Nushrat Jahan Dity

Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes

Muhammad M. Rahman, K. M. Furkan Uddin, Nesreen K. Al‐Jezawi et al. · Molecular Genetics & Genomic Medicine · 2019 · 17 citations · Full text

Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh

Hosneara Akter, Mohammad Shahnoor Hossain, Nushrat Jahan Dity et al. · npj Genomic Medicine · 2021 · 17 citations · Full text

Novel mutations in actionable breast cancer genes by targeted sequencing in an ethnically homogenous cohort

Hosneara Akter, Nasima Sultana, Nazrana Martuza et al. · BMC Medical Genetics · 2019 · 15 citations · Full text

Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

Hosneara Akter, Muhammad Mizanur Rahman, Shaoli Sarker et al. · Frontiers in Genetics · 2023 · 15 citations · Full text

An <i> <scp>ANKRD</scp> 26 </i> nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

K. M. Furkan Uddin, Md Robed Amin, Sabbiha Nadia Majumder et al. · Clinical Case Reports · 2018 · 14 citations · Full text