X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (337) 337
Publication (101) 101
Book Review (14) 14
Book Chapter (7) 7
Conference Proceeding (7) 7
Magazine Article (2) 2
Newspaper Article (2) 2
Data Set (1) 1
Patent (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (207) 207
humans (201) 201
schizophrenia (165) 165
psychiatry (124) 124
genome-wide association study (104) 104
schizophrenia - genetics (104) 104
female (96) 96
male (95) 95
genetic predisposition to disease (81) 81
adult (73) 73
genetics & heredity (72) 72
genetic aspects (69) 69
genetics (69) 69
genomics (69) 69
bipolar disorder (68) 68
neurosciences (68) 68
genome-wide association (66) 66
article (65) 65
polymorphism, single nucleotide (64) 64
risk factors (59) 59
middle aged (58) 58
research (58) 58
case-control studies (52) 52
polymorphism, single nucleotide - genetics (52) 52
genomes (51) 51
genotype (49) 49
risk (42) 42
mental disorders (41) 41
neuroscience (39) 39
psychosis (37) 37
studies (37) 37
genes (35) 35
genetic predisposition to disease - genetics (35) 35
phenotype (34) 34
aged (33) 33
analysis (33) 33
association (33) 33
metaanalysis (33) 33
cognition (31) 31
gene expression (30) 30
common variants (29) 29
genes & society (29) 29
brain (28) 28
population (28) 28
young adult (28) 28
disease (27) 27
adolescent (26) 26
alleles (26) 26
biochemistry & molecular biology (26) 26
bipolar disorder - genetics (26) 26
genetic research (26) 26
loci (26) 26
multidisciplinary sciences (26) 26
medical research (25) 25
meta-analysis (24) 24
schizophrenic psychology (24) 24
neuropsychological tests (23) 23
single nucleotide polymorphisms (22) 22
genetic variation (21) 21
genome-wide association studies (21) 21
gwas (21) 21
medicin och hälsovetenskap (21) 21
autism (20) 20
gene (20) 20
health aspects (20) 20
medical and health sciences (20) 20
memory (20) 20
variants (20) 20
heritability (19) 19
magnetic resonance imaging (19) 19
psychotic disorders - genetics (19) 19
schizophrenia - pathology (19) 19
european continental ancestry group - genetics (18) 18
physiological aspects (18) 18
susceptibility (18) 18
medicine (17) 17
susceptibility loci (17) 17
consortia (16) 16
linkage disequilibrium (16) 16
abridged index medicus (15) 15
biology (15) 15
development and progression (15) 15
expression (15) 15
gene frequency (15) 15
genetic loci (15) 15
haplotypes (15) 15
schizophrenia - physiopathology (15) 15
aged, 80 and over (14) 14
disorders (14) 14
genome-wide association study - methods (14) 14
mutation (14) 14
schizophrenia - epidemiology (14) 14
disease susceptibility (13) 13
psychiatric status rating scales (13) 13
psychiatric-disorders (13) 13
usage (13) 13
family (12) 12
genetic variation - genetics (12) 12
genome, human (12) 12
genotype & phenotype (12) 12
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Schizophrenia Research, ISSN 0920-9964, 2014, Volume 160, Issue 1, pp. e1 - e2
Journal Article
Journal Article
Schizophrenia Research, ISSN 0920-9964, 2014, Volume 153, pp. S72 - S72
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
PLoS ONE, ISSN 1932-6203, 11/2011, Volume 6, Issue 11, pp. e26488 - e26488
Psychiatric disorders such as schizophrenia and autism are characterised by cellular disorganisation and dysconnectivity across the brain and can be caused by... 
MOLECULAR CHARACTERIZATION | BEHAVIORAL ABNORMALITIES | LAMINA-RESTRICTED PROJECTION | HIPPOCAMPAL MOSSY FIBERS | RECEPTOR HYPOFUNCTION | ADOLESCENT-ONSET SCHIZOPHRENIA | BIOLOGY | SCHIZOPHRENIA-SUSCEPTIBILITY LOCUS | WHITE-MATTER ABNORMALITIES | BIPOLAR DISORDER | INTERSTITIAL DELETION | Limbic System - pathology | Humans | Memory | Prefrontal Cortex - physiopathology | Male | Mental Disorders - complications | Gait - physiology | Mice, Neurologic Mutants | Prefrontal Cortex - pathology | Mental Disorders - genetics | Anxiety - complications | Limbic System - physiopathology | Female | Nerve Net - physiopathology | Semaphorins - genetics | Disease Models, Animal | Limbic System - growth & development | Mice, Inbred C57BL | Anxiety - psychology | Anxiety - physiopathology | Behavior, Animal - physiology | Mutation - genetics | Mental Disorders - physiopathology | Mental Disorders - psychology | Phenotype | Animals | Mice | Locomotion - physiology | Psychological aspects | Autism | Brain | Neurons | Analysis | Physiological aspects | Schizophrenia | Genetic aspects | Clozapine | Neurosciences | Animal models | Neuroleptics | Mental disorders | Genes | Disorders | Nervous system | Genomes | Health physics | Neurodevelopmental disorders | Defects | Proteins | Psychosis | Rodents | Genetics | Physiology | Psychopathology | Narcotics | EEG | Exploratory behavior | Cortex | Behavior disorders | Pattern recognition | Object recognition | Mutants | Brain research | Lamination | Anxieties | Neural networks | Psychopharmacology | Mutation | Short term memory | Psychiatry | Organizational aspects | Index Medicus
