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1. Full Text CNVs conferring risk of autism or schizophrenia affect cognition in controls
by Stefansson, Hreinn and Meyer-Lindenberg, Andreas and Steinberg, Stacy and Magnusdottir, Brynja and Morgen, Katrin and Arnarsdottir, Sunna and Bjornsdottir, Gyda and Walters, G. Bragi and Jonsdottir, Gudrun A and Doyle, Orla M and Tost, Heike and Grimm, Oliver and Kristjansdottir, Solveig and Snorrason, Heimir and Davidsdottir, Solveig R and Gudmundsson, Larus J and Jonsson, Gudbjorn F and Stefansdottir, Berglind and Helgadottir, Isafold and Haraldsson, Magnus and Jonsdottir, Birna and Thygesen, Johan H and Schwarz, Adam J and Didriksen, Michael and Stensbøl, Tine B and Brammer, Michael and Kapur, Shitij and Halldorsson, Jonas G and Hreidarsson, Stefan and Saemundsen, Evald and Sigurdsson, Engilbert and Stefansson, Kari
Nature (London), ISSN 0028-0836, 2014, Volume 505, Issue 7483, pp. 361 - 366
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Brain - anatomy & histology | Humans | Middle Aged | Male | Brain - abnormalities | Case-Control Studies | Iceland | Brain - metabolism | Young Adult | Fertility - genetics | Schizophrenia - genetics | Cognition - physiology | Adult | Female | Autistic Disorder - genetics | Chromosome Deletion | Genetic Predisposition to Disease | Chromosomes, Human - genetics | DNA Copy Number Variations - genetics | Chromosomes, Human, Pair 15 - genetics | Dyslexia - genetics | Neuropsychological Tests | Magnetic Resonance Imaging | Phenotype | Adolescent | Heterozygote | Learning Disorders - genetics | Aged | Autism | Copy number variations | Physiological aspects | Schizophrenia | Dyslexia | Genetic aspects | Cognition | Research | Population | Cognition & reasoning | Disease | Memory | Index Medicus
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2. Full Text A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains
by Ranlund, Siri and Calafato, Stella and Thygesen, Johan H and Lin, Kuang and Cahn, Wiepke and Crespo-Facorro, Benedicto and Zwarte, Sonja M. C and Diez, Alvaro and Di Forti, Marta and Iyegbe, Conrad and Jablensky, Assen and Jones, Rebecca and Hall, Mei-Hua and Kahn, Rene and Kalaydjieva, Luba and Kravariti, Eugenia and McDonald, Colm and McIntosh, Anew M and McQuillin, Anew and Picchioni, Marco and Prata, Diana P and Rujescu, Dan and Schulze, Katja and Shaikh, Madiha and Toulopoulou, Timothea and van Haren, Neeltje and van Os, Jim and Vassos, Evangelos and Walshe, Muriel and Lewis, Cathryn and Murray, Robin M and Powell, John and Bramon, Elvira and WTCCC2 and PEIC and GROUP
American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 01/2018, Volume 177, Issue 1, pp. 21 - 34
Humans | Family/psychology | Genetic Predisposition to Disease/genetics | Male | schizophrenia | bipolar disorder | Polymorphism, Single Nucleotide/genetics | Psychotic Disorders/genetics | Adult | Female | Event-Related Potentials, P300 | Endophenotypes/blood | Schizophrenia/genetics | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group/genetics | cognition | WHITE-MATTER | EEG | Europe | Risk Factors | UNAFFECTED 1ST-DEGREE RELATIVES | Brain/physiology | Multifactorial Inheritance/genetics | Bipolar Disorder/genetics | Neuropsychological Tests | MAUDSLEY FAMILY | single nucleotide polymorphism (SNP) | EVENT-RELATED POTENTIALS | PSYCHIATRIC-DISORDERS | GENETIC OVERLAP | EDINBURGH HIGH-RISK | Cognition/physiology | Australia | WORKING-MEMORY | Genetics & Heredity | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Family - psychology | Multifactorial Inheritance - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Bipolar Disorder - genetics | Brain - physiology | Psychotic Disorders - genetics | Schizophrenia - genetics | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Endophenotypes - blood | Medical research | Usage | Schizophrenia | Medicine, Experimental | Bipolar disorder | Genetic aspects | Risk factors | Statistical analysis | Mental disorders | Cognitive ability | Event-related potentials | Auditory evoked potentials | Genetic diversity | Psychosis | Genetic variance | Genotyping | Auditory discrimination learning | Ventricle | Structure-function relationships | Index Medicus
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3. Full Text Cognitive performance of GBA mutation carriers with early-onset PD The CORE-PD study
by Alcalay, R.N and Caccappolo, E and Mejia-Santana, H and Tang, M.-X and Rosado, L and Reilly, M. Orbe and Ruiz, D and Ross, B and Verbitsky, M and Kisselev, S and Louis, E and Comella, C and Colcher, A and Jennings, D and Nance, M and Bressman, S and Scott, W.K and Tanner, C and Mickel, S and Andrews, H and Waters, C and Fahn, S and Cote, L and Frucht, S and Ford, B and Rezak, M and Novak, K and Friedman, J.H and Pfeiffer, R and Marsh, L and Hiner, B and Siderowf, A and Payami, H and Molho, E and Factor, S and Ottman, R and Clark, L.N and Marder, K
Neurology, ISSN 0028-3878, 05/2012, Volume 78, Issue 18, pp. 1434 - 1440
