about
Investigating the effects of copy number variants on reading and language performance.H3M2: detection of runs of homozygosity from whole-exome sequencing data.Detection of runs of homozygosity from whole exome sequencing data: state of the art and perspectives for clinical, population and epidemiological studies.Genome-wide screening for DNA variants associated with reading and language traitsNext-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.Neuroimaging genetic analyses of novel candidate genes associated with reading and language.A genetic epidemiology study of Congenital Adrenal Hyperplasia in Italy.Estimating the allele frequency of autosomal recessive disorders through mutational records and consanguinity: the Homozygosity Index (HI).Hypnotizability and Catechol-O-Methyltransferase (COMT) polymorphysms in Italians.The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population.Persistence and transmission of recessive deafness and sign language: new insights from village sign languages.Reply to ten Kate et al.The homozygosity index (HI) approach reveals high allele frequency for Wilson disease in the Sardinian population.Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity.Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaZBTB12 DNA methylation is associated with coagulation- and inflammation-related blood cell parameters: findings from the Moli-family cohortRevisiting the link between platelets and depression through genetic epidemiology: new insights from platelet distribution widthMediterranean diet and mortality in the elderly: a prospective cohort study and a meta-analysisLifestyle and biological factors influence the relationship between mental health and low-grade inflammationMachine Learning Approaches for the Estimation of Biological Aging: The Road Ahead for Population StudiesWhole Exome Sequencing Study of Parkinson Disease and Related Endophenotypes in the Italian PopulationMultivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youthNew challenges from Covid-19 pandemic: an unexpected opportunity to enlighten the link between viral infections and brain disorders?
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description
hulumtues
@sq
onderzoeker
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researcher
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ricercatore
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հետազոտող
@hy
name
Alessandro Gialluisi
@ast
Alessandro Gialluisi
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Alessandro Gialluisi
@es
Alessandro Gialluisi
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type
label
Alessandro Gialluisi
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Alessandro Gialluisi
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Alessandro Gialluisi
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Alessandro Gialluisi
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prefLabel
Alessandro Gialluisi
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Alessandro Gialluisi
@en
Alessandro Gialluisi
@es
Alessandro Gialluisi
@nl
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P2798
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