Biblio

Found 18 results
Filters: Author is Pattaro, Cristian  [Clear All Filters]
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.
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.
Gögele M, Pattaro C, Fuchsberger C, Minelli C, Pramstaller PP, Wjst M.  2011.  Heritability analysis of life span in a semi-isolated population followed across four centuries reveals the presence of pleiotropy between life span and reproduction.. J Gerontol A Biol Sci Med Sci. 66(1):26-37.
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.
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.