Lista de obras -

8-Oxoguanine DNA-glycosylase repair activity and expression: a comparison between cryopreserved isolated lymphocytes and EBV-derived lymphoblastoid cell lines.

artículo científico publicado en 2010

A genome-wide association study for malignant mesothelioma risk.

artículo científico publicado en 2013

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

scientific journal article

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

artículo científico publicado en 2010

Association Between Aryl Hydrocarbon Receptor Genotype and Survival in Soft Tissue Sarcoma

scientific article published on 01 October 2004

Association between Beta1 -Adrenergic Receptor Polymorphism and Risk of ICD Shock in Heart Failure Patients.

artículo científico publicado en 2016

Association between total number of deaths, diabetes mellitus, incident cancers, and haplotypes in chromosomal region 8q24 in a prospective study

artículo científico publicado en 2012

Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults

Association study of the I/D polymorphism and plasma angiotensin-converting enzyme (ACE) as risk factors for stent restenosis.

artículo científico publicado en 2004

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Author Correction: Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

scientific article published in Scientific Reports

B-vitamins intake, DNA-methylation of One Carbon Metabolism and homocysteine pathway genes and myocardial infarction risk: the EPICOR study

artículo científico publicado en 2013

Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study.

artículo científico publicado en 2003

Correction: genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.

artículo científico publicado en 2015

DNA Methylation of FKBP5 as Predictor of Overall Survival in Malignant Pleural Mesothelioma

artículo científico publicado en 2020

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

artículo científico publicado en 2016

DNA repair gene expression level in peripheral blood and tumour tissue from non-small cell lung cancer and head and neck squamous cell cancer patients.

artículo científico publicado en 2012

Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome

artículo científico publicado en 2009

ERCC1 haplotypes modify bladder cancer risk: a case-control study

artículo científico publicado en 2010

Effect of angiotensin-converting enzyme inhibition on restenosis after coronary stenting

article

Epigenetic Signatures at AQP3 and SOCS3 Engage in Low-Grade Inflammation across Different Tissues

artículo científico publicado en 2016

Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity

artículo científico publicado en 2016

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene

artículo científico publicado en 2011

Gene-asbestos interaction in malignant pleural mesothelioma susceptibility.

artículo científico publicado en 2015

Gene-specific DNA methylation profiles and LINE-1 hypomethylation are associated with myocardial infarction risk

artículo científico publicado en 2015

Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.

artículo científico publicado en 2013

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

scientific journal article

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

artículo científico publicado en 2014

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

artículo científico publicado en 2011

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

artículo científico publicado en 2021

Germline mutations in DNA repair genes predispose asbestos-exposed patients to malignant pleural mesothelioma

artículo científico publicado en 2017

Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

artículo científico publicado en 2016

Inference on germline BAP1 mutations and asbestos exposure from the analysis of familial and sporadic mesothelioma in a high-risk area

artículo científico publicado en 2014

Inter-individual variation in nucleotide excision repair pathway is modulated by non-synonymous polymorphisms in ERCC4 and MBD4 genes.

artículo científico publicado en 2013

Interaction between gene polymorphisms of nitric oxide synthase and renin-angiotensin system in the progression of membranous glomerulonephritis.

artículo científico publicado en 2004

Lactase persistence and bitter taste response: instrumental variables and mendelian randomization in epidemiologic studies of dietary factors and cancer risk

artículo científico publicado en 2007

Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

artículo científico publicado en 2017

Novel epigenetic changes unveiled by monozygotic twins discordant for smoking habits.

artículo científico publicado en 2015

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

artículo científico publicado en 2016

Peripheral blood DNA methylation as potential biomarker of Malignant Pleural Mesothelioma in asbestos-exposed subjects

artículo científico publicado en 2018

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

scientific article published on 29 October 2019

Polymorphisms in DNA repair genes as risk factors for asbestos-related malignant mesothelioma in a general population study.

artículo científico

Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer

artículo científico publicado en 2009

Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients. Italian Group of Renal Immunopathology

scientific article published on 01 December 1998

Polymorphisms in the XRCC1 gene modify survival of bladder cancer patients treated with chemotherapy

artículo científico publicado en 2013

Role of TGF-beta1 haplotypes in the occurrence of myocardial infarction in young Italian patients.

artículo científico publicado en 2008

Role of the 12q24.12 locus in the onset of preeclampsia: an Italian case-control study.

artículo científico publicado en 2011

Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection.

artículo científico publicado en 2014

Seventy-five nuclear DNA polymorphisms in an Italian sample: a comparative worldwide study.

artículo científico publicado en 1997

Synergistic effect of renin-angiotensin system and nitric oxide synthase genes polymorphisms in pre-eclampsia

article

Telomerase activity, telomere length and hTERT DNA methylation in peripheral blood mononuclear cells from monozygotic twins with discordant smoking habits.

artículo científico

Telomere length variation in juvenile acute myocardial infarction.

