X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (77) 77
Publication (12) 12
Book Review (3) 3
Book / eBook (2) 2
Conference Proceeding (2) 2
Patent (2) 2
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (34) 34
humans (30) 30
female (15) 15
male (15) 15
schizophrenia (15) 15
genome-wide association (12) 12
genomes (12) 12
bipolar disorder (11) 11
genome-wide association study (11) 11
genes (10) 10
genomics (10) 10
genotype (10) 10
adult (9) 9
risk (9) 9
risk factors (9) 9
aged (8) 8
case-control studies (8) 8
gene expression (8) 8
genetic predisposition to disease (8) 8
genetics (8) 8
metaanalysis (8) 8
middle aged (8) 8
psychiatry (8) 8
alzheimer's disease (7) 7
bipolar disorder - genetics (7) 7
consortia (7) 7
disease (7) 7
genetics & heredity (7) 7
multidisciplinary sciences (7) 7
neurosciences (7) 7
studies (7) 7
aged, 80 and over (6) 6
alzheimers disease (6) 6
analysis (6) 6
genetic aspects (6) 6
genetic predisposition to disease - genetics (6) 6
genome-wide association studies (6) 6
linkage disequilibrium (6) 6
loci (6) 6
mental disorders (6) 6
phenotype (6) 6
polymorphism, single nucleotide (6) 6
research (6) 6
schizophrenia - genetics (6) 6
alzheimer disease - genetics (5) 5
article (5) 5
biotechnology & applied microbiology (5) 5
cognitive ability (5) 5
common variants (5) 5
genome-wide association study - methods (5) 5
gwas (5) 5
medical research (5) 5
neurology (5) 5
polymorphism, single nucleotide - genetics (5) 5
adolescent (4) 4
algorithms (4) 4
biochemical research methods (4) 4
cancer (4) 4
cardiovascular (4) 4
clinical neurology (4) 4
comorbidity (4) 4
development and progression (4) 4
disorders (4) 4
etiology (4) 4
expression (4) 4
family (4) 4
genetic loci (4) 4
genetic loci - genetics (4) 4
genetic research (4) 4
genetic variation (4) 4
genotype imputation (4) 4
genotypes (4) 4
heritability (4) 4
immunity (4) 4
mental depression (4) 4
odds ratio (4) 4
original (4) 4
proteins (4) 4
psykiatri (4) 4
research article (4) 4
set (4) 4
single-nucleotide polymorphism (4) 4
alleles (3) 3
biochemistry (3) 3
biochemistry & molecular biology (3) 3
bioinformatics (3) 3
brain (3) 3
cardiac & cardiovascular systems (3) 3
cell biology (3) 3
clinical medicine (3) 3
cognitive neuroscience (3) 3
dementia (3) 3
disease susceptibility (3) 3
epilepsy, generalized - genetics (3) 3
fatigue (3) 3
genealogy (3) 3
genetic analysis (3) 3
genetics of the nervous system (3) 3
health aspects (3) 3
health risk assessment (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


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 | Index Medicus | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2017, Volume 12, Issue 2, pp. e0171595 - e0171595
Journal Article
Nature Communications, ISSN 2041-1723, 03/2014, Volume 5, Issue 1, pp. 3339 - 3339
Journal Article
by Sims, Rebecca and Van Der Lee, Sven J and Naj, Adam C and Bellenguez, Céline and Badarinarayan, Nandini and Jakobsdottir, Johanna and Kunkle, Brian W and Boland, Anne and Raybould, Rachel and Bis, Joshua C and Martin, Eden R and Grenier-Boley, Benjamin and Heilmann-Heimbach, Stefanie and Chouraki, Vincent and Kuzma, Amanda B and Sleegers, Kristel and Vronskaya, Maria and Ruiz, Agustin and Graham, Robert R and Olaso, Robert and Hoffmann, Per and Grove, Megan L and Vardarajan, Badri N and Hiltunen, Mikko and Nöthen, Markus M and White, Charles C and Hamilton-Nelson, Kara L and Epelbaum, Jacques and Maier, Wolfgang and Choi, Seung-Hoan and Beecham, Gary W and Dulary, Cécile and Herms, Stefan and Smith, Albert V and Funk, Cory C and Derbois, Céline and Forstner, Andreas J and Ahmad, Shahzad and Li, Hongdong and Bacq, Delphine and Harold, Denise and Satizabal, Claudia L and Valladares, Otto and Squassina, Alessio and Thomas, Rhodri and Brody, Jennifer A and Qu, Liming and Sánchez-Juan, Pascual and Morgan, Taniesha and Wolters, Frank J and Zhao, Yi and Garcia, Florentino Sanchez and Denning, Nicola and Fornage, Myriam and Malamon, John and Naranjo, Maria Candida Deniz and Majounie, Elisa and Mosley, Thomas H and Dombroski, Beth and Wallon, David and Lupton, Michelle K and Dupuis, Josée and Whitehead, Patrice and Fratiglioni, Laura and Medway, Christopher and Jian, Xueqiu and Mukherjee, Shubhabrata and