X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (120) 120
Patent (55) 55
Publication (18) 18
Conference Proceeding (6) 6
Book Chapter (3) 3
Magazine Article (3) 3
Book Review (2) 2
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (52) 52
humans (48) 48
genetics & heredity (25) 25
schizophrenia (24) 24
male (23) 23
genetic aspects (20) 20
genetics (20) 20
female (19) 19
schizophrenia - genetics (18) 18
psychiatry (17) 17
research (17) 17
article (15) 15
human necessities (15) 15
polymorphism, single nucleotide - genetics (14) 14
autism (13) 13
genome-wide association study (13) 13
genotype (13) 13
physics (13) 13
analysis (12) 12
case-control studies (12) 12
genomics (12) 12
multidisciplinary sciences (12) 12
risk factors (12) 12
genetic predisposition to disease - genetics (11) 11
health aspects (11) 11
phenotype (11) 11
adult (10) 10
autistic disorder - genetics (10) 10
genes (10) 10
linkage disequilibrium (10) 10
mental disorders (10) 10
mutation (10) 10
studies (10) 10
performing operations (9) 9
transporting (9) 9
child (8) 8
china (8) 8
family health (8) 8
fixed constructions (8) 8
genetic predisposition to disease (8) 8
genome-wide association (8) 8
alleles (7) 7
animals (7) 7
association (7) 7
blasting (7) 7
foods or foodstuffs (7) 7
gene expression (7) 7
genetic research (7) 7
genomes (7) 7
heating (7) 7
life sciences (7) 7
lighting (7) 7
measuring (7) 7
mechanical engineering (7) 7
mutation - genetics (7) 7
polymorphism, single nucleotide (7) 7
risk (7) 7
testing (7) 7
their treatment, not covered by other classes (7) 7
variants (7) 7
weapons (7) 7
[ sdv.gen ] life sciences [q-bio]/genetics (6) 6
aged (6) 6
autistic disorder (6) 6
development and progression (6) 6
disease (6) 6
gene (6) 6
gene mutations (6) 6
genetic variation - genetics (6) 6
methods (6) 6
middle aged (6) 6
multifactorial inheritance - genetics (6) 6
mutations (6) 6
neurology (6) 6
neurosciences (6) 6
pedigree (6) 6
psykiatri (6) 6
agriculture (5) 5
brain (5) 5
brain - metabolism (5) 5
electricity (5) 5
exons (5) 5
genetic linkage (5) 5
medical and health sciences (5) 5
medicin och hälsovetenskap (5) 5
mental-retardation (5) 5
metaanalysis (5) 5
psychosis (5) 5
schizophrenia - pathology (5) 5
spectrum disorders (5) 5
traits (5) 5
usage (5) 5
adolescent (4) 4
age of onset (4) 4
amino acid sequence (4) 4
animal husbandry (4) 4
biotechnology & applied microbiology (4) 4
bipolar disorder (4) 4
bipolar disorder - genetics (4) 4
chemistry (4) 4
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


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 Neale, Benjamin M and Neale, Benjamin M and Kou, Yan and Samocha, Kaitlin E and Liu, Li and Lim, Elaine and Ma'Ayan, Avi and Rossin, Elizabeth and Samocha, Kaitlin E and Kirby, Andrew and Fromer, Menachem and Sabo, Aniko and Lin, Chiao-Feng and Daly, Mark J and Stevens, Christine and Rossin, Elizabeth and Kirby, Andrew and Wang, Li-San and Makarov, Vladimir and Flannick, Jason and Polak, Paz and Fromer, Menachem and Shakir, Khalid and Yoon, Seungtai and Maguire, Jared and Fennell, Tim and Garimella, Kiran and Crawford, Emily L and Banks, Eric and Campbell, Nicholas G and Poplin, Ryan and Geller, Evan T and Valladares, Otto and Gabriel, Stacey and Schafer, Chad and De Pristo, Mark and Sunyaev, Shamil and Liu, Han and Daly, Mark J and Zhao, Tuo and Cai, Guiqing and Lihm, Jayon and Dannenfelser, Ruth and Jabado, Omar and Peralta, Zuleyma and Nagaswamy, Uma and Muzny, Donna and Reid, Jeffrey G and Newsham, Irene and Wu, Yuanqing and Lewis, Lora and Han, Yi and Voight, Benjamin F and Lim, Elaine and Rossin, Elizabeth and Kirby, Andrew and Flannick, Jason and Fromer, Menachem and Shakir, Khalid and Fennell, Tim and Garimella, Kiran and Banks, Eric and Poplin, Ryan and Gabriel, Stacey and Depristo, Mark and Wimbish, Jack R and Boone, Braden E and Levy, Shawn E and Betancur, Catalina and Sunyaev, Shamil and Boerwinkle, Eric and Buxbaum, Joseph D and Cook Jr, Edwin H and Devlin, Bernie and Gibbs, Richard A and Roeder, Kathryn and Schellenberg, Gerard D and Sutcliffe, James S and Daly, Mark J
Nature, ISSN 0028-0836, 05/2012, Volume 484, Issue 7397, pp. 242 - 246
Journal Article
