List of works - Simonetta Guarrera

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

scientific article published on 4 November 2010

A genome-wide association study for malignant mesothelioma risk.

scientific article published in July 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

scientific article

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.

scientific article

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

scientific article published on 20 February 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.

scientific article published in October 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

scientific article

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

scientific article published in July 2003

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

scientific article published on 3 June 2015

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

scientific article published on 21 November 2020

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

scientific article published on 12 December 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.

scientific article

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

scientific article

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

scientific article published on 12 January 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

scientific article

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

scientific article published on 21 December 2016

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

scientific article

Gene-asbestos interaction in malignant pleural mesothelioma susceptibility.

scientific article published on 2 July 2015

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

scientific article

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

scientific article

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

scientific article published on 6 October 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

scientific article published on 26 May 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

scientific article published on 19 December 2011

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

scientific article

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

scientific article published on 4 July 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

scientific article published on 4 January 2016

Immunogenetics of Henoch-Schoenlein disease ⬇️

scientific article published on October 1, 1997

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

scientific article published on 18 September 2014

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

scientific article published in September 2013

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

scientific article published in March 2004

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

scientific article

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

scientific article published on 20 September 2017

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

scientific article published on 4 June 2015

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

scientific article published on 28 November 2016

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

scientific article published on 05 November 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.

scientific article published on 27 March 2006

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

scientific article published on 25 August 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

scientific article published on 25 April 2013

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

scientific article

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

scientific article published on 29 November 2011

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

scientific article published on 20 March 2014

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

scientific article published in April 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.

scientific article published on 26 August 2017

Telomere length variation in juvenile acute myocardial infarction.

scientific article

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

scientific article

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.

scientific article

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

scientific article published on 26 January 2011

List of works by Simonetta Guarrera

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

Immunogenetics of Henoch-Schoenlein disease ⬇️

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