Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
humans (27) 27
index medicus (27) 27
calculating (22) 22
computing (22) 22
counting (22) 22
physics (22) 22
genome-wide association study (18) 18
information and communication technology [ict] specially adaptedfor specific application fields (17) 17
computer systems based on specific computational models (16) 16
schizophrenia (16) 16
genetics & heredity (15) 15
article (13) 13
research (13) 13
electric digital data processing (12) 12
genomes (12) 12
genome-wide association (11) 11
handling record carriers (11) 11
presentation of data (11) 11
recognition of data (11) 11
record carriers (11) 11
schizophrenia - genetics (11) 11
genomics (10) 10
polymorphism, single nucleotide - genetics (10) 10
genetic aspects (9) 9
multidisciplinary sciences (9) 9
analysis (7) 7
animals (7) 7
base sequence (7) 7
case-control studies (7) 7
expression (7) 7
genetic predisposition to disease (7) 7
genetics (7) 7
mental disorders (7) 7
methods (7) 7
studies (7) 7
biochemistry & molecular biology (6) 6
consortia (6) 6
disease (6) 6
gene expression (6) 6
genes (6) 6
genetic research (6) 6
phenotype (6) 6
risk (6) 6
risk factors (6) 6
susceptibility loci (6) 6
genetic predisposition to disease - genetics (5) 5
genome-wide association studies (5) 5
genotype (5) 5
health aspects (5) 5
healthcare informatics, i.e. information and communicationtechnology [ict] specially adapted for the handling orprocessing of medical or healthcare data (5) 5
metaanalysis (5) 5
multifactorial inheritance - genetics (5) 5
polymorphism, single nucleotide (5) 5
traits (5) 5
bipolar disorder (4) 4
brain (4) 4
brain - metabolism (4) 4
cell biology (4) 4
conserved sequence (4) 4
data processing systems or methods, specially adapted foradministrative, commercial, financial, managerial, supervisoryor forecasting purposes (4) 4
disorders (4) 4
electric communication technique (4) 4
electricity (4) 4
enhancer elements, genetic - genetics (4) 4
genetic variation (4) 4
genetic variation - genetics (4) 4
genome-wide association study - methods (4) 4
identification (4) 4
linkage disequilibrium (4) 4
medical research (4) 4
mice (4) 4
mutation (4) 4
odds ratio (4) 4
psychiatry (4) 4
rna (4) 4
rna, messenger - genetics (4) 4
schizophrenia - pathology (4) 4
statistics (4) 4
systems or methods specially adapted for administrative,commercial, financial, managerial, supervisory or forecastingpurposes, not otherwise provided for (4) 4
transmission of digital information, e.g. telegraphiccommunication (4) 4
variants (4) 4
alleles (3) 3
architecture (3) 3
autism (3) 3
binding sites (3) 3
body-mass index (3) 3
chromatin - genetics (3) 3
common variants (3) 3
comorbidity (3) 3
computer simulation (3) 3
epigenesis, genetic - genetics (3) 3
epigenetic inheritance (3) 3
evolution (3) 3
female (3) 3
gene (3) 3
gene loci (3) 3
genetic loci (3) 3
genome, human (3) 3
gwas (3) 3
haplotypes (3) 3
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

Science, ISSN 0036-8075, 12/2005, Volume 310, Issue 5755, pp. 1817 - 1821
Journal Article
Nature, ISSN 0028-0836, 02/2015, Volume 518, Issue 7539, pp. 337 - 343
Journal Article
by Roadmap Epigenomics Consortium, Epigenomics Consortium and Kundaje, Anshul and Meuleman, Wouter and Ernst, Jason and Bilenky, Misha and Yen, Angela and Heravi-Moussavi, Alireza and Kheradpour, Pouya and Zhang, Zhizhuo and Wang, Jianrong and Ziller, Michael J and Amin, Viren and Whitaker, John W and Schultz, Matthew D and Ward, Lucas D and Sarkar, Abhishek and Quon, Gerald and Sandstrom, Richard S and Eaton, Matthew L and Wu, Yi-Chieh and Pfenning, Andreas R and Wang, Xinchen and Claussnitzer, Melina and Liu, Yaping and Coarfa, Cristian and Harris, R. Alan and Shoresh, Noam and Epstein, Charles B and Gjoneska, Elizabeta and Leung, Danny and Xie, Wei and Hawkins, R. David and Lister, Ryan and Hong, Chibo and Gascard, Philippe and Mungall, Andrew J and Moore, Richard and Chuah, Eric and Tam, Angela and Canfield, Theresa K and Hansen, R. Scott and Kaul, Rajinder and Sabo, Peter J and Bansal, Mukul S and Carles, Annaick and Dixon, Jesse R and Farh, Kai-How and Feizi, Soheil and Karlic, Rosa and Kim, Ah-Ram and Kulkarni, Ashwinikumar and Li, Daofeng and Lowdon, Rebecca and Elliott, Ginell and Mercer, Tim R and Neph, Shane J and Onuchic, Vitor and Polak, Paz and Rajagopal, Nisha and Ray, Pradipta and Sallari, Richard C and Siebenthall, Kyle T and Sinnott-Armstrong, Nicholas A and Stevens, Michael and Thurman, Robert E and Wu, Jie and Zhang, Bo and Zhou, Xin and Beaudet, Arthur E and Boyer, Laurie A and De Jager, Philip L and Farnham, Peggy J and Fisher, Susan J and Haussler, David and Jones, Steven J. M and Li, Wei and Marra, Marco A and McManus, Michael T and Sunyaev, Shamil and Thomson, James A and Tlsty, Thea D and Tsai, Li-Huei and Wang, Wei and Waterland, Robert A and Zhang, Michael Q and Chadwick, Lisa H and Bernstein, Bradley E and Costello, Joseph F and Ecker, Joseph R and Hirst, Martin and Meissner, Alexander and Milosavljevic, Aleksandar and Ren, Bing and Stamatoyannopoulos, John A and Wang, Ting and Kellis, Manolis and Roadmap Epigenomics Consortium
Nature, ISSN 0028-0836, 02/2015, Volume 518, Issue 7539, pp. 317 - 329
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
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
Journal Article