Disease Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE Depression in multiple sclerosis: effect of brain derived neurotrophic factor Val66Met polymorphism and disease perception. 26756166 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE The Val(66)Met polymorphism has opposite effects on hippocampal circuitry underlying episodic memory in Multiple Sclerosis patients and healthy controls. 23593393 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE The val(66)met polymorphism alters the function of the BDNF protein, and has along with rs56164415 previously been reported to be associated with MS. We genotyped BDNF SNPs val(66)met and rs56164415 in 2149 Norwegian MS patients and 2747 healthy controls. 22341604 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE The effects of BDNF Val66Met polymorphism on brain function in controls and patients with multiple sclerosis: an imaging genetic study. 19874854 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE BDNF A196G and C270T gene polymorphisms and susceptibility to multiple sclerosis in the Polish population. Gender differences. 18061279 2008
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE To investigate the association of the rs6265 (Val66Met) single nucleotide polymorphism (SNP) of brain-derived neurotrophic factor (BDNF) with brain morphometry and functional status as measured by quantitative magnetic resonance imaging (MRI) and neurocognitive testing in multiple sclerosis (MS) patients. 17656372 2007
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
0.070 GeneticVariation BEFREE The BDNF-Val66Met polymorphism: implications for susceptibility to multiple sclerosis and severity of disease. 16046000 2005