المؤلفون: Stein, Jason L, Medland, Sarah E, Bernard, Manon, Nauck, Matthias, Nöthen, Markus M., Olvera, Rene L, Pandolfo, Massimo, Pike, G Bruce, Puls, Ralf, Reinvang, Ivar, Rentería, Miguel E, Rietschel, Marcella, Roffman, Joshua L, Brown, Andrew A, Royle, Natalie A, Rujescu, Dan, Savitz, Jonathan, Schnack, Hugo G, Schnell, Knut, Seiferth, Nina, Smith, Colin, Steen, Vidar M, Valdés Hernández, Maria C, Van den Heuvel, Martijn, Cannon, Dara M, van der Wee, Nic J, Van Haren, Neeltje E M, Veltman, Joris A, Völzke, Henry, Walker, Robert, Westlye, Lars T, Whelan, Christopher D, Agartz, Ingrid, Boomsma, Dorret I, Cavalleri, Gianpiero L, Chakravarty, M Mallar, Dale, Anders M, Djurovic, Srdjan, Drevets, Wayne C, Hagoort, Peter, Hall, Jeremy, Heinz, Andreas, Jack, Clifford R, Foroud, Tatiana M, Le Hellard, Stephanie, Macciardi, Fabio, Christoforou, Andrea, Montgomery, Grant W, Poline, Jean Baptiste, Porteous, David J, Sisodiya, Sanjay M, Starr, John M, Sussmann, Jessika, Toga, Arthur W, Veltman, Dick J, Walter, Henrik, Weiner, Michael W, Domin, Martin, Initiative, Alzheimer's Disease Neuroimaging, Consortium, EPIGEN, Consortium, IMAGEN, Group, Saguenay Youth Study, Bis, Joshua C, Ikram, M Arfan, Smith, Albert V, Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Grimm, Oliver, Launer, Lenore J, DeCarli, Charles, Seshadri, Sudha, Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology, Andreassen, Ole A, Apostolova, Liana G, Bastin, Mark E, Blangero, John, Brunner, Han G, Buckner, Randy L, Hollinshead, Marisa, Cichon, Sven, Coppola, Giovanni, de Zubicaray, Greig I, Deary, Ian J, Donohoe, Gary, de Geus, Eco J C, Espeseth, Thomas, Fernández, Guillén, Glahn, David C, Grabe, Hans J, Holmes, Avram J, Hardy, John, Hulshoff Pol, Hilleke E, Jenkinson, Mark, Kahn, René S, McDonald, Colm, McIntosh, Andrew M, McMahon, Francis J, McMahon, Katie L, Meyer-Lindenberg, Andreas, Morris, Derek W, Homuth, Georg, Müller-Myhsok, Bertram, Nichols, Thomas E, Ophoff, Roel A, Paus, Tomas, Pausova, Zdenka, Penninx, Brenda W, Potkin, Steven G, Sämann, Philipp G, Saykin, Andrew J, Schumann, Gunter, Vasquez, Alejandro Arias, Hottenga, Jouke-Jan, Smoller, Jordan W, Wardlaw, Joanna M, Weale, Michael E, Martin, Nicholas G, Franke, Barbara, Wright, Margaret J, Thompson, Paul M, Consortium, Enhancing Neuro Imaging Genetics through Meta-Analysis, Weiner, Michael, Aisen, Paul, Langan, Camilla, Petersen, Ronald, Jagust, William, Trojanowki, John Q, Beckett, Laurel, Green, Robert C, Morris, John, Liu, Enchi, Lopez, Lorna M, Montine, Tom, Gamst, Anthony, Thomas, Ronald G, Donohue, Michael, Walter, Sarah, Gessert, Devon, Sather, Tamie, Hansell, Narelle K, Harvey, Danielle, Kornak, John, Dale, Anders, Bernstein, Matthew, Felmlee, Joel, Fox, Nick, Hwang, Kristy S, Thompson, Paul, Schuff, Norbert, Alexander, Gene, Bandy, Dan, Koeppe, Robert A, Foster, Norm, Reiman, Eric M, Chen, Kewei, Mathis, Chet, Kim, Sungeun, Cairns, Nigel J, Taylor-Reinwald, Lisa, Trojanowki, J. Q., Shaw, Les, Lee, Virginia M Y, Korecka, Magdalena, Crawford, Karen, Neu, Scott, Laje, Gonzalo, Potkin, Steven, Shen, Li, Kachaturian, Zaven, Frank, Richard, Snyder, Peter J, Molchan, Susan, Kaye, Jeffrey, Quinn, Joseph, Lee, Phil H, Lind, Betty, Dolen, Sara, Schneider, Lon S, Pawluczyk, Sonia, Spann, Bryan M, Brewer, James, Vanderswag, Helen, Heidebrink, Judith L, Lord, Joanne L, Liu, Xinmin, Johnson, Kris, Doody, Rachelle S, Villanueva-Meyer, Javier, Chowdhury, Munir, Stern, Yaakov, Honig, Lawrence S, Bell, Karen L, Morris, John C, Ances, Beau, Carroll, Maria, Loth, Eva, Leon, Sue, Mintun, Mark A, Schneider, Stacy, Marson, Daniel, Griffith, Randall, Clark, David, Grossman, Hillel, Mitsis, Effie, Romirowsky, Aliza, deToledo-Morrell, Leyla, Hibar, Derrek P, Lourdusamy, Anbarasu, Shah, Raj C, Duara, Ranjan, Varon, Daniel, Roberts, Peggy, Albert, Marilyn, Onyike, Chiadi, Kielb, Stephanie, Rusinek, Henry, de Leon, Mony J, Glodzik, Lidia, Mattingsdal, Morten, De Santi, Susan, Doraiswamy, P Murali, Petrella, Jeffrey R, Coleman, R Edward, Arnold, Steven E, Karlawish, Jason H, Wolk, David, Smith, Charles D, Jicha, Greg, Hardy, Peter, Mohnke, Sebastian, Lopez, Oscar L, Oakley, MaryAnn, Simpson, Donna M, Porsteinsson, Anton P, Goldstein, Bonnie S, Martin, Kim, Makino, Kelly M, Ismail, M Saleem, Mulnard, Ruth A, Thai, Gaby, Maniega, Susana Muñoz, Mc-Adams-Ortiz, Catherine, Womack, Kyle, Mathews, Dana, Quiceno, Mary, Diaz-Arrastia, Ramon, King, Richard, Weiner, Myron, Martin-Cook, Kristen, DeVous, Michael, Levey, Allan I, Nho, Kwangsik, Lah, James J, Cellar, Janet S, Burns, Jeffrey M, Anderson, Heather S, Swerdlow, Russell H, Apostolova, Liana, Lu, Po H, Bartzokis, George, Silverman, Daniel H S, Graff-Radford, Neill R, Nugent, Allison C, Parfitt, Francine, Johnson, Heather, Farlow, Martin R, Hake, Ann Marie, Matthews, Brandy R, Herring, Scott, van Dyck, Christopher H, Carson, Richard E, MacAvoy, Martha G, Chertkow, Howard, O'Brien, Carol, Bergman, Howard, Hosei, Chris, Black, Sandra, Stefanovic, Bojana, Caldwell, Curtis, Hsiung, Ging-Yuek Robin, Feldman, Howard, Mudge, Benita, Assaly, Michele, Kertesz, Andrew, Papmeyer, Martina, Rogers, John, Trost, Dick, Bernick, Charles, Munic, Donna, Kerwin, Diana, Mesulam, Marek-Marsel, Lipowski, Kristina, Wu, Chuang-Kuo, Johnson, Nancy, Sadowsky, Carl, Pütz, Benno, Martinez, Walter, Villena, Teresa, Turner, Raymond Scott, Johnson, Kathleen, Reynolds, Brigid, Sperling, Reisa A, Johnson, Keith A, Marshall, Gad, Frey, Meghan, Yesavage, Jerome, Ramasamy, Adaikalavan, Taylor, Joy L, Lane, Barton, Rosen, Allyson, Tinklenberg, Jared, Sabbagh, Marwan, Belden, Christine, Jacobson, Sandra, Kowall, Neil, Killiany, Ronald, Budson, Andrew E, Senstad, Rudy E, Rasmussen, Jerod, Norbash, Alexander, Johnson, Patricia Lynn, Obisesan, Thomas O, Wolday, Saba, Bwayo, Salome K, Lerner, Alan, Hudson, Leon, Ogrocki, Paula, Fletcher, Evan, Carmichael, Owen, Rijpkema, Mark, Olichney, John, Kittur, Smita, Borrie, Michael, Lee, T-Y, Bartha, Rob, Johnson, Sterling, Asthana, Sanjay, Carlsson, Cynthia M, Risacher, Shannon L, Preda, Adrian, Nguyen, Dana, Tariot, Pierre, Fleisher, Adam, Reeder, Stephanie, Bates, Vernice, Capote, Horacio, Rainka, Michelle, Scharre, Douglas W, Kataki, Maria, Roddey, J Cooper, Zimmerman, Earl A, Celmins, Dzintra, Brown, Alice D, Pearlson, Godfrey D, Blank, Karen, Anderson, Karen, Santulli, Robert B, Schwartz, Eben S, Sink, Kaycee M, Rose, Emma J, Williamson, Jeff D, Garg, Pradeep, Watkins, Franklin, Ott, Brian R, Querfurth, Henry, Tremont, Geoffrey, Salloway, Stephen, Malloy, Paul, Correia, Stephen, Rosen, Howard J, Ryten, Mina, Miller, Bruce L, Mintzer, Jacobo, Longmire, Crystal Flynn, Spicer, Kenneth, Finger, Elizabeth, Rachinsky, Irina, Drost, Dick, Cavalleri, Gianpiero, Alhusaini, Saud, Delanty, Norman, Whelan, Christopher, Sisodiya, Sanjay, Kasperaviciute, Dalia, Matarin, Mar, Depondt, Chantal, Goldstein, David B, Heinzen, Erin L, Shianna, Kevin, Sprooten, Emma, Radtke, Rodney, Ottmann, Ruth, Sergievsky, G. H., Schumann, G., Conrod, P., Reed, L., Barker, G., Williams, S., Loth, E., Struve, M., Strengman, Eric, Lourdusamy, A., Cattrell, A., Nymberg, C., Topper, L., Smith, L., Havatzias, S., Stueber, K., Mallik, C., Stacey, D., Wong, C Peng, Teumer, Alexander, Werts, H., Andrew, C., Desrivieres, S., Heinz, A., Gallinat, J., Häke, I., Ivanov, N., Klär, A., Reuter, J., Winkler, Anderson M, Trabzuni, Daniah, Palafox, C., Hohmann, C., Schilling, C., Lüdemann, K., Romanowski, A., Ströhle, A., Wolff, E., Rapp, M., Ittermann, B., Brühl, R., Turner, Jessica, Ihlenfeld, A., Walaszek, B., Schubert, F., Garavan, H., Connolly, C., Jones, J., Lalor, E., McCabe, E., Ní Shiothcháin, A., Whelan, R., van Eijk, Kristel, Spanagel, R., Leonardi-Essmann, F., Sommer, W., Flor, H., Vollstaedt-Klein, S., Nees, F., Banaschewski, T., Poustka, L., Steiner, S., Mann, K., van Erp, Theo G M, Buehler, M., Rietschel, M., Stolzenburg, E., Schmal, C., Schirmbeck, F., Paus, T., Gowland, P., Heym, N., Lawrence, C., Newman, C., van Tol, Marie-Jose, Pausova, Z., Smolka, M., Huebner, T., Ripke, S., Mennigen, E., Muller, K., Ziesch, V., Büchel, C., Bromberg, U., Fadai, T., Wittfeld, Katharina, Lueken, L., Yacubian, J., Finsterbusch, J., Martinot, J. L., Artiges, E., Bordas, N., de Bournonville, S., Bricaud, Z., Gollier Briand, F., Lemaitre, H., Wolf, Christiane, Massicotte, J., Miranda, R., Paillère Martinot, M. L., Penttilä, J., Poline, J. B., Barbot, A., Schwartz, Y., Lalanne, C., Frouin, V., Thyreau, B., Woudstra, Saskia, Dalley, J., Mar, A., Robbins, T., Subramaniam, N., Theobald, D., Richmond, N., de Rover, M., Molander, A., Jordan, E., Robinson, E., Aleman, Andre, Hipolata, L., Moreno, M., Arroyo, M., Stephens, D., Ripley, T., Crombag, H., Pena, Y., Lathrop, M., Zelenika, D., Heath, S., Lanzerath, D., Heinrichs, B., Spranger, T., Fuchs, B., Speiser, C., Resch, F., Haffner, J., Parzer, P., Brunner, R., Klaassen, A., Toro, Roberto, Almasy, Laura, Klaassen, I., Constant, P., Mignon, X., Thomsen, T., Zysset, S., Vestboe, A., Ireland, J., Rogers, J., Binder, Elisabeth B, Chakravarty, Mallar, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Shulman, Joshua M, Brohawn, David G, Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F J, DeStefano, Anita L, Lambert, Jean-Charles, Cantor, Rita M, Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A, Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H, Enzinger, Christian, Danoy, Patrick, Carless, Melanie A, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A, de Bruijn, Renée F A G, Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J, Corvin, Aiden, Chibnik, Lori B, Gislason, Gauti K, Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B, Phan, Thanh G, Oostra, Ben A, Nalls, Michael A, Uitterlinden, Andre G, Czisch, Michael, Au, Rhoda, Elbaz, Alexis, Beare, Richard J, van Swieten, John C, Lopez, Oscar, Harris, Tamara B, Chouraki, Vincent, Breteler, Monique M B, De Jager, Philip L, Becker, James T, Curran, Joanne E, Knopman, David, Fazekas, Franz, Wolf, Philip A, van der Lugt, Aad, Longstreth, W. T., Brown, Mathew A, Bennett, David A, van Duijn, Cornelia M, Davies, Gail, Mosley, Thomas H, Schmidt, Reinhold, de Almeida, Marcio A A, Appel, Katja, Duggirala, Ravi, Dyer, Thomas D, Erk, Susanne, Fagerness, Jesen, Fox, Peter T, Freimer, Nelson B, Gill, Michael, Göring, Harald H H, Bartecek, Richard, Hagler, Donald J, Hoehn, David, Holsboer, Florian, Hoogman, Martine, Hosten, Norbert, Jahanshad, Neda, Johnson, Matthew P, Kent, Jack W, Kochunov, Peter, Bergmann, Ørjan, Lancaster, Jack L, Lawrie, Stephen M, Liewald, David C, Mandl, René, Mattheisen, Manuel, Meisenzahl, Eva, Melle, Ingrid, Moses, Eric K, Mühleisen, Thomas W

