| Nr. | Year OPEN | Title | users say> | rate good | rate bad | no link | Citation |
PTENNeoplasia (Inherited)Multiple hereditary infundibulocystic basal cell carcinomaCowden s syndromeColon and rectum (Neoplasia)Data base (Medicine Biology Pharmacology)Fumarate hydrataseNeuroendocrine system (Neoplasia)Stomach (Neoplasia)ChemopreventionFamilial adenomatous polyposisLynch syndromePreventive surgeryVon Hippel Lindau syndromeMammary gland (Neoplasia)Ovary (Neoplasia)Carney s complexGastrointestinal stromal cell tumor GISTNervous system (Neoplasia Paraganglioma)Runx1 AML1DNA (Repair and Toxicology)MSH6Leukemia and lymphoma (BASKET)Endometrium (Neoplasia)Kidney (Neoplasm)Thyroid (Neoplasia)Sleep apnea (central)PHOX2BAnemia (Fanconi s anemia)| 1 | 2006 | Mucocutaneous neuromas: an underrecognized manifestation of PTEN hamartoma-tumor syndrome. | 
| + | - | nl | Arch Dermatol 142(5):625-32 (2006) |
| 2 | 1999 | Multiple hereditary infundibulocystic basal cell carcinomas: a genodermatosis different from nevoid basal cell carcinoma syndrome. | 
| + | - | nl | Arch Dermatol 135(10):1227-35 (1999) |
| 3 | 2002 | Cowden disease or multiple hamartoma syndrome--cutaneous clue to internal malignancy. | 
| + | - | nl | Eur J Dermatol 12(5):411-21 (2002) |
| 4 | 2008 | Extracolonic manifestations of hereditary colorectal cancer syndromes. | 
| + | - | nl | Clin Colon Rectal Surg 21(4):263-72 (2008) |
| 5 | 2008 | The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. | 
| + | - | nl | BMC Med Genet 9(-):20 (2008) |
| 6 | 2008 | BRCA1/2 associated hereditary breast cancer. | 
| + | - | nl | J Zhejiang Univ Sci B 9(2):85-9 (2008) |
| 7 | 1982 | Multiple primary carcinomas of the colon and associated extracolonic primary malignant tumors. | 
| + | - | nl | Ann Surg 195(4):501-7 (1982) |
| 8 | 2007 | Selected aspects of inherited susceptibility to prostate cancer and tumours of different site of origin. | 
| + | - | nl | Hered Cancer Clin Pract 5(3):164-79 (2007) |
| 9 | 1998 | Recommendations for medical management of hereditary breast and ovarian cancer: the French National Ad Hoc Committee. | 
| + | - | nl | Ann Oncol 9(9):939-50 (1998) |
| 10 | 1979 | Hereditary cancer: ascertainment and management. | 
| + | - | nl | CA Cancer J Clin 29(4):216-32 (1979) |
| 11 | 2008 | Inherited pancreatic endocrine tumor syndromes: advances in molecular pathogenesis, diagnosis, management, and controversies. | 
| + | - | nl | Cancer 113(7 Suppl):1807-43 (2008) |
| 12 | 2008 | Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy. | 
| + | - | nl | Cancer 112(12):2655-63 (2008) |
| 13 | 1999 | Chemoprevention in hereditary colorectal cancer syndromes. | 
| + | - | nl | Cancer 86(11 Suppl):2551-63 (1999) |
| 14 | 1999 | Genetic testing and counseling for hereditary forms of colorectal cancer. | 
| + | - | nl | Cancer 86(11 Suppl):2540-50 (1999) |
| 15 | 1999 | Clinical challenges in management of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer. | 
| + | - | nl | Cancer 86(11 Suppl):2533-9 (1999) |
| 16 | 1999 | Managing hereditary ovarian cancer risk. | 
| + | - | nl | Cancer 86(11 Suppl):2517-24 (1999) |
| 17 | 1999 | Prophylactic mastectomy and inherited predisposition to breast carcinoma. | 
| + | - | nl | Cancer 86(11 Suppl):2502-16 (1999) |
| 18 | 1999 | Inherited genetic predisposition in breast cancer. A population-based perspective. | 
| + | - | nl | Cancer 86(11 Suppl):2493-501 (1999) |
| 19 | 1999 | Genetic cancer risk assessment. Putting it all together. | 
| + | - | nl | Cancer 86(11 Suppl):2483-92 (1999) |
| 20 | 1999 | Von Hippel-Lindau syndrome. A pleomorphic condition. | 
| + | - | nl | Cancer 86(11 Suppl):2478-82 (1999) |
| 21 | 1999 | The genetics of hereditary melanoma and nevi. 1998 update. | 
| + | - | nl | Cancer 86(11 Suppl):2464-77 (1999) |
