X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (32) 32
index medicus (30) 30
autism (23) 23
genetics (18) 18
male (18) 18
psychiatry (18) 18
article (17) 17
female (17) 17
schizophrenia (17) 17
genetics & heredity (16) 16
mental disorders (14) 14
neurosciences (14) 14
phenotype (12) 12
risk factors (12) 12
child (11) 11
genetic aspects (11) 11
life sciences (11) 11
adult (10) 10
autistic disorder - genetics (10) 10
genetic predisposition to disease (10) 10
genomes (8) 8
research (8) 8
adolescent (7) 7
association (7) 7
disorders (7) 7
genetic variation (7) 7
genome-wide association study (7) 7
mental-retardation (7) 7
child, preschool (6) 6
chromosome deletion (6) 6
de-novo mutations (6) 6
duplication (6) 6
genomics (6) 6
mental disorders - genetics (6) 6
schizophrenia - genetics (6) 6
spectrum disorders (6) 6
child development disorders, pervasive - genetics (5) 5
dna copy number variations (5) 5
dna copy number variations - genetics (5) 5
family (5) 5
genome-wide association (5) 5
heritability (5) 5
intellectual disability (5) 5
population (5) 5
psykiatri (5) 5
sequence deletion (5) 5
[ sdv.gen ] life sciences [q-bio]/genetics (4) 4
[sdv.gen]life sciences [q-bio]/genetics (4) 4
analysis (4) 4
animals (4) 4
autism spectrum disorder - genetics (4) 4
bipolar disorder (4) 4
brain (4) 4
brain - metabolism (4) 4
children (4) 4
deletion (4) 4
developmental disabilities - genetics (4) 4
gene expression (4) 4
genes (4) 4
genetic predisposition to disease - genetics (4) 4
hidden-markov model (4) 4
identification (4) 4
intellectual disability - genetics (4) 4
middle aged (4) 4
neurology (4) 4
neurons and cognition (4) 4
pervasive developmental disorders (4) 4
polymorphism, single nucleotide (4) 4
autism spectrum disorder (3) 3
autism spectrum disorders (3) 3
autistic disorder - physiopathology (3) 3
chromosomes (3) 3
chromosomes, human, pair 15 - genetics (3) 3
clinical medicine (3) 3
clinical neurology (3) 3
cnvs (3) 3
copy number variation (3) 3
deletion syndrome (3) 3
etiology (3) 3
gene deletion (3) 3
gene dosage (3) 3
gene duplication (3) 3
genetic research (3) 3
genetic risk (3) 3
genome-wide association study - methods (3) 3
genotype (3) 3
health aspects (3) 3
heterogeneity (3) 3
human (3) 3
individuals (3) 3
klinisk medicin (3) 3
liability (3) 3
mice (3) 3
multifactorial inheritance - genetics (3) 3
mutation (3) 3
neuroscience (3) 3
proteins (3) 3
proximal 15q (3) 3
quantitative trait, heritable (3) 3
siblings (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Weiner, Daniel J and Wigdor, Emilie M and Ripke, Stephan and Walters, Raymond K and Kosmicki, Jack A and Grove, Jakob and Samocha, Kaitlin E and Goldstein, Jacqueline I and Okbay, Aysu and Bybjerg-Grauholm, Jonas and Werge, Thomas and Hougaard, David M and Taylor, Jacob and Skuse, David and Devlin, Bernie and Anney, Richard and Sanders, Stephan J and Bishop, Somer and Mortensen, Preben Bo and Børglum, Anders D and Smith, George Davey and Daly, Mark J and Robinson, Elise B and Bækvad-Hansen, Marie and Dumont, Ashley and Hansen, Christine and Hansen, Thomas F and Howrigan, Daniel and Mattheisen, Manuel and Moran, Jennifer and Mors, Ole and Nordentoft, Merete and Nørgaard-Pedersen, Bent and Poterba, Timothy and Poulsen, Jesper and Stevens, Christine and Anttila, Verneri and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A Jeremy and Wijsman, Ellen M and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Van Engeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne G and Pedersen, Carsten B and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Murtha, Michael T and Mouga, Susana and Morrow, Eric M and DeLuca, Daniel Moreno and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and ... and Psychiat Genomics Consortium and iPSYCH-Broad Autism Grp and iPSYCH-Broad Autism Group and Psychiatric Genomics Consortium Autism Group and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 978 - 985
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
Neuron, ISSN 0896-6273, 06/2011, Volume 70, Issue 5, pp. 863 - 885
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
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 10/2019, Volume 58, Issue 10, pp. S364 - S364
Journal Article
Neuron, ISSN 0896-6273, 09/2015, Volume 87, Issue 6, pp. 1215 - 1233
Journal Article
by Maier, Wolfgang and Maier, Robert and Moser, Gerhard and Chen, Guo-Bo and Ripke, Stephan and Absher, Devin and Agartz, Ingrid and Akil, Huda and Amin, Farooq and Andreassen, Ole A and Anjorin, Adebayo and Anney, Richard and Arking, Dan E and Asherson, Philip and Azevedo, Maria H and Backlund, Lena and Badner, Judith A and Bailey, Anthony J and Banaschewski, Tobias and Barchas, Jack D and Barnes, Michael R and Barrett, Thomas B and Bass, Nicholas and Battaglia, Agatino and Bauer, Michael and Bayés, Mònica and Bellivier, Frank and Bergen, Sarah E and Berrettini, Wade and Betancur, Catalina and Bettecken, Thomas and Biederman, Joseph and Binder, Elisabeth B and Black, Donald W and Blackwood, Douglas H.R and Bloss, Cinnamon S and Boehnke, Michael and Boomsma, Dorret I and Breen, Gerome and Breuer, René and Bruggeman, Richard and Buccola, Nancy G and Buitelaar, Jan K and Bunney, William E and Buxbaum, Joseph D and Byerley, William F and Caesar, Sian and Cahn, Wiepke and Cantor, Rita M and Casas, Miguel and Chakravarti, Aravinda and Chambert, Kimberly and Choudhury, Khalid and Cichon, Sven and Cloninger, C. Robert and Collier, David A and Cook, Edwin H and Coon, Hilary and Cormand, Bru and Cormican, Paul and Corvin, Aiden and Coryell, William and Coryell, William H and Craddock, Nicholas and Craig, David W and Craig, Ian W and Crosbie, Jennifer and Cuccaro, Michael L and Curtis, David and Czamara, Darina and Daly, Mark J and Datta, Susmita and Dawson, Geraldine and Day, Richard and De Geus, Eco J and Degenhardt, Franziska and Devlin, Bernie and Djurovic, Srdjan and Donohoe, Gary J and Doyle, Alysa E and Duan, Jubao and Dudbridge, Frank and Duketis, Eftichia and Ebstein, Richard P and Edenberg, Howard J and Elia, Josephine and Ennis, Sean and Etain, Bruno and Fanous, Ayman and Faraone, Stephen V and Farmer, Anne E and Ferrier, I. Nicol and Flickinger, Matthew and Fombonne, Eric and Foroud, Tatiana and Frank, Josef and Franke, Barbara and Fraser, Christine and Freedman, Robert and Freimer, Nelson B and ... and Psychiat Genomics Consortium and Cross-Disorder Working Group of the Psychiatric Genomics Consortium and Institute of Neuroscience and Physiology and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy and Institutionen för neurovetenskap och fysiologi
The American Journal of Human Genetics, ISSN 0002-9297, 02/2015, Volume 96, Issue 2, pp. 283 - 294
Journal Article