about
Saami and Berbers--an unexpected mitochondrial DNA link.Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europeThe molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene poolY-chromosome and mtDNA polymorphisms in Iraq, a crossroad of the early human dispersal and of post-Neolithic migrationsFrom surnames to the history of Y chromosomes: the Sardinian population as a paradigmThe 49a,f haplotype 11 is a new marker of the EU19 lineage that traces migrations from northern regions of the Black Sea"GenotypeColour": colour visualisation of SNPs and CNVsNew copy number variations in schizophrenia.Mitochondrial DNA haplogroups do not play a role in the variable phenotypic presentation of the A3243G mutation.Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement.Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality ConsortiumCombined DOCK8 and CLEC7A mutations causing immunodeficiency in 3 brothers with diarrhea, eczema, and infections.Proteasome system dysregulation and treatment resistance mechanisms in major depressive disorder.De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay.The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis.Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathwaysRole of allelic variants of FK506-binding protein 51 (FKBP5) gene in the development of anxiety disorders.Study on GRIA2, GRIA3 and GRIA4 genes highlights a positive association between schizophrenia and GRIA3 in female patients.Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sample.Compound heterozygosity for a hemizygous rare missense variant (rs141999351) and a large CNV deletion affecting the FSTL5 gene in a patient with schizophrenia.Copy number variants in attention-deficit hyperactive disorderThe effect of childhood trauma on blood transcriptome expression in major depressive disorderAnalysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorderITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiencyMitochondrial DNA haplogroups and age at onset of schizophreniaA novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzymeAuthor Correction: A novel homozygous mutation in GAD1 gene described in a schizophrenic patient impairs activity and dimerization of GAD67 enzymeAssessment of haptoglobin alleles in autism spectrum disorders
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Chiara Magri
@ast
Chiara Magri
@en
Chiara Magri
@es
Chiara Magri
@nl
type
label
Chiara Magri
@ast
Chiara Magri
@en
Chiara Magri
@es
Chiara Magri
@nl
prefLabel
Chiara Magri
@ast
Chiara Magri
@en
Chiara Magri
@es
Chiara Magri
@nl
P106
P1153
6701337681
P21
P31
P496
0000-0001-9933-8666