المساهمون: David Geffen School of Medicine [Los Angeles], University of California [Los Angeles] (UCLA), University of California-University of California, Queensland Institute of Medical Research, Radboud University Medical Center [Nijmegen], Yale University School of Medicine, Génétique Humaine et Fonctions Cognitives, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Universität Greifswald - University of Greifswald, Universität Heidelberg [Heidelberg], University Medical Center [Utrecht], University of Oslo (UiO), University of Toronto, National University of Ireland [Galway] (NUI Galway), Montreal Neurological Institute and Hospital, McGill University = Université McGill [Montréal, Canada], University of Bergen (UiB), Harvard University [Cambridge], VU University Amsterdam, University of Edinburgh, Structure et Réactivité des Systèmes Moléculaires Complexes (SRSMC), Institut de Chimie du CNRS (INC)-Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS), Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], National Institutes of Health [Bethesda] (NIH), Department of Forensic and Neurodevelopmental Sciences, King‘s College London, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Georgia State University, University System of Georgia (USG), Department of Psychiatry and Human Behavior [Irvine], University of California [Irvine] (UCI), Leiden University Medical Center (LUMC), Dundee Technopole, CXR Biosciences Ltd, University of Groningen [Groningen], Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland (RCSI), Department of Genetics, Southwest Foundation for Biomedical Research, Bijvoet Center of Biomolecular Research [Utrecht], Utrecht University [Utrecht], Neurology Division, Beaumont Hospital, Dublin 9, Ireland, Beaumont Hospital, The University of Texas Health Science Center at Houston (UTHealth), Center for Neurobehavioral Genetics, Max Planck Institute of Psychiatry, Max-Planck-Gesellschaft, Department of Computer Science, Durham University, Laboratoire des symbioses tropicales et méditerranéennes (UMR LSTM), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Université Montpellier 1 (UM1)-Institut de Recherche pour le Développement (IRD)-Institut National de la Recherche Agronomique (INRA)-Université Montpellier 2 - Sciences et Techniques (UM2)-Université de Montpellier (UM)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Charité - UniversitätsMedizin = Charité - University Hospital [Berlin], University of California, Institute of Neurology [London], University College of London [London] (UCL), University of California [San Francisco] (UCSF), Department of Medicine, University of Washington [Seattle], Erasmus University Medical Center [Rotterdam] (Erasmus MC), Centre Émile Durkheim (CED), Sciences Po Bordeaux - Institut d'études politiques de Bordeaux (IEP Bordeaux)-Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Università degli Studi di Salermo, Università degli Studi di Salerno (UNISA), School of Psychology, University of Queensland, University of Queensland [Brisbane], Hartford Hospital, Lancaster University, Centre for Advanced Imaging, McConnell Brain Imaging Centre (MNI), McGill University = Université McGill [Montréal, Canada]-McGill University = Université McGill [Montréal, Canada], Stanley Center for Psychiatric Research, Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston]-Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Faculteit Medische Wetenschappen/UMCG, Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Perceptual and Cognitive Neuroscience (PCN), Biological Psychology, Neuroscience Campus Amsterdam - Brain Imaging, EMGO+ - Mental Health, EPIGEN Consortium, IMAGENConsortium, Saguenay Youth Study Group, the Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium, Psychiatry, NCA - Brain Imaging, EMGO - Mental health, Vrije universiteit = Free university of Amsterdam [Amsterdam] (VU), Virology, Epidemiology, Clinical Chemistry, Erasmus MC other, Radiology & Nuclear Medicine, University of California (UC)-University of California (UC), Yale School of Medicine [New Haven, Connecticut] (YSM), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Universität Heidelberg [Heidelberg] = Heidelberg University, Harvard University, Vrije Universiteit Amsterdam [Amsterdam] (VU), University of California [Irvine] (UC Irvine), Universiteit Leiden, University of California (UC), University of California [San Francisco] (UC San Francisco), Università degli Studi di Salerno = University of Salerno (UNISA), University of Iceland [Reykjavik], McGill University, University of Bergen (UIB), Université de Lorraine (UL)-Centre National de la Recherche Scientifique (CNRS), Bijvoet Center of Biomolecular Research, Charité - Universitätsmedizin Berlin / Charite - University Medicine Berlin, UMR5116, Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS)-Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), McGill University-McGill University

