List of works - Silvia Galbiati

10. Circulating Nucleic Acids as Diagnostic Tool

scientific article published on 03 April 2008

A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia

scientific article published in January 2008

A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer

scientific article

Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator gene

scientific article published in January 2009

COLD-PCR and Innovative Microarray Substrates for Detecting and Genotyping MPL Exon 10 W515 Substitutions

scientific article published on 11 October 2012

COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.

scientific article published on 24 February 2016

Cellular microchimerism as a lifelong physiologic status in parous women: An immunologic basis for its amplification in patients with systemic sclerosis

scientific article published on 01 April 2003

Communicating Down syndrome risk according to maternal age: "1-in-X" effect on perceived risk.

scientific article published on 9 June 2015

Correlation of fetal DNA levels in maternal plasma with Doppler status in pathological pregnancies

scientific article

DNA microarray-based solid-phase PCR on copoly (DMA-NAS-MAPS) silicon coated slides: An example of relevant clinical application.

scientific article published in December 2015

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

scientific article published on 10 June 2004

Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA-Mediated Enriched PCR

scientific article published on 01 September 2006

Droplet digital polymerase chain reaction for DNMT3A and IDH1/2 mutations to improve early detection of acute myeloid leukemia relapse after allogeneic hematopoietic stem cell transplantation.

scientific article published on 24 December 2015

Evaluation of a panel of circulating DNA, RNA and protein potential markers for pathologies of pregnancy

scholarly article by Silvia Galbiati et al published 1 January 2010 in Clinical Chemistry and Laboratory Medicine

Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseases

scientific article published in June 2004

Fetal DNA detection in maternal plasma throughout gestation

Fetal DNA in Maternal Plasma in Twin Pregnancies

scientific article published on 01 September 2003

Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.

scientific article published on 16 April 2012

Further considerations concerning non-invasive prenatal diagnosis of craniosynostosis based on the identification of an 18 bp deletion in the TWIST1 gene by COLD-PCR.

scientific article

HIF1A and MIF as potential predictive mRNA biomarkers of pre-eclampsia: a longitudinal prospective study in high risk population

scientific article

High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasma

scientific article published on 01 January 2009

High-throughput mutational screening for beta-thalassemia by single-nucleotide extension

scientific article published on 01 December 2007

Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case report.

scientific article

International Interlaboratory Digital PCR Study Demonstrating High Reproducibility for the Measurement of a Rare Sequence Variant

scientific article published on 9 December 2016

Membrane-binding peptides for extracellular vesicles on-chip analysis

scientific article published on 17 April 2020

New trend in non-invasive prenatal diagnosis

scientific article published on 23 December 2014

No evidence of fetal DNA persistence in maternal plasma after pregnancy

article

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.

scientific article

Predictive biomarkers of pre-eclampsia and effectiveness of preventative interventions for the disease

scientific article published on 26 April 2014

Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract

scientific article published on 01 February 2003

Prospective evaluation of RASSF1A cell-free DNA as a biomarker of pre-eclampsia

scientific article

Scanning mutations of the 5'UTR regulatory sequence of l-ferritin by denaturing high-performance liquid chromatography: identification of new mutations

scientific article published on 01 April 2003

Workshop report on the extraction of foetal DNA from maternal plasma

article

List of works by Silvia Galbiati

10. Circulating Nucleic Acids as Diagnostic Tool

A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia

A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer

Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator gene

COLD-PCR and Innovative Microarray Substrates for Detecting and Genotyping MPL Exon 10 W515 Substitutions

COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.

Cellular microchimerism as a lifelong physiologic status in parous women: An immunologic basis for its amplification in patients with systemic sclerosis

Communicating Down syndrome risk according to maternal age: "1-in-X" effect on perceived risk.

Correlation of fetal DNA levels in maternal plasma with Doppler status in pathological pregnancies

DNA microarray-based solid-phase PCR on copoly (DMA-NAS-MAPS) silicon coated slides: An example of relevant clinical application.

Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations.

Different Approaches for Noninvasive Prenatal Diagnosis of Genetic Diseases Based on PNA-Mediated Enriched PCR

Droplet digital polymerase chain reaction for DNMT3A and IDH1/2 mutations to improve early detection of acute myeloid leukemia relapse after allogeneic hematopoietic stem cell transplantation.

Evaluation of a panel of circulating DNA, RNA and protein potential markers for pathologies of pregnancy

Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseases

Fetal DNA detection in maternal plasma throughout gestation

Fetal DNA in Maternal Plasma in Twin Pregnancies

Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.

Further considerations concerning non-invasive prenatal diagnosis of craniosynostosis based on the identification of an 18 bp deletion in the TWIST1 gene by COLD-PCR.

HIF1A and MIF as potential predictive mRNA biomarkers of pre-eclampsia: a longitudinal prospective study in high risk population

High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasma

High-throughput mutational screening for beta-thalassemia by single-nucleotide extension

Identification of an 18 bp deletion in the TWIST1 gene by CO-amplification at lower denaturation temperature-PCR (COLD-PCR) for non-invasive prenatal diagnosis of craniosynostosis: first case report.

International Interlaboratory Digital PCR Study Demonstrating High Reproducibility for the Measurement of a Rare Sequence Variant

Membrane-binding peptides for extracellular vesicles on-chip analysis

New trend in non-invasive prenatal diagnosis

No evidence of fetal DNA persistence in maternal plasma after pregnancy

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.

Predictive biomarkers of pre-eclampsia and effectiveness of preventative interventions for the disease

Prevalence of hereditary hyperferritinemia-cataract syndrome in blood donors and patients with cataract

Prospective evaluation of RASSF1A cell-free DNA as a biomarker of pre-eclampsia

Scanning mutations of the 5'UTR regulatory sequence of l-ferritin by denaturing high-performance liquid chromatography: identification of new mutations

Workshop report on the extraction of foetal DNA from maternal plasma