Author

Daniela D’Agostino

McGill UniversityORCID 0000-0003-1837-9357Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:imputation· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. James BarkovichiD· 1 shared Adam J. ShapiroiD· 1 shared Alban C. ZiegleriD· 1 shared Alejandro Mejía‐GarcíaiD· 1 shared Alex Diaz-PapkovichiD· 1 shared Alexandra AfenjariD· 1 shared Allan Micheil InnesiD· 1 shared Amy Sarah Kimball· 1 shared

Activity by Year

2020-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

A. James BarkovichORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintMar 13, 2025

Using the ancestral recombination graph to study the history of rare variants in founder populations

Alejandro Mejía‐García, Alex Diaz-Papkovich, Guillaume Sillon…·Simon Gravel

This paper uses ancestral recombination graphs to impute and trace rare variants in founder populations, showing high accuracy in mutation age and regional frequency estimation.

6 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsNeuronPeer-reviewedMar 4, 2020

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang…·Elliott H. Sherr

This study identifies DDX3X mutations as causing neurodevelopmental disorders by disrupting RNA metabolism and neurogenesis during fetal cortical development.

213 citationstop 1%

humanmouse

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