المصدر: Nature genetics 44, 552-561 (2012). doi:10.1038/ng.2250
Nature Genetics
Nature Genetics, Nature Publishing Group, 2012, 44 (5), pp.552-561. ⟨10.1038/ng.2250⟩
Nature Genetics, 44(5), 552-+. Nature Publishing Group
Nature Genetics, 44(5), 552-561. Nature Publishing Group
Nature Genetics, 44, 552-61
Stein, J L, Medland, S E, Arias-Vasquez, A, Hibar, D P, Senstad, R E, Winkler, A M, Toro, R, Appel, K, Bartecek, R, Bergmann, O, Hottenga, J J, Boomsma, D I, Montgomery, G W, de Geus, E J C, Hulshoff Pol, H E, Kahn, R S, Penninx, B W J H, Sämann, P G, Saykin, A J, Schumann, G, Smoller, J W, Wardlaw, J M, Weale, M E, Martin, N G, Franke, B, Wright, M J & Thompson, P M 2012, ' Identification of common variants associated with human hippocampal and intracranial volumes ', Nature Genetics, vol. 44, no. 5, pp. 552-561 . https://doi.org/10.1038/ng.2250Test
Nature genetics 44(5), 552-561 (2012). doi:10.1038/ng.2250
Nature Genetics, 44, 5, pp. 552-61
Nature Genetics, 44(5), 552
Stein, J L, Medland, S E, Vasquez, A A, Hibar, D P, Senstad, R E, Winkler, A M, Toro, R, Appel, K, Bartecek, R, Bergmann, O, Bernard, M, Brown, A A, Cannon, D M, Chakravarty, M M, Christoforou, A, Domin, M, Grimm, O, Hollinshead, M, Holmes, A J, Homuth, G, Hottenga, J-J, Langan, C, Lopez, L M, Hansell, N K, Hwang, K S, Kim, S, Laje, G, Lee, P H, Liu, X, Loth, E, Lourdusamy, A, Mattingsdal, M, Mohnke, S, Maniega, S M, Nho, K, Nugent, A C, Davies, G, Lawrie, S M, Liewald, D C, Royle, N A, Smith, C, Valdés Hernández, M C, Hall, J, Porteous, D J, Starr, J M, Sussmann, J, Bastin, M E, Deary, I J & McIntosh, A M & Wardlaw, J M 2012, ' Identification of common variants associated with human hippocampal and intracranial volumes ', Nature Genetics, vol. 44, no. 5, pp. 552-561 . https://doi.org/10.1038/ng.2250Test
Nature Genetics, 2012, 44 (5), pp.552-561. ⟨10.1038/ng.2250⟩
Nature Genetics; Vol 44

