Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5663
Gene Symbol: PSEN1
PSEN1
0.300 GermlineCausalMutation disease ORPHANET Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation. 11094121 2000
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.390 GeneticVariation disease BEFREE PGRN mutations at 17q21 may occur in apparently sporadic frontotemporal lobar dementia with ubiquitinated inclusions cases and in cases presenting with either primary progressive aphasia or the behavioral variant of frontotemporal dementia. 17522386 2007
Entrez Id: 788
Gene Symbol: SLC25A20
SLC25A20
0.010 GeneticVariation disease BEFREE Three of them carried the CACT deletion in exon 7 and their clinical diagnosis was behavioral variant Frontotemporal Dementia. 19683260 2009
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
0.390 GeneticVariation disease BEFREE The same mutation was recently described in a case of progressive non-fluent aphasia, but the prominent presenting feature in tau gene mutation cases is the behavioral variant of frontotemporal dementia, with typical symmetrical frontotemporal atrophy. 20598713 2010
Entrez Id: 54664
Gene Symbol: TMEM106B
TMEM106B
0.300 SusceptibilityMutation disease ORPHANET TMEM106B a novel risk factor for frontotemporal lobar degeneration. 21614538 2011
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
0.390 Biomarker disease BEFREE The asymptomatic MAPT subjects and subjects with bvFTD showed altered functional connectivity in the DMN, with reduced in-phase connectivity in lateral temporal lobes and medial prefrontal cortex, compared to controls. 21849646 2011
Entrez Id: 2521
Gene Symbol: FUS
FUS
0.020 GeneticVariation disease BEFREE We identified 2 novel heterozygous missense mutations in FUS: P106L (g.22508384C>T) in a patient with behavioral variant frontotemporal dementia (bvFTD) and Q179H in several members of a family with behavioral variant FTD. 21943958 2012
Entrez Id: 2521
Gene Symbol: FUS
FUS
0.020 Biomarker disease BEFREE This patient demonstrates the striking focality associated with FUS neuropathology in patients with bvFTD. 22060063 2012
Entrez Id: 25978
Gene Symbol: CHMP2B
CHMP2B
0.300 SusceptibilityMutation disease ORPHANET Frontotemporal dementia: implications for understanding Alzheimer disease. 22355793 2012
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.390 GeneticVariation disease BEFREE Herein, we describe the clinical, neuropathological, and genetic findings in a case of autosomal dominant behavioral variant of frontotemporal dementia (bvFTD) with asymmetrical parkinsonism and prominent visuospatial deficits that carries a novel GRN mutation. 22366770 2012
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 Biomarker disease BEFREE Here we show that the large Lund pedigree with behavioral variant of frontotemporal dementia previously described with this disorder has an expansion in the recently described C9ORF72 locus on chromosome 9. 22483864 2012
Entrez Id: 4137
Gene Symbol: MAPT
MAPT
0.390 GeneticVariation disease BEFREE Microtubule-associated protein tau gene mutations have been the first ones identified, and are generally associated with early onset (40-50 years) and with the bvFTD phenotype. 22532172 2012
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 GeneticVariation disease BEFREE Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations. 22571983 2012
Entrez Id: 348
Gene Symbol: APOE
APOE
0.020 GeneticVariation disease BEFREE Inside this region of 16.3 kb, LD (r2 = 0.14) between TOMM40 (rs157590) and APOE (rs429358) was observed in PPA, but not in bvFTD and in controls. 22710912 2012
Entrez Id: 341
Gene Symbol: APOC1
APOC1
0.010 GeneticVariation disease BEFREE LD (r2 = 0.35) between TOMM40 (rs2075650) and APOC1 (rs1064725) was observed in PPA, but not in controls and in bvFTD. 22710912 2012
Entrez Id: 10452
Gene Symbol: TOMM40
TOMM40
0.010 GeneticVariation disease BEFREE Inside this region of 16.3 kb, LD (r2 = 0.14) between TOMM40 (rs157590) and APOE (rs429358) was observed in PPA, but not in bvFTD and in controls. 22710912 2012
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 Biomarker disease BEFREE Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers. 22766732 2012
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 GeneticVariation disease BEFREE Behavioral variant frontotemporal dementia due to C9orf72 expansion displays some phenotypic heterogeneity and may be associated with hallucinations, parkinsonism, focal dystonia, and posterior brain atrophy. 22964910 2012
Entrez Id: 23435
Gene Symbol: TARDBP
TARDBP
0.040 GeneticVariation disease BEFREE The TDP-43 p.N267S substitution has been previously implicated in both amyotrophic lateral sclerosis and behavioral variant frontotemporal dementia. 23231971 2013
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 GeneticVariation disease BEFREE C9orf72 -associated FTLD most often presents with early-onset behavioral variant frontotemporal dementia with disinhibition as the prominent feature, with or without amyotrophic lateral sclerosis. 23338682 2013
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 SusceptibilityMutation disease ORPHANET Neuroimaging and biochemical markers in the three variants of primary progressive aphasia. 23392204 2013
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.390 SusceptibilityMutation disease ORPHANET Neuroimaging and biochemical markers in the three variants of primary progressive aphasia. 23392204 2013
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.390 GeneticVariation disease BEFREE The clinical presentation of the GRN A9D missense mutation is not restricted to behavioral variant frontotemporal dementia and may include aphasia, extrapyramidal features, and, notably, amyotrophic lateral sclerosis. 23596077 2013
Entrez Id: 203228
Gene Symbol: C9orf72
C9orf72
0.400 SusceptibilityMutation disease ORPHANET Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review. 23597030 2013
Entrez Id: 2896
Gene Symbol: GRN
GRN
0.390 SusceptibilityMutation disease ORPHANET Clinic, neuropathology and molecular genetics of frontotemporal dementia: a mini-review. 23597030 2013