A community-based study of insomnia in Hong Kong Chinese children: Prevalence, risk factors and familial aggregation

Autor: Zhang, Jihui, Li, A.M., Kong, A.P.S., Lai, K.Y.C., Tang, N.L.S., Wing, Y.K.

Publikováno v: In Sleep Medicine 2009 10(9):1040-1046

RANTES G-401A polymorphism is associated with allergen sensitization and FEV1 in Chinese children

Autor: Leung, T.F. ^*, Tang, N.L.S., Lam, C.W.K., Li, A.M., Fung, S.L.M., Chan, I.H.S., Wong, G.W.K.

Publikováno v: In Respiratory Medicine February 2005 99(2):216-219

Assessment of the genetic and clinical determinants of fracture risk : genome wide association and mendelian randomisation study

Autor: Trajanoska, Katerina, Morris, John A., Oei, Ling, Zheng, Hou Feng, Evans, David M., Kiel, Douglas P., Ohlsson, Claes, Richards, J.B., Rivadeneira, Fernando, Forgett, V., Leong, A., Ahmad, O.S., Laurin, C., Mokry, L.E., Ross, S., Elks, C.E., Bowden, J., Warrington, N.M., Kleinman, A., Willems, S.M., Wright, D., Day, F.R., Murray, A., Ruth, K.S., Tsilidis, K.K., Ackert-Bicknell, C.L., Bassett, J.H.D., van der Eerden, B.C.J., Gautvik, K., Reppe, S., Williams, G.R., Medina-Gómez, C., Estrada, K., Amin, N., Enneman, A.W., Li, G., Liu, C.T., Liu, Y., Xiao, S.M., Lee, S.H., Koh, J.M., Tang, N.L.S., Cummings, S.R., Brown, M., de Groot, L., Jukema, J.W., Lips, P., van Meurs, J.B.J., Smith, A.V., Tian, S.

Publikováno v: British medical journal
BMJ. 2018 Aug 29;362:k3225
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
BMJ
BMJ (Online), 362
Skovsager Andersen, M, Frost, M & GEFOS/GENOMOS consortium and the 23andMe research team 2018, ' Assessment of the genetic and clinical determinants of fracture risk : genome wide association and mendelian randomisation study ', B M J, vol. 362, k3225 . https://doi.org/10.1136/bmj.k3225
Trajanoska, K, Morris, J A, Oei, L, Zheng, H-F, Evans, D M, Kiel, D P, Ohlsson, C, Richards, J B, Rivadeneira, F, GEFOS/GENOMOS consortium and the 23andMe research team & Langdahl, B L 2018, ' Assessment of the genetic and clinical determinants of fracture risk : genome wide association and mendelian randomisation study ', B M J, vol. 362, k3225 . https://doi.org/10.1136/bmj.k3225
The BMJ
Trajanoska, K, Morris, J A, Oei, L, Zheng, H F, Evans, D M, Kiel, D P, Ohlsson, C, Richards, J B, Rivadeneira, F, Forgett, V, Leong, A, Ahmad, O S, Laurin, C, Mokry, L E, Ross, S, Elks, C E, Bowden, J, Warrington, N M, Kleinman, A, Willems, S M, Wright, D, Day, F R, Murray, A, Ruth, K S, Tsilidis, K K, Ackert-Bicknell, C L, Bassett, J H D, van der Eerden, B C J, Gautvik, K, Reppe, S, Williams, G R, Medina-Gómez, C, Estrada, K, Amin, N, Bis, J C, Breda, S, Chasman, Demissie, S, Enneman, A W, Hsu, Y H, Ingvarsson, T, Kähönen, M, Kammerer, C, Moayyeri, A, Eriksson, J, Lee, S H, Christiansen, C, Brown, M & Duncan, E L & Spector, T D 2018, ' Assessment of the genetic and clinical determinants of fracture risk : Genome wide association and mendelian randomisation study ', The BMJ, vol. 362, k3225 . https://doi.org/10.1136/bmj.k3225
BMJ-British medical journal, 362:k3225. BMJ Publishing Group
BMJ (Online) 362 (2018)

OBJECTIVES: To identify the genetic determinants of fracture risk and assess the role of 15 clinical risk factors on osteoporotic fracture risk.
DESIGN: Meta-analysis of genome wide association studies (GWAS) and a two-sample mendelian randomisa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b4153e310e4e3f623a156fb95f602e1
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-151426

Total daily energy expenditure in wasted chronic obstructive pulmonary disease patients.

Autor: Tang, N.L.S., Chung, M.L., Elia, M., Hui, E., Lum, C.M., Luk, J.K.H., Jones, M.G., Woo, J.

