Author

Mst. Noorjahan Begum

International Centre for Diarrhoeal Disease ResearchORCID 0000-0001-7975-9383Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Evolutionary Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:whole-genome sequencing· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:mixed model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Fahmida ChowdhuryiD· 1 shared Firdausi QadriiD· 1 shared Kaiissar MannooriD· 1 shared Md Tarikul IslamiD· 1 shared Md. Shaheen Alam· 1 shared Mohammad JubairiD· 1 shared Muhammad TalhaiD· 1 shared Mustafizur RahmaniD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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Focal author (center)Selected co-authorORCID co-authorUnlinked name

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1 shared paperEvolutionary Biology

Fahmida ChowdhuryORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genomic Surveillance of Respiratory Syncytial Virus among Patients with Acute Respiratory Infection through Hospital-Based Influenza Surveillance Platforms in Bangladesh, August 2024-December 2025

Md. Shaheen Alam, Yeasir Karim, Mustafizur Rahman, Rubel Howlader, Tanzim Rahman, Muhammad Talha, Fahmida Chowdhury, Mohammad Jubair, Mst. Noorjahan Begum

This study conducts whole-genome sequencing of RSV in Bangladesh, characterizing genetic diversity and vaccine targets, and deposits genomes in GISAID.

bioRxiv · Jul 3, 2026 · PreprintEvolutionary Biology

Molecular Investigation of TSHR gene in Bangladeshi Congenital Hypothyroid patients

Mst. Noorjahan Begum, Rumana Mahtarin, Md Tarikul Islam, Sinthyia Ahmed, Tasnia Kawsar Konika, Kaiissar Mannoor, Sharif Akhteruzzaman, Firdausi Qadri

The paper identifies two TSHR gene mutations in congenital hypothyroid patients and evaluates their impact on drug binding and protein stability using computational methods.

PLoS ONE · Aug 10, 2023Peer-reviewedGenetics