by Pinto, Dalila and Delaby, Elsa and Merico, Daniele and Barbosa, Mafalda and Merikangas, Alison and Klei, Lambertus and Thiruvahindrapuram, Bhooma and Xu, Xiao and Ziman, Robert and Wang, Zhuozhi and Vorstman, Jacob A.S and Thompson, Ann and Regan, Regina and Pilorge, Marion and Pellecchia, Giovanna and Pagnamenta, Alistair T and Oliveira, Guiomar and Oliveira, Bárbara and Marshall, Christian R and Magalhaes, Tiago R and Lowe, Jennifer K and Howe, Jennifer L and Griswold, Anthony J and Gilbert, John and Duketis, Eftichia and Dombroski, Beth A and De Jonge, Maretha V and Cuccaro, Michael and Crawford, Emily L and Correia, Catarina T and Conroy, Judith and Conceição, Inês C and Chiocchetti, Andreas G and Casey, Graham and Casey, Jillian P and Cai, Guiqing and Cabrol, Christelle and Bolshakova, Nadia and Bacchelli, Elena and Anney, Richard and Gallinger, Steven and Cotterchio, Michelle and Zwaigenbaum, Lonnie and Wittemeyer, Kerstin and Wing, Kirsty and Wallace, Simon and van Engeland, Herman and Tryfon, Ana and Thomson, Susanne and Soorya, Latha and Rogé, Bernadette and Roberts, Wendy and Poustka, Fritz and Mouga, Susana and Minshew, Nancy and McInnes, L. Alison and McGrew, Susan G and Lord, Catherine and Leboyer, Marion and Le Couteur, Ann S and Kolevzon, Alexander and Jiménez González, Patricia and Jacob, Suma and Holt, Richard and Guter, Stephen and Green, Jonathan and Green, Andrew and Gillberg, Christopher and Fernandez, Bridget A and Duque, Frederico and Delorme, Richard and Dawson, Geraldine and Chaste, Pauline and Café, Cátia and Brennan, Sean and Bourgeron, Thomas and Bolton, Patrick F and Bölte, Sven and Bernier, Raphael and Baird, Gillian and Bailey, Anthony J and Anagnostou, Evdokia and Almeida, Joana and Wijsman, Ellen M and Vieland, Veronica J and Vicente, Astrid M and Schellenberg, Gerard D and Pericak-Vance, Margaret and Paterson, Andrew D and Parr, Jeremy R and Nurnberger, John I and Monaco, Anthony P and Maestrini, Elena and Klauck, Sabine M and Hakonarson, Hakon and Haines, Jonathan L and Geschwind, Daniel H and Freitag, Christine M and Folstein, Susan E and Ennis, Sean and ... and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
The American Journal of Human Genetics, ISSN 0002-9297, 05/2014, Volume 94, Issue 5, pp. 677 - 694
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
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 9/2014, Volume 111, Issue 37, pp. 13529 - 13534
Delineating the molecular basis of individual differences in the stress response is critical to understanding the pathophysiology and treatment of... 
Datasets | Transcription factors | Animal models | Post traumatic stress disorder | Amygdala | Genes | Military psychiatry | Biological markers | Blood | Hippocampus | transcription regulation | POSTTRAUMATIC-STRESS-DISORDER | HIGH-DOSE CORTICOSTERONE | preventive treatment | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | NEUROSCIENCE | MECHANISMS | predator stress | psychiatry | NR3C1 | PTSD | BIOMARKERS | SOCIAL DEFEAT | GENE-EXPRESSION | ANIMAL-MODELS | Corticosterone - pharmacology | Signal Transduction | Amygdala - metabolism | Receptors, Glucocorticoid - blood | Male | Gene Expression Profiling | Sex Characteristics | Gene Regulatory Networks | Rats, Sprague-Dawley | Behavior, Animal | Brain - metabolism | Hippocampus - metabolism | Predatory Behavior - drug effects | Stress Disorders, Post-Traumatic - blood | Animals | Stress Disorders, Post-Traumatic - drug therapy | Receptors, Glucocorticoid - genetics | Brain - pathology | Female | Corticosterone - therapeutic use | Stress Disorders, Post-Traumatic - genetics | Brain | Protein research | Corticosteroids | Brain research | Blood-brain barrier | Genetic aspects | Cellular signal transduction | Research | Gene expression | Health aspects | Injuries | Tissue | Rodents | Biomarkers | Trauma | Index Medicus | Anxiety Disorders | Biochemical Markers | Neurobiology | Arousal | Genetic Markers | Conditioned Emotional Responses | Animal Models | Resilience | Biological Sciences
Journal Article
Nature, ISSN 0028-0836, 05/2009, Volume 459, Issue 7246, pp. 569 - 573
Journal Article
2000, Di 1 ban., A collection of theses on contemporary cinema, ISBN 9787810049092, 4, 7, 345
Book
The American Journal of Human Genetics, ISSN 0002-9297, 2011, Volume 88, Issue 2, pp. 201 - 206
Increasingly, mutations in genes causing Mendelian disease will be supported by individual and small families only; however, exome sequencing studies have thus... 
DIPHOSPHATE SYNTHASE |