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: Stephan Ripke, A. Di Florio, Gustavo Turecki, N Bass, Ian Jones, Laura J. Scott, Lisa Hall, Martin Hautzinger, Tracy Air, Sarah Knott, Marcella Rietschel, Christel M. Middeldorp, Patrick J. Brennan, John Strauss, Nicholas G. Martin, Bertram Müller-Myhsok, Tony Davis, Andreas Reif, Katherine Gordon-Smith, Céline S. Reinbold, Urs Heilbronner, Anders Juréus, Stefan Kloiber, Andrew McQuillin, Dan Rujescu, N. Dahmen, Fermin Mayoral-Cleries, Richard M. Myers, Abdel Abdellaoui, Franck Bellivier, Gunnar Morken, Sarah E. Bergen, Manolis Kogevinas, Dorret I. Boomsma, Thomas G. Schulze, Arian Mobascher, Stefanie Heilmann-Heimbach, Sascha B. Fischer, Christine Fraser, Y. Milaneschi, Michael Conlon O'Donovan, Susan L. McElroy, Klaus Lieb, B.W.J.H. Penninx, Helmut Vedder, Fabian Streit, Piotr M. Czerski, Swapnil Awasthi, Lilijana Oruc, Caroline M. Nievergelt, Michael Bauer, Jana Strohmaier, Qingqin S. Li, Bernhard T. Baune, Roel A. Ophoff, S. E. Medland, Marco P. Boks, Gulja Babadjanova, Mark A. Frye, Christian Schmahl, M. M. Nöthen, Nicholas John Craddock, John B. Vincent, Douglas Blackwood, Marion Leboyer, Franziska Degenhardt, C. E. Schwarze, Henriette N. Buttenschøn, Tiffany A. Greenwood, Ole A. Andreassen, Toni-Kim Clarke, Loes M. Olde Loohuis, Scott D. Gordon, Björn H. Schott, Stephanie H. Witt, Stefan Roepke, John I. Nurnberger, S Van der Auwera, Lisa Jones, James D. McKay, André Tadić, Mikael Landén, Guy A. Rouleau, Monika Budde, Grant C.B. Sinnamon, Enda M. Byrne, Bruno Etain, Darja Schendel, Andreas J. Forstner, Cristiana Cruceanu, Srdjan Djurovic, Sara A. Paciga, Ney Alliey-Rodriguez, Joanna Hauser, Enrico Domenici, Peter Hoffmann, Elaine K. Green, Stéphane Jamain, Markus Schwarz, Marian L. Hamshere, Christian Witt, E.J.C. de Geus, Andrew M. McIntosh, Sven Cichon, Ole Mors, Jolanta Lissowska, Josef Frank, Pablo Cervantes, G. Kirov, Howard J. Edenberg, Ina Giegling, Grant W. Montgomery, Lydie Dietl, Martin Preisig, M. J. Owen, Martin Alda, David Curtis, Eli A. Stahl, Gonneke Willemsen, Udo Dannlowski, Rolf Adolfsson, Janice M. Fullerton, Jose Guzman-Parra, Elliot S. Gershon, Peter Holmans, Hans-Jörgen Grabe, Hualin S. Xi, Jens Treutlein, Fabio Rivas, James B. Potash, Martin Bohus, Naomi R. Wray, René S. Kahn, Katrin Gade, Sarah Kittel-Schneider, Anders D. Børglum, Susanne Lucae, Jouke-Jan Hottenga, Joanna M. Biernacka, Liz Forty, Margitta Borrmann-Hassenbach, Martin Jungkunz, Andrea Pfennig, Jutta Kammerer-Ciernioch, Maria Grigoroiu-Serbanescu, Peter R. Schofield, Stefan Herms, Amy Perry, Shashi Hitturlingappa, Markus Leber, Thomas W. Mühleisen, Philip B. Mitchell, Andrew Bethell, Huda Akil

المساهمون: Biological Psychology, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Mental Health, APH - Methodology, Environmental Policy Analysis, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Psychiatry, Amsterdam Neuroscience - Complex Trait Genetics, APH - Digital Health, Bipolar Disorders Working Group of the Psychiatric Genomics Consortium, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Variabilité de réponse aux Psychotropes (VariaPsy - U1144), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hopital Saint-Louis [AP-HP] (AP-HP), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Centre International de Recherche contre le Cancer - International Agency for Research on Cancer (CIRC - IARC), Organisation Mondiale de la Santé / World Health Organization Office (OMS / WHO), Université Paris-Est Créteil Val-de-Marne - Faculté de médecine (UPEC Médecine), Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Duchange, Nathalie

