文章名稱引用次數(shù)

• The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice15
• Physician interpretation of variants of uncertain significance14
• Hereditary gastric cancer: what's new? Update 2013-201811
• Recent advances in Lynch syndrome10
• Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic10
• Germline CDH1 mutations are a significant contributor to the high frequency of early-onset diffuse gastric cancer cases in New Zealand Mori9
• Moving into the mainstream: healthcare professionals' views of implementing treatment focussed genetic testing in breast cancer care8
• Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European8
• Association between miR-146a rs2910164 polymorphism and specific cancer susceptibility: an updated meta-analysis8
• An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review7