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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Authors :
Stephen W. Scherer
Mònica Gratacòs
Kari Stefansson
Muriel Holder
Unnur Thorsteinsdottir
Lukas Forer
Katharina M. Roetzer
Josette Lucas
Claudia Schurmann
Satu Kaksonen
Armand Valsesia
Carina Wallgren-Pettersson
Barbara Leube
Alexandra I. F. Blakemore
Alexandre Moerman
Marco Belfiore
Anne Faudet
Dominique Gaillard
Roberto Ravazzolo
Dominique Bonneau
Marjo-Riitta Järvelin
Yongguo Yu
Louis Vallée
Bénédicte Demeer
Sophie Visvikis-Siest
Frédérique Béna
Brigitte H. W. Faas
Benoit Arveiler
Georg Homuth
Charles Coutton
Bénédicte de Fréminville
Giorgio Gimelli
Xavier Estivill
Richard I. Fisher
Stefania Gimelli
Wendy Roberts
Jacques S. Beckmann
Emilie Landais
Orah S. Platt
Robin G. Walters
Gudmar Thorleifsson
Alexandre Reymond
Anna-Liisa Hartikainen
Solenn Legallic
James F. Gusella
Peter Vollenweider
Gian Paolo Ramelli
Tõnu Esko
Boris Keren
Nine V A M Knoers
Fanny Morice-Picard
Dominique Campion
Odile Boute
Evica Rajcan-Separovic
Rolph Pfundt
Nathalie Bednarek
Martine Doco-Fenzy
Suzanne M E Lewis
Gérard Didelot
Mylène Beri
Engilbert Sigurdsson
Véronique Satre
Audrey Labalme
Carola Tengstrom
Florian Kronenberg
Florence Petit
Simon Zwolinksi
Philippe Froguel
Paul Elliott
Dorothée Cailley
Christian R. Marshall
Bruno Leheup
Klaus Dieterich
Janina S. Ried
Sylvie Jaillard
Armand Bottani
Stylianos E. Antonarakis
Elisabetta Lapi
Jean-Christophe Cuvellier
Robert M. Witwicki
Gérard Waeber
Christèle Dubourg
Marion Gérard
Lachlan J. M. Coin
Magalie Barth
Anita Kloss-Brandstätter
Vincent Mooser
Cristóbal Richart
Giuseppe Merla
Bénédicte Duban-Bedu
Yiping Shen
Ants Kurg
Audrey Guilmatre
Juliane Hoyer
Susana Jiménez-Murcia
Mafalda Mucciolo
Bai-Lin Wu
Alessandra Ferrarini
Séverine Drunat
Yves Alembik
Páll Magnússon
Han G. Brunner
Maria Antonietta Mencarelli
Dominique Descamps
R. Frank Kooy
Azzedine Aboura
Valérie Layet
Sven Bergmann
Thomas Meitinger
Peter M. Kroisel
Nathalie Van der Aa
Olivier Guillin
Michèle Mathieu-Dramard
Zoltán Kutalik
Elisabeth Flori
Laurent Pasquier
André Reis
Noam D. Beckmann
Bertrand Isidor
Delphine Héron
Philippe Jonveaux
Sergi Villatoro Gomez
Ann Nordgren
José Manuel Fernández-Real
Florence Fellmann
Fernando Fernández-Aranda
Laurence Faivre
Dimitri J. Stavropoulos
Katrin Männik
Christian Gieger
Evald Saemundsen
Agnès Guichet
Jean-Marie Cuisset
R. Touraine
Laura Bernardini
Marie-Ange Delrue
Alessandra Renieri
Omar Gustafsson
Flore Zufferey
David A. Koolen
Massimiliano Rossi
Jacqueline Chrast
Ghislaine Plessis
Faida Walha
Joris Andrieux
Ellen van Binsbergen
Albert David
Catherine Vincent-Delorme
Cédric Le Caignec
Jean Chiesa
Ndeye Coumba Ndiaye
Geraldine Joly Helas
Damien Sanlaville
Anita Rauch
Louise Harewood
Mark I. McCarthy
Bridget A. Fernandez
Sébastien Jacquemont
Hreinn Stefansson
Anneke T. Vulto-van Silfhout
Zdenek Jaros
Matthias Nauck
Hans J. Grabe
Sonia Bouquillon
Mieke M. van Haelst
Andres Metspalu
Loyse Hippolyte
Patrick Callier
Bert B.A. de Vries
Francisco J. Tinahones
Nicole de Leeuw
Julia S. El-Sayed Moustafa
Claudine Rieubland
Kay D. MacDermot
Vittoria Disciglio
Henry Völzke
Caroline Rooryck
Bettina Blaumeiser
Danielle Martinet
Marie-Claude Addor
Bruno Delobel
Jacquemont, S
Reymond, A
Zufferey, F
Harewood, L
Walters, Rg
Kutalik, Z
Martinet, D
Shen, Y
Valsesia, A
Beckmann, Nd
Thorleifsson, G
Belfiore, M
Bouquillon, S
Campion, D
de Leeuw, N
de Vries, Bb
Esko, T
Fernandez, Ba
Fernández-Aranda, F
Fernández-Real, Jm
Gratacòs, M
Guilmatre, A
Hoyer, J
Jarvelin, Mr
Kooy, Rf
Kurg, A
Le Caignec, C
Männik, K
Platt, O
Sanlaville, D
Van Haelst, Mm
Villatoro Gomez, S
Walha, F
Wu, Bl
Yu, Y
Aboura, A
Addor, Mc
Alembik, Y
Antonarakis, Se
Arveiler, B
Barth, M
Bednarek, N
Béna, F
Bergmann, S
Beri, M
Bernardini, L
Blaumeiser, B
Bonneau, D
Bottani, A
Boute, O
Brunner, Hg
Cailley, D
Callier, P
Chiesa, J
Chrast, J
Coin, L
Coutton, C
Cuisset, Jm
Cuvellier, Jc
David, A
de Freminville, B
Delobel, B
Delrue, Ma
Demeer, B
Descamps, D
Didelot, G
Dieterich, K
Disciglio, V
Doco-Fenzy, M
Drunat, S
Duban-Bedu, B
Dubourg, C
El-Sayed Moustafa, J
Elliott, P
Faas, Bh
Faivre, L
Faudet, A
Fellmann, F
Ferrarini, A
Fisher, R
Flori, E
Forer, L
Gaillard, D
Gerard, M
Gieger, C
Gimelli, S
Gimelli, G
Grabe, Hj
Guichet, A
Guillin, O
Hartikainen, Al
Heron, D
Hippolyte, L
Holder, M
Homuth, G
Isidor, B
Jaillard, S
Jaros, Z
