Volpato CB - Search Results

1

Silencing of CCR4-NOT complex subunits affects heart structure and function.

Elmén L, Volpato CB, Kervadec A, Pineda S, Kalvakuri S, Alayari NN, Foco L, Pramstaller PP, Ocorr K, Rossini A, Cammarato A, Colas AR, Hicks AA, Bodmer R. Elmén L, et al. Among authors: volpato cb. Dis Model Mech. 2020 Jul 20;13(7):dmm044727. doi: 10.1242/dmm.044727. Dis Model Mech. 2020. PMID: 32471864 Free PMC article.

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

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

7

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

8

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

9

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

10

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.

Sotoodehnia N, Isaacs A, de Bakker PI, Dörr M, Newton-Cheh C, Nolte IM, van der Harst P, Müller M, Eijgelsheim M, Alonso A, Hicks AA, Padmanabhan S, Hayward C, Smith AV, Polasek O, Giovannone S, Fu J, Magnani JW, Marciante KD, Pfeufer A, Gharib SA, Teumer A, Li M, Bis JC, Rivadeneira F, Aspelund T, Köttgen A, Johnson T, Rice K, Sie MP, Wang YA, Klopp N, Fuchsberger C, Wild SH, Mateo Leach I, Estrada K, Völker U, Wright AF, Asselbergs FW, Qu J, Chakravarti A, Sinner MF, Kors JA, Petersmann A, Harris TB, Soliman EZ, Munroe PB, Psaty BM, Oostra BA, Cupples LA, Perz S, de Boer RA, Uitterlinden AG, Völzke H, Spector TD, Liu FY, Boerwinkle E, Dominiczak AF, Rotter JI, van Herpen G, Levy D, Wichmann HE, van Gilst WH, Witteman JC, Kroemer HK, Kao WH, Heckbert SR, Meitinger T, Hofman A, Campbell H, Folsom AR, van Veldhuisen DJ, Schwienbacher C, O'Donnell CJ, Volpato CB, Caulfield MJ, Connell JM, Launer L, Lu X, Franke L, Fehrmann RS, te Meerman G, Groen HJ, Weersma RK, van den Berg LH, Wijmenga C, Ophoff RA, Navis G, Rudan I, Snieder H, Wilson JF, Pramstaller PP, Siscovick DS, Wang TJ, Gudnason V, van Duijn CM, Felix SB, Fishman GI, Jamshidi Y, Stricker BH, Samani NJ, Kääb S, Arking… See abstract for full author list ➔ Sotoodehnia N, et al. Among authors: volpato cb. Nat Genet. 2010 Dec;42(12):1068-76. doi: 10.1038/ng.716. Epub 2010 Nov 14. Nat Genet. 2010. PMID: 21076409 Free PMC article.

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