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1. Full Text Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance
by Huentelman, Matthew J and Papassotiropoulos, Andreas and Craig, David W and Hoerndli, Frederic J and Pearson, John V and Huynh, Kim-Dung and Corneveaux, Jason and Hänggi, Jürgen and Mondadori, Christian R.A and Buchmann, Andreas and Reiman, Eric M and Henke, Katharina and de Quervain, Dominique J.-F and Stephan, Dietrich A
Human Molecular Genetics, ISSN 0964-6906, 06/2007, Volume 16, Issue 12, pp. 1469 - 1477
Little is known about the genes and proteins involved in the process of human memory. To identify genetic factors related to human episodic memory performance,... 
COMPLEX HUMAN-DISEASES | HIPPOCAMPUS | MILD MENTAL IMPAIRMENT | DELETED REGION | ALZHEIMERS-DISEASE | POOLED DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | MEDIAL TEMPORAL-LOBE | GENETICS & HEREDITY | NEUROBLASTOMA | IDENTIFICATION | ASSOCIATION | Calcium-Binding Proteins - metabolism | Brain - anatomy & histology | Humans | Memory | Middle Aged | Genotype | Male | Brain - metabolism | Magnetic Resonance Imaging | Animals | Adolescent | Alleles | Mental Recall - physiology | Trans-Activators - genetics | Adult | Female | Trans-Activators - metabolism | Mice | Polymorphism, Single Nucleotide | Genome | Calcium-Binding Proteins - genetics | Cohort Studies
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2. Full Text Common Kibra Alleles Are Associated with Human Memory Performance
by Andreas Papassotiropoulos and Dietrich A. Stephan and Matthew J. Huentelman and Frederic J. Hoerndli and David W. Craig and John V. Pearson and Kim-Dung Huynh and Fabienne Brunner and Jason Corneveaux and David Osborne and M. Axel Wollmer and Amanda Aerni and Daniel Coluccia and Jürgen Hänggi and Christian R. A. Mondadori and Andreas Buchmann and Eric M. Reiman and Richard J. Caselli and Katharina Henke and Dominique J.-F. de Quervain
Science, ISSN 0036-8075, 10/2006, Volume 314, Issue 5798, pp. 475 - 478
Human memory is a polygenic trait. We performed a genome-wide screen to identify memory-related gene variants. A genomic locus encoding the brain protein KIBRA... 
Haplotypes | Temporal lobe | Magnetic resonance imaging | Memory | Coordinate systems | Reports | Memory recall | Population genetics | Hippocampus | Genotypes | Human genetics | HIPPOCAMPUS | PROTEIN-KINASE-C | ACTIVATION | POPULATION STRATIFICATION | MULTIDISCIPLINARY SCIENCES | POLYMORPHISM | COGNITION | Hippocampus - chemistry | United States | Humans | Middle Aged | Male | Proteins - analysis | Brain - physiology | Phosphoproteins | Adult | Female | Proteins - physiology | Gene Expression | Membrane Proteins - genetics | Attention | Intracellular Signaling Peptides and Proteins | Genotype | Reverse Transcriptase Polymerase Chain Reaction | Switzerland | Proteins - genetics | Magnetic Resonance Imaging | Animals | Adolescent | Alleles | Brain Chemistry | Mice | Polymorphism, Single Nucleotide | Hippocampus - physiology | Calcium-Binding Proteins - genetics | Cohort Studies | Allelomorphism | Research | Complementation (Genetics) | Analysis
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3. Full Text Common brain disorders are associated with heritable patterns of apparent aging of the brain
by Kaufmann, Tobias and van der Meer, Dennis and Doan, Nhat Trung and Schwarz, Emanuel and Lund, Martina J and Agartz, Ingrid and Alnæs, Dag and Barch, Deanna M and Baur-Streubel, Ramona and Bertolino, Alessano and Bettella, Francesco and Beyer, Mona K and Bøen, Erlend and Borgwardt, Stefan and Brandt, Christine L and Buitelaar, Jan and Celius, Elisabeth G and Cervenka, Simon and Conzelmann, Annette and Córdova-Palomera, Aldo and Dale, Anders M and de Quervain, Dominique J. F and Carlo, PasqualeDi and Djurovic, Srdjan and Dørum, Erlend S and Eisenacher, Sarah and Elvsåshagen, Torbjørn and Espeseth, Thomas and Fatouros-Bergman, Helena and Flyckt, Lena and Franke, Barbara and Frei, Oleksan and Haatveit, Beathe and Håberg, Asta K and Harbo, Hanne F and Hartman, Catharina A and Heslenfeld, Dirk and Hoekstra, Pieter J and Høgestøl, Einar A and Jernigan, Terry L and Jonassen, Rune and Jönsson, Erik G and Kirsch, Peter and Kłoszewska, Iwona and Kolskår, Knut K and Lanø, Nils Inge and Hellard, StephanieLe and Lesch, Klaus-Peter and Lovestone, Simon and Oosterlaan, Jaap and Karolinska Schizophrenia Project K and Karolinska Schizophrenia Project (KaSP) and Medicinska fakulteten and Institutionen för integrativ medicinsk biologi (IMB) and Umeå centrum för funktionell hjärnavbildning (UFBI) and Institutionen för strålningsvetenskaper and Umeå universitet
Nature neuroscience, ISSN 1097-6256, 2019, Volume 22, Issue 10, pp. 1617 - 1623
Common risk factors for psychiatric and other brain disorders are likely to converge on biological pathways influencing the development and maintenance of... 
