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Jennifer Dackor

Researcher at University of North Carolina at Chapel Hill

Publications -  9
Citations -  1699

Jennifer Dackor is an academic researcher from University of North Carolina at Chapel Hill. The author has contributed to research in topics: Epidermal growth factor receptor & Body mass index. The author has an hindex of 8, co-authored 9 publications receiving 1601 citations. Previous affiliations of Jennifer Dackor include Research Triangle Park.

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Journal ArticleDOI

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Helena Furberg, +123 more
- 01 May 2010 - 
TL;DR: A meta-analyses of several smoking phenotypes within cohorts of the Tobacco and Genetics Consortium found the strongest association was a synonymous 15q25 SNP in the nicotinic receptor gene CHRNA3, and three loci associated with number of cigarettes smoked per day were identified.

A genome-wide association study of anorexia nervosa

Vesna Boraska, +175 more
TL;DR: The accrual of large genotyped AN case-control samples should be an immediate priority for the field, suggesting that true findings exist but the sample, the largest yet reported, was underpowered for their detection.
Journal ArticleDOI

A common biological basis of obesity and nicotine addiction

Thorgeir E. Thorgeirsson, +316 more
TL;DR: The results strongly point to a common biological basis of the regulation of theregulation of the authors' appetite for tobacco and food, and thus the vulnerability to nicotine addiction and obesity, and the effect of single-nucleotide polymorphisms affecting body mass index (BMI).
Journal ArticleDOI

Placental and embryonic growth restriction in mice with reduced function epidermal growth factor receptor alleles

TL;DR: It is suggested that Egfrwa2 homozygous embryos model EGFR-mediated intrauterine growth restriction in humans and differential expression in the placenta of Glut3, a glucose transporter essential for normal embryonic growth, may contribute to strain-dependent differences in intrauterne growth restriction caused by reduced EGFR activity.