| 22 | 2007 | New issues in genetic counseling of hereditary colon cancer. | 
| + | - | nl | Clin Cancer Res 13(22 Pt 2):6857s-61s (2007) |
| 23 | 2004 | Recognition and management of hereditary breast cancer syndromes. | 
| + | - | nl | Oncologist 9(1):13-24 (2004) Thull DL |
| 24 | 1987 | Genetics of cancer predisposition. | 
| + | - | nl | Cancer Res 47(21):5518-27 (1987) |
| 25 | 2002 | Why have we failed to find the low penetrance genetic constituents of common cancers? | 
| + | - | nl | Cancer Epidemiol Biomarkers Prev 11(12):1544-9 (2002) |
| 26 | 2009 | Diagnosis and management of hereditary colorectal cancer syndromes: Lynch syndrome as a model. | 
| + | - | nl | CMAJ 181(5):273-80 (2009) |
| 27 | 2008 | Cancer surveillance based on imaging techniques in carriers of BRCA1/2 gene mutations: a systematic review. | 
| + | - | nl | Br J Radiol 81(963):172-9 (2008) |
| 28 | 2004 | Hereditary cancer: guidelines in clinical practice--general overview. | 
| + | - | nl | Ann Oncol 15 Suppl 4(-):iv121-5 (2004) |
| 29 | 2004 | Hereditary cancer: guidelines in clinical practice. Colorectal cancer genetics. | 
| + | - | nl | Ann Oncol 15 Suppl 4(-):iv127-31 (2004) |
| 30 | 2004 | Hereditary cancer: guidelines in clinical practice. Breast and ovarian cancer genetics. | 
| + | - | nl | Ann Oncol 15 Suppl 4(-):iv133-8 (2004) |
| 31 | 2010 | Genetic counselling for hereditary predisposition to ovarian and breast cancer. | 
| + | - | nl | Ann Oncol 21 Suppl 7(-):vii334-8 (2010) |
| 32 | 2009 | Familial colorectal cancer risk: ESMO clinical recommendations. | 
| + | - | nl | Ann Oncol 20 Suppl 4(-):51-3 (2009) |
| 33 | 2009 | Carney triad: a syndrome featuring paraganglionic, adrenocortical, and possibly other endocrine tumors. | 
| + | - | nl | J Clin Endocrinol Metab 94(10):3656-62 (2009) |
| 34 | 2011 | Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency. | 
| + | - | nl | Haematologica 96(12):1892-4 (2011) |
| 35 | 2010 | Constitutional mismatch repair deficiency and childhood leukemia/lymphoma--report on a novel biallelic MSH6 mutation. | 
| + | - | nl | Haematologica 95(5):841-4 (2010) |
| 36 | 2010 | Constitutional mismatch repair-deficiency syndrome. | 
| + | - | nl | Haematologica 95(5):699-701 (2010) Wimmer K |
| 37 | 2010 | Hereditary myeloproliferative disorders. | 
| + | - | nl | Haematologica 95(1):6-8 (2010) |
| 38 | 2007 | Genetic susceptibility to lymphoma. | 
| + | - | nl | Haematologica 92(7):960-9 (2007) |
| 39 | 2011 | BRCA and beyond: A genome-first approach to familial breast cancer risk assessment. | 
| + | - | nl | Discov Med 12(66):433-43 (2011) |
| 40 | 2010 | The inherited genetics of ovarian and endometrial cancer. | 
| + | - | nl | Curr Opin Genet Dev 20(3):231-8 (2010) |
| 41 | 2010 | Candidate gene association studies: successes and failures. | 
| + | - | nl | Curr Opin Genet Dev 20(3):257-61 (2010) |
| 42 | 2010 | Advances in the genetics of familial renal cancer. | 
| + | - | nl | Oncologist 15(6):532-8 (2010) |
| 43 | 2009 | Genetic aspects of familial thyroid cancer. | 
| + | - | nl | Oncologist 14(6):571-7 (2009) |
| 44 | 2009 | Hereditary kidney cancer: unique opportunity for disease-based therapy. | 
| + | - | nl | Cancer 115(10 Suppl):2252-61 (2009) |
| 45 | 2010 | An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management. | 
| + | - | nl | Am J Respir Crit Care Med 181(6):626-44 (2010) |
| 46 | 2010 | Susceptibility pathways in Fanconi's anemia and breast cancer. | 
| + | - | nl | N Engl J Med 362(20):1909-19 (2010) |
| 47 | 2003 | Hereditary colorectal cancer. | 
| + | - | nl | N Engl J Med 348(10):919-32 (2003) |
| 48 | 2011 | Hereditary breast and ovarian cancer: new genes, new treatments, new concepts. | 
| + | - | nl | Dtsch Arztebl Int 108(19):323-30 (2011) |
| 49 | 2004 | Inherited forms of renal cell carcinoma. | 
| + | - | nl | Scand J Surg 93(2):103-11 (2004) |