MULTIPLE-SCLEROSIS | MRI | SCHIZOPHRENIA | LOCI | NEUROSCIENCES | ALZHEIMERS | AGE | Medical colleges | Brain | Medical imaging equipment | Neurophysiology | Pleiotropy | Functional anatomy | Magnetic resonance imaging | Disorders | Aging | Neurodevelopmental disorders | Risk analysis | Risk factors | Structure-function relationships | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
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4. Full Text DAT1 polymorphism is associated with risk taking in the Balloon Analogue Risk Task (BART)
by Mata, Rui and Hau, Robin and Papassotiropoulos, Andreas and Hertwig, Ralph
PLoS ONE, ISSN 1932-6203, 06/2012, Volume 7, Issue 6, p. e39135
Twin-studies suggest that a significant portion of individual differences in the propensity to take risks resides in people's genetic make-up and there is... 
IMAGING GENETICS | AVAILABILITY | GENOTYPE | VARIABLE NUMBER | MULTIDISCIPLINARY SCIENCES | VNTR POLYMORPHISM | PROPENSITY | PERSONALITY-TRAIT | DOPAMINE TRANSPORTER GENE | IMPULSIVITY | BRAIN | Humans | Middle Aged | Genotype | Male | Tandem Repeat Sequences | Dopamine Plasma Membrane Transport Proteins - genetics | Polymorphism, Genetic | Young Adult | Risk-Taking | Adolescent | Adult | Female | 3' Untranslated Regions | Genetic aspects | Genetic polymorphisms | Behavior | Brain | Neurosciences | Genes | Risk | Family medical history | Gene polymorphism | Neostriatum | Reinforcement | Dopamine transporter | Food | Dopamine receptors | Impulsivity | Sensitivity analysis | Dopamine | Analogue | Decision making | Alcoholism | Risk taking | Carriers | Studies | 3' Untranslated regions | Alleles | Transporter | Polymorphism
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5. Full Text Human genome–guided identification of memory-modulating drugs
by Andreas Papassotiropoulos and Christiane Gerhards and Angela Heck and Sandra Ackermann and Amanda Aerni and Nathalie Schicktanz and Bianca Auschra and Philippe Demougin and Eva Mumme and Thomas Elbert and Verena Ertl and Leo Gschwind and Edveena Hanser and Kim-Dung Huynh and Frank Jessen and Iris-Tatjana Kolassa and Annette Milnik and Paolo Paganetti and Klara Spalek and Christian Vogler and Andreas Muhs and Andrea Pfeifer and Dominique J.-F. de Quervain
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 11/2013, Volume 110, Issue 46, pp. E4369 - E4374
In the last decade there has been an exponential increase in knowledge about the genetic basis of complex human traits, including neuropsychiatric disorders.... 
