Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Richardson, T.G."'
Autor:
Porcu, E., Claringbould, A., Weihs, A., Lepik, K., Richardson, T.G., Völker, U., Santoni, F.A., Teumer, A., Franke, L., Reymond, A., Kutalik, Z.
Publikováno v:
Genome medicine, 14(1):89. BMC
Genome medicine, vol. 14, no. 1, pp. 89
Genome medicine, vol. 14, no. 1, pp. 89
Background: The genetic underpinning of sexual dimorphism is very poorly understood. The prevalence of many diseases differs between men and women, which could be in part caused by sex-specific genetic effects. Nevertheless, only a few published geno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d50252f71a9669906563cc0ae801d151
https://pubmed.ncbi.nlm.nih.gov/35953856
https://pubmed.ncbi.nlm.nih.gov/35953856
Autor:
Harris, S.E., Corley, J., Wojczynski, M.K., Nauck, M., Levy, D., Gu, C., Sorensen, T.I.A., Noordam, R., Guo, X., Hill, W.D., Chen, Y.-D.I., Liu, C., Yao, J., Kraja, A.T., Daw, E.W., Irvin, M.R., Christensen, C., Newman, A.B., Hansen, T., Hudson, G., Zeng, D., Wu, H., Uitterlinden, A.G., Wareham, N.J., Perls, T.T., Grarup, N., Broeckel, U., Luan, J., Fu, M., Hemani, G., de Mutsert, R., Lin, S.J., Wilson, J.G., Jorgensen, M.E., Witte, D.R., Have, C.T., Ribel-Madsen, R., Wang, Y., Love-Gregory, L.D., Bowden, D.W., Province, M.A., Rotter, J.I., Taylor, A.M., Hunt, S.C., Thyagarajan, B., Goodarzi, M.O., Ridker, P.M., Torp-Pedersen, C., Ligthart, S., Starr, J.M., Feitosa, M.F., Arnett, D.K., de Haan, H.G., Jorgensen, T., Weeke, P.E., Graff, M., de las Fuentes, L., Justice, A.E., Hayward, C., Kerrison, N.D., Pedersen, O., Bonnelykke, K., Perry, J.A., Fetterman, J.L., Hai, Y., Malik, A.N., Vestergaard, H., Cropp, C.D., Ryan, K.A., Christensen, K., The Population Sciences Branch, NHLBI/NIH, Armasu, S.M., Langenberg, C., Forouhi, N.G., Yang, W., Teumer, A., Rodriguez, S., Kardia, S.L.R., Qi, Q., Becker, D.M., Baranski, T.J., Yanek, L.R., Rao, D.C., Fernandez, E.P., Lin, K.-H., Li-Gao, R., Sofer, T., Nohr, E.A., Larson, N.B., Sheu, W.H.-H., Elliott, P., An, P., Schnurr, T.M., Gu, Z., Taylor, K.D., Davies, G., Kilpelainen, T.O., Lee, W.-J., Patki, A., Barve, R.A., Brandslund, I., Sandow, K., Weiss, S., Wang, L., Stergiakouli, E., Mathias, R.A., Ghanbari, M., Tiwari, H.K., Rivadeneira, F., Davila-Roman, V.G., de Andrade, M., North, K.E., Richardson, T.G., Horta, B.L., Bielinski, S.J., Linneberg, A., Young, K., Argos, M., Dehghan, A., Chasman, D.I., Mook-Kanamori, D.O., Vaidya, D., Petersmann, A., Scott, R.A., Meigs, J.B., Ahluwalia, T.S., Gao, H., Rosendaal, F.R., Chakravarti, A., van Heemst, D., Cox, S.R., Williams, C., Pankow, J., Giulianini, F., Weir, B.S., Jonsson, A.E., Hartwig, F.P., Rohde, R., Ikram, M.A., Homuth, G., Lee, J.H., Deary, I.J., Erzurumluoglu, A.M., Chu, A.Y., Emery, L.S., Franco, O.H., Ong, K.K., Arking, D.E., Loos, R.J.F., Tzoulaki, I., Pattie, A., Timpson, N.J., Turner, S.T.
Mitochondria (MT), the major site of cellular energy production, are under dual genetic control by 37 mitochondrial DNA (mtDNA) genes and numerous nuclear genes (MT-nDNA). In the CHARGEmtDNA+ Consortium, we studied genetic associations of mtDNA and M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6df8acf77c79d7e455f9a9e396af51ad
Autor:
Richardson, T.G., Minica, C.C., Heron, J., Tavare, J., MacKenzie, A., Day, I., Lewis, G., Hickman, M., Vink, J.M., Gelernter, J., Kranzler, H.R., Farrer, L.A., Munafò, M., Wynick, D.
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 165(8), 654-664. Wiley-Liss Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Richardson, T G, Minica, C C, Heron, J, Tavare, J, MacKenzie, A, Day, I, Lewis, G, Hickman, M, Vink, J M, Gelernter, J, Kranzler, H R, Farrer, L A, Munafò, M & Wynick, D 2014, ' Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 165, no. 8, pp. 654-664 . https://doi.org/10.1002/ajmg.b.32270
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Richardson, T G, Minica, C C, Heron, J, Tavare, J, MacKenzie, A, Day, I, Lewis, G, Hickman, M, Vink, J M, Gelernter, J, Kranzler, H R, Farrer, L A, Munafò, M & Wynick, D 2014, ' Evaluating the role of a galanin enhancer genotype on a range of metabolic, depressive and addictive phenotypes ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 165, no. 8, pp. 654-664 . https://doi.org/10.1002/ajmg.b.32270
There is a large body of pre-clinical and some clinical data to link the neuropeptide galanin to a range of physiological and pathological functions that include metabolism, depression, and addiction. An enhancer region upstream of the human GAL tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1f87016766918b4fd416836e247419ed
https://research.vu.nl/en/publications/d86bc806-d289-482e-803c-a8179ed00e30
https://research.vu.nl/en/publications/d86bc806-d289-482e-803c-a8179ed00e30