Daniela Turchetti - Concepedia

Author

Daniela Turchetti

Also Known As

Amanda B. Spurdle, D Turchetti, D. Turchetti, D., Turchetti, DANIELA TURCHETTI, Daniela TURCHETTI, Daniela Turchetti, Turchetti, Daniela

176

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

University of Bologna IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola Istituti di Ricovero e Cura a Carattere Scientifico University of Modena and Reggio Emilia Azienda USL di Bologna

About

Daniela Turchetti is an author at University of Bologna specializing in medicine, pathology, and oncology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	20	767
2	Public Health	8	8	415
3	Arts	1	1	23
4	Education	1	1	28
5	Language Studies	1	1	28

Daniela Turchetti

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Multicenter Surveillance of Women at High Genetic Breast Cancer Risk Using Mammography, Ultrasonography, and Contrast-Enhanced Magnetic Resonance Imaging (the High Breast Cancer Risk Italian 1 Study) Francesco Sardanelli, Franca Podo, Filippo Santoro, Investigative Radiology	2010	333
Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study Nicoletta Resta, Daniela Pierannunzio, Gennaro Mariano Lenato, Digestive and Liver Disease Cancer RiskCancer EpidemiologyGenetic DisorderMedicineGenetics	2013	153
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study Aung Ko Win, James G. Dowty, Jeanette C. Reece, The Lancet Oncology Lynch SyndromeRetrospective Cohort StudyCancer RiskCancer EpidemiologyMedicine	2021	112
CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma Marta Betti, Anna Aspesi, Alessandra Biasi, Cancer Letters MedicineMelanomaPathologyCancer GeneticsMolecular Diagnostics	2016	74
<i>MYO7A</i> mutation screening in Usher syndrome type I patients from diverse origins Teresa Jaijo, Elena Aller, Magdalena Beneyto, Journal of Medical Genetics	2007	70
Breast cancer screening in women at increased risk according to different family histories: an update of the Modena Study Group experience Laura Cortesi, Daniela Turchetti, Isabella Marchi, BMC Cancer	2006	57
ARID1A and CTNNB1/β-Catenin Molecular Status Affects the Clinicopathologic Features and Prognosis of Endometrial Carcinoma: Implications for an Improved Surrogate Molecular Classification Antonio De Leo, Dario de Biase, Jacopo Lenzi, Cancers	2021	51
Clinical genetic testing for familial melanoma in Italy: A cooperative study William Bruno, Paola Ghiorzo, Linda Battistuzzi, Journal of the American Academy of Dermatology Genetic TestingMedicineFamilial MelanomaGenetic EpidemiologyMelanoma	2009	47
Favourable ten-year overall survival in a Caucasian population with high probability of hereditary breast cancer Laura Cortesi, Cristina Masini, Claudia Cirilli, BMC Cancer	2010	47
Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome Linda A.J. Hendricks, Nicoline Hoogerbrugge, Arjen R. Mensenkamp, JNCI Journal of the National Cancer Institute	2022	45

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