مصطلحات موضوعية: Netherlands Twin Register (NTR), Pathology, 110 012 Social cognition of verbal communication, [SDV]Life Sciences [q-bio], Hippocampus, Genome-wide association study, DCN PAC - Perception action and control, Hippocampal formation, physiopathology [Brain], Bioinformatics, 0302 clinical medicine, 130 000 Cognitive Neurology & Memory, TEMPORAL-LOBE EPILEPSY, 110 014 Public activities, Renal disorder [IGMD 9], 0303 health sciences, medicine.diagnostic_test, Translational research Immune Regulation [ONCOL 3], Brain, Human brain, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], ALZHEIMERS-DISEASE, medicine.anatomical_structure, Brain size, genetics [Chromosomes, Human, Pair 12], genetics [Polymorphism, Single Nucleotide], Biomarker (medicine), NA+/H+ EXCHANGER, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Genetic Markers, medicine.medical_specialty, 110 000 Neurocognition of Language, DCN MP - Plasticity and memory, A neurocomputational model for the Processing of Linguistic Utterances based on the Unification-Space architecture [110 007 PLUS], BRAIN VOLUME, UNIFIED APPROACH, 110 013 Binding and the MUC-model, Neuroimaging, Biology, GENOTYPE IMPUTATION, Polymorphism, Single Nucleotide, Article, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], 03 medical and health sciences, AUTOMATED SEGMENTATION, Meta-Analysis as Topic, SDG 3 - Good Health and Well-being, ddc:570, FUNCTIONAL IMPLICATIONS, Genetics, medicine, Humans, GENOME-WIDE ASSOCIATION, 030304 developmental biology, Chromosomes, Human, Pair 12, Magnetic resonance imaging, Genetic Loci, physiopathology [Hippocampus], 110 009 The human brain and Chinese prosody, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], HUMAN HEIGHT, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8111baa0f5f935359719e49c7b34423fTest
https://research.vu.nl/en/publications/a1783293-b8fa-444d-8373-02190b79846bTest