Jiménez-Murcia, S
Helas, Gj
Jonveaux, P
Kaksonen, S
Keren, B
Kloss-Brandstätter, A
Knoers, Nv
Koolen, Da
Kroisel, Pm
Kronenberg, F
Labalme, A
Landais, E
Lapi, E
Layet, V
Legallic, S
Leheup, B
Leube, B
Lewis, S
Lucas, J
Macdermot, Kd
Magnusson, P
Marshall, C
Mathieu-Dramard, M
Mccarthy, Mi
Meitinger, T
Mencarelli, Ma
Merla, G
Moerman, A
Mooser, V
Morice-Picard, F
Mucciolo, M
Nauck, M
Ndiaye, Nc
Nordgren, A
Pasquier, L
Petit, F
Pfundt, R
Plessis, G
Rajcan-Separovic, E
Ramelli, Gp
Rauch, A
Ravazzolo, R
Reis, A
Renieri, A
Richart, C
Ried, J
Rieubland, C
Roberts, W
Roetzer, Km
Rooryck, C
Rossi, M
Saemundsen, E
Satre, V
Schurmann, C
Sigurdsson, E
Stavropoulos, Dj
Stefansson, H
Tengström, C
Thorsteinsdóttir, U
Tinahones, Fj
Touraine, R
Vallée, L
van Binsbergen, E
Van der Aa, N
Vincent-Delorme, C
Visvikis-Siest, S
Vollenweider, P
Völzke, H
Vulto-van Silfhout, At
Waeber, G
Wallgren-Pettersson, C
Witwicki, Rm
Zwolinksi, S
Andrieux, J
Estivill, X
Gusella, Jf
Gustafsson, O
Metspalu, A
Scherer, Sw
Stefansson, K
Blakemore, Ai
Beckmann, J
Froguel, P
Faculteit Medische Wetenschappen/UMCG
Service de génétique médicale
Centre Hospitalier Universitaire Vaudois [Lausanne] (CHUV)
Center for Integrative Genomics - Institute of Bioinformatics, Génopode (CIG)
Swiss Institute of Bioinformatics [Lausanne] (SIB)
Université de Lausanne = University of Lausanne (UNIL)-Université de Lausanne = University of Lausanne (UNIL)
Department of Genomics of Common Disease
Imperial College London
Department of Medical Genetics
Université de Lausanne = University of Lausanne (UNIL)
Laboratory Medicine
Boston Children's Hospital
Center for Human Genetic Research
Massachusetts General Hospital [Boston]
Ludwig Institute for Cancer Research
deCODE Genetics
deCODE genetics [Reykjavik]
Laboratoire de Génétique Médicale
Hôpital Jeanne de Flandre [Lille]-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
Génétique médicale et fonctionnelle du cancer et des maladies neuropsychiatriques
Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Estonian Genome and Medicine
University of Tartu
Department of human genetics
Radboud University Medical Center [Nijmegen]-Nijmegen Centre for Molecular Life Sciences-Institute for Genetic and Metabolic Disorders
Institute of Molecular and Cell Biology
Disciplines of Genetics and Medicine
Memorial University of Newfoundland = Université Memorial de Terre-Neuve [St. John's, Canada] (MUN)
Department of Psychiatry (IDIBELL)
CIBERobn Fisiopatología de la Obesidad y Nutrición-University Hospital of Bellvitge
Section of Diabetes, Endocrinology and Nutrition
University Hospital of Girona-Biomedical Research Institute 'Dr Josep Trueta'-CIBERobn Fisiopatología de la Obesidad y Nutrición
Center for Genomic Regulation (CRG-UPF)
CIBER de Epidemiología y Salud Pública (CIBERESP)
Institute of Human Genetics [Erlangen, Allemagne]
Friedrich-Alexander Universität Erlangen-Nürnberg (FAU)
Department of child and adolescent health
University of Oulu-Institute of Health Sciences and Biocenter Oulu-National Institute for Health and Welfare [Helsinki]
Antwerp University Hospital [Edegem] (UZA)
CHU Trousseau [APHP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Service de cytogénétique constitutionnelle
Hospices Civils de Lyon (HCL)-CHU de Lyon-Centre Neuroscience et Recherche
University Medical Center [Utrecht]
Institutes of Biomedical Science
Fudan University [Shanghai]-Children's Hospital
Shanghai Children's Medical Center
Département de génétique
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Robert Debré-Université Paris Diderot - Paris 7 (UPD7)
Service de cytogénétique
CHU Strasbourg-Hôpital de Hautepierre [Strasbourg]
Génétique médicale
Hôpitaux Universitaires de Genève (HUG)
Maladies Rares - Génétique et Métabolisme (MRGM)
Université Bordeaux Segalen - Bordeaux 2-Hôpital Pellegrin-Service de Génétique Médicale du CHU de Bordeaux
Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin
Service de génétique [Angers]
Université d'Angers (UA)-Centre Hospitalier Universitaire d'Angers (CHU Angers)
PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM)
Université de Reims Champagne-Ardenne (URCA)
Department of Molecular Genetics
Weizmann Institute of Science [Rehovot, Israël]
Service de Génétique [CHRU Nancy]
Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)
Mendel Laboratory
