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1. Full Text From the genetic architecture to synaptic plasticity in autism spectrum disorder
by Bourgeron, Thomas
Nature reviews. Neuroscience, ISSN 1471-003X, 08/2015, Volume 16, Issue 9, pp. 551 - 563
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Child Development Disorders, Pervasive - metabolism | Neuronal Plasticity - genetics | Neuronal Plasticity - physiology | Synapses - metabolism | Child Development Disorders, Pervasive - genetics | Humans | Child Development Disorders, Pervasive - diagnosis | Brain - pathology | Synapses - genetics | Synapses - pathology | Brain - physiology | Neuroplasticity | Gene mutations | Pervasive developmental disorders | Development and progression | Genetic aspects | Disease susceptibility | Identification and classification | Autism | Index Medicus | Life Sciences | Brain | Human health and pathology | Neuronal Plasticity | Genetics | Child Development Disorders, Pervasive | Synapses | Human genetics | Psychiatrics and mental health
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2. Full Text The GABAA Receptor as a Therapeutic Target for Neurodevelopmental Disorders
by Braat, Sien and Kooy, R. Frank
Neuron (Cambridge, Mass.), ISSN 0896-6273, 06/2015, Volume 86, Issue 5, pp. 1119 - 1130
Fragile X Syndrome - genetics | Child Development Disorders, Pervasive - metabolism | Developmental Disabilities - drug therapy | Developmental Disabilities - metabolism | Humans | GABA Modulators - administration & dosage | Nervous System Diseases - drug therapy | Fragile X Syndrome - metabolism | Developmental Disabilities - genetics | Nervous System Diseases - genetics | Child Development Disorders, Pervasive - drug therapy | Fragile X Syndrome - drug therapy | Rett Syndrome - metabolism | Rett Syndrome - drug therapy | Animals | Child Development Disorders, Pervasive - genetics | GABA Modulators - metabolism | Receptors, GABA-A - genetics | Nervous System Diseases - metabolism | Receptors, GABA-A - metabolism | Drug Delivery Systems - trends | Rett Syndrome - genetics | Index Medicus
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3. Full Text Pervasive developmental disorders in children of hyperandrogenic women with polycystic ovary syndrome: a longitudinal case–control study
by Palomba, Stefano and Marotta, Rosa and Di Cello, Annalisa and Russo, Tiziana and Falbo, Angela and Orio, Francesco and Tolino, Achille and Zullo, Fulvio and Esposito, Rosa and Sala, Giovanni Battista La
Clinical endocrinology (Oxford), ISSN 0300-0664, 12/2012, Volume 77, Issue 6, pp. 898 - 904
Life Sciences & Biomedicine | Endocrinology & Metabolism | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Endocrinopathies | General aspects | Medical sciences | Vertebrates: endocrinology | Child Development Disorders, Pervasive - epidemiology | Prenatal Exposure Delayed Effects | Humans | Pregnancy Complications | Risk Factors | Child, Preschool | Child Development Disorders, Pervasive - etiology | Male | Autistic Disorder - epidemiology | Case-Control Studies | Pregnancy | Amniotic Fluid - chemistry | Hyperandrogenism - complications | Polycystic Ovary Syndrome - complications | Testosterone - analysis | Child Development Disorders, Pervasive - diagnosis | Sex Factors | Female | Autistic Disorder - diagnosis | Child | Longitudinal Studies | Women | Testosterone | Medical research | Child development | Pregnant women | Stein-Leventhal syndrome | Analysis | Medicine, Experimental | Children | Health aspects | Polycystic ovary syndrome | Index Medicus
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4. Full Text Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development
by Bernier, Raphael and Golzio, Christelle and Xiong, Bo and Stessman, Holly A and Coe, Bradley P and Penn, Osnat and Witherspoon, Kali and Gerdts, Jennifer and Baker, Carl and Vulto-van Silfhout, Anneke T and Schuurs-Hoeijmakers, Janneke H and Fichera, Marco and Bosco, Paolo and Buono, Serafino and Alberti, Antonino and Failla, Pinella and Peeters, Hilde and Steyaert, Jean and Vissers, Lisenka E.L.M and Francescatto, Ludmila and Mefford, Heather C and Rosenfeld, Jill A and Bakken, Trygve and O’Roak, Brian J and Pawlus, Matthew and Moon, Randall and Shendure, Jay and Amaral, David G and Lein, Ed and Rankin, Julia and Romano, Corrado and de Vries, Bert B.A and Katsanis, Nicholas and Eichler, Evan E