المؤلفون: Josep Antoni Ramos-Quiroga, Christian Jacob, Andrea Boreatti-Hümmer, Noèlia Fernàndez-Castillo, Mònica Bayés, C.C. Kan, Miguel Casas, Philip Asherson, Klaus-Peter Lesch, Cristina Sánchez-Mora, Monika Heine, Bru Cormand, Nuria Gómez-Barros, Helene Barone Halleland, Lambertus A. Kiemeney, Jan Haavik, Ole Bernt Fasmer, E.T. Landaas, Marta Ribasés, Martine Hoogman, Andreas Reif, Angelien Heister, Anne Halmøy, Per M. Knappskog, Rosa Bosch, Stephen V. Faraone, Alejandro Arias Vasquez, Jan K. Buitelaar, Barbara Franke, Jasmin Romanos, A. Marije Boonstra, Stefan Johansson, J. J. Sandra Kooij

المساهمون: Clinical Child and Family Studies, Clinical Neuropsychology, LEARN! - Brain, learning and development, Department of Psychology, Education and Child Studies

المصدر: Neuropsychopharmacology, 35, 656-664. Nature Publishing Group
Neuropsychopharmacology, 35, 656-64
Neuropsychopharmacology
Neuropsychopharmacology, 35, 3, pp. 656-64
Boonstra, A M, Franke, B, Vasquez, A A, Johansson, S, Hoogman, M, Romanos, J & Boreatti-Hümmer, A 2010, ' Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD ', Neuropsychopharmacology, vol. 35, pp. 656-664 . https://doi.org/10.1038/npp.2009.170Test

