Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nushrat Jahan Dity"'
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:
Hosneara Akter, Mohammad Shahnoor Hossain, Nushrat Jahan Dity, Md. Atikur Rahaman, K. M. Furkan Uddin, Nasna Nassir, Ghausia Begum, Reem Abdel Hameid, Muhammad Sougatul Islam, Tahrima Arman Tusty, Mohammad Basiruzzaman, Shaoli Sarkar, Mazharul Islam, Sharmin Jahan, Elaine T. Lim, Marc Woodbury-Smith, Dimitri James Stavropoulos, Darren D. O’Rielly, Bakhrom K. Berdeiv, A. H. M. Nurun Nabi, Mohammed Nazmul Ahsan, Stephen W. Scherer, Mohammed Uddin
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
Abstract Collectively, rare genetic diseases affect a significant number of individuals worldwide. In this study, we have conducted whole-exome sequencing (WES) and identified underlying pathogenic or likely pathogenic variants in five children with
Externí odkaz:
https://doaj.org/article/be7577baefe0449d9e32b34e4247a672
Autor:
Hosneara Akter, Nasima Sultana, Nazrana Martuza, Aaysha Siddiqua, Nushrat Jahan Dity, Md. Atikur Rahaman, Bisan Samara, Ahmed Sayeed, Mohammed Basiruzzaman, Mohammad Mizanur Rahman, Md. Rashidul Hoq, Md. Robed Amin, Md. Abdul Baqui, Marc Woodbury-Smith, K. M. Furkan Uddin, Syed S. Islam, Rayhana Awwal, Bakhrom K. Berdiev, Mohammed Uddin
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
Abstract Background Genetic testing is becoming an essential tool for breast cancer (BC) diagnosis and treatment pathway, and particularly important for early detection and cancer prevention. The purpose of this study was to explore the diagnostic yi
Externí odkaz:
https://doaj.org/article/9bdce28b3b1c42458c72576dcbbb9633
Autor:
Mazharul Islam, Ghausia Begum, Tahrima Arman Tusty, Nushrat Jahan Dity, Shaoli Sarkar, Marc Woodbury-Smith, Hosneara Akter, Md. Atikur Rahaman, Mohammed Uddin, Bakhrom K. Berdeiv, Reem Abdel Hameid, Mohammad Basiruzzaman, K. M. Furkan Uddin, Sharmin Jahan, Darren D. O’Rielly, Elaine T. Lim, Mohammed Nazmul Ahsan, A.H.M. Nurun Nabi, Stephen W. Scherer, Mohammad Shahnoor Hossain, Dimitri J. Stavropoulos, Nasna Nassir, Muhammad Sougatul Islam
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-9 (2021)
NPJ Genomic Medicine
NPJ Genomic Medicine
Collectively, rare genetic diseases affect a significant number of individuals worldwide. In this study, we have conducted whole-exome sequencing (WES) and identified underlying pathogenic or likely pathogenic variants in five children with rare gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44258f66cfe98db8636f7f00ecdd6040
https://doaj.org/article/be7577baefe0449d9e32b34e4247a672
https://doaj.org/article/be7577baefe0449d9e32b34e4247a672
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:
Abdul Aleem, Mohammad Ali, Wahida Khanam, Robed Amin, Narsis Rahman, AB Ziauddin Hossain, K. M. Furkan Uddin, Suprovath Kumar Sarker, Nushrat Jahan Dity, Laila Anjuman Banu, Hosneara Akter, Nasima Sultana, Abdul Baqui
Publikováno v:
Bangladesh Journal of Medicine. 30:24-29
Introduction: Autism Spectrum Disorder (ASD) is a neurodevelopmental disorder. Due to long term impairment, high genetic component (heritability> 90%), lack of effective prevention and treatment, ASD has been prioritized for genetic studies. Studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f9878e383ecafaf6597f48a54493bb6
https://doi.org/10.3329/bjmed.v30i1.39919
https://doi.org/10.3329/bjmed.v30i1.39919
Autor:
M. D. Abdul Baqui, Atikur Rahaman, Robed Amin, Mohammed Uddin, Mohammad Abdul Aleem, Muhammad Mizanur Rahman, Nushrat Jahan Dity, Sabbiha Nadia Majumder, Stephen W. Scherer, K. M. Furkan Uddin, Marc Woodbury-Smith, Hosneara Akter
Publikováno v:
Clinical Case Reports
Key Clinical Message Epidermodysplasia verruciformis (EV) is an extremely rare hereditary skin disease characterized by an abnormal susceptibility to the human papilloma virus (HPV) with an increased risk of cutaneous malignancy. Here we report the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2100ba8241ef52da8bf24bc51213478
https://doi.org/10.1002/ccr3.1595
https://doi.org/10.1002/ccr3.1595
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
Autor:
Marc Woodbury-Smith, Hosneara Akter, Mohammed Basiruzzaman, Md. Abdul Baqui, Bisan Samara, Aaysha Siddiqua, Mohammed Uddin, Mohammad Mizanur Rahman, Nazrana Martuza, K. M. Furkan Uddin, Md. Atikur Rahaman, Bakhrom K Berdiev, Ahmed Sayeed, Nushrat Jahan Dity, Syed S. Islam, Nasima Sultana, Md. Robed Amin, Rayhana Awwal, Md. Rashidul Hoq
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
Background Genetic testing is becoming an essential tool for breast cancer (BC) diagnosis and treatment pathway, and particularly important for early detection and cancer prevention. The purpose of this study was to explore the diagnostic yield of ta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d23dd8d2b3d154c54dd0e321bde23dc
https://doi.org/10.1186/s12881-019-0881-0
https://doi.org/10.1186/s12881-019-0881-0