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Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe...

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4106235

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

About this item

Full title

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

Publisher

New York: Nature Publishing Group US

Journal title

Nature genetics, 2013-05, Vol.45 (5), p.513-517

Language

English

Formats

Publication information

Publisher

New York: Nature Publishing Group US

More information

Scope and Contents

Contents

Sadaf Farooqi, Inês Barroso and colleagues report genome-wide SNP and CNV association analyses for severe obesity in children, selected at the extreme of the distribution for body mass index. They identify four loci newly associated with severe obesity, an enrichment of rare CNVs in severely obese cases and overlap in the loci associated with sever...

Alternative Titles

Full title

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4106235

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4106235

Other Identifiers

ISSN

1061-4036

E-ISSN

1546-1718

DOI

10.1038/ng.2607

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