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1. Full Text Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
by Weiner, Daniel J and Wigdor, Emilie M and Ripke, Stephan and Walters, Raymond K and Kosmicki, Jack A and Grove, Jakob and Samocha, Kaitlin E and Goldstein, Jacqueline I and Okbay, Aysu and Bybjerg-Grauholm, Jonas and Werge, Thomas and Hougaard, David M and Taylor, Jacob and Skuse, David and Devlin, Bernie and Anney, Richard and Sanders, Stephan J and Bishop, Somer and Mortensen, Preben Bo and Børglum, Anders D and Smith, George Davey and Daly, Mark J and Robinson, Elise B and Bækvad-Hansen, Marie and Dumont, Ashley and Hansen, Christine and Hansen, Thomas F and Howrigan, Daniel and Mattheisen, Manuel and Moran, Jennifer and Mors, Ole and Nordentoft, Merete and Nørgaard-Pedersen, Bent and Poterba, Timothy and Poulsen, Jesper and Stevens, Christine and Anttila, Verneri and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A Jeremy and Wijsman, Ellen M and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Van Engeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne G and Pedersen, Carsten B and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Murtha, Michael T and Mouga, Susana and Morrow, Eric M and DeLuca, Daniel Moreno and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and ... and Psychiat Genomics Consortium and iPSYCH-Broad Autism Grp and iPSYCH-Broad Autism Group and Psychiatric Genomics Consortium Autism Group and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 07/2017, Volume 49, Issue 7, pp. 978 - 985
Autism spectrum disorder (ASD) risk is influenced by common polygenic and de novo variation. We aimed to clarify the influence of polygenic risk for ASD and to... 
DE-NOVO | VARIANTS | GENETIC RISK | GENETICS & HEREDITY | MUTATIONS | SIMONS SIMPLEX COLLECTION | GENOME-WIDE ASSOCIATION | INSIGHTS | Autism Spectrum Disorder - genetics | Sequence Deletion | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Risk Factors | Family Health | Genetics, Behavioral | Male | Educational Status | Intelligence - genetics | Multifactorial Inheritance | Intellectual Disability - genetics | Genetic Variation | Phenotype | Ethnic Groups - genetics | Schizophrenia - genetics | Autism Spectrum Disorder - epidemiology | Adult | Female | Child | Cohort Studies | Family | Genetic aspects | Genetic transformation | Research | Risk factors | Pervasive developmental disorders | Mental disorders | Intellectual disabilities | Disorders | Schizophrenia | Risk | Genomes | Cases (containers) | Subgroups | Educational attainment | Children & youth | Proteins | Studies | Consortia | Autism | Parents & parenting | Etiology | Population | Mutation | Children | Psychiatry | Life Sciences | Neurons and Cognition | Neurologi | disease | biology | insights | variants | Genetics & Heredity | de-novo | Neurology | mutations | general-population | genetic risk | genome-wide association | loci
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2. 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
Aggression is an evolutionary conserved behavior present in most species including humans. Inadequate aggression can lead to long-term detrimental personal and... 
animal models | genetic association studies | aggression | epigenetics | CALLOUS-UNEMOTIONAL TRAITS | PSYCHIATRY | NITRIC-OXIDE SYNTHASE | SEROTONIN-RELATED GENES | NONAGGRESSIVE ANTISOCIAL-BEHAVIOR | PERVASIVE CHILDHOOD AGGRESSION | BORDERLINE PERSONALITY-DISORDER | BETA-HYDROXYLASE ACTIVITY | GENETICS & HEREDITY | INDUCED INTERMALE AGGRESSION | ANDROGEN RECEPTOR GENE | PITUITARY-ADRENAL AXIS | 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
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3. Full Text Genetics of autistic disorders: review and clinical implications
by Freitag, Christine M and Staal, Wouter and Klauck, Sabine M and Duketis, Eftichia and Waltes, Regina
European Child & Adolescent Psychiatry, ISSN 1018-8827, 3/2010, Volume 19, Issue 3, pp. 169 - 178
Twin and family studies in autistic disorders (AD) have elucidated a high heritability of AD. In this literature review, we will present an overview on... 
Autistic disorder | Linkage | Copy number variation | Medicine & Public Health | Mutation | Psychiatry | Whole genome association | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | SPECTRUM DISORDERS | CHINESE HAN POPULATION | REELIN GENE | PERVASIVE DEVELOPMENTAL DISORDERS | CHROMOSOMAL REARRANGEMENTS | SOCIAL-BEHAVIOR | FRAGILE-X-SYNDROME | PEDIATRICS | COPY NUMBER VARIANTS | STRUCTURAL VARIATION | GENOME-WIDE ASSOCIATION | 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 | Review
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4. Full Text Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders
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 1553-7390, 02/2012, 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... 