Publikováno v: European Journal of Clinical Nutrition. Apr2002, Vol. 56 Issue 4, p282. 6p. 3 Charts.

Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci

Autor: Reppe, S. Wang, Y. Thompson, W.K. McEvoy, L.K. Schork, A.J. Zuber, V. LeBlanc, M. Bettella, F. Mills, I.G. Desikan, R.S. Djurovic, S. Gautvik, K.M. Dale, A.M. Andreassen, O.A. Estrada, K. Styrkarsdottir, U. Evangelou, E. Hsu, Y.-H. Duncan, E.L. Ntzani, E.E. Oei, L. Albagha, O.M.E. Amin, N. Kemp, J.P. Koller, D.L. Li, G. Liu, C.-T. Minster, R.L. Moayyeri, A. Vandenput, L. Willner, D. Xiao, S.-M. Yerges-Armstrong, L.M. Zheng, H.-F. Alonso, N. Eriksson, J. Kammerer, C.M. Kaptoge, S.K. Leo, P.J. Thorleifsson, G. Wilson, S.G. Wilson, J.F. Aalto, V. Alen, M. Aragaki, A.K. Aspelund, T. Center, J.R. Dailiana, Z. Duggan, D.J. Garcia, M. Garcia-Giralt, N. Giroux, S. Hallmans, G. Hocking, L.J. Husted, L.B. Jameson, K.A. Khusainova, R. Kim, G.S. Kooperberg, C. Koromila, T. Kruk, M. Laaksonen, M. Lacroix, A.Z. Lee, S.H. Leung, P.C. Lewis, J.R. Masi, L. Mencej-Bedrac, S. Nguyen, T.V. Nogues, X. Patel, M.S. Prezelj, J. Rose, L.M. Scollen, S. Siggeirsdottir, K. Smith, A.V. Svensson, O. Trompet, S. Trummer, O. Van Schoor, N.M. Woo, J. Zhu, K. Balcells, S. Brandi, M.L. Buckley, B.M. Cheng, S. Christiansen, C. Cooper, C. Dedoussis, G. Ford, I. Frost, M. Goltzman, D. González-Macías, J. Kähönen, M. Karlsson, M. Khusnutdinova, E. Koh, J.-M. Kollia, P. Langdahl, B.L. Leslie, W.D. Lips, P. Ljunggren, Ö. Lorenc, R.S. Marc, J. Mellström, D. Obermayer-Pietsch, B. Olmos, J.M. Pettersson-Kymmer, U. Reid, D.M. Riancho, J.A. Ridker, P.M. Rousseau, F. Slagboom, P.E. Tang, N.L.S. Urreizti, R. Van Hul, W. Viikari, J. Zarrabeitia, M.T. Aulchenko, Y.S. Castano-Betancourt, M. Grundberg, E. Herrera, L. Ingvarsson, T. Johannsdottir, H. Kwan, T. Li, R. Luben, R. Medina-Gómez, C. Palsson, S.Th. Rotter, J.I. Sigurdsson, G. Van Meurs, J.B.J. Verlaan, D. Williams, F.M.K. Wood, A.R. Zhou, Y. Pastinen, T. Raychaudhuri, S. Cauley, J.A. Chasman, D.I. Clark, G.R. Cummings, S.R. Danoy, P. Dennison, E.M. Eastell, R. Eisman, J.A. Gudnason, V. Hofman, A. Jackson, R.D. Jones, G. Jukema, J.W. Khaw, K.-T. Lehtimäki, T. Liu, Y. Lorentzon, M. McCloskey, E. Mitchell, B.D. Nandakumar, K. Nicholson, G.C. Oostra, B.A. Peacock, M. Pols, H.A.P. Prince, R.L. Raitakari, O. Reid, I.R. Robbins, J. Sambrook, P.N. Sham, P.C. Shuldiner, A.R. Tylavsky, F.A. Van Duijn, C.M. Wareham, N.J. Cupples, L.A. Econs, M.J. Evans, D.M. Harris, T.B. Kung, A.W.C. Psaty, B.M. Reeve, J. Spector, T.D. Streeten, E.A. Zillikens, M.C. Thorsteinsdottir, U. Ohlsson, C. Karasik, D. Richards, J.B. Brown, M.A. Stefansson, K. Uitterlinden, A.G. Ralston, S.H. Ioannidis, J.P.A. Kiel, D.P. Rivadeneira, F. GEFOS Consortium

Bone Mineral Density (BMD) is a highly heritable trait, but genome-wide association studies have identified few genetic risk factors. Epidemiological studies suggest associations between BMD and several traits and diseases, but the nature of the sugg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::5500e40958c884c9002d18428bc97e0e
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3056830