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Biological Psychiatry, ISSN 0006-3223, 05/2018, Volume 83, Issue 9, pp. S5 - S5
Journal Article
Schizophrenia Bulletin, ISSN 0586-7614, 04/2018, Volume 44, Issue suppl_1, pp. S188 - S188
Abstract Background Transcription at enhancers is a widespread phenomenon, which produces so-called enhancer RNA (eRNA) and occurs in an activity dependent... 
Abstracts
Journal Article
European Neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S773 - S773
To better understand the role of CREs in neuropsychiatric disorders we have applied the Assay for Transposase Accessible Chromatin followed by sequencing... 
Medical colleges | Nervous system diseases | Chromatin | Neurons | Genes | Fluorescence | Schizophrenia | DNA binding proteins | Genetic transcription | Protein binding | Neurophysiology
Journal Article
Book
by Savage, Jeanne E and Jansen, Philip R and Stringer, Sven and Watanabe, Kyoko and Bryois, Julien and De Leeuw, Christiaan A and Nagel, Mats and Awasthi, Swapnil and Barr, Peter B and Coleman, Jonathan R. I and Grasby, Katrina L and Hammerschlag, Anke R and Kaminski, Jakob A and Karlsson, Robert and Krapohl, Eva and Lam, Max and Nygaard, Marianne and Reynolds, Chandra A and Trampush, Joey W and Young, Hannah and Zabaneh, Delilah and Hägg, Sara and Hansell, Narelle K and Karlsson, Ida K and Linnarsson, Sten and Montgomery, Grant W and Muñoz-Manchado, Ana B and Quinlan, Erin B and Schumann, Gunter and Skene, Nathan G and Webb, Bradley T and White, Tonya and Arking, Dan E and Avramopoulos, Dimitrios and Bilder, Robert M and Bitsios, Panos and Burdick, Katherine E and Cannon, Tyrone D and Chiba-Falek, Ornit and Christoforou, Andrea and Cirulli, Elizabeth T and Congdon, Eliza and Corvin, Aiden and Davies, Gail and Deary, Ian J and Derosse, Pamela and Dickinson, Dwight and Djurovic, Srdjan and Donohoe, Gary and Conley, Emily Drabant and Eriksson, Johan G and Espeseth, Thomas and Freimer, Nelson A and Giakoumaki, Stella and Giegling, Ina and Gill, Michael and Glahn, David C and Hariri, Ahmad R and Hatzimanolis, Alex and Keller, Matthew C and Knowles, Emma and Koltai, Deborah and Konte, Bettina and Lahti, Jari and Le Hellard, Stephanie and Lencz, Todd and Liewald, David C and London, Edythe and Lundervold, Astri J and Malhotra, Anil K and Melle, Ingrid and Morris, Derek and Need, Anna C and Ollier, William and Palotie, Aarno and Payton, Antony and Pendleton, Neil and Poldrack, Russell A and Räikkönen, Katri and Reinvang, Ivar and Roussos, Panos and Rujescu, Dan and Sabb, Fred W and Scult, Matthew A and Smeland, Olav B and Smyrnis, Nikolaos and Starr, John M and Steen, Vidar M and Stefanis, Nikos C and Straub, Richard E and Sundet, Kjetil and Tiemeier, Henning and Voineskos, Aristotle N and Weinberger, Daniel R and Widen, Elisabeth and Yu, Jin and Abecasis, Goncalo and Andreassen, Ole A and Breen, Gerome and Christiansen, Lene and ...
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 912 - 919
Intelligence is highly heritable(1) and a major determinant of human health and well-being(2). Recent genome-wide meta-analyses have identified 24 genomic loci... 
