18 results for author:"Grundy S.M." in Literature citations
Results Customize
› Repeat search in UniProtKB (2)
| Adiponectin as an independent predictor of the presence and degree of hepatic steatosis in the Dallas Heart Study. Turer A.T., Browning J.D., Ayers C.R., Das S.R., Khera A., Vega G.L., Grundy S.M., Scherer P.E. J. Clin. Endocrinol. Metab. 97:E982-6(2012) · Mapped (3) |
| ENPP1/PC-1 K121Q and other predictors of posttransplant diabetes. Szuszkiewicz M., Bell J., Vazquez M., Adams-Huet B., Grundy S.M., Chandalia M., Abate N. Metab Syndr Relat Disord 9:25-29(2011) · Mapped (4) |
| Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Wellcome Trust Case Control Consortium Arterioscler. Thromb. Vasc. Biol. 30:2264-2276(2010) · Mapped (51) |
| Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. Ling H., Waterworth D.M., Stirnadel H.A., Pollin T.I., Barter P.J., Kesaniemi Y.A., Mahley R.W., McPherson R., Waeber G., Bersot T.P. et al. Obesity (Silver Spring) 17:737-744(2009) · Mapped (10) |
| LDL-cholesterol concentrations: a genome-wide association study. Wellcome Trust Case Control Consortium Lancet 371:483-491(2008) · Mapped (21) |
| Ethnic differences in the frequency of ENPP1/PC1 121Q genetic variant in the Dallas Heart Study cohort. Chandalia M., Grundy S.M., Adams-Huet B., Abate N. J. Diabetes Complicat. 21:143-148(2007) · Mapped (4) |
| Mechanisms of disease: Ectonucleotide pyrophosphatase phosphodiesterase 1 as a 'gatekeeper' of insulin receptors. Abate N., Chandalia M., Di Paola R., Foster D.W., Grundy S.M., Trischitta V. Nat Clin Pract Endocrinol Metab 2:694-701(2006) · Mapped (4) |
| Sex differences in the association between leptin and CRP: results from the Dallas Heart Study. Abdullah S.M., Khera A., Leonard D., Das S.R., Canham R.M., Kamath S.A., Vega G.L., Grundy S.M., McGuire D.K., de Lemos J.A. Atherosclerosis 195:404-410(2007) · Mapped (8) |
| Role of genetic polymorphism peroxisome proliferator-activated receptor-gamma2 Pro12Ala on ethnic susceptibility to diabetes in South-Asian and Caucasian subjects: Evidence for heterogeneity. Radha V., Vimaleswaran K.S., Babu H.N., Abate N., Chandalia M., Satija P., Grundy S.M., Ghosh S., Majumder P.P., Deepa R. et al. Diabetes Care 29:1046-1051(2006) · Mapped (9) |
| Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels. Cohen J.C., Pertsemlidis A., Fahmi S., Esmail S., Vega G.L., Grundy S.M., Hobbs H.H. Proc. Natl. Acad. Sci. U.S.A. 103:1810-1815(2006) · Mapped (2) |
| ENPP1/PC-1 K121Q polymorphism and genetic susceptibility to type 2 diabetes. Abate N., Chandalia M., Satija P., Adams-Huet B., Grundy S.M., Sandeep S., Radha V., Deepa R., Mohan V. Diabetes 54:1207-1213(2005) · Mapped (4) |
| Genetic polymorphism PC-1 K121Q and ethnic susceptibility to insulin resistance. Abate N., Carulli L., Cabo-Chan A. Jr., Chandalia M., Snell P.G., Grundy S.M. J. Clin. Endocrinol. Metab. 88:5927-5934(2003) · UniProtKB (1) · Mapped (8) |
| Sources of variability in genetic association studies: insights from the analysis of hepatic lipase (LIPC). Shohet R.V., Vega G.L., Bersot T.P., Mahley R.W., Grundy S.M., Guerra R., Cohen J.C. Hum. Mutat. 19:536-542(2002) · Mapped (4) |
| Heritability of plasma noncholesterol sterols and relationship to DNA sequence polymorphism in ABCG5 and ABCG8. Berge K.E., von Bergmann K., Lutjohann D., Guerra R., Grundy S.M., Hobbs H.H., Cohen J.C. J. Lipid Res. 43:486-494(2002) · Mapped (4) |
| Three polymorphisms associated with low hepatic lipase activity are common in African Americans. Nie L., Niu S., Vega G.L., Clark L.T., Tang A., Grundy S.M., Cohen J.C. J. Lipid Res. 39:1900-1903(1998) · Mapped (4) |
| Obesity in db and ob animals leads to impaired hepatic very low density lipoprotein secretion and differential secretion of apolipoprotein B-48 and B-100. Li X., Grundy S.M., Patel S.B. J. Lipid Res. 38:1277-1288(1997) · Mapped (23) |
| A hepatic lipase (LIPC) allele associated with high plasma concentrations of high density lipoprotein cholesterol. Guerra R., Wang J., Grundy S.M., Cohen J.C. Proc. Natl. Acad. Sci. U.S.A. 94:4532-4537(1997) · Mapped (4) |
| Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100. Soria L.F., Ludwig E.H., Clarke H.R.G., Vega G.L., Grundy S.M., McCarthy B.J. Proc. Natl. Acad. Sci. U.S.A. 86:587-591(1989) · UniProtKB (1) · Mapped (11) |