Author

Shankar Rengasamy Venugopalan

Tufts UniversityORCID 0000-0001-7762-0572Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Aline Lourenço PetriniD· 2 shared Jeffrey Clark MurrayiD· 2 shared Ligiane Alves Machado‐PaulaiD· 2 shared Lina M. Moreno‐UribeiD· 2 shared Michael S. ChimentiiD· 2 shared Patrick John BrehenyiD· 2 shared Shareef M. DabdoubiD· 2 shared Waheed A. AwotoyeiD· 2 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Aline Lourenço PetrinORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicineHuman Molecular GeneticsPeer-reviewedJan 1, 2026

Genetic and Epigenetic Contributors to Cleft Laterality: Evidence from Monozygotic Mirror Twins and Replication Cohorts

Aline Lourenço Petrin, Waheed A. Awotoye, Christina Spencer…·Lina M. Moreno‐Uribe

This study identifies genetic and epigenetic factors contributing to cleft laterality using monozygotic twins and replication cohorts, finding methylation differences in ARID5B, ZFP57, and HOOK2 associated with cleft side and severity.

DOI 10.1093/hmg/ddag088

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintFeb 7, 2024

Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum

Aline Lourenço Petrin, Ligiane Alves Machado‐Paula, Ashley Hinkle…·Lina M. Moreno Uribe

The paper identifies rare mutations in SIX1, PDGFRA, and KDR/VEGFR2 associated with OAVS phenotypes through whole genome sequencing and statistical analysis of a family.

DOI 10.1101/2024.02.07.24301824

humanwhole-genome sequencing

𝕏 PostBluesky