15Q13.3 MICRODELETIONS | SNP GENOTYPING DATA | DE-NOVO MUTATIONS | MENTAL-RETARDATION | HIDDEN-MARKOV MODEL | SCAFFOLDING PROTEIN SHANK3 | GENETICS & HEREDITY | RECURRENT MICRODELETIONS | PSYCHIATRIC-DISORDERS | POSTSYNAPTIC DENSITY | COPY-NUMBER VARIATION | 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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5. Full Text Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
by Anney, Richard J. L and Ripke, Stephan and Anttila, Verneri and Grove, Jakob and Holmans, Peter and Huang, Hailiang and Klei, Lambertus and Lee, Phil H and Medland, Sarah E and Neale, Benjamin and Robinson, Elise and Weiss, Lauren A and Zwaigenbaum, Lonnie and Yu, Timothy W and Wittemeyer, Kerstin and Willsey, A.Jeremy and Wijsman, Ellen M and Werge, Thomas and Wassink, Thomas H and Waltes, Regina and Walsh, Christopher A and Wallace, Simon and Vorstman, Jacob A. S and Vieland, Veronica J and Vicente, Astrid M and Vanengeland, Herman and Tsang, Kathryn and Thompson, Ann P and Szatmari, Peter and Svantesson, Oscar and Steinberg, Stacy and Stefansson, Kari and Stefansson, Hreinn and State, Matthew W and Soorya, Latha and Silagadze, Teimuraz and Scherer, Stephen W and Schellenberg, Gerard D and Sandin, Sven and Sanders, Stephan J and Saemundsen, Evald and Rouleau, Guy A and Rogé, Bernadette and Roeder, Kathryn and Roberts, Wendy and Reichert, Jennifer and Reichenberg, Abraham and Rehnström, Karola and Regan, Regina and Poustka, Fritz and Poultney, Christopher S and Piven, Joseph and Pinto, Dalila and Pericak-Vance, Margaret A and Pejovic-Milovancevic, Milica and Pedersen, Marianne Giørtz and Pedersen, Carsten Bøcker and Paterson, Andrew D and Parr, Jeremy R and Pagnamenta, Alistair T and Oliveira, Guiomar and Nurnberger, John I and Nordentoft, Merete and Murtha, Michael T and Mouga, Susana and Mortensen, Preben Bo and Mors, Ole and Morrow, Eric M and Moreno-De-Luca, Daniel and Monaco, Anthony P and Minshew, Nancy and Merikangas, Alison and McMahon, William M and McGrew, Susan G and Mattheisen, Manuel and Martsenkovsky, Igor and Martin, Donna M and Mane, Shrikant M and Magnusson, Pall and Magalhaes, Tiago and Maestrini, Elena and Lowe, Jennifer K and Lord, Catherine and Levitt, Pat and Martin, Christa Lese and Ledbetter, David H and Leboyer, Marion and Lecouteur, Ann S and Ladd-Acosta, Christine and Kolevzon, Alexander and Klauck, Sabine M and Jacob, Suma and Iliadou, Bozenna and Hultman, Christina M and Hougaard, David M and Hertz-Picciotto, Irva and Hendren, Robert and Hansen, Christine Søholm and Haines, Jonathan L and Guter, Stephen J and ... and Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Molecular Autism, ISSN 2040-2392, 05/2017, Volume 8, Issue 1, pp. 21 - 17
Background: Over the past decade genome-wide association studies (GWAS) have been applied to aid in the understanding of the biology of traits. The success of... 
Gene-set analysis | Genome-wide association study | Genetic correlation | Neurodevelopment | Schizophrenia | Heritability | Autism spectrum disorder | Meta-analysis | MENTAL-RETARDATION | NEUROSCIENCES | FOXP1 | INTELLECTUAL DISABILITY | RISK LOCI | GENETICS & HEREDITY | COMMON | SCAN | COPY NUMBER VARIATION | LINKAGE | GENOME-WIDE ASSOCIATION | REVEALS | Autism Spectrum Disorder - genetics | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Plasma Membrane Calcium-Transporting ATPases - genetics | Membrane Proteins - genetics | Humans | Repressor Proteins - genetics | Male | Genetic Loci | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Carrier Proteins - genetics | Schizophrenia - genetics | Schizophrenia - diagnosis | Schizophrenia - physiopathology | Female | Autism Spectrum Disorder - diagnosis | Autism Spectrum Disorder - physiopathology | Genetic aspects | Research | Genetic susceptibility | Risk factors | Pervasive developmental disorders | Autism | Genomes | Gene expression | Life Sciences | Genetics | Autism spectrum disorder, Genome-wide association study, Meta-analysis, Genetic correlation, Heritability, Gene-set analysis, Schizophrenia, Neurodevelopment | genetic | Neurologi | asperger-syndrome | resource exchange | Genetics & Heredity | Neurosciences & Neurology | pervasive developmental disorders | Neurology | copy number variation | neuronal migration | risk loci | de-novo mutations | genome-wide association | mental-retardation | intellectual disability
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