Giovanna Bianchi Scarrà

Giovanna Bianchi Scarrà

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Giovanna Bianchi Scarrà

Giovanna Bianchi Scarrà

Publications by authors named "Giovanna Bianchi Scarrà"

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Functional analysis of a CDKN2A 5'UTR germline variant associated with pancreatic cancer development.

PLoS One 2017 7;12(12):e0189123. Epub 2017 Dec 7.

Genetics of Rare Cancers, Department of Internal Medicine and Medical Specialties (DiMI), University of Genoa and Ospedale Policlinico San Martino, Genoa, Italy.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0189123PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720692PMC
December 2017

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.

Nat Genet 2015 Sep 3;47(9):987-995. Epub 2015 Aug 3.

Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.

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http://dx.doi.org/10.1038/ng.3373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557485PMC
September 2015

Histologic features of melanoma associated with CDKN2A genotype.

J Am Acad Dermatol 2015 Mar 13;72(3):496-507.e7. Epub 2015 Jan 13.

Department of Pathology and Laboratory Medicine at the Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.

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http://dx.doi.org/10.1016/j.jaad.2014.11.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333073PMC
March 2015

The effect on melanoma risk of genes previously associated with telomere length.

J Natl Cancer Inst 2014 Oct 17;106(10). Epub 2014 Sep 17.

Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, Leeds Cancer Research UK Centre, University of Leeds, Leeds, UK (MMI, DTB, JCT, MHa, JRM, JANB, JHB); Oncogenomics (NKH), Genetic Epidemiology (NGM), Inflammatory Bowel Diseases Laboratory (GLRS), Cancer Control Group (DCW), Statistical Genetics (SM, MHL), and Molecular Epidemiology (GWM), QIMR Berghofer Medical Research Institute, Brisbane, Australia; INSERM, UMR-946, Genetic Variation and Human Diseases Unit, Paris, France (MB, FD); Université Paris Diderot, Sorbonne Paris Cité, Institut Universitaire d'Hématologie, Paris, France (MB, FD); Cancer Epidemiology and Services Research, Sydney School of Public Health, University of Sydney, Australia (AEC); Department of Oncology, University of Cambridge, Cambridge, UK (AMD, PDPP); Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX (JEL); Centre for Genetic Origins of Health and Disease, Faculty of Medicine, Dentistry and Health Sciences, University of Western Australia, Crawley, Australia (EKM, SVW); Centre for Cancer Biomarkers CCBIO (LAA) and Gade Laboratory for Pathology (AM), Department of Clinical Medicine, University of Bergen, Bergen, Norway; Department of Pathology, Haukeland University Hospital, Bergen, Norway (LAA); Department of Pathology, Molecular Pathology (PAA) and Department of Dermatology (PH), Oslo University Hospital, Rikshospitalet, Oslo, Norway; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Service de Dermatologie, Université Paris Descartes, Paris, France (MFA); Department of Dermatology (EA) and Oncogenics Unit (EA, EF), Sheba Medical Center, Tel Hashomer, Sackler Faculty of Medicine, Tel Aviv, Israel (EA); Department of Internal Medicine and Medical Specialties, University of Genoa, Genoa, Italy (GBS, EFPG); Laboratory of Genetics of Rare Hereditary Cancers, San Martino-IST Research Hospital, Genoa, Italy (GBS, EFPG); Division of Cancer Epidemiology and Gene

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https://genepi.qimr.edu.au/contents/p/staff/IlesMM_JNCI_EPUB
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http://jnci.oxfordjournals.org/cgi/doi/10.1093/jnci/dju267
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http://dx.doi.org/10.1093/jnci/dju267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196080PMC
October 2014

Clinical utility gene card for: Gorlin syndrome--update 2013.

Eur J Hum Genet 2013 Oct 30;21(10). Epub 2013 Jan 30.

Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.

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http://dx.doi.org/10.1038/ejhg.2012.299DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778338PMC
October 2013

A variant in FTO shows association with melanoma risk not due to BMI.

Nat Genet 2013 Apr 3;45(4):428-32, 432e1. Epub 2013 Mar 3.

