PubRank

Familial cancer (Fam Cancer)

Journal PubWeight™ 705.32‹?›

Top papers

Rank Title Year PubWeight™‹?›
1 Lynch syndrome genes. 2005 1.94
2 Attenuated familial adenomatous polyposis (AFAP). A review of the literature. 2003 1.93
3 Hereditary colorectal cancer syndromes: molecular genetics, genetic counseling, diagnosis and management. 2007 1.82
4 Current ideas in desmoid tumours. 2006 1.82
5 Methylation not a frequent "second hit" in tumors with germline BRCA mutations. 2009 1.78
6 Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer. 2007 1.77
7 The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch syndrome: from bench to bedside. 2007 1.76
8 Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma. 2010 1.68
9 Promoter hypermethylation frequency and BRAF mutations distinguish hereditary non-polyposis colon cancer from sporadic MSI-H colon cancer. 2004 1.66
10 BRCA1 and BRCA2: chemosensitivity, treatment outcomes and prognosis. 2006 1.65
11 Familial breast cancer: an investigation into the outcome of treatment for early stage disease. 2001 1.62
12 HNPCC and sporadic MSI-H colorectal cancer: a review of the morphological similarities and differences. 2004 1.60
13 Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures. 2005 1.58
14 The use of preventive measures among healthy women who carry a BRCA1 or BRCA2 mutation. 2005 1.57
15 The incidence of Lynch syndrome. 2005 1.56
16 Imaging of pheochromocytoma and paraganglioma. 2005 1.49
17 Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome. 2005 1.47
18 Gene-related cancer spectrum in families with hereditary non-polyposis colorectal cancer (HNPCC). 2007 1.45
19 Hereditary diffuse gastric cancer: association with lobular breast cancer. 2008 1.45
20 Prolactin levels, breast-feeding and milk production in a cohort of young healthy women from high-risk breast cancer families: implications for breast cancer risk. 2007 1.43
21 Prophylactic oophorectomy in Ontario. 2001 1.41
22 Evolution of the nomenclature for the hereditary colorectal cancer syndromes. 2005 1.40
23 Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies. 2007 1.39
24 Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations. 2012 1.39
25 Recommendations to improve identification of hereditary and familial colorectal cancer in Europe. 2009 1.38
26 Family history is a significant risk factor for pancreatic cancer: results from a systematic review and meta-analysis. 2008 1.36
27 The genetics of FAP and FAP-like syndromes. 2006 1.34
28 Paragangliomas of the head and neck: diagnosis and treatment. 2005 1.33
29 Psychological impact of genetic counseling for familial cancer: a systematic review and meta-analysis. 2006 1.30
30 Improved survival in BRCA2 carriers with ovarian cancer. 2007 1.30
31 Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics. 2011 1.30
32 The InSiGHT database: utilizing 100 years of insights into Lynch syndrome. 2013 1.27
33 The tumor spectrum in the Lynch syndrome. 2005 1.27
34 Communicating genetic risk information within families: a review. 2010 1.26
35 Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program. 2017 1.26
36 Cancer variation associated with the position of the mutation in the BRCA2 gene. 2004 1.25
37 Guidelines for disclosing genetic information to family members: from development to use. 2006 1.23
38 Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome. 2011 1.23
39 Restorative proctocolectomy and ileal pouch-anal anastomosis for familial adenomatous polyposis revisited. 2006 1.21
40 Diagnosis and management of BHD-associated kidney cancer. 2013 1.20
41 Frequency of familial colon cancer and hereditary nonpolyposis colorectal cancer (Lynch syndrome) in a large population database. 2005 1.20
42 Cancer risk in Lynch Syndrome. 2013 1.19
43 Cancer risk in mismatch repair gene mutation carriers. 2001 1.19
44 PALB2 mutations in familial breast and pancreatic cancer. 2011 1.18
45 Health-related direct-to-consumer genetic testing: a review of companies' policies with regard to genetic testing in minors. 2009 1.18
46 A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han. 2010 1.17
47 High prevalence of two BRCA1 mutations, 4154delA and 5382insC, in Latvia. 2005 1.17
48 Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors. 2013 1.16
49 Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations. 2005 1.16
50 Informing one's family about genetic testing for hereditary non-polyposis colorectal cancer (HNPCC): a retrospective exploratory study. 2005 1.15
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