المؤلفون: Alessandro Serretti, Julien Mendlewicz, Joseph Zohar, Chiara Fabbri, Diego Albani, Stuart Montgomery, Alexander Kautzky, Siegfried Kasper, Daniel Souery

المصدر: European Neuropsychopharmacology. 29:S934-S935

مصطلحات موضوعية: Pharmacology, business.industry, Genome-wide association study, Disease, medicine.disease, Bioinformatics, Psychiatry and Mental health, Mitotic cell cycle, Neurology, medicine, Major depressive disorder, Pharmacology (medical), Human genome, Neurology (clinical), business, Treatment-resistant depression, Biological Psychiatry, Exome sequencing, Genetic association

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b20221dc1715d7f896d49cab8f0da678Test
https://doi.org/10.1016/j.euroneuro.2017.08.274Test

المؤلفون: Thomas G. Schulze, Eduard Vieta, Melissa J. Green, Jakob Grove, Ingrid Melle, Preben Bo Mortensen, Nicholas J. Schork, Thorgeir E. Thorgeirsson, Jonas Bybjerg-Grauholm, Margit Burmeister, Peter R. Schofield, Szabolcs Szelinger, Fermín Mayoral, Katherine Gordon-Smith, Qingqin S. Li, Claire O'Donovan, Josep Antoni Ramos-Quiroga, Derek W. Morris, Douglas M. Ruderfer, Stefan Herms, Huckins Lm, Martin Hautzinger, Eline J. Regeer, Sebastian Zöllner, Gustavo Turecki, Christine Søholm Hansen, Helena Medeiros, Laura J. Scott, Annelie Nordin Adolfsson, Helmut Vedder, Thomas W. Weickert, Nelson B. Freimer, Céline S. Reinbold, James McKay, Cathryn M. Lewis, Eric R. Gamazon, Frank Bellivier, Marie B¾kvad-Hansen, Srdjan Djurovic, Chun Chieh Fan, Ole A. Andreassen, Solveig K. Sieberts, Jack D. Barchas, David Curtis, Elaine K. Green, Tatiana Foroud, Shaun Purcell, Mette A. Peters, Joanna M. Biernacka, Fabian Streit, Alan F. Schatzberg, James L. Kennedy, Tiffany A. Greenwood, Bertram Müller-Myhsok, Robin Kramer, Swapnil Awasthi, Jordan W. Smoller, Cristina Sánchez-Mora, George Kirov, Ulrik Fredrik Malt, Gabriel E. Hoffman, Liz Forty, Pablo Cervantes, Jose Guzman Parra, Nicholas G. Martin, William Byerley, J. Raymond DePaulo, Martin Alda, Anil P.S. Ori, Menachem Fromer, William E. Bunney, Valentina Escott-Price, Judith A. Badner, Danielle Posthuma, Judith Allardyce, M. Ribasés, Manolis Kogevinas, Stephanie H. Witt, Anne T. Spijker, James A. Knowles, Simon Xi, Jun Li, Francis J. McMahon, Nancy J. Cox, Marcella Rietschel, Markus Leber, Laura M. Huckins, John I. Nurnberger, M. Casas, Marco P. Boks, Maria Hipolito, Evaristus A. Nwulia, Gerome Breen, Franziska Degenhardt, Janice M. Fullerton, Carlos N. Pato, Urs Heilbronner, Piotr M. Czerski, Michael Steffens, Monika Budde, Nicholas John Craddock, Katrin Gade, Bernie Devlin, Sarah Kittel-Schneider, Enrico Domenci, Weihua Guan, Sarah E. Bergen, Fan Meng, Eystein Stordal, Janet L. Sobell, Naomi R. Wray, Engilbert Sigurdsson, Marion Leboyer, Sven Cichon, Pamela Sklar, Bruno Etain, Richard M. Myers, Melvin G. McInnis, Steve McCarroll, Nicholas Bass, Christine Fraser, Thomas W. Mühleisen, Anna Maaser, Patrick F. Sullivan, Mark A. Frye, Amanda Dobbyn, John P. Rice, Amy Perry, Wei Xu, Thomas Damm Als, Anders D. Børglum, Anna C. Koller, Michael Conlon O'Donovan, Pamela B. Mahon, Sara A. Paciga, Douglas Blackwood, Michael Bauer, Fernando S. Goes, Susanne Lucae, Markus M. Nöthen, Josef Frank, Grant W. Montgomery, Scott D. Gordon, Philip B. Mitchell, Hoang T. Nguyen, Huda Akil, Chunyu Liu, Stanley J. Watson, Allan H. Young, Roel A. Ophoff, Caroline M. Nievergelt, John B. Vincent, Robert Karlsson, Kari Stefansson, Thomas Werge, Niamh Mullins, William A. Scheftner, Elliot S. Gershon, Peter McGuffin, Ralph Kupka, Mikael Landén, Matthew Flickinger, Claudia Giambartolomei, Carsten Bøcker Pedersen, Michael John Owen, Diego Albani, Hae Kyung Im, Andres Metspalu, Gunnar Morken, Panos Roussos, Tõnu Esko, Andrew M. McIntosh, Vishwajit L. Nimgaonkar, Per Hoffmann, Olav B. Smeland, Stéphane Jamain, Ole Mors, Vahram Haroutunian, Anders Juréus, Shawn Levy, Roy H. Perlis, Whitney McFadden, James Boocock, Ney Alliey-Rodriguez, Stacy Steinberg, Paul D. Shilling, Arne E. Vaaler, David Craig, Sarah E. Medland, Donald J. MacIntyre, William Coryell, Jens Treutlein, Joanna Hauser, Cynthia Shannon Weickert, Jana Strohmaier, Guy A. Rouleau, Michele T. Pato, John R. Kelsoe, Arianna Di Florio, Radhika Kandaswamy, David M. Hougaard, Toni-Kim Clarke, Susan L. McElroy, Ian Jones, Sarah Knott, Tatyana Shehktman, Wade H. Berrettini, John Strauss, Anders M. Dale, Peter P. Zandi, Andreas Reif, Claire Slaney, Julie Garnham, Margarita Rivera, Michael Gill, Lisa Jones, Cristiana Cruceanu, Sascha B. Fischer, Marian L. Hamshere, Lilijana Oruc, Weiqing Wang, Eli A. Stahl, Wolfgang Maier, Peng Zhang, Hreinn Stefansson, Ingrid Agartz, Bernhard T. Baune, Esben Agerbo, Alessandro Serretti, Robert C. Thompson, Ketil J. Oedegaard, William Lawson, Merete Nordentoft, Jacob Lawrence, Fabio Rivas, James B. Potash, Aiden Corvin, Christina M. Hultman, Maria Grigoroiu-Serbanescu, Marianne Giørtz Pedersen, Michael Boehnke, René S. Kahn, Lili Milani, Jurgen Del-Favero, Veera M. Rajagopal, Jolanta Lissowska, Howard J. Edenberg, Udo Dannlowski, Rolf Adolfsson, Andrea Pfennig, Adebayo Anjorin, Torbjørn Elvsåshagen

