Gianfrancesco F - Search Results

1

Identification of sixteen novel candidate genes for late onset Parkinson's disease.

Gialluisi A, Reccia MG, Modugno N, Nutile T, Lombardi A, Di Giovannantonio LG, Pietracupa S, Ruggiero D, Scala S, Gambardella S; International Parkinson’s Disease Genomics Consortium (IPDGC); Iacoviello L, Gianfrancesco F, Acampora D, D'Esposito M, Simeone A, Ciullo M, Esposito T. Gialluisi A, et al. Among authors: gianfrancesco f. Mol Neurodegener. 2021 Jun 21;16(1):35. doi: 10.1186/s13024-021-00455-2. Mol Neurodegener. 2021. PMID: 34148545 Free PMC article.

2

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation.

D'Esposito M, Ciccodicola A, Gianfrancesco F, Esposito T, Flagiello L, Mazzarella R, Schlessinger D, D'Urso M. D'Esposito M, et al. Among authors: gianfrancesco f. Nat Genet. 1996 Jun;13(2):227-9. doi: 10.1038/ng0696-227. Nat Genet. 1996. PMID: 8640232

3

Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome.

Gianfrancesco F, Esposito T, Ruini L, Houlgatte R, Nagaraja R, D'Esposito M, Rocchi M, Auffray C, Schlessinger D, D'Urso M, Forabosco A. Gianfrancesco F, et al. Gene. 1997 Mar 18;187(2):179-84. doi: 10.1016/s0378-1119(96)00743-3. Gene. 1997. PMID: 9099878

4

Characterization of the murine orthologue of a novel human subtelomeric multigene family.

Gianfrancesco F, Falco G, Esposito T, Rocchi M, D'Urso M. Gianfrancesco F, et al. Cytogenet Cell Genet. 2001;94(1-2):98-100. doi: 10.1159/000048796. Cytogenet Cell Genet. 2001. PMID: 11701968 No abstract available.

5

[Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis].

Gianfrancesco F, Esposito T. Gianfrancesco F, et al. Minerva Med. 2005 Dec;96(6):409-16. Minerva Med. 2005. PMID: 16518303 Review. Italian.

6

Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.

Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F. Gianfrancesco F, et al. Am J Med Genet B Neuropsychiatr Genet. 2007 Jul 5;144B(5):691-5. doi: 10.1002/ajmg.b.30381. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440989

7

DDX11L: a novel transcript family emerging from human subtelomeric regions.

Costa V, Casamassimi A, Roberto R, Gianfrancesco F, Matarazzo MR, D'Urso M, D'Esposito M, Rocchi M, Ciccodicola A. Costa V, et al. Among authors: gianfrancesco f. BMC Genomics. 2009 May 28;10:250. doi: 10.1186/1471-2164-10-250. BMC Genomics. 2009. PMID: 19476624 Free PMC article.

8

Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility.

Formicola D, Aloia A, Sampaolo S, Farina O, Diodato D, Griffiths LR, Gianfrancesco F, Di Iorio G, Esposito T. Formicola D, et al. Among authors: gianfrancesco f. BMC Med Genet. 2010 Jun 25;11:103. doi: 10.1186/1471-2350-11-103. BMC Med Genet. 2010. PMID: 20579352 Free PMC article.

9

piR_015520 belongs to Piwi-associated RNAs regulates expression of the human melatonin receptor 1A gene.

Esposito T, Magliocca S, Formicola D, Gianfrancesco F. Esposito T, et al. Among authors: gianfrancesco f. PLoS One. 2011;6(7):e22727. doi: 10.1371/journal.pone.0022727. Epub 2011 Jul 26. PLoS One. 2011. PMID: 21818375 Free PMC article.

10

Giant cell tumor occurring in familial Paget's disease of bone: report of clinical characteristics and linkage analysis of a large pedigree.

Gianfrancesco F, Rendina D, Merlotti D, Esposito T, Amyere M, Formicola D, Muscariello R, De Filippo G, Strazzullo P, Nuti R, Vikkula M, Gennari L. Gianfrancesco F, et al. J Bone Miner Res. 2013 Feb;28(2):341-50. doi: 10.1002/jbmr.1750. J Bone Miner Res. 2013. PMID: 22936311 Free article.

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