Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 CausalMutation disease CGI
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE BRAF mutations in thyroid tumors are restricted to papillary carcinomas and anaplastic or poorly differentiated carcinomas arising from papillary carcinomas. 14602780 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE We analyzed BRAF gene mutation at codon 599 in thyroid tumors using mutant-allele-specific PCR and in 10 thyroid tumor cell lines by DNA sequencing of the PCR-amplified exon 15. 12907632 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN BRAF mutation in papillary thyroid carcinoma. 12697856 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. 12670889 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTC-RAS-BRAF signaling pathway in papillary thyroid carcinoma. 12670889 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE We analyzed exons 11 and 15 of BRAF gene in six human thyroid cancer cell lines and 207 paraffin-embedded thyroid tumor tissues. 12970315 2003
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE Low prevalence of BRAF mutations in radiation-induced thyroid tumors in contrast to sporadic papillary carcinomas. 15145515 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE We examined BRAF(T1796A) in 21 patients with thyroid tumors using leftover cells in the needle at the preoperative FNAB. 15671769 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease LHGDN These data clearly confirm that BRAF(V599E) is the more common genetic alteration found to date in adult sporadic PTCs, that it is unique for this thyroid cancer histotype, and that it might drive the development of PTCs of the classic papillary subtype. 15126572 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE These data clearly confirm that BRAF(V599E) is the more common genetic alteration found to date in adult sporadic PTCs, that it is unique for this thyroid cancer histotype, and that it might drive the development of PTCs of the classic papillary subtype. 15126572 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE In the present study, the genetic analysis of BRAF in an Italian cohort of 65 thyroid tumours with corresponding normal tissues and 21 thyroid benign disorders is reported. 15272920 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN Alternative mutations of BRAF, RET and NTRK1 are associated with similar but distinct gene expression patterns in papillary thyroid cancer. 15273715 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 PosttranslationalModification disease BEFREE A similar inverse correlation of RASSF1A methylation with BRAF mutation was seen in thyroid tumor cell lines. 14996725 2004
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN Mutational activation of BRAF is not a major event in sporadic childhood papillary thyroid carcinoma. 15968271 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE BRAF copy number gains in thyroid tumors detected by fluorescence in situ hybridization. 16199894 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE BRAF mutation occurs later in thyroid tumor progression and is restricted mainly to PTC and anaplastic thyroid carcinoma. 15980887 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 Biomarker disease BEFREE Oncogenic AKAP9-BRAF fusion is a novel mechanism of MAPK pathway activation in thyroid cancer. 15630448 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE The BRAF(V600E) mutation was detected in tumour samples from 31 of 60 conventional micro-PTC patients (52%), but was not detected in patients with other types of thyroid tumours. 16268813 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE The aim of this study was the quantitative assessment of promoter hypermethylation and its relation to the BRAF mutation in thyroid tumors. 15840741 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN BRAF mutation predicts a poorer clinical prognosis for papillary thyroid cancer. 16174717 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN Molecular classification of papillary thyroid carcinoma: distinct BRAF, RAS, and RET/PTC mutation-specific gene expression profiles discovered by DNA microarray analysis. 16007166 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 PosttranslationalModification disease BEFREE Alterations of the BRAF gene in thyroid tumors. 16299399 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease LHGDN BRAF mutation occurs later in thyroid tumor progression and is restricted mainly to PTC and anaplastic thyroid carcinoma. 15980887 2005
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.700 GeneticVariation disease BEFREE We isolated genomic DNA from primary thyroid tumors and paired lymph node metastases and performed direct sequencing of exon 15 of the BRAF gene mutation that carries the T1799A mutation. 15998781 2005