Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
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| Title: | Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity. |
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| Authors: | Selvanayagam T; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada., Walker S; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada., Gazzellone MJ; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada., Kellam B; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada., Cytrynbaum C; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada., Stavropoulos DJ; Department of Pediatric Laboratory Medicine, Genome Diagnostics, The Hospital for Sick Children, Toronto, ON, Canada., Li P; Division of Endocrinology, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada., Birken CS; Division of Pediatric Medicine, Hospital for Sick Children, Toronto, ON, Canada.; Department of Pediatrics, University of Toronto, Toronto, ON, Canada., Hamilton J; Division of Endocrinology, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.; Department of Pediatrics, University of Toronto, Toronto, ON, Canada., Weksberg R; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada. rweksb@sickkids.ca.; Division of Clinical & Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada. rweksb@sickkids.ca.; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada. rweksb@sickkids.ca.; Department of Pediatrics, University of Toronto, Toronto, ON, Canada. rweksb@sickkids.ca., Scherer SW; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada. stephen.scherer@sickkids.ca.; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, ON, Canada. stephen.scherer@sickkids.ca.; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada. stephen.scherer@sickkids.ca.; McLaughlin Centre, University of Toronto, Toronto, ON, Canada. stephen.scherer@sickkids.ca. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2018 Nov; Vol. 26 (11), pp. 1588-1596. Date of Electronic Publication: 2018 Jul 05. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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