GENERAL COGNITIVE FUNCTION | CONSORTIUM | TEST BATTERIES | GWAS | ANNOTATION | GENETICS & HEREDITY | RISK | LOCI | EDUCATIONAL-ATTAINMENT | TRAITS | HERITABILITY | Genetic Predisposition to Disease | Humans | Middle Aged | Adolescent | Female | Male | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Intelligence - genetics | Quantitative Trait Loci | Brain - physiology | Brain | Chromatin | Neurosciences | Intelligence | Synaptogenesis | Mental disorders | Genomics | Genes | Cognitive ability | Schizophrenia | Association analysis | Nervous system | Identification | Mapping | Genomes | Genetic effects | Annotations | Coding | Genetic analysis | Neostriatum | Alzheimer's disease | Bioinformatics | Neurodegenerative diseases | Neurons | Attention deficit hyperactivity disorder | Causation | Gene expression | Spiny neurons | Loci | Educational attainment | Meta-analysis | Quantitative trait loci | Neurological diseases | Studies | Pyramidal cells | Gene loci | Gene mapping | Alzheimers disease | Hippocampus | Medical and Health Sciences | Medicin och hälsovetenskap | Alzheimer disease | Article | nervous system development | genetic association | gene location | schizophrenia | Klinisk medicin | pleiotropy | gene mapping | genetic correlation | priority journal | human | Neurologi | corpus striatum | hippocampus | synapse | chromatin | heredity | genetic variability | intelligence | pyramidal nerve cell | gene locus | Mendelian randomization analysis | Clinical Medicine | Neurology | expression quantitative trait locus | medium spiny neuron | genome-wide association study | attention deficit disorder | exon | conserved sequence | gene expression
Journal Article
by Davies, Gail and Lam, Max and Harris, Sarah E and Trampush, Joey W and Luciano, Michelle and Hill, W. David and Hagenaars, Saskia P and Ritchie, Stuart J and Marioni, Riccardo E and Fawns-Ritchie, Chloe and Liewald, David C. M and Okely, Judith A and Ahola-Olli, Ari V and Barnes, Catriona L. K and Bertram, Lars and Bis, Joshua C and Burdick, Katherine E and Christoforou, Andrea and Derosse, Pamela and Djurovic, Srdjan and Espeseth, Thomas and Giakoumaki, Stella and Giddaluru, Sudheer and Gustavson, Daniel E and Hayward, Caroline and Hofer, Edith and Ikram, M. Arfan and Karlsson, Robert and Knowles, Emma and Lahti, Jari and Leber, Markus and Li, Shuo and Mather, Karen A and Melle, Ingrid and Morris, Derek and Oldmeadow, Christopher and Palviainen, Teemu and Payton, Antony and Pazoki, Raha and Petrovic, Katja and Reynolds, Chandra A and Sargurupremraj, Muralidharan and Scholz, Markus and Smith, Jennifer A and Smith, Albert V and Terzikhan, Natalie and Thalamuthu, Anbupalam and Trompet, Stella and Van Der Lee, Sven J and Ware, Erin B and Windham, B. Gwen and Wright, Margaret J and Yang, Jingyun and Yu, Jin and Ames, David and Amin, Najaf and Amouyel, Philippe and Andreassen, Ole A and Armstrong, Nicola J and Assareh, Amelia A and Attia, John R and Attix, Deborah and Avramopoulos, Dimitrios and Bennett, David A and Böhmer, Anne C and Boyle, Patricia A and Brodaty, Henry and Campbell, Harry and Cannon, Tyrone D and Cirulli, Elizabeth T and Congdon, Eliza and Conley, Emily Drabant and Corley, Janie and Cox, Simon R and Dale, Anders M and Dehghan, Abbas and Dick, Danielle and Dickinson, Dwight and Eriksson, Johan G and Evangelou, Evangelos and Faul, Jessica D and Ford, Ian and Freimer, Nelson A and Gao, He and Giegling, Ina and Gillespie, Nathan A and Gordon, Scott D and Gottesman, Rebecca F and Griswold, Michael E and Gudnason, Vilmundur and Harris, Tamara B and Hartmann, Annette M and Hatzimanolis, Alex and Heiss, Gerardo and Holliday, Elizabeth G and Joshi, Peter K and Kähönen, Mika and Kardia, Sharon L. R and Karlsson, Ida and Kleineidam, Luca and ...
