Author

N. Raja

National Institutes of Health

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 Cell Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:differential expression· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Amy E. RobertsiD· 2 shared Beth A. KozeliD· 2 shared Carolyn Β. MervisiD· 2 shared D. Liu· 2 shared Elisa BiaminoiD· 2 shared Gabriella Maria SqueoiD· 2 shared Giuseppe MerlaiD· 2 shared J. A. Freeman· 2 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Amy E. RobertsORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotyping

D. Liu, Carolyn Β. Mervis, Mark David Levin, Elisa Biamino, Maria Francesca Bedeschi, Maria Cristina Digilio, Gabriella Maria Squeo, Roberta Villa, Sharon Osgood, J. A. Freeman, N. Raja, Giuseppe Merla, Amy E. Roberts, Colleen A. Morris, Lucy R. Osborne, Beth A. Kozel

The paper develops polygenic risk scores for surgical supravalvar aortic stenosis using variants from Williams syndrome patients, achieving high AUC and low misclassification rates.

medRxiv · Sep 17, 2024 · PreprintGenetic & Genomic Medicine

Pathway analysis identifies novel non-synonymous variants contributing to extreme vascular outcomes in Williams-Beuren syndrome

D. Liu, Charles John Billington, N. Raja, Zoë C. Wong, Mark David Levin, Wolfgang Resch, Camille Alba, Daniel N. Hupalo, Elisa Biamino, Maria Francesca Bedeschi, Maria Cristina Digilio, Gabriella Maria Squeo, R. Villa, Phoebe C. R. Parrish, Russell H. Knutsen, , Beth A. Kozel

The paper identifies novel non-synonymous variants associated with extreme vascular outcomes in Williams-Beuren syndrome through whole-genome sequencing and pathway analysis.

medRxiv · Sep 21, 2022 · PreprintGenetic & Genomic Medicine

Exosomes isolated from two different cell lines using three different isolation techniques show variation in physical and molecular characteristics

M. Dash, N. RAJA, K. Palaniyandi, S. Ramalingam, S. Sahabudeen

This study compares three exosome isolation techniques from cancer cell lines, finding variations in yield, purity, and molecular characteristics.

bioRxiv · Jun 6, 2020Cell Biology