Author

Dhanya Vettiatil

Albert Einstein College of Medicine

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:differential expression· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Research Focus:cell type annotation· 1 Assay:DNA methylation· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Anjana SoorajkumariD· 2 shared Erika Pedrosa· 2 shared Herbert M. LachmaniD· 2 shared Janet L. CunninghamiD· 2 shared Jennifer FrankovichiD· 2 shared Peter J. van der SpekiD· 2 shared Alexandra QuezadaiD· 1 shared Allan Schornagel· 1 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 28 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Anjana SoorajkumarORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 30, 2026

Ultrarare Variants in Genes Involved in Intestinal Microbiota and Permeability Homeostasis in Youth with Developmental and Neuropsychiatric Deteriorations

Jennifer Frankovich, Robert Dubin, Chetna Natarajan…·Herbert M. Lachman

The paper identifies ultrarare genetic variants in intestinal homeostasis genes in youth with neuropsychiatric deteriorations and gastrointestinal symptoms, suggesting a potential link to disease pathogenesis.

DOI 10.64898/2026.05.29.26353976

humanDNA methylation

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Genetic & Genomic MedicineDevelopmental NeurosciencePeer-reviewedFeb 9, 2026

Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders

Dhanya Vettiatil, Anjana Soorajkumar, Robert A. Dubin…·Herbert M. Lachman

The paper identifies ultrarare variants in DNA damage repair and mitochondrial genes in pediatric neuropsychiatric syndromes and neurodevelopmental disorders, linking them to innate immune pathways and gut microbiome homeostasis.

1 citation

humanwhole-exome sequencing

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NeurosciencePROTEOMICSPeer-reviewedJun 9, 2025

Multi-omics identification of extracellular components of the fetal monkey and human neocortex.

Felipe Vilicich, Dhanya Vettiatil, Seth Kattapong‐Graber…·Simone Sidoli

The paper identifies extracellular components in the developing fetal neocortex of humans and non-human primates using multi-omics approaches.

DOI 10.1002/pmic.202400385

humannon-human primate

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