Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 213
Gene Symbol: ALB
ALB
0.010 Biomarker disease BEFREE Increased cerebrospinal fluid albumin and immunoglobulin A fractions forecast cortical atrophy and longitudinal functional deterioration in relapsing-remitting multiple sclerosis. 29226779 2019
Entrez Id: 7439
Gene Symbol: BEST1
BEST1
0.010 Biomarker disease BEFREE In Duchenne and Becker muscular dystrophies (DMD, BMD) cortical atrophy is associated with minimal ventricular dilatation and WM abnormalities. 31105770 2019
Entrez Id: 1756
Gene Symbol: DMD
DMD
0.010 Biomarker disease BEFREE In Duchenne and Becker muscular dystrophies (DMD, BMD) cortical atrophy is associated with minimal ventricular dilatation and WM abnormalities. 31105770 2019
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
0.010 Biomarker disease BEFREE The rate of cortical atrophy was higher in the DMF group (-2.4%) compared to NAT (-2.1%, <i>p</i> < 0.05) group. 31417557 2019
Entrez Id: 345643
Gene Symbol: MCIDAS
MCIDAS
0.010 Biomarker disease BEFREE Regional THK-5351 uptake correlated more strongly with cortical atrophy in AD compared with MCI, thereby demonstrating a close relationship between the neuro-pathologic process and cortical atrophy. 31834916 2019
Entrez Id: 30849
Gene Symbol: PIK3R4
PIK3R4
0.010 GeneticVariation disease BEFREE Finally, we report that mutations in VPS15 are associated with cortical atrophy and epilepsy in humans. 29311744 2018
Entrez Id: 2266
Gene Symbol: FGG
FGG
0.010 GeneticVariation disease BEFREE Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report. 29769041 2018
Entrez Id: 443
Gene Symbol: ASPA
ASPA
0.010 Biomarker disease BEFREE Genetic suppression of N-acetyl-l-aspartate (NAA) synthesis, previously shown to block brain vacuolation in aspartoacylase-deficient mice, also prevents neuron loss and cerebral cortical atrophy in these mice. 28077719 2017
Entrez Id: 10563
Gene Symbol: CXCL13
CXCL13
0.010 AlteredExpression disease BEFREE BAFF Index and CXCL13 levels in the cerebrospinal fluid associate respectively with intrathecal IgG synthesis and cortical atrophy in multiple sclerosis at clinical onset. 28095856 2017
Entrez Id: 10673
Gene Symbol: TNFSF13B
TNFSF13B
0.010 AlteredExpression disease BEFREE BAFF Index and CXCL13 levels in the cerebrospinal fluid associate respectively with intrathecal IgG synthesis and cortical atrophy in multiple sclerosis at clinical onset. 28095856 2017
Entrez Id: 3485
Gene Symbol: IGFBP2
IGFBP2
0.010 GeneticVariation disease BEFREE We then test cAGE's association with serum insulin-like growth factor binding protein 2 (IGF-BP2), which has previously been associated with age-related cognitive changes in animals, and with cortical atrophy in older humans. 26043140 2015
Entrez Id: 5744
Gene Symbol: PTHLH
PTHLH
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 23336
Gene Symbol: SYNM
SYNM
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 2534
Gene Symbol: FYN
FYN
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 5354
Gene Symbol: PLP1
PLP1
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 25824
Gene Symbol: PRDX5
PRDX5
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 57026
Gene Symbol: PDXP
PDXP
0.010 GeneticVariation disease BEFREE MRI revealed a significantly smaller brain volume in PLP-SYN mice at 12 months, which further decreased at 18 months together with increased volume of ventricles and cortical atrophy. 24243499 2014
Entrez Id: 6908
Gene Symbol: TBP
TBP
0.010 Biomarker disease BEFREE The SCA17 clinical phenotype includes characteristics associated with cerebellar and cortical atrophy such as ataxia, dementia, epilepsy, chorea and parkinsonian features. 21710129 2011
Entrez Id: 6855
Gene Symbol: SYP
SYP
0.010 AlteredExpression disease BEFREE The FTLD up-regulation of synaptophysin is disease specific (P < 0.0001), and is not influenced by age (P = 0.787) or cortical atrophy (P = 0.248). 21073671 2011
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
0.010 Biomarker disease BEFREE An excess of senile plaques (beta-amyloid protein) and neurofibrillary tangles (tau protein), ventricular enlargement, and cortical atrophy characterizes it. 16246446 2005
Entrez Id: 627
Gene Symbol: BDNF
BDNF
0.020 GeneticVariation disease BEFREE We also observed an interaction effect on brain structure between the BDNF and APOE genotypes: cortical atrophy was associated with harboring the apoliprotein E (APOE) ε4 allele only in BDNF val/met subjects (both in HC and PD groups). 31202861 2019
Entrez Id: 23435
Gene Symbol: TARDBP
TARDBP
0.020 Biomarker disease BEFREE This short report clarifies the heterogeneity of structural magnetic resonance imaging (MRI) findings in seven demented patients due to pathologically accumulated TAR DNA-binding protein-43 (TDP-43) protein using visual analyses including visual rating scales (i.e., global cortical atrophy and medial temporal atrophy scales). 31520153 2019
Entrez Id: 627
Gene Symbol: BDNF
BDNF
0.020 AlteredExpression disease BEFREE We postulate that exercise will attenuate cortical atrophy and synaptic loss inherent to neurodegenerative disorders - many of which also exhibit aberrant down-regulation of BDNF. 30326283 2018
Entrez Id: 23435
Gene Symbol: TARDBP
TARDBP
0.020 Biomarker disease BEFREE The distribution of TDP-43 inclusions and microglial activation in right temporal language regions showed concordance with anatomic distribution of cortical atrophy and clinical presentation. 29305438 2018
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
0.030 Biomarker disease BEFREE Here, we aim to forecast longitudinal magnetic resonance imaging (MRI)-driven cortical atrophy and clinical disability from cerebrospinal fluid (CSF) markers. 29226779 2019