Author

Carolina Cappi

Icahn School of Medicine at Mount SinaiORCID 0000-0001-6661-3756Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1 Genomics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 5 Research Focus:gene regulatory network inference· 2 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Assay:whole-exome sequencing· 2 Research Focus:variant calling· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Eurı́pedes Constantino MigueliD· 3 shared Gwyneth C. ZaiiD· 3 shared James L. KennedyiD· 3 shared Bernadette CulleniD· 2 shared Cristina BarlassinaiD· 2 shared Donald W. BlackiD· 2 shared Dongmei YuiD· 2 shared Edwin H. CookiD· 2 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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3 shared papersGenomics

Eurı́pedes Constantino MiguelORCID

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Author profile →

5 papers

Recent·Most cited

Genetic & Genomic MedicineResearch at the University of Copenhagen (University of Copenhagen)Peer-reviewedJan 1, 2025

Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder

Nora I Strom, Zachary F Gerring, Marco Galimberti…·Bjarne K. A. Hansen

This study identifies 30 genome-wide significant loci for obsessive-compulsive disorder (OCD) using a large GWAS, linking risk to specific brain cell types and shared genetic risk with other psychiatric and non-psychiatric traits.

9 citations

humanGWAS summary statistics

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintMay 19, 2023

Ultra-rare de novo damaging coding variants are enriched in attention-deficit/hyperactivity disorder and identify risk genes

Emily Olfson, Luís C. Farhat, Wenzhong Liu…·Thomas V. Fernandez

This paper identifies ultra-rare de novo damaging variants in ADHD cases and finds KDM5B as a high-confidence risk gene, along with enriched biological pathways.

2 citations

humanwhole-exome sequencing

𝕏 PostBluesky

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

𝕏 PostBluesky

NeuroscienceBMC PsychiatryPeer-reviewedJul 20, 2020

Cognitive performance in children and adolescents at high-risk for obsessive-compulsive disorder

Elisa Teixeira Bernardes, Leonardo Cardoso Saraiva, Marina de Marco e Souza…·Marcelo C. Batistuzzo

The paper investigates cognitive performance in children and adolescents at high-risk for OCD compared to healthy controls, finding impairments in processing speed and IQ discrepancy.

15 citations

humanstatistical model

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GeneticsbioRxivPreprintSep 21, 2017

De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autism

Carolina Cappi, Melody E. Oliphant, Zsanett Péter…·Thomas V. Fernandez

The paper identifies de novo damaging mutations in OCD and finds overlap with autism genes, suggesting shared genetic risk.

7 citations

humanwhole-exome sequencing

𝕏 PostBluesky