مصطلحات موضوعية: Genotype, Expression quantitative trait loci, medicine, Genome-wide association study, Locus (genetics), Bipolar disorder, Computational biology, Biology, medicine.disease, Phenotype, Genetic architecture, Imputation (genetics)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b2a419d5c19d7df0ad2b9219c5ea139Test
https://doi.org/10.1101/222786Test

المؤلفون: Daniel Souery, Diego Albani, Concetta Crisafulli, Alessandro Serretti, Armando Chierchia, Julien Mendlewicz, Rosalba Martines, Chiara Fabbri, Alberto Chiesa, Othman Sentissi, Gianluigi Forloni, Giovanni de Girolamo, Raffaella Calati

المساهمون: Fabbri, C., Souery, D., Calati, R., Crisafulli, C., Chierchia, A., Albani, D., Forloni, G., Chiesa, A., Martines, R., Sentissi, O., Mendlewicz, J., De Girolamo, G., Serretti, A., Fabbri, C, Souery, D, Calati, R, Crisafulli, C, Chierchia, A, Albani, D, Forloni, G, Chiesa, A, Martines, R, Sentissi, O, Mendlewicz, J, De Girolamo, G, Serretti, A

المصدر: Journal of Neural Transmission. 122:43-58

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Bipolar Disorder, Drug-Related Side Effects and Adverse Reactions, Genotype, medicine.drug_class, Side effect Gene Pharmacogenetics Antipsychotic Antidepressant Mood stabilizer, medicine.medical_treatment, Sp4 Transcription Factor, Single-nucleotide polymorphism, Genome-wide association study, Pharmacology, Catechol O-Methyltransferase, Polymorphism, Single Nucleotide, Treatment of bipolar disorder, Glycogen Synthase Kinase 3, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Receptor, Serotonin, 5-HT2A, Bipolar disorder, Antipsychotic, Biological Psychiatry, Aged, Psychotropic Drugs, Glycogen Synthase Kinase 3 beta, business.industry, Brain-Derived Neurotrophic Factor, Psychotropic Drug, Nuclear Receptor Subfamily 1, Group F, Member 1, Mood stabilizer, Middle Aged, medicine.disease, Psychiatry and Mental health, Neurology, Antidepressant, Female, Neurology (clinical), Drug-Related Side Effects and Adverse Reaction, business, Pharmacogenetics, Genome-Wide Association Study, Human, Signal Transduction

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76c8502479309bda21a434997152fc27Test
https://doi.org/10.1007/s00702-014-1290-3Test

المؤلفون: Diego Albani, Koen Schruers, Daniel Souery, Alexander Kautzky, Alessandro Serretti, Chiara Fabbri, Julien Mendlewicz, Vilma Mantovani, Ilaria Raimondi, Filippo Corponi, Stuart Montgomery, Joseph Zohar, Carlotta Pia Cristalli, Gianluigi Forloni, Siegfried Kasper

المساهمون: RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, Fabbri, Chiara, Corponi, Filippo, Albani, Diego, Raimondi, Ilaria, Forloni, Gianluigi, Schruers, Koen, Kasper, Siegfried, Kautzky, Alexander, Zohar, Joseph, Souery, Daniel, Montgomery, Stuart, Cristalli, Carlotta Pia, Mantovani, Vilma, Mendlewicz, Julien, Serretti, Alessandro

المصدر: Progress in Neuro-Psychopharmacology & Biological Psychiatry, 81, 203-210. Elsevier Science

