Daniela Turchetti

DNABERT: pre-trained Bidirectional Encoder Representations from Transformers model for DNA-language in genome

Olaparib for Metastatic Breast Cancer in Patients with a Germline BRCA Mutation

Breast cancer

Triple-negative breast cancer molecular subtyping and treatment progress

Single-cell-resolution transcriptome map of human, chimpanzee, bonobo, and macaque brains

Microsatellite Instability in Colorectal Cancer

Olaparib: First Global Approval

Effective gene expression prediction from sequence by integrating long-range interactions

Pancreatic cancer

Combined Screening With Ultrasound and Mammography vs Mammography Alone in Women at Elevated Risk of Breast Cancer

Beyond Standard Mammographic Screening: Mammography at Age Extremes, Ultrasound, and MR Imaging

Microsatellite instability: an update

Machine learning applications in cancer prognosis and prediction

Worse Breast Cancer Prognosis of BRCA1/BRCA2 Mutation Carriers: What's the Evidence? A Systematic Review with Meta-Analysis

Human Brain Evolution: Harnessing the Genomics (R)evolution to Link Genes, Cognition, and Behavior

Predictive Models for Breast Cancer Susceptibility from Multiple Single Nucleotide Polymorphisms

Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas

Magnetic Resonance Imaging Improves Breast Screening Sensitivity in BRCA Mutation Carriers Age ≥ 50 Years: Evidence From an Individual Patient Data Meta-Analysis

Incidence and Outcome of BRCA Mutations in Unselected Patients with Triple Receptor-Negative Breast Cancer

Breast cancer screening in women at increased risk according to different family histories: an update of the Modena Study Group experience

Favourable ten-year overall survival in a Caucasian population with high probability of hereditary breast cancer

T[20] repeat in the 3′-untranslated region of the MT1X gene: a marker with high sensitivity and specificity to detect microsatellite instability in colorectal cancer

MYO7A mutation screening in Usher syndrome type I patients from diverse origins

A de novo nonsense mutation of PAX6 gene in a patient with aniridia, ataxia, and mental retardation

Hereditary risk of breast cancer: not only BRCA.

BRCA-Associated Ovarian Cancer: From Molecular Genetics to Risk Management