Mouse model implicates GNB3 duplication in a childhood obesity syndrome
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Mouse model implicates GNB3 duplication in a childhood obesity syndrome
Authors
Keywords
-
Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 110, Issue 37, Pages 14990-14994
Publisher
Proceedings of the National Academy of Sciences
Online
2013-08-27
DOI
10.1073/pnas.1305999110
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity
- (2013) Eleanor Wheeler et al. NATURE GENETICS
- Nontelomeric Role for Rap1 in Regulating Metabolism and Protecting against Obesity
- (2013) Frank Yeung et al. Cell Reports
- Molecular Basis of Obesity: Current Status and Future Prospects
- (2012) Helene Choquet et al. CURRENT GENOMICS
- Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations
- (2012) C. Robberecht et al. GENOME RESEARCH
- A genome-wide association meta-analysis identifies new childhood obesity loci
- (2012) NATURE GENETICS
- Leptin revisited: its mechanism of action and potential for treating diabetes
- (2012) Roberto Coppari et al. NATURE REVIEWS DRUG DISCOVERY
- A recurrent translocation is mediated by homologous recombination between HERV-H elements
- (2012) Karen E Hermetz et al. Molecular Cytogenetics
- A Duplication CNV That Conveys Traits Reciprocal to Metabolic Syndrome and Protects against Diet-Induced Obesity in Mice and Men
- (2012) Melanie Lacaria et al. PLoS Genetics
- An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities
- (2011) Erin B. Kaminsky et al. GENETICS IN MEDICINE
- Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes
- (2011) Z. Ou et al. GENOME RESEARCH
- Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements
- (2011) Yue Luo et al. HUMAN MOLECULAR GENETICS
- A copy number variation morbidity map of developmental delay
- (2011) Gregory M Cooper et al. NATURE GENETICS
- Ten years of leptin replacement therapy
- (2011) G. Paz-Filho et al. Obesity Reviews
- The GNB3 C825T polymorphism as a pharmacogenetic marker in the treatment of hypertension, obesity, and depression
- (2011) Stefanie Klenke et al. Pharmacogenetics and Genomics
- A Genome-wide Study Reveals Copy Number Variants Exclusive to Childhood Obesity Cases
- (2010) Joseph T. Glessner et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine
- (2010) Alexandra I. F. Blakemore et al. Annals of the New York Academy of Sciences
- Overgrowth
- (2010) C. F. Verge et al. ARCHIVES OF DISEASE IN CHILDHOOD
- Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity
- (2010) Ruxandra Bachmann-Gagescu et al. GENETICS IN MEDICINE
- Rai1 haploinsufficiency causes reduced Bdnf expression resulting in hyperphagia, obesity and altered fat distribution in mice and humans with no evidence of metabolic syndrome
- (2010) Brooke Burns et al. HUMAN MOLECULAR GENETICS
- A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
- (2010) R. G. Walters et al. NATURE
- Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
- (2010) Elizabeth K Speliotes et al. NATURE GENETICS
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
- (2009) Helen V. Firth et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Duplication hotspots, rare genomic disorders, and common disease
- (2009) Heather C Mefford et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Trisomy 12p and Monosomy 4p: Phenotype–Genotype Correlation
- (2009) Daniela Gambel Benussi et al. Genetic Testing and Molecular Biomarkers
- Large, rare chromosomal deletions associated with severe early-onset obesity
- (2009) Elena G. Bochukova et al. NATURE
- Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity
- (2008) Gudmar Thorleifsson et al. NATURE GENETICS
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
- (2008) Cristen J Willer et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search