Emanuela Lucci‐Cordisco

The spectrum of<i>WRN</i>mutations in Werner syndrome patients

Shurong Huang, Lin Lee, Nancy Hanson et al. · Human Mutation · 2006 · 223 citations · Full text

A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer

Alessandra Viel, Alessandro Bruselles, Ettore Meccia et al. · EBioMedicine · 2017 · 223 citations · Full text

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 et al. · Digestive and Liver Disease · 2013 · 153 citations · Full text

Cancer Risk, Cancer Epidemiology, Genetic Disorder +12

Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification

Michael T. Parsons, Emma Tudini, Hongyan Li et al. · Human Mutation · 2019 · 148 citations · Full text

Genetics, Genetic Epidemiology, Pathology +25

Identification of Muir–Torre syndrome among patients with sebaceous tumors and keratoacanthomas

Giovanni Ponti, Lorena Losi, Carmela Di Gregorio et al. · Cancer · 2005 · 142 citations · Full text