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Journal of Obesity
Volume 2015, Article ID 623431, 7 pages
http://dx.doi.org/10.1155/2015/623431
Research Article

A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity

1Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
2Cardiovascular Genetics Division, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
3Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84112, USA
4ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT, USA
5Department of Genetic Medicine, Weill Cornell Medical College in Qatar, Doha, Qatar

Received 18 August 2015; Accepted 20 December 2015

Academic Editor: Eric Doucet

Copyright © 2015 Sandra J. Hasstedt et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [5 citations]

The following is the list of published articles that have cited the current article.

  • Ana Carolina Proen?a da Fonseca, Claudio Mastronardi, Angad Johar, Mauricio Arcos-Burgos, and Gilberto Paz-Filho, “Genetics of non-syndromic childhood obesity and the use of high-throughput DNA sequencing technologies,” Journal of Diabetes and its Complications, 2017. View at Publisher · View at Google Scholar
  • Herman E. Wyandt, Golder N. Wilson, and Vijay S. Tonkpp. 1–490, 2017. View at Publisher · View at Google Scholar
  • Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk, Herman E. Wyandt, Golder N. Wilson, and Vijay S. Tonk, “A CNV Catalogue,” Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis, pp. 235–417, 2017. View at Publisher · View at Google Scholar
  • Man Li, Jacob Carey, Stephen Cristiano, Katalin Susztak, Josef Coresh, Eric Boerwinkle, Wen Hong L. Kao, Terri H. Beaty, Anna Köttgen, and Robert B. Scharpf, “Genome-Wide Association of Copy Number Polymorphisms and Kidney Function,” Plos One, vol. 12, no. 1, pp. e0170815, 2017. View at Publisher · View at Google Scholar
  • Liwen Hu, Xinyue Yao, Hairong Huang, Zhong Guo, Xi Chen, Yang Xu, Yi Shen, Biao Xu, and Demin Li, “Clinical significance of germline copy number variation in susceptibility of human diseases,” Journal of Genetics and Genomics, 2018. View at Publisher · View at Google Scholar