Title	Publication Date	Language	Citations
A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han	2010/08/01	English	77
Pancreatic cancer and the FAMMM syndrome	2007/11/09	English	76
CDH1 germline mutations and hereditary lobular breast cancer	2016/01/13	English	75
The prognostic value of MGMT promoter methylation in Glioblastoma multiforme: a meta-analysis	2013/02/09	English	74
Genetic counseling and cascade genetic testing in Lynch syndrome	2016/03/11	English	73
Hereditary diffuse gastric cancer: association with lobular breast cancer	2007/11/29	English	73
Update multiple endocrine neoplasia type 2	2010/01/20	English	73
Desmoid Tumors – a Characterization of Patients Seen at Mayo Clinic 1976–1999	2006/06/01	English	73
Use of Microsatellite Instability and Immunohistochemistry Testing for the Identification of Individuals at Risk for Lynch Syndrome	2005/09/01	English	72
Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families	2013/08/11	English	70
Clinical Description of the Lynch Syndrome [Hereditary Nonpolyposis Colorectal Cancer (HNPCC)]	2005/09/01	English	70
Gastric cancer in FAP: a concerning rise in incidence	2017/02/09	English	70
The Tumor Spectrum in the Lynch Syndrome	2005/09/01	English	68
Preparing individuals to communicate genetic test results to their relatives: report of a randomized control trial	2013/02/19	English	68
CTNNB1-mutant colorectal carcinomas with immediate invasive growth: a model of interval cancers in Lynch syndrome	2016/03/09	English	67
Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study	2016/02/20	English	66
Lynch syndrome-associated neoplasms: a discussion on histopathology and immunohistochemistry	2013/02/24	English	65
Diagnosis and management of BHD-associated kidney cancer	2013/05/24	English	64
Recent advances in Lynch syndrome	2019/01/09	English	64
Psychological Impact of Genetic Counseling for Familial Cancer: A Systematic Review and Meta-Analysis	2006/03/01	English	64
Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia	2007/02/28	English	63
The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice	2018/05/30	English	63
The genetics of FAP and FAP-like syndromes	2006/09/01	English	62
Syndrome of Early Onset Colon Cancers, Hematologic Malignancies & Features of Neurofibromatosis in HNPCC Families with Homozygous Mismatch Repair Gene Mutations	2005/11/01	English	62
The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation	2005/06/01	English	61
Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures	2005/11/01	English	60
Routine TP53 testing for breast cancer under age 30: ready for prime time?	2012/08/01	English	60
The History of Lynch Syndrome	2013/04/02	English	59
Inversion of exons 1–7 of the MSH2 gene is a frequent cause of unexplained Lynch syndrome in one local population	2013/10/11	English	58
Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma	2010/11/17	English	58