Year |
Citation |
Score |
2014 |
Cooke Bailey JN, Palmer ND, Ng MC, Bonomo JA, Hicks PJ, Hester JM, Langefeld CD, Freedman BI, Bowden DW. Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans. Human Genetics. 133: 769-79. PMID 24385048 DOI: 10.1007/S00439-013-1415-Z |
0.758 |
|
2012 |
Cooke JN, Ng MC, Palmer ND, An SS, Hester JM, Freedman BI, Langefeld CD, Bowden DW. Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans. Diabetes Care. 35: 287-92. PMID 22275441 DOI: 10.2337/Dc11-0957 |
0.75 |
|
2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.68 |
|
2012 |
Hester JM, Wing MR, Li J, Palmer ND, Xu J, Hicks PJ, Roh BH, Norris JM, Wagenknecht LE, Langefeld CD, Freedman BI, Bowden DW, Ng MC. Implication of European-derived adiposity loci in African Americans. International Journal of Obesity (2005). 36: 465-73. PMID 21750520 DOI: 10.1038/Ijo.2011.131 |
0.809 |
|
2012 |
Ng MC, Hester JM, Wing MR, Li J, Xu J, Hicks PJ, Roh BH, Lu L, Divers J, Langefeld CD, Freedman BI, Palmer ND, Bowden DW. Genome-wide association of BMI in African Americans. Obesity (Silver Spring, Md.). 20: 622-7. PMID 21701570 DOI: 10.1038/Oby.2011.154 |
0.826 |
|
2011 |
McDonough CW, Palmer ND, Hicks PJ, Roh BH, An SS, Cooke JN, Hester JM, Wing MR, Bostrom MA, Rudock ME, Lewis JP, Talbert ME, Blevins RA, Lu L, Ng MC, et al. A genome-wide association study for diabetic nephropathy genes in African Americans. Kidney International. 79: 563-72. PMID 21150874 DOI: 10.1038/Ki.2010.467 |
0.662 |
|
2011 |
Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD, Freedman BI, Ng MC, Bowden DW. 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. PMID 20980453 DOI: 10.2337/Db10-0134 |
0.855 |
|
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