artículo científico publicado en 2012

The Italian genome reflects the history of Europe and the Mediterranean basin

artículo científico publicado en 2015

The TDI-FP Assay in Human Y Chromosome SNP Haplotyping

scientific article published on 01 January 2004

Unsuitability of lymphoblastoid cell lines as surrogate of cryopreserved isolated lymphocytes for the analysis of DNA double-strand break repair activity.

artículo científico publicado en 2009

XRCC1 and ERCC1 variants modify malignant mesothelioma risk: A case–control study

artículo científico publicado en 2011

Lista de obras de

8-Oxoguanine DNA-glycosylase repair activity and expression: a comparison between cryopreserved isolated lymphocytes and EBV-derived lymphoblastoid cell lines.

A genome-wide association study for malignant mesothelioma risk.

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Association Between Aryl Hydrocarbon Receptor Genotype and Survival in Soft Tissue Sarcoma

Association between Beta1 -Adrenergic Receptor Polymorphism and Risk of ICD Shock in Heart Failure Patients.

Association between total number of deaths, diabetes mellitus, incident cancers, and haplotypes in chromosomal region 8q24 in a prospective study

Association of maternal prenatal smoking GFI1-locus and cardio-metabolic phenotypes in 18,212 adults

Association study of the I/D polymorphism and plasma angiotensin-converting enzyme (ACE) as risk factors for stent restenosis.

Associations of autozygosity with a broad range of human phenotypes

Author Correction: Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

B-vitamins intake, DNA-methylation of One Carbon Metabolism and homocysteine pathway genes and myocardial infarction risk: the EPICOR study

Combination of DNA repair gene single nucleotide polymorphisms and increased levels of DNA adducts in a population-based study.

Correction: genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.

DNA Methylation of FKBP5 as Predictor of Overall Survival in Malignant Pleural Mesothelioma

DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases

DNA repair gene expression level in peripheral blood and tumour tissue from non-small cell lung cancer and head and neck squamous cell cancer patients.

Differential Greek and northern African migrations to Sicily are supported by genetic evidence from the Y chromosome

ERCC1 haplotypes modify bladder cancer risk: a case-control study

Effect of angiotensin-converting enzyme inhibition on restenosis after coronary stenting

Epigenetic Signatures at AQP3 and SOCS3 Engage in Low-Grade Inflammation across Different Tissues

Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity

European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene

Gene-asbestos interaction in malignant pleural mesothelioma susceptibility.

Gene-specific DNA methylation profiles and LINE-1 hypomethylation are associated with myocardial infarction risk

Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase

Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation

Germline mutations in DNA repair genes predispose asbestos-exposed patients to malignant pleural mesothelioma

Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry

Inference on germline BAP1 mutations and asbestos exposure from the analysis of familial and sporadic mesothelioma in a high-risk area

Inter-individual variation in nucleotide excision repair pathway is modulated by non-synonymous polymorphisms in ERCC4 and MBD4 genes.

Interaction between gene polymorphisms of nitric oxide synthase and renin-angiotensin system in the progression of membranous glomerulonephritis.

Lactase persistence and bitter taste response: instrumental variables and mendelian randomization in epidemiologic studies of dietary factors and cancer risk

Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

Novel epigenetic changes unveiled by monozygotic twins discordant for smoking habits.

PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Peripheral blood DNA methylation as potential biomarker of Malignant Pleural Mesothelioma in asbestos-exposed subjects

Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9

Polymorphisms in DNA repair genes as risk factors for asbestos-related malignant mesothelioma in a general population study.

Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer

Polymorphisms in angiotensin-converting enzyme gene and severity of renal disease in Henoch-Schoenlein patients. Italian Group of Renal Immunopathology

Polymorphisms in the XRCC1 gene modify survival of bladder cancer patients treated with chemotherapy

Role of TGF-beta1 haplotypes in the occurrence of myocardial infarction in young Italian patients.

Role of the 12q24.12 locus in the onset of preeclampsia: an Italian case-control study.

Sardinians genetic background explained by runs of homozygosity and genomic regions under positive selection.

Seventy-five nuclear DNA polymorphisms in an Italian sample: a comparative worldwide study.

Synergistic effect of renin-angiotensin system and nitric oxide synthase genes polymorphisms in pre-eclampsia

Telomerase activity, telomere length and hTERT DNA methylation in peripheral blood mononuclear cells from monozygotic twins with discordant smoking habits.

Telomere length variation in juvenile acute myocardial infarction.

The Italian genome reflects the history of Europe and the Mediterranean basin

The TDI-FP Assay in Human Y Chromosome SNP Haplotyping

Unsuitability of lymphoblastoid cell lines as surrogate of cryopreserved isolated lymphocytes for the analysis of DNA double-strand break repair activity.

XRCC1 and ERCC1 variants modify malignant mesothelioma risk: A case–control study