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Science Translational Medicine, ISSN 1946-6234, 01/2014, Volume 6, Issue 221, pp. 221 - ec22
Journal Article
Science Translational Medicine, ISSN 1946-6234, 10/2013, Volume 5, Issue 209
Journal Article
Science Translational Medicine, ISSN 1946-6234, 08/2013, Volume 5, Issue 197
Journal Article
Science Translational Medicine, ISSN 1946-6234, 09/2013, Volume 5, Issue 203
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2004, Volume 75, Issue 3, pp. 353 - 362
Journal Article
Current Opinion in Neurobiology, ISSN 0959-4388, 2014, Volume 30, Issue 1, pp. 131 - 138
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 2016, Volume 17, Issue 6, pp. 353 - 364
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2017, Volume 100, Issue 4, pp. 635 - 649
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2015, Volume 47, Issue 11, pp. 1236 - 1241
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1371 - 1379
Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present... 
Internal Medicine | POPULATION | DEPRESSION | MEDICINE, GENERAL & INTERNAL | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | METAANALYSIS | GENE-EXPRESSION | SCHIZOPHRENIA | CACNA1C | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | Child Development Disorders, Pervasive - epidemiology | Genome-Wide Association Study | Humans | Genetic Loci - genetics | Logistic Models | Bipolar Disorder - genetics | Depressive Disorder, Major - epidemiology | Schizophrenia - epidemiology | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Depressive Disorder, Major - genetics | Age of Onset | Polymorphism, Single Nucleotide - genetics | Adult | Child | Bipolar Disorder - epidemiology | Attention Deficit Disorder with Hyperactivity - epidemiology | Physiological aspects | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Medical research | Calcium channels | Genes | Depression, Mental | Genomics | Schizophrenia | Bipolar disorder | Child psychopathology | Quantitative genetics | Autism | Medicine, Experimental | Genetic research | Single nucleotide polymorphisms | Studies | Genetics | Children & youth | Attention deficit disorder | Enrichment | Brain | Calcium | Disease | Mental disorders | Hyperactivity | Mental health | Disorders | Genomes | Single-nucleotide polymorphism | Mental depression | Consortia | Datasets | Calcium signalling | Genetic effects | Signal transduction | Regression models | Autopsy | Classification | Psychopathology | Children | Chromosomes | Genotypes | Phenotypes | Channel gating | Attention deficit hyperactivity disorder | Calcium channels (voltage-gated) | Behavior disorders | Regression analysis | Risk analysis | Loci | Quantitative trait loci | Government grants | Calcium channels (L-type) | Diagnostic systems | Polygenic inheritance | Psychiatry | Polymorphism | Neurosciences | Calcium Channels | Pervasive | Attention Deficit Disorder with Hyperactivity | L-Type | Child Development Disorders | Depressive Disorder | Genetic Loci | Single Nucleotide | epidemiology | genetics | Bipolar Disorder | Major | Neurovetenskaper
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 01/2014, Volume 111, Issue 4, pp. E455 - E464
Genetic studies have revealed thousands of loci predisposing to hundreds of human diseases and traits, revealing important biological pathways and defining... 
POPULATION | CONTRIBUTE | ALLELES | mapping disease genes | LOW-FREQUENCY | MULTIDISCIPLINARY SCIENCES | statistical genetics | LOCI | power analysis | GENES | SEQUENCE | MUTATIONS | SPECTRUM | SELECTION | Genetic Variation | Genetic Predisposition to Disease | Genome-Wide Association Study | Mutation | Gene Frequency | Humans | Genetics | Hypotheses | Genes | Analysis | Biological Sciences | PNAS Plus
Journal Article
Nature genetics, ISSN 1061-4036, 4/2019, Volume 51, Issue 4, pp. 584 - 591
Polygenic risk scores (PRS) are poised to improve biomedical outcomes via precision medicine. However, the major ethical and scientific challenge surrounding... 
population genetics | diversity | health disparities | statistical genetics | genetic risk prediction | polygenic risk scores
Journal Article
Journal Article