مصطلحات موضوعية: Adult, Male, Internationality, Adolescent, Neurogenetics, Single-nucleotide polymorphism, Aetiology, screening and detection [ONCOL 5], Minisatellite Repeats, behavioral disciplines and activities, Genomic disorders and inherited multi-system disorders [IGMD 3], Young Adult, Genotype, mental disorders, Perception and Action [DCN 1], Humans, Allele, Child, Aged, Retrospective Studies, Dopamine transporter, Genetic association, Pharmacology, Genetics, Mental Health [NCEBP 9], Dopamine Plasma Membrane Transport Proteins, biology, Haplotype, Age Factors, Middle Aged, Psychiatry and Mental health, Variable number tandem repeat, Haplotypes, Evaluation of complex medical interventions [NCEBP 2], Attention Deficit Disorder with Hyperactivity, biology.protein, Female, Original Article, Psychology, Functional Neurogenomics [DCN 2]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29744e6ff2e43fb7186e3c81377c1406Test
https://research.vu.nl/en/publications/555998a5-de2c-439b-a9ba-22feb2c9f6aaTest

المؤلفون: S Gloudemans, Nicoline Hoogerbrugge, Jan C. Oosterwijk, Danielle Bodmer, K Ansink, AH van der Hout, M.J.L. Ligtenberg

المساهمون: Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON)

المصدر: British Journal of Cancer
British Journal of Cancer, 95, 6, pp. 757-62
British Journal of Cancer, 95, 757-62
British Jounal of Cancer, 95(6), 757-762. Nature Publishing Group

مصطلحات موضوعية: Cancer Research, Genetics and epigenetic pathways of disease [NCMLS 6], SCORING SYSTEM, FAMILY-HISTORY, Cohort Studies, Statistics, Cutoff, Medicine, Molecular diagnosis, prognosis and monitoring [UMCN 1.2], RISK, Genetics, Ovarian Neoplasms, BRCA1 Protein, WOMEN, GERMLINE MUTATIONS, Middle Aged, PREVALENCE, Pedigree, ovarian cancer, Oncology, Growth and differentiation [NCMLS 3], Mutation (genetic algorithm), Female, Risk assessment, probability model, Adult, Risk management tools, Breast Neoplasms, Risk Assessment, Sensitivity and Specificity, OVARIAN-CANCER, Genomic disorders and inherited multi-system disorders [IGMD 3], Molecular epidemiology [NCEBP 1], Breast cancer, breast cancer, Translational research [ONCOL 3], Predictive Value of Tests, BREAST-CANCER, Humans, Genetic Predisposition to Disease, Selection (genetic algorithm), Probability, Retrospective Studies, BRCA2 Protein, Models, Statistical, Hereditary cancer and cancer-related syndromes [ONCOL 1], business.industry, Patient Selection, BRCA mutation, CANCER-SUSCEPTIBILITY GENES, Genetics and Genomics, medicine.disease, BRCA1, BRCA2, PREDICTION MODELS, Mutation, business, Predictive modelling

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c91cb990bb38281963a634238ccc915Test
http://europepmc.org/articles/PMC2360521Test

المؤلفون: Reif, A., Nguyen, T.T., Weissflog, L., Jacob, C.P., Romanos, M., Renner, T.J., Buttenschon, H.N., Kittel-Schneider, S., Gessner, A., Weber, H., Neuner, M., Gross-Lesch, S., Zamzow, K., Kreiker, S., Walitza, S., Meyer, J., Freitag, C.M., Bosch, R., Casas, M., Gomez, N., Ribases, M., Bayes, M., Buitelaar, J.K., Kiemeney, L.A.L.M., Kooij, J.J., Kan, C.C., Hoogman, M., Johansson, S., Jacobsen, K.K., Knappskog, P.M., Fasmer, O.B., Asherson, P., Warnke, A., Grabe, H.J., Mahler, J., Teumer, A., Volzke, H., Mors, O.N., Schafer, H., Ramos-Quiroga, J.A., Cormand, B., Haavik, J., Franke, B., Lesch, K.P.

المصدر: Neuropsychopharmacology, 36, 11, pp. 2318-27

مصطلحات موضوعية: 110 012 Social cognition of verbal communication, 150 000 MR Techniques in Brain Function, DCN 1: Perception and Actions NCEBP 9: Mental Health, DCN 2: Functional Neurogenomics, IGMD 3: Genomic disorders and inherited multi-system disorders, IGMD 3: Genomic disorders and inherited multi-system disorders DCN 2: Functional Neurogenomics, NCEBP 1: Molecular epidemiology ONCOL 5: Aetiology, screening and detection, NCEBP 9: Mental health, psy, demo