PTSD | Emotional memory | Pharmacology | POSTTRAUMATIC-STRESS-DISORDER | MULTIDISCIPLINARY SCIENCES | DIPHENHYDRAMINE | RISK | GENE SET ANALYSIS | RECONSOLIDATION BLOCKADE | PSYCHOMOTOR PERFORMANCE | emotional memory | pharmacology | SEDATION | PSYCHIATRIC-DISORDERS | WIDE ASSOCIATION | GSA-SNP | Diphenhydramine - pharmacology | Memory - drug effects | Oligonucleotides - genetics | Humans | Drug Discovery - methods | Genotype | Logistic Models | Male | Fluorometry | Switzerland | Genome, Human - genetics | Cross-Over Studies | Young Adult | Stress Disorders, Post-Traumatic - drug therapy | Polymerase Chain Reaction | Polymorphism, Single Nucleotide - genetics | Adult | Female | Interviews as Topic | Survivors - psychology | Stress Disorders, Post-Traumatic - genetics | Data Mining - methods | Memory - physiology | Biological Sciences | PNAS Plus
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6. Full Text Associations among child abuse, mental health, and epigenetic modifications in the proopiomelanocortin gene (POMC): A study with children in Tanzania
by Hecker, Tobias and Radtke, Karl M and Hermenau, Katharin and Papassotiropoulos, Andreas and Elbert, Thomas
Development and Psychopathology, ISSN 0954-5794, 11/2016, Volume 28, Issue 4, pp. 1401 - 1412
Child abuse is associated with a number of emotional and behavioral problems. Nevertheless, it has been argued that these adverse consequences may not hold for... 
PHYSICAL ABUSE | GLUCOCORTICOID-RECEPTOR | DNA METHYLATION | CORPORAL PUNISHMENT | PSYCHOLOGY, DEVELOPMENTAL | PSYCHIATRIC-DISORDERS | STRESS | PROMOTER | BETA-ENDORPHIN | DIFFICULTIES QUESTIONNAIRE | MALTREATMENT | Epigenetics | Child abuse & neglect | Mental health
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7. Full Text Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder
by Schwarz, E and Doan, N.T and Pergola, G and Westlye, L.T and Kaufmann, T and Wolfers, T and Brecheisen, R and Quarto, T and Ing, A.J and Carlo, P. di and Gurholt, T.P and Harms, R.L and Noirhomme, Q and Moberget, T and Agartz, I and Aneassen, O.A and Bellani, M and Bertolino, A and Blasi, G and Brambilla, P and Buitelaar, J.K and Cervenka, S and Flyckt, L and Frangou, S and Franke, B and Hall, J and Heslenfeld, D.J and Kirsch, P and McIntosh, A.M and Nothen, M.M and Papassotiropoulos, A and Quervain, D.J. de and Rietschel, M and Schumann, G and Tost, H and Witt, S.H and Zink, M and Meyer-Lindenberg, A and IMAGEMEND Consortium and Karolinska Schizophrenia Project and IMAGEMEND Consortium, Karolinska Schizophrenia Project (KaSP) Consortium and The IMAGEMEND Consortium, Karolinska Schizophrenia Project (KaSP) Consortium
Translational Psychiatry, ISSN 2158-3188, 2019, Volume 9, Issue 1, pp. 12 - 13
Schizophrenia is a severe mental disorder characterized by numerous subtle changes in brain structure and function. Machine learning allows exploring the... 
MRI SCANS | METAANALYSIS | PSYCHIATRY | VOLUME | LIKELIHOOD ESTIMATION | SEGMENTATION | RISK | CLASSIFICATION | 1ST-EPISODE | DEFICITS | Attention Deficit Disorder with Hyperactivity - physiopathology | Humans | Middle Aged | Bipolar Disorder - physiopathology | Male | Schizophrenia - diagnostic imaging | Machine Learning | Case-Control Studies | Gray Matter - diagnostic imaging | Young Adult | Magnetic Resonance Imaging | Attention Deficit Disorder with Hyperactivity - diagnostic imaging | Bipolar Disorder - diagnostic imaging | Schizophrenia - physiopathology | Gray Matter - physiopathology | Adolescent | Adult | Female | Schizophrenia | Bipolar disorder | Nuclear magnetic resonance--NMR | Artificial intelligence
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8. Full Text Better memory and neural efficiency in young apolipoprotein E ε4 carriers
by Mondadori, Christian R. A and De Quervain, Dominique J.-F and Buchmann, Andreas and Mustovic, Henrietta and Wollmer, M. Axel and Schmidt, Conny F and Boesiger, Peter and Hock, Christoph and Nitsch, Roger M and Papassotiropoulos, Andreas and Henke, Katharina
Cerebral Cortex, ISSN 1047-3211, 08/2007, Volume 17, Issue 8, pp. 1934 - 1947
Learning | Neuroimaging | Functional magnetic resonance imaging | APOE gene | Alzheimer's disease | Hippocampus
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9. Full Text Predicting emotional arousal and emotional memory performance from an identical brain network
by Loos, Eva and Egli, Tobias and Coynel, David and Fastenrath, Matthias and Freytag, Virginie and Papassotiropoulos, Andreas and de Quervain, Dominique J.-F and Milnik, Annette
NeuroImage, ISSN 1053-8119, 04/2019, Volume 189, pp. 459 - 467
Encoding and retrieval of emotionally arousing stimuli depend on the activation of multiple interconnected brain regions, with people showing differences in... 
