检索结果 - Giegling, I

The human metabolic profile reflects macro- and micronutrient intake distinctly according to fasting time 由 Sedlmeier, A., Kluttig, A., Giegling, I., Prehn, C., Adamski, J., Kastenmüller, G., Lacruz, M. E.

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Association of VSNL1 with schizophrenia, frontal cortical function, and biological significance for its gene product as a modulator of cAMP levels and neuronal morphology 由 Braunewell, K H, Dwary, A D, Richter, F, Trappe, K, Zhao, C, Giegling, I, Schönrath, K, Rujescu, D

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Elevated cytokine expression in the orbitofrontal cortex of victims of suicide 由 Tonelli, L. H., Stiller, J., Rujescu, D., Giegling, I., Schneider, B., Maurer, K., Schnabel, A., Möller, H.-J., Chen, H. H., Postolache, T. T.

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Instability of personal human metabotype is linked to all-cause mortality 由 Lacruz, M. E., Kluttig, A., Tiller, D., Medenwald, D., Giegling, I., Rujescu, D., Prehn, C., Adamski, J., Greiser, K. H., Kastenmüller, G.

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Schizophrenia shows a unique metabolomics signature in plasma 由 He, Y, Yu, Z, Giegling, I, Xie, L, Hartmann, A M, Prehn, C, Adamski, J, Kahn, R, Li, Y, Illig, T, Wang-Sattler, R, Rujescu, D

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Steroid sulfatase is a potential modifier of cognition in attention deficit hyperactivity disorder 由 Stergiakouli, E, Langley, K, Williams, H, Walters, J, Williams, N M, Suren, S, Giegling, I, Wilkinson, L S, Owen, M J, O'Donovan, M C, Rujescu, D, Thapar, A, Davies, W

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Expression analysis in a rat psychosis model identifies novel candidate genes validated in a large case–control sample of schizophrenia 由 Ingason, A, Giegling, I, Hartmann, A M, Genius, J, Konte, B, Friedl, M, Ripke, S, Sullivan, P F, St. Clair, D, Collier, D A, O'Donovan, M C, Mirnics, K, Rujescu, D

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Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets 由 Degenhardt, F, Priebe, L, Meier, S, Lennertz, L, Streit, F, Witt, S H, Hofmann, A, Becker, T, Mössner, R, Maier, W, Nenadic, I, Sauer, H, Mattheisen, M, Buizer-Voskamp, J, Ophoff, R A, Rujescu, D, Giegling, I, Ingason, A, Wagner, M, Delobel, B, Andrieux, J, Meyer-Lindenberg, A, Heinz, A, Walter, H, Moebus, S, Corvin, A, Rietschel, M, Nöthen, M M, Cichon, S

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia 由 Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia 由 Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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Erratum: Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia 由 Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking 由 Terracciano, A, Esko, T, Sutin, A R, de Moor, M H M, Meirelles, O, Zhu, G, Tanaka, T, Giegling, I, Nutile, T, Realo, A, Allik, J, Hansell, N K, Wright, M J, Montgomery, G W, Willemsen, G, Hottenga, J-J, Friedl, M, Ruggiero, D, Sorice, R, Sanna, S, Cannas, A, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Cucca, F, Krueger, R F, Lahti, J, Luciano, M, Smoller, J W, van Duijn, C M, Abecasis, G R, Boomsma, D I, Ciullo, M, Costa, P T, Ferrucci, L, Martin, N G, Metspalu, A, Rujescu, D, Schlessinger, D, Uda, M

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia 由 Ingason, A, Rujescu, D, Cichon, S, Sigurdsson, E, Sigmundsson, T, Pietiläinen, OPH, Buizer-Voskamp, JE, Strengman, E, Francks, C, Muglia, P, Gylfason, A, Gustafsson, O, Olason, PI, Steinberg, S, Hansen, T, Jakobsen, KD, Rasmussen, HB, Giegling, I, Möller, H-J, Hartmann, A, Crombie, C, Fraser, G, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Bramon, E, Kiemeney, LA, Franke, B, Murray, R, Vassos, E, Toulopoulou, T, Mühleisen, TW, Tosato, S, Ruggeri, M, Djurovic, S, Andreassen, OA, Zhang, Z, Werge, T, Ophoff, RA, Rietschel, M, Nöthen, MM, Petursson, H, Stefansson, H, Peltonen, L, Collier, D, Stefansson, K, St Clair, DM

