Mohammad Shboul
Jordan University of Science and Technology(JO)
Publications by Year
Research Areas
Connective tissue disorders research, Genetic and Kidney Cyst Diseases, Genomic variations and chromosomal abnormalities, RNA Research and Splicing, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → Mutations in PYCR1 cause cutis laxa with progeroid features(2009)252 cited
- → TMEM237 Is Mutated in Individuals with a Joubert Syndrome Related Disorder and Expands the Role of the TMEM Family at the Ciliary Transition Zone(2011)199 cited
- → Genome-wide CRISPR-Cas9 Screen Identifies Leukemia-Specific Dependence on a Pre-mRNA Metabolic Pathway Regulated by DCPS(2018)142 cited
- → Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number(2014)100 cited
- → Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program(2015)98 cited
- → Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling(2010)94 cited
- → C5orf42 is the major gene responsible for OFD syndrome type VI(2013)89 cited
- → Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma(2012)86 cited
- → Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1(2012)83 cited
- → Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells(2017)83 cited