Genomic insights into Rett syndrome-like features in Bangladeshi participants
This genetic study of clinically diagnosed Bangladeshi RTT participants identifies new genes involved in the etiology of RTT-like phenotypes and expands the phenotypic spectrum of known genes linked to neurodevelopmental disorders.
Authors
- AHM Nurun Nabi (ORCID: https://orcid.org/0000-0002-0504-6556)
- Nasna Nassir (ORCID: https://orcid.org/0000-0002-8883-9630)
- Bassam Jamalalail
- Mohammed J. Uddin (ORCID: https://orcid.org/0000-0001-6867-5803)
- Amirul Islam (ORCID: https://orcid.org/0000-0003-3897-3302)
- Binte Zehra
- Shaoli Sarker
- Marc Woodbury‐Smith (ORCID: https://orcid.org/0000-0002-0593-8917)
- Ankur Ganguly (ORCID: https://orcid.org/0000-0002-1893-6478)
- Tamannyat Binte Eshaque
- Hosneara Akter (ORCID: https://orcid.org/0000-0003-0777-5426)
- Nor’Aishah Hasan (ORCID: https://orcid.org/0000-0003-1945-1170)
- K. M. Furkan Uddin (ORCID: https://orcid.org/0000-0001-7322-1988)
- Rabeya Akter Mim
- Muhammad Mizanur Rahman (ORCID: https://orcid.org/0000-0002-9225-7617)
- Shah Hossain (ORCID: https://orcid.org/0000-0003-1989-9389)
- Atikur Rahaman (ORCID: https://orcid.org/0000-0003-1261-4520)
- Masuma Afrin Taniya
- Farjana Binta Omar
Institutions
- Bangladesh Medical University (BD)
- Queen's University (CA)
- University of Dhaka (BD)
- International Centre for Diarrhoeal Disease Research (BD)
- Bangladesh Shishu (Children) Hospital & Institute (BD)
- Genome Canada (CA)
- Mohammed Bin Rashid University of Medicine and Health Sciences (AE)
- Child Health Research Foundation (BD)
- Holy Family Red Crescent Medical College
- Newcastle University (GB)
- Dhaka Medical College and Hospital (BD)
Publication Details
- Journal
- Genetics in Medicine Open
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1016/j.gimo.2025.103438
- Citations
- 2
- Primary Topic
- Genetics and Neurodevelopmental Disorders
- Type
- article
- Field-Weighted Citation Impact
- 3.63
Funders
- Al Jalila Foundation