Journal article
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Abstract
Genetic link to obesityObesity is a highly heritable disorder but the genetic associations reported to date account for only a small percentage of the inherited variation in body mass index. Two groups report deletions on chromosome16p11.2 that may explain part of the 'missing heritability' in terms of 'high-penetrance' mutations that are rare but when present are very often associated with severe obesity. This is in contrast to more common …
Authors
Walters RG; Jacquemont S; Valsesia A; de Smith AJ; Martinet D; Andersson J; Falchi M; Chen F; Andrieux J; Lobbens S
Journal
Nature, Vol. 463, No. 7281, pp. 671–675
Publisher
Springer Nature
Publication Date
February 2010
DOI
10.1038/nature08727
ISSN
0028-0836
Fields of Research (FoR)
Medical Subject Headings (MeSH)
AdolescentAdultAge of OnsetAgingBody Mass IndexCase-Control StudiesChildChromosome DeletionChromosomes, Human, Pair 16Cognition DisordersCohort StudiesEuropeFemaleGenome-Wide Association StudyHeterozygoteHumansInheritance PatternsMaleMutationObesityPenetranceReproducibility of ResultsSex CharacteristicsYoung Adult