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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
Journal of Medical Genetics, ISSN 0022-2593, 10/2012, Volume 49, Issue 10, pp. 660 - 668
Journal Article
by Martin-Brevet, Sandra and Rodríguez-Herreros, Borja and Nielsen, Jared A and Moreau, Clara and Modenato, Claudia and Maillard, Anne M and Pain, Aurélie and Richetin, Sonia and Jønch, Aia E and Qureshi, Abid Y and Zürcher, Nicole R and Conus, Philippe and Addor, Marie-Claude and Andrieux, Joris and Arveiler, Benoît and Baujat, Geneviève and Sloan-Béna, Frédérique and Belfiore, Marco and Bonneau, Dominique and Bouquillon, Sonia and Boute, Odile and Brusco, Alfredo and Busa, Tiffany and Caberg, Jean-Hubert and Campion, Dominique and Colombert, Vanessa and Cordier, Marie-Pierre and David, Albert and Debray, François-Guillaume and Delrue, Marie-Ange and Doco-Fenzy, Martine and Dunkhase-Heinl, Ulrike and Edery, Patrick and Fagerberg, Christina and Faivre, Laurence and Forzano, Francesca and Genevieve, David and Gérard, Marion and Giachino, Daniela and Guichet, Agnès and Guillin, Olivier and Héron, Delphine and Isidor, Bertrand and Jacquette, Aurélia and Jaillard, Sylvie and Journel, Hubert and Keren, Boris and Lacombe, Didier and Lebon, Sébastien and Le Caignec, Cédric and Lemaître, Marie-Pierre and Lespinasse, James and Mathieu-Dramart, Michèle and Mercier, Sandra and Mignot, Cyril and Missirian, Chantal and Petit, Florence and Pilekær Sørensen, Kristina and Pinson, Lucile and Plessis, Ghislaine and Prieur, Fabienne and Rooryck-Thambo, Caroline and Rossi, Massimiliano and Sanlaville, Damien and Schlott Kristiansen, Britta and Schluth-Bolard, Caroline and Till, Marianne and Van Haelst, Mieke and Van Maldergem, Lionel and Alupay, Hanalore and Aaronson, Benjamin and Ackerman, Sean and Ankenman, Katy and Anwar, Ayesha and Atwell, Constance and Bowe, Alexandra and Beaudet, Arthur L and Benedetti, Marta and Berg, Jessica and Berman, Jeffrey and Berry, Leandra N and Bibb, Audrey L and Blaskey, Lisa and Brennan, Jonathan and Brewton, Christie M and Buckner, Randy and Buckner, Randy L and Bukshpun, Polina and Burko, Jordan and Cali, Phil and Cerban, Bettina and Chang, Yishin and Cheong, Maxwell and Chow, Vivian and Chu, Zili and Chudnovskaya, Darina and Cornew, Lauren and Dale, Corby and Dell, John and Dempsey, Allison G and ... and 16p11 2 European Consorti and Simons Variation Individuals and Simons Variation in Individuals Project (VIP) Consortium and 16p11.2 European Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Biological Psychiatry, ISSN 0006-3223, 08/2018, Volume 84, Issue 4, pp. 253 - 264
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 08/2015, Volume 23, Issue 8, pp. 1010 - 1018
Journal Article
Archives of Disease in Childhood - Fetal and Neonatal Edition, ISSN 1359-2998, 10/2019, p. fetalneonatal-2019-317121
ObjectiveAlveolar capillary dysplasia (ACD) is one of the causes of pulmonary hypertension. Its diagnosis is histological but new pathogenetic data have... 
Journal Article
Cardiology in the Young, ISSN 1047-9511, 04/2015, Volume 25, Issue 4, pp. 712 - 717
Journal Article
by Cárdenas-de-la-Parra, Alonso and Martin-Brevet, Sandra and Moreau, Clara and Rodriguez-Herreros, Borja and Fonov, Vladimir S and Maillard, Anne M and Zürcher, Nicole R and Marie-Claude, Addor and Joris, Andrieux and Benoît, Arveiler and Geneviève, Baujat and Frédérique, Sloan-Béna and Marco, Belfiore and Dominique, Campion and Dominique, Bonneau and Sonia, Bouquillon and Odile, Boute and Alfredo, Brusco and Tiffany, Busa and Jean-Hubert, Caberg and Vanessa, Colombert and Marie-Pierre, Cordier and Marie-Pierre, Lemaître and Albert, David and François-Guillaume, Debray and Marie-Ange, Delrue and Martine, Doco-Fenzy and Ulrike, Dunkhase-Heinl and Patrick, Edery and Christina, Fagerberg and Laurence, Faivre and Francesca, Forzano and David, Genevieve and Marion, Gérard and Daniela, Giachino and Agnès, Guichet and Olivier, Guillin and Delphine, Héron and Bertrand, Isidor and Aurélia, Jacquette and Sylvie, Jaillard and Hubert, Journel and Boris, Keren and Didier, Lacombe and Sébastien, Lebon and Cédric, Le Caignec and James, Lespinasse and Michèle, Mathieu-Dramart and Sandra, Mercier and Cyril, Mignot and Chantal, Missirian and Florence, Petit and Kristina, Pilekær Sørensen and Lucile, Pinson and Ghislaine, Plessis and Fabienne, Prieur and Caroline, Schluth-Bolard and Caroline, Rooryck-Thambo and Massimiliano, Rossi and Damien, Sanlaville and Britta, Schlott Kristiansen and Marianne, Till and Mieke, Van Haelst and Lionel, Van Maldergem and Hadjikhani, Nouchine and Beckmann, Jacques S and Reymond, Alexandre and Draganski, Bogdan and Jacquemont, Sébastien and Collins, D. Louis and 16p11.2 European Consortium
NeuroImage, ISSN 1053-8119, 12/2019, Volume 203, p. 116155
Most of human genome is present in two copies (maternal and paternal). However, segments of the genome can be deleted or duplicated, and many of these genomic... 
Genetics | 16p11.2 Copy number variants | Neurodevelopmental disorders | Imaging | Normative growth trajectories | Brain development | Neuroimaging | Adolescence | Pediatrics | Medical research | Brain architecture | Mental disorders | Copy number | Genomes | Grants | Anatomy | Substantia alba | Datasets | Consortia | Brain research | Child development | Clonal deletion | Quality control | Population | Children | Morphometry | Age
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 11/2014, Volume 23, Issue 22, pp. 6069 - 6080
Journal Article