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1. Full Text Synaptic, transcriptional and chromatin genes disrupted in autism
by De Rubeis, Silvia and He, Xin and Goldberg, Arthur P and Poultney, Christopher S and Samocha, Kaitlin and Cicek, A. Ercument and Kou, Yan and Liu, Li and Fromer, Menachem and Walker, Susan and Singh, Tarjinder and Klei, Lambertus and Kosmicki, Jack and Fu, Shih-Chen and Aleksic, Branko and Biscaldi, Monica and Bolton, Patrick F and Brownfeld, Jessica M and Cai, Jinlu and Campbell, Nicholas G and Carracedo, Angel and Chahrour, Maria H and Chiocchetti, Andreas G and Coon, Hilary and Crawford, Emily L and Crooks, Lucy and Curran, Sarah R and Dawson, Geraldine and Duketis, Eftichia and Fernandez, Bridget A and Gallagher, Louise and Geller, Evan and Guter, Stephen J and Hill, R. Sean and Ionita-Laza, Iuliana and Gonzalez, Patricia Jimenez and Kilpinen, Helena and Klauck, Sabine M and Kolevzon, Alexander and Lee, Irene and Lei, Jing and Lehtimäki, Terho and Lin, Chiao-Feng and Ma'ayan, Avi and Marshall, Christian R and McInnes, Alison L and Neale, Benjamin and Owen, Michael J and Ozaki, Norio and Parellada, Mara and Parr, Jeremy R and Purcell, Shaun and Puura, Kaija and Rajagopalan, Deepthi and Rehnström, Karola and Reichenberg, Abraham and Sabo, Aniko and Sachse, Michael and Sanders, Stephan J and Schafer, Chad and Schulte-Rüther, Martin and Skuse, David and Stevens, Christine and Szatmari, Peter and Tammimies, Kristiina and Valladares, Otto and Voran, Annette and Wang, Li-San and Weiss, Lauren A and Willsey, A. Jeremy and Yu, Timothy W and Yuen, Ryan K. C and Cook, Edwin H and Freitag, Christine M and Gill, Michael and Hultman, Christina M and Lehner, Thomas and Palotie, Aarno and Schellenberg, Gerard D and Sklar, Pamela and State, Matthew W and Sutcliffe, James S and Walsh, Christopher A and Scherer, Stephen W and Zwick, Michael E and Barrett, Jeffrey C and Cutler, David J and Roeder, Kathryn and Devlin, Bernie and Daly, Mark J and Buxbaum, Joseph D and Homozygosity Mapping Collaborative and DDD Study and Autism Sequencing Consortium and UK10K Consortium and The Autism Sequencing Consortium and The DDD Study and Homozygosity Mapping Collaborative for Autism
Nature (London), ISSN 0028-0836, 11/2014, Volume 515, Issue 7526, pp. 209 - 215
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Gene mutations | Analysis | Pervasive developmental disorders | Research | Genetic transcription | Nucleotide sequencing | Health aspects | DNA sequencing | Studies | Autism | Neurosciences | Chromatin | Mutation | Genes | Index Medicus | Medicin och hälsovetenskap
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2. Full Text Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
by Lim, Elaine T and Uddin, Mohammed and De Rubeis, Silvia and Chan, Yingleong and Kamumbu, Anne S and Zhang, Xiaochang and D'Gama, Alissa M and Kim, Sonia N and Hill, Robert Sean and Goldberg, Arthur P and Poultney, Christopher and Minshew, Nancy J and Kushima, Itaru and Aleksic, Branko and Ozaki, Norio and Parellada, Mara and Arango, Celso and Penzol, Maria J and Carracedo, Angel and Kolevzon, Alexander and Hultman, Christina M and Weiss, Lauren A and Fromer, Menachem and Chiocchetti, Andreas G and Freitag, Christine M and Church, George M and Scherer, Stephen W and Buxbaum, Joseph D and Walsh, Christopher A and Autism Sequencing Consortium
Nature neuroscience, ISSN 1097-6256, 09/2017, Volume 20, Issue 9, pp. 1217 - 1224
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Autism Spectrum Disorder - genetics | Genetic Predisposition to Disease - genetics | Humans | Databases, Genetic - trends | Mosaicism | Genetic Variation - genetics | Zygote - physiology | Mutation, Missense - genetics | Development and progression | Genetic aspects | Gene mutations | Health aspects | Pervasive developmental disorders | Autism | Amygdala | Exons | Genes | Genomes | Mutation | Neurodevelopmental disorders | Damage | Gene expression | Disorders | Index Medicus | Genetic Variation | Life Sciences | Genetic Predisposition to Disease | Zygote | Databases, Genetic | Autism Spectrum Disorder | Genetics | Mutation, Missense | Medicin och hälsovetenskap
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3. 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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4. Full Text Recessive gene disruptions in autism spectrum disorder
by Doan, Ryan N and Lim, Elaine T and De Rubeis, Silvia and Betancur, Catalina and Cutler, David J and Chiocchetti, Andreas G and Overman, Lynne M and Soucy, Aubrie and Goetze, Susanne and Freitag, Christine M and Daly, Mark J and Walsh, Christopher A and Buxbaum, Joseph D and Yu, Timothy W and Autism Sequencing Consortium
Nature genetics, ISSN 1061-4036, 07/2019, Volume 51, Issue 7, pp. 1092 - 1098
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Allelic Imbalance | Autism Spectrum Disorder - genetics | Genetic Predisposition to Disease | Genes, Recessive - genetics | Humans | Female | Male | Mutation, Missense | Genome, Human | Case-Control Studies | Cohort Studies | Whole Exome Sequencing | Haplotypes | ETS protein | USH2A protein | Transcription factors | Circuits | Genes | Genomics | Genomes | Gene expression | Gene sequencing | Autism | Missense mutation | Brain research | Mutation | Disruption | Females | Index Medicus | Autism Spectrum Disorder | Genes, Recessive | Life Sciences
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5. Full Text Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD
by Palladino, Viola Stella and Chiocchetti, Andreas G and Frank, Lukas and Haslinger, Denise and McNeill, Rhiannon and Radtke, Franziska and Till, Andreas and Haupt, Simone and Brüstle, Oliver and Günther, Katharina and Edenhofer, Frank and Hoffmann, Per and Reif, Andreas and Kittel-Schneider, Sarah
Journal of clinical medicine, ISSN 2077-0383, 12/2020, Volume 9, Issue 12, p. 4092
ADHD | hiPSC | disease modelling | mitochondria | PARK2
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6. Full Text Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults
by Biere, Silvia and Kranz, Thorsten M and Matura, Silke and Petrova, Kristiyana and Streit, Fabian and Chiocchetti, Andreas G and Grimm, Oliver and Brum, Murielle and Brunkhorst-Kanaan, Natalie and Oertel, Viola and Malyshau, Aliaksandr and Pfennig, Andrea and Bauer, Michael and Schulze, Thomas G and Kittel-Schneider, Sarah and Reif, Andreas
Frontiers in psychiatry, ISSN 1664-0640, 10/2020, Volume 11, pp. 552532 - 552532
Life Sciences & Biomedicine | Psychiatry | Science & Technology | Bipolar disorder | Genetic aspects | Adults | Risk factors | early recognition | genetic phenotypes | ADHD | bipolar disorder | depression | polygenic risk score
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