المؤلفون: Gallagher, CS, Mäkinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Järvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR, Hinds, DA, Tung, JY, 23andMe Research Team, Perry, JRB, Lind, PA, Painter, JN, Martin, NG, Morris, AP, Chasman, DI, Missmer, SA, Zondervan, KT, Morton, CC

مصطلحات موضوعية: Adult, Ataxia Telangiectasia Mutated Proteins, Endometriosis, Female, Forkhead Box Protein O1, Genome-Wide Association Study, Humans, Leiomyoma, Mendelian Randomization Analysis, Menorrhagia, Middle Aged, Polymorphism, Single Nucleotide, Proportional Hazards Models, Receptor, Fibroblast Growth Factor, Type 4, Signal Transduction, Telomerase, Uterine Neoplasms, White People

وصف الملف: Electronic; application/pdf

العلاقة: https://www.repository.cam.ac.uk/handle/1810/298690Test

الإتاحة: https://doi.org/10.17863/CAM.45747Test
https://www.repository.cam.ac.uk/handle/1810/298690Test

المؤلفون: Gallagher, CS, Makinen, N, Harris, HR, Rahmioglu, N, Uimari, O, Cook, JP, Shigesi, N, Ferreira, T, Velez-Edwards, DR, Edwards, TL, Mortlock, S, Ruhioglu, Z, Day, F, Becker, CM, Karhunen, V, Martikainen, H, Jarvelin, M-R, Cantor, RM, Ridker, PM, Terry, KL, Buring, JE, Gordon, SD, Medland, SE, Montgomery, GW, Nyholt, DR, Hinds, DA, Tung, JY, Perry, JRB, Lind, PA, Painter, JN, Martin, NG, Morris, AP, Chasman, DI, Missmer, SA, Zondervan, KT, Morton, CC, Agee, M, Alipanahi, B, Auton, A, Bell, RK, Bryc, K, Elson, SL, Fontanillas, P, Furlotte, NA, Huber, KE, Kleinman, A, Litterman, NK, McIntyre, MH, Mountain, JL, Noblin, ES, Northover, CAM, Pitts, SJ, Sathirapongsasuti, JF, Sazonova, OV, Shelton, JF, Shringarpure, S, Tian, C, Vacic, V, Wilson, CH

المساهمون: UNIVERSITY OF OULU

المصدر: 11 ; 1

مصطلحات موضوعية: Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, CANCER SUSCEPTIBILITY LOCI, TRANSCRIPTION FACTOR FKHR, RISK-FACTORS, EXPRESSION, FOXO1, METAANALYSIS, MECHANISM, VARIANTS, GROWTH, CELLS, Adult, Ataxia Telangiectasia Mutated Proteins, Endometriosis, European Continental Ancestry Group, Female, Forkhead Box Protein O1, Genome-Wide Association Study, Humans, Leiomyoma, Mendelian Randomization Analysis, Menorrhagia, Middle Aged, Polymorphism, Single Nucleotide, Proportional Hazards Models, Receptor, Fibroblast Growth Factor

العلاقة: Nature Communications; http://hdl.handle.net/10044/1/85467Test; Nil

الإتاحة: https://doi.org/10.1038/s41467-019-12536-4Test
http://hdl.handle.net/10044/1/85467Test

