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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, 08/2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | 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 | Index Medicus | 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
Nature genetics, ISSN 1546-1718, 02/2017, Volume 49, Issue 4, pp. 515 - 526
Gene-disruptive mutations contribute to the biology of neurodevelopmental disorders (NDDs), but most of the related pathogenic genes are not known. We... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Autistic Disorder - genetics | Phenotype | Humans | Female | Male | Developmental Disabilities - genetics | Mutation - genetics | Intellectual Disability - genetics | Consortia | Autism | Councils | Intellectual disabilities | Genes | Mutation | Siblings | Index Medicus
Journal Article
The New England journal of medicine, ISSN 1533-4406, 03/2018, Volume 378, Issue 13, pp. 1189 - 1199
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2009, Volume 46, Issue 9, pp. 577 - 584
Journal Article
06/2015
..., falls die extrapolierte Rotationsenergie unter dem vorbestimmten Schwellenwert liegt. A method for controlling an internal combustion engine having a crankshaft... 
MECHANICAL ENGINEERING | WEAPONS | BLASTING | COMBUSTION ENGINES | HEATING | CONTROLLING COMBUSTION ENGINES | LIGHTING | HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
Patent
Human molecular genetics, ISSN 0964-6906, 10/2007, Volume 16, Issue 2, pp. R150 - R158
A relationship between fragile sites, specific genomic regions visible as gaps or breaks on cultivated chromosomes, and human disease has been proposed many... 
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Fragile X Syndrome - genetics | Base Sequence | Humans | Chromosome Fragile Sites | DNA Replication | Female | Male | Genome, Human | Chromosome Disorders - genetics | Trinucleotide Repeat Expansion | Evolution, Molecular | Index Medicus
Journal Article