مصطلحات موضوعية: Male, Candidate gene, HPA-AXIS, Pharmacogenomic Variants, STAR-ASTERISK-D, Antidepressant, Genome-wide association study, Gene, Depressive Disorder, Treatment-Resistant, 0302 clinical medicine, SCHIZOPHRENIA, GWAS, Pharmacology (medical), Genetics, MAJOR DEPRESSIVE DISORDER, Pharmacogenetic, Genetic Pleiotropy, BIPOLAR DISORDER, Antidepressants, Middle Aged, Psychiatry and Mental health, Treatment Outcome, Neurology, Pharmacogenomic Variant, COMPREHENSIVE METAANALYSIS, Major depressive disorder, Female, FKBP5, Treatment-resistant depression, Human, Adult, medicine.medical_specialty, Single-nucleotide polymorphism, Genetic Association Studie, Biology, Calcium Channel, Polymorphism, Single Nucleotide, Tacrolimus Binding Proteins, 03 medical and health sciences, medicine, Humans, Genetic Predisposition to Disease, ANK3, GENOME-WIDE ASSOCIATION, Psychiatry, Genetic Association Studies, TREATMENT RESPONSE, Biological Psychiatry, Genetic association, Pharmacology, Depressive Disorder, Major, Tacrolimus Binding Protein, medicine.disease, 030227 psychiatry, Pharmacogenetics, Genetic marker, ANK3 GENE, Calcium Channels, Neurology (clinical), TREATMENT OUTCOMES, 030217 neurology & neurosurgery

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01b93669d52cfdc1e433af67c1e9a86fTest
https://doi.org/10.1016/j.euroneuro.2017.12.093Test

المؤلفون: Euijung Ryu, Danfeng Chen, Allan H. Young, Olav B. Smeland, James McKay, Frank Bellivier, Qingqin S. Li, Yunpeng Wang, Tõnu Esko, Bertram Müller-Myhsok, Weiqing Wang, Thomas W. Weickert, Joanna M. Biernacka, Ralph W. Kupka, Claire O'Donovan, Josep Antoni Ramos-Quiroga, Marian L. Hamshere, Derek W. Morris, Douglas M. Ruderfer, Stephan Ripke, Nelson B. Freimer, Tatiana Foroud, Shaun Purcell, Ashley Dumont, Shawn Levy, Dominic Holland, Joanna Hauser, Anders D. Børglum, Liz Forty, Alan F. Schatzberg, Christine Fraser, Jennifer M. Whitehead Pavlides, William E. Bunney, Merete Nordentoft, Andres Metspalu, Gunnar Morken, Susanne Lucae, Roy H. Perlis, Anne T. Spijker, Richard A. Belliveau, Sarah E. Bergen, Fan Meng, Eduard Vieta, Cynthia Shannon Weickert, J. Raymond DePaulo, Martin Alda, Lina Martinsson, Melvin G. McInnis, Jacob Lawrence, Markus Leber, James A. Knowles, Franziska Degenhardt, Melissa J. Green, Jaqueline Goldstein, Amanda Dobbyn, Radhika Kandaswamy, Steve McCarroll, Katrin Gade, Jack D. Barchas, Christina M. Hultman, Sarah Kittel-Schneider, Martin Hautzinger, Maria Hipolito, Louise Frisén, Kari Stefansson, Michael Conlon O'Donovan, Markus M. Nöthen, Eline J. Regeer, Jens Treutlein, Robert Karlsson, Ian Jones, Nicholas G. Martin, William A. Scheftner, Caroline M. Nievergelt, Marta Ribasés, Simone de Jong, Szabolcs Szelinger, Thomas W. Mühleisen, Michele T. Pato, Manuel Mattheisen, Maciej Trzaskowski, Urs Heilbronner, Diane Gage, Jakob Grove, Ingrid Melle, Ole A. Andreassen, Claudia Giambartolomei, Kimberly Chambert, Arne E. Vaaler, William Coryell, Peter R. Schofield, Preben Bo Mortensen, Roel A. Ophoff, Fabian Streit, Manolis Kogevinas, Ingrid Agartz, John Strauss, James L. Kennedy, Anders M. Dale, Stefan Herms, Douglas Blackwood, Torbjørn Elvsåshagen, Bernhard T. Baune, Grant W. Montgomery, Andreas Reif, Fabio Rivas, Andrew McQuillin, Jordan W. Smoller, Chun Chieh Fan, James B. Potash, Jun Li, Ketil J. Oedegaard, David Curtis, Martin Schalling, John R. Kelsoe, Valentina Escott-Price, Sascha B. Fischer, Tatyana Shehktman, Jonathan R. I. Coleman, Stanley J. Watson, Donald J. MacIntyre, Tune H. Pers, Eystein Stordal, Richard M. Myers, Jose Guzman-Parra, Danielle Posthuma, John I. Nurnberger, William Lawson, Janet L. Sobell, Felecia Cerrato, Judith A. Badner, Elliot S. Gershon, Gerome Breen, Naomi R. Wray, Thomas Werge, Lilijana Oruc, Claire Slaney, Anil P.S. Ori, Alexander W. Charney, Marianne Giørtz Pedersen, Marie Bækvad-Hansen, Michael Boehnke, Marcella Rietschel, George Kirov, Aiden Corvin, Piotr M. Czerski, Peter Holmans, Michael Steffens, Margarita Rivera, Maria Grigoroiu-Serbanescu, René S. Kahn, Laura M. Huckins, Monika Budde, Michael Gill, Lili Milani, Christiaan de Leeuw, Peng Zhang, Nicholas Bass, Jana Strohmaier, John P. Rice, Wei Xu, Cristiana Cruceanu, Vassily Trubetskoy, Philip B. Mitchell, Helena Medeiros, Thomas Damm Als, Anna C. Koller, Huda Akil, Jessica S. Johnson, Toni-Kim Clarke, Janice M. Fullerton, Guy A. Rouleau, Fernando S. Goes, Weihua Guan, Wolfgang Maier, Pamela Sklar, Diego Albani, Laura J. Scott, Pamela B. Mahon, Anna Maaser, Katherine Gordon-Smith, Urban Ösby, Jurgen Del-Favero, Jolanta Lissowska, Howard J. Edenberg, Sven Cichon, Annelie Nordin Adolfsson, Julie Garnham, Josef Frank, Hoang T. Nguyen, Michael Bauer, Helmut Vedder, Vishwajit L. Nimgaonkar, Loes M. Olde Loohuis, Thomas G. Schulze, Cristina Sánchez-Mora, Udo Dannlowski, Rolf Adolfsson, Benjamin M. Neale, Verneri Antilla, Andrea Pfennig, John B. Vincent, Niamh Mullins, Per Hoffmann, Peter McGuffin, Erlend Bøen, Ney Alliey-Rodriguez, Adebayo Anjorin, Fermín Mayoral, Arianna Di Florio, Claire Churchhouse, David M. Hougaard, Nicholas J. Schork, Tiffany A. Greenwood, Carlos N. Pato, Thorgeir E. Thorgeirsson, Nicholas John Craddock, Stephanie H. Witt, Liam Abbott, Swapnil Awasthi, Miquel Casas, Jonas Bybjerg-Grauholm, Cathryn M. Lewis, Srdjan Djurovic, Bruno Etain, Margit Burmeister, Phil Lee, Elaine K. Green, Sara A. Paciga, Lena Backlund, Engilbert Sigurdsson, Patrick F. Sullivan, Amy Perry, Pablo Cervantes, Marco P. Boks, Catharina Lavebratt, Andrew M. McIntosh, Panos Roussos, Enda M. Byrne, Alexander Richards, Eli A. Stahl, Stéphane Jamain, Hreinn Stefansson, Ole Mors, Esben Agerbo, Susan L. McElroy, Wade H. Berrettini, Peter P. Zandi, Lisa Jones, Andreas J. Forstner, Alessandro Serretti, Céline S. Reinbold, Robert C. Thompson, Matthew Flickinger, William Byerley, Michael John Owen, Helena Gaspar, Francis J. McMahon, David St Clair, Mark A. Frye, Christine Søholm Hansen, Scott D. Gordon, Mikael Landén, Gustavo Turecki, Simon Xi, Evaristus A. Nwulia, Anders Juréus, James Boocock, Stacy Steinberg, Paul D. Shilling, David Craig, Mark J. Daly, Sarah E. Medland, Marion Leboyer, Chunyu Liu, Carsten Bøcker Pedersen, Sebastian Zöllner

