Author

J. Velilla

Brigham and Women's HospitalORCID 0000-0002-1282-4467Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:bacteria (other)· 1 Organism:human· 1 Assay:protein structure· 1 Research Focus:protein structure prediction· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Rachelle GaudetiD· 2 shared Ágnes Tóth-PetróczyiD· 1 shared Alexis H. BennettiD· 1 shared Basil T. DarrasiD· 1 shared Brigham Genomic Medicine· 1 shared Claire A GrosgogeatiD· 1 shared David Z RudneriD· 1 shared Elicia A. EstrellaiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersMicrobiology

Rachelle GaudetORCID

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2 papers

Recent·Most cited

MicrobiologybioRxivPreprintNov 2, 2026

Structure of Bacillus cereus ZmaM, a peptidase-ABC transporter that secretes and activates zwittermicin A

Gerardo E Zavala, José A Velilla, Richard M Walsh…·Rachelle Gaudet

The paper structures ZmaM, a type II peptidase-ABC transporter in B. cereus, showing it activates and exports zwittermicin A by coordinating peptidase and transporter modules.

DOI 10.64898/2026.10.31.763113

bacteria (other)protein structure

𝕏 PostBluesky

GeneticsNeurology GeneticsPeer-reviewedMar 7, 2019

Homozygous TRPV4 mutation causes congenital distal spinal muscular atrophy and arthrogryposis

J. Velilla, Michael Mario Marchetti, Ágnes Tóth-Petróczy…·Vandana Gupta

This study identifies a homozygous TRPV4 mutation as a cause of congenital spinal muscular atrophy and arthrogryposis through whole exome sequencing and functional analysis.

25 citations

humanwhole-exome sequencing

𝕏 PostBluesky