يعرض 1 - 10 نتائج من 38 نتيجة بحث عن '"Chen, Y.D.I."', وقت الاستعلام: 2.10s تنقيح النتائج
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    المساهمون: Butterworth, Adam [0000-0002-6915-9015], Howson, Joanna [0000-0001-7618-0050], Chowdhury, Rajiv [0000-0003-4881-5690], Surendran, Praveen [0000-0002-4911-6077], Di Angelantonio, Emanuele [0000-0001-8776-6719], Danesh, John [0000-0003-1158-6791], Apollo - University of Cambridge Repository

    المصدر: Nature Genetics, 49(10), 1450
    Nature genetics
    Nature genetics, vol 49, iss 10

    مصطلحات موضوعية: 0301 basic medicine, endocrine system diseases, EPIC-Interact Consortium, Genome-wide association study, Coronary Disease, Type 2 diabetes, ACID-BINDING PROTEIN, Comorbidity, 030204 cardiovascular system & hematology, VARIANTS, Cardiovascular, Bioinformatics, Medical and Health Sciences, 0302 clinical medicine, Risk Factors, 2.1 Biological and endogenous factors, ARTERY-DISEASE, Molecular Targeted Therapy, Aetiology, health care economics and organizations, 11 Medical and Health Sciences, Genetics & Heredity, RISK, Metabolic Syndrome, 0303 health sciences, CHD Exome+ Consortium, Diabetes, Single Nucleotide, Biological Sciences, 3. Good health, Europe, Heart Disease, MENDELIAN RANDOMIZATION, Medical genetics, Life Sciences & Biomedicine, Type 2, Metabolic Networks and Pathways, Asian Continental Ancestry Group, medicine.medical_specialty, endocrine system, Asia, education, European Continental Ancestry Group, Mutation, Missense, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, White People, EPIC-CVD Consortium, GENETIC ARCHITECTURE, 03 medical and health sciences, Asian People, Clinical Research, Mendelian randomization, Diabetes Mellitus, Genetics, Genetic predisposition, medicine, Humans, Genetic Predisposition to Disease, Obesity, Genetic variability, cardiovascular diseases, Polymorphism, GENOME-WIDE ASSOCIATION, Heart Disease - Coronary Heart Disease, Metabolic and endocrine, METAANALYSIS, AP2, 030304 developmental biology, Science & Technology, Human Genome, nutritional and metabolic diseases, Odds ratio, 06 Biological Sciences, medicine.disease, HLA-DRB5 Chains, Michigan Biobank, 030104 developmental biology, ATHEROSCLEROSIS, Diabetes Mellitus, Type 2, Genetic Loci, Mutation, Missense, human activities, Biomarkers, Genome-Wide Association Study, Developmental Biology

    وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

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    المصدر: Aging Cell, 16(4), 898-898

