Author

Smriti Mishra

National Neurosciences CentreORCID 0000-0002-4793-050XUnclaimed ORCID profile · follow to get notified of new preprints

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:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:genome assembly· 1 Assay:GWAS summary statistics· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Arindam Biswas· 3 shared Atanu BiswasiD· 3 shared Dipanwita SadhukhaniD· 3 shared Subhra Prakash HuiiD· 3 shared Tapas Kumar BanerjeeiD· 3 shared Biman Kanti RayiD· 2 shared Gargi Podder· 2 shared Parama Mitra· 2 shared

Activity by Year

2023-2023 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Arindam Biswas

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3 papers

Recent·Most cited

Genetic Variations and Altered Blood mRNA Level of Circadian Genes and BDNF as Risk Factors of Post-Stroke Cognitive Impairment among Eastern Indians

Dipanwita Sadhukhan, Arindam Biswas, Smriti Mishra, Koustav Chatterjee, Daytee Maji, Parama Mitra, Priyanka Mukherjee, Gargi Podder, Biman Kanti Ray, Atanu Biswas, Tapas Kumar Banerjee, Subhra Prakash Hui, Ishani Deb

The paper identifies genetic variants and expression changes in circadian genes and BDNF associated with post-stroke cognitive impairment in Eastern Indians.

NeuroMolecular Medicine · Oct 9, 2023Peer-reviewedNeuroscience

Evaluation of Apolipoprotein e4 allele as susceptible factor for neurodegenerative diseases among Eastern Indians

Dipanwita Sadhukhan, Smriti Mishra, Priyanka Mukherjee, Atanu Biswas, Subhra Prakash Hui, Tapas Kumar Banerjee, Arindam Biswas

The paper evaluates the association of Apolipoprotein E4 allele with neurodegenerative diseases in Eastern Indians, finding significant links with disease subtypes, age at onset, and family history.

medRxiv · Jun 21, 2023 · PreprintGenetic & Genomic Medicine

Arg4810Lys Mutation in RNF213 among Eastern Indian Non-MMD Ischemic Stroke Patients: A Genotype-Phenotype Correlation

Dipanwita Sadhukhan, Parama Mitra, Smriti Mishra, Arunima Roy, Gargi Podder, Biman Kanti Ray, Atanu Biswas, Subhra Prakash Hui, Tapas Kumar Banerjee, Arindam Biswas

This study identifies the Arg4810Lys RNF213 variant in Eastern Indian non-MMD ischemic stroke patients, finding its association with family history, earlier onset, and recurrent stroke, but not cognitive decline.

medRxiv · May 30, 2023 · PreprintGenetic & Genomic Medicine