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Diseases of striated muscles. Neuromuscular diseases | Olfaction Disorders - genetics | Glucosylceramidase - genetics | Genetic Testing | Memory Disorders - genetics | Humans | Middle Aged | Dementia - diagnosis | Male | Memory Disorders - diagnosis | Olfaction Disorders - diagnosis | Dementia - genetics | Basal Ganglia Diseases - genetics | DNA Mutational Analysis | beta-Glucosidase - genetics | Basal Ganglia Diseases - diagnosis | Mental Status Schedule | Adult | Cognitive Dysfunction - genetics | Female | Cognitive Dysfunction - diagnosis | Depressive Disorder - genetics | Depressive Disorder - diagnosis | Protein-Serine-Threonine Kinases - genetics | Genotype | Parkinson Disease - genetics | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 | Neuropsychological Tests | Phenotype | Parkinson Disease - diagnosis | Ubiquitin-Protein Ligases - genetics | Genetic Carrier Screening | Index Medicus | Abridged Index Medicus | Executive function | Demography | Parkinson's disease | Neurodegenerative diseases | Memory | spatial memory | Attention | Cognitive ability | Risk factors | Dementia disorders | Glucosylceramidase | Parkin protein | Mutation | LRRK2 protein | Age | Genotypes | Movement disorders | 165 | 201 | 205
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4. How children learn to read
: current issues and new directions in the integration of cognition, neurobiology and genetics of reading and dyslexia research and practice
by Pugh, Ken and McCardle, Peggy D
2009, The extraordinary brain series, ISBN 1848728433, xxxiii, 343
Physiological aspects | Dyslexia | Reading | Reading, Psychology of | Cognition in children | Psychology of | Cognitive Development
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5. Full Text Neuron-specific chromatin remodeling: A missing link in epigenetic mechanisms underlying synaptic plasticity, memory, and intellectual disability disorders
by Vogel-Ciernia, Annie and Wood, Marcelo A
Neuropharmacology, ISSN 0028-3908, 05/2014, Volume 80, pp. 18 - 27
Intellectual disability disorder | Long-term potentiation | Epigenetics | Long-term memory | Nucleosome remodeling | Autism spectrum disorder | Chromatin remodeling | Pharmacology & Pharmacy | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory Disorders - physiopathology | Autistic Disorder - physiopathology | Autistic Disorder - metabolism | Memory Disorders - genetics | Epigenesis, Genetic | Humans | Memory | Actins - metabolism | Brain - enzymology | Memory Disorders - metabolism | Cognition Disorders - metabolism | Actins - genetics | Brain - metabolism | DNA-Binding Proteins - metabolism | Nucleosomes - enzymology | Neurons - metabolism | Nuclear Proteins - genetics | DNA Helicases - genetics | Autistic Disorder - genetics | Cognition Disorders - physiopathology | Chromosomal Proteins, Non-Histone - metabolism | Gene Expression Regulation | Chromatin Assembly and Disassembly | Nucleosomes - metabolism | Nuclear Proteins - metabolism | Cognition Disorders - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | DNA Helicases - metabolism | Animals | Models, Biological | Neuronal Plasticity | Neurons - enzymology | Intellectual Disability - etiology | Mutation | Chromatin | Neurons | Genes | Histones | Schizophrenia | Gene expression | Index Medicus | chromatin remodeling | intellectual disability disorder | autism spectrum disorder | nucleosome remodeling | long-term memory | epigenetics | long-term potentiation
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6. Full Text Hydrogen Sulfide Ameliorates Homocysteine-Induced Alzheimer’s Disease-Like Pathology, Blood–Brain Barrier Disruption, and Synaptic Disorder
by Kamat, Pradip K and Kamat, Pradip K and Kyles, Philip and Kyles, Philip and Kalani, Anuradha and Kalani, Anuradha and Tyagi, Neetu and Tyagi, Neetu
Molecular neurobiology, ISSN 0893-7648, 5/2016, Volume 53, Issue 4, pp. 2451 - 2467
Cerebrovascular pathology | Neurology | Neurosciences | Biomedicine | Blood–brain barrier dysfunction | Alzheimer’s disease | Neurobiology | Homocysteine | Cell Biology | Dementia | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Memory - drug effects | Glial Fibrillary Acidic Protein - genetics | Cadherins - metabolism | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Blood-Brain Barrier - physiopathology | Claudin-5 - metabolism | Microvessels - pathology | Male | Synapses - pathology | Glial Fibrillary Acidic Protein - metabolism | RNA, Messenger - metabolism | Antigens, CD - genetics | Alzheimer Disease - pathology | Antigens, CD - metabolism | Matrix Metalloproteinase 9 - metabolism | Cadherins - genetics | Synapses - drug effects | Alzheimer Disease - physiopathology | Hydrogen Sulfide - pharmacology | Cerebrovascular Circulation - drug effects | Matrix Metalloproteinase 2 - metabolism | Mice, Inbred C57BL | RNA, Messenger - genetics | Alzheimer Disease - drug therapy | Microvessels - drug effects | Claudin-5 - genetics | Cystathionine beta-Synthase - metabolism | Permeability | Blood-Brain Barrier - drug effects | Nerve Tissue Proteins - genetics | Blood-Brain Barrier - metabolism | Gene Expression Regulation - drug effects | Nerve Tissue Proteins - metabolism | Blood-Brain Barrier - pathology | Hydrogen Sulfide - therapeutic use | Intercellular Adhesion Molecule-1 - metabolism | Animals | Intercellular Adhesion Molecule-1 - genetics | Avoidance Learning - drug effects | Alzheimer Disease - genetics | Dizocilpine Maleate - pharmacology | Hydrogen sulfide | Methyl aspartate | Brain | RNA | Neurons | Intermediate filament proteins | Alzheimer's disease | Index Medicus | cerebrovascular pathology | dementia | blood brain barrier dysfunction
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