Biblio

Found 24 results
Filters: Author is Hicks, Andrew A  [Clear All Filters]
2013
Do R, Willer CJ, Schmidt EM, Sengupta S, Gao C, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J et al..  2013.  Common variants associated with plasma triglycerides and risk for coronary artery disease.. Nat Genet. 45(11):1345-52.
Willer CJ, Schmidt EM, Sengupta S, Peloso GM, Gustafsson S, Kanoni S, Ganna A, Chen J, Buchkovich ML, Mora S et al..  2013.  Discovery and refinement of loci associated with lipid levels.. Nat Genet. 45(11):1274-83.
Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T et al..  2013.  Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.. Nat Genet. 45(2):145-54.
Berndt SI, Gustafsson S, Mägi R, Ganna A, Wheeler E, Feitosa MF, Justice AE, Monda KL, Croteau-Chonka DC, Day FR et al..  2013.  Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.. Nat Genet. 45(5):501-12.
Hoed Mden, Eijgelsheim M, Esko T, Brundel BJJM, Peal DS, Evans DM, Nolte IM, Segrè AV, Holm H, Handsaker RE et al..  2013.  Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.. Nat Genet. 45(6):621-31.
Minelli C, De Grandi A, Weichenberger CX, Gögele M, Modenese M, Attia J, Barrett JH, Boehnke M, Borsani G, Casari G et al..  2013.  Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.. Genet Epidemiol. 37(2):205-13.
Porcu E, Medici M, Pistis G, Volpato CB, Wilson SG, Cappola AR, Bos SD, Deelen J, den Heijer M, Freathy RM et al..  2013.  A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.. PLoS Genet. 9(2):e1003266.
Pichler I, Del Greco M F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M et al..  2013.  Serum iron levels and the risk of Parkinson disease: a mendelian randomization study.. PLoS Med. 10(6):e1001462.
Thompson JR, Gögele M, Weichenberger CX, Modenese M, Attia J, Barrett JH, Boehnke M, De Grandi A, Domingues FS, Hicks AA et al..  2013.  SNP prioritization using a Bayesian probability of association.. Genet Epidemiol. 37(2):214-21.
2011
Demirkan A, Amin N, Isaacs A, Jarvelin M-R, Whitfield JB, Wichmann H-E, Kyvik K O, Rudan I, Gieger C, Hicks AA et al..  2011.  Genetic architecture of circulating lipid levels.. Eur J Hum Genet. 19(7):813-9.
Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang S-J et al..  2011.  Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.. Nature. 478(7367):103-9.
Del Greco M F, Pattaro C, Luchner A, Pichler I, Winkler T, Hicks AA, Fuchsberger C, Franke A, Melville SA, Peters A et al..  2011.  Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.. Hum Mol Genet. 20(8):1660-71.
Pichler I, Minelli C, Sanna S, Tanaka T, Schwienbacher C, Naitza S, Porcu E, Pattaro C, Busonero F, Zanon A et al..  2011.  Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.. Hum Mol Genet. 20(6):1232-40.
Volpato CB, De Grandi A, Gögele M, Taliun D, Fuchsberger C, Facheris MF, Minelli C, Pattaro C, Pramstaller PP, Hicks AA.  2011.  Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27.. J Med Genet. 48(8):549-56.
Dehghan A, Dupuis J, Barbalic M, Bis JC, Eiriksdottir G, Lu C, Pellikka N, Wallaschofski H, Kettunen J, Henneman P et al..  2011.  Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.. Circulation. 123(7):731-8.
Gieger C, Radhakrishnan A, Cvejic A, Tang W, Porcu E, Pistis G, Serbanovic-Canic J, Elling U, Goodall AH, Labrune Y et al..  2011.  New gene functions in megakaryopoiesis and platelet formation.. Nature. 480(7376):201-8.
Oexle K, Ried JS, Hicks AA, Tanaka T, Hayward C, Bruegel M, Gögele M, Lichtner P, Müller-Myhsok B, Döring A et al..  2011.  Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.. Hum Mol Genet. 20(5):1042-7.
Facheris MF, Hicks AA, Minelli C, Hagenah JM, Kostic V, Campbell S, Hayward C, Volpato CB, Pattaro C, Vitart V et al..  2011.  Variation in the uric acid transporter gene SLC2A9 and its association with AAO of Parkinson's disease.. J Mol Neurosci. 43(3):246-50.