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Journal of Medical Genetics, ISSN 0022-2593, 11/2014, Volume 51, Issue 11, pp. 724 - 736
Journal Article
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 Article
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2013, Volume 21, Issue 6, pp. 602 - 612
The 2q37 locus is one of the most commonly deleted subtelomeric regions. Such a deletion has been identified in 4100 patients by telomeric fluorescence in situ... 
brachydactyly | AHO-like syndrome | overweight | 2q37-deletion syndrome | intellectual disability | genotype-phenotype correlation | OSTEODYSTROPHY-LIKE PHENOTYPE | MOLECULAR CHARACTERIZATION | AUTISM | PROLACTIN-RELEASING PEPTIDE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CANDIDATE REGION | 2Q37.3 DELETION | GENE | MENTAL-RETARDATION SYNDROME | ARRAY-CGH | GENETICS & HEREDITY | DUPLICATION | Overweight - complications | Humans | Child, Preschool | Intellectual Disability - complications | Male | Intellectual Disability - genetics | Fibrous Dysplasia, Polyostotic - genetics | Young Adult | Chromosomes, Human, Pair 2 - genetics | Adult | Female | Behavior | Fibrous Dysplasia, Polyostotic - complications | Child | Chromosome Deletion | Genetic Association Studies | Chromosome Disorders - complications | Overweight - genetics | Chromosome Mapping | DNA Copy Number Variations - genetics | Comparative Genomic Hybridization | Brachydactyly - genetics | Adolescent | Brachydactyly - complications | Chromosome Disorders - genetics | Intellectual disabilities | Body weight | Hybridization | Gene deletion | French language | Literature reviews | Genotype & phenotype | Databases | Language | Clonal deletion | Cell cycle | Fluorescence in situ hybridization | Genetics | Period 2 protein | Brachydactyly | Genotypes | Seizures | Obesity | Phenotypes | Calpain | Gene expression | Chromosome 2 | Autism | Osteodystrophy | Collaboration | Life Sciences | genotype–phenotype correlation
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