| Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.010 | Biomarker | phenotype | BEFREE | This revealed multiple F-FDG avid tumors with localization pattern suggesting multiple primary neoplasms of different origin rather than disseminated paraganglioma. | 27824319 | 2017 | ||||
|
0.010 | Biomarker | phenotype | BEFREE | Hence, 15-PGDH in normal-appearing colorectal mucosa can be a useful biomarker of field effect for the prediction of sporadic synchronous neoplasms. | 23960441 | 2013 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | To study the association of SULT1A1*2 polymorphism with tobacco-related cancers (TRCs), a case-control study comprising 132 patients with multiple primary neoplasm (MPN) involving TRC and 198 cancer-free controls was carried out. | 18854828 | 2008 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | In this study conducted amongst Indian male tobacco users with upper aero-digestive tract (UADT) squamous carcinoma, 30 patients with multiple primary neoplasms (MPN) were compared with 28 age and sex matched patients with a single primary neoplasm (SPN) for various environmental factors (form of tobacco use, alcohol, radiotherapy for index cancer) and genetic parameters (family history of UADT cancers and GSTT1/GSTM1 genotype). | 14662420 | 2004 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | Glutathione S-transferase M1 or T1 null genotype as a risk factor for developing multiple primary neoplasms in the upper aero-digestive tract, in Indian males using tobacco. | 14662420 | 2004 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | Glutathione S-transferase M1 or T1 null genotype as a risk factor for developing multiple primary neoplasms in the upper aero-digestive tract, in Indian males using tobacco. | 14662420 | 2004 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | We screened germline mutations of mismatch repair genes hMLH1 and hMSH2 in a patient with multiple primary neoplasms (multiple stomach cancers, colon cancer and brain tumor) in a cancer clustered HNPCC family. | 12110639 | 2002 | ||||
|
0.010 | GeneticVariation | phenotype | BEFREE | We screened germline mutations of mismatch repair genes hMLH1 and hMSH2 in a patient with multiple primary neoplasms (multiple stomach cancers, colon cancer and brain tumor) in a cancer clustered HNPCC family. | 12110639 | 2002 |