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 2098 - 16
General cognitive function is a prominent and relatively stable human trait that is associated with many important life outcomes. We combine cognitive and... 
COMMON VARIANTS | METAANALYSIS | REACTION-TIME | PROCESSING SPEED | MULTIDISCIPLINARY SCIENCES | INTELLIGENCE DIFFERENCES | SCHIZOPHRENIA | DCDC2 | DISCOVERY | GENOME-WIDE ASSOCIATION | REVEALS | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Humans | Middle Aged | Genetic Loci - genetics | Neurodegenerative Diseases - genetics | Neurodevelopmental Disorders - genetics | Reaction Time - genetics | Young Adult | Mental Disorders - genetics | Adolescent | Aged, 80 and over | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Adult | Aged | Hypertension | Brain | Cognitive ability | Genomes | Gene expression | Neurodevelopmental disorders | Loci | Consortia | Illnesses | Mathematical analysis | Reaction time | Heritability | Gene loci | Polygenic inheritance | brain cortex | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | osteoarthritis | Article | heart infarction | Klinisk medicin | lung cancer | identification method | longevity | grip strength | angina pectoris | genetic correlation | human | major depression | Neurologi | cognition | data set | aged | brain | gene locus | Clinical Medicine | Neurology | genome | vision | genetic analysis | controlled study | response time | adolescent | nervous system disorder | adult | hypertension | gene expression
Journal Article
Neuron, ISSN 0896-6273, 12/2014, Volume 84, Issue 5, pp. 997 - 1008
Three-dimensional chromosomal conformations regulate transcription by moving enhancers and regulatory elements into spatial proximity with target genes. Here... 
CYTOCHROME-C | DE-NOVO MUTATIONS | SYNAPTIC-TRANSMISSION | GENOME-WIDE | SCHIZOPHRENIA RISK | ENERGY-METABOLISM | ENHANCER FUNCTION | SUBUNIT GENES | NEUROSCIENCES | PREFRONTAL CORTEX | MAMMALIAN GENOMES | Chromatin - metabolism | Humans | Middle Aged | Receptors, N-Methyl-D-Aspartate - metabolism | Male | Schizophrenia - pathology | Cerebral Cortex - cytology | Cerebral Cortex - ultrastructure | Receptors, N-Methyl-D-Aspartate - genetics | Neurons - ultrastructure | Schizophrenia - genetics | Antipsychotic Agents - therapeutic use | Receptors, N-Methyl-D-Aspartate - chemistry | HEK293 Cells | Aged, 80 and over | Cognition - physiology | Female | Neurons - metabolism | Chromatin - drug effects | Animals, Newborn | Mice, Inbred C57BL | Cells, Cultured | Gene Expression Regulation - physiology | Mice, Transgenic | Signal Transduction - genetics | Transcription Factors - genetics | Cognition - drug effects | Transcription Factors - metabolism | Animals | Polymorphism, Single Nucleotide - genetics | Aged | Mice | Antipsychotic Agents - pharmacology | Schizophrenia - drug therapy | Computer science | Methyl aspartate | Chromatin | Liability (Law) | Genes | Transferases | Genomics | Stem cells | Cognition | Glutamate | Gene expression | Genetic polymorphisms | Medical colleges | Neurons | DNA binding proteins | Genetic transcription | Neurosciences | Editing | Genomes | Grants | Experiments | Proteins | Brain research | Cognition & reasoning | Rodents | Chromosomes | Deoxyribonucleic acid--DNA
Journal Article
Biological Psychiatry, ISSN 0006-3223, 2008, Volume 64, Issue 3, pp. 235 - 240
Background The dopamine D3 receptor (DRD3 ) is suspected to modulate prepulse inhibition (PPI) in animals and humans, but definite conclusions cannot be drawn... 
Psychiatry | startle | healthy males | Dopamine | sensorimotor gating | Ser9Gly polymorphism | DRD
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e39243
Journal Article