Volpato CB - Search Results

1

Variation in the uric acid transporter gene SLC2A9 and its association with AAO of Parkinson's disease.

Facheris MF, Hicks AA, Minelli C, Hagenah JM, Kostic V, Campbell S, Hayward C, Volpato CB, Pattaro C, Vitart V, Wright A, Campbell H, Klein C, Pramstaller PP. Facheris MF, et al. Among authors: volpato cb. J Mol Neurosci. 2011 Mar;43(3):246-50. doi: 10.1007/s12031-010-9409-y. Epub 2010 Jun 30. J Mol Neurosci. 2011. PMID: 20589538

2

Restless legs syndrome: epidemiological and clinicogenetic study in a South Tyrolean population isolate.

Vogl FD, Pichler I, Adel S, Pinggera GK, Bracco S, De Grandi A, Volpato CB, Aridon P, Mayer T, Meitinger T, Klein C, Casari G, Pramstaller PP. Vogl FD, et al. Among authors: volpato cb. Mov Disord. 2006 Aug;21(8):1189-95. doi: 10.1002/mds.20922. Mov Disord. 2006. PMID: 16685686

3

Linkage analysis identifies a novel locus for restless legs syndrome on chromosome 2q in a South Tyrolean population isolate.

Pichler I, Marroni F, Volpato CB, Gusella JF, Klein C, Casari G, De Grandi A, Pramstaller PP. Pichler I, et al. Among authors: volpato cb. Am J Hum Genet. 2006 Oct;79(4):716-23. doi: 10.1086/507875. Epub 2006 Aug 14. Am J Hum Genet. 2006. PMID: 16960808 Free PMC article.

4

Population isolates in South Tyrol and their value for genetic dissection of complex diseases.

Marroni F, Pichler I, De Grandi A, Volpato CB, Vogl FD, Pinggera GK, Bailey-Wilson JE, Pramstaller PP. Marroni F, et al. Among authors: volpato cb. Ann Hum Genet. 2006 Nov;70(Pt 6):812-21. doi: 10.1111/j.1469-1809.2006.00274.x. Ann Hum Genet. 2006. PMID: 17044856

5

Genetic structure in contemporary south Tyrolean isolated populations revealed by analysis of Y-chromosome, mtDNA, and Alu polymorphisms.

Pichler I, Mueller JC, Stefanov SA, De Grandi A, Volpato CB, Pinggera GK, Mayr A, Ogriseg M, Ploner F, Meitinger T, Pramstaller PP. Pichler I, et al. Among authors: volpato cb. Hum Biol. 2006 Aug;78(4):441-64. doi: 10.1353/hub.2006.0057. Hum Biol. 2006. PMID: 17278620

6

The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives.

Pattaro C, Marroni F, Riegler A, Mascalzoni D, Pichler I, Volpato CB, Dal Cero U, De Grandi A, Egger C, Eisendle A, Fuchsberger C, Gögele M, Pedrotti S, Pinggera GK, Stefanov SA, Vogl FD, Wiedermann CJ, Meitinger T, Pramstaller PP. Pattaro C, et al. Among authors: volpato cb. BMC Med Genet. 2007 Jun 5;8:29. doi: 10.1186/1471-2350-8-29. BMC Med Genet. 2007. PMID: 17550581 Free PMC article.

7

Exclusion of linkage to chromosome 14q in a large South Tyrolean family with Idiopathic Basal Ganglia Calcification (IBGC).

Volpato CB, De Grandi A, Buffone E, Pichler I, Gebert U, Schifferle G, Schönhuber R, Pramstaller PP. Volpato CB, et al. Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1319-22. doi: 10.1002/ajmg.b.30748. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18361429

8

ParkScreen: a low-cost rapid linkage marker panel for Parkinson's disease.

De Grandi A, Volpato CB, Bedin E, Pattaro C, Marroni F, Pichler I, Hicks AA, Casari G, Pramstaller PP. De Grandi A, et al. Among authors: volpato cb. J Mol Neurosci. 2009 Sep;39(1-2):235-41. doi: 10.1007/s12031-009-9193-8. Epub 2009 Mar 25. J Mol Neurosci. 2009. PMID: 19319700

9

2q37 as a susceptibility locus for idiopathic basal ganglia calcification (IBGC) in a large South Tyrolean family.

Volpato CB, De Grandi A, Buffone E, Facheris M, Gebert U, Schifferle G, Schönhuber R, Hicks A, Pramstaller PP. Volpato CB, et al. J Mol Neurosci. 2009 Nov;39(3):346-53. doi: 10.1007/s12031-009-9287-3. J Mol Neurosci. 2009. PMID: 19757205

10

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.

Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Mägi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpeläinen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Lango Allen H, Weyant RJ, Wheeler E, Wood AR; MAGIC; Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Smith AV, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proença C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman … See abstract for full author list ➔ Heid IM, et al. Among authors: volpato cb. Nat Genet. 2010 Nov;42(11):949-60. doi: 10.1038/ng.685. Epub 2010 Oct 10. Nat Genet. 2010. PMID: 20935629 Free PMC article.

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