Mayana Zatz
Human Genome Sciences (United States)(US)Inserm(FR)Universidade de São Paulo(BR)Université Paris Cité(FR)Universidade Cidade de São Paulo(BR)Stem Cell Institute(PA)Faculdade de Medicina de Jundiaí(BR)Institut des Maladies Génétiques Imagine(FR)Medical University of Vienna(AT)Universidade São Francisco(BR)Rockefeller University(US)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Genetic Neurodegenerative Diseases, Neurogenetic and Muscular Disorders Research, Cardiomyopathy and Myosin Studies, Mosquito-borne diseases and control
Most-Cited Works
- → A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B(1998)681 cited
- → Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths(2021)617 cited
- → Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene(1996)422 cited
- → Multipotent Stem Cells from Umbilical Cord: Cord Is Richer than Blood!(2007)391 cited
- → Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin(2000)333 cited
- → Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice(2013)326 cited