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Gasparini, Paolo
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Preferred name
Gasparini, Paolo
Main Affiliation
Email
paolo.gasparini@burlo.trieste.it
ORCID
Scopus Author ID
22634397400
Researcher ID
B-6173-2014
Research Output
Now showing 1 - 10 of 11
- PublicationSPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
; ; ; ; - PublicationGenetic dissection of temperament personality traits in Italian isolates
; ; ; - PublicationDietary Macronutrient Composition in Relation to Circulating HDL and Non-HDL Cholesterol
; ; - PublicationHearing function: Identification of new candidate genes further explaining the complexity of this sensory ability
; ; ; ; - PublicationNatural human knockouts and Mendelian disorders: deep phenotyping in Italian isolates
; ; ; ; ; ; - PublicationGenome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
; ; ; ; ; ; - PublicationRuns of homozygosity are associated with staging of periodontitis in isolated populations
; ; ; ; - PublicationSystematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique
; ; ; - PublicationTaste perception and expression in stomach of bitter taste receptor tas2r38 in obese and lean subjects
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