المساهمون: APH - Mental Health, Psychiatry, Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Reproduction & Development (AR&D), Stahl E.A., Breen G., Forstner A.J., McQuillin A., Ripke S., Trubetskoy V., Mattheisen M., Wang Y., Coleman J.R.I., Gaspar H.A., de Leeuw C.A., Steinberg S., Pavlides J.M.W., Trzaskowski M., Byrne E.M., Pers T.H., Holmans P.A., Richards A.L., Abbott L., Agerbo E., Akil H., Albani D., Alliey-Rodriguez N., Als T.D., Anjorin A., Antilla V., Awasthi S., Badner J.A., Baekvad-Hansen M., Barchas J.D., Bass N., Bauer M., Belliveau R., Bergen S.E., Pedersen C.B., Boen E., Boks M.P., Boocock J., Budde M., Bunney W., Burmeister M., Bybjerg-Grauholm J., Byerley W., Casas M., Cerrato F., Cervantes P., Chambert K., Charney A.W., Chen D., Churchhouse C., Clarke T.-K., Coryell W., Craig D.W., Cruceanu C., Curtis D., Czerski P.M., Dale A.M., de Jong S., Degenhardt F., Del-Favero J., DePaulo J.R., Djurovic S., Dobbyn A.L., Dumont A., Elvsashagen T., Escott-Price V., Fan C.C., Fischer S.B., Flickinger M., Foroud T.M., Forty L., Frank J., Fraser C., Freimer N.B., Frisen L., Gade K., Gage D., Garnham J., Giambartolomei C., Pedersen M.G., Goldstein J., Gordon S.D., Gordon-Smith K., Green E.K., Green M.J., Greenwood T.A., Grove J., Guan W., Guzman-Parra J., Hamshere M.L., Hautzinger M., Heilbronner U., Herms S., Hipolito M., Hoffmann P., Holland D., Huckins L., Jamain S., Johnson J.S., Jureus A., Kandaswamy R., Karlsson R., Kennedy J.L., Kittel-Schneider S., Knowles J.A., Kogevinas M., Koller A.C., Kupka R., Lavebratt C., Lawrence J., Lawson W.B., Leber M., Lee P.H., Levy S.E., Li J.Z., Liu C., Lucae S., Maaser A., MacIntyre D.J., Mahon P.B., Maier W., Martinsson L., McCarroll S., McGuffin P., McInnis M.G., McKay J.D., Medeiros H., Medland S.E., Meng F., Milani L., Montgomery G.W., Morris D.W., Muhleisen T.W., Mullins N., Nguyen H., Nievergelt C.M., Adolfsson A.N., Nwulia E.A., O'Donovan C., Loohuis L.M.O., Ori A.P.S., Oruc L., Osby U., Perlis R.H., Perry A., Pfennig A., Potash J.B., Purcell S.M., Regeer E.J., Reif A., Reinbold C.S., Rice J.P., Rivas F., Rivera M., Roussos P., Ruderfer D.M., Ryu E., Sanchez-Mora C., Schatzberg A.F., Scheftner W.A., Schork N.J., Shannon Weickert C., Shehktman T., Shilling P.D., Sigurdsson E., Slaney C., Smeland O.B., Sobell J.L., Soholm Hansen C., Spijker A.T., St Clair D., Steffens M., Strauss J.S., Streit F., Strohmaier J., Szelinger S., Thompson R.C., Thorgeirsson T.E., Treutlein J., Vedder H., Wang W., Watson S.J., Weickert T.W., Witt S.H., Xi S., Xu W., Young A.H., Zandi P., Zhang P., Zollner S., Adolfsson R., Agartz I., Alda M., Backlund L., Baune B.T., Bellivier F., Berrettini W.H., Biernacka J.M., Blackwood D.H.R., Boehnke M., Borglum A.D., Corvin A., Craddock N., Daly M.J., Dannlowski U., Esko T., Etain B., Frye M., Fullerton J.M., Gershon E.S., Gill M., Goes F., Grigoroiu-Serbanescu M., Hauser J., Hougaard D.M., Hultman C.M., Jones I., Jones L.A., Kahn R.S., Kirov G., Landen M., Leboyer M., Lewis C.M., Li Q.S., Lissowska J., Martin N.G., Mayoral F., McElroy S.L., McIntosh A.M., McMahon F.J., Melle I., Metspalu A., Mitchell P.B., Morken G., Mors O., Mortensen P.B., Muller-Myhsok B., Myers R.M., Neale B.M., Nimgaonkar V., Nordentoft M., Nothen M.M., O'Donovan M.C., Oedegaard K.J., Owen M.J., Paciga S.A., Pato C., Pato M.T., Posthuma D., Ramos-Quiroga J.A., Ribases M., Rietschel M., Rouleau G.A., Schalling M., Schofield P.R., Schulze T.G., Serretti A., Smoller J.W., Stefansson H., Stefansson K., Stordal E., Sullivan P.F., Turecki G., Vaaler A.E., Vieta E., Vincent J.B., Werge T., Nurnberger J.I., Wray N.R., Di Florio A., Edenberg H.J., Cichon S., Ophoff R.A., Scott L.J., Andreassen O.A., Kelsoe J., Sklar P., eQTLGen Consortium, BIOS Consortium, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, Complex Trait Genetics

