المؤلفون: Michael Bauer, Susanne Moebus, Gulja Babadjanova, Guy A. Rouleau, Sascha B. Fischer, Markus Schwarz, Gustavo Turecki, Wolfgang Maier, Helmut Vedder, Marcella Rietschel, Fabio Rivas, Jana Strohmaier, André Lacour, Catherine Laprise, Lilia I. Abramova, Alexey Polonikov, Nicholas G. Martin, Jolanta Lissowska, Lilijana Oruc, Andreas Reif, Joanna Hauser, Scott D. Gordon, Lorena M. Schenk, James McKay, Alexander S. Tiganov, Markus M. Nöthen, Grant W. Montgomery, Bertram Müller-Myhsok, Susanne Lucae, Neonila Szeszenia-Dabrowska, Martin Alda, Galina Pantelejeva, Céline S. Reinbold, Cristiana Cruceanu, Lejla Pojskic, Manolis Kogevinas, Thomas G. Schulze, Paul Grof, Alexander Chuchalin, Stephanie H. Witt, Jens Treutlein, Manuel Mattheisen, Sven Cichon, Janice M. Fullerton, Andreas J. Forstner, Fabian Streit, Elza Khusnutdinova, Martin Hautzinger, Paul Brennan, Sarah E. Medland, Fermín Mayoral, Anna Maaser, Piotr M. Czerski, Franziska Degenhardt, Per Hoffmann, Markus Leber, Valery Krasnov, Thomas W. Mühleisen, Peter R. Schofield, Stefan Herms, Philip B. Mitchell, Andrea Pfennig, Jutta Kammerer-Ciernioch, Maria Grigoroiu-Serbanescu

المساهمون: Nofer Institute of Occupational Medicine

المصدر: Mühleisen, T W, Reinbold, C S, Forstner, A J, Abramova, L I, Alda, M, Babadjanova, G, Bauer, M, Brennan, P, Chuchalin, A, Cruceanu, C, Czerski, P M, Degenhardt, F, Fischer, S B, Fullerton, J M, Gordon, S D, 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, N G, Mattheisen, M, Mayoral, F, McKay, J D, Medland, S E, Mitchell, P B, Moebus, S, Montgomery, G W, Müller-Myhsok, B, Oruc, L, Pantelejeva, G, Pfennig, A, Pojskic, L, Polonikov, A, Reif, A, Rivas, F, Rouleau, G A, Schenk, L M, Schofield, P R, Schwarz, M, Streit, F, Strohmaier, J, Szeszenia-Dabrowska, N, Tiganov, A S, Treutlein, J, Turecki, G, Vedder, H, Witt, S H, Schulze, T G, Rietschel, M, Nöthen, M M & Cichon, S 2018, ' Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder ', Journal of Affective Disorders, vol. 228, pp. 20-25 . https://doi.org/10.1016/j.jad.2017.11.068Test
JOURNAL OF AFFECTIVE DISORDERS
Journal of affective disorders 228, 20-25 (2018). doi:10.1016/j.jad.2017.11.068

مصطلحات موضوعية: 0301 basic medicine, Male, Bipolar Disorder, Pathway analysis, Receptor, ErbB-2, Medizin, Gene Expression, Genome-wide association study, genetics [GRB2 Adaptor Protein], 0302 clinical medicine, Neurodevelopmental disorder, Gene expression, GRB2 protein, human, physiology [Genes, erbB-2], growth & development [Brain], Brain, Psychiatry and Mental health, Clinical Psychology, Phenotype, metabolism [RNA], Female, Psychology, Algorithms, Signal Transduction, metabolism [Receptor, ErbB-2], physiopathology [Bipolar Disorder], Bipolar disorder, Computational biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, medicine, Humans, Genetic Predisposition to Disease, ddc:610, Gene, Genetic association, GRB2 Adaptor Protein, metabolism [Bipolar Disorder], metabolism [GRB2 Adaptor Protein], NCAM signaling for neurite out-growth, RNA, Genes, erbB-2, medicine.disease, GRB2 events in ERBB2 signaling, 030104 developmental biology, metabolism [Brain], Multiple comparisons problem, Neuroscience, 030217 neurology & neurosurgery, genetics [Bipolar Disorder], Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::781902b10c019e8809d65f79d25f156bTest
https://pure.au.dk/portal/da/publications/gene-set-enrichment-analysis-and-expression-pattern-exploration-implicate-an-involvement-of-neurodevelopmental-processes-in-bipolar-disorderTest(6f342b86-fe24-4c5c-a884-5522ec0636d0).html