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Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 (FGFR2) 由 O’Donovan, M.C., Norton, N., Williams, H., Peirce, T., Moskvina, V., Nikolov, I., Hamshere, M., Carroll, L., Georgieva, L., Dwyer, S, Holmans, P., Marchini, J. L., Spencer, C.C.A., Howie, B., Leung, H-T., Giegling, I., Hartmann, A.M., Möller, H.-J., Morris, D.W., Shi, Y., Feng, G., Hoffmann, P., Propping, P., Vasilescu, C., Maier, W., Rietschel, M., Zammit, S., Schumacher, J., Quinn, E.M., Schulze, T.G., Iwata, N., Ikeda, M., Darvasi, A., Shifman, S., He, L., Duan, J., Sanders, A.R., Levinson, D.F., Adolfsson, R., Ösby, U., Terenius, Lars, Jönsson, Erik G, Cichon, S., Nöthen, M. M., Gill, M., Corvin, A.P., Rujescu, D., Gejman, P.V., Kirov, G., Craddock, N., Williams, N.M., Owen, M.J.

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia 由 Chen, X, Lee, G, Maher, BS, Fanous, AH, Chen, J, Zhao, Z, Guo, A, van den Oord, E, Sullivan, PF, Shi, J, Levinson, DF, Gejman, PV, Sanders, A, Duan, J, Owen, MJ, Craddock, NJ, O’Donovan, MC, Blackman, J, Lewis, D, Kirov, GK, Qin, W, Schwab, S, Wildenauer, D, Chowdari, K, Nimgaonkar, V, Straub, RE, Weinberger, DR, O’Neill, FA, Walsh, D, Bronstein, M, Darvasi, A, Lencz, T, Malhotra, AK, Rujescu, D, Giegling, I, Werge, T, Hansen, T, Ingason, A, Nöethen, MM, Rietschel, M, Cichon, S, Djurovic, S, Andreassen, OA, Cantor, RM, Ophoff, R, Corvin, A, Morris, DW, Gill, M, Pato, CN, Pato, MT, Macedo, A, Gurling, HMD, McQuillin, A, Pimm, J, Hultman, C, Lichtenstein, P, Sklar, P, Purcell, SM, Scolnick, E, St Clair, D, Blackwood, DHR, Kendler, KS

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Expanding the range of ZNF804A variants conferring risk of psychosis 由 Steinberg, S, Mors, O, Børglum, AD, Gustafsson, O, Werge, T, Mortensen, PB, Andreassen, OA, Sigurdsson, E, Thorgeirsson, TE, Böttcher, Y, Olason, P, Ophoff, RA, Cichon, S, Gudjonsdottir, IH, Pietiläinen, OPH, Nyegaard, M, Tuulio-Henriksson, A, Ingason, A, Hansen, T, Athanasiu, L, Suvisaari, J, Lonnqvist, J, Paunio, T, Hartmann, A, Jürgens, G, Nordentoft, M, Hougaard, D, Norgaard-Pedersen, B, Breuer, R, Möller, H-J, Giegling, I, Glenthøj, B, Rasmussen, HB, Mattheisen, M, Bitter, I, Réthelyi, JM, Sigmundsson, T, Fossdal, R, Thorsteinsdottir, U, Ruggeri, M, Tosato, S, Strengman, E, Kiemeney, LA, Melle, I, Djurovic, S, Abramova, L, Kaleda, V, Walshe, M, Bramon, E, Vassos, E, Li, T, Fraser, G, Walker, N, Toulopoulou, T, Yoon, J, Freimer, NB, Cantor, RM, Murray, R, Kong, A, Golimbet, V, Jönsson, EG, Terenius, L, Agartz, I, Petursson, H, Nöthen, MM, Rietschel, M, Peltonen, L, Rujescu, D, Collier, DA, Stefansson, H, St Clair, D, Stefansson, K

