Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 GeneticVariation BEFREE Diffuse Tract Damage in CADASIL Is Correlated with Global Cognitive Impairment. 31484188

2019

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE We obtained 3.0T MRI and neuropsychological data on processing speed, the main cognitive deficit in CADASIL. 31524338

2019

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 GeneticVariation BEFREE The most common symptoms of CADASIL are small ischemic strokes and/or transient ischemic attacks and cognitive impairment, appearing in middle age, that may progress to frank vascular dementia. 29478611

2018

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE <b>Background:</b> It remains unclear whether the degree of white matter tract damage or cerebral hypoperfusion can better predict global cognitive impairment in CADASIL. 30692942

2018

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE We report an individual with MS and CADASIL presenting with cognitive decline at age 25. 29449082

2018

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE The finding suggests that a disturbed neurogenic process due to Notch3-dependent micromilieu changes might be one vascular-independent mechanism contributing to cognitive decline observed in CADASIL. 28345617

2017

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 GeneticVariation BEFREE We recently reported a patient with parkinsonism and cognitive impairment and with evidence of diffuse white matter changes on imaging, carrying a NOTCH3 nonsense mutation in exon 3 (c.307C>T), and suggested that such a hypomorphic NOTCH3 mutation was likely to be pathogenic. 26216120

2015

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 GeneticVariation BEFREE Cognitive decline is one of the clinical hallmarks of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a cerebrovascular disease caused by NOTCH3 mutations. 19139365

2009

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE CADASIL is a hereditary arteriopathy causing recurrent strokes and cognitive decline. 19372454

2009

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL. 17272761

2007

Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.400 Biomarker BEFREE CADASIL is an autosomal dominant arteriopathy characterised by diffuse white matter lesions and small subcortical infarcts on neuroimaging and a variable combination of recurrent cerebral ischaemic episodes, cognitive deficits, migraine with aura and psychiatric symptoms. 17690848

2007