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by Leblond, Claire S and Heinrich, Jutta and Delorme, Richard and Proepper, Christian and Betancur, Catalina and Huguet, Guillaume and Konyukh, Marina and Chaste, Pauline and Ey, Elodie and Rastam, Maria and Anckarsäter, Henrik and Nygren, Gudrun and Gillberg, I. Carina and Melke, Jonas and Toro, Roberto and Regnault, Beatrice and Fauchereau, Fabien and Mercati, Oriane and Lemière, Nathalie and Skuse, David and Poot, Martin and Holt, Richard and Monaco, Anthony P and Järvelä, Irma and Kantojärvi, Katri and Vanhala, Raija and Curran, Sarah and Collier, David A and Bolton, Patrick and Chiocchetti, Andreas and Klauck, Sabine M and Poustka, Fritz and Freitag, Christine M and Waltes, Regina and Kopp, Marnie and Duketis, Eftichia and Bacchelli, Elena and Minopoli, Fiorella and Ruta, Liliana and Battaglia, Agatino and Mazzone, Luigi and Maestrini, Elena and Sequeira, Ana F and Oliveira, Barbara and Vicente, Astrid and Oliveira, Guiomar and Pinto, Dalila and Scherer, Stephen W and Zelenika, Diana and Delepine, Marc and Lathrop, Mark and Bonneau, Dominique and Guinchat, Vincent and Devillard, Françoise and Assouline, Brigitte and Mouren, Marie-Christine and Leboyer, Marion and Gillberg, Christopher and Boeckers, Tobias M and Bourgeron, Thomas and Gillberg Neuropsychiatry Centre and Göteborgs universitet and Gothenburg University and Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi and Gillbergcentrum and Sahlgrenska Academy and Sahlgrenska akademin and Institute of Neuroscience and Physiology, Department of Pharmacology
PLoS genetics, ISSN 1553-7404, 2012, Volume 8, Issue 2, p. e1002521
Autism spectrum disorders (ASD) are a heterogeneous group of neurodevelopmental disorders with a complex inheritance pattern. While many rare variants in... 
SYNAPTIC PROTEINS | RARE DE-NOVO | MENTAL-RETARDATION | HIDDEN-MARKOV MODEL | SCAFFOLDING PROTEIN SHANK3 | GENETICS & HEREDITY | RECURRENT MICRODELETIONS | 15Q13.3 | POSTSYNAPTIC DENSITY | COPY-NUMBER VARIATION | CRITICAL REGION | Humans | Child, Preschool | Male | Neurons - cytology | Synapses - genetics | Synapses - pathology | Tissue Distribution | Protein Isoforms - metabolism | Adult | Female | Child | Cell Line | Gene Dosage - genetics | Receptors, Nicotinic - metabolism | RNA Splice Sites - genetics | Alternative Splicing - genetics | Gene Expression Regulation | Nerve Tissue Proteins - genetics | Child Development Disorders, Pervasive - genetics | Adaptor Proteins, Signal Transducing - genetics | Adaptor Proteins, Signal Transducing - metabolism | Receptors, Nicotinic - genetics | Protein Isoforms - genetics | Sequence Deletion - genetics | alpha7 Nicotinic Acetylcholine Receptor | Autism | Gene mutations | Physiological aspects | Genetic aspects | Research | Risk factors | Prevalence studies (Epidemiology) | Medical research | Genetics | Mutation | Genes | Sequence Deletion | RNA Splice Sites | Receptors, Nicotinic | Alternative Splicing | Neurons | Nerve Tissue Proteins | Gene Dosage | Life Sciences | Adaptor Proteins, Signal Transducing | Protein Isoforms | Child Development Disorders, Pervasive | Synapses | Pervasive | Cytology | Child Development Disorders | Receptors | Psykiatri | Preschool | Metabolism | Adaptor Proteins | Nicotinic | Pathology | Signal Transducing | Psychiatry
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Medicine & Science in Sports & Exercise, ISSN 0195-9131, 05/2019, Volume 51, Issue 5, pp. 920 - 929
INTRODUCTIONThis 24-month study aimed to determine whether exercise intervention added to weight loss treatment at 6 months is effective for weight loss and... 
SPORT SCIENCES | RISK | INSULIN SENSITIVITY | WEIGHT MAINTENANCE | OBESITY | LIFE-STYLE | REDUCTION | OVERWEIGHT | RESISTANCE | PHYSICAL-ACTIVITY | GLUCOSE METABOLISM | HEART-RATE | OBESE INDIVIDUALS | PHYSICAL ACTIVITY | GLUCOSE-TOLERANCE | Exercise | Health aspects | Weight loss maintenance | Reducing diets | Methods | Weight loss
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Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 01/2015, Volume 57, Issue 1, pp. 75 - 80
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2002, Volume 71, Issue 4, pp. 777 - 790
Journal Article
Developmental medicine and child neurology, ISSN 0012-1622, 9/2001, Volume 43, Issue 9, pp. 614 - 616
Autism is a behaviourally defined syndrome characterized by disturbances of social interaction and communication and restrictions of behaviour patterns and... 
Original Articles | SYSTEM | STAGE | INFANTILE-AUTISM | SIZE | CNS | PEDIATRICS | SERUM | BRAIN | CLINICAL NEUROLOGY | Predictive Value of Tests | Insulin-Like Growth Factor I - cerebrospinal fluid | Autistic Disorder - cerebrospinal fluid | Humans | Child, Preschool | Infant | Male | Reference Values | Autistic Disorder - etiology | Radioimmunoassay | Female | Autistic Disorder - diagnosis | Child
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 8/2016, Volume 46, Issue 8, pp. 2780 - 2784
... Timonen-Soivio 1,2 • Raija Vanhala 2 • Heli Malm 1,3 • Susanna Hinkka-Yli-Saloma ¨ ki 1 • Mika Gissler 1,5 • Alan Brown 4,6 • Andre Sourander 1,4 Published online: 21... 
Pediatrics | Child and School Psychology | Neurosciences | Public Health | Single gene disorders | Syndromic autism | Psychology | Chromosomal abnormalities | Autism spectrum disorder | POPULATION | SPECTRUM DISORDER | PSYCHOLOGY, DEVELOPMENTAL | BOYS | GENETIC-DISORDERS | ASSOCIATION | Autism | Gender Differences | Correlation | Comparative Analysis | Congenital Impairments | Comorbidity | Pervasive Developmental Disorders | Finland | Foreign Countries | Children | Symptoms (Individual Disorders) | Prevalence | Humans | Child, Preschool | Male | Autistic Disorder - epidemiology | Autistic Disorder - psychology | Case-Control Studies | Nervous System Malformations - epidemiology | Syndrome | Nervous System Malformations - diagnosis | Adult | Female | Registries | Autistic Disorder - diagnosis | Child | Finland - epidemiology | Nervous System Malformations - psychology | Cohort Studies | Autistic children | Medical examination | Hospital discharged | Congenital defects | Intellectual disabilities | Alcohol | Systematic review | Clinical evaluation | Birth place | Population | Public health | Genetic disorders | Congenital diseases | Statistical analysis | Sotos syndrome | Autistic spectrum disorders | Residence | Associations | Children & youth | Studies | Neurology | Hospitals | Surveillance | Neurofibromatosis | Men | Rehabilitation | Childbirth | Developmental disabilities | Child & adolescent psychiatry | Index Medicus
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 07/2009, Volume 150B, Issue 5, pp. 741 - 746
Journal Article