Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi populationShaoli Sarker, Mohammed Uddin, Mohammad Kawsar Ali et al.|Scientific Reports|2023Cited by 11
Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohortHosneara Akter, Mohammed Uddin, Atikur Rahaman et al.|Genetics in Medicine|2024Cited by 8
Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting regionRabeya Akter Mim, Anjana Soorajkumar, Noor Kosaji et al.|Brain and Behavior|2024Cited by 7
Genomic insights into Rett syndrome-like features in Bangladeshi participantsHosneara Akter, Mohammed Uddin, Muhammad Mizanur Rahman et al.|Genetics in Medicine Open|2025Cited by 2
Genetic landscape of primary ovarian insufficiency in Bangladeshi women through whole exome sequencingHasna Hena Pervin, Mohammed Uddin, Rabeya Akter Mim et al.|Clinica Chimica Acta|2025Cited by 0