المصدر: Nature Genetics
NATURE GENETICS
eQTLGen Consortium, BIOS Consortium & the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Nature Genetics, 51(5), 793-803. Nature Publishing Group
Nature genetics
Nature Genetics, 51(5), 793. Nature Publishing Group
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H L A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B C, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Casas, M, Cerrato, F, Cervantes, P, Chambert, K, Charney, A W, Kupka, R, Posthuma, D, Stefánsson, H, Ophoff, R A, Scott, L J, Andreassen, O A, Kelsoe, J, Sklar, P & the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Pedersen, M G, Grove, J, Xu, W, Zhang, P, Børglum, A D, Mors, O, Mortensen, P B & eQTLGen Consortium 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Stahl, E A, Breen, G, Forstner, A J, Mcquillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, De Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-grauholm, J, Byerley, W, Casas, M, Cerrato, F, Cervantes, P, Chambert, K, Charney, A W, Chen, D, Churchhouse, C, Clarke, T, Coryell, W, Craig, D W, Cruceanu, C, Curtis, D, Czerski, P M, Dale, A M, De Jong, S, Degenhardt, F, Del-favero, J, Depaulo, J R, Djurovic, S, Dobbyn, A L, Dumont, A, Elvsåshagen, T, Escott-price, V, Fan, C C, Fischer, S B, Flickinger, M, Foroud, T M, Forty, L, Frank, J, Fraser, C, Freimer, N B, Frisén, L, Gade, K, Gage, D, Garnham, J, Giambartolomei, C, Pedersen, M G, Goldstein, J, Gordon, S D, Gordon-smith, K, Green, E K, Green, M J, Greenwood, T A, Grove, J, Guan, W, Guzman-parra, J, Hamshere, M L, Hautzinger, M, Heilbronner, U, Herms, S, Hipolito, M, Hoffmann, P, Holland, D, Huckins, L, Jamain, S, Johnson, J S, Juréus, A, Kandaswamy, R, Karlsson, R, Kennedy, J L, Kittel-schneider, S, Knowles, J A, Kogevinas, M, Koller, A C, Kupka, R, Lavebratt, C, Lawrence, J, Lawson, W B, Leber, M, Lee, P H, Levy, S E, Li, J Z, Liu, C, Lucae, S, Maaser, A, Macintyre, D J, Mahon, P B, Maier, W, Martinsson, L, Mccarroll, S, Mcguffin, P, Mcinnis, M G, Mckay, J D, Medeiros, H, Medland, S E, Meng, F, Milani, L, Montgomery, G W, Morris, D W, Mühleisen, T W, Mullins, N, Nguyen, H, Nievergelt, C M, Adolfsson, A N, Nwulia, E A, O’donovan, C, Loohuis, L M O, Ori, A P S, Oruc, L, Ösby, U, Perlis, R H, Perry, A, Pfennig, A, Potash, J B, Purcell, S M, Regeer, E J, Reif, A, Reinbold, C S, Rice, J P, Rivas, F, Rivera, M, Roussos, P, Ruderfer, D M, Ryu, E, Sánchez-mora, C, Schatzberg, A F, Scheftner, W A, Schork, N J, Shannon Weickert, C, Shehktman, T, Shilling, P D, Sigurdsson, E, Slaney, C, Smeland, O B, Sobell, J L, Søholm Hansen, C, Spijker, A T, St Clair, D, Steffens, M, Strauss, J S, Streit, F, Strohmaier, J, Szelinger, S, Thompson, R C, Thorgeirsson, T E, Treutlein, J, Vedder, H, Wang, W, Watson, S J, Weickert, T W, Witt, S H, Xi, S, Xu, W, Young, A H, Zandi, P, Zhang, P, Zöllner, S, Adolfsson, R, Agartz, I, Alda, M, Backlund, L, Baune, B T, Bellivier, F, Berrettini, W H, Biernacka, J M, Blackwood, D H R, Boehnke, M, Børglum, A D, Corvin, A, Craddock, N, Daly, M J, Dannlowski, U, Esko, T, Etain, B, Frye, M, Fullerton, J M, Gershon, E S, Gill, M, Goes, F, Grigoroiu-serbanescu, M, Hauser, J, Hougaard, D M, Hultman, C M, Jones, I, Jones, L A, Kahn, R S, Kirov, G, Landén, M, Leboyer, M, Lewis, C M, Li, Q S, Lissowska, J, Martin, N G, Mayoral, F, Mcelroy, S L, Mcintosh, A M, Mcmahon, F J, Melle, I, Metspalu, A, Mitchell, P B, Morken, G, Mors, O, Mortensen, P B, Müller-myhsok, B, Myers, R M, Neale, B M, Nimgaonkar, V, Nordentoft, M, Nöthen, M M, O’donovan, M C, Oedegaard, K J, Owen, M J, Paciga, S A, Pato, C, Pato, M T, Posthuma, D, Ramos-quiroga, J A, Ribasés, M, Rietschel, M, Rouleau, G A, Schalling, M, Schofield, P R, Schulze, T G, Serretti, A, Smoller, J W, Stefansson, H, Stefansson, K, Stordal, E, Sullivan, P F, Turecki, G, Vaaler, A E, Vieta, E, Vincent, J B, Werge, T, Nurnberger, J I, Wray, N R, Di Florio, A, Edenberg, H J, Cichon, S, Ophoff, R A, Scott, L J, Andreassen, O A, Kelsoe, J & Sklar, P 2019, ' Genome-wide association study identifies 30 loci associated with bipolar disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test
Online: 1546-1718
Stahl, E A, Breen, G, Forstner, A J, McQuillin, A, Ripke, S, Trubetskoy, V, Mattheisen, M, Wang, Y, Coleman, J R I, Gaspar, H A, de Leeuw, C A, Steinberg, S, Pavlides, J M W, Trzaskowski, M, Byrne, E M, Pers, T H, Holmans, P A, Richards, A L, Abbott, L, Agerbo, E, Akil, H, Albani, D, Alliey-Rodriguez, N, Als, T D, Anjorin, A, Antilla, V, Awasthi, S, Badner, J A, Bækvad-Hansen, M, Barchas, J D, Bass, N, Bauer, M, Belliveau, R, Bergen, S E, Pedersen, C B, Bøen, E, Boks, M P, Boocock, J, Budde, M, Bunney, W, Burmeister, M, Bybjerg-Grauholm, J, Byerley, W, Casas, M, de Jong, S, Kandaswamy, R, McGuffin, P, Mullins, N & Young, A H & Lewis, C M 2019, ' Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder ', Nature Genetics, vol. 51, no. 5, pp. 793-803 . https://doi.org/10.1038/s41588-019-0397-8Test

