De Grandi A - Search Results

1

A catalog of genetic loci associated with kidney function from analyses of a million individuals.

Wuttke M, Li Y, Li M, Sieber KB, Feitosa MF, Gorski M, Tin A, Wang L, Chu AY, Hoppmann A, Kirsten H, Giri A, Chai JF, Sveinbjornsson G, Tayo BO, Nutile T, Fuchsberger C, Marten J, Cocca M, Ghasemi S, Xu Y, Horn K, Noce D, van der Most PJ, Sedaghat S, Yu Z, Akiyama M, Afaq S, Ahluwalia TS, Almgren P, Amin N, Ärnlöv J, Bakker SJL, Bansal N, Baptista D, Bergmann S, Biggs ML, Biino G, Boehnke M, Boerwinkle E, Boissel M, Bottinger EP, Boutin TS, Brenner H, Brumat M, Burkhardt R, Butterworth AS, Campana E, Campbell A, Campbell H, Canouil M, Carroll RJ, Catamo E, Chambers JC, Chee ML, Chee ML, Chen X, Cheng CY, Cheng Y, Christensen K, Cifkova R, Ciullo M, Concas MP, Cook JP, Coresh J, Corre T, Sala CF, Cusi D, Danesh J, Daw EW, de Borst MH, De Grandi A, de Mutsert R, de Vries APJ, Degenhardt F, Delgado G, Demirkan A, Di Angelantonio E, Dittrich K, Divers J, Dorajoo R, Eckardt KU, Ehret G, Elliott P, Endlich K, Evans MK, Felix JF, Foo VHX, Franco OH, Franke A, Freedman BI, Freitag-Wolf S, Friedlander Y, Froguel P, Gansevoort RT, Gao H, Gasparini P, Gaziano JM, Giedraitis V, Gieger C, Girotto G, Giulianini F, Gögele M, Gordon SD, Gudbjartsson DF, Gudnason V, Hal… See abstract for full author list ➔ Wuttke M, et al. Among authors: de borst mh, de grandi a, de mutsert r, de vries apj. Nat Genet. 2019 Jun;51(6):957-972. doi: 10.1038/s41588-019-0407-x. Epub 2019 May 31. Nat Genet. 2019. PMID: 31152163 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: de grandi a. 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: de grandi a. 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: de grandi a. 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: de grandi a. 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: de grandi a. 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. Among authors: de grandi a. 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. 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

Parkin gene modifies the effect of RLS4 on the age at onset of restless legs syndrome (RLS).

Pichler I, Marroni F, Pattaro C, Lohmann K, de Grandi A, Klein C, Hicks AA, Pramstaller PP. Pichler I, et al. Among authors: de grandi a. Am J Med Genet B Neuropsychiatr Genet. 2010 Jan 5;153B(1):350-5. doi: 10.1002/ajmg.b.30988. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19526454

10

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. Among authors: de grandi a. J Mol Neurosci. 2009 Nov;39(3):346-53. doi: 10.1007/s12031-009-9287-3. J Mol Neurosci. 2009. PMID: 19757205

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

47 results

Search Page