Pictures | fMRI | Encoding | MVPA | Recognition | ANXIETY | DISORDERS | NEUROSCIENCES | NEUROIMAGING | RETRIEVAL | MODELS | CORTEX | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | AMYGDALA-HIPPOCAMPAL CONNECTIVITY | VALENCE | Neurosciences | Mental illness | Memory | Analysis | Brain | Young adults | Amygdala | Mental disorders | Scanners | Brain mapping | Perceptions | Emotions | Post traumatic stress disorder | Ratings & rankings | Arousal | Functional magnetic resonance imaging | Parietal lobe | Behavior
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10. Full Text The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val(158)Met Polymorphism
by Kolassa, IT and Kolassa, S and Ertl, V and Papassotiropoulos, A and De Quervain, DJF
BIOLOGICAL PSYCHIATRY, ISSN 0006-3223, 02/2010, Volume 67, Issue 4, pp. 304 - 308
Background: The risk for posttraumatic stress disorder (PTSD) depends on the number of traumatic event types experienced in a dose-response relationship, but... 
post-traumatic stress disorder | FUNCTIONAL POLYMORPHISM | ENVIRONMENT INTERACTION | COMT GENE | refugees | GENOTYPE | ANXIETY | PSYCHIATRY | NEUROSCIENCE | SCHIZOPHRENIA | genetic polymorphisms | NEUROSCIENCES | FEAR | risk | PHARMACOGENETICS | COMT polymorphism | AMYGDALA | Genetic Predisposition to Disease | Humans | Life Change Events | Middle Aged | Risk Factors | Africa | Probability | Male | Catechol O-Methyltransferase - genetics | Chi-Square Distribution | Young Adult | Adolescent | Adult | Female | Valine - genetics | Aged | Polymorphism, Single Nucleotide | Stress Disorders, Post-Traumatic - genetics | Methionine - genetics | Multiple Traumatic Events | Etiology | Neuroanatomy | Survivors | Genetic Markers | Refugees | PTSD (DSM-IV) | Rwandans | Genocide | Biologic Markers | Neurophysiology
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11. Full Text Association of KIBRA with episodic and working memory: A meta‐analysis
by Milnik, Annette and Heck, Angela and Vogler, Christian and Heinze, Hans‐Jochen and de Quervain, Dominique J.‐F and Papassotiropoulos, Andreas
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 12/2012, Volume 159B, Issue 8, pp. 958 - 969
WWC1 was first implicated in human cognition through a genome wide association study in 2006 that reported an association of the intronic single nucleotide... 
rs17070145 | common variant | single nucleotide polymorphism | human | WWC1 | Human | Common variant | Rs17070145 | Single nucleotide polymorphism | VARIANTS | PSYCHIATRY | ALZHEIMERS-DISEASE | PERFORMANCE | SCHIZOPHRENIA | POLYMORPHISM | HEIGHT | HERITABILITY | MESSENGER-RNA | FAMILIES | GENETICS & HEREDITY | GENETIC INFLUENCES | Genome-Wide Association Study | Humans | Middle Aged | Memory, Episodic | Male | Cognition | Phosphoproteins - genetics | Learning | Neuropsychological Tests | Young Adult | Adolescent | Alleles | Aged, 80 and over | Adult | Female | Aged | Polymorphism, Single Nucleotide | Memory, Short-Term | Intracellular Signaling Peptides and Proteins - genetics | Nervous system diseases | Neurosciences | Analysis | Short-term memory | Universities and colleges | Societies | Associations, institutions, etc | Psychiatric services
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12. Full Text Microarray-based maps of copy-number variant regions in European and Sub-Saharan populations
by Vogler, Christian and Gschwind, Leo and Röthlisberger, Benno and Huber, Andreas and Filges, Isabel and Miny, Peter and Auschra, Bianca and Stetak, Attila and Demougin, Philippe and Vukojevic, Vanja and Kolassa, Iris-Tatjana and Elbert, Thomas and de Quervain, Dominique J.-F and Papassotiropoulos, Andreas
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 12, p. e15246
The genetic basis of phenotypic variation can be partially explained by the presence of copy-number variations (CNVs). Currently available methods for CNV... 