مصطلحات موضوعية: Male, Bipolar Disorder, Bipolar I disorder, Schizophrenia/genetics, LD SCORE REGRESSION, Genome-wide association study, VARIANTS, Bipolar II disorder, 0302 clinical medicine, SCHIZOPHRENIA, GWAS, Psychotic Disorders/genetics, Non-U.S. Gov't, RISK, Genetics, 0303 health sciences, HERITABILITY, Research Support, Non-U.S. Gov't, Systems Biology, Major/genetics, Single Nucleotide, 3. Good health, Schizophrenia, Major depressive disorder, Female, Case-Control Studie, Depressive Disorder, Major/genetics, Human, Psychosis, GENES, Biology, Psychotic Disorder, Research Support, Polymorphism, Single Nucleotide, Article, Bipolar Disorder/classification, N.I.H, 03 medical and health sciences, SDG 3 - Good Health and Well-being, medicine, Journal Article, POLYGENICITY, Humans, Genetic Predisposition to Disease, Bipolar disorder, Polymorphism, METAANALYSIS, 030304 developmental biology, Intramural, Depressive Disorder, Major, Depressive Disorder, Genetic heterogeneity, Research Support, N.I.H., Intramural, medicine.disease, INDIVIDUALS, Psychotic Disorders, Genetic Loci, Case-Control Studies, Human medicine, 030217 neurology & neurosurgery, Genome-Wide Association Study, Meta-Analysis

