Author

Alessandro Gialluisi

Istituto Neurologico MediterraneoORCID 0000-0002-7388-4463Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:differential expression· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Clyde FrancksiD· 3 shared Bruce F. PenningtoniD· 2 shared John C. DeFries· 2 shared Richard K. OlsoniD· 2 shared Shelley D. Smith· 2 shared Simon E. FisheriD· 2 shared Andrew K. Adams· 1 shared Andrew P. MorrisiD· 1 shared

Activity by Year

2016-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 42 mutual co-author links

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3 shared papersGenetics

Clyde FrancksORCID

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3 papers

Recent·Most cited

GenomicsTranslational PsychiatryPeer-reviewedFeb 11, 2019

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia.

Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber…·Gerd Schulte‐Körne

The paper conducts a GWAS to identify genetic variants associated with a cognitive predictor of dyslexia, finding significant associations with variants near MIR924HG and NKAIN3.

105 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintNov 16, 2017

Multivariate genome-wide association study of rapid automatized naming and rapid alternating stimulus in Hispanic and African American youth.

Dongnhu T. Truong, Andrew K. Adams, Richard Boada…·Jeffrey R. Gruen

This paper identifies a genetic locus on chromosome 10q23.31 associated with RAN, RAS, and reading-related performance in Hispanic and African American youth.

4 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivJun 22, 2016

Finding functional disease-associated non-coding variation using next-generation sequencing

Paolo Devanna, Xiaowei Sylvia Chen, Joses Ho…·Sonja C Vernes

The paper identifies a non-coding variant in a microRNA binding site associated with language impairment using whole exome sequencing data from a cohort of children.

DOI 10.1038/mp.2017.30

humanwhole-exome sequencing

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