المصدر: Translational Psychiatry
Translational Psychiatry, 7(6). Nature Publishing Group
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 J, Strohmaier, J, Abdellaoui, A, Adolfsson, R, Air, T M, Akil, H, Lopezz de Alda, M, Alliey-Rodriguez, N, Andreassen, O A, Babadjanova, G, Bass, N J, Bauer, M, Baune, B T, Bellivier, F, Bergen, S E, 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, de Geus, E J C, Fischer, S B, Hottenga, J-J, Middeldorp, C M, Milaneschi, Y, Penninx, B W J H, Willemsen, G & Bipolar Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia ', Translational Psychiatry, vol. 7, no. 6, pp. e1155 . https://doi.org/10.1038/tp.2017.115Test
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, Borglum, A D, Borrmann-Hassenbach, M, Brennan, P, Budde, M, Buttenschon, 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, Jureus, A, Kahn, R S, Kammerer-Ciernioch, J, Kirov, G, Kittel-Schneider, S, Kloiber, S, Knott, S V, Kogevinas, M, Landen, 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, Muehleisen, T W, Mueller-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, Noethen, M M, Ripke, S, Mobascher, A, Rujescu, D, Lieb, K, Roepke, S, Schmahl, C, Bohus, M & Rietschel, M 2017, ' Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia ', Translational Psychiatry, vol. 7 . https://doi.org/10.1038/tp.2017.115Test
TRANSLATIONAL PSYCHIATRY
Translational Psychiatry, 7. Nature Publishing Group
Translational psychiatry, vol. 7, no. 6, pp. e1155
Translational Psychiatry, Nature Pub. Group, 2017, 7 (6), pp.e1155. ⟨10.1038/tp.2017.115⟩
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, Borglum, A D, Borrmann-Hassenbach, M, Brennan, P, Budde, M, Buttenschon, 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 & McIntosh, A M 2017, ' Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia ', Translational Psychiatry, vol. 7, 1155 . https://doi.org/10.1038/tp.2017.115Test
Translational Psychiatry 7(6), e1155-(2017). doi:10.1038/tp.2017.115
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, Fischer, S B, Gade, K, Hall, L S, Hoffmann, P, Jones, L A, Li, Q S, Mors, O, Schwarz, M, Stahl, E A, Witt, C C & Bipolar Disorders Working Group of the Psychiatric Genomics Consortium 2017, ' Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia ', Translational Psychiatry, vol. 7, no. 6, pp. e1155 . https://doi.org/10.1038/tp.2017.115Test
Translational psychiatry

مصطلحات موضوعية: Netherlands Twin Register (NTR), Male, Linkage disequilibrium, Multifactorial Inheritance, Bipolar Disorder, FEATURES, [SDV.MHEP.PSM] Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, Genome-wide association study, 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit, MESH: Genotype, 0302 clinical medicine, Borderline Personality Disorder, MESH: Bipolar Disorder, Borderline personality disorder, Genetics, RISK, Psychiatry, MESH: Aged, MESH: Middle Aged, PSYCHOPATHOLOGY, MESH: Genetic Predisposition to Disease, Middle Aged, MESH: Case-Control Studies, 3. Good health, FAMILY, Psychiatry and Mental health, Schizophrenia, MESH: Young Adult, Female, Original Article, medicine.symptom, Psychology, SET, TRAITS, Adolescent, Adult, Aged, Bipolar Disorder/genetics, Borderline Personality Disorder/genetics, Case-Control Studies, Depressive Disorder, Major/genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Schizophrenia/genetics, Young Adult, Clinical psychology, MESH: Depressive Disorder, Major, TWIN, BF, Impulsivity, Psykiatri, 03 medical and health sciences, Cellular and Molecular Neuroscience, medicine, Journal Article, ddc:610, Bipolar disorder, Biological Psychiatry, METAANALYSIS, MESH: Borderline Personality Disorder, MESH: Adolescent, Depressive Disorder, Major, MESH: Humans, MESH: Adult, medicine.disease, Comorbidity, MESH: Male, MESH: Schizophrenia, 030227 psychiatry, [SDV.MHEP.PSM]Life Sciences [q-bio]/Human health and pathology/Psychiatrics and mental health, MESH: Genome-Wide Association Study, PATTERNS, RC0321, DPYD, MESH: Multifactorial Inheritance, COMORBIDITY, MESH: Female, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::feef93fa89a41f8b57dbe34156009307Test
https://doi.org/10.17169/refubium-24737Test

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: Gulja Babadjanova, Sergey Petrov, Andrea Rivera, Bernhard H. F. Weber, Lars G. Fritsche, Sheila A. Fisher

المصدر: British Journal of Ophthalmology. 91:576-578

مصطلحات موضوعية: Male, Linkage disequilibrium, Population, Biology, Linkage Disequilibrium, Russia, Macular Degeneration, Cellular and Molecular Neuroscience, Risk Factors, Polymorphism (computer science), medicine, Humans, Genetic Predisposition to Disease, Allele, education, Aged, Genetics, education.field_of_study, Polymorphism, Genetic, Chromosomes, Human, Pair 10, Homozygote, Case-control study, World View, Chromosome, Macular degeneration, medicine.disease, eye diseases, Sensory Systems, Ophthalmology, Case-Control Studies, Complement Factor H, Factor H, Female, sense organs

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d346cb5c40b3ad2f8039c25ddc0649c2Test
https://doi.org/10.1136/bjo.2006.105577Test

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