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document; image/pdf; STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a01aab7c8cdaf13b3f435a46eef431f1Test
https://doi.org/10.1038/s41588-019-0397-8Test

المؤلفون: Filippo Martinelli Boneschi, Giacomo Giacalone, Giuseppe Magnani, Gloria Biella, Elisabetta Coppi, Roberto Santangelo, Paola Brambilla, Federica Esposito, Sara Lupoli, Francesca Clerici, Luisa Benussi, Roberta Ghidoni, Daniela Galimberti, Rosanna Squitti, Annamaria Confaloni, Sabrina Pichler, Manuel Mayhaus, Matthias Riemenschneider, Claudio Mariani, Giancarlo Comi, Elio Scarpini, Giuliano Binetti, Gianluigi Forloni, Massimo Franceschi, Diego Albani, BRUNO, Giuseppe

المساهمون: Filippo Martinelli, Boneschi, Giacomo, Giacalone, Giuseppe, Magnani, Gloria, Biella, Elisabetta, Coppi, Roberto, Santangelo, Paola, Brambilla, Federica, Esposito, Sara, Lupoli, Francesca, Clerici, Luisa, Benussi, Roberta, Ghidoni, Daniela, Galimberti, Rosanna, Squitti, Annamaria, Confaloni, Bruno, Giuseppe, Sabrina, Pichler, Manuel, Mayhau, Matthias, Riemenschneider, Claudio, Mariani, Giancarlo, Comi, Elio, Scarpini, Giuliano, Binetti, Gianluigi, Forloni, Massimo, Franceschi, Diego, Albani

مصطلحات موضوعية: acetylcholinesterase inhibitor, alzheimer's disease, genetic, genome-wide association study, pharmacogenomics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23374588; info:eu-repo/semantics/altIdentifier/wos/WOS:000317417100032; volume:34; issue:6; firstpage:1711e7; lastpage:1711e13; numberofpages:7; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/11573/515444Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84875240626

الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2012.12.008Test
http://hdl.handle.net/11573/515444Test

المؤلفون: Giovanni de Girolamo, Julia C. Stingl, R Calati, J. Zohar, Daniel Souery, Alzbeta Juven-Wetzler, David Gurwitz, Chiara Fabbri, Marco Calabrò, Stuart Montgomery, Siegfried Kasper, Alessandro Serretti, Julien Mendlewicz, Concetta Crisafulli, Gianluigi Forloni, Rosalba Martines, Diego Albani

المساهمون: Fabbri, C., Crisafulli, C., Gurwitz, D., Stingl, J., Calati, R., Albani, D., Forloni, G., Calabrò, M., Martines, R., Kasper, S., Zohar, J., Juven-Wetzler, A., Souery, D., Montgomery, S., Mendlewicz, J., Girolamo, G.D., Serretti, A, Fabbri, C, Crisafulli, C, Gurwitz, D, Stingl, J, Calati, R, Albani, D, Forloni, G, Calabro, M, Martines, R, Kasper, S, Zohar, J, Juven-Wetzler, A, Souery, D, Montgomery, S, Mendlewicz, J, Girolamo, G

مصطلحات موضوعية: Male, L1, Genotype, Neuronal, Cell Adhesion Molecules, Neuronal, Integrin, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, CHL1, GAP-43 Protein, Cell Adhesion, Genetics, Humans, Polymorphism, Cell adhesion, Gene, Pharmacology, Depressive Disorder, Major, Depressive Disorder, Cell adhesion molecule, Integrin beta3, Major, Single Nucleotide, Middle Aged, Genes, antidepressant response, treatment-resistant depression, STAR*D, Phenotype, Antidepressive Agents, Antidepressive Agents, Biomarkers, Cell Adhesion, Cell Adhesion Molecules, Cell Adhesion Molecules, Neuronal, Depressive Disorder, Major, Female, GAP-43 Protein, Genome-Wide Association Study, Genotype, Humans, Integrin beta3, Male, Middle Aged, Polymorphism, Single Nucleotide, Molecular Medicine, Genetics, Pharmacology, biology.protein, Molecular Medicine, Female, Cell Adhesion Molecules, Biomarkers, Genome-Wide Association Study

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e074febec684ec194d764b93fa5c75deTest
http://hdl.handle.net/11570/3106179Test

المؤلفون: Daniela Galimberti, Francesco Lescai, Carlo Gabelli, Sandro Sorbi, Roberta Ghidoni, Aurelia Santoro, Diego Albani, Chiara Pirazzini, Giuseppe D'Agostino, Federica Esposito, Alessandra Codemo, Filippo Martinelli Boneschi, Gaetano Crepaldi, Elio Scarpini, Maurizio Cardelli, Claudio Franceschi, Fabrizio Tagliavini, Giuliano Binetti, Luisa Benussi, Francesca Marchegiani, Cristina Ruaro, Gianluigi Forloni, Fabiola Olivieri, Andrea Maria Chiamenti, Benedetta Nacmias

المساهمون: Lescai F., Chiamenti A.M., Codemo A., Pirazzini C., D'Agostino G., Ruaro C., Ghidoni R., Benussi L., Galimberti D., Esposito F., Marchegiani F., Cardelli M., Olivieri F., Nacmias B., Sorbi S., Tagliavini F., Albani D., Boneschi F.M., Binetti G., Santoro A., Forloni G., Scarpini E., Crepaldi G., Gabelli C., Franceschi C.