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
Schizophrenia Research, ISSN 0920-9964, 2008, Volume 102, Issue 1, pp. 184 - 184
Journal Article
by Hibar, Derrek and Stein, J.L and Rentería, Miguel and Arias-Vásquez, Alejano and Desrivières, Sylvane and Jahanshad, Neda and Toro, Roberto and Wittfeld, Katharina and Abramovic, Lucija and Andersson, Micael and Aribisala, Benjamin and Armstrong, Nicola J and Bernard, Manon and Bohlken, Marc M and Boks, Marco and Bralten, Linda and Brown, Anew and Chakravarty, M. Mallar and Chen, Qiang and Ching, Christopher and Cuellar-Partida, Gabriel and Braber, Anouk and Giddaluru, Sudheer and Goldman, Aaron L and Grimm, Oliver and Guadalupe, Tulio and Hass, Johanna and Woldehawariat, Girma and Holmes, Avram and Hoogman, Martine and Janowitz, Deborah and Jia, Tianye and Kim, Shinseog and Klein, Marieke and Kraemer, Bernd and Lee, Phil H and Olde Loohuis, Loes M and Luciano, Michelle and MacAre, Christine and Mather, R and Mattheisen, Manuel and Milaneschi, Yuri and Nho, Kwangsik and Papmeyer, Martina and Ramasamy, Adaikalavan and Risacher, Shannon and Roiz-Santiañez, Roberto and Rose, Emma and Salami, Alireza and Sämann, Philipp and Schmaal, Lianne and Schork, Nicholas and Shin, Jean and Strike, Vanessa and Teumer, Alexander and Van Donkelaar, Marjolein M. J and Eijk, Kristel and Walters, Raymond and Westlye, Lars and Whelan, Christopher and Winkler, Anderson and Zwiers, Marcel and Alhusaini, Saud and Athanasiu, Lavinia and Ehrlich, Stefan and Hakobjan, Marina and Hartberg, Cecilie B and Haukvik, Unn and Heister, Angelien J. G. A. M and Hoehn, David and Kasperaviciute, Dalia and Liewald, David C and Lopez, Lorna and Makkinje, Remco R. R and Matarin, Mar and Naber, Marlies A. M and Reese McKay, D and Needham, Margaret and Nugent, Allison and Pütz, Benno and Royle, Natalie and Shen, Li and Sprooten, Roy and Trabzuni, Danyah and Van Der Marel, Saskia S. L and Van Hulzen, Kimm J. E and Walton, Esther and Björnsson, Asgeir and Almasy, Laura and Ames, David and Arepalli, Sampath and Assareh, A.A and Bastin, Mark and Brodaty, Henry and Bulayeva, Kazima and Carless, Melanie and Cichon, Sven and Corvin, Aiden and Curran, Joanne and Czisch, Michael and ... and EPIGEN and SYS and Alzheimers Dis Neuroimaging and CHARGE Consortium and IMAGEN and Alzheimer’s Disease Neuroimaging Initiative and The Alzheimer’s Disease Neuroimaging Initiative and The CHARGE Consortium and Stockholms universitet and Centrum för forskning om äldre och åldrande (ARC), (tills m KI) and Samhällsvetenskapliga fakulteten
Nature: international weekly journal of science, ISSN 0028-0836, 04/2015, Volume 520, Issue 7546, pp. 224 - 229
Journal Article
by Marshall, Christian R and Howrigan, Daniel P and Merico, Daniele and Thiruvahinapuram, Bhooma and Wu, Wenting and Greer, Douglas S and Antaki, Danny and Shetty, Aniket and Holmans, Peter A and Pinto, Dalila and Gujral, Madhusudan and Brandler, William M and Malhotra, Dheeraj and Wang, Zhouzhi and Fajarado, Karin V Fuentes and Maile, Michelle S and Ripke, Stephan and Agartz, Ingrid and Albus, Margot and Alexander, Madeline and Amin, Farooq and Atkins, Joshua and Bacanu, Silviu A and Belliveau, Richard A and Bergen, Sarah E and Bertalan, Marcelo and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Bulik-Sullivan, Brendan 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 Catts, Stanley V and Chambert, Kimberley D and Cheng, Wei and Cloninger, C Robert and Cohen, David and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and Del Favero, Jurgen and DeLisi, Lynn E and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farh, Kai-How and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedman, Joseph I and Forstner, Aneas J and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Gershon, Elliot S and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Gratten, Jacob and de Haan, Lieuwe 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 Huang, Hailiang and Ikeda, Masashi and Joa, Inge and Kähler, Anna K and ... and Schizophrenia Working Grp and Psychosis Endophenotypes and CNV and Psychosis Endophenotypes International Consortium and CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 27 - 35
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of schizophrenia (SCZ). However, genome-wide investigation of the... 
DUPLICATIONS | AUTISM | GENE | CNVS | GENETICS & HEREDITY | RISK | DISORDERS | 16P11.2 | PHENOTYPES | MUTATIONS | REARRANGEMENTS | Genetic Predisposition to Disease | Genome-Wide Association Study | Schizophrenia - genetics | Genetic Markers - genetics | Humans | Risk Factors | Genetic Loci - genetics | Female | Genotype | Male | DNA Copy Number Variations - genetics |