Gene | Score gda | Association Type | Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
0.200 | GeneticVariation | disease | BEFREE | Glucose metabolism in the brain in LMNB1-related autosomal dominant leukodystrophy. | 30192380 | 2019 | ||||
|
0.200 | Biomarker | disease | BEFREE | Lamin B1 mediated demyelination: Linking Lamins, Lipids and Leukodystrophies. | 27854160 | 2016 | ||||
|
0.200 | GeneticVariation | disease | BEFREE | LMNB1-related autosomal-dominant leukodystrophy: Clinical and radiological course. | 26053668 | 2015 | ||||
|
0.200 | AlteredExpression | disease | BEFREE | Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts. | 24858279 | 2014 | ||||
|
0.200 | Biomarker | disease | BEFREE | Lamin B1 mediates cell-autonomous neuropathology in a leukodystrophy mouse model. | 23676464 | 2013 | ||||
|
0.200 | Biomarker | disease | BEFREE | Prior to this report, such a phenotype had been speculated to represent an entity different from lamin B1-duplicated leukodystrophy. | 23681646 | 2013 | ||||
|
0.200 | GeneticVariation | disease | BEFREE | Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression. | 23649844 | 2013 | ||||
|
0.200 | GeneticVariation | disease | BEFREE | A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutations. | 19961535 | 2010 | ||||
|
0.200 | GeneticVariation | disease | BEFREE | Duplication in LMNB1 encoding lamin B1 causes autosomal dominant leukodystrophy and mutations in LMNB2 encoding lamin B2 are associated with acquired partial lipodystrophy. | 17467691 | 2007 | ||||
|
0.200 | GeneticVariation | disease | BEFREE | Lamin B1 duplications cause autosomal dominant leukodystrophy. | 16951681 | 2006 | ||||
|
0.200 | Biomarker | disease | HPO |