S. Tognazzo

发表

A computerised cancer registration network in the Veneto region, north-east of Italy: a pilot study.

L. Simonato, P. Zambon, S. Rodella, 1996, British Journal of Cancer.

Quality control of automatically defined cancer cases by the automated registration system of the Venetian Tumour Registry. Quality control of cancer cases automatically registered.

P. Zambon, S. Guzzinati, C. Stocco, 2005, European journal of public health.

Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

W. Chung, P. Hall, V. Pankratz, 2013, PLoS genetics.

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Yurii B. Shvetsov, Simon G. Coetzee, A. Whittemore, 2015, Nature Genetics.

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Lara E Sucheston-Campbell, Simon G. Coetzee, Lara E. Sucheston-Campbell, 2017, Nature Genetics.

CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment

Silvio C. E. Tosatto, S. Tognazzo, S. Tosatto, 2014, Human mutation.

Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members

A. Spurdle, C. Lázaro, S. Tognazzo, 2012, Breast Cancer Research and Treatment.

Factor XIIIA-V34L and Factor XIIIB-H95R Gene Variants: Effects on Survival in Myocardial Infarction Patients

R. Ferrari, M. Valgimigli, S. Tognazzo, 2007, Molecular medicine.

Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

Annette Lee, W. Chung, R. Nussbaum, 2018, Human mutation.

Italian cancer figures--Report 2015

D. Costarelli, S. Rosso, L. Bisanti, 2016 .

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3

W. Chung, R. Nussbaum, F. Couch, 2016, Breast Cancer Research and Treatment.

Coexistence of Factor V G1691A and Factor II G20210A Gene Mutations in a Thrombotic Family Is Associated with Recurrence and Early Onset of Venous Thrombosis

S. Tognazzo, D. Gemmati, A. Ongaro, 2001, Pathophysiology of Haemostasis and Thrombosis.

Vision loss after PDT.

F. Parmeggiani, S. Tognazzo, D. Gemmati, 2006, Ophthalmology.

A common mutation in the gene for coagulation factor XIII‐A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases

S. Tognazzo, D. Gemmati, A. Ongaro, 2001, American journal of hematology.

Polymorphisms in the CCR5 promoter region influence disease progression in perinatally human immunodeficiency virus type 1-infected children.

S. Tognazzo, S. Tognazzo, R. Bertorelle, 2001, The Journal of infectious diseases.

Factor XIIIA-V 34 L and Factor XIIIB-H 95 R Gene Variants : Effects on Survival in Myocardial Infarction Patients

R. Ferrari, M. Valgimigli, S. Tognazzo, 2007 .

Italian cancer figures, report 2014: Prevalence and cure of cancer in Italy.

Coviello, Taranto, D. Costarelli, 2014, Epidemiologia e prevenzione.

[Italian cancer figures, report 2010: Cancer prevalence in Italy. Patients living with cancer, long-term survivors and cured patients].

D. Costarelli, S. Rosso, L. Bisanti, 2010, Epidemiologia e prevenzione.

Value of platelet reactivity in predicting response to treatment and clinical outcome in patients undergoing primary coronary intervention: insights into the STRATEGY Study.

R. Ferrari, M. Valgimigli, S. Tognazzo, 2006, Journal of the American College of Cardiology.

Prevalence of factor XIII Val34Leu polymorphism in patients affected by spontaneous subconjunctival hemorrhage.

F. Parmeggiani, S. Tognazzo, D. Gemmati, 2004, American journal of ophthalmology.

Prognostic role of factor XIII gene variants in nonhealing venous leg ulcers.

S. Tognazzo, D. Gemmati, P. Zamboni, 2006, Journal of vascular surgery.

The factor V Glu1608Lys mutation is recurrent in familial thrombophilia

S. Tognazzo, M. Pinotti, F. Bernardi, 2005, Journal of thrombosis and haemostasis : JTH.

Serum Iron and Matrix Metalloproteinase‐9 Variations in Limbs Affected by Chronic Venous Disease and Venous Leg Ulcers

S. Tognazzo, D. Gemmati, P. Zamboni, 2005, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Italian cancer figures, report 2012: Cancer in children and adolescents.

D. Costarelli, S. Rosso, L. Bisanti, 2013, Epidemiologia e prevenzione.

Influence of gene polymorphisms in ulcer healing process after superficial venous surgery.

S. Tognazzo, D. Gemmati, P. Zamboni, 2006, Journal of vascular surgery.

Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy

S. Tognazzo, V. Chiarion-Sileni, A. Vecchiato, 2011, Pigment cell & melanoma research.

The overlapping of local iron overload and HFE mutation in venous leg ulcer pathogenesis.

