Author

Alexei Stortchevoi

Broad InstituteORCID 0000-0001-9916-4344Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Approach:statistical model· 3 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1

Frequent Co-Authors

Ashok RagavendraniD· 3 shared Dadi GaoiD· 3 shared Michael E. TalkowskiiD· 3 shared Benjamin CurralliD· 2 shared Elisabetta MoriniiD· 2 shared Rachita YadaviD· 2 shared Ryan L. CollinsiD· 2 shared Serkan ErdiniD· 2 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Ashok RagavendranORCID

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3 papers

Recent·Most cited

GenomicsThe American Journal of Human GeneticsPeer-reviewedSep 23, 2022

Tissue and cell-type specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models

Derek J.C. Tai, Parisa Razaz, Serkan Erdin…·James F. Gusella

This study identifies molecular and functional changes in mouse and human models of 16p11.2 reciprocal genomic disorder, revealing context-specific disruptions in energy metabolism, RNA processing, and neuronal development.

38 citationstop 4%

mousehuman

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Developmental BiologyJournal of genetics and genomics/Journal of Genetics and GenomicsPeer-reviewedDec 9, 2021

Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage.

Elisabetta Morini, Dadi Gao, Emily M. Logan…·Susan Slaugenhaupt

This study investigates the role of ELP1 in neuronal development by analyzing transcriptomes of mouse embryos with varying ELP1 levels, finding that ELP1 regulates gene expression and neuronal development.

10 citations

mousebulk RNA-seq

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GenomicsCellPeer-reviewedJan 1, 2018

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

Tatsiana Aneichyk, William T. J. Hendriks, Rachita Yadav…·Michael E. Talkowski

This study identifies the causal mechanism of X-linked Dystonia-Parkinsonism (XDP) by integrating genome and transcriptome assembly, revealing a SVA insertion causing intron retention and TAF1 dysfunction.

230 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky