Author

Humberto Nicolini

National Institute of Genomic MedicineORCID 0000-0003-2494-0067Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

James A. KnowlesiD· 2 shared Abby J. FyeriD· 1 shared Alexander W. CharneyiD· 1 shared Aline S. SampaioiD· 1 shared Ana Gabriela HounieiD· 1 shared Anders JuréusiD· 1 shared Andrew D. PatersoniD· 1 shared Ann E. PulveriD· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenomics

James A. KnowlesORCID

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2 papers

Recent·Most cited

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

GeneticsBiological PsychiatryPeer-reviewedDec 19, 2018

Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases

Alexander W. Charney, Eli A. Stahl, Elaine Green…·Pamela B. Sklar

The study finds that rare copy number variants (CNVs) contribute to bipolar disorder risk primarily in schizoaffective disorder bipolar type cases, with differences in CNV burden and schizophrenia polygenic risk scores between subtypes.

69 citationstop 4%

humanstatistical model

𝕏 PostBluesky