Common genetic variation in obesity, lipid transfer genes and risk of Metabolic Syndrome: Results from IDEFICS/I.Family study and meta-analysis.

Nagrani, Rajini; Foraita, Ronja; Gianfagna, Francesco; Iacoviello, Licia; Marild, Staffan; Michels, Nathalie; Molnár, Dénes; Moreno, Luis; Russo, Paola; Veidebaum, Toomas; Ahrens, Wolfgang; Marron, Manuela

Nagrani, Rajini; Foraita, Ronja; Gianfagna, Francesco; Iacoviello, Licia; Marild, Staffan; Michels, Nathalie; Molnár, Dénes; Moreno, Luis; Russo, Paola; Veidebaum, Toomas; Ahrens, Wolfgang; Marron, Manuela.

Afiliación

Nagrani R; Leibniz Institute for Prevention Research and Epidemiology - BIPS, Bremen, Germany. rajni.nagrani@gmail.com.
Foraita R; Leibniz Institute for Prevention Research and Epidemiology - BIPS, Bremen, Germany.
Gianfagna F; Mediterranea Cardiocentro, Napoli, Italy.
Iacoviello L; EPIMED Research Center, Department of Medicine and Surgery, University of Insubria, Varese, Italy.
Marild S; IRCCS Istituto Neurologico Mediterraneo Neuromed, Pozzilli, Italy.
Michels N; Department of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Molnár D; Department of Public Health and Primary Care, Ghent University, 9000, Ghent, Belgium.
Moreno L; Department of Paediatrics, Medical School, University of Pécs, Pécs, Hungary.
Russo P; GENUD (Growth, Exercise, Nutrition, and Development) Research Group, University of Zaragoza, Zaragoza, Spain.
Veidebaum T; Institute of Food Sciences, National Research Council, Avellino, Italy.
Ahrens W; National Institute for Health Development, Tallinn, Estonia.
Marron M; Leibniz Institute for Prevention Research and Epidemiology - BIPS, Bremen, Germany.

Sci Rep ; 10(1): 7189, 2020 04 28.

Article en En | MEDLINE | ID: mdl-32346024

Asunto(s)

Dioxigenasa FTO Dependiente de Alfa-Cetoglutarato/genética; Proteínas de Transferencia de Ésteres de Colesterol/genética; Cromosomas Humanos Par 16/genética; Síndrome Metabólico/genética; Obesidad Infantil/genética; Polimorfismo de Nucleótido Simple; Adulto; Niño; Preescolar; Familia; Femenino; Humanos; Masculino; Factores de Riesgo

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 16 / Polimorfismo de Nucleótido Simple / Síndrome Metabólico / Proteínas de Transferencia de Ésteres de Colesterol / Obesidad Infantil / Dioxigenasa FTO Dependiente de Alfa-Cetoglutarato Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Sci Rep Año: 2020 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido

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