Search Filters
Format Format
Subjects Subjects
Subjects Subjects
Sort by Item Count (A-Z)
Filter by Count
schizophrenia (29) 29
humans (28) 28
index medicus (28) 28
schizophrenia - genetics (21) 21
genome-wide association study (18) 18
research (16) 16
female (14) 14
genetic aspects (14) 14
genetics & heredity (14) 14
male (14) 14
genetic predisposition to disease (13) 13
genomics (13) 13
polymorphism, single nucleotide (13) 13
psychiatry (13) 13
article (12) 12
genetics (12) 12
genome-wide association (12) 12
genotype (12) 12
polymorphism, single nucleotide - genetics (12) 12
alleles (11) 11
mental disorders (11) 11
genomes (10) 10
risk factors (10) 10
case-control studies (9) 9
genetic predisposition to disease - genetics (9) 9
metaanalysis (9) 9
neurosciences (9) 9
single nucleotide polymorphisms (9) 9
adult (8) 8
association (8) 8
bipolar disorder (8) 8
genetic research (8) 8
risk (7) 7
studies (7) 7
aged (6) 6
analysis (6) 6
brain (6) 6
disease (6) 6
genes (6) 6
biochemistry & molecular biology (5) 5
common variants (5) 5
consortia (5) 5
gene (5) 5
genome-wide association study - methods (5) 5
health aspects (5) 5
linkage disequilibrium (5) 5
middle aged (5) 5
multidisciplinary sciences (5) 5
multifactorial inheritance - genetics (5) 5
odds ratio (5) 5
phenotype (5) 5
psychosis (5) 5
susceptibility (5) 5
usage (5) 5
variants (5) 5
cortex (4) 4
development and progression (4) 4
european continental ancestry group - genetics (4) 4
gene expression (4) 4
gene frequency (4) 4
genetic loci (4) 4
genome, human (4) 4
loci (4) 4
meta-analysis (4) 4
mutation (4) 4
phenotypes (4) 4
population (4) 4
sample size (4) 4
traits (4) 4
accuracy (3) 3
biology (3) 3
bipolar disorder - genetics (3) 3
brain - metabolism (3) 3
computer simulation (3) 3
de-novo mutations (3) 3
gene expression - genetics (3) 3
genealogy (3) 3
genetic variation - genetics (3) 3
genotype & phenotype (3) 3
gwas (3) 3
haplotypes (3) 3
heritability (3) 3
identification (3) 3
linkage (3) 3
medical research (3) 3
medicine, experimental (3) 3
methods (3) 3
psychology, multidisciplinary (3) 3
schizophrenia - epidemiology (3) 3
schizophrenia - immunology (3) 3
schizophrenia - pathology (3) 3
schizophrenic psychology (3) 3
snps (3) 3
statistics (3) 3
susceptibility loci (3) 3
young adult (3) 3
abridged index medicus (2) 2
anxiety - genetics (2) 2
anxiety - psychology (2) 2
architecture (2) 2
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range

Schizophrenia Research and Treatment, ISSN 2090-2085, 2017, Volume 2017, pp. 5763094 - 8
Literature suggests that the effect of winter birth on vulnerability to schizophrenia might be mediated by increased expression of proinflammatory cytokines... 
Cytokines | Analysis | Genes | Genetic research | Schizophrenia | Development and progression | Genetic aspects | Health aspects
Journal Article
Spanish Journal of Psychology, ISSN 1138-7416, 05/2009, Volume 12, Issue 1, p. 46
Palabras clave: reconocimiento de afecto, cognicion, esquizofrenia, personalidad esquizotipica 
Genetic research | Genetic aspects | Actors | Liability (Law) | Actresses
Journal Article
Neuropsychobiology, ISSN 0302-282X, 07/2018, Volume 76, Issue 3, pp. 143 - 150
Background: Visual word recognition is one of the central topics in cognitive psychology and cognitive neuroscience. Genetic factors are known to contribute to... 
Journal Article
Spanish Journal of Psychology, ISSN 1138-7416, 11/2009, Volume 12, Issue 2, p. 696
Cuidar a un miembro de la familia con un trastorno psicotico es considerado como uno de los estresores mas significativos y los familiares de una persona que... 
Phenols | Anopheles | Serotonin | Genes
Journal Article
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
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Journal Article
by Pardiñas, Antonio F and Holmans, Peter and Pocklington, Andrew J and Escott-Price, Valentina and Ripke, Stephan and Carrera, Noa and Legge, Sophie E and Bishop, Sophie and Cameron, Darren and Hamshere, Marian L and Han, Jun and Hubbard, Leon and Lynham, Amy and Mantripragada, Kiran and Rees, Elliott and MacCabe, James H and McCarroll, Steven A and Baune, Bernhard T and Breen, Gerome and Byrne, Enda M and Dannlowski, Udo and Eley, Thalia C and Hayward, Caroline and Martin, Nicholas G and McIntosh, Andrew M and Plomin, Robert and Porteous, David J and Wray, Naomi R and Caballero, Armando and Geschwind, Daniel H and Huckins, Laura M and Ruderfer, Douglas M and Santiago, Enrique and Sklar, Pamela and Stahl, Eli A and Won, Hyejung and Agerbo, Esben and Als, Thomas D and Andreassen, Ole A and Bækvad-Hansen, Marie and Mortensen, Preben Bo and Pedersen, Carsten Bøcker and Børglum, Anders D and Bybjerg-Grauholm, Jonas and Djurovic, Srdjan and Durmishi, Naser and Pedersen, Marianne Giørtz and Golimbet, Vera and Grove, Jakob and Hougaard, David M and Mattheisen, Manuel and Molden, Espen and Mors, Ole and Nordentoft, Merete and Pejovic-Milovancevic, Milica and Sigurdsson, Engilbert and Silagadze, Teimuraz and Hansen, Christine Søholm and Stefansson, Kari and Stefansson, Hreinn and Steinberg, Stacy and Tosato, Sarah and Werge, Thomas and Harold, Denise and Sims, Rebecca and Gerrish, Amy and Chapman, Jade and Abraham, Richard and Hollingworth, Paul and Pahwa, Jaspreet and Denning, Nicola and Thomas, Charlene and Taylor, Sarah and Powell, John and Proitsi, Petroula and Lupton, Michelle and Lovestone, Simon and Passmore, Peter and Craig, David and McGuinness, Bernadette and Johnston, Janet and Todd, Stephen and Maier, Wolfgang and Jessen, Frank and Heun, Reiner and Schurmann, Britta and Ramirez, Alfredo and Becker, Tim and Herold, Christine and Lacour, André and Drichel, Dmitriy and Nothen, Markus and Goate, Alison and Cruchaga, Carlos and Nowotny, Petra and Morris, John C and Mayo, Kevin and O'Donovan, Michael and Owen, Michael and Williams, Julie and ... and GERAD1 Consortium and CRESTAR Consortium
Nature Genetics, ISSN 1061-4036, 03/2018, Volume 50, Issue 3, pp. 381 - 389
Journal Article