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Mohammed Uddin

Researcher Next ID · RN-019441

Researcher · Biochemistry, Genetics and Molecular Biology

University of California, Riverside

Riverside, United Arab Emirates

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Not currently recruitingFunding unknown
Works count
197
Citation count
13,418
H-index
44
i10-index
82

Research interests

Biochemistry, Genetics and Molecular Biology
Neuroscience
Medicine
Genomic variations and chromosomal abnormalities
Genetics and Neurodevelopmental Disorders
Autism Spectrum Disorder Research
Genomics and Rare Diseases
SARS-CoV-2 and COVID-19 Research

Publications

  • Studying severe long COVID to understand post-infectious disorders beyond COVID-19

    Nature Medicine · 2022 · https://doi.org/10.1038/s41591-022-01766-7

  • SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions

    Viruses · 2020 · 10.3390/v12050526

  • Artificial intelligence for precision medicine in neurodevelopmental disorders

    npj Digital Medicine · 2019 · 10.1038/s41746-019-0191-0

  • OTUD7A Regulates Neurodevelopmental Phenotypes in the 15q13.3 Microdeletion Syndrome

    The American Journal of Human Genetics · 2018 · 10.1016/j.ajhg.2018.01.006

  • Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder

    Nature Neuroscience · 2017 · 10.1038/nn.4598

  • Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

    Nature Neuroscience · 2017 · https://doi.org/10.1038/nn.4524

  • Genome-wide characteristics of de novo mutations in autism

    npj Genomic Medicine · 2016 · 10.1038/npjgenmed.2016.27

  • Whole-genome sequencing of quartet families with autism spectrum disorder

    Nature Medicine · 2015 · 10.1038/nm.3792

  • Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

    JAMA · 2015 · 10.1001/jama.2015.10078

  • Sonic hedgehog (Shh) signaling promotes tumorigenicity and stemness via activation of epithelial-to-mesenchymal transition (EMT) in bladder cancer

    Molecular Carcinogenesis · 2015 · 10.1002/mc.22300

  • Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder

    Nature Genetics · 2014 · 10.1038/ng.2980

  • Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

    The American Journal of Human Genetics · 2013 · 10.1016/j.ajhg.2013.06.012

  • Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

    Human Molecular Genetics · 2013 · 10.1093/hmg/ddt669

Current projects

    No projects listed.