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Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature

Overview of attention for article published in Current Genomics, May 2011
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Title
Structural Chromosome Abnormalities Associated with Obesity: Report of Four New subjects and Review of Literature
Published in
Current Genomics, May 2011
DOI 10.2174/138920211795677930
Pubmed ID
Authors

Majed J Dasouki, Erin L Youngs, Karine Hovanes

Abstract

Obesity in humans is a complex polygenic trait with high inter-individual heritability estimated at 40-70%. Candidate gene, DNA linkage and genome-wide association studies (GWAS) have allowed for the identification of a large set of genes and genomic regions associated with obesity. Structural chromosome abnormalities usually result in congenital anomalies, growth retardation and developmental delay. Occasionally, they are associated with hyperphagia and obesity rather than growth delay. We report four new individuals with structural chromosome abnormalities involving 10q22.3-23.2, 16p11.2 and Xq27.1-q28 chromosomal regions with early childhood obesity and developmental delay. We also searched and summarized the literature for structural chromosome abnormalities reported in association with childhood obesity.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 2 6%
Italy 1 3%
Unknown 33 92%

Demographic breakdown

Readers by professional status Count As %
Researcher 9 25%
Student > Ph. D. Student 7 19%
Student > Bachelor 4 11%
Other 4 11%
Student > Doctoral Student 2 6%
Other 6 17%
Unknown 4 11%
Readers by discipline Count As %
Medicine and Dentistry 10 28%
Agricultural and Biological Sciences 7 19%
Biochemistry, Genetics and Molecular Biology 4 11%
Neuroscience 4 11%
Social Sciences 3 8%
Other 4 11%
Unknown 4 11%