Istituto di Ricovero e Cura a Carattere Scientifico, Ospedale Casa Sollievo della Sofferenza [San Giovanni Rotondo] (IRCCS)
Service de Génétique clinique
Laboratoire de cytogénétique (CHU de Dijon)
Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)
Laboratoire de Cytogénétique
Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
Département de génétique et procréation
Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-faculté de médecine-pharmacie
AGeing and IMagery (AGIM)
Université Pierre Mendès France - Grenoble 2 (UPMF)-Université Joseph Fourier - Grenoble 1 (UJF)-École Pratique des Hautes Études (EPHE)
Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)
Laboratoire de biochimie et génétique moléculaire
CHU Grenoble
Service de Neuropédiatrie
Hôpital Roger Salengro [Lille]-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
Service de génétique
Centre Hospitalier Universitaire de Saint-Etienne [CHU Saint-Etienne] (CHU ST-E)
Centre de Génétique Chromosomique
Hôpital Saint Vincent de Paul-Groupement des Hôpitaux de l'Institut Catholique de Lille (GHICL)
Université catholique de Lille (UCL)-Université catholique de Lille (UCL)
CHU Amiens-Picardie
Centre Hospitalier de Béthune (CH Béthune)
GHT de l'Artois
Service de Génétique Clinique
Department of Biotechnology
Università degli Studi di Siena = University of Siena (UNISI)-Medical Genetics
Service de Génétique
Centre Hospitalier Universitaire de Reims (CHU Reims)-Hôpital Maison Blanche-IFR 53
Université de Reims Champagne-Ardenne (URCA)-Université de Reims Champagne-Ardenne (URCA)
Institut de Génétique et Développement de Rennes (IGDR)
Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)
Department of Epidemiology and Public Health
Department of Human Genetics [Nijmegen]
Radboud University Medical Center [Nijmegen]
Department of Experimental Cardiology
Academic Medical Center - Academisch Medisch Centrum [Amsterdam] (AMC)
University of Amsterdam [Amsterdam] (UvA)-University of Amsterdam [Amsterdam] (UvA)-Heart Failure Research Center (HFRC)
CHU Pitié-Salpêtrière [AP-HP]
Institute of human genetics
International Centre for Life
Division of genetic epidemiology
HMNC Brain Health-Molecular and Clinical Pharmacology-Innsbruck Medical University = Medizinische Universität Innsbruck (IMU)
Institute of Experimental Medicine
Czech Academy of Sciences [Prague] (CAS)
Department of Obstetrics and Gynecology
University of Oulu-Institute of Clinical Medicine
Laboratorio di citogenetica
G. Gaslini Institute
Department of Psychiatry and Psychotherapy
Universität Greifswald - University of Greifswald
Interfaculty Institute for Genetics and Functional Genomics
Abteilung für Kinder und Jugendheilkunde
Landesklinikum Waldviertel Zwettl
Service de génétique [Rouen]
CHU Rouen
Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)
The Habilitation Unit of Folkhalsan
Medical University Graz
Medical Genetics Unit
Children's Hospital Anna Meyer
Unité de Cytogénétique et Génétique Médicale
Groupe Hospitalier du Havre-Hôpital Gustave Flaubert
Service de Médecine Infantile III et Génétique Clinique [CHRU Nancy]
Institute of Human Genetics and Anthropology
Heinrich-Heine University Hospital Duesseldorf
Child and Family Research Institute-University of British Columbia (UBC)
North West Thames Regional Genetics Service
Northwick Park & St Marks Hospital
Child and Adolescent Psychiatry
Landspitali University Hospital
Program in Genetics and Genomic Biology
Hospital for Sick Children-University of Toronto McLaughlin Centre
Oxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM)
University of Oxford
The Wellcome Trust Centre for Human Genetics [Oxford]
Institute of Human Genetics
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz Zentrum München = German Research Center for Environmental Health
Genetics, GlaxoSmithKline R&D
GlaxoSmithKline
Institute of Clinical Chemistry and Laboratory Medicine
Génétique cardiovasculaire (GC)
Université Henri Poincaré - Nancy 1 (UHP)
Molecular Medicine and Surgery department
Karolinska Institutet [Stockholm]
Service de Génétique [CHU Caen]
Université de Caen Normandie (UNICAEN)
Normandie Université (NU)-Normandie Université (NU)-CHU Caen
Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN)
Department of Pathology
Division of pediatrics
Ospedale San Giovanni
Institute of Medical Genetics
Universität Zürich [Zürich] = University of Zurich (UZH)
Department of pediatrics and CEBR
