlí, J V, Toledo, E, Martínez-González, M A, Ruiz-Canela, M

    Published in European journal of preventive cardiology (01-06-2021)
    “…Abstract Aims The association between caffeinated coffee consumption and atrial fibrillation remains unclear. Recent studies suggest an inverse association…”
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    PPAR-α L162V and PGC-1 G482S gene polymorphisms, but not PPAR-γ P12A, are associated with alcohol consumption in a Spanish Mediterranean population by Francès, F., Verdú, F., Portolés, O., Castelló, A., Sorlí, J.V., Guillen, M., Corella, D.

    Published in Clinica chimica acta (01-12-2008)
    “…Peroxisome Proliferator-Activated Receptors (PPARs) and its co-activators are regulatory elements of the cellular lipid homeostasis and have been associated…”
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    Register and clinical follow-up of patients with Peutz-Jeghers syndrome in Valencia by Rodríguez Lagos, F A, Sorlí Guerola, J V, Romero Martínez, I M, Codoñer Franch, P

    “…Peutz-Jeghers syndrome is a rare autosomal dominant inherited disease caused by a germline mutation of the STK11/LKB1 gene, located on chromosome 19p13.3. It…”
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    Gender specific associations of the Trp64Arg mutation in the beta3-adrenergic receptor gene with obesity-related phenotypes in a Mediterranean population: interaction with a common lipoprotein lipase gene variation by Corella, D, Guillén, M, Portolés, O, Sorlí, J V, Alonso, V, Folch, J, Sáiz, C

    Published in Journal of internal medicine (01-10-2001)
    “…To investigate the association between the Trp64Arg beta3-adrenergic receptor (ADRB3) mutation and obesity-related phenotypes in a Mediterranean Spanish…”
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