Genomic insights from a deeply phenotyped highly consanguineous neurodevelopmental disorders cohortHosneara Akter, Mohammed Uddin, Md. Adnan Morshed 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