Università degli studi di Genova = University of Genoa (UniGe)-G. Gaslini Institute
Department of Internal Medicine
Universitat Rovira i Virgili-University Hospital Juan XXIII-Instituto Salud Carlos III-Ciber Fisiopatologia Obesidad y Nutricion (CIBEROBN)
Division of Human Genetics
Department of Paediatrics, Inselspital-University of Bern
Autism Research Unit
The Hospital for sick children [Toronto] (SickKids)-University of Toronto
State Diagnostic
Counseling Center
University of Iceland [Reykjavik]
Department of Pediatric Laboratory Medicine
Hospital for Sick Children
Genetic Services
Rinnekoti Research Foundation
Department of Endocrinology and Nutrition
Instituto Salud Carlos III-Clinic Hospital of Virgen de la Victoria-Ciber Fisiopatologia y Nutricion (CIBEROBN)
Centre de Maladies Rares
Anomalies du Développement Nord de France-CH Arras - CHRU Lille
Institute for Community Medicine
Department of Medical and Clinical Genetics [Helsinki]
Haartman Institute [Helsinki]
Faculty of Medecine [Helsinki]
Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Faculty of Medecine [Helsinki]
Helsingin yliopisto = Helsingfors universitet = University of Helsinki-Helsingin yliopisto = Helsingfors universitet = University of Helsinki
The Centre for Applied Genomics, Toronto
The Hospital for sick children [Toronto] (SickKids)-University of Toronto-Department of Molecular Genetics-McLaughlin Centre
Institut de biologie de Lille - UMS 3702 (IBL)
Institut Pasteur de Lille
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Université de Lille-Centre National de la Recherche Scientifique (CNRS)
This work was supported by the Leenaards Foundation Prize (SJ, DM and AR), the Jérôme Lejeune Foundation (AR), the Telethon Action Suisse Foundation (AR), the Swiss National Science Foundation (AR, JSB, SB and SEA), a SNSF Sinergia grant (SJ, DM, SB, JSB and AR), the European Commission anEUploidy Integrated Project grant 037627 (AR, SB, XE, HGB and SEA), the Ludwig Institute for Cancer Research (AV), the Swiss Institute of Bioinformatics (SB, ZK), an Imperial College Dept of Medicine PhD studentship (JSe-SM), the Comprehensive Biomedical Research Centre, Imperial College Healthcare NHS Trust, and the National Institute for Health Research (PE), the Wellcome Trust and the Medical Research Council (AIFB and PF), the Instituto de Salud Carlos III (ISCIII)-FIS, the German Mental Retardation Network funded through a grant of the German Federal Ministry of Education and Research (NGFNplus 01GS08160) to A Reis and European Union-FEDER (PI081714, PS09/01778), SAF2008-02278 (XE, MG, FFA), the Belgian National Fund for Scientific Research - Flanders (NVA, RFK), the Dutch Organisation for Health Research and Development (ZONMW grant 917-86-319) and Hersenstichting Nederland (BBAdV), grant 81000346 from the Chinese National Natural Science Foundation (YGY), the Simons Foundation Autism Research Initiative, Autism Speaks and NIH grant GM061354 (JFG), and the OENB grant 13059 (AK-B). YS holds a Young Investigator Award from the Children's Tumor Foundation and Catalyst Award from Harvard Medical School, and BLW, a Fudan Scholar Research Award from Fudan University, a grant from Chinese National '973' project on Population and Health (2010CB529601) and a grant from Science and Technology Council of Shanghai (09JC1402400). ERS and SL, recipients of the Michael Smith Foundation for Health Research Scholar award, acknowledge the CIHR MOP 74502 operational grant. EGCUT received support from the EU Centre of Excellence in Genomics and FP7 grants #201413 and #245536, from Estonian Government SF0180142s08, SF0180026s09 and SF0180027s10 (AM, KM, AK). The Helmholtz Zentrum Munich and the State of Bavaria financed KORA, also supported by the German National Genome Research Network (NGFN-2 and NGFNPlus: 01GS0823), the German Federal Ministry of Education and Research (BMBF), and the Munich Center of Health Sciences (MC Health, LMUinnovativ). CIBEROBN and CIBERESP are initiatives of ISCIII (Spain). SWS holds the GlaxoSmithKline-Canadian Institutes of Health (CIHR) Chair in Genetics, Genomics at the University of Toronto and the Hospital for Sick Children and is supported by Genome Canada and the McLaughlin Centre. deCODE was funded in part by NIH grant MH071425 (KS), EU grant HEALTH-2007-2.2.1-10-223423 (Project PsychCNV) and EU grant IMI-JU-NewMeds.