Section of Epidemiology and Biostatistics, Leeds Institute of Molecular Medicine, Leeds Cancer Research UK Centre, St. James's University Hospital, Leeds, UK.

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https://genepi.qimr.edu.au/contents/p/staff/Iles_etal_Nature
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http://www.nature.com/doifinder/10.1038/ng.2571
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http://dx.doi.org/10.1038/ng.2571DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3640814PMC
April 2013

Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes.

J Cutan Pathol 2012 Mar 12;39(3):366-71. Epub 2011 Nov 12.

Division of Dermatology, Department of Internal Medicine, University of Modena and Reggio Emilia, Modena, Italy.

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http://dx.doi.org/10.1111/j.1600-0560.2011.01813.xDOI Listing
March 2012

Genome-wide association study identifies three new melanoma susceptibility loci.

Nat Genet 2011 Oct 9;43(11):1108-13. Epub 2011 Oct 9.

Section of Epidemiology and Biostatistics, Leeds Institute of Molecular Medicine, Leeds Cancer Research UK Centre, St James’s University Hospital, Leeds, UK.

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http://dx.doi.org/10.1038/ng.959DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3251256PMC
October 2011

Clinical utility gene card for: Gorlin syndrome.

Eur J Hum Genet 2011 Aug 9;19(8). Epub 2011 Feb 9.

Department of Surgical Sciences, University of Foggia, Foggia, Italy.

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http://dx.doi.org/10.1038/ejhg.2011.9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3172938PMC
August 2011

Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma.

Hum Mol Genet 2010 Apr 21;19(8):1479-91. Epub 2010 Jan 21.

Unit of Molecular Mutagenesis and DNA Repair, National Institute for Cancer Research IST, 16132 Genoa, Italy.

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http://dx.doi.org/10.1093/hmg/ddq022DOI Listing
April 2010

MDM2 SNP309 genotype influences survival of metastatic but not of localized neuroblastoma.

Pediatr Blood Cancer 2009 Oct;53(4):576-83

Molecular Mutagenesis and DNA Repair Unit, National Cancer Research Institute, Genoa, Italy.

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http://dx.doi.org/10.1002/pbc.22132DOI Listing
October 2009

Analysis of cultured human melanocytes based on polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P loci.

J Invest Dermatol 2009 Feb 24;129(2):392-405. Epub 2008 Jul 24.

Melanogenix Group, Institute for Molecular Bioscience, University of Queensland, Queensland, Australia.

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http://dx.doi.org/10.1038/jid.2008.211DOI Listing
February 2009

No evidence for linkage with melanoma in Italian melanoma-prone families.

Cancer Epidemiol Biomarkers Prev 2008 Jul;17(7):1838-40

Division of Cancer Epidemiology and Genetics, Genetic Epidemiology Branch, National Cancer Institute, NIH, Bethesda, MD 20892-7236, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-08-0264DOI Listing
July 2008

Increased risk of colorectal adenomas in Italian subjects carrying the p53 PIN3 A2-Pro72 haplotype.

Digestion 2006 20;74(3-4):228-35. Epub 2007 Mar 20.

Unit of Molecular Mutagenesis, National Institute for Cancer Research, Genoa, Italy.

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http://dx.doi.org/10.1159/000100966DOI Listing
August 2007

Genetics of melanoma susceptibility.

Forum (Genova) 2003 ;13(2):114-22; quiz 187

Department of Oncology, Biology and Genetics, University of Genova, Viale Benedetto XV, 6 - 16132 Genova, Italy.

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February 2005

Novel MC1R variants in Ligurian melanoma patients and controls.

Hum Mutat 2004 Jul;24(1):103

Dipartimento di Oncologia, Biologia e Genetica, Università degli Studi di Genova, 16132, Italy.

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http://dx.doi.org/10.1002/humu.9253DOI Listing
July 2004

Genetic testing for melanoma.

Lancet Oncol 2002 Nov;3(11):653-4

Westmead Institute for Cancer Research, University of Sydney, Westmead Millennium Institute, New South Wales, 2145, Australia.

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http://dx.doi.org/10.1016/s1470-2045(02)00894-xDOI Listing
November 2002