Author

Valentina Ciullo

Fondazione Santa LuciaORCID 0000-0002-4095-7806Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Valentina Ciullo1 paper

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Lea Karatheodoris DavisiD· 2 shared Abby J. FyeriD· 1 shared Ahmad A. BeydouniD· 1 shared Alica M. GoldmaniD· 1 shared Aline S. SampaioiD· 1 shared Alison AndersoniD· 1 shared Ana Gabriela HounieiD· 1 shared Andrew D. PatersoniD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Lea Karatheodoris DavisORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineNature NeurosciencePeer-reviewedOct 1, 2024

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Epi25 Collaborative, Siwei Chen, Bassel W Abou-Khalil…·Alica M. Goldman

This study identifies shared and distinct ultra-rare genetic risk factors for epilepsy subtypes using whole-exome sequencing of 20,979 patients and 33,444 controls.

72 citationstop 1%

humanwhole-exome sequencing

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GenomicsTranslational PsychiatryPeer-reviewedFeb 2, 2021

Genome-wide Association Study of Pediatric Obsessive-Compulsive Traits: Shared Genetic Risk between Traits and Disorder

Christie L. Burton, Mathieu Lemire, Bowei Xiao…·Andrew D. Paterson

This study identifies a genome-wide significant variant for OC traits and shows shared genetic risk between OC traits and OCD.

50 citations

humanGWAS summary statistics

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