Effectiveness of an integrated approach to reduce perinatal mortality: recent experiences from Matlab, Bangladesh by Rahman, Anisur, Moran, Allisyn, Pervin, Jesmin, Rahman, Aminur, Rahman, Monjur, Yeasmin, Sharifa, Begum, Hosneara, Rashid, Harunor, Yunus, Mohammad, Hruschka, Daniel, Arifeen, Shams E, Streatfield, Peter K, Sibley, Lynn, Bhuiya, Abbas, Koblinsky, Marge

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A Child with Pyopericardium by Hassan, Tariq, Rahim, Mahibur, Nahar, Nazmun, Mollah, Abid Hossain, Begum, Hosneara

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Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome by Begum, Ghausia, Albanna, Ammar, Bankapur, Asma, Nassir, Nasna, Tambi, Richa, Berdiev, Bakhrom K, Akter, Hosneara, Karuvantevida, Noushad, Kellam, Barbara, Alhashmi, Deena, Sung, Wilson W L, Thiruvahindrapuram, Bhooma, Alsheikh-Ali, Alawi, Scherer, Stephen W, Uddin, Mohammed

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Whole exome sequencing uncovered highly penetrant recessive mutations for a spectrum of rare genetic pediatric diseases in Bangladesh by Akter, Hosneara, Hossain, Mohammad Shahnoor, Dity, Nushrat Jahan, Rahaman, Md. Atikur, Furkan Uddin, K. M., Nassir, Nasna, Begum, Ghausia, Hameid, Reem Abdel, Islam, Muhammad Sougatul, Tusty, Tahrima Arman, Basiruzzaman, Mohammad, Sarkar, Shaoli, Islam, Mazharul, Jahan, Sharmin, Lim, Elaine T., Woodbury-Smith, Marc, Stavropoulos, Dimitri James, O’Rielly, Darren D., Berdeiv, Bakhrom K., Nurun Nabi, A. H. M., Ahsan, Mohammed Nazmul, Scherer, Stephen W., Uddin, Mohammed

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Single Cell Transcriptomic and Genomic Characterization of Brugada Syndrome Associated Genes by Tambi, Richa, Abdel Hameid, Reem, Bankapur, Asma, Nassir, Nasna, Begum, Ghausia, Zehra, Binte, Akter, Hosneara, Alsheikh‐Ali, Alawi, Uddin, Mohammed, Berdiev, Bakhrom

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SARS‐CoV‐2 May Hijack GPCR Signaling Pathways to Compromise Lung Ion and Fluid Transport by Abdel Hameid, Reem, Tambi, Richa, Nassir, Nasna, Begum, Ghausia, Zehra, Binte, Akter, Hosneara, Cormet‐Boyaka, Estelle, Kuebler, Wolfgang, Uddin, Mohammed, Berdiev, Bakhrom

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Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders by Akter, Hosneara, Rahman, Muhammad Mizanur, Sarker, Shaoli, Basiruzzaman, Mohammed, Islam, Md Mazharul, Rahaman, Md Atikur, Rahaman, Md Ashiquir, Eshaque, Tamannyat Binte, Dity, Nushrat Jahan, Sarker, Shouvik, Amin, Md Robed, Hossain, Mohammad Monir, Lopa, Maksuda, Jahan, Nargis, Hossain, Shafaat, Islam, Amirul, Mondol, Ashaduzzaman, Faruk, Md Omar, Saha, Narayan, Kundu, Gopen Kumar, Kanta, Shayla Imam, Kazal, Rezaul Karim, Fatema, Kanij, Rahman, Md Ashrafur, Hasan, Maruf, Hossain Mollah, Md Abid, Hosen, Md Ismail, Karuvantevida, Noushad, Begum, Ghausia, Zehra, Binte, Nassir, Nasna, Nabi, A H M Nurun, Uddin, K M Furkan, Uddin, Mohammed

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Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19 by Nassir, Nasna, Tambi, Richa, Bankapur, Asma, Al Heialy, Saba, Karuvantevida, Noushad, Khansaheb, Hamda Hassan, Zehra, Binte, Begum, Ghausia, Hameid, Reem Abdel, Ahmed, Awab, Deesi, Zulfa, Alkhajeh, Abdulmajeed, Uddin, K.M. Furkan, Akter, Hosneara, Safizadeh Shabestari, Seyed Ali, Almidani, Omar, Islam, Amirul, Gaudet, Mellissa, Kandasamy, Richard Kumaran, Loney, Tom, Tayoun, Ahmad Abou, Nowotny, Norbert, Woodbury-Smith, Marc, Rahman, Proton, Kuebler, Wolfgang M., Yaseen Hachim, Mahmood, Casanova, Jean-Laurent, Berdiev, Bakhrom K., Alsheikh-Ali, Alawi, Uddin, Mohammed

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Mutational Landscape of Autism Spectrum Disorder Brain Tissue by Woodbury-Smith, Marc, Lamoureux, Sylvia, Begum, Ghausia, Nassir, Nasna, Akter, Hosneara, O'Rielly, Darren D, Rahman, Proton, Wintle, Richard F, Scherer, Stephen W, Uddin, Mohammed

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Analyzing single cell transcriptome data from severe COVID-19 patients by Nassir, Nasna, Tambi, Richa, Bankapur, Asma, Karuvantevida, Noushad, Khansaheb, Hamdah Hassan, Zehra, Binte, Begum, Ghausia, Hameid, Reem Abdel, Ahmed, Awab, Deesi, Zulfa, Alkhajeh, Abdulmajeed, Uddin, K.M.Furkan, Akter, Hosneara, Safizadeh Shabestari, Seyed Ali, Gaudet, Mellissa, Hachim, Mahmood Yaseen, Alsheikh-Ali, Alawi, Berdiev, Bakhrom K., Al Heialy, Saba, Uddin, Mohammed

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Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes by Rahman, Muhammad M., Uddin, KM Furkan, Al Jezawi, Nesreen K., Karuvantevida, Noushad, Akter, Hosneara, Dity, Nushrat J., Rahaman, Md. Ashiquir, Begum, Maksuda, Rahaman, Md. Atikur, Baqui, Md. Abdul, Salwa, Zeena, Islam, Serajul, Woodbury‐Smith, Marc, Basiruzzaman, Mohammed, Uddin, Mohammed

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