about
Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 functionGenome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanicsEvidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity.Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer's disease data set.Identical twins with the C9orf72 repeat expansion are discordant for ALSMutation analysis of patients with neurodegenerative disorders using NeuroX arrayCoding mutations in SORL1 and Alzheimer diseaseInbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer diseaseRare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci.Novel GRN Mutations in Patients with Corticobasal SyndromeRole of p73 in Alzheimer disease: lack of association in mouse models or in human cohortsIndependent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.Investigation of c9orf72 in 4 neurodegenerative disorders.Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion.Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly.A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.Mutation analysis of CHCHD10 in different neurodegenerative diseasesSegmental duplications in genome-wide significant loci and housekeeping genes; warning for GAPDH and ACTB.Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism.Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations.Genetic Variations in ABCA7 Can Increase Secreted Levels of Amyloid-β40 and Amyloid-β42 Peptides and ABCA7 Transcription in Cell Culture Models.MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis.Fcγ Receptor Polymorphisms Do Not Predict Response to Intravenous Immunoglobulin in Myasthenia Gravis
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description
hulumtues
@sq
researcher
@en
ricercatore
@it
wetenschapper
@nl
հետազոտող
@hy
name
Mahdi Ghani
@ast
Mahdi Ghani
@en
Mahdi Ghani
@es
Mahdi Ghani
@nl
Mahdi Ghani
@sl
type
label
Mahdi Ghani
@ast
Mahdi Ghani
@en
Mahdi Ghani
@es
Mahdi Ghani
@nl
Mahdi Ghani
@sl
prefLabel
Mahdi Ghani
@ast
Mahdi Ghani
@en
Mahdi Ghani
@es
Mahdi Ghani
@nl
Mahdi Ghani
@sl
P106
P1153
55314299200
P21
P214
373155042706472401209
P31
P496
0000-0001-6455-7199
P569
2000-01-01T00:00:00Z
P735
P7859
viaf-373155042706472401209