S. Tognazzo, D. Gemmati, P. Zamboni, 2006, Free radical biology & medicine.

Factor XIII Contrasts the Effects of Metalloproteinases in Human Dermal Fibroblast Cultured Cells

S. Tognazzo, D. Gemmati, P. Zamboni, 2004, Vascular and endovascular surgery.

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.

Stefania Tommasi, Laura Cortesi, Mads Thomassen, 2019, Cancer research.

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

D. Steinemann, F. Couch, B. Bonanni, 2020, Genetics in Medicine.

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus

A. Whittemore, L. Kiemeney, S. Cross, 2016, Nature Communications.

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

D. Steinemann, F. Couch, B. Bonanni, 2016, PloS one.

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

J. S. Hoffman, W. Chung, V. Pankratz, 2012, Human mutation.

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Mads Thomassen, Stephen Fox, Dieter Niederacher, 2011, Breast Cancer Research.

Segregation analysis of the BRCA2 c.9227G>T variant in multiple families suggests a pathogenic role in breast and ovarian cancer predisposition

S. Tognazzo, M. Montagna, S. Agata, 2020, Scientific Reports.

Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

Katherine M. Tucker, Sebastian A. Wagner, Kelly J. Sullivan, 2019, Human Mutation.

Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-Hodgkin's lymphoma in adults.

S. Tognazzo, D. Gemmati, F. Rodeghiero, 2004, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

W. Chung, D. Steinemann, F. Couch, 2019, British Journal of Cancer.

Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.

S. Tognazzo, D. Gemmati, P. Zamboni, 2005, Journal of vascular surgery.

Factor XIII V34L polymorphism modulates the risk of chronic venous leg ulcer progression and extension

S. Tognazzo, D. Gemmati, P. Zamboni, 2004, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

D. Steinemann, F. Couch, O. Olopade, 2017, Journal of Clinical Oncology.

Efficacy of risk-reducing salpingo-oophorectomy in BRCA1-2 variants and clinical outcomes of follow-up in patients with isolated serous tubal intraepithelial carcinoma (STIC).

S. Tognazzo, M. Noventa, C. Saccardi, 2021, Gynecologic oncology.

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Lara E Sucheston-Campbell, Simon G. Coetzee, Dennis J. Hazelett, 2017, Nature Genetics.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Christiana Kartsonaki, Mads Thomassen, Etienne Rouleau, 2011, Human molecular genetics.

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Eliseos J. Mucaki, F. Couch, B. Bonanni, 2015, Human molecular genetics.

Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

W. Chung, P. Hall, V. Pankratz, 2013, PLoS Genetics.

Association of breast cancer risk in BRCA 1 and BRCA 2 mutation carriers with genetic variants showing differential allelic expression

R. Nussbaum, F. Couch, O. Olopade, 2016 .

DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

Olufunmilayo I. Olopade, Mads Thomassen, Torben A. Kruse, 2014, PLoS genetics.

The bloodsucking arthropod bite as possible cofactor in the transmission of human herpesvirus-8 infection and in the expression of Kaposi's sarcoma disease.

P. Zambon, S. Guzzinati, S. Tognazzo, 2002, Parassitologia.

Methylenetetrahydrofolate reductase C677T and A1298C gene variants in adult non-Hodgkin's lymphoma patients: association with toxicity and survival.

S. Tognazzo, D. Gemmati, M. D. Della Porta, 2007, Haematologica.

Italian cancer figures, report 2013: Multiple tumours.

Adamo, D. Costarelli, S. Rosso, 2013, Epidemiologia e prevenzione.

Incidence trends of colorectal cancer in the early 2000s in Italy. Figures from the IMPATTO study on colorectal cancer screening

M. Zorzi, S. Baracco, S. Guzzinati, 2015 .

The reduced sensitivity of the ProC® Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk

S. Tognazzo, D. Gemmati, A. Ongaro, 2001, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

CLINICAL RESEARCH Interventional Cardiology Value of Platelet Reactivity in Predicting Response to Treatment and Clinical Outcome in Patients Undergoing Primary Coronary Intervention Insights Into the STRATEGY Study

R. Ferrari, M. Valgimigli, S. Tognazzo, 2006 .

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Yurii B. Shvetsov, Simon G. Coetzee, Dennis J. Hazelett, 2014, Nature Genetics.

FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor.

Eliseos J. Mucaki, F. Couch, B. Bonanni, 2015, Human molecular genetics.

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers.

V. Pankratz, F. Couch, T. Rebbeck, 2011, Human molecular genetics.

Common breast cancer susceptibility alleles are associated with tumor subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

B. Bonanni, O. Olopade, B. Karlan, 2012 .

Contribution of susceptibility gene variants to melanoma risk in families from the Veneto region of Italy

S. Tognazzo, V. Chiarion-Sileni, A. Vecchiato, 2011, Pigment Cell & Melanoma Research.

DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

A. Whittemore, D. Steinemann, F. Couch, 2014, PLoS genetics.