Centre de génomique intégrative
Université de Lausanne (UNIL)
Swiss Institute of Bioinformatics (SIB)
Swiss Institute of Bioinformatics
Memorial University of Newfoundland [St. John's]
Friedrich Alexander University [Erlangen-Nürnberg]
Service d'ORL et de Chirurgie Cervicofaciale
Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP]
Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-Hôpital Robert Debré-Université Paris Diderot - Paris 7 (UPD7)
Weizmann Institute of Science
IRCCS Casa Sollievo della Sofferenza Hospital
Centre Hospitalier Régional Universitaire de Nîmes (CHRU Nîmes)
Université Pierre Mendès France - Grenoble 2 (UPMF)-Université Joseph Fourier - Grenoble 1 (UJF)-École pratique des hautes études (EPHE)-Centre National de la Recherche Scientifique (CNRS)
Hôpital Roger Salengro-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
CHU Saint-Etienne-Hôpital nord
Hôpital Saint Vincent de Paul-GHICL
Centre hospitalier de Béthune
Università degli Studi di Siena (UNISI)-Medical Genetics
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-IFR140-Centre National de la Recherche Scientifique (CNRS)
Department of Human Genetics, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen
Service de Génétique Cytogénétique et Embryologie [CHU Pitié-Salpêtrière]
Assistance publique - Hôpitaux de Paris (AP-HP) (APHP)-CHU Pitié-Salpêtrière [APHP]
Innsbruck Medical University [Austria] (IMU)-HMNC Brain Health-Molecular and Clinical Pharmacology
Czech Academy of Sciences [Prague] (ASCR)
University of Oxford [Oxford]
Technische Universität München [München] (TUM)-Helmholtz-Zentrum München (HZM)-German Research Center for Environmental Health
University of Zürich [Zürich] (UZH)
Universita degli studi di Genova -G. Gaslini Institute
University of Toronto-The Hospital for Sick Children
University of Helsinki-University of Helsinki-Faculty of Medecine [Helsinki]
University of Helsinki-University of Helsinki
University of Toronto-The Hospital for Sick Children-Department of Molecular Genetics-McLaughlin Centre
Institut de biologie de Lille - IBL (IBLI)
Université de Lille, Sciences et Technologies-Institut Pasteur de Lille
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Université de Lille, Droit et Santé-Centre National de la Recherche Scientifique (CNRS)
Human genetics
Amsterdam Neuroscience - Complex Trait Genetics
Amsterdam Reproduction & Development (AR&D)
De Villemeur, Hervé
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Université Pierre Mendès France - Grenoble 2 (UPMF)-Université Joseph Fourier - Grenoble 1 (UJF)-École pratique des hautes études (EPHE)
Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.