المؤلفون: Peter R. Schofield, Sandra Meier, Stefan Herms, Paul Brennan, Susanne Moebus, Jana Strohmaier, Paul Grof, Nicholas G. Martin, Grant W. Montgomery, Adam Wright, Susanne Lucae, Maria Grigoroiu-Serbanescu, Alexey Polonikov, Peter Propping, Stephanie H. Witt, Andreas J. Forstner, Joanna Hauser, Fabio Rivas, Markus Leber, René Breuer, Piotr M. Czerski, Johannes Schumacher, Manolis Kogevinas, Neonila Szeszenia-Dabrowska, Scott D. Gordon, Sven Cichon, Jolanta Lissowska, Wolfgang Maier, Tim Becker, Alexander S. Tiganov, Thomas W. Mühleisen, Andreas Reif, Manuel Mattheisen, Michael Bauer, Galina Pantelejeva, Thomas G. Schulze, Philip B. Mitchell, Jens Treutlein, André Lacour, Marcella Rietschel, Lilia I. Abramova, Valery Krasnow, Andrea Pfennig, Martin Alda, Alexander Chuchalin, Lutz Priebe, Per Hoffmann, Janice M. Fullerton, Jutta Kammerer-Ciernioch, Markus M. Nöthen, Fermín Mayoral, Helmut Vedder, M.P. Schwarz, Gulja Babadjanova, Guy A. Rouleau, Franziska Degenhardt, Elza Khusnutdinova, Martin Hautzinger, James McKay, Bertram Müller-Myhsok, Catherine Laprise, Gustavo Turecki, Sarah E. Medland

المصدر: Nature Communications 5(1), 3339 (2014). doi:10.1038/ncomms4339
Mühleisen, T W, Leber, M, Schulze, T G, Strohmaier, J, Degenhardt, F, Treutlein, J, Mattheisen, M, Forstner, A J, Schumacher, J, Breuer, R, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, S H, Reif, A, Müller-Myhsok, B, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Moebus, S, Priebe, L, Czerski, P M, Hauser, J, Lissowska, J, Szeszenia-Dabrowska, N, Brennan, P, McKay, J D, Wright, A, Mitchell, P B, Fullerton, J M, Schofield, P R, Montgomery, G W, Medland, S E, Gordon, S D, Martin, N G, Krasnow, V, Chuchalin, A, Babadjanova, G, Pantelejeva, G, Abramova, L I, Tiganov, A S, Polonikov, A, Khusnutdinova, E, Alda, M, Grof, P, Rouleau, G A, Turecki, G, Laprise, C, Rivas, F, Mayoral, F, Kogevinas, M, Grigoroiu-Serbanescu, M, Propping, P, Becker, T, Rietschel, M, Nöthen, M M & Cichon, S 2014, ' Genome-wide association study reveals two new risk loci for bipolar disorder ', Nature Communications, vol. 5, pp. 3339 . https://doi.org/10.1038/ncomms4339Test
Nature Communications 5, 3339 (2014). doi:10.1038/ncomms4339

مصطلحات موضوعية: Male, Bipolar Disorder, Medizin, General Physics and Astronomy, Locus (genetics), Genome-wide association study, Single-nucleotide polymorphism, Disease, Biology, methods [Genome-Wide Association Study], Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, adenylyl cyclase 2, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, ANK3, genetics [Genetic Predisposition to Disease], Genetic association, Genetics, Multidisciplinary, genetics [Adenylyl Cyclases], General Chemistry, medicine.disease, Mental illness, 3. Good health, genetics [Polymorphism, Single Nucleotide], Female, ddc:500, genetics [Bipolar Disorder], Genome-Wide Association Study, Adenylyl Cyclases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4299677c5f4a942ff0d5e886163ed29aTest
https://doi.org/10.1038/ncomms4339Test