HUMAN GENOME | GENE | ARRAY-CGH | DISEASE | SUSCEPTIBILITY | BIOLOGY | SEGMENTAL DUPLICATIONS | HAPLOTYPE | EVOLUTIONARY HISTORY | STRUCTURAL VARIATION | European Continental Ancestry Group - genetics | Oligonucleotide Array Sequence Analysis | Humans | Rwanda | Genotype | Gene Dosage | Switzerland | Genetic Variation | Algorithms | Sensitivity and Specificity | Models, Genetic | Polymorphism, Single Nucleotide | African Continental Ancestry Group - genetics | Genome, Human | Cluster Analysis | Genetic aspects | Single nucleotide polymorphisms | Genes | Genomics | Populations | Laboratories | Phenotypic variations | Feasibility studies | Mental health | Genomes | Genetic diversity | Single-nucleotide polymorphism | Population genetics | Medicine | Studies | Hospitals | Maps | Spiders | Population | Gene mapping | Localization | Polymorphism
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13. Full Text NTRK2 Methylation is negatively related to traumatic memory and PTSD risk in traumatized individuals and to episodic memory in healthy subjects
by Vukojevic, Vanja and Ghaffari, Navid and Kolassa, Iris and Wilker, Sarah and Elbert, Thomas and Papassotiropoulos, Andreas and de Quervain, Dominique
Psychoneuroendocrinology, ISSN 0306-4530, 09/2019, Volume 107, pp. 72 - 72
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14. Full Text S1-04-05: Genetics of human memory
by Papassotiropoulos, Andreas
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 2008, Volume 4, Issue 4, pp. T105 - T106
Neurology
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15. Full Text The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism
by Kolassa, Iris-Tatjana and Kolassa, Stephan and Ertl, Verena and Papassotiropoulos, Andreas and De Quervain, Dominique J.-F
Biological Psychiatry, ISSN 0006-3223, 02/2010, Volume 67, Issue 4, pp. 304 - 308
Background: The risk for posttraumatic stress disorder (PTSD) depends on the number of traumatic event types experienced in a dose-response relationship, but... 
post-traumatic stress disorder | risk | refugees | genetic polymorphisms | COMT polymorphism
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16. Full Text Converging Genetic and Functional Brain Imaging Evidence Links Neuronal Excitability to Working Memory, Psychiatric Disease, and Brain Activity
by Heck, Angela and Fastenrath, Matthias and Ackermann, Sandra and Auschra, Bianca and Bickel, Horst and Coynel, David and Gschwind, Leo and Jessen, Frank and Kaduszkiewicz, Hanna and Maier, Wolfgang and Milnik, Annette and Pentzek, Michael and Riedel-Heller, Steffi G and Ripke, Stephan and Spalek, Klara and Sullivan, Patrick and Vogler, Christian and Wagner, Michael and Weyerer, Siegfried and Wolfsgruber, Steffen and de Quervain, Dominique J.-F and Papassotiropoulos, Andreas
Neuron, ISSN 0896-6273, 03/2014, Volume 81, Issue 5, pp. 1203 - 1213
Working memory, the capacity of actively maintaining task-relevant information during a cognitive task, is a heritable trait. Working memory deficits are... 
SYSTEM | RISK LOCI | CIRCUITRY | SET ANALYSIS | CEREBELLUM | SCHIZOPHRENIA | REGISTRATION | BIPOLAR DISORDER | COGNITION | NEUROSCIENCES | GENOME-WIDE ASSOCIATION | Humans | Magnetic Resonance Imaging - methods | Male | Memory, Short-Term - physiology | Cerebellum - physiology | Healthy Volunteers | Brain - physiology | Case-Control Studies | Young Adult | Calcium Channels - physiology | Algorithms | Schizophrenia - genetics | Schizophrenia - physiopathology | Cognition - physiology | Adult | Female | Parietal Lobe - physiology | Aged | Genome-Wide Association Study - methods | Calcium Channels - genetics | Prefrontal Cortex - physiology | Brain | Neurosciences | Neurons | Genes | Genomics | Short-term memory | Schizophrenia | Genetic research | Disease susceptibility | Genetic aspects | Attention deficit disorder | Proteins | Studies | Neural networks | Bipolar disorder | Genomes | Kinases | Gene expression | Binding sites | Data bases
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