A New Set of in Silico Tools to Support the Interpretation of ATM Missense Variants Using Graphical Analysis.

Opportunistic genetic screening increases the diagnostic yield and is medically valuable for care of patients and their relatives with hereditary cancer.

Toxic Tire Wear Compounds (6PPD-Q and 4-ADPA) Detected in Airborne Particulate Matter Along a Highway in Mississippi, USA.

Occupational exposure to pesticides and endometrial cancer in the Screenwide case-control study.

MTHFR C677T and A1298C polymorphism's effect on risk of colorectal cancer in Lynch syndrome.

Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome.

Recommendations for the classification of germline variants in the exonuclease domain of POLE and POLD1.

Evaluation of Somatic Mutations in Urine Samples as a Noninvasive Method for the Detection and Molecular Classification of Endometrial Cancer.

SEOM clinical guideline on heritable TP53-related cancer syndrome (2022).

ATG2A-mediated bridge-like lipid transport regulates lipid droplet accumulation.

Evaluation of somatic mutations in cervicovaginal samples as a non-invasive method for the detection and molecular classification of endometrial cancer.

Cost-effectiveness analysis of molecular testing in minimally invasive samples to detect endometrial cancer in women with postmenopausal bleeding.

Highly Sensitive Microsatellite Instability and Immunohistochemistry Assessment in Endometrial Aspirates as a Tool for Cancer Risk Individualization in Lynch Syndrome.

Constitutional MLH1 Methylation Is a Major Contributor to Mismatch Repair-Deficient, MLH1-Methylated Colorectal Cancer in Patients Aged 55 Years and Younger.

Real-world evidence of nivolumab for non-small-cell lung cancer in a developing country.