Author

Aniket Shetty

Johns Hopkins UniversityORCID 0000-0003-2353-9589Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 1 Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Bhooma ThiruvahindrapuramiD· 2 shared Dalila PintoiD· 2 shared Daniele MericoiD· 2 shared Elizabeth Bevilacqua· 2 shared Guiqing Cai· 2 shared Ingrid AgartziD· 2 shared Madeline Alexander· 2 shared Madhusudan GujraliD· 2 shared

Activity by Year

2016-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Bhooma ThiruvahindrapuramORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineCell GenomicsPeer-reviewedJul 6, 2023

Schizophrenia-associated somatic copy number variants from 12,834 cases reveal contribution to risk and recurrent, isoform-specific NRXN1 disruptions

Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese…·Brandon K. Wormley

This study identifies somatic copy number variants (sCNVs) in schizophrenia cases, revealing their contribution to risk and specific NRXN1 disruptions.

47 citationstop 2%

humanwhole-genome sequencing

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BioinformaticsbioRxivPreprintMar 2, 2017

Genome-wide association study of asthma in individuals of African ancestry reveals novel asthma susceptibility loci

Michelle Daya, Nicholas M. Rafaels, Sameer Chavan…·Maria Yazdanbakhsh

This study identifies novel asthma susceptibility loci in individuals of African ancestry through genome-wide association analysis and admixture mapping.

DOI 10.1101/112953

humanGWAS summary statistics

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GeneticsNature GeneticsPeer-reviewedNov 21, 2016

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

Christian Marshall, Daniel Howrigan, Daniele Merico…·Rita Ca

This study identifies eight genome-wide significant CNV loci associated with schizophrenia using a large cohort of 41,321 subjects.

DOI 10.1038/ng.3725

humanwhole-genome sequencing

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