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1دورية أكاديمية
المؤلفون: Mühleisen, TW, Reinbold, CS, Forstner, AJ, Abramova, LI, Alda, M, Babadjanova, G, Bauer, M, Brennan, P, Chuchalin, A, Cruceanu, C, Czerski, PM, Degenhardt, F, Fischer, SB, Fullerton, JM, Gordon, SD, Grigoroiu-Serbanescu, M, Grof, P, Hauser, J, Hautzinger, M, Herms, S, Hoffmann, P, Kammerer-Ciernioch, J, Khusnutdinova, E, Kogevinas, M, Krasnov, V, Lacour, A, Laprise, C, Leber, M, Lissowska, J, Lucae, S, Maaser, A, Maier, W, Martin, NG, Mattheisen, M, Mayoral, F, McKay, JD, Medland, SE, Mitchell, PB, Moebus, S, Montgomery, GW, Müller-Myhsok, B, Oruc, L, Pantelejeva, G, Pfennig, A, Pojskic, L, Polonikov, A, Reif, A, Rivas, F, Rouleau, GA, Schenk, LM, Schofield, PR, Schwarz, M, Streit, F, Strohmaier, J, Szeszenia-Dabrowska, N, Tiganov, AS, Treutlein, J, Turecki, G, Vedder, H, Witt, SH, Schulze, TG, Rietschel, M, Nöthen, MM, Cichon, S
المصدر: urn:ISSN:0165-0327 ; urn:ISSN:1573-2517 ; Journal of Affective Disorders, 228, 20-25
مصطلحات موضوعية: Neurosciences, Serious Mental Illness, Genetics, Biotechnology, Human Genome, Bipolar Disorder, Brain Disorders, Mental Health, 2 Aetiology, 2.1 Biological and endogenous factors, Algorithms, Brain, Female, GRB2 Adaptor Protein, Gene Expression, Genes, erbB-2, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Phenotype, Polymorphism, Single Nucleotide, RNA, Receptor, Signal Transduction, GRB2 events in ERBB2 signaling, NCAM signaling for neurite out-growth, Neurodevelopmental disorder
وصف الملف: application/pdf
العلاقة: http://hdl.handle.net/1959.4/unsworks_49676Test; https://unsworks.unsw.edu.au/bitstreams/4bfc82b1-a667-4881-9a9c-144ea89d129e/downloadTest; https://doi.org/10.1016/j.jad.2017.11.068Test
الإتاحة: https://doi.org/10.1016/j.jad.2017.11.068Test
http://hdl.handle.net/1959.4/unsworks_49676Test
https://unsworks.unsw.edu.au/bitstreams/4bfc82b1-a667-4881-9a9c-144ea89d129e/downloadTest -
2دورية أكاديمية
المؤلفون: Forstner, AJ, Hecker, J, Hofmann, A, Maaser, A, Reinbold, CS, Mühleisen, TW, Leber, M, Strohmaier, J, Degenhardt, F, Treutlein, J, Mattheisen, M, Schumacher, J, Streit, F, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, SH, Reif, A, Müller-Myhsok, B, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Moebus, S, Schenk, LM, Fischer, SB, Sivalingam, S, Czerski, PM, Hauser, J, Lissowska, J, Szeszenia-Dabrowska, N, Brennan, P, McKay, JD, Wright, A, Mitchell, PB, Fullerton, JM, Schofield, PR, Montgomery, GW, Medland, SE, Gordon, SD, Martin, NG, Krasnov, V, Chuchalin, A, Babadjanova, G, Pantelejeva, G, Abramova, LI, Tiganov, AS, Polonikov, A, Khusnutdinova, E, Alda, M, Cruceanu, C, Rouleau, GA, Turecki, G, Laprise, C, Rivas, F, Mayoral, F, Kogevinas, M, Grigoroiu-Serbanescu, M, Becker, T, Schulze, TG, Rietschel, M, Cichon, S, Fier, H, Nöthen, MM, Schofield, Peter
المساهمون: Walss-Bass, Consuelo
المصدر: urn:ISSN:1932-6203 ; PLoS ONE, 12, 2, e0171595
مصطلحات موضوعية: Mental Health, Schizophrenia, Prevention, Serious Mental Illness, Brain Disorders, Human Genome, Biotechnology, Neurosciences, Genetics, Bipolar Disorder, 2 Aetiology, 2.1 Biological and endogenous factors, Genetic Linkage, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Risk, Signal Transduction
وصف الملف: application/pdf
العلاقة: http://hdl.handle.net/1959.4/unsworks_44893Test; https://unsworks.unsw.edu.au/bitstreams/327bea5c-73ff-4f53-8891-6c6736bffd1b/downloadTest; https://doi.org/10.1371/journal.pone.0171595Test
الإتاحة: https://doi.org/10.1371/journal.pone.0171595Test
http://hdl.handle.net/1959.4/unsworks_44893Test
https://unsworks.unsw.edu.au/bitstreams/327bea5c-73ff-4f53-8891-6c6736bffd1b/downloadTest