Gian Antonio Danieli

Biochemistry, Genetics and Molecular Biology · Life Sciences

34h-index7.4kcitations94works0.02yr avg
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Research Topics

Muscle Physiology and Disorders(22), Cardiovascular Effects of Exercise(21), Cardiomyopathy and Myosin Studies(18), RNA Research and Splicing(16), Sports injuries and prevention(12)

Publications94 total

Stephen J. Gould: The Scientific Legacy
2013· 8 cited
Functional analysis reveals splicing mutations of the CASQ2 gene in patients with CPVT: implication for genetic counselling and clinical management
Human Mutation·2011· 14 cited
TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources
BMC Genomics·2011· 32 citedOpen Access
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy
European Journal of Human Genetics·2010· 27 citedOpen Access
Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy
Journal of the American College of Cardiology·2010· 314 cited
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Heart Rhythm·2009· 183 cited
The Two Cultures: Shared Problems
2009· 11 cited
General Discussion on the Themes of the First Section
2009
Motif discovery in promoters of genes co-localized and co-expressed during myeloid cells differentiation
Nucleic Acids Research·2008· 18 citedOpen Access
Screening di mutazioni patogene nei quattro geni più frequentemente implicati nella cardiomiopatia ipertrofica
Research Padua Archive (University of Padua)·2008
DNA resequencing array for mutation detection in hypertrophic cardiomyopathy
Research Padua Archive (University of Padua)·2008
Novel definition files for human GeneChips based on GeneAnnot
BMC Bioinformatics·2007· 109 citedOpen Access
Advances in Genetics: Dominant Forms
2007· 6 cited
Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro
BMC Medical Genetics·2007· 79 citedOpen Access
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities
EP Europace·2007· 49 citedOpen Access
Genomic expression during human myelopoiesis
BMC Genomics·2007· 31 citedOpen Access
REEF: searching REgionally Enriched Features in genomes
BMC Bioinformatics·2006· 40 citedOpen Access
Desmosomal Dysfunction due to Mutations in Desmoplakin Causes Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Circulation Research·2006· 318 citedOpen Access
Mutations in Desmoglein-2 Gene Are Associated With Arrhythmogenic Right Ventricular Cardiomyopathy
Circulation·2006· 572 citedOpen Access
Computational reconstruction of the human skeletal muscle secretome
Proteins Structure Function and Bioinformatics·2005· 136 cited
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Frequent Co-authors

Alessandra Rampazzo(19), Andrea Nava(15), Stefania Bortoluzzi(15), Barbara Bauce(13), Cristina Basso(11), Gaetano Thiene(11), Giorgia Beffagna(10), Natascia Tiso(8), Libero Vitiello(6), Alessandro Coppe(6), Rosanna Zimbello(5), Jeffrey A. Towbin(5), Alessandra Lorenzon(5), C. Angelini(5), Gerolamo Lanfranchi(5), Luciano Daliento(4), Fabio d’Alessi(4), Alessia Bagattin(4), Francesco Mari(4), Sérgio Ferrari(4)