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by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 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) 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
by D’Angelo, Debra and Lebon, Sébastien and Chen, Qixuan and Martin-Brevet, Sandra and Snyder, LeeAnne Green and Hippolyte, Loyse and Hanson, Ellen and Maillard, Anne M and Faucett, W. Andrew and Macé, Aurélien and Pain, Aurélie and Bernier, Raphael and Chawner, Samuel J. R. A and David, Albert and Andrieux, Joris and Aylward, Elizabeth and Baujat, Genevieve and Caldeira, Ines and Conus, Philippe and Ferrari, Carrina and Forzano, Francesca and Gérard, Marion and Goin-Kochel, Robin P and Grant, Ellen and Hunter, Jill V and Isidor, Bertrand and Jacquette, Aurélia and Jønch, Aia E and Keren, Boris and Lacombe, Didier and Le Caignec, Cédric and Martin, Christa Lese and Männik, Katrin and Metspalu, Andres and Mignot, Cyril and Mukherjee, Pratik and Owen, Michael J and Passeggeri, Marzia and Rooryck-Thambo, Caroline and Rosenfeld, Jill A and Spence, Sarah J and Steinman, Kyle J and Tjernagel, Jennifer and Van Haelst, Mieke and Shen, Yiping and Draganski, Bogdan and Sherr, Elliott H and Ledbetter, David H and van den Bree, Marianne B. M and Beckmann, Jacques S and Spiro, John E and Reymond, Alexandre and Jacquemont, Sébastien and Chung, Wendy K and Cardiff Univ Experiences Children and Simons Variation Individuals Proje and 16p112 European Consortium and Simons Variation in Individuals Project (VIP) Consortium and 16p11.2 European Consortium and Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study and for the Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, the 16p11.2 European Consortium, and the Simons Variation in Individuals Project (VIP) Consortium
JAMA Psychiatry, ISSN 2168-622X, 01/2016, Volume 73, Issue 1, pp. 20 - 30
IMPORTANCE: The 16p11.2 BP4-BP5 duplication is the copy number variant most frequently associated with autism spectrum disorder (ASD), schizophrenia, and... 
DE-NOVO | INFANTILE SPASMS | AUTISM | PSYCHIATRY | COPY NUMBER VARIATIONS | SCHIZOPHRENIA | DISORDERS | PHENOTYPES | SPECTRUM | ASSOCIATION | DELETION | Chromosome Disorders - epidemiology | Microcephaly - genetics | Chromosome Duplication | Humans | Middle Aged | Child, Preschool | Male | Cognition | Developmental Disabilities - genetics | Cerebellum - abnormalities | Schizophrenic Psychology | Microcephaly - epidemiology | Case-Control Studies | Chromosome Disorders - psychology | DNA Copy Number Variations | Epilepsy - epidemiology | Intellectual Disability - genetics | Young Adult | Schizophrenia - genetics | Autism Spectrum Disorder - epidemiology | Adult | Epilepsy - genetics | Female | Nervous System Malformations - genetics | Child | Chromosomes, Human, Pair 16 - genetics | Intellectual Disability - epidemiology | Autistic Disorder - genetics | Chromosome Deletion | Autism Spectrum Disorder - genetics | Comorbidity | Autism Spectrum Disorder - psychology | Autistic Disorder - epidemiology | Schizophrenia - epidemiology | Autistic Disorder - psychology | Nervous System Malformations - epidemiology | Developmental Disabilities - epidemiology | Adolescent | Intellectual Disability - psychology | Chromosome Disorders - genetics | Cohort Studies | Body mass index | Genetic aspects | Analysis | Risk factors | Pervasive developmental disorders
Journal Article
Clinical Genetics, ISSN 0009-9163, 09/2012, Volume 82, Issue 3, pp. 248 - 255
Journal Article
by Walters, R.G and Jacquemont, S and Valsesia, A and De Smith, A.J and Martinet, D and Andersson, J and Falchi, M and Chen, F and Andrieux, J and Lobbens, S and Delobel, B and Stutzmann, F and El-Sayed Moustafa, J.S and Chèvre, J.-C and Lecoeur, C and Vatin, V and Bouquillon, S and Buxton, J.L and Boute, O and Holder-Espinasse, M and Cuisset, J.-M and Lemaitre, M.-P and Ambresin, A.-E and Brioschi, A and Gaillard, M and Giusti, V and Fellmann, F and Ferrarini, A and Hadjikhani, N and Campion, D and Guilmatre, A and Goldenberg, A and Calmels, N and Mandel, J.-L and Le Caignec, C and David, A and Isidor, B and Cordier, M.-P and Dupuis-Girod, S and Labalme, A and Sanlaville, D and Béri-Dexheimer, M and Jonveaux, P and Leheup, B and Õunap, K and Bochukova, E.G and Henning, E and Keogh, J and Ellis, R.J and MacDermot, K.D and Van Haelst, M.M and Vincent-Delorme, C and Plessis, G and Touraine, R and Philippe, A and Malan, V and Mathieu-Dramard, M and Chiesa, J and Blaumeiser, B and Kooy, R.F and Caiazzo, R and Pigeyre, M and Balkau, B and Sladek, R and Bergmann, S and Mooser, V and Waterworth, D and Reymond, A and Vollenweider, P and Waeber, G and Kurg, A and Palta, P and Esko, T and Metspalu, A and Nelis, M and Elliott, P and Hartikainen, A.-L and McCarthy, M.I and Peltonen, L and Carlsson, L and Jacobson, P and Sjöström, L and Huang, N and Hurles, M.E and O'Rahilly, S and Farooqi, I.S and Männik, K and Jarvelin, M.-R and Pattou, F and Meyre, D and Walley, A.J and Coin, L.J.M and Blakemore, A.I.F and Froguel, P and Beckmann, J.S and Sahlgrenska akademin and Institute of Medicine, Department of Molecular and Clinical Medicine and Institutionen för medicin, avdelningen för molekylär och klinisk medicin and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
Nature, ISSN 0028-0836, 02/2010, Volume 463, Issue 7281, pp. 671 - 675
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2013, Volume 50, Issue 8, pp. 507 - 514
Journal Article
American Journal of Medical Genetics. Part A, ISSN 1552-4825, 2012, Volume 158A, Issue 7, pp. 1633 - 1640
Journal Article
Clinical Genetics, ISSN 0009-9163, 08/2010, Volume 78, Issue 2, pp. 149 - 161
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 06/2010, Volume 47, Issue 6, pp. 377 - 384
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 02/2012, Volume 49, Issue 2, pp. 104 - 109
Journal Article