Other departments
Reymond, Alexandre
Antonarakis, Stylianos
Sloan Bena, Frédérique
Bottani, Armand
Callier, Patrick
Gimelli, Stefania
Merla, Giuseppe
Vollenweider, Peter
Université de Lausanne (UNIL)-Université de Lausanne (UNIL)
Centre National de la Recherche Scientifique (CNRS)-École pratique des hautes études (EPHE)
Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université Joseph Fourier - Grenoble 1 (UJF)-Université Pierre Mendès France - Grenoble 2 (UPMF)
Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)
Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM)-Helmholtz-Zentrum München (HZM)-German Research Center for Environmental Health
CHU Caen
Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Université de Caen Normandie (UNICAEN)
University of Toronto-The Hospital for sick children [Toronto] (SickKids)-Department of Molecular Genetics-McLaughlin Centre
Université de Lille-Institut Pasteur de Lille
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Centre National de la Recherche Scientifique (CNRS)
Source :
Nature, 478, 97-U111. Nature Publishing Group, Nature, 478, 7367, pp. 97-102, Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R G, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N D, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B B A, Esko, T, Fernandez, B A, Fernández-Aranda, F, Fernández-Real, J M, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, M-R, Kooy, R F, Kurg, A, Le Caignec, C, Männik, K, Platt, O S, Sanlaville, D, Van Haelst, M M, Villatoro Gomez, S, Walha, F, Wu, B-L, Yu, Y, Aboura, A, Addor, M-C, Alembik, Y, Antonarakis, S E, Arveiler, B, Barth, M, Bednarek, N, Béna, F, Bergmann, S, Beri, M, Bernardini, L, Blaumeiser, B, Bonneau, D, Bottani, A, Boute, O, Brunner, H G, Cailley, D, Callier, P, Chiesa, J, Chrast, J, Coin, L, Coutton, C, Cuisset, J-M, Cuvellier, J-C, David, A, de Freminville, B, Delobel, B, Delrue, M-A, Demeer, B, Descamps, D, Didelot, G, Dieterich, K, Disciglio, V, Doco-Fenzy, M, Drunat, S, Duban-Bedu, B, Dubourg, C, El-Sayed Moustafa, J S, Elliott, P, Faas, B H W, Faivre, L, Faudet, A, Fellmann, F, Ferrarini, A, Fisher, R, Flori, E, Forer, L, Gaillard, D, Gerard, M, Gieger, C, Gimelli, S, Gimelli, G, Grabe, H J, Guichet, A, Guillin, O, Hartikainen, A-L, Heron, D, Hippolyte, L, Holder, M, Homuth, G, Isidor, B, Jaillard, S, Jaros, Z, Jiménez-Murcia, S, Helas, G J, Jonveaux, P, Kaksonen, S, Keren, B, Kloss-Brandstätter, A, Knoers, N V A M, Koolen, D A, Kroisel, P M, Kronenberg, F, Labalme, A, Landais, E, Lapi, E, Layet, V, Legallic, S, Leheup, B, Leube, B, Lewis, S, Lucas, J, MacDermot, K D, Magnusson, P, Marshall, C, Mathieu-Dramard, M, McCarthy, M I, Meitinger, T, Mencarelli, M A, Merla, G, Moerman, A, Mooser, V, Morice-Picard, F, Mucciolo, M, Nauck, M, Ndiaye, N C, Nordgren, A, Pasquier, L, Petit, F, Pfundt, R, Plessis, G, Rajcan-Separovic, E, Ramelli, G P, Rauch, A, Ravazzolo, R, Reis, A, Renieri, A, Richart, C, Ried, J S, Rieubland, C, Roberts, W, Roetzer, K M, Rooryck, C, Rossi, M, Saemundsen, E, Satre, V, Schurmann, C, Sigurdsson, E, Stavropoulos, D J, Stefansson, H, Tengström, C, Thorsteinsdóttir, U, Tinahones, F J, Touraine, R, Vallée, L, van Binsbergen, E, Van der Aa, N, Vincent-Delorme, C, Visvikis-Siest, S, Vollenweider, P, Völzke, H, Vulto-van Silfhout, A T, Waeber, G, Wallgren-Pettersson, C, Witwicki, R M, Zwolinksi, S, Andrieux, J, Estivill, X, Gusella, J F, Gustafsson, O, Metspalu, A, Scherer, S W, Stefansson, K, Blakemore, A I F, Beckmann, J S & Froguel, P 2011, ' Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus ', Nature, vol. 478, no. 7367, pp. 97-102 . https://doi.org/10.1038/nature10406, Nature, Nature, 2011, 478 (7367), pp.97-102. ⟨10.1038/nature10406⟩, Nature, Nature Publishing Group, 2011, 478 (7367), pp.97-102. ⟨10.1038/nature10406⟩, Nature, 478(7367), 97-102. Nature Publishing Group, Nature; Vol 478, Nature, 478(7367), 97-U111. Nature Publishing Group, Nature, Vol. 478, No 7367 (2011) pp. 97-102, Nature, vol. 478, no. 7367, pp. 97-102, Nature, 478, 97-102
Publication Year :
2011

Abstract

