Author

S.N. Deshpande

Post Graduate Institute of Medical Education and Research

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

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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bittianda Kuttapa ThelmaiD· 1 shared Jibin JohniD· 1 shared Prachi KukshaliD· 1 shared Ricardo HarripauliD· 1 shared Triptish Bhatia AiD· 1 shared Vishwajit Laxmikant NimgaonkariD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

6 top collaborators · 15 mutual co-author links

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1 shared paperGenetics

Bittianda Kuttapa ThelmaORCID

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1 paper

Recent·Most cited

Oligogenic rare variant contributions in schizophrenia and their convergence with genes harboring de novo mutations in schizophrenia, autism, and intellectual disability: Evidence from multiplex families

Jibin John, Prachi Kukshal, Triptish Bhatia A, Ricardo Harripaul, Vishwajit Laxmikant Nimgaonkar, S.N. Deshpande, Bittianda Kuttapa Thelma

The paper identifies inherited rare variants in schizophrenia families, showing enrichment in neurodevelopmental pathways and convergence with genes linked to de novo mutations in schizophrenia, autism, and intellectual disability.

bioRxiv · Nov 12, 2019 · PreprintGenetics