List of works - Elvezia Maria Paraboschi

A frequent oligogenic involvement in congenital hypothyroidism.

scientific article published on 21 April 2017

ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

scientific article published on 02 April 2020

Abiotic ligation of DNA oligomers templated by their liquid crystal ordering

scientific article

Corrigendum: Abiotic ligation of DNA oligomers templated by their liquid crystal ordering

scientific article published on 17 June 2015

DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease

scientific article published on 24 November 2021

Exploring the global landscape of genetic variation in coagulation factor XI deficiency.

scientific article published on 14 June 2017

Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains

scientific article published on 14 December 2017

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

scientific article

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients

scientific article published on December 2011

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.

scientific article published on 21 October 2014

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

scientific article

Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay

scientific article published on 30 November 2014

Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiency

scientific article published on 26 May 2011

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

scientific article

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.

scientific article

Molecular investigation of 41 patients affected by coagulation factor XI deficiency.

scientific article published on 27 November 2017

Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia

scientific article published on 09 December 2011

Phase behavior and critical activated dynamics of limited-valence DNA nanostars

scientific article published on 09 September 2013

The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis.

scientific article published on 07 March 2017

miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA.

scientific article published on 14 February 2017

List of works by Elvezia Maria Paraboschi

A frequent oligogenic involvement in congenital hypothyroidism.

ACE2 and TMPRSS2 variants and expression as candidates to sex and country differences in COVID-19 severity in Italy

Abiotic ligation of DNA oligomers templated by their liquid crystal ordering

Corrigendum: Abiotic ligation of DNA oligomers templated by their liquid crystal ordering

DNA Methylation Signature in Monozygotic Twins Discordant for Psoriatic Disease

Exploring the global landscape of genetic variation in coagulation factor XI deficiency.

Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains

Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

Genetic association and altered gene expression of mir-155 in multiple sclerosis patients

Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.

Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis.

Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay

Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiency

Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern.

Molecular investigation of 41 patients affected by coagulation factor XI deficiency.

Notch1 regulates chemotaxis and proliferation by controlling the CC-chemokine receptors 5 and 9 in T cell acute lymphoblastic leukaemia

Phase behavior and critical activated dynamics of limited-valence DNA nanostars

The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis.

miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA.