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Journal of Biomedical Informatics, ISSN 1532-0464, 10/2019, Volume 98, p. 103273
In recent years, the technological advances for capturing genetic variation in large populations led to the identification of large numbers of putative or... 
Complex diseases | Semantic similarity | Functional enrichment analysis | Genetic variants
Journal Article
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
by Gillberg, Christopher and Kolevzon, Alexander and Nelson, Stanley F and Sansom, Katherine and Casallo, Guillermo and Miller, Judith and Brennan, Sean and Leboyer, Marion and Bacchelli, Elena and Delorme, Richard and Fombonne, Eric and Hallmayer, Joachim and Green, Jonathan and Pickles, Andrew and Heron, Elizabeth A and Salt, Jeff and Battaglia, Agatino and Klauck, Sabine M and McDougle, Christopher J and Mahoney, William and Noor, Abdul and Cytrynbaum, Cheryl and Sato, Daisuke and Almeida, Joana and Korvatska, Olena and Dawson, Geraldine and Bierut, Laura J and Coon, Hilary and Rickaby, Jessica and Freitag, Christine M and Roeder, Kathryn and Bader, Gary D and Wijsman, Ellen M and Vincent, John B and Hakonarson, Hakon and Segurado, Ricardo and Paton, Tara and Roge, Bernadette and Ennis, Sean and Kim, Cecilia and Monaco, Anthony P and Paterson, Andrew D and Crossett, Andrew and McGrath, Jane and Carson, Andrew R and Le Couteur, Ann and Cook, Edwin H and Chung, Brian H.Y and Cuccaro, Michael L and Van Engeland, Herman and Conroy, Judith and Holt, Richard and Strawbridge, Christina and Kustanovich, Vlad and Migita, Ohsuke and Stoppioni, Vera and Igliozzi, Roberta and Poustka, Fritz and Stein, Olaf and Posey, David J and Sheffield, Val C and Duque, Frederico and Parrini, Barbara and Berney, Tom and Hus, Vanessa and Baird, Gillian and Duketis, Eftichia and Soorya, Latha and Corsello, Christina and Drmic, Irene and Sousa, Inês and Abrahams, Brett S and Thomson, Susanne and Lajonchere, Clara M and Tsiantis, John and Pinto, Dalila and Green, Andrew and Hughes, Gillian and Mantoulan, Carine and Betancur, Catalina and Volkmar, Fred and Poustka, Annemarie and Shah, Naisha and Bryson, Susan E and Munson, Jeff and Tancredi, Raffaella and Nygren, Gudrun and Wittemeyer, Kerstin and Merikangas, Alison and Oliveira, Guiomar and Farrar, Penny and Maestrini, Elena and Liu, Xiao-Qing and Gallagher, Louise and McConachie, Helen and Zurawiecki, Danielle and Schellenberg, Gerard D and Glessner, Joseph T and Lord, Catherine and Piven, Joseph and ... and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature, ISSN 0028-0836, 07/2010, Volume 466, Issue 7304, pp. 368 - 372
Journal Article
by Pinto, Dalila and Delaby, Elsa and Merico, Daniele and Barbosa, Mafalda and Merikangas, Alison and Klei, Lambertus and Thiruvahindrapuram, Bhooma and Xu, Xiao and Ziman, Robert and Wang, Zhuozhi and Vorstman, Jacob A.S and Thompson, Ann and Regan, Regina and Pilorge, Marion and Pellecchia, Giovanna and Pagnamenta, Alistair T and Oliveira, Guiomar and Oliveira, Bárbara and Marshall, Christian R and Magalhaes, Tiago R and Lowe, Jennifer K and Howe, Jennifer L and Griswold, Anthony J and Gilbert, John and Duketis, Eftichia and Dombroski, Beth A and De Jonge, Maretha V and Cuccaro, Michael and Crawford, Emily L and Correia, Catarina T and Conroy, Judith and Conceição, Inês C and Chiocchetti, Andreas G and Casey, Graham and Casey, Jillian P and Cai, Guiqing and Cabrol, Christelle and Bolshakova, Nadia and Bacchelli, Elena and Anney, Richard and Gallinger, Steven and Cotterchio, Michelle and Zwaigenbaum, Lonnie and Wittemeyer, Kerstin and Wing, Kirsty and Wallace, Simon and van Engeland, Herman and Tryfon, Ana and Thomson, Susanne and Soorya, Latha and Rogé, Bernadette and Roberts, Wendy and Poustka, Fritz and Mouga, Susana and Minshew, Nancy and McInnes, L. Alison and McGrew, Susan G and Lord, Catherine and Leboyer, Marion and Le Couteur, Ann S and Kolevzon, Alexander and Jiménez González, Patricia and Jacob, Suma and Holt, Richard and Guter, Stephen and Green, Jonathan and Green, Andrew and Gillberg, Christopher and Fernandez, Bridget A and Duque, Frederico and Delorme, Richard and Dawson, Geraldine and Chaste, Pauline and Café, Cátia and Brennan, Sean and Bourgeron, Thomas and Bolton, Patrick F and Bölte, Sven and Bernier, Raphael and Baird, Gillian and Bailey, Anthony J and Anagnostou, Evdokia and Almeida, Joana and Wijsman, Ellen M and Vieland, Veronica J and Vicente, Astrid M and Schellenberg, Gerard D and Pericak-Vance, Margaret and Paterson, Andrew D and Parr, Jeremy R and Nurnberger, John I and Monaco, Anthony P and Maestrini, Elena and Klauck, Sabine M and Hakonarson, Hakon and Haines, Jonathan L and Geschwind, Daniel H and Freitag, Christine M and Folstein, Susan E and Ennis, Sean and ... and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
