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  1. 1
    Artificial intelligence for precision medicine in neurodevelopmental disorders

    Artificial intelligence for precision medicine in neurodevelopmental disorders por Mohammed Uddin, Yujiang Wang, Marc Woodbury‐Smith

    Publicado em 2019
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  2. 2
    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES

    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES por Mohammed Uddin Rasheed, Nooruddin Thajuddin, Parveez Ahamed, Zelalem Teklemariam, Kaiser Jamil

    Publicado em 2014
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  3. 3
    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES

    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES por Rasheed, Mohammed Uddin, Thajuddin, Nooruddin, Ahamed, Parveez, Teklemariam, Zelalem, Jamil, Kaiser

    Publicado em 2014
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  4. 4
    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES

    ANTIMICROBIAL DRUG RESISTANCE IN STRAINS OF Escherichia coli ISOLATED FROM FOOD SOURCES por Rasheed, Mohammed Uddin, Thajuddin, Nooruddin, Ahamed, Parveez, Teklemariam, Zelalem, Jamil, Kaiser

    Publicado em 2014
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  5. 5
    SARS-CoV-2 may hijack GPCR signaling pathways to dysregulate lung ion and fluid transport

    SARS-CoV-2 may hijack GPCR signaling pathways to dysregulate lung ion and fluid transport por Reem Abdel Hameid, Estelle Cormet‐Boyaka, Wolfgang M. Kuebler, Mohammed Uddin, Bakhrom K. Berdiev

    Publicado em 2021
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  6. 6
    Genetic contributions to autism spectrum disorder

    Genetic contributions to autism spectrum disorder por Alexandra Havdahl, Maria Niarchou, Anna Starnawska, Mohammed Uddin, Celia van der Merwe, Varun Warrier

    Publicado em 2021
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  7. 7
    Evolutionary constrained genes associated with autism spectrum disorder across 2,054 nonhuman primate genomes

    Evolutionary constrained genes associated with autism spectrum disorder across 2,054 nonhuman primate genomes por Yukiko Kikuchi, Mohammed Uddin, Joris A. Veltman, Sara Wells, Christopher Morris, Marc Woodbury‐Smith

    Publicado em 2025
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  8. 8
    SNCA and TPPP transcripts increase in oligodendroglial cytoplasmic inclusions in multiple system atrophy

    SNCA and TPPP transcripts increase in oligodendroglial cytoplasmic inclusions in multiple system atrophy por Tomoya Kon, Shelley L. Forrest, Seojin Lee, Jun Li, Helen Chasiotis, Nasna Nassir, Mohammed Uddin, Anthony E. Lang, Gábor G. Kovács

    Publicado em 2024
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  9. 9
    Tissue engineering the retinal ganglion cell nerve fiber layer

    Tissue engineering the retinal ganglion cell nerve fiber layer por Karl E. Kador, Ramon B. Montero, Praseeda Venugopalan, Jonathan Hertz, Allison N. Zindell, Daniel A. Valenzuela, Mohammed Uddin, Erin Lavik, Kenneth J. Muller, Fotios M. Andreopoulos, Jeffrey L. Goldberg

    Publicado em 2013
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  10. 10
    Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes

    Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes por Ruchi Jain, Sathishkumar Ramaswamy, Divinlal Harilal, Mohammed Uddin, Tom Loney, Norbert Nowotny, Hanan Al Suwaidi, Rupa Varghese, Zulfa Deesi, Abdulmajeed Alkhajeh, Hamda Khansaheb, Alawi Alsheikh‐Ali, Ahmad Abou Tayoun

    Publicado em 2020
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  11. 11
    Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy

    Cell-specific MAPT gene expression is preserved in neuronal and glial tau cytopathologies in progressive supranuclear palsy por Shelley L. Forrest, Seojin Lee, Nasna Nassir, Iván Martínez-Valbuena, Valerie Sackmann, Jun Li, Awab Ahmed, Maria Carmela Tartaglia, Lars M. Ittner, Anthony E. Lang, Mohammed Uddin, Gábor G. Kovács

    Publicado em 2023
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  12. 12
    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes

    Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes por Marc Woodbury‐Smith, Rob Nicolson, Mehdi Zarrei, Ryan K. C. Yuen, Susan Walker, Jennifer Howe, Mohammed Uddin, Ny Hoang, Janet A. Buchanan, Christina Chrysler, Ann Thompson, Peter Szatmari, Stephen W. Scherer

    Publicado em 2017
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  13. 13
    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly

    Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly por Marc Woodbury‐Smith, Éric Deneault, Ryan K. C. Yuen, Susan Walker, Mehdi Zarrei, Giovanna Pellecchia, Jennifer Howe, Ny Hoang, Mohammed Uddin, Christian R. Marshall, Christina Chrysler, Ann Thompson, Péter Szatmári, Stephen W. Scherer

    Publicado em 2017
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  14. 14
    The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traits

    The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traits por Rosie Watts, Tanith Archibald, Pippa Hembry, Maxine Howard, Cate Kelly, Rachel Loomes, Laura Markham, Harry Moss, Alfonce Munuve, Anca Oros, Amy Siddall, Charlotte Rhind, Mohammed Uddin, Zain Ahmad, Rachel Bryant‐Waugh, Christopher Hübel

    Publicado em 2023
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  15. 15
    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions

    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions por Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmad Al Marzouqi, Afaf Kamal Eldin, Nabeel H. M. Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh‐Ali, Abiola Senok

    Publicado em 2020
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  16. 16
    Copy number variation in Han Chinese individuals with autism spectrum disorder

    Copy number variation in Han Chinese individuals with autism spectrum disorder por Matthew J. Gazzellone, Xue Zhou, Anath C. Lionel, Mohammed Uddin, Bhooma Thiruvahindrapuram, Shuang Liang, Caihong Sun, Jia Wang, Mingyang Zou, Kristiina Tammimies, Susan Walker, Thanuja Selvanayagam, John Wei, Zhuozhi Wang, Lijie Wu, Stephen W. Scherer

    Publicado em 2014
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  17. 17
    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions

    SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions por Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmed H. Hassan Al-Marzouqi, Afaf Kamal Eldin, Nabeel H. M. Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh‐Ali, Abiola Senok

    Publicado em 2020
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  18. 18
    Overexpression of sonic hedgehog in the triple negative breast cancer: clinicopathological characteristics of high burden breast cancer patients from Bangladesh

    Overexpression of sonic hedgehog in the triple negative breast cancer: clinicopathological characteristics of high burden breast cancer patients from Bangladesh por Abu Shadat Mohammod Noman, Mohammed Uddin, Md. Zillur Rahman, Mohammad Nayeem, Sharmin Alam, Zehedina Khatun, Md Wahiduzzaman, Afrin Sultana, Md Lutfur Rahman, M. Y. Ali, Dipta Barua, Imtiaz Ahmed, M. S. Islam, Abdelilah Aboussekhra, Herman Yeger, Walid A. Farhat, Syed S. Islam

    Publicado em 2016
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  19. 19
    Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases

    Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases por Shruti Sinha, Fatma Rabea, Sathishkumar Ramaswamy, Ikram Chekroun, Maha El Naofal, Ruchi Jain, Roudha Alfalasi, Nour Halabi, Sawsan Yaslam, Massomeh Sheikh Hassani, Shruti Shenbagam, Alan Taylor, Mohammed Uddin, Mohamed A. Almarri, Stefan S. du Plessis, Alawi Alsheikh‐Ali, Ahmad Abou Tayoun

    Publicado em 2025
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  20. 20
    Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation

    Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation por Matthew J. Gazzellone, Mehdi Zarrei, Christie L. Burton, Susan Walker, Mohammed Uddin, S.‐M. Shaheen, Julie Coste, Rageen Rajendram, Reva Schachter, Marlena Colasanto, Gregory L. Hanna, David R. Rosenberg, Noam Soreni, Kate D. Fitzgerald, Christian R. Marshall, Janet A. Buchanan, Daniele Merico, Paul Arnold, Stephen W. Scherer

    Publicado em 2016
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