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Nature (London), ISSN 1476-4687, 2013, Volume 505, Issue 7483, pp. 361 - 366
Journal Article
Journal Article
by Stefansson, Hreinn and Ophoff, Roel A and Steinberg, Stacy and Andreassen, Ole A and Cichon, Sven and Rujescu, Dan and Werge, Thomas and Pietiläinen, Olli P. H and Mors, Ole and Mortensen, Preben B and Sigurdsson, Engilbert and Gustafsson, Omar and Nyegaard, Mette and Tuulio-Henriksson, Annamari and Ingason, Andres and Hansen, Thomas and Suvisaari, Jaana and Lonnqvist, Jouko and Paunio, Tiina and Børglum, Anders D and Hartmann, Annette and Fink-Jensen, Anders and Nordentoft, Merete and Hougaard, David and Norgaard-Pedersen, Bent and Böttcher, Yvonne and Olesen, Jes and Breuer, René and Möller, Hans-Jürgen and Giegling, Ina and Rasmussen, Henrik B and Timm, Sally and Mattheisen, Manuel and Bitter, István and Réthelyi, János M and Magnusdottir, Brynja B and Sigmundsson, Thordur and Olason, Pall and Masson, Gisli and Gulcher, Jeffrey R and Haraldsson, Magnus and Fossdal, Ragnheidur and Thorgeirsson, Thorgeir E and Thorsteinsdottir, Unnur and Ruggeri, Mirella and Tosato, Sarah and Franke, Barbara and Strengman, Eric and Kiemeney, Lambertus A and Melle, Ingrid and Djurovic, Srdjan and Abramova, Lilia and Kaleda, Vasily and Sanjuan, Julio and de Frutos, Rosa and Bramon, Elvira and Vassos, Evangelos and Fraser, Gillian and Ettinger, Ulrich and Picchioni, Marco and Walker, Nicholas and Toulopoulou, Timi and Need, Anna C and Ge, Dongliang and Lim Yoon, Joeng and Shianna, Kevin V and Freimer, Nelson B and Cantor, Rita M and Murray, Robin and Kong, Augustine and Golimbet, Vera and Carracedo, Angel and Arango, Celso and Costas, Javier and Jönsson, Erik G and Terenius, Lars and Agartz, Ingrid and Petursson, Hannes and Nöthen, Markus M and Rietschel, Marcella and Matthews, Paul M and Muglia, Pierandrea and Peltonen, Leena and St Clair, David and Goldstein, David B and Stefansson, Kari and Collier, David A and Genetic Risk and Outcome in Psychosis (GROUP) and GROUP
Nature (London), ISSN 1476-4687, 2009, Volume 460, Issue 7256, pp. 744 - 747
Journal Article
by Jacquemont, Sébastien and Reymond, Alexandre and Zufferey, Flore and Harewood, Louise and Walters, Robin G and Kutalik, Zoltán and Martinet, Danielle and Shen, Yiping and Valsesia, Armand and Beckmann, Noam D and Thorleifsson, Gudmar and Belfiore, Marco and Bouquillon, Sonia and Campion, Dominique and de Leeuw, Nicole and de Vries, Bert B. A and Esko, Tõnu and Fernandez, Bridget A and Fernández-Aranda, Fernando and Fernández-Real, José Manuel and Gratacòs, Mònica and Guilmatre, Audrey and Hoyer, Juliane and Jarvelin, Marjo-Riitta and Frank Kooy, R and Kurg, Ants and Le Caignec, Cédric and Männik, Katrin and Platt, Orah S and Sanlaville, Damien and Van Haelst, Mieke M and Villatoro Gomez, Sergi and Walha, Faida and Wu, Bai-lin and Yu, Yongguo and Aboura, Azzedine and Addor, Marie-Claude and Alembik, Yves and Antonarakis, Stylianos E and Arveiler, Benoît and Barth, Magalie and Bednarek, Nathalie and Béna, Frédérique and Bergmann, Sven and Beri, Mylène and Bernardini, Laura and Blaumeiser, Bettina and Bonneau, Dominique and Bottani, Armand and Boute, Odile and Brunner, Han G and Cailley, Dorothée and Callier, Patrick