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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 | Index Medicus | Abridged Index Medicus | 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
Science Translational Medicine, ISSN 1946-6234, 06/2013, Volume 5, Issue 191, pp. 191 - 191ec107
Journal Article
Science Translational Medicine, ISSN 1946-6234, 04/2013, Volume 5, Issue 179, pp. 179 - 179ec57
Journal Article
Science Translational Medicine, ISSN 1946-6234, 12/2013, Volume 5, Issue 215, pp. 215 - 215ec206
Journal Article
Science Translational Medicine, ISSN 1946-6234, 10/2013, Volume 5, Issue 209, pp. 209 - 209ec180
What can you learn from sequencing seven genes? Flannick et al. have done just this in genes that carry mutations causing maturity-onset diabetes of the young... 
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 | Index Medicus | Biological Sciences | PNAS Plus
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Journal Article
by O'Dushlaine, Colm and Rossin, Lizzy and Lee, Phil H and Duncan, Laramie and Parikshak, Neelroop N and Newhouse, Stephen and Ripke, Stephan and Neale, Benjamin M and Purcell, Shaun M and Posthuma, Danielle and Nurnberger, John I and Lee, S. Hong and Faraone, Stephen V and Perlis, Roy H and Mowry, Bryan J and Thapar, Anita and Goddard, Michael E and Witte, John S and Absher, Devin and Agartz, Ingrid and Akil, Huda and Amin, Farooq and Aneassen, Ole A and Anjorin, Adebayo and Anney, Richard and Anttila, Verneri and Arking, Dan E and Asherson, Philip and Azevedo, Maria H and Backlund, Lena and Badner, Judith A and Bailey, Anthony J and Banaschewski, Tobias and Barchas, Jack D and Barnes, Michael R and Barrett, Thomas B and Bass, Nicholas and Battaglia, Agatino and Bauer, Michael and Bayés, Mònica and Bellivier, Frank and Bergen, Sarah E and Berrettini, Wade and Betancur, Catalina and Bettecken, Thomas and Biederman, Joseph and Binder, Elisabeth B and Black, Donald W and Blackwood, Douglas H. R and Bloss, Cinnamon S and Boehnke, Michael and Boomsma, Dorret I and Breuer, René and Bruggeman, Richard and Cormican, Paul and Buccola, Nancy G and Buitelaar, Jan K and Bunney, William E and Buxbaum, Joseph D and Byerley, William F and Byrne, Enda M and Caesar, Sian and Cahn, Wiepke and Cantor, Rita M and Casas, Miguel and Chakravarti, Aravinda and Chambert, Kimberly and Choudhury, Khalid and Cichon, Sven and Mattheisen, Manuel and Cloninger, C. Robert and Collier, David A and Cook, Edwin H and Coon, Hilary and Cormand, Bru and Corvin, Aiden and Coryell, William H and Craig, David W and Craig, Ian W and Crosbie, Jennifer and Cuccaro, Michael L and Curtis, David and Czamara, Darina and Datta, Susmita and Dawson, Geraldine and Day, Richard and de Geus, Eco J and Degenhardt, Franziska and Djurovic, Srdjan and Donohoe, Gary J and Doyle, Alysa E and Duan, Jubao and Dudbridge, Frank and Duketis, Eftichia and Ebstein, Richard P and Edenberg, Howard J and Elia, Josephine and Ennis, Sean and Etain, Bruno and Fanous, Ayman and ... and Network & Pathway Anal Subgrp Psyc and IIBDGC and Network and Pathway Analysis Subgroup of Psychiatric Genomics Consortium and The Network and Pathway Analysis Subgroup of the Psychiatric Genomics Consortium and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature neuroscience, ISSN 1097-6256, 2015, Volume 18, Issue 2, pp. 199 - 209
Journal Article
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
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