Author

Soumitra Barua

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· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Addie May I. Nesbitt· 1 shared Andrew E. TimmsiD· 1 shared Angela M. BardiD· 1 shared Avni SantaniiD· 1 shared Chelsea M. PaganiD· 1 shared David S. JardineiD· 1 shared Diego A. MartineziD· 1 shared Edwin A. MitchelliD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Addie May I. Nesbitt

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1 paper

Recent·Most cited

Known pathogenic gene variants and new candidates detected in Sudden Unexpected Infant Death using Whole Genome Sequencing

Angela M. Bard, Lindsay V. Clark, Erdal Coşgun, Kimberly A. Aldinger, Andrew E. Timms, Lely A. Quina, Juan Lavista Ferres, David S. Jardine, Elisabeth A. Haas, Tatiana M. Becker, Chelsea M. Pagan, Avni Santani, Diego A. Martinez, Soumitra Barua, Zakkary McNutt, , Jan‐Marino Ramirez

This study identifies known pathogenic variants and new candidates in SUID using WGS, highlighting genetic factors related to heart disease and redox metabolism.

American Journal of Medical Genetics Part A · Jun 19, 2024Peer-reviewedGenetic & Genomic Medicine