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1. Full Text The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms
by Waltes, Regina and Chiocchetti, Andreas G and Freitag, Christine M
American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 07/2016, Volume 171, Issue 5, pp. 650 - 675
animal models | genetic association studies | aggression | epigenetics | Genetics & Heredity | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Aggression - physiology | Neuroendocrine Cells | Dopamine | Genetic Association Studies | Serotonin | Humans | Risk Factors | Aggression - psychology | Gene-Environment Interaction | Behavior, Animal | Animals | Epigenesis, Genetic - genetics | Social Behavior | Genome-Wide Association Study - methods | Genetic research | Epigenetic inheritance | Analysis | Index Medicus
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2. Full Text Genetics of autistic disorders: review and clinical implications
by Freitag, Christine M and Freitag, Christine M and Staal, Wouter and Staal, Wouter and Klauck, Sabine M and Klauck, Sabine M and Duketis, Eftichia and Duketis, Eftichia and Waltes, Regina and Waltes, Regina
European child & adolescent psychiatry, ISSN 1018-8827, 3/2010, Volume 19, Issue 3, pp. 169 - 178
Autistic disorder | Linkage | Copy number variation | Medicine & Public Health | Mutation | Psychiatry | Whole genome association | Pediatrics | Social Sciences | Life Sciences & Biomedicine | Psychology | Psychology, Developmental | Science & Technology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Diseases in Twins - genetics | Humans | Chromosome Mapping | Genetic Counseling | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | DNA Mutational Analysis | Genetic Markers - genetics | Adolescent | Child Development Disorders, Pervasive - diagnosis | DNA Copy Number Variations - physiology | Cytogenetic Analysis | Child | Autism | Anopheles | Genetic counseling | Oncology, Experimental | Medical genetics | Psychotherapy | Genetic aspects | Research | Cancer | Index Medicus | Review
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3. Full Text Human RAD50 Deficiency in a Nijmegen Breakage Syndrome-like Disorder
by Waltes, Regina and Kalb, Reinhard and Gatei, Magtouf and Kijas, Amanda W and Stumm, Markus and Sobeck, Alexandra and Wieland, Britta and Varon, Raymonda and Lerenthal, Yaniv and Lavin, Martin F and Schindler, Detlev and Dörk, Thilo
American journal of human genetics, ISSN 0002-9297, 05/2009, Volume 84, Issue 5, pp. 605 - 616
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Nijmegen Breakage Syndrome - pathology | Genetic Predisposition to Disease | Tumor Suppressor Proteins - metabolism | Signal Transduction | Cell Survival | Humans | Radiation Tolerance | Cell Cycle Proteins - metabolism | Cells, Cultured | DNA Repair Enzymes - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Nijmegen Breakage Syndrome - genetics | DNA-Binding Proteins - deficiency | DNA-Binding Proteins - metabolism | DNA Repair Enzymes - metabolism | Germ-Line Mutation | Adult | Female | Heterozygote | DNA Damage | Chromosomal Instability | DNA Repair Enzymes - deficiency | Protein-Serine-Threonine Kinases - metabolism | Medical colleges | Immunoglobulins | Molecular genetics | Nuclear radiation | DNA damage | DNA synthesis | Automated teller machines | Mental illness | Proteins | Genetic disorders | Mutation | Medical disorders | Genes | Deoxyribonucleic acid--DNA | Index Medicus
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4. Full Text Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
by Waltes, Regina and Duketis, Eftichia and Knapp, Michael and Anney, Richard J. L and Huguet, Guillaume and Schlitt, Sabine and Jarczok, Tomasz A and Sachse, Michael and Kämpfer, Laura M and Kleinböck, Tina and Poustka, Fritz and Bölte, Sven and Schmötzer, Gabriele and Voran, Anette and Huy, Ellen and Meyer, Jobst and Bourgeron, Thomas and Klauck, Sabine M and Freitag, Christine M and Chiocchetti, Andreas G
Human genetics, ISSN 0340-6717, 6/2014, Volume 133, Issue 6, pp. 781 - 792
Human Genetics | Gene Function | Molecular Medicine | Biomedicine | Metabolic Diseases | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Child Development Disorders, Pervasive - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 4 - metabolism | Humans | Child, Preschool | Male | Fragile X Mental Retardation Protein - metabolism | Genotyping Techniques | Calcium-Calmodulin-Dependent Protein Kinase Type 4 - genetics | Neuronal Plasticity - genetics | Female | Child | Genetic Predisposition to Disease | Signal Transduction | Child Development Disorders, Pervasive - pathology | Risk Factors | Gene Expression Regulation | European Continental Ancestry Group | Child Development Disorders, Pervasive - genetics | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Alleles | Protein Binding | Fragile X Mental Retardation Protein - genetics | Polymorphism, Single Nucleotide | Adaptor Proteins, Signal Transducing - metabolism | Child Development Disorders, Pervasive - ethnology | Autism | Family | RNA | Genes | Genomics | Risk factors | Index Medicus | Calcium-Calmodulin-Dependent Protein Kinase Type 4 | Psychiatrics and mental health | Fragile X Mental Retardation Protein | Life Sciences | Human health and pathology | Adaptor Proteins, Signal Transducing | Neuronal Plasticity | Child Development Disorders, Pervasive | Cognitive science | Medicin och hälsovetenskap
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5. Full Text Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range
by Waltes, Regina and Gfesser, Johannes and Haslinger, Denise and Schneider-Momm, Katja and Biscaldi, Monica and Voran, Anette and Freitag, Christine M and Chiocchetti, Andreas G
Journal of Neural Transmission, ISSN 0300-9564, 9/2014, Volume 121, Issue 9, pp. 1107 - 1116
Neurology | Common variant | Neurosciences | Repetitive behaviour | Medicine & Public Health | High-functioning autism | Association analysis | Transmission disequilibrium testing | Pharmacology/Toxicology | Psychiatry | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Psychiatric Status Rating Scales | Child Development Disorders, Pervasive - genetics | Humans | Female | Logistic Models | Male | Polymorphism, Single Nucleotide | Genotyping Techniques | Child | Nucleocytoplasmic Transport Proteins - genetics | Cohort Studies | Autism | RNA | Glutamate | Risk factors | Index Medicus
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