    وصف الملف: application/pdf

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    المؤلفون: Wain, L.V., Verwoert, G.C., O'Reilly, P.F., Shi, G., Johnson, T., Johnson, A.D., Bochud, M., Rice, K.M., Henneman, P., Smith, A.V., Ehret, G.B., Amin, N., Larson, M.G., Mooser, V., Hadley, D., Dorr, M., Bis, J.C., Aspelund, T., Esko, T., Janssens, A.C.J.W., Zhao, J.H., Heath, S., Laan, M., Fu, J.Y., Pistis, G., Luan, J.A., Arora, P., Lucas, G., Pirastu, N., Pichler, I., Jackson, A.U., Webster, R.J., Zhang, F., Peden, J.F., Schmidt, H., Tanaka, T., Campbell, H., Igl, W., Milaneschi, Y., Hottenga, J.J., Vitart, V., Chasman, D.I., Trompet, S., Bragg-Gresham, J.L., Alizadeh, B.Z., Chambers, J.C., Guo, X.Q., Lehtimaki, T., Kuhnel, B., Lopez, L.M., Polasek, O., Boban, M., Nelson, C.P., Morrison, A.C., Pihur, V., Ganesh, S.K., Hofman, A., Kundu, S., Mattace-Raso, F.U.S., Rivadeneira, F., Sijbrands, E.J.G., Uitterlinden, A.G., Hwang, S.J., Vasan, R.S., Wang, T.J., Bergmann, S., Vollenweider, P., Waeber, G., Laitinen, J., Pouta, A., Zitting, P., McArdle, W.L., Kroemer, H.K., Volker, U., Volzke, H., Glazer, N.L., Taylor, K.D., Harris, T.B., Alavere, H., Haller, T., Keis, A., Tammesoo, M.L., Aulchenko, Y., Barroso, I., Khaw, K.T., Galan, P., Hercberg, S., Lathrop, M., Eyheramendy, S., Org, E., Sober, S., Lu, X.W., Nolte, I.M., Penninx, B.W., Corre, T., Masciullo, C., Sala, C., Groop, L., Voight, B.F., Melander, O., O'Donnell, C.J., Salomaa, V., d'Adamo, A.P., Fabretto, A., Faletra, F., Ulivi, S., Greco, M.F. del, Facheris, M., Collins, F.S., Bergman, R.N., Beilby, J.P., Hung, J., Musk, A.W., Mangino, M., Shin, S.Y., Soranzo, N., Watkins, H., Goel, A., Hamsten, A., Gider, P., Loitfelder, M., Zeginigg, M., Hernandez, D., Najjar, S.S., Navarro, P., Wild, S.H., Corsi, A.M., Singleton, A., Geus, E.J.C. de, Willemsen, G., Parker, A.N., Rose, L.M., Buckley, B., Stott, D., Orru, M., Uda, M., Klauw, M.M. van der, Zhang, W.H., Li, X.Z., Scott, J., Chen, Y.D.I., Burke, G.L., Kahonen, M., Viikari, J., Doring, A., Meitinger, T., Davies, G., Starr, J.M., Emilsson, V., Plump, A., Lindeman, J.H., Hoen, P.A.C. 't, Konig, I.R., Felix, J.F., Clarke, R., Hopewell, J.C., Ongen, H., Breteler, M., Debette, S., DeStefano, A.L., Fornage, M., Mitchell, G.F., Smith, N.L., Holm, H., Stefansson, K., Thorleifsson, G., Thorsteinsdottir, U., Samani, N.J., Preuss, M., Rudan, I., Hayward, C., Deary, I.J., Wichmann, H.E., Raitakari, O.T., Palmas, W., Kooner, J.S., Stolk, R.P., Jukema, J.W., Wright, A.F., Boomsma, D.I., Bandinelli, S., Gyllensten, U.B., Wilson, J.F., Ferrucci, L., Schmidt, R., Farrall, M., Spector, T.D., Palmer, L.J., Tuomilehto, J., Pfeufer, A., Gasparini, P., Siscovick, D., Altshuler, D., Loos, R.J.F., Toniolo, D., Snieder, H., Gieger, C., Meneton, P., Wareham, N.J., Oostra, B.A., Metspalu, A., Launer, L., Rettig, R., Strachan, D.P., Beckmann, J.S., Witteman, J.C.M., Erdmann, J., Dijk, K.W. van, Boerwinkle, E., Boehnke, M., Ridker, P.M., Jarvelin, M.R., Chakravarti, A., Abecasis, G.R., Gudnason, V., Newton-Cheh, C., Levy, D., Munroe, P.B., Psaty, B.M., Caulfield, M.J., Rao, D.C., Tobin, M.D., Elliott, P., Duijn, C.M. van, LifeLines Cohort Study, EchoGen Consortium, AortaGen Consortium, CHARGE Consortium Heart Failure, KidneyGen Consortium, CKDGen Consortium, Cardiogenics Consortium, CardioGram

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