Si S. An, Ph.D.

Affiliations: 
2012 Biochemistry and Molecular Biology Wake Forest University, Winston-Salem, NC, United States 
Area:
Genetics, Biochemistry, Pathology
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"Si An"

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Donald W. Bowden grad student 2012 Wake Forest
 (Genetic variants of ADIPOQ and association with plasma adiponectin levels, type 2 diabetes, glucose homeostasis and adiposity.)
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Publications

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Hellwege JN, Palmer ND, Mark Brown W, et al. (2015) Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels. Human Genetics. 134: 203-13
Cox AJ, Lambird JE, An SS, et al. (2013) Variants in adiponectin signaling pathway genes show little association with subclinical CVD in the diabetes heart study. Obesity (Silver Spring, Md.). 21: E456-62
An SS, Palmer ND, Hanley AJ, et al. (2013) Estimating the contributions of rare and common genetic variations and clinical measures to a model trait: adiponectin. Genetic Epidemiology. 37: 13-24
An SS, Hanley AJ, Ziegler JT, et al. (2012) Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study. Molecular Genetics and Metabolism. 107: 721-8
Cooke JN, Ng MC, Palmer ND, et al. (2012) Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans. Diabetes Care. 35: 287-92
Palmer ND, McDonough CW, Hicks PJ, et al. (2012) A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202
McDonough CW, Palmer ND, Hicks PJ, et al. (2011) A genome-wide association study for diabetic nephropathy genes in African Americans. Kidney International. 79: 563-72
Palmer ND, Hester JM, An SS, et al. (2011) Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Diabetes. 60: 662-8
Bowden DW, An SS, Palmer ND, et al. (2010) Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study. Human Molecular Genetics. 19: 4112-20
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