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GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium 由 Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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Erratum: GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium 由 Trampush, J W, Yang, M L Z, Yu, J, Knowles, E, Davies, G, Liewald, D C, Starr, J M, Djurovic, S, Melle, I, Sundet, K, Christoforou, A, Reinvang, I, DeRosse, P, Lundervold, A J, Steen, V M, Espeseth, T, Räikkönen, K, Widen, E, Palotie, A, Eriksson, J G, Giegling, I, Konte, B, Roussos, P, Giakoumaki, S, Burdick, K E, Payton, A, Ollier, W, Horan, M, Chiba-Falek, O, Attix, D K, Need, A C, Cirulli, E T, Voineskos, A N, Stefanis, N C, Avramopoulos, D, Hatzimanolis, A, Arking, D E, Smyrnis, N, Bilder, R M, Freimer, N A, Cannon, T D, London, E, Poldrack, R A, Sabb, F W, Congdon, E, Conley, E D, Scult, M A, Dickinson, D, Straub, R E, Donohoe, G, Morris, D, Corvin, A, Gill, M, Hariri, A R, Weinberger, D R, Pendleton, N, Bitsios, P, Rujescu, D, Lahti, J, Le Hellard, S, Keller, M C, Andreassen, O A, Deary, I J, Glahn, D C, Malhotra, A K, Lencz, T

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Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia 由 Witt, S H, Streit, F, Jungkunz, M, Frank, J, Awasthi, S, Reinbold, C S, Treutlein, J, Degenhardt, F, Forstner, A J, Heilmann-Heimbach, S, Dietl, L, Schwarze, C E, Schendel, D, Strohmaier, J, Abdellaoui, A, Adolfsson, R, Air, T M, Akil, H, Alda, M, Alliey-Rodriguez, N, Andreassen, O A, Babadjanova, G, Bass, N J, Bauer, M, Baune, B T, Bellivier, F, Bergen, S, Bethell, A, Biernacka, J M, Blackwood, D H R, Boks, M P, Boomsma, D I, Børglum, A D, Borrmann-Hassenbach, M, Brennan, P, Budde, M, Buttenschøn, H N, Byrne, E M, Cervantes, P, Clarke, T-K, Craddock, N, Cruceanu, C, Curtis, D, Czerski, P M, Dannlowski, U, Davis, T, de Geus, E J C, Di Florio, A, Djurovic, S, Domenici, E, Edenberg, H J, Etain, B, Fischer, S B, Forty, L, Fraser, C, Frye, M A, Fullerton, J M, Gade, K, Gershon, E S, Giegling, I, Gordon, S D, Gordon-Smith, K, Grabe, H J, Green, E K, Greenwood, T A, Grigoroiu-Serbanescu, M, Guzman-Parra, J, Hall, L S, Hamshere, M, Hauser, J, Hautzinger, M, Heilbronner, U, Herms, S, Hitturlingappa, S, Hoffmann, P, Holmans, P, Hottenga, J-J, Jamain, S, Jones, I, Jones, L A, Juréus, A, Kahn, R S, Kammerer-Ciernioch, J, Kirov, G, Kittel-Schneider, S, Kloiber, S, Knott, S V, Kogevinas, M, Landén, M, Leber, M, Leboyer, M, Li, Q S, Lissowska, J, Lucae, S, Martin, N G, Mayoral-Cleries, F, McElroy, S L, McIntosh, A M, McKay, J D, McQuillin, A, Medland, S E, Middeldorp, C M, Milaneschi, Y, Mitchell, P B, Montgomery, G W, Morken, G, Mors, O, Mühleisen, T W, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nurnberger, J I, O'Donovan, M C, Loohuis, L M O, Ophoff, R, Oruc, L, Owen, M J, Paciga, S A, Penninx, B W J H, Perry, A, Pfennig, A, Potash, J B, Preisig, M, Reif, A, Rivas, F, Rouleau, G A, Schofield, P R, Schulze, T G, Schwarz, M, Scott, L, Sinnamon, G C B, Stahl, E A, Strauss, J, Turecki, G, Van der Auwera, S, Vedder, H, Vincent, J B, Willemsen, G, Witt, C C, Wray, N R, Xi, H S, Tadic, A, Dahmen, N, Schott, B H, Cichon, S, Nöthen, M M, Ripke, S, Mobascher, A, Rujescu, D, Lieb, K, Roepke, S, Schmahl, C, Bohus, M, Rietschel, M

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