The American Journal of Human Genetics, ISSN 0002-9297, 05/2014, Volume 94, Issue 5, pp. 677 - 694
Journal Article
by Traylor, Matthew, MSc and Farrall, Martin, FRCPath and Holliday, Elizabeth G, PhD and Sudlow, Cathie, FRCP and Hopewell, Jemma C, PhD and Cheng, Yu-Ching, PhD and Fornage, Myriam, PhD and Ikram, M Arfan, MD and Malik, Rainer, PhD and Bevan, Steve, PhD and Thorsteinsdottir, Unnur, PhD and Nalls, Mike A, PhD and Longstreth, WT, MD and Wiggins, Kerri L, MS and Yadav, Sunaina, MSc and Parati, Eugenio A, MD and DeStefano, Anita L, PhD and Worrall, Bradford B, MD and Kittner, Steven J, MD and Khan, Muhammad Saleem, MSc and Reiner, Alex P, MD and Helgadottir, Anna, MD and Achterberg, Sefanja, PhD and Fernandez-Cadenas, Israel, PhD and Abboud, Sherine, MD and Schmidt, Reinhold, MD and Walters, Matthew, MD and Chen, Wei-Min, PhD and Ringelstein, E Bernd, MD and O'Donnell, Martin, MD and Ho, Weang Kee, PhD and Pera, Joanna, MD and Lemmens, Robin, MD and Norrving, Bo, MD and Higgins, Peter, MRCP and Benn, Marianne, MD and Sale, Michele, PhD and Kuhlenbäumer, Gregor, MD and Doney, Alexander S F, PhD and Vicente, Astrid M, PhD and Delavaran, Hossein, MD and Algra, Ale, MD and Davies, Gail, PhD and Oliveira, Sofia A, PhD and Palmer, Colin N A, PhD and Deary, Ian, PhD and Schmidt, Helena, MD and Pandolfo, Massimo, MD and Montaner, Joan, MD and Carty, Cara, PhD and de Bakker, Paul I W, PhD and Kostulas, Konstantinos, MD and Ferro, Jose M, MD and van Zuydam, Natalie R, MSc and Valdimarsson, Einar, MD and Nordestgaard, Børge G, MD and Lindgren, Arne, MD and Thijs, Vincent, MD and Slowik, Agnieszka, MD and Saleheen, Danish, MD and Paré, Guillaume, MD and Berger, Klaus, MD and Thorleifsson, Gudmar, PhD and Hofman, Albert, MD and Mosley, Thomas H, PhD and Mitchell, Braxton D, PhD and Furie, Karen, MD and Clarke, Robert, FRCP and Levi, Christopher, MD and Seshadri, Sudha, MD and Gschwendtner, Andreas, MD and Boncoraglio, Giorgio B, MD and Sharma, Pankaj, PhD and Bis, Joshua C, PhD and Gretarsdottir, Solveig, PhD and Psaty, Bruce M and Rothwell, Peter M, FMedSci and Rosand, Jonathan, MD and Meschia, James F, MD and Stefansson, Kari, MD and Dichgans, Martin, MD and Markus, Hugh S, Dr and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and EpiHealth: Epidemiology for Health and Lund University and Neurologi, Lund and Lunds universitet and Neurology, Lund
The Lancet Neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
by Lee, Shermin and Ripke, S and Neale, B.M and Faraone, S.V and Purcell, S.M and Perlis, R.H and Mowry, B.J and Thapar, A and Goddard, M.E and Witte, J.S and Absher, D and Agartz, I and Akil, H and Amin, F and Aneassen, O.A and Anjorin, A and Anney, R and Anttila, V and Arking, D.E and Asherson, P and Azevedo, M.H and Backlund, L and Badner, J.A and Bailey, A.J and Banaschewski, T and Barchas, J.D and Barnes, M.R and Barrett, T.B and Bass, N and Battaglia, A and Bauer, M and Bayes, M and Bellivier, F and Bergen, S.E and Berrettini, W and Betancur, C and Bettecken, T and Biederman, J and Binder, E.B and Black, D.W and Blackwood, D.H and Bloss, C.S and Boehnke, M and Boomsma, D.I and Breen, G and Breuer, R and Bruggeman, R and Cormican, P and Buccola, N.G and Buitelaar, J.K and Bunney, W.E and Buxbaum, J.D and Byerley, W.F and Byrne, E.M and Caesar, S and Cahn, W and Cantor, R.M and Casas, M and Chakravarti, A and Chambert, K and Choudhury, K and Cichon, S and Cloninger, C.R and Collier, D.A and Cook, E.H and Coon, H and Cormand, B and Corvin, A and Coryell, W.H and Craig, D.W and Craig, I.W and Crosbie, J and Cuccaro, M.L and Curtis, D and Czamara, D and Datta, S and Dawson, G and Day, R and Geus, E.J. de and Degenhardt, F and Djurovic, S and Donohoe, G.J and Doyle, A.E and Duan, J and Dudbridge, F and Duketis, E and Ebstein, R.P and Edenberg, H.J and Elia, J and Ennis, S and Etain, B and Fanous, A and Farmer, A.E and Ferrier, I.N and Flickinger, M and Fombonne, E and Foroud, T and Frank, J and Franke, B and et al and Cross-Disorder Grp Psychiat Genomi and Int Inflammatory Bowel Dis Genetic and Cross-Disorder Group of the Psychiatric Genomics Consortium
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 9, pp. 984 - 994
Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across... 
ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | CROHNS-DISEASE | DEFICIT HYPERACTIVITY DISORDER | COMMON SNPS | GENETICS & HEREDITY | SCHIZOPHRENIA | RISK | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | HERITABILITY | Usage | Genetic aspects | Research | Single nucleotide polymorphisms | Psychoses | Genomics | Life Sciences | Biochemistry, Molecular Biology
Journal Article