العلاقة: http://hdl.handle.net/2066/95784Test

الإتاحة: http://hdl.handle.net/2066/95784Test

المؤلفون: Sullivan, P., Andreassen, Ole A, Anney, Richard J L, Asherson, Philip, Ashley-Koch, Allison, Blackwood, Douglas, Boomsma, Dorret I, Breen, Gerome, Buitelaar, Jan, Bulik, Cynthia M, Cichon, Sven, Collier, David, Corvin, Aiden, Craddock, Nicholas, DeLisi, Lynn E, Ebstein, Richard, Edenberg, Howard J, Estivill, Xavier, Faraone, Stephen V, Farmer, Anne E, Fernandez-Aranda, Fernando, Flint, Jonathan, Foroud, Tatiana, Franke, Barbara, Gelernter, Joel, Gill, Michael, Grabe, Hans J, Hamilton, Steven P, Hickie, Ian B, Hoogendijk, Witte, Jablensky, Assen, Kalaydjieva, Luba, Kaprio, Jaakko, Kas, Martien, Keller, Matthew, Kelsoe, John, Kendler, Kenneth S, Kennedy, Martin, Kent, Lindsey, Klump, Kelly, Knowles, James A, Levinson, Douglas F, Lewis, Cathryn M, Lichtenstein, Paul, Lucae, Susanne, Martin, Nicholas G, McCarroll, Steve, McGough, James, McGrath, John J, McGuffin, Peter, Mitchell, Philip, Mowry, Bryan, Muglia, Pierandrea, Müller-Myhsok, Bertram, Neale, Benjamin, Nöthen, Markus, Nurnberger, John I, Oades, Robert D., O'Donovan, Michael, Ophoff, Roel, Owen, Michael, Pato, Carlos N, Pato, Michele T, Penninx, Brenda W, Perlis, Roy H, Porjesz, Bernice, Posthuma, Danielle, Potash, James B, Preisig, Martin, Reichborn-Kjennerud, Ted, Rice, John P, Rietschel, Marcella, Riley, Brien, Ripke, Stephan, Rothenberger, Aribert, Rujescu, Dan, Santangelo, Susan L, Schachar, Russell, Schellenberg, Gerard D, Scherer, Stephen W, Schofield, Peter, Schulze, Thomas G, Sklar, Pamela, Smoller, Jordan W, Stefansson, Hreinn, Stefansson, Kari, Todorov, Alexandre, Tozzi, Federica, Tzeng, Jung-Ying, van den Oord, Edwin J. C. G., Vorstman, Jacob A S, Wang, Kai, Weissman, Myrna M, Werge, Thomas, Wray, Naomi R, Zeggini, Eleftheria

المساهمون: Psychiatry, Human genetics, EMGO - Mental health, NCA - Attention & Cognition, Functional Genomics, Biological Psychology, Neuroscience Campus Amsterdam - Attention & Cognition, EMGO+ - Mental Health

المصدر: Molecular Psychiatry, 17(1), 2-3. Nature Publishing Group
Sullivan, P F, Penninx, B W J H, Boomsma, D I & Posthuma, D 2012, ' Don't give up on GWAS ', Molecular Psychiatry, vol. 17, no. 1, pp. 2-3 . https://doi.org/10.1038/mp.2011.94Test
Molecular Psychiatry, 17, 2-3
Molecular Psychiatry, 17, 1, pp. 2-3

مصطلحات موضوعية: Netherlands Twin Register (NTR), Mental Disorders, Medizin, Genomic disorders and inherited multi-system disorders [DCN PAC - Perception action and control IGMD 3], Article, Genomic disorders and inherited multi-system disorders DCN MP - Plasticity and memory [IGMD 3], Cellular and Molecular Neuroscience, Psychiatry and Mental health, Financial Support, Humans, DCN PAC - Perception action and control NCEBP 9 - Mental health, Psychology, Molecular Biology, Humanities, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcd9e9fa4ae4d6c843b1f96fc08bdd3cTest
https://doi.org/10.1038/mp.2011.94Test

المؤلفون: Asherson, P., Zhou, K., Anney, R., Franke, B., Buitelaar, J.K., Ebstein, R.P., Gill, M., Altink, M.E., Arnold, R., Boer, F., Brookes, K., Buschgens, C.J.M., Butler, L., Cambell, D., Chen, W., Christiansen, H., Feldman, L.B., Fleischman, K., Fliers, E.A., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriels, I., Johansson, L., Lubetzki, I., Marco, R., Medad, S., Minderaa, R.B., Mulas, F., Muller, U., Mulligan, A., Neale, B., Rijsdijk, F., Rabin, K., Lambregts-Rommelse, N.N.J., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Xu, X., Banaschewski, T., Sonuga-Barke, E.J.S., Eisenberg, J., Manor, I., Miranda, A., Oades, R.D., Roeyers, H., Rothenberger, A., Sergeant, J.A., Steinhausen, H.C., Taylor, E., Thompson, M., Faraone, S.V.

المصدر: Molecular Psychiatry, 13, 5, pp. 514-21

مصطلحات موضوعية: DCN 1: Perception and Action, DCN 2: Functional Neurogenomics, DCN 3: Neuroinformatics, IGMD 3: Genomic disorders and inherited multi-system disorders, NCEBP 9: Mental health, NCMLS 6: Genetics and epigenetic pathways of disease, UMCN 3.2: Cognitive neurosciences, UMCN 5.1: Genetic defects of metabolism, demo, envir

العلاقة: http://hdl.handle.net/2066/69343Test

الإتاحة: http://hdl.handle.net/2066/69343Test

المؤلفون: J. van Reeuwijk, L. De Meirleir, J Ranells, G Gillessen Kaesbach, Maciej Adamowicz, Emmanuelle Lemyre, I Salafsky, Jolanta Sykut-Cegielska, Eva Morava, Han G. Brunner, Peter Meinecke, Zsolt Urban, Ron A. Wevers, Dirk J. Lefeber

المساهمون: Pediatrics

المصدر: European Journal of Human Genetics, 16, 1, pp. 28-35
European Journal of Human Genetics, 16, 28-35