Cell (Cambridge), ISSN 0092-8674, 07/2014, Volume 158, Issue 2, pp. 263 - 276
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Megalencephaly - pathology | Humans | Child, Preschool | Molecular Sequence Data | Child Development Disorders, Pervasive - physiopathology | Male | Macaca mulatta | Brain - growth & development | DNA-Binding Proteins - metabolism | Female | Gastrointestinal Tract - innervation | Child | Child Development Disorders, Pervasive - classification | Amino Acid Sequence | Child Development Disorders, Pervasive - pathology | Zebrafish Proteins - metabolism | Gastrointestinal Tract - physiopathology | Zebrafish | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Transcription Factors - metabolism | Sequence Alignment | Animals | Child Development Disorders, Pervasive - genetics | Adolescent | Brain - pathology | Mutation | Zebrafish Proteins - genetics | Autism | Analysis | Genetic aspects | Medical colleges | Hospitals | Comorbidity | Genomics | Medical genetics | Index Medicus | dysmorphology | zebrafish modeling | enteric neurons | midbrain expansion | macrocephaly | gastrointestinal defect | autism subtypes | forebrain | Autism spectrum disorder
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5. Full Text SHANK proteins: Roles at the synapse and in autism spectrum disorder
by Monteiro, Patricia and Feng, Guoping
Nature reviews. Neuroscience, ISSN 1471-003X, 03/2017, Volume 18, Issue 3, pp. 147 - 157
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Nerve Tissue Proteins - metabolism | Autism Spectrum Disorder - genetics | Child Development Disorders, Pervasive - metabolism | Animals | Synapses - metabolism | Child Development Disorders, Pervasive - genetics | Autism Spectrum Disorder - metabolism | Humans | Neurons - metabolism | Mutation - genetics | Psychological aspects | Cellular proteins | Care and treatment | Pervasive developmental disorders | Neural transmission | Development and progression | Genetic aspects | Gene expression | Health aspects | Autism | Index Medicus
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6. Full Text SHANK1 Deletions in Males with Autism Spectrum Disorder
by Sato, Daisuke and Lionel, Anath C and Leblond, Claire S and Prasad, Aparna and Pinto, Dalila and Walker, Susan and O'Connor, Irene and Russell, Carolyn and Drmic, Irene E and Hamdan, Fadi F and Michaud, Jacques L and Endris, Volker and Roeth, Ralph and Delorme, Richard and Huguet, Guillaume and Leboyer, Marion and Rastam, Maria and Gillberg, Christopher and Lathrop, Mark and Stavropoulos, Dimitri J and Anagnostou, Evdokia and Weksberg, Rosanna and Fombonne, Eric and Zwaigenbaum, Lonnie and Fernandez, Bridget A and Roberts, Wendy and Rappold, Gudrun A and Marshall, Christian R and Bourgeron, Thomas and Szatmari, Peter and Scherer, Stephen W and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
American journal of human genetics, ISSN 0002-9297, 05/2012, Volume 90, Issue 5, pp. 879 - 887
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Psychology. Psychoanalysis. Psychiatry | Infantile autism | Psychopathology. Psychiatry | Medical genetics | Developmental disorders | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Child clinical studies | Sequence Deletion | Europe | Humans | Child, Preschool | Child Development Disorders, Pervasive - physiopathology | Male | Synapses - genetics | Nerve Tissue Proteins - genetics | DNA Copy Number Variations | Intellectual Disability - genetics | Intellectual Disability - physiopathology | Nerve Tissue Proteins - metabolism | Canada | Synapses - metabolism | Child Development Disorders, Pervasive - genetics | Pedigree | Adolescent | Adult | Female | Neurons - metabolism | Mutation | Child | Autism | Gene mutations | Genetic susceptibility | Genetic variation | Causes of | Protein biosynthesis | Genetic aspects | Research | Proteins | Development and progression | Sex discrimination | Molecular genetics | Analysis | Genetics | Neurons | Chromosomes | Index Medicus | Data processing | Models | Nerve Tissue Proteins | Psychiatrics and mental health | Life Sciences | Human health and pathology | Child Development Disorders, Pervasive | Cognitive science | Intellectual Disability | Synapses | Report | Pervasive | Preschool | Child Development Disorders | Metabolism | Physiopathology | Psykiatri | Psychiatry | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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