Gian Antonio Danieli
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Explore the profile of Gian Antonio Danieli including associated specialties, affiliations and a list of published articles.
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32
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1438
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Recent Articles
1.
Roux-Buisson N, Rendu J, Denjoy I, Guicheney P, Goldenberg A, David N, et al.
Hum Mutat
. 2011 May;
32(9):995-9.
PMID: 21618644
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and severe arrhythmogenic disorder. Although usually transmitted in a recessive form, few cases of dominant mutations have been reported. Thirteen mutations in...
2.
Lenzi L, Facchin F, Piva F, Giulietti M, Pelleri M, Frabetti F, et al.
BMC Genomics
. 2011 Feb;
12:121.
PMID: 21333005
Background: Several tools have been developed to perform global gene expression profile data analysis, to search for specific chromosomal regions whose features meet defined criteria as well as to study...
3.
De Bortoli M, Beffagna G, Bauce B, Lorenzon A, Smaniotto G, Rigato I, et al.
Eur J Hum Genet
. 2010 Mar;
18(7):776-82.
PMID: 20197793
Mutations in genes encoding desmosomal proteins have been reported to cause arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D), an autosomal-dominant disease characterised by progressive myocardial atrophy with fibro-fatty replacement. We screened 112...
4.
Xu T, Yang Z, Vatta M, Rampazzo A, Beffagna G, Pilichou K, et al.
J Am Coll Cardiol
. 2010 Feb;
55(6):587-97.
PMID: 20152563
Objectives: The aim of this study was to define the genetic basis of arrhythmogenic right ventricular cardiomyopathy (ARVC). Background: Arrhythmogenic right ventricular cardiomyopathy, characterized by right ventricular fibrofatty replacement and...
5.
Bauce B, Nava A, Beffagna G, Basso C, Lorenzon A, Smaniotto G, et al.
Heart Rhythm
. 2010 Feb;
7(1):22-9.
PMID: 20129281
Background: Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a progressive cardiomyopathy showing a wide clinical spectrum in terms of clinical expressions and prognoses. Objective: This study sought to estimate the occurrence...
6.
Coppe A, Ferrari F, Bisognin A, Danieli G, Ferrari S, Bicciato S, et al.
Nucleic Acids Res
. 2008 Dec;
37(2):533-49.
PMID: 19059999
Genes co-expressed may be under similar promoter-based and/or position-based regulation. Although data on expression, position and function of human genes are available, their true integration still represents a challenge for...
7.
Ferrari F, Bortoluzzi S, Coppe A, Sirota A, Safran M, Shmoish M, et al.
BMC Bioinformatics
. 2007 Nov;
8:446.
PMID: 18005434
Background: Improvements in genome sequence annotation revealed discrepancies in the original probeset/gene assignment in Affymetrix microarray and the existence of differences between annotations and effective alignments of probes and transcription...
8.
Beffagna G, De Bortoli M, Nava A, Salamon M, Lorenzon A, Zaccolo M, et al.
BMC Med Genet
. 2007 Oct;
8:65.
PMID: 17963498
Background: Mutations in genes encoding desmosomal proteins have been reported to cause arrhythmogenic right ventricular cardiomyopathy (ARVC), an autosomal dominant disease characterised by progressive myocardial atrophy with fibro-fatty replacement. We...
9.
Ferrari F, Bortoluzzi S, Coppe A, Basso D, Bicciato S, Zini R, et al.
BMC Genomics
. 2007 Aug;
8:264.
PMID: 17683550
Background: Human myelopoiesis is an exciting biological model for cellular differentiation since it represents a plastic process where multipotent stem cells gradually limit their differentiation potential, generating different precursor cells...
10.
Frigo G, Rampazzo A, Bauce B, Pilichou K, Beffagna G, Danieli G, et al.
Europace
. 2007 Apr;
9(6):391-7.
PMID: 17442746
Aims: To describe a patient showing monomorphic ventricular tachycardia, ECG aspect of Brugada syndrome, and structural heart abnormalities due to a homozygous missense mutation in SCN5A. Methods And Results: Thirteen...