Biblio

Found 25 results
Filters: Author is Tanaka, Toshiko  [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.
Parsa A, Fuchsberger C, Köttgen A, O'Seaghdha CM, Pattaro C, de Andrade M, Chasman DI, Teumer A, Endlich K, Olden M et al..  2013.  Common variants in mendelian kidney disease genes and their association with renal function.. J Am Soc Nephrol. 24(12):2105-17.
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.
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.
O'Seaghdha CM, Wu H, Yang Q, Kapur K, Guessous I, Zuber AMercier, Köttgen A, Stoudmann C, Teumer A, Kutalik Z et al..  2013.  Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.. PLoS Genet. 9(9):e1003796.
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.
2011
Böger CA, Chen M-H, Tin A, Olden M, Köttgen A, de Boer IH, Fuchsberger C, O'Seaghdha CM, Pattaro C, Teumer A et al..  2011.  CUBN is a gene locus for albuminuria.. J Am Soc Nephrol. 22(3):555-70.
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.
Wain LV, Verwoert GC, O'Reilly PF, Shi G, Johnson T, Johnson AD, Bochud M, Rice KM, Henneman P, Smith AV et al..  2011.  Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.. Nat Genet. 43(10):1005-11.
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.
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.
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.
Kilpeläinen TO, Qi L, Brage S, Sharp SJ, Sonestedt E, Demerath E, Ahmad T, Mora S, Kaakinen M, Sandholt C H et al..  2011.  Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children.. PLoS Med. 8(11):e1001116.