مصطلحات موضوعية: Male, Systemic disease, medicine.medical_specialty, Pathology, cutis laxa syndrome, Glycosylation, Energy and redox metabolism [NCMLS 4], Genetics and epigenetic pathways of disease [NCMLS 6], Hearing loss, Central nervous system, Genes, Recessive, Biology, Neuroinformatics [DCN 3], Cutis Laxa, Genomic disorders and inherited multi-system disorders [IGMD 3], Internal medicine, Genetics, medicine, Perception and Action [DCN 1], Humans, Abnormalities, Multiple, isoelectric focusing, Child, Genetics (clinical), Genetic heterogeneity, Infant, Syndrome, Glycostation disorders [IGMD 4], medicine.disease, Phenotype, Neuromuscular development and genetic disorders [UMCN 3.1], Pedigree, Endocrinology, medicine.anatomical_structure, Palpebral fissure, Mitochondrial medicine [IGMD 8], Genetic defects of metabolism [UMCN 5.1], Child, Preschool, Female, glycosylation defect, medicine.symptom, Congenital disorder of glycosylation, Metabolism, Inborn Errors, Cutis laxa, Immunity, infection and tissue repair [NCMLS 1]

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f54df43fb286e2c958ad3929c16252d9Test
https://hdl.handle.net/20.500.14017/77a97e3e-58b3-4672-8827-9b29485f396eTest

المؤلفون: Sarina G. Kant, Marjolein Kriek, Johan T. den Dunnen, Nicolette S. den Hollander, Arie van Haeringen, Gert-Jan B. van Ommen, Irina N. Snoeck, Marja W. Wessels, Christian Gilissen, Emmelien Aten, Yvonne Hilhorst-Hofstee, Martijn H. Breuning, Claudia A. L. Ruivenkamp, Rowida Almomani, Gijs W. E. Santen, Maartje Nielsen, Els A. J. Peeters, Yu Sun

المساهمون: Public Health, Clinical Genetics, Obstetrics & Gynecology

المصدر: Nature Genetics, 44, 4, pp. 379-80
Nature Genetics, 44, 379-80
Nature Genetics, 44(4), 379-380
Nature Genetics, 44(4), 379-380. Nature Publishing Group
Nature Genetics; Vol 44

مصطلحات موضوعية: Male, DNA Copy Number Variations, Micrognathism, Biology, medicine.disease_cause, Chromatin remodeling, Speech Disorders, 03 medical and health sciences, 0302 clinical medicine, Intellectual Disability, Intellectual disability, Genetics, medicine, otorhinolaryngologic diseases, Humans, Abnormalities, Multiple, Child, Coffin–Siris syndrome, Exome sequencing, 030304 developmental biology, Sequence Deletion, 0303 health sciences, Mutation, Middle Aged, medicine.disease, Chromatin Assembly and Disassembly, SWI/SNF, Chromatin, DNA-Binding Proteins, Child, Preschool, Face, Female, Haploinsufficiency, Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6], Hand Deformities, Congenital, 030217 neurology & neurosurgery, Neck, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3be728aba94bdcbf3ae5b386d0c74e70Test
https://pure.eur.nl/en/publications/809bb501-cf77-49aa-bc85-7c9c0ce89ac9Test

المؤلفون: C. R. Srikumari Srisailapathy, Kausik Ray, Richard J.H. Smith, Konrad Noben-Trauth, Nikoletta Charizopoulou, Margit Schraders, Ronald J.C. Admiraal, Jeffrey R. Holt, Joseph R. Latoche, Arabandi Ramesh, Harold R. Neely, John K. Northup, Hannie Kremer, Andrea Lelli, Michael S. Hildebrand, Jaap Oostrik

المصدر: Nature Communications
Nature Communications, 2, 201-201
Nature Communications, 2, pp. 201-201

مصطلحات موضوعية: Hearing loss, Hearing Loss, Sensorineural, DNA Mutational Analysis, Immunoblotting, Mutation, Missense, General Physics and Astronomy, Mice, Transgenic, Biology, medicine.disease_cause, Mechanotransduction, Cellular, General Biochemistry, Genetics and Molecular Biology, Article, Genomic disorders and inherited multi-system disorders [IGMD 3], 03 medical and health sciences, Mice, 0302 clinical medicine, Hair Cells, Auditory, medicine, otorhinolaryngologic diseases, Missense mutation, Animals, Humans, Inner ear, Genetic Predisposition to Disease, Mechanotransduction, Spiral ganglion, Crosses, Genetic, 030304 developmental biology, Adaptor Proteins, Signal Transducing, Genetics, 0303 health sciences, Mutation, Analysis of Variance, Multidisciplinary, Hearing Tests, General Chemistry, medicine.disease, Immunohistochemistry, Genetics and epigenetic pathways of disease Neuroinformatics [NCMLS 6], medicine.anatomical_structure, Acoustic Stimulation, Genetics and epigenetic pathways of disease Functional Neurogenomics [NCMLS 6], Sensorineural hearing loss, Hair cell, sense organs, medicine.symptom, Carrier Proteins, Neuroscience, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae2212602474ceea84e1c011aeb52dd8Test
http://europepmc.org/articles/PMC3105340Test