المؤلفون: Chambers, J.C., Zhang, W., Sehmi, J., Li, X., Wass, M.N., Van der Harst, P., Holm, H., Sanna, S., Kavousi, M., Baumeister, S.E., Coin, L.J., Deng, G., Gieger, C., Heard-Costa, N.L., Hottenga, J.J., Kühnel, B., Kumar, V., Lagou, V., Liang, L., Luan, J., Vidal, P.M., Mateo Leach, I., O'Reilly, P.F., Peden, J.F., Rahmioglu, N., Soininen, P., Speliotes, E.K., Yuan, X., Thorleifsson, G., Alizadeh, B.Z., Atwood, L.D., Borecki, I.B., Brown, M.J., Charoen, P., Cucca, F., Das, D., de Geus, E.J., Dixon, A.L., Döring, A., Ehret, G., Eyjolfsson, G.I., Farrall, M., Forouhi, N.G., Friedrich, N., Goessling, W., Gudbjartsson, D.F., Harris, T.B., Hartikainen, A.L., Heath, S., Hirschfield, G.M., Hofman, A., Homuth, G., Hyppönen, E., Janssen, H.L., Johnson, T., Kangas, A.J., Kema, I.P., Kühn, J.P., Lai, S., Lathrop, M., Lerch, M.M., Li, Y., Liang, T.J., Lin, J.P., Loos, R.J., Martin, N.G., Moffatt, M.F., Montgomery, G.W., Munroe, P.B., Musunuru, K., Nakamura, Y., O'Donnell, C.J., Olafsson, I., Penninx, B.W., Pouta, A., Prins, B.P., Prokopenko, I., Puls, R., Ruokonen, A., Savolainen, M.J., Schlessinger, D., Schouten, J.N., Seedorf, U., Sen-Chowdhry, S., Siminovitch, K.A., Smit, J.H., Spector, T.D., Tan, W., Teslovich, T.M., Tukiainen, T., Uitterlinden, A.G., Van der Klauw, M.M., Vasan, R.S., Wallace, C., Wallaschofski, H., Wichmann, H.E., Willemsen, G., Würtz, P., Xu, C., Yerges-Armstrong, L.M., Abecasis, G.R., Ahmadi, K.R., Boomsma, D.I., Caulfield, M., Cookson, W.O., van Duijn, C.M., Froguel, P., Matsuda, K., McCarthy, M.I., Meisinger, C., Mooser, V., Pietiläinen, K.H., Schumann, G., Snieder, H., Sternberg, M.J., Stolk, R.P., Thomas, H.C., Thorsteinsdottir, U., Uda, M., Waeber, G., Wareham, N.J., Waterworth, D.M., Watkins, H., Whitfield, J.B., Witteman, J.C., Wolffenbuttel, B.H., Fox, C.S., Ala-Korpela, M., Stefansson, K., Vollenweider, P., Völzke, H., Schadt, E.E., Scott, J., Järvelin, M.R., Elliott, P., Kooner, J.S.

المساهمون: Alcohol Genome-wide Association (AlcGen) Consortium, Diabetes Genetics Replication and Meta-analyses (DIAGRAM+) Study, Genetic Investigation of Anthropometric Traits (GIANT) Consortium, Global Lipids Genetics Consortium, Genetics of Liver Disease (GOLD) Consortium, International Consortium for Blood Pressure (ICBP-GWAS), Meta-analyses of Glucose and Insulin-Related Traits Consortium (MAGIC), Voight, B.F., Scott, L.J., Steinthorsdottir, V., Morris, A.P., Dina, C., Welch, R.P., Zeggini, E., Huth, C., Aulchenko, Y.S., Thorleifsson, G., McCulloch, L.J., Ferreira, T., Grallert, H., Amin, N., Wu, G., Willer, C.J., Raychaudhuri, S., McCarroll, S.A., Langenberg, C., Hofmann, O.M., Dupuis, J., Qi, L., Segrè, A.V., van Hoek, M., Navarro, P., Ardlie, K., Balkau, B., Benediktsson, R., Bennett, A.J., Blagieva, R., Boerwinkle, E., Bonnycastle, L.L., Bengtsson Boström, K., Bravenboer, B., Bumpstead, S., Burtt, N.P., Charpentier, G., Chines, P.S., Cornelis, M., Couper, D.J., Crawford, G., Doney, A.S., Elliott, K.S., Elliott, A.L., Erdos, M.R., Fox, C.S., Franklin, C.S., Ganser, M., Gieger, C., Grarup, N., Green, T., Griffin, S., Groves, C.J., Guiducci, C., Hadjadj, S., Hassanali, N., Herder, C., Isomaa, B., Jackson, A.U., Johnson, P.R., Jørgensen, T., Kao, W.H., Klopp, N., Kong, A., Kraft, P., Kuusisto, J., Lauritzen, T., Li, M., Lieverse, A., Lindgren, C.M., Lyssenko, V., Marre, M., Meitinger, T., Midthjell, K., Morken, M.A., Narisu, N., Nilsson, P., Owen, K.R., Payne, F., Perry, J.R., Petersen, A.K., Platou, C., Proença, C., Prokopenko, I., Rathmann, W., William Rayner, N., Robertson, N.R., Rocheleau, G., Roden, M., Sampson, M.J., Saxena, R., Shields, B.M., Shrader, P.

المصدر: Nature genetics, vol. 43, no. 11, pp. 1131-1138

مصطلحات موضوعية: Enzymes/blood, Enzymes/genetics, Genome-Wide Association Study, Humans, Liver/enzymology, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/22001757; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; https://serval.unil.ch/notice/serval:BIB_C64416CF49EETest; urn:issn:1061-4036; https://serval.unil.ch/resource/serval:BIB_C64416CF49EE.P001/REF.pdfTest

الإتاحة: https://doi.org/10.1038/ng.970Test
https://serval.unil.ch/notice/serval:BIB_C64416CF49EETest
https://serval.unil.ch/resource/serval:BIB_C64416CF49EE.P001/REF.pdfTest