المصدر: Lescai, F, Chiamenti, A M, Codemo, A, Pirazzini, C, D'Agostino, G, Ruaro, C, Ghidoni, R, Benussi, L, Galimberti, D, Esposito, F, Marchegiani, F, Cardelli, M, Olivieri, F, Nacmias, B, Sorbi, S, Tagliavini, F, Albani, D, Boneschi, F M, Binetti, G, Santoro, A, Forloni, G, Scarpini, E, Crepaldi, G, Gabelli, C & Franceschi, C 2011, ' An APOE haplotype associated with decreased epsilon4 expression increases the risk of late onset Alzheimer's disease. ', Journal of Alzheimer's Disease, bind 24, nr. 2, s. 235-245 . https://doi.org/10.3233/JAD-2011-101764Test

مصطلحات موضوعية: Apolipoprotein E, Male, Linkage disequilibrium, GENETICS, Apolipoprotein E4, Late onset, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Alzheimer Disease, Risk Factors, medicine, Humans, Genetic Predisposition to Disease, Longitudinal Studies, Allele, Genetics, Chi-Square Distribution, General Neuroscience, Haplotype, Age Factors, General Medicine, Single Nucleotide, medicine.disease, POLYMORPHISM, Psychiatry and Mental health, Clinical Psychology, Haplotypes, Italy, Female, Geriatrics and Gerontology, Alzheimer's disease, Age of onset, Genome-Wide Association Study

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3931898515aece2adef5d73df7a618Test
https://pubmed.ncbi.nlm.nih.gov/21206004Test

المؤلفون: Roberta Ghidoni, Diego Albani, Elio Scarpini, Francesca Marchegiani, Claudio Franceschi, Francesco Lescai, Esposito Federica, Luisa Benussi, Silvia Bagnoli, Daniela Galimberti, Chiara Pirazzini, Gianluigi Forloni, Aurelia Santoro, Giuseppe D'Agostino, Filippo Martinelli Boneschi, Giuliano Binetti, Sandro Sorbi, Fabrizio Tagliavini, Benedetta Nacmias, Pierluigi Quadri, Fabiola Olivieri, Maurizio Cardelli

المساهمون: Lescai F., Pirazzini C., D'Agostino G., Santoro A., Ghidoni R., Benussi L., Galimberti D., Federica E., Marchegiani F., Cardelli M., Olivieri F., Nacmias B., Sorbi S., Bagnoli S., Tagliavini F., Albani D., Boneschi F.M., Binetti G., Forloni G., Quadri P., Scarpini E., Franceschi C.

المصدر: Lescai, F, Pirazzini, C, D'Agostino, G, Santoro, A, Ghidoni, R, Benussi, L, Galimberti, D, Federica, E, Marchegiani, F, Cardelli, M, Olivieri, F, Nacmias, B, Sorbi, S, Bagnoli, S, Tagliavini, F, Albani, D, Boneschi, F M, Binetti, G, Forloni, G, Quadri, P, Scarpini, E & Franceschi, C 2010, ' Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients. ', Journal of Alzheimer's Disease, bind 21, nr. 2, s. 385-388 . https://doi.org/10.3233/JAD-2010-091516Test

مصطلحات موضوعية: Apolipoprotein E, Oncology, Male, medicine.medical_specialty, Genotype, Apolipoprotein E4, Single-nucleotide polymorphism, Alzheimer Disease, genetics, Logistic regression, Polymorphism, Single Nucleotide, White People, Alzheimer Disease, Internal medicine, Apolipoprotein E4, genetics, medicine, SNP, Humans, Allele, PCDH11X, Aged, Genetics, European Continental Ancestry Group, genetics, business.industry, General Neuroscience, Haplotype, General Medicine, Middle Aged, Cadherins, Protocadherins, Cadherins, genetics, Psychiatry and Mental health, Clinical Psychology, Logistic Models, Italy, Female, Geriatrics and Gerontology, business, Genome-Wide Association Study

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::018bb3756a922ced11be06c86e7ac228Test
https://pubmed.ncbi.nlm.nih.gov/20555150Test

المؤلفون: Diego, Albani, Angelica, Vittori, Sara, Batelli, Letizia, Polito, Stefania, De Mauro, Daniela, Galimberti, Elio, Scarpini, Carlo, Lovati, Claudio, Mariani, Gianluigi, Forloni

المصدر: European neurology. 62(2)

مصطلحات موضوعية: Male, Serotonin Plasma Membrane Transport Proteins, Polymorphism, Genetic, Parkinson Disease, Sequence Analysis, DNA, Middle Aged, Polymorphism, Single Nucleotide, Logistic Models, Haplotypes, Italy, Risk Factors, Mutation, Odds Ratio, Humans, Female, Genetic Predisposition to Disease, Promoter Regions, Genetic, Aged, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::ed6d30d95c0d5d2f0fcb9a5b9e08ede2Test
https://pubmed.ncbi.nlm.nih.gov/19521089Test