Resultados da busca - Nöthen, MM

072 Covid-19 and male androgenetic alopecia: Systematic investigation of a potential epidemiological and genetic association por Henne, S.K., Hochfeld, L.M., Maj, C., Nöthen, M.M., Heilmann-Heimbach, S.

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Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder por Schulze, TG, Detera-Wadleigh, SD, Akula, N, Gupta, A, Kassem, L, Steele, J, Pearl, J, Strohmaier, J, Breuer, R, Schwarz, M, Propping, P, Nöthen, MM, Cichon, S, Schumacher, J, Rietschel, M, McMahon, FJ

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder por Baum, AE, Akula, N, Cabanero, M, Cardona, I, Corona, W, Klemens, B, Schulze, TG, Cichon, S, Rietschel, M, Nöthen, MM, Georgi, A, Schumacher, J, Schwarz, M, Jamra, R Abou, Höfels, S, Propping, P, Satagopan, J, Detera-Wadleigh, SD, Hardy, J, McMahon, FJ

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia por 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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Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susc... por Li, M, Luo, X-j, Rietschel, M, Lewis, CM, Mattheisen, M, Müller-Myhsok, B, Jamain, S, Leboyer, M, Landén, M, Thompson, PM, Cichon, S, Nöthen, MM, Schulze, TG, Sullivan, PF, Bergen, SE, Donohoe, G, Morris, DW, Hargreaves, A, Gill, M, Corvin, A, Hultman, C, Toga, AW, Shi, L, Lin, Q, Shi, H, Gan, L, Meyer-Lindenberg, A, Czamara, D, Henry, C, Etain, B, Bis, JC, Ikram, MA, Fornage, M, Debette, S, Launer, LJ, Seshadri, S, Erk, S, Walter, H, Heinz, A, Bellivier, F, Stein, JL, Medland, SE, Vasquez, A Arias, Hibar, DP, Franke, B, Martin, NG, Wright, MJ, Su, B

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Expanding the range of ZNF804A variants conferring risk of psychosis por 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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