To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) ≤ 18.5 kg per m(2) in adults and ≤ -2 standard deviations from the mean in children, is the main sign of a series of heterogeneous clinical conditions including failure to thrive, feeding and eating disorder and/or anorexia nervosa. In contrast to obesity, few genetic variants underlying these clinical conditions have been reported. We previously showed that hemizygosity of a ∼600-kilobase (kb) region on the short arm of chromosome 16 causes a highly penetrant form of obesity that is often associated with hyperphagia and intellectual disabilities. Here we show that the corresponding reciprocal duplication is associated with being underweight. We identified 138 duplication carriers (including 132 novel cases and 108 unrelated carriers) from individuals clinically referred for developmental or intellectual disabilities (DD/ID) or psychiatric disorders, or recruited from population-based cohorts. These carriers show significantly reduced postnatal weight and BMI. Half of the boys younger than five years are underweight with a probable diagnosis of failure to thrive, whereas adult duplication carriers have an 8.3-fold increased risk of being clinically underweight. We observe a trend towards increased severity in males, as well as a depletion of male carriers among non-medically ascertained cases. These features are associated with an unusually high frequency of selective and restrictive eating behaviours and a significant reduction in head circumference. Each of the observed phenotypes is the converse of one reported in carriers of deletions at this locus. The phenotypes correlate with changes in transcript levels for genes mapping within the duplication but not in flanking regions. The reciprocal impact of these 16p11.2 copy-number variants indicates that severe obesity and being underweight could have mirror aetiologies, possibly through contrasting effects on energy balance. Leenaards Foundation Jerome Lejeune Foundation Telethon Action Suisse Foundation Swiss National Science Foundation European Commission 037627 QLG1-CT-2000-01643 Ludwig Institute for Cancer Research Swiss Institute of Bioinformatics Imperial College Department of Medicine Comprehensive Biomedical Research Centre Imperial College Healthcare NHS Trust National Institute for Health Research Wellcome Trust Medical Research Council Instituto de Salud Carlos III (ISCIII)-FIS German Mental Retardation Network German Federal Ministry of Education and Research NGFNplus 01GS08160 European Union PI081714 PS09/01778 201413 245536 info:eu-repo/grantAgreement/EC/FP7/223423 Belgian National Fund for Scientific Research, Flanders Dutch Organisation for Health Research and Development (ZON-MW) 917-86-319 Hersenstichting Nederland (B.B.A.d.V.) Chinese National Natural Science Foundation 81000346 Simons Foundation Autism Research Initiative Autism Speaks NIH GM061354 MH071425 Oesterreichische Nationalbank (OENB) 13059 Children's Tumor Foundation Harvard Medical School Fudan University Chinese National '973' project on Population and Health 2010CB529601 Science and Technology Council of Shanghai 09JC1402400 Michael Smith Foundation for Health CIHR MOP 74502 Estonian Government SF0180142s08 SF0180026s09 SF0180027s10 Helmholtz Zentrum Munich State of Bavaria German National Genome Research Network 01GS0823 German Federal Ministry of Education and Research (BMBF) Munich Center of Health Sciences (MC Health, LMUinnovativ) Genome Canada McLaughlin Centre Academy of Finland 104781 120315 129269 1114194 University Hospital Oulu Biocenter University of Oulu, Finland 75617 NHLBI 5R01HL087679-02 1RL1MH083268-01 NIH/NIMH 5R01MH63706:02 ENGAGE project Medical Research Council, UK G0500539 G0600705 Academy of Finland Biocentrum Helsinki SAF2008-02278 HEALTH-F4-2007-201413

Subjects

Subjects :
Male
Aging
Transcription, Genetic
Adolescent
Adult
Aged
Body Height
Body Mass Index
Case-Control Studies
Child
Child, Preschool
Chromosomes, Human, Pair 16
Cohort Studies
Comparative Genomic Hybridization
Developmental Disabilities
Energy Metabolism
Europe
Female
Gene Dosage
Gene Duplication
Gene Expression Profiling
Genetic Predisposition to Disease
Genome-Wide Association Study
Head
Heterozygote
Humans
Infant
Infant, Newborn
Mental Disorders
Middle Aged
Mutation
North America
Obesity
Phenotype
RNA, Messenger
Sequence Deletion
Thinness
Young Adult
Physiology
RNA, Messenger/analysis/genetics
Genome-wide association study
HIDDEN-MARKOV MODEL
0302 clinical medicine
Sequence Deletion/genetics
ddc:576.5
0303 health sciences
education.field_of_study
Body Height/genetics
Genetic Predisposition to Disease/genetics
[SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism
3. Good health
population characteristics
Chromosomes, Human, Pair 16/genetics
