1 - 25 of 121 results for author:"Collins F.S." in Literature citations
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| Hyperglycemia and a common variant of GCKR are associated with the levels of eight amino acids in 9,369 Finnish men. Stancakova A., Civelek M., Saleem N.K., Soininen P., Kangas A.J., Cederberg H., Paananen J., Pihlajamaki J., Bonnycastle L.L., Morken M.A. et al. Diabetes 61:1895-1902(2012) · Mapped (4) |
| Human longevity and common variations in the LMNA gene: a meta-analysis. Conneely K.N., Capell B.C., Erdos M.R., Sebastiani P., Solovieff N., Swift A.J., Baldwin C.T., Budagov T., Barzilai N., Atzmon G. et al. Aging Cell 11:475-481(2012) · Mapped (11) |
| Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes. Rees M.G., Ng D., Ruppert S., Turner C., Beer N.L., Swift A.J., Morken M.A., Below J.E., Blech I., Mullikin J.C. et al. J. Clin. Invest. 122:205-217(2012) · Mapped (4) |
| Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk. Rees M.G., Wincovitch S., Schultz J., Waterstradt R., Beer N.L., Baltrusch S., Collins F.S., Gloyn A.L. Diabetologia 55:114-122(2012) · Mapped (7) |
| Progerin and telomere dysfunction collaborate to trigger cellular senescence in normal human fibroblasts. Cao K., Blair C.D., Faddah D.A., Kieckhaefer J.E., Olive M., Erdos M.R., Nabel E.G., Collins F.S. J. Clin. Invest. 121:2833-2844(2011) · Mapped (11) |
| Genetic analysis of complex traits in the emerging Collaborative Cross. Aylor D.L., Valdar W., Foulds-Mathes W., Buus R.J., Verdugo R.A., Baric R.S., Ferris M.T., Frelinger J.A., Heise M., Frieman M.B. et al. Genome Res. 21:1213-1222(2011) · Mapped (30) |
| Protein farnesylation inhibitors cause donut-shaped cell nuclei attributable to a centrosome separation defect. Verstraeten V.L., Peckham L.A., Olive M., Capell B.C., Collins F.S., Nabel E.G., Young S.G., Fong L.G., Lammerding J. Proc. Natl. Acad. Sci. U.S.A. 108:4997-5002(2011) · Mapped (11) |
| Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Procardis Consortium Nat. Genet. 42:937-948(2010) · Mapped (6) |
| Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Heid I.M., Jackson A.U., Randall J.C., Winkler T.W., Qi L., Steinthorsdottir V., Thorleifsson G., Zillikens M.C., Speliotes E.K., Magi R. et al. Nat. Genet. 42:949-960(2010) · Mapped (60) |
| A role for coding functional variants in HNF4A in type 2 diabetes susceptibility. DIAGRAM Consortium Diabetologia 54:111-119(2011) · Mapped (9) |
| Common variants at 10 genomic loci influence hemoglobin A(1)(C) levels via glycemic and nonglycemic pathways. Soranzo N., Sanna S., Wheeler E., Gieger C., Radke D., Dupuis J., Bouatia-Naji N., Langenberg C., Prokopenko I., Stolerman E. et al. Diabetes 59:3229-3239(2010) · Mapped (36) |
| Biological, clinical and population relevance of 95 loci for blood lipids. Teslovich T.M., Musunuru K., Smith A.V., Edmondson A.C., Stylianou I.M., Koseki M., Pirruccello J.P., Ripatti S., Chasman D.I., Willer C.J. et al. |
| Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. GIANT Consortium Nat. Genet. 42:579-589(2010) · Mapped (17) |
| Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans. Ingelsson E., Langenberg C., Hivert M.F., Prokopenko I., Lyssenko V., Dupuis J., Magi R., Sharp S., Jackson A.U., Assimes T.L. et al. Diabetes 59:1266-1275(2010) · Mapped (29) |
| New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. DIAGRAM Consortium Nat. Genet. 42:105-116(2010) · Mapped (94) |
| Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Saxena R., Hivert M.F., Langenberg C., Tanaka T., Pankow J.S., Vollenweider P., Lyssenko V., Bouatia-Naji N., Dupuis J., Jackson A.U. et al. Nat. Genet. 42:142-148(2010) · Mapped (48) |
| A progeria mutation reveals functions for lamin A in nuclear assembly, architecture, and chromosome organization. Taimen P., Pfleghaar K., Shimi T., Moller D., Ben-Harush K., Erdos M.R., Adam S.A., Herrmann H., Medalia O., Collins F.S. et al. Proc. Natl. Acad. Sci. U.S.A. 106:20788-20793(2009) · Mapped (11) |
| Alternative splicing of TCF7L2 gene in omental and subcutaneous adipose tissue and risk of type 2 diabetes. Prokunina-Olsson L., Kaplan L.M., Schadt E.E., Collins F.S. PLoS ONE 4:e7231-e7231(2009) · Mapped (31) |
| No association between a candidate TCF7L2 variant and risk of breast or ovarian cancer. Goode E.L., Szabo C., Prokunina-Olsson L., Vierkant R.A., Fredericksen Z.S., Collins F.S., White K.L., Schmidt M., Fridley B.L., Couch F.J. BMC Cancer 9:312-312(2009) · Mapped (31) |
| Tissue-specific alternative splicing of TCF7L2. Prokunina-Olsson L., Welch C., Hansson O., Adhikari N., Scott L.J., Usher N., Tong M., Sprau A., Swift A., Bonnycastle L.L. et al. Hum. Mol. Genet. 18:3795-3804(2009) · Mapped (31) |
| Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. Wellcome Trust Case Control Consortium PLoS Genet. 5:e1000508-e1000508(2009) · Mapped (11) |
| Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men. Stancakova A., Kuulasmaa T., Paananen J., Jackson A.U., Bonnycastle L.L., Collins F.S., Boehnke M., Kuusisto J., Laakso M. Diabetes 58:2129-2136(2009) · Mapped (79) |
| Genome-wide association study identifies eight loci associated with blood pressure. Wellcome Trust Case Control Consortium Nat. Genet. 41:666-676(2009) · Mapped (91) |
| In vitro hematopoietic differentiation of mouse embryonic stem cells requires the tumor suppressor menin and is mediated by Hoxa9. Novotny E., Compton S., Liu P.P., Collins F.S., Chandrasekharappa S.C. Mech. Dev. 126:517-522(2009) · Mapped (6) |
| Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Wellcome Trust Case Control Consortium Nat. Genet. 41:25-34(2009) · Mapped (30) |