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Silvia Pulignani

Observed names: PULIGNANI, SILVIA, Pulignani Silvia, S Pulignani
ORCID: 0000-0003-2097-3160
Observed ORCID: 0000-0003-2097-3160
OpenAlex ID: A5058988154
Congenital Heart Disease: The Crossroads of Genetics, Epigenetics and Environment
2014 · Cecilia Vecoli, Silvia Pulignani, et al. · Current Genomics · 98
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Maternal and Paternal Environmental Risk Factors, Metabolizing GSTM1 and GSTT1 Polymorphisms, and Congenital Heart Disease
2011 · Monica Cresci, Ilenia Foffa, et al. · The American Journal of Cardiology · 73
Prognostic value of mitochondrial DNA4977 deletion and mitochondrial DNA copy number in patients with stable coronary artery disease
2018 · Cecilia Vecoli, Andrea Borghini, et al. · Atherosclerosis · 42
Altered DNA methylation indicates an oscillatory flow mediated epithelial-to-mesenchymal transition signature in ascending aorta of patients with bicuspid aortic valve
2018 · Hanna M. Björck, Lei Du, et al. · Scientific Reports · 40
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Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease
2018 · Silvia Pulignani, Cecilia Vecoli, et al. · Pediatric Cardiology · 32
Genetic and Epigenetic Mechanisms Linking Air Pollution and Congenital Heart Disease
2016 · Cecilia Vecoli, Silvia Pulignani, et al. · Journal of Cardiovascular Development and Disease · 31
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Radiobiological Effectiveness of Ultrashort Laser-Driven Electron Bunches: Micronucleus Frequency, Telomere Shortening and Cell Viability
2016 · Maria Grazia Andreassi, Andrea Borghini, et al. · Radiation Research · 30
Independent and Combined Effects of Telomere Shortening and mtDNA4977 Deletion on Long-term Outcomes of Patients with Coronary Artery Disease
2019 · Cecilia Vecoli, Andrea Borghini, et al. · International Journal of Molecular Sciences · 26
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Holt–Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: Functional characterization of a de novo TBX5 mutation
2014 · Anwar Baban, Letizia Pitto, et al. · American Journal of Medical Genetics Part A · 26
Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects
2013 · Saverio Sabina, Silvia Pulignani, et al. · Journal of Molecular and Cellular Cardiology · 24
miRNome Profiling in Bicuspid Aortic Valve-Associated Aortopathy by Next-Generation Sequencing
2017 · Andrea Borghini, Ilenia Foffa, et al. · International Journal of Molecular Sciences · 22
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Maternal Environmental Exposure, Infant GSTP1 Polymorphism, and Risk of Isolated Congenital Heart Disease
2012 · Monica Cresci, Ilenia Foffa, et al. · Pediatric Cardiology · 17
3’UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease
2016 · Silvia Pulignani, Cecilia Vecoli, et al. · Revista Española de Cardiología (English Edition) · 14
Influence of genetic polymorphisms in DICER and XPO5 genes on the risk of coronary artery disease and circulating levels of vascular miRNAs
2019 · Andrea Borghini, Silvia Pulignani, et al. · Thrombosis Research · 12
LESM: a laser-driven sub-MeV electron source delivering ultra-high dose rate on thin biological samples
2016 · L Labate, M G Andreassi, et al. · Journal of Physics D Applied Physics · 11
MicroRNAs and Congenital Heart Disease: Where Are We Now?
2018 · Silvia Pulignani, Maria Grazia Andreassi · Revista Española de Cardiología (English Edition) · 9
Lack of Association of the 3′-UTR Polymorphism (rs1017) in the ISL1 Gene and Risk of Congenital Heart Disease in the White Population
2012 · Monica Cresci, Cecilia Vecoli, et al. · Pediatric Cardiology · 9
microRNAs in bicuspid aortic valve associated aortopathy: Recent advances and future perspectives
2019 · Silvia Pulignani, Andrea Borghini, et al. · Journal of Cardiology · 8
Functional characterization and circulating expression profile of dysregulated microRNAs in BAV-associated aortopathy
2019 · Silvia Pulignani, Andrea Borghini, et al. · Heart and Vessels · 7
El papel de los microARN en las cardiopatías congénitas: qué sabemos
2018 · Silvia Pulignani, Maria Grazia Andreassi · Revista Española de Cardiología · 7
Los polimorfismos de nucleótido único y los haplotipos de la región 3’UTR del gen GATA4 contribuyen al riesgo genético de cardiopatía congénita
2016 · Silvia Pulignani, Cecilia Vecoli, et al. · Revista Española de Cardiología · 7
Screening genetico di Gata4 e Nkx2,5 nelle cardiopatie congenite: cinque casi familiari
2011 · Silvia Pulignani, Ilenia Foffa, et al. · Recenti Progressi in Medicina · 4
A Functional Aryl Hydrocarbon Receptor Genetic Variant, Alone and in Combination with Parental Exposure, is a Risk Factor for Congenital Heart Disease
2017 · Silvia Pulignani, Andrea Borghini, et al. · Cardiovascular Toxicology · 3
Genetics of congenital heart defects: is it not all in the DNA?
2012 · Silvia Pulignani, Monica Cresci, et al. · Translational research · 3
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[A novel lamin A/C mutation in a family with dilated cardiomyopathy and a strong history of sudden cardiac death].
2010 · Maria Grazia Andreassi, Nicoletta Botto, et al. · PubMed · 1
Works count: 34
Citation count: 556
H-index: 13
I10-index: 15
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