X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (160) 160
humans (130) 130
psychiatry (114) 114
schizophrenia (112) 112
male (89) 89
female (84) 84
bipolar disorder (76) 76
adult (69) 69
neurosciences (55) 55
mental disorders (49) 49
middle aged (45) 45
psychosis (45) 45
risk factors (45) 45
genome-wide association (44) 44
genomes (44) 44
genome-wide association study (43) 43
analysis (41) 41
brain (39) 39
metaanalysis (39) 39
risk (39) 39
genetic aspects (38) 38
young adult (38) 38
article (37) 37
genetics (37) 37
magnetic resonance imaging (37) 37
genomics (36) 36
research (36) 36
multidisciplinary sciences (34) 34
genetics & heredity (33) 33
adolescent (32) 32
studies (32) 32
polymorphism, single nucleotide (31) 31
schizophrenia - genetics (31) 31
medical research (29) 29
neuroimaging (29) 29
clinical medicine (27) 27
medical and health sciences (27) 27
medicin och hälsovetenskap (27) 27
aged (25) 25
medicine, experimental (25) 25
case-control studies (24) 24
genetic predisposition to disease (24) 24
bipolar disorder - genetics (23) 23
loci (23) 23
psykiatri (22) 22
consortia (21) 21
cognition (20) 20
cognitive ability (20) 20
genes (20) 20
medicine (20) 20
neuroscience (20) 20
research article (20) 20
genotype (19) 19
health aspects (19) 19
phenotype (19) 19
heritability (18) 18
brain research (17) 17
comorbidity (17) 17
meta-analysis (17) 17
polymorphism, single nucleotide - genetics (17) 17
variants (17) 17
gwas (16) 16
klinisk medicin (16) 16
schizophrenic psychology (16) 16
science (16) 16
usage (16) 16
clinical neurology (15) 15
gene expression (15) 15
genome-wide association studies (15) 15
hospitals (15) 15
memory (15) 15
neurology (15) 15
neuropsychological tests (15) 15
basic medicine (14) 14
medicinska och farmaceutiska grundvetenskaper (14) 14
population (14) 14
autism (13) 13
disease (13) 13
disorders (13) 13
genetic research (13) 13
mental health (13) 13
pleiotropy (13) 13
single nucleotide polymorphisms (13) 13
single-nucleotide polymorphism (13) 13
association (12) 12
bipolar disorder - psychology (12) 12
common variants (12) 12
diagnosis (12) 12
genetic variation (12) 12
medical genetics (12) 12
physiological aspects (12) 12
psychiatric status rating scales (12) 12
abnormalities (11) 11
age (11) 11
child (11) 11
cohort studies (11) 11
cortex (11) 11
epidemiology (11) 11
genetic variance (11) 11
genome-wide association study - methods (11) 11
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


ISSN 1932-6203, 2018
The genome-wide association study of the Psychiatric Genomics Consortium identified over one hundred schizophrenia susceptibility loci. The number of... 
Journal Article
ISSN 0340-6717, 2019
In recent years, genome-wide association study (GWAS) sample sizes have become larger, the statistical power has improved and thousands of trait-associated... 
Journal Article
ISSN 0002-953X, 2018
Objective: Antipsychotic drugs were incidentally discovered in the 1950s, but their mechanisms of action are still not understood. Better understanding of... 
Journal Article
ISSN 0022-3077, 2017
Current-source density (CSD) analysis is a well-established method for analyzing recorded local field potentials (LFPs), that is, the low-frequency part of... 
Journal Article
ISSN 0010-440X, 2018
Background: Theory of mind (ToM) can be divided into cognitive and affective ToM, and a distinction can be made between overmentalizing and undermentalizing... 
Journal Article
ISSN 2045-2322, 2018
Memory is indispensable for normal cognitive functioning, and the ability to store and retrieve information is central to mental health and disease. The... 
Journal Article
ISSN 2045-2322, 2018
Vitamin D and folate defciency are considered risk factors for schizophrenia and bipolar disorders, but it is unknown how vitamin D and folate infuence the... 
Journal Article
ISSN 1932-6203, 2017
An altered processing of emotions may contribute to a reduced ability for social interaction and communication in autism spectrum disorder, ASD. We... 
Journal Article
ISSN 1662-4548, 2019
Background: Alzheimer’s disease (AD) and bipolar disorder (BIP) are complex traits influenced by numerous common genetic variants, most of which remain to be... 
Journal Article
ISSN 0920-9964, 2018
Background A potential link between increase in total cholesterol and triglycerides and clinical improvement has been observed during antipsychotic drug... 
Journal Article
ISSN 0033-2917, 2017
Background Schizophrenia (SZ) and bipolar disorder (BD) are heritable, polygenic disorders with shared clinical and genetic components, suggesting a psychosis... 
Journal Article
ISSN 1932-6203, 2017
Heart rate variability (HRV) has become an increasingly popular index of cardiac autonomic control in the biobehavioral sciences due to its relationship with... 
Journal Article
ISSN 1422-0067, 2017
Clinical genetic testing (CGT) of children with autism spectrum disorder (ASD) may have positive and negative effects. Knowledge about parents’ attitudes is... 
genetic counselling | ASD | Asperger syndrome | clinical genetic testing | attitudes | ethics | autism | parents
Journal Article
ISSN 1095-9572, 2014
Valuable stimuli are invariably localized in space. While our knowledge regarding the neural networks supporting value assignment and comparisons is... 
fMRI | Amygdala | Anterior cingulate cortex | Spatial coding
Journal Article
ISSN 0001-690X, 2015
Objective: We investigated whether elevated plasma levels of immune markers were associated with verbal memory and hippocampal subfield volumes in patients... 
Journal Article
ISSN 2045-2322, 2016
Heart rate variability (HRV) has become central to biobehavioral models of self-regulation and interpersonal interaction. While research on healthy populations... 
Journal Article
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Journal Article
ISSN 1471-2164, 2015
Background: The genotype information carried by Genome-wide association studies (GWAS) seems to have the potential to explain more of the 'missing... 
Genome-wide association study | Polygenic | Conditional false discovery rate | Genomic enrichment | miRNA
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.