23 results for author:"Palmer N." in Literature citations
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| Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans. Cooke J.N., Ng M.C., Palmer N.D., An S.S., Hester J.M., Freedman B.I., Langefeld C.D., Bowden D.W. Diabetes Care 35:287-292(2012) · Mapped (31) |
| SIRT6 in mouse spermatogenesis is modulated by diet-induced obesity. Palmer N.O., Fullston T., Mitchell M., Setchell B.P., Lane M. Reprod. Fertil. Dev. 23:929-939(2011) · Mapped (2) |
| Implication of European-derived adiposity loci in African Americans. Hester J.M., Wing M.R., Li J., Palmer N.D., Xu J., Hicks P.J., Roh B.H., Norris J.M., Wagenknecht L.E., Langefeld C.D. et al. Int J Obes (Lond) 36:465-473(2012) · Mapped (10) |
| Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. Freedman B.I., Langefeld C.D., Lu L., Divers J., Comeau M.E., Kopp J.B., Winkler C.A., Nelson G.W., Johnson R.C., Palmer N.D. et al. PLoS Genet. 7:e1002150-e1002150(2011) · Mapped (12) |
| Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant. Palmer N.D., Hester J.M., An S.S., Adeyemo A., Rotimi C., Langefeld C.D., Freedman B.I., Ng M.C., Bowden D.W. Diabetes 60:662-668(2011) · Mapped (31) |
| 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. Bowden D.W., An S.S., Palmer N.D., Brown W.M., Norris J.M., Haffner S.M., Hawkins G.A., Guo X., Rotter J.I., Chen Y.D. et al. Hum. Mol. Genet. 19:4112-4120(2010) · Mapped (3) |
| Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans. Lewis J.P., Palmer N.D., Ellington J.B., Divers J., Ng M.C., Lu L., Langefeld C.D., Freedman B.I., Bowden D.W. Genomics 96:211-219(2010) · Mapped (23) |
| Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study. Engelman C.D., Meyers K.J., Ziegler J.T., Taylor K.D., Palmer N.D., Haffner S.M., Fingerlin T.E., Wagenknecht L.E., Rotter J.I., Bowden D.W. et al. J. Steroid Biochem. Mol. Biol. 122:186-192(2010) · Mapped (8) |
| Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study. Palmer N.D., Mychaleckyj J.C., Langefeld C.D., Ziegler J.T., Williams A.H., Bryer-Ash M., Bowden D.W. Diabetes Res. Clin. Pract. 87:69-76(2010) · Mapped (9) |
| Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study. Sutton B.S., Palmer N.D., Langefeld C.D., Xue B., Proctor A., Ziegler J.T., Haffner S.M., Norris J.M., Bowden D.W. Diabetes 58:1457-1462(2009) · Mapped (2) |
| Phenotype-genotype correlations in autosomal dominant retinitis pigmentosa caused by RHO, D190N. Tsui I., Chou C.L., Palmer N., Lin C.S., Tsang S.H. Curr. Eye Res. 33:1014-1022(2008) · Mapped (1) |
| Comprehensive dissection of PDGF-PDGFR signaling pathways in PDGFR genetically defined cells. Wu E., Palmer N., Tian Z., Moseman A.P., Galdzicki M., Wang X., Berger B., Zhang H., Kohane I.S. |
| Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans. Palmer N.D., Langefeld C.D., Bryer-Ash M., Rotter J.I., Taylor K.D., Bowden D.W. J. Clin. Endocrinol. Metab. 93:4979-4983(2008) · Mapped (6) |
| Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1. Bento J.L., Palmer N.D., Zhong M., Roh B., Lewis J.P., Wing M.R., Pandya H., Freedman B.I., Langefeld C.D., Rich S.S. et al. Genomics 92:226-234(2008) · Mapped (24) |
| Association analysis of the ephrin-B2 gene in African-Americans with end-stage renal disease. Hicks P.J., Staten J.L., Palmer N.D., Langefeld C.D., Ziegler J.T., Keene K.L., Sale M.M., Bowden D.W., Freedman B.I. Am. J. Nephrol. 28:914-920(2008) · Mapped (2) |
| Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies. Lewis J.P., Palmer N.D., Hicks P.J., Sale M.M., Langefeld C.D., Freedman B.I., Divers J., Bowden D.W. Diabetes 57:2220-2225(2008) · Mapped (42) |
| Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study. Palmer N.D., Goodarzi M.O., Langefeld C.D., Ziegler J., Norris J.M., Haffner S.M., Bryer-Ash M., Bergman R.N., Wagenknecht L.E., Taylor K.D. et al. Diabetes 57:1093-1100(2008) · Mapped (4) |
| Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans. Palmer N.D., Lehtinen A.B., Langefeld C.D., Campbell J.K., Haffner S.M., Norris J.M., Bergman R.N., Goodarzi M.O., Rotter J.I., Bowden D.W. J. Clin. Endocrinol. Metab. 93:304-309(2008) · Mapped (31) |
| The uncoupling protein 1 gene, UCP1, is expressed in mammalian islet cells and associated with acute insulin response to glucose in African American families from the IRAS Family Study. Sale M.M., Hsu F.C., Palmer N.D., Gordon C.J., Keene K.L., Borgerink H.M., Sharma A.J., Bergman R.N., Taylor K.D., Saad M.F. et al. BMC Endocr Disord 7:1-1(2007) · Mapped (3) |
| Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study. Palmer N.D., Bento J.L., Mychaleckyj J.C., Langefeld C.D., Campbell J.K., Norris J.M., Haffner S.M., Bergman R.N., Bowden D.W. Diabetes 53:3013-3019(2004) · Mapped (4) |
| Association of protein tyrosine phosphatase 1B gene polymorphisms with type 2 diabetes. Bento J.L., Palmer N.D., Mychaleckyj J.C., Lange L.A., Langefeld C.D., Rich S.S., Freedman B.I., Bowden D.W. Diabetes 53:3007-3012(2004) · Mapped (4) |
| A bacterial genome in flux: the twelve linear and nine circular extrachromosomal DNAs in an infectious isolate of the Lyme disease spirochete Borrelia burgdorferi. Casjens S., Palmer N., van Vugt R., Huang W.M., Stevenson B., Rosa P., Lathigra R., Sutton G.G., Peterson J.D., Dodson R.J. et al. Mol. Microbiol. 35:490-516(2000) · UniProtKB (265) |
| Genomic sequence of a Lyme disease spirochaete, Borrelia burgdorferi. Fraser C.M., Casjens S., Huang W.M., Sutton G.G., Clayton R.A., Lathigra R., White O., Ketchum K.A., Dodson R.J., Hickey E.K. et al. Nature 390:580-586(1997) · UniProtKB (1,289) |