Keller, Lina and Brown, Kristelle and Lin, Honghuang and Cantwell, Laura B and Panza, Francesco and McGuinness, Bernadette and Moreno-Grau, Sonia and Burgess, Jeremy D and Solfrizzi, Vincenzo and Proitsi, Petra and Adams, Hieab H and Allen, Mariet and Seripa, Davide and Pastor, Pau and Cupples, L Adrienne and Price, Nathan D and Hannequin, Didier and Frank-García, Ana and Levy, Daniel and Chakrabarty, Paramita and Caffarra, Paolo and Giegling, Ina and Beiser, Alexa S and Giedraitis, Vilmantas and Hampel, Harald and Garcia, Melissa E and Wang, Xue and Lannfelt, Lars and Mecocci, Patrizia and Eiriksdottir, Gudny and Crane, Paul K and Pasquier, Florence and Boccardi, Virginia and ... and EADI and GERAD PERADES and ARUKConsortium and CHARGE and ADGC and GERAD/PERADES, CHARGE, ADGC, EADI and ARUK Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 09/2017, Volume 49, Issue 9, pp. 1373 - 1384
Journal Article
PLoS genetics, ISSN 1553-7390, 2014, Volume 10, Issue 6, pp. e1004345 - e1004345
Journal Article
by Brainstorm Consortium and 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 Kamboh, M Ilyas and Larson, Eric B and Rogaeva, Ekaterina and St George-Hyslop, Peter and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Demirci, F Yesim and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John SK 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 Chaim 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 ...
Science (New York, N.Y.), ISSN 0036-8075, 2018, Volume 360, Issue 6395, p. 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and share symptoms, provoking debate about their etiologic overlap. We quantified... 
Genetic Variation | Brainstorm Consortium | Phenotype | Genome-Wide Association Study | Quantitative Trait, Heritable | Humans | Risk Factors | Mental Disorders | Brain Diseases
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 9/2017, Volume 54, Issue 7, pp. 5166 - 5176
Journal Article
by Ruderfer, Douglas M and Ripke, Stephan and McQuillin, Andrew and Boocock, James and Stahl, Eli A and Pavlides, Jennifer M. Whitehead and Mullins, Niamh and Charney, Alexander W and Ori, Anil P.S and Loohuis, Loes M. Olde and Domenici, Enrico and Di Florio, Arianna and Papiol, Sergi and Kalman, Janos L and Trubetskoy, Vassily and Adolfsson, Rolf and Agartz, Ingrid and Agerbo, Esben and Akil, Huda and Albani, Diego and Albus, Margot and Alda, Martin and Alexander, Madeline and Alliey-Rodriguez, Ney and Als, Thomas D and Amin, Farooq and Anjorin, Adebayo and Arranz, Maria J and Awasthi, Swapnil and Bacanu, Silviu A and Badner, Judith A and Baekvad-Hansen, Marie and Bakker, Steven and Band, Gavin and Barchas, Jack D and Barroso, Ines and Bass, Nicholas and Bauer, Michael and Baune, Bernhard T and Begemann, Martin and Bellenguez, Celine and Belliveau, Richard A and Bellivier, Frank and Bender, Stephan and Bene, Judit and Bergen, Sarah E and Berrettini, Wade H and Bevilacqua, Elizabeth and Biernacka, Joanna M and Bigdeli, Tim B and Black, Donald W and Blackburn, Hannah and Blackwell, Jenefer M and Blackwood, Douglas H.R and Pedersen, Marianne Giortz and Pedersen, Carsten Bocker and Boehnke, Michael and Boks, Marco and Borglum, Anders D and Bramon, Elvira and Breen, Gerome and Brown, Matthew A and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Budde, Monika and Bulik-Sullivan, Brendan and Bumpstead, Suzannah J and Bunney, William and Burmeister, Margit and Buxbaum, Joseph D and Bybjerg-Grauholm, Jonas and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Casas, Miquel and Casas, Juan P and Catts, Stanley V and Cervantes, Pablo and Chambert, Kimberley D and Chan, Raymond C.K and Chen, Eric Y.H and Chen, Ronald Y.L and Cheng, Wei and Cheung, Eric F.C and Chong, Siow Ann and Clarke, Toni-Kim and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Coleman, Jonathan R.I and Collier, David A and Cormican, Paul and Coryell, William and Craddock, Nicholas and ... and Psychosis Endophenotypes Inter and Psychiat Genomics Consortium and Wellcome Trust Case-Control and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium. Electronic address: douglas.ruderfer@vanderbilt.edu
Cell, ISSN 0092-8674, 06/2018, Volume 173, Issue 7, pp. 1705 - 1715.e16
Journal Article