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Including Lynch syndrome in personalized prognostication and follow-up of stage II and III colon cancer

Annals of oncology, 2017-10, Vol.28 (10), p.2620-2621

2017

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The genetics of inherited predispositions to colorectal polyps: a quick guide for clinicians

Colorectal disease, 2015-01, Vol.17 (s1), p.3-9

2015

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Multiple Approach to the Exploration of Genotype-Phenotype Correlations in Familial Adenomatous Polyposis

Journal of clinical oncology, 2003-05, Vol.21 (9), p.1698-1707

2003

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Association of low-penetrance alleles with male breast cancer risk and clinicopathological characteristics: results from a multicenter study in Italy

Breast cancer research and treatment, 2013-04, Vol.138 (3), p.861-868

2013

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962: Association of SULT1A1 Arg213His polymorphism with male breast cancer risk: a case−control study in Italy

European journal of cancer (1990), 2014-07, Vol.50, p.S234-S235

2014

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Familial adenomatous polyposis: genetics and epidemiology

Techniques in coloproctology, 2004-12, Vol.8 Suppl 2 (S2), p.s305-s308

Varesco, L

2004

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Association of SULT1A1 Arg[sup.213]His polymorphism with male breast cancer risk: results from a multicenter study in Italy

Breast cancer research and treatment, 2014-12, Vol.148 (3), p.623

2014

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Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Clinical genetics, 2005-11, Vol.68 (5), p.442-447

2005

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Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis

International journal of cancer, 2001-03, Vol.95 (2), p.102-107

2001

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Performance of BOADICEA and BRCAPRO genetic models and of empirical criteria based on cancer family history for predicting BRCA mutation carrier probabilities: A retrospective study in a sample of Italian cancer genetics clinics

Breast (Edinburgh), 2013-12, Vol.22 (6), p.1130-1135

2013

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Association of SULT1A1 Arg213His polymorphism with male breast cancer risk: results from a multicenter study in Italy

Breast cancer research and treatment, 2014-12, Vol.148 (3), p.623-628

2014

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Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis

Gastroenterology (New York, N.Y. 1943), 1996-04, Vol.110 (4), p.1020-1027

1996

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Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy

Familial cancer, 2012-03, Vol.11 (1), p.41-47

2012

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The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011)

BioMed research international, 2013-01, Vol.2013, p.739010-8

2013

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P-205 Streamlining the diagnostic pathway for Lynch syndrome in colorectal cancer patients: A ten-year experience in a single Italian center

Annals of oncology, 2023-06, Vol.34, p.S88-S89

2023

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A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family

Journal of medical genetics, 2001-12, Vol.38 (12), p.863-867

2001

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PD-9 Universal screening for Lynch syndrome: Reflex testing to improve appropriateness of genetic counseling and diagnosis

Annals of oncology, 2020-07, Vol.31, p.S214-S215

2020

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PP9 GERMLINE NONSYNONYMOUS VARIANT OF APC GENE IN A PATIENT WITH MULTIPLE COLORECTAL ADENOMAS

Digestive and liver disease, 2009, Vol.41, p.S207-S207

2009

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Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

American journal of human genetics, 1996-02, Vol.58 (2), p.300-307

1996

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TP53 germline mutation testing in early onset breast cancer

Annals of oncology, 2016-09, Vol.27, p.iv71

2016

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Impact of Surgery on the Development of Duodenal Cancer in Patients with Familial Adenomatous Polyposis

Diseases of the colon & rectum, 2006-12, Vol.49 (12), p.1860-1866

2006

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Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas

International journal of cancer, 2004-05, Vol.109 (5), p.680-684

2004

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Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis

American journal of human genetics, 1993-02, Vol.52 (2), p.280-285

1993

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Association of SULT1A1 Arg^sup 213^His polymorphism with male breast cancer risk: results from a multicenter study in Italy

Breast cancer research and treatment, 2014-12, Vol.148 (3), p.623

2014

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Including Lynch syndrome in personalized prognostication and follow-up of stage II and III colon cancer

The genetics of inherited predispositions to colorectal polyps: a quick guide for clinicians

Multiple Approach to the Exploration of Genotype-Phenotype Correlations in Familial Adenomatous Polyposis

Association of low-penetrance alleles with male breast cancer risk and clinicopathological characteristics: results from a multicenter study in Italy

962: Association of SULT1A1 Arg213His polymorphism with male breast cancer risk: a case−control study in Italy

Familial adenomatous polyposis: genetics and epidemiology

Association of SULT1A1 Arg[sup.213]His polymorphism with male breast cancer risk: results from a multicenter study in Italy

Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations

Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis

Performance of BOADICEA and BRCAPRO genetic models and of empirical criteria based on cancer family history for predicting BRCA mutation carrier probabilities: A retrospective study in a sample of Italian cancer genetics clinics

Association of SULT1A1 Arg213His polymorphism with male breast cancer risk: results from a multicenter study in Italy

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis

Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy

The Italian National External Quality Assessment Program in Molecular Genetic Testing: Results of the VII Round (2010-2011)

P-205 Streamlining the diagnostic pathway for Lynch syndrome in colorectal cancer patients: A ten-year experience in a single Italian center

A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family

PD-9 Universal screening for Lynch syndrome: Reflex testing to improve appropriateness of genetic counseling and diagnosis

PP9 GERMLINE NONSYNONYMOUS VARIANT OF APC GENE IN A PATIENT WITH MULTIPLE COLORECTAL ADENOMAS

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16

An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers

TP53 germline mutation testing in early onset breast cancer

Impact of Surgery on the Development of Duodenal Cancer in Patients with Familial Adenomatous Polyposis

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas

Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis

Association of SULT1A1 Arg^sup 213^His polymorphism with male breast cancer risk: results from a multicenter study in Italy

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