and Chiesa, Jean and Chrast, Jacqueline and Coin, Lachlan and Coutton, Charles and Cuisset, Jean-Marie and Cuvellier, Jean-Christophe and David, Albert and de Freminville, Bénédicte and Delobel, Bruno and Delrue, Marie-Ange and Demeer, Bénédicte and Descamps, Dominique and Didelot, Gérard and Dieterich, Klaus and Disciglio, Vittoria and Doco-Fenzy, Martine and Drunat, Séverine and Duban-Bedu, Bénédicte and Dubourg, Christèle and El-Sayed Moustafa, Julia S and Elliott, Paul and Faas, Brigitte H. W and Faivre, Laurence and Faudet, Anne and Fellmann, Florence and Ferrarini, Alessandra and Fisher, Richard and Flori, Elisabeth and Forer, Lukas and Gaillard, Dominique and Gerard, Marion and Gieger, Christian and Gimelli, Stefania and Gimelli, Giorgio and Grabe, Hans J and Guichet, Agnès and Guillin, Olivier and Hartikainen, Anna-Liisa and Heron, Délphine and Hippolyte, Loyse and Holder, Muriel and Homuth, Georg and Isidor, Bertrand and Jaillard, Sylvie and Jaros, Zdenek and Jiménez-Murcia, Susana and Joly Helas, Géraldine and ...
Nature (London), ISSN 1476-4687, 2011, Volume 478, Issue 7367, pp. 97 - 102
.... In contrast to obesity, few genetic variants underlying these clinical conditions have been reported... 
DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article
American journal of medical genetics. Part B, Neuropsychiatric genetics, ISSN 1552-4841, 2018, Volume 177, Issue 1, pp. 21 - 34
This large multi‐center study investigates the relationships between genetic risk for schizophrenia and bipolar disorder, and multi... 
Humans | Family/psychology | Genetic Predisposition to Disease/genetics | Male | schizophrenia | bipolar disorder | Polymorphism, Single Nucleotide/genetics | Psychotic Disorders/genetics | Adult | Female | Event-Related Potentials, P300 | Endophenotypes/blood | Schizophrenia/genetics | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group/genetics | cognition | WHITE-MATTER | EEG | Europe | Risk Factors | UNAFFECTED 1ST-DEGREE RELATIVES | Brain/physiology | Multifactorial Inheritance/genetics | Bipolar Disorder/genetics | Neuropsychological Tests | MAUDSLEY FAMILY | single nucleotide polymorphism (SNP) | EVENT-RELATED POTENTIALS | PSYCHIATRIC-DISORDERS | GENETIC OVERLAP | EDINBURGH HIGH-RISK | Cognition/physiology | Australia | WORKING-MEMORY | PSYCHOPHYSIOLOGICAL ENDOPHENOTYPES | WIDE ASSOCIATION ANALYSIS | PSYCHIATRY | 1ST-EPISODE SCHIZOPHRENIA | GENETICS & HEREDITY | INTERMEDIATE PHENOTYPES | Family - psychology | Multifactorial Inheritance - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Bipolar Disorder - genetics | Brain - physiology | Psychotic Disorders - genetics | Schizophrenia - genetics | Cognition - physiology | Polymorphism, Single Nucleotide - genetics | Endophenotypes - blood | Medical research | Usage | Schizophrenia | Medicine, Experimental | Bipolar disorder | Genetic aspects | Risk factors | Statistical analysis | Mental disorders | Cognitive ability | Event-related potentials | Auditory evoked potentials | Genetic diversity | Psychosis | Genetic variance | Genotyping | Auditory discrimination learning | Ventricle | Structure-function relationships
Journal Article
Nature (London), ISSN 1476-4687, 2014, Volume 511, Issue 7510, pp. 421 - 427
Journal Article