Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Md. Ashiquir Rahaman"'
Autor:
Hosneara Akter, Muhammad Mizanur Rahman, Shaoli Sarker, Mohammed Basiruzzaman, Md. Mazharul Islam, Md. Atikur Rahaman, Md. Ashiquir Rahaman, Tamannyat Binte Eshaque, Nushrat Jahan Dity, Shouvik Sarker, Md. Robed Amin, Mohammad Monir Hossain, Maksuda Lopa, Nargis Jahan, Shafaat Hossain, Amirul Islam, Ashaduzzaman Mondol, Md Omar Faruk, Narayan Saha, Gopen kumar Kundu, Shayla Imam Kanta, Rezaul Karim Kazal, Kanij Fatema, Md. Ashrafur Rahman, Maruf Hasan, Md. Abid Hossain Mollah, Md. Ismail Hosen, Noushad Karuvantevida, Ghausia Begum, Binte Zehra, Nasna Nassir, A. H. M. Nurun Nabi, K. M. Furkan Uddin, Mohammed Uddin
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Copy number variations (CNVs) play a critical role in the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://doaj.org/article/990779ba5a7e42dc992125e6354c08cc
Autor:
Muhammad M. Rahman, KM Furkan Uddin, Nesreen K. Al Jezawi, Noushad Karuvantevida, Hosneara Akter, Nushrat J. Dity, Md. Ashiquir Rahaman, Maksuda Begum, Md. Atikur Rahaman, Md. Abdul Baqui, Zeena Salwa, Serajul Islam, Marc Woodbury‐Smith, Mohammed Basiruzzaman, Mohammed Uddin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Intellectual disability (ID) is a complex condition that can impact multiple domains of development. The genetic contribution to ID’s etiology is significant, with more than 100 implicated genes and loci currently identified. Th
Externí odkaz:
https://doaj.org/article/6991731ee49c418aabb747b9a403609a
Publikováno v:
International Perspectives in Psychology. 10:172-179
Abstract. This study is a content analysis of women's experiences during the COVID-19 (coronavirus) pandemic in Bangladesh, using a unique data set from Bangladesh's only emotional support and suicide prevention helpline. Each call to the helpline ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93582b23e6ae25d6ebb222149ef860c6
https://doi.org/10.1027/2157-3891/a000018
https://doi.org/10.1027/2157-3891/a000018
Autor:
Manzoor Hussain, Md. Abdul Baqui, Shaoli Sarker, Maksuda Lopa, Nargis Jahan, Mohammad Ghaziuddin, Mohammed Uddin, Md. Omar Faruk, Costanza Colombi, Mohammad Mizanur Rahman, K. M. Furkan Uddin, Darren D. O’Rielly, Narayan Saha, Marc Woodbury-Smith, Mohammed Basiruzzaman, M. A. K. Azad Chowdhury, Ammar AlBanna, Mazharul Islam, Selina Parvin Keya, Md. Ashiquir Rahaman
Publikováno v:
Journal of Autism and Developmental Disorders. 51:2392-2401
This study explored the physical and clinical phenotype of Bangladeshi children with autism spectrum disorder (ASD). A totally of 283 children who were referred for screening and administered Module 1 of the Autism Diagnostic Observation Schedule (AD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c584f1e1cb9c89f3f06cc011a58070
https://doi.org/10.1007/s10803-020-04703-0
https://doi.org/10.1007/s10803-020-04703-0
Autor:
Muhammad Mizanur Rahman, Hosneara Akter, Md. Ashiquir Rahaman, Md. Abid Hossain Mollah, Nushrat Jahan Dity, A.H.M. Nurun Nabi, Ashaduzzaman Mondol, Md. Robed Amin, Mohammed Basiruzzaman, Ghausia Begum, Maruf Hasan, Rezaul Karim Kazal, Narayan Saha, Gopenkumar Kundu, Md. Atikur Rahaman, Md. Ismail Hosen, Zehra Binte Ashraf, Amirul Islam, Maksuda Lopa, Shayla Imam Kanta, Mazharul M. Islam, Nargis Jahan, Mohammed Uddin, Shaoli Sarker, Md. Ashrafur Rahman, Shouvik Sarker, Omar Faruk, Tamannyat Binte Eshaque, Shafaat Hossain, K. M. Furkan Uddin, Noushad Karuvantevida, Monir Hossain, Nasna Nassir, Kanij Fatema
Background: Copy number variations (CNVs) play a critical role into the pathogenesis of neurodevelopmental disorders (NDD) among children. In this study, we aim to identify clinically relevant CNVs, genes and their phenotypic characteristics in an et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe1434565d248ccaf955acafc2020fd2
https://doi.org/10.21203/rs.3.rs-948388/v1
https://doi.org/10.21203/rs.3.rs-948388/v1
Autor:
Serajul Islam, Nesreen K. Al Jezawi, Md. Atikur Rahaman, Mohammed Uddin, Zeena Salwa, Mohammed Basiruzzaman, Md. Ashiquir Rahaman, Nushrat Jahan Dity, Md. Abdul Baqui, Maksuda Begum, Muhammad Mizanur Rahman, Noushad Karuvantevida, Marc Woodbury-Smith, Hosneara Akter, K. M. Furkan Uddin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Intellectual disability (ID) is a complex condition that can impact multiple domains of development. The genetic contribution to ID’s etiology is significant, with more than 100 implicated genes and loci currently identified. The majorit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28aa791fa32aee654f1514fbca33b7e
https://doaj.org/article/6991731ee49c418aabb747b9a403609a
https://doaj.org/article/6991731ee49c418aabb747b9a403609a