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

المؤلفون: Anne Farmer, Roel A. Ophoff, Peter McGuffin, Lilia I. Abramova, Mads V. Hollegaard, Ole Mors, Omar Gustafsson, Thomas W. Mühleisen, Evangelos Vassos, Srdjan Djurovic, Gulja Babadjanova, Marcella Rietschel, Markus M. Nöthen, Gunnar Morken, Anders D. Børglum, Carmen C. Diaconu, David A. Collier, Lambertus A. Kiemeney, Kari Stefansson, M. Ruggeri, Ingrid Melle, Maria Grigoroiu-Serbanescu, Preben Bo Mortensen, Hreinn Stefansson, István Bitter, Ole A. Andreassen, Stacy Steinberg, Leonard H. van den Berg, Thomas Werge, Barbara Franke, Ruud van Winkel, Dan Rujescu, Vera Golimbet, Gerome Breen, János Réthelyi, Piotr M. Czerski, Joanna Hauser, Sarah Tosato, I. Alex Rubino, Olli Pietiläinen, Erik G. Jönsson, David St Clair, Sven Cichon, Gunter Kenis, Ditte Demontis, Engilbert Sigurdsson, Marc De Hert

المساهمون: Psychiatrie & Neuropsychologie, RS: MHeNs School for Mental Health and Neuroscience, Amsterdam Neuroscience, Adult Psychiatry

المصدر: Biological Psychiatry, 72(8), 645-650. Elsevier Science
Biological psychiatry 72(8), 645-650 (2012). doi:10.1016/j.biopsych.2012.02.040
Biological Psychiatry, 72, 645-50
Biological Psychiatry
Biological Psychiatry, 72, 8, pp. 645-50
Biological Psychiatry; Vol 72
Vassos, E, Steinberg, S, Cichon, S, Breen, G, Sigurdsson, E, Andreassen, O A, Djurovic, S, Morken, G, Grigoroiu-Serbanescu, M, Diaconu, C C, Czerski, P M, Hauser, J, Babadjanova, G, Abramova, L I, Mühleisen, T W, Nöthen, M M, Rietschel, M, McGuffin, P, Clair, D S, Gustafsson, O, Melle, I, Pietiläinen, O P H, Ruggeri, M, Tosato, S, Werge, T, Ophoff, R A, Rujescu, D, Børglum, A D, Mors, O, Mortensen, P B, Demontis, D, Hollegaard, M V, van Winkel, R, Kenis, G, De Hert, M, Réthelyi, J M, Bitter, I, Rubino, I A, Golimbet, V, Kiemeney, L A, van den Berg, L H, Franke, B, Jönsson, E G, Farmer, A, Stefansson, H, Stefansson, K, Collier, D A & GROUP Consortium 2012, ' Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder ', Biological Psychiatry, vol. 72, no. 8, pp. 645-650 . https://doi.org/10.1016/j.biopsych.2012.02.040Test
Biological psychiatry, 72(8), 645-650. Elsevier USA

مصطلحات موضوعية: Male, Linkage disequilibrium, Genome-wide association study, Aetiology, screening and detection [ONCOL 5], Linkage Disequilibrium, PBRM1, statistics & numerical data [Databases, Genetic], 0302 clinical medicine, Gene Frequency, genome-wide association, bipolar disorder, PBRM1, SGENE, Databases, Genetic, Odds Ratio, genetics [Schizophrenia], genetics, SGENE, Genetics, bipolar disorder, 0303 health sciences, epidemiology [Europe], Single Nucleotide, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], Europe, genetics [European Continental Ancestry Group], Pair 3, genetics [Chromosomes, Human, Pair 3], genetics [Polymorphism, Single Nucleotide], Female, Chromosomes, Human, Pair 3, Human, Genotype, European Continental Ancestry Group, 3p21.1, Locus (genetics), Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Chromosomes, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], 03 medical and health sciences, Databases, Bipolar Disorder, Humans, Genome-Wide Association Study, Schizophrenia, Genetic Predisposition to Disease, Genetic, medicine, ddc:610, Bipolar disorder, Polymorphism, Allele frequency, Settore MED/25 - Psichiatria, Biological Psychiatry, Molecular epidemiology Aetiology, screening and detection [NCEBP 1], 030304 developmental biology, Genetic association, Odds ratio, medicine.disease, schizophrenia, genome-wide association, polybromo 1, genetics [Bipolar Disorder], 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d15e99571768e434114e1470a2a68bTest
https://cris.maastrichtuniversity.nl/en/publications/85b8f1b8-3b89-4bdc-8aa2-6539e0f2766dTest

المؤلفون: Franziska Degenhardt, Jana Strohmaier, Thomas W. Mühleisen, Sven Cichon, René Breuer, Markus M. Nöthen, Britta Haenisch, Christian Hammer, Beate Niesler, Lilijana Oruc, Marcella Rietschel, Gulja Babadjanova, S H Witt, Manuel Mattheisen, Ralph Röth, M Grigoroiu-Serbanescu, Gudrun A. Rappold, Joanna Hauser, Fabio Rivas

المصدر: Translational Psychiatry 2(4), e103-e103 (2012). doi:10.1038/tp.2012.30
Translational Psychiatry 2, e103 (2012). doi:10.1038/tp.2012.30
Translational Psychiatry

مصطلحات موضوعية: HTR3B, Male, Bipolar Disorder, HTR3, 5-HT3, Genome-wide association study, Comorbidity, Bioinformatics, 0302 clinical medicine, genetics [Genetic Predisposition to Disease], Genetics, 0303 health sciences, biology, Brain, Human brain, Anxiety Disorders, genetics [Genetic Variation], Europe, Psychiatry and Mental health, medicine.anatomical_structure, metabolism [Fetus], Phenotype, genetics [Receptors, Serotonin, 5-HT3], genetics [Polymorphism, Single Nucleotide], Original Article, Female, Adult, Genotype, genetics [Anxiety Disorders], HTR3A protein, human, Single-nucleotide polymorphism, BPAD, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cellular and Molecular Neuroscience, genetics [RNA, Messenger], Fetus, Sex Factors, embryology [Brain], medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, ddc:610, RNA, Messenger, Biological Psychiatry, Alleles, 030304 developmental biology, Genetic association, Gene Expression Profiling, association, Case-control study, Genetic Variation, Odds ratio, medicine.disease, bipolar, metabolism [Brain], Case-Control Studies, biology.protein, Receptors, Serotonin, 5-HT3, 030217 neurology & neurosurgery, genetics [Bipolar Disorder], Genome-Wide Association Study, HTR3B protein, human

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::664d88832c17302b88e99aeabe29ce89Test