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All papers authored by Daniela Turchetti

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2022 Benedetta Bertonazzi, Daniela Turchetti

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ORCID

Outcomes of support groups for carriers of BRCA 1/2 pathogenic variants and their relatives: a systematic review

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2021 Lea Godino

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, Daniela Turchetti

ORCID

, Leigh Jackson

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, Catherine Hennessy

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, Heather Skirton

ORCID

Genetic counselling as a route to enhanced autonomy: using a sequential mixed methods research approach to develop a theory regarding presymptomatic genetic testing for young adults at risk of inherited cancer syndromes

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2020 Maria Luisa Di Pietro, Drieda Zaçe

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, Alessia Orfino, Francesca Romana Di Raimo, Andrea Poscia, Elisabetta de Matteis, Daniela Turchetti

ORCID

ORCID

, Benedetta Bertonazzi, Marzena Franiuk, Carla Bruzzone, Liliana Varesco

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, Emanuela Lucci-Cordisco, Maurizio Genuardi

ORCID

Correction: Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach

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Maria Luisa Di Pietro, Drieda Zaçe

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, Alessia Orfino, Francesca Romana Di Raimo, Andrea Poscia, Elisabetta de Matteis, Daniela Turchetti

ORCID

ORCID

, Benedetta Beronazzi, Benedetta Bertonazzi, Marzena Franiuk, Carla Bruzzone, Liliana Varesco

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, Emanuela Lucci-Cordisco, Maurizio Genuardi

ORCID

Intrafamilial communication of hereditary breast and ovarian cancer genetic information in Italian women: towards a personalised approach

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2016 Milena Paneque

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, Daniela Turchetti

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, Leigh Jackson, Peter Lunt, Elisa Houwink, Heather Skirton

A systematic review of interventions to provide genetics education for primary care

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2015 Lea Godino

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, Elisabetta Razzaboni, Margherita Bianconi, Daniela Turchetti

ORCID

Impact of Genetic Counseling in Women with a Family History of Breast Cancer in Italy

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Pamela Magini, Monica Poscente, Simona Ferrari, Manuela Vargiolu, Elena Bacchelli, Claudio Graziano, Anita Wischmeijer, Daniela Turchetti

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, Elisabetta Malaspina, Valentina Marchiani, Duccio Maria Cordelli

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, Emilio Franzoni, Giovanni Romeo, Marco Seri

Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration

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Lea Godino

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, Daniela Turchetti

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, Leigh Jackson, Catherine Hennessy, Heather Skirton

Impact of presymptomatic genetic testing on young adults: a systematic review

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Lea Godino

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, Eva Pompilii, Federica D'Anna, Antonio M. Morselli-Labate, Elena Nardi

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, Marco Seri, Nicola Rizzo, Gianluigi Pilu, Daniela Turchetti

ORCID

Attitudes of women of advanced maternal age undergoing invasive prenatal diagnosis and the impact of genetic counselling

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2014 Francesca Crucianelli, Rossella Tricarico, Daniela Turchetti

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, Greta Gorelli, Francesca Gensini, Roberta Sestini, Laura Giunti, Monica Pedroni, Maurizio Ponz de Leon, Serenella Civitelli, Maurizio Genuardi

MLH1constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria

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Pamela Magini, Tommaso Pippucci, I.-Chun Tsai, I. Chun Tsai, Simona Coppola, Emilia Stellacci, Anna Bartoletti-Stella, Daniela Turchetti

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, Claudio Graziano, Giovanna Cenacchi, Iria Neri, Duccio Maria Cordelli

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, Valentina Marchiani, Rosalba Bergamaschi, Giuseppe Gasparre and 9 other authors

A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype

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Laura Maria Pradella, Cecilia Evangelisti, Claudia Ligorio, Claudio Ceccarelli, Iria Neri, Roberta Zuntini, Laura Benedetta Amato, Simona Ferrari, Alberto Maria Martelli, Giuseppe Gasparre, Daniela Turchetti

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A novel deleterious PTEN mutation in a patient with early-onset bilateral breast cancer

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2013 Lea Godino

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, Daniela Turchetti

ORCID

, Heather Skirton

A systematic review of factors influencing uptake of invasive fetal genetic testing by pregnant women of advanced maternal age

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Linda Battistuzzi, Rosagemma Ciliberti, William Bruno

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, Daniela Turchetti

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, Liliana Varesco, Francesco De Stefano

Communication of Clinically Useful Next-Generation Sequencing Results to At-Risk Relatives of Deceased Research Participants: Toward Active Disclosure?

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L. Varesco, V. Viassolo

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, A. Viel, V. Gismondi, P. Radice

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, M. Montagna, E. Alducci, L. Della Puppa, C. Oliani, S. Tommasi, M. A. Caligo, C. Vivanet, M. Zuradelli, P. Mandich, M. G. Tibiletti and 7 other authors

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

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Annamaria Pollio, Aldo Tomasi, Stefania Seidenari, Giovanni Pellacani, Monica Rodolfo

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, Simona Frigerio, Andrea Maurichi, Daniela Turchetti

ORCID

, Sara Bassoli, Cristel Ruini, Giovanni Ponti

Malignant and benign tumors associated with multiple primary melanomas: just the starting block for the involvement ofMITF, PTENandCDKN2Ain multiple cancerogenesis?

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Maurizio Ponz de Leon, Nicoletta Resta, Daniela Pierannunzio, Stella A. Lenato Gm, Gennaro Mariano Lenato

ORCID

, Lenato Gm, Alessandro Stella, Riccardo Capocaccia, Rosanna Bagnulo, Patrizia Lastella, Susca Fc, Francesco Claudio Susca, Cristina Bozzao, Daria Carmela Loconte, Loconte Dc and 24 other authors

Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: Results of an Italian multicenter study

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Laura Maria Pradella, Martin Lang, Ivana Kurelac, Elisa Mariani, Flora Guerra, Roberta Zuntini, Giovanni Tallini, Alan MacKay, Jorge S. Reis-Filho, Marco Seri, Daniela Turchetti

ORCID

, Giuseppe Gasparre

Where Birt–Hogg–Dubé meets Cowden Syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours

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2012 Lea Godino

ORCID

, Daniela Turchetti

ORCID

, Heather Skirton

Knowledge of genetics and the role of the nurse in genetic health care: a survey of Italian nurses

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Laura Cortesi, Arcangela De Nicolo, Veronica Medici, Marco Marino, Daniela Turchetti

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, Laura Maria Pradella, Giulio Rossi, Emilio Parisini

ORCID

, Massimo Federico

Collective evidence supports neutrality of BRCA1 V1687I, a novel sequence variant in the conserved THV motif of the first BRCT repeat

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