Author

Nihar Ranjan Mishra

All India Institute of Medical Sciences, KalyaniORCID 0000-0002-5280-4719Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biochemistry· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:protein folding & dynamics· 1 Assay:proteomics· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Kalyan GoswamiiD· 2 shared Aastha BaliyaniD· 1 shared Amit Kumar MandaliD· 1 shared Anbu Kayalvizhi C.· 1 shared Atanu Kumar DuttaiD· 1 shared Jayeeta Bhowmick· 1 shared Neha YadaviD· 1 shared Niladri Sekhar BhuniaiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersBiochemistry

Kalyan GoswamiORCID

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2 papers

Recent·Most cited

BiochemistrybioRxivPreprintJun 7, 2026

Structural insights into the inhibition of sickle hemoglobin polymerization by asymmetric hemoglobin tetramer HbFS (α2γβS)

Aastha Baliyan, Neha Yadav, Nihar Ranjan Mishra…·Amit Kumar Mandal

This study investigates how elevated fetal hemoglobin (HbF) inhibits sickle hemoglobin (HbS) polymerization using mass spectrometry techniques, revealing conformational changes in HbFS that reduce polymerization.

DOI 10.64898/2026.06.03.729826

humanproteomics

Genetic & Genomic MedicinemedRxivPreprintSep 13, 2022

Exome re-analysis driven by deep phenotyping increases diagnostic yield

Atanu Kumar Dutta, Niladri Sekhar Bhunia, Rohit Bhowmick…·Anbu Kayalvizhi C.

Re-analyzing negative exome sequencing data with deep phenotyping identifies pathogenic variants in two patients with suspected Mendelian diseases.

DOI 10.1101/2022.09.13.22279858

humanwhole-exome sequencing