Human
Locus (genetics)
Gene Duplication/genetics
Article
03 medical and health sciences
Genetic
education
SNP GENOTYPING DATA
Thinness/genetics
[SDV.GEN]Life Sciences [q-bio]/Genetics
Pair 16
Case-control study
nutritional and metabolic diseases
social sciences
medicine.disease
DEPENDENT PROBE AMPLIFICATION
Human medicine
Body mass index
030217 neurology & neurosurgery
Messenger
Obesity/genetics
FAILURE-TO-THRIVE
[SDV.GEN] Life Sciences [q-bio]/Genetics
Head/anatomy & histology
METABOLIC SYNDROME
[SDV.MHEP.EM] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism
2. Zero hunger
Genetics
Multidisciplinary
TIME QUANTITATIVE PCR
Failure to thrive
medicine.symptom
Underweight
Transcription
geographic locations
Mutation/genetics
Population
Biology
Chromosomes
150 000 MR Techniques in Brain Function
medicine
Preschool
030304 developmental biology
COPY NUMBER VARIATION
Mental Disorders/genetics
Energy Metabolism/genetics
RELATIVE QUANTIFICATION
Gene Dosage/genetics
Newborn
BODY-MASS INDEX
CIRCULAR BINARY SEGMENTATION
RNA
Genetics and epigenetic pathways of disease Genomic disorders and inherited multi-system disorders [NCMLS 6]
human activities
Developmental Disabilities/genetics

Details

ISSN :
00280836, 14764687, and 14764679
Database :
OpenAIRE
Journal :
Nature, 478, 97-U111. Nature Publishing Group, Nature, 478, 7367, pp. 97-102, Jacquemont, S, Reymond, A, Zufferey, F, Harewood, L, Walters, R G, Kutalik, Z, Martinet, D, Shen, Y, Valsesia, A, Beckmann, N D, Thorleifsson, G, Belfiore, M, Bouquillon, S, Campion, D, de Leeuw, N, de Vries, B B A, Esko, T, Fernandez, B A, Fernández-Aranda, F, Fernández-Real, J M, Gratacòs, M, Guilmatre, A, Hoyer, J, Jarvelin, M-R, Kooy, R F, Kurg, A, Le Caignec, C, Männik, K, Platt, O S, Sanlaville, D, Van Haelst, M M, Villatoro Gomez, S, Walha, F, Wu, B-L, Yu, Y, Aboura, A, Addor, M-C, Alembik, Y, Antonarakis, S E, Arveiler, B, Barth, M, Bednarek, N, Béna, F, Bergmann, S, Beri, M, Bernardini, L, Blaumeiser, B, Bonneau, D, Bottani, A, Boute, O, Brunner, H G, Cailley, D, Callier, P, Chiesa, J, Chrast, J, Coin, L, Coutton, C, Cuisset, J-M, Cuvellier, J-C, David, A, de Freminville, B, Delobel, B, Delrue, M-A, Demeer, B, Descamps, D, Didelot, G, Dieterich, K, Disciglio, V, Doco-Fenzy, M, Drunat, S, Duban-Bedu, B, Dubourg, C, El-Sayed Moustafa, J S, Elliott, P, Faas, B H W, Faivre, L, Faudet, A, Fellmann, F, Ferrarini, A, Fisher, R, Flori, E, Forer, L, Gaillard, D, Gerard, M, Gieger, C, Gimelli, S, Gimelli, G, Grabe, H J, Guichet, A, Guillin, O, Hartikainen, A-L, Heron, D, Hippolyte, L, Holder, M, Homuth, G, Isidor, B, Jaillard, S, Jaros, Z, Jiménez-Murcia, S, Helas, G J, Jonveaux, P, Kaksonen, S, Keren, B, Kloss-Brandstätter, A, Knoers, N V A M, Koolen, D A, Kroisel, P M, Kronenberg, F, Labalme, A, Landais, E, Lapi, E, Layet, V, Legallic, S, Leheup, B, Leube, B, Lewis, S, Lucas, J, MacDermot, K D, Magnusson, P, Marshall, C, Mathieu-Dramard, M, McCarthy, M I, Meitinger, T, Mencarelli, M A, Merla, G, Moerman, A, Mooser, V, Morice-Picard, F, Mucciolo, M, Nauck, M, Ndiaye, N C, Nordgren, A, Pasquier, L, Petit, F, Pfundt, R, Plessis, G, Rajcan-Separovic, E, Ramelli, G P, Rauch, A, Ravazzolo, R, Reis, A, Renieri, A, Richart, C, Ried, J S, Rieubland, C, Roberts, W, Roetzer, K M, Rooryck, C, Rossi, M, Saemundsen, E, Satre, V, Schurmann, C, Sigurdsson, E, Stavropoulos, D J, Stefansson, H, Tengström, C, Thorsteinsdóttir, U, Tinahones, F J, Touraine, R, Vallée, L, van Binsbergen, E, Van der Aa, N, Vincent-Delorme, C, Visvikis-Siest, S, Vollenweider, P, Völzke, H, Vulto-van Silfhout, A T, Waeber, G, Wallgren-Pettersson, C, Witwicki, R M, Zwolinksi, S, Andrieux, J, Estivill, X, Gusella, J F, Gustafsson, O, Metspalu, A, Scherer, S W, Stefansson, K, Blakemore, A I F, Beckmann, J S & Froguel, P 2011, ' Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus ', Nature, vol. 478, no. 7367, pp. 97-102 . https://doi.org/10.1038/nature10406, Nature, Nature, 2011, 478 (7367), pp.97-102. ⟨10.1038/nature10406⟩, Nature, Nature Publishing Group, 2011, 478 (7367), pp.97-102. ⟨10.1038/nature10406⟩, Nature, 478(7367), 97-102. Nature Publishing Group, Nature; Vol 478, Nature, 478(7367), 97-U111. Nature Publishing Group, Nature, Vol. 478, No 7367 (2011) pp. 97-102, Nature, vol. 478, no. 7367, pp. 97-102, Nature, 478, 97-102
Accession number :
edsair.doi.dedup.....0e62f829b873e55fff944148463fb1d3
Full Text :
https://doi.org/10.1038/nature10406