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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureHippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's diseaseHERVs expression in Autism Spectrum DisordersSubcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortiumThe ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic dataGenetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophreniaIdentifying gene regulatory networks in schizophreniaGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisA two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisHuntington's disease cerebrospinal fluid seeds aggregation of mutant huntingtin.The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approachAHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaSupport for EKN1 as the susceptibility locus for dyslexia on 15q21The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkersEnabling collaborative research using the Biomedical Informatics Research Network (BIRN)Applications of the pipeline environment for visual informatics and genomics computationsGenome-wide meta-analyses identify three loci associated with primary biliary cirrhosisA genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.Epigenetic reprogramming of cortical neurons through alteration of dopaminergic circuits.MYO1E mutations and childhood familial focal segmental glomerulosclerosis.The perfect neuroimaging-genetics-computation storm: collision of petabytes of data, millions of hardware devices and thousands of software toolsSNPLims: a data management system for genome wide association studies.Lack of association between the T-->C 267 serotonin 5-HT6 receptor gene (HTR6) polymorphism and prediction of response to clozapine in schizophrenia.PP2A-Bgamma subunit and KCNQ2 K+ channels in bipolar disorder.A tumor suppressor locus in familial and sporadic chordoma maps to 1p36.Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene.Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleApplication of pharmacogenetics to psychotic disorders: the first consensus conference. The Consensus Group for Outcome Measures in Psychoses for Pharmacological Studies.alpha- and beta-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy.Pharmacogenetics of antipsychotic treatment: lessons learned from clozapine.No interaction of GABA(A) alpha-1 subunit and dopamine receptor D4 exon 3 genes in symptomatology of major psychoses.SNP-based pathway enrichment analysis for genome-wide association studiesAssociation between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort.Association of the type 2 diabetes mellitus susceptibility gene, TCF7L2, with schizophrenia in an Arab-Israeli family sampleAn unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: a common expansion locus.Reelin gene alleles and susceptibility to autism spectrum disorders.Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse.Social adjustment and self-esteem of bipolar patients: a multicentric study.Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.
P50
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P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Fabio Macciardi
@ast
Fabio Macciardi
@en
Fabio Macciardi
@es
Fabio Macciardi
@fr
Fabio Macciardi
@nl
Fabio Macciardi
@sl
type
label
Fabio Macciardi
@ast
Fabio Macciardi
@en
Fabio Macciardi
@es
Fabio Macciardi
@fr
Fabio Macciardi
@nl
Fabio Macciardi
@sl
prefLabel
Fabio Macciardi
@ast
Fabio Macciardi
@en
Fabio Macciardi
@es
Fabio Macciardi
@fr
Fabio Macciardi
@nl
Fabio Macciardi
@sl
P1053
N-3768-2014
P106
P1153
24